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2025-05-09 16:59:01, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_030582 5910 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens collagen, type XVIII, alpha 1 (COL18A1), transcript
variant 1, mRNA.
ACCESSION NM_030582 NM_016214
VERSION NM_030582.3 GI:110611234
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 5910)
AUTHORS Li,M., Liu,F., Sun,P., Gao,Y., Chen,H., Liu,H., Wang,M., Chen,J.
and Zhao,Y.
TITLE Correlations between serum levels of vascular endothelial growth
factor and endostatin with clinical pathological characteristics of
patients with gastrointestinal cancers
JOURNAL Hepatogastroenterology 59 (118), 1865-1868 (2012)
PUBMED 22819906
REMARK GeneRIF: Report pre/postoperative endostatin levels in surgically
treated gastrointestinal cancers.
REFERENCE 2 (bases 1 to 5910)
AUTHORS Sunshine,S.B., Dallabrida,S.M., Durand,E., Ismail,N.S., Bazinet,L.,
Birsner,A.E., Sohn,R., Ikeda,S., Pu,W.T., Kulke,M.H.,
Javaherian,K., Zurakowski,D., Folkman,J.M. and Rupnick,M.
TITLE Endostatin lowers blood pressure via nitric oxide and prevents
hypertension associated with VEGF inhibition
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 109 (28), 11306-11311 (2012)
PUBMED 22733742
REMARK GeneRIF: Endostatin lowers blood pressure via nitric oxide and
prevents hypertension associated with VEGF inhibition
REFERENCE 3 (bases 1 to 5910)
AUTHORS Melville SA, Buros J, Parrado AR, Vardarajan B, Logue MW, Shen L,
Risacher SL, Kim S, Jun G, DeCarli C, Lunetta KL, Baldwin CT,
Saykin AJ and Farrer LA.
CONSRTM Alzheimer's Disease Neuroimaging Initiative
TITLE Multiple loci influencing hippocampal degeneration identified by
genome scan
JOURNAL Ann. Neurol. 72 (1), 65-75 (2012)
PUBMED 22745009
REFERENCE 4 (bases 1 to 5910)
AUTHORS Chen,Y., Liang,B., Zhao,Y.J., Wang,S.C., Fan,Y.B. and Wu,G.P.
TITLE Transcription expression and clinical significance of vascular
endothelial growth factor mRNA and endostatin mRNA in pleural
effusions of patients with lung cancer
JOURNAL Diagn. Cytopathol. 40 (4), 287-291 (2012)
PUBMED 22431315
REMARK GeneRIF: The detection of VEGF mRNA and endostatin mRNA appears to
be suitable for distinguishing carcinoma cells from reactive
mesothelial cells in pleural effusions, they could be useful to
diagnose the pleural micrometastasis.
REFERENCE 5 (bases 1 to 5910)
AUTHORS Wu,X., Wu,J., Xin,Z., Wang,H., Zhu,X., Pan,L., Li,Z., Li,H. and
Liu,Y.
TITLE A 3' UTR SNP in COL18A1 is associated with susceptibility to HBV
related hepatocellular carcinoma in Chinese: three independent
case-control studies
JOURNAL PLoS ONE 7 (3), E33855 (2012)
PUBMED 22461898
REMARK GeneRIF: Findings indicate that COL18A1 rs7499 may contribute to
the risk of Hepatocellular carcinoma (HCC) in Han Chinese.
REFERENCE 6 (bases 1 to 5910)
AUTHORS Ding,Y.H., Javaherian,K., Lo,K.M., Chopra,R., Boehm,T.,
Lanciotti,J., Harris,B.A., Li,Y., Shapiro,R., Hohenester,E.,
Timpl,R., Folkman,J. and Wiley,D.C.
TITLE Zinc-dependent dimers observed in crystals of human endostatin
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 95 (18), 10443-10448 (1998)
PUBMED 9724722
REFERENCE 7 (bases 1 to 5910)
AUTHORS Saarela,J., Ylikarppa,R., Rehn,M., Purmonen,S. and Pihlajaniemi,T.
TITLE Complete primary structure of two variant forms of human type XVIII
collagen and tissue-specific differences in the expression of the
corresponding transcripts
JOURNAL Matrix Biol. 16 (6), 319-328 (1998)
PUBMED 9503365
REFERENCE 8 (bases 1 to 5910)
AUTHORS Sertie,A.L., Quimby,M., Moreira,E.S., Murray,J., Zatz,M.,
Antonarakis,S.E. and Passos-Bueno,M.R.
TITLE A gene which causes severe ocular alterations and occipital
encephalocele (Knobloch syndrome) is mapped to 21q22.3
JOURNAL Hum. Mol. Genet. 5 (6), 843-847 (1996)
PUBMED 8776601
REFERENCE 9 (bases 1 to 5910)
AUTHORS Oh,S.P., Kamagata,Y., Muragaki,Y., Timmons,S., Ooshima,A. and
Olsen,B.R.
TITLE Isolation and sequencing of cDNAs for proteins with multiple
domains of Gly-Xaa-Yaa repeats identify a distinct family of
collagenous proteins
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 91 (10), 4229-4233 (1994)
PUBMED 8183893
REFERENCE 10 (bases 1 to 5910)
AUTHORS Oh,S.P., Warman,M.L., Seldin,M.F., Cheng,S.D., Knoll,J.H.,
Timmons,S. and Olsen,B.R.
TITLE Cloning of cDNA and genomic DNA encoding human type XVIII collagen
and localization of the alpha 1(XVIII) collagen gene to mouse
chromosome 10 and human chromosome 21
JOURNAL Genomics 19 (3), 494-499 (1994)
PUBMED 8188291
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BX322561.1, BC063833.1 and
AF018082.1.
This sequence is a reference standard in the RefSeqGene project.
On Jul 20, 2006 this sequence version replaced gi:18765744.
Summary: This gene encodes the alpha chain of type XVIII collagen.
This collagen is one of the multiplexins, extracellular matrix
proteins that contain multiple triple-helix domains (collagenous
domains) interrupted by non-collagenous domains. The
proteolytically produced C-terminal fragment of type XVIII collagen
is endostatin, a potent antiangiogenic protein. Mutations in this
gene are associated with Knobloch syndrome. The main features of
this syndrome involve retinal abnormalities, so type XVIII collagen
may play an important role in retinal structure and in neural tube
closure. Alternatively spliced transcript variants encoding
different isoforms have been found for this gene. [provided by
RefSeq, Sep 2008].
Transcript Variant: This variant (1) is generated from an alternate
promoter. It lacks an in-frame segment in the 5' exon, as compared
to variant 3. The resulting isoform (1) lacks an internal segment
in the N-terminus, as compared to isoform 3.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AF018081.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025083 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-667 BX322561.1 14592-15258
668-3998 BC063833.1 142-3472
3999-5910 AF018082.1 3497-5408
FEATURES Location/Qualifiers
source 1..5910
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="21"
/map="21q22.3"
gene 1..5910
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/note="collagen, type XVIII, alpha 1"
/db_xref="GeneID:80781"
/db_xref="HGNC:2195"
/db_xref="MIM:120328"
exon 1..667
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
CDS 22..4572
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/note="isoform 1 precursor is encoded by transcript
variant 1; endostatin; collagen alpha-1(XVIII) chain;
antiangiogenic agent; multi-functional protein MFP"
/codon_start=1
/product="collagen alpha-1(XVIII) chain isoform 1
precursor"
/protein_id="NP_085059.2"
/db_xref="GI:110611235"
/db_xref="CCDS:CCDS42972.1"
/db_xref="GeneID:80781"
/db_xref="HGNC:2195"
/db_xref="MIM:120328"
/translation="
MAPYPCGCHILLLLFCCLAAARANLLNLNWLWFNNEDTSHAATTIPEPQGPLPVQPTADTTTHVTPRNGSTEPATAPGSPEPPSELLEDGQDTPTSAESPDAPEENIAGVGAEILNVAKGIRSFVQLWNDTVPTESLARAETLVLETPVGPLALAGPSSTPQENGTTLWPSRGIPSSPGAHTTEAGTLPAPTPSPPSLGRPWAPLTGPSVPPPSSERISEEVGLLQLLGDPPPQQVTQTDDPDVGLAYVFGPDANSGQVARYHFPSLFFRDFSLLFHIRPATEGPGVLFAITDSAQAMVLLGVKLSGVQDGHQDISLLYTEPGAGQTHTAASFRLPAFVGQWTHLALSVAGGFVALYVDCEEFQRMPLARSSRGLELEPGAGLFVAQAGGADPDKFQGVIAELKVRRDPQVSPMHCLDEEGDDSDGASGDSGSGLGDARELLREETGAALKPRLPAPPPVTTPPLAGGSSTEDSRSEEVEEQTTVASLGAQTLPGSDSVSTWDGSVRTPGGRVKEGGLKGQKGEPGVPGPPGRAGPPGSPCLPGPPGLPCPVSPLGPAGPALQTVPGPQGPPGPPGRDGTPGRDGEPGDPGEDGKPGDTGPQGFPGTPGDVGPKGDKGDPGVGERGPPGPQGPPGPPGPSFRHDKLTFIDMEGSGFGGDLEALRGPRGFPGPPGPPGVPGLPGEPGRFGVNSSDVPGPAGLPGVPGREGPPGFPGLPGPPGPPGREGPPGRTGQKGSLGEAGAPGHKGSKGAPGPAGARGESGLAGAPGPAGPPGPPGPPGPPGPGLPAGFDDMEGSGGPFWSTARSADGPQGPPGLPGLKGDPGVPGLPGAKGEVGADGVPGFPGLPGREGIAGPQGPKGDRGSRGEKGDPGKDGVGQPGLPGPPGPPGPVVYVSEQDGSVLSVPGPEGRPGFAGFPGPAGPKGNLGSKGERGSPGPKGEKGEPGSIFSPDGGALGPAQKGAKGEPGFRGPPGPYGRPGYKGEIGFPGRPGRPGMNGLKGEKGEPGDASLGFGMRGMPGPPGPPGPPGPPGTPVYDSNVFAESSRPGPPGLPGNQGPPGPKGAKGEVGPPGPPGQFPFDFLQLEAEMKGEKGDRGDAGQKGERGEPGGGGFFGSSLPGPPGPPGPRGYPGIPGPKGESIRGQPGPPGPQGPPGIGYEGRQGPPGPPGPPGPPSFPGPHRQTISVPGPPGPPGPPGPPGTMGASSGVRLWATRQAMLGQVHEVPEGWLIFVAEQEELYVRVQNGFRKVQLEARTPLPRGTDNEVAALQPPVVQLHDSNPYPRREHPHPTARPWRADDILASPPRLPEPQPYPGAPHHSSYVHLRPARPTSPPAHSHRDFQPVLHLVALNSPLSGGMRGIRGADFQCFQQARAVGLAGTFRAFLSSRLQDLYSIVRRADRAAVPIVNLKDELLFPSWEALFSGSEGPLKPGARIFSFDGKDVLRHPTWPQKSVWHGSDPNGRRLTESYCETWRTEAPSATGQASSLLGGRLLGQSAASCHHAYIVLCIENSFMTASK
"
sig_peptide 22..90
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 91..4569
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/product="collagen alpha-1(XVIII) chain isoform 1"
misc_feature 127..573
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/note="Domain of Unknown Function (DUF959); Region:
DUF959; pfam06121"
/db_xref="CDD:114818"
misc_feature 760..1248
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/note="Laminin G domain; Laminin G-like domains are
usually Ca++ mediated receptors that can have binding
sites for steroids, beta1 integrins, heparin, sulfatides,
fibulin-1, and alpha-dystroglycans. Proteins that contain
LamG domains serve a variety of...; Region: LamG; cl00102"
/db_xref="CDD:206838"
misc_feature <2515..2640
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/note="Collagen triple helix repeat (20 copies); Region:
Collagen; pfam01391"
/db_xref="CDD:189968"
misc_feature 4039..4551
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/note="Endostatin-like domain; the angiogenesis inhibitor
endostatin is a C-terminal fragment of collagen XV/XVIII,
a proteoglycan/collagen found in vessel walls and basement
membranes; this domain has a compact globular fold similar
to that of C-type lectins; Region: Endostatin-like;
cd00247"
/db_xref="CDD:29322"
misc_feature order(4132..4134,4159..4161,4177..4179,4204..4209,
4216..4218,4402..4407,4435..4437)
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/note="putative ligand binding site [chemical binding];
other site"
/db_xref="CDD:29322"
variation 50
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:368343259"
variation 77
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:7277693"
variation 103
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375363285"
variation 111
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200976185"
variation 112
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369389768"
variation 141
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:914230"
variation 152
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199984023"
variation 156
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:368696106"
variation 163
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:61749002"
variation 167
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="t"
/db_xref="dbSNP:61735029"
variation 192
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200354859"
variation 200
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199929202"
variation 211
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373586271"
variation 220
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375087150"
variation 257..258
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="c"
/db_xref="dbSNP:375958675"
variation 260
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:61739237"
variation 312
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201529109"
variation 321
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370812546"
variation 324
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:149777818"
variation 333
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:377623821"
variation 337
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375714903"
variation 345
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370000815"
variation 351
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:374634058"
variation 352
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:114139997"
variation 369
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:62000459"
variation 393
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372080967"
variation 394
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200559406"
variation 419
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:368269918"
variation 451
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:61759533"
variation 523
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:201773944"
variation 535
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:368985827"
variation 536
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200284308"
variation 538
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:62000960"
variation 558
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:73386835"
variation 559
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:148957774"
variation 561
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:373353645"
variation 581
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:142892701"
variation 592
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369474928"
variation 603
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372854150"
variation 609
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:199717521"
variation 621
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:201419516"
variation 622
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199725915"
variation 660
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2236451"
exon 668..1212
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 679
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375719577"
variation 687
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:115800039"
variation 711
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:190083327"
variation 717
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373105258"
variation 727
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375009748"
variation 737
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:200842530"
variation 747
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372731688"
variation 748
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:377002382"
variation 778
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370054491"
variation 787
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:374084790"
variation 802
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:76658745"
variation 803
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:371058906"
variation 849
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:149578781"
variation 856
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199918230"
variation 857
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375588763"
variation 858
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368228266"
variation 871
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:112855834"
variation 876
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:201508976"
variation 897
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:61735014"
variation 902
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:373861758"
variation 905
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367715239"
variation 913
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:200702024"
variation 928
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:376829205"
variation 953
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368606628"
variation 954
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372142063"
variation 981
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:17004775"
variation 1011
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367852328"
variation 1012
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201833726"
variation 1021
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375242667"
variation 1028
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369275624"
variation 1029
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372556095"
variation 1035
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377547341"
variation 1049
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376036984"
variation 1057
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:144281842"
variation 1071
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:76754353"
variation 1139
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2236453"
variation 1159
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370834739"
variation 1161
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:374980607"
variation 1164
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:17004776"
variation 1165
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373735265"
variation 1173
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:373748503"
variation 1174
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201116208"
variation 1185
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:76148908"
variation 1187
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:376944366"
exon 1213..1299
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1215
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:369219412"
variation 1221
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:189093550"
variation 1228
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:60162212"
variation 1232
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:200168928"
variation 1237
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375001641"
variation 1238
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201095161"
variation 1252
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:202012055"
variation 1254
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:149772252"
variation 1275
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369721525"
exon 1300..1359
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1304
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:200073359"
variation 1320
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:374330522"
variation 1328
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:368233273"
variation 1332
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371736290"
variation 1336
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376722572"
variation 1337
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:62000965"
exon 1360..1489
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1362
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:145912433"
variation 1364
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375414087"
variation 1365
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368376035"
variation 1389
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2230686"
variation 1397
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375411877"
variation 1398
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2230687"
variation 1402
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:192075600"
variation 1407
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2230688"
variation 1433
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201652671"
variation 1434
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:183924183"
variation 1435
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:138471288"
variation 1448
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372308402"
variation 1458
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376715250"
variation 1472
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:200230216"
variation 1473
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:141548934"
variation 1476
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:17338853"
variation 1481
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:200882031"
variation 1486
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:369289615"
variation 1487
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:372726135"
exon 1490..1566
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1523
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372492704"
variation 1531
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375058072"
variation 1558
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:367882523"
exon 1567..1782
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1569
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372133935"
variation 1570
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:76547444"
variation 1573
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369413748"
variation 1604
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372859456"
variation 1612
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370176315"
variation 1618
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369114408"
variation 1619
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373030953"
variation 1633
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:62000458"
variation 1657
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377028409"
variation 1667
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371330320"
variation 1698
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:374344376"
variation 1704
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:2230689"
variation 1755
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370965213"
variation 1764
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375400196"
variation 1773
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367951949"
variation 1776
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370283993"
variation 1782
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368902481"
exon 1783..1809
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1785
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:13046486"
variation 1786
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200553372"
variation 1809
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:185296216"
exon 1810..1872
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1815
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:368594049"
variation 1818
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:183085141"
variation 1822
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375265466"
variation 1827
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:113540632"
variation 1836
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1131100"
variation 1851
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:1131101"
variation 1853
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201414473"
variation 1866
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:1131102"
exon 1873..1959
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1884
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201380467"
variation 1903
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:373670175"
variation 1948
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376357877"
variation 1951
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:61738822"
exon 1960..2013
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 1989
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2236467"
variation 1990
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375852929"
variation 1996
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:369917403"
variation 2013
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:373106775"
exon 2014..2172
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2021
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:371292624"
variation 2044
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375739796"
variation 2068
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368194132"
variation 2070
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:112723616"
variation 2071
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375045387"
variation 2096
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:367836626"
variation 2101
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:79292579"
variation 2103
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:200106008"
variation 2108..2109
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="c"
/db_xref="dbSNP:35603970"
variation 2110
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368600244"
variation 2116
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:61737706"
variation 2118
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372703675"
variation 2134
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375198952"
variation 2142
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369409660"
exon 2173..2235
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2176
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375417533"
variation 2184
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:376461054"
variation 2195
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:373536407"
variation 2203
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370509732"
variation 2235
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:181807938"
exon 2236..2262
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2244
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:75222922"
variation 2248
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201476017"
exon 2263..2394
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2321
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199823547"
variation 2385
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370138639"
exon 2395..2457
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2400
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369792535"
variation 2412
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376114537"
variation 2413
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368967629"
variation 2426
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:371586411"
variation 2432
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377286160"
variation 2442
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370015560"
variation 2443
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:181012655"
exon 2458..2484
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2466
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199523495"
variation 2481
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:11702425"
exon 2485..2520
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2496
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367928373"
variation 2497
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:371970491"
variation 2510
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376627920"
variation 2511
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:61731167"
variation 2517
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372310838"
exon 2521..2592
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2542
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:62000962"
variation 2544
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:375695180"
variation 2556
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:185089648"
variation 2559
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:62000963"
variation 2564..2565
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="c"
/db_xref="dbSNP:35277478"
exon 2593..2628
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2595
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375058430"
variation 2618
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:367841049"
exon 2629..2718
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2646
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:373006940"
variation 2652
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376084472"
variation 2660
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370141116"
variation 2661
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373318899"
variation 2664
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377652187"
variation 2678
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:79980197"
variation 2680
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375408962"
variation 2682
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:377533410"
variation 2688
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370417664"
variation 2697
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:374390595"
variation 2699
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367570320"
variation 2704
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372801767"
variation 2709
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:374522196"
exon 2719..2748
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2727
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201512380"
variation 2734
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:116111018"
variation 2741
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:377720407"
variation 2744
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:58380358"
exon 2749..2775
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2753
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201805043"
variation 2757
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:115470104"
variation 2764
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:372137898"
variation 2775
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199910738"
exon 2776..2838
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2790
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376292745"
variation 2815
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370009347"
variation 2828
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370673713"
exon 2839..2913
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2854
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371808014"
variation 2865
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:373455911"
variation 2901
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:2230693"
exon 2914..2940
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2921
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367994730"
variation 2922
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:371966493"
variation 2938
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376597265"
variation 2939
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367551698"
exon 2941..2994
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 2949
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:139122081"
variation 2953
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201566264"
variation 2957
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376924299"
variation 2994
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200147240"
exon 2995..3069
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3003
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375606333"
variation 3012
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:368730788"
variation 3013
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372658384"
variation 3038
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375575507"
variation 3039
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:369390092"
variation 3051
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377601838"
exon 3070..3138
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3071
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:377444691"
variation 3079
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372552105"
variation 3129
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376919554"
exon 3139..3181
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3139
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:200779516"
variation 3157
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372312684"
variation 3162
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:374530279"
exon 3182..3244
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3184
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:371993501"
variation 3193
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377290522"
variation 3205
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:374976416"
variation 3210
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369139821"
variation 3224
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:373528509"
variation 3234
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:191481067"
exon 3245..3288
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3254
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:201753320"
variation 3255
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:190374248"
variation 3263..3265
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="ttc"
/db_xref="dbSNP:371849586"
variation 3266
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="ttc"
/db_xref="dbSNP:78636159"
exon 3289..3420
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3328
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372982447"
variation 3342
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:11544970"
variation 3343
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:187721798"
variation 3348
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:11544971"
variation 3360
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370771189"
variation 3376..3393
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="ggcccccccggcccccca"
/db_xref="dbSNP:201180574"
variation 3383
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="cggcccccc"
/db_xref="dbSNP:72301048"
variation 3385..3393
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="ggcccccca"
/db_xref="dbSNP:149296338"
variation 3393
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:28696990"
variation 3397
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="cccccaggc"
/db_xref="dbSNP:11276732"
variation 3398
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="cccaggccc"
/db_xref="dbSNP:56328291"
variation 3399..3400
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="cccaggccc"
/db_xref="dbSNP:78227997"
variation 3401
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:202106628"
exon 3421..3565
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3442
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371106773"
variation 3448
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:374058652"
variation 3480
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:368077149"
variation 3481
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:371933414"
variation 3486
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375548890"
variation 3487
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:376598650"
variation 3489
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:367549674"
variation 3499
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372973695"
variation 3500
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200299380"
variation 3513
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369702868"
variation 3534
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:367651350"
variation 3554
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375478181"
exon 3566..3639
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3574
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201381498"
variation 3588
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370656151"
variation 3627
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375254978"
variation 3628
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:367825934"
exon 3640..3768
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3659
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:199718927"
variation 3676..3681
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="caggtg"
/db_xref="dbSNP:201754608"
variation 3685
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200427354"
variation 3694
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201265799"
variation 3711
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:371774034"
variation 3735
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376728632"
variation 3747
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:374911370"
variation 3748
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:369018715"
variation 3750
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377152291"
exon 3769..3801
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3782
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:200839439"
variation 3783
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:12483761"
variation 3794
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:199583095"
exon 3802..4047
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 3826
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:76086392"
variation 3863
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:187670025"
variation 3866
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:374207420"
variation 3868
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377620137"
variation 3893
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:112359725"
variation 3904
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:113268527"
variation 3910
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372741290"
variation 3931
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375753362"
variation 3932
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370102608"
variation 3939
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377093259"
variation 3958
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:199836125"
variation 3971
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:372765303"
variation 3981
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375601931"
variation 3996
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:150227889"
variation 3999
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:1050351"
variation 4032
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370921955"
exon 4048..4245
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 4062
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:374326288"
variation 4080
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:9980939"
variation 4083
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376208451"
variation 4084
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:369592585"
variation 4089
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:373470254"
variation 4091
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200484625"
variation 4101
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370643343"
variation 4131
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372559352"
variation 4148
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375590764"
variation 4159
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371038039"
variation 4161
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:114276639"
variation 4162
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:144147445"
variation 4176
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370750158"
variation 4177
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:374880663"
variation 4182
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368134801"
variation 4198
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:369304666"
variation 4201
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:371989063"
variation 4208
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:200043539"
variation 4212
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:367565307"
variation 4217
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201006742"
variation 4220
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:377226690"
variation 4224
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:369895316"
variation 4225
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:77326997"
variation 4233
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:2838952"
exon 4246..4361
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 4254
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:372684121"
variation 4271
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:375813847"
variation 4287
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:368913533"
variation 4295
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373537140"
variation 4302
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:199498978"
variation 4308
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371424181"
variation 4309
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:374321733"
variation 4315
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:199908300"
variation 4330
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:12483377"
variation 4333
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375269967"
variation 4342
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:202104330"
exon 4362..5894
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/inference="alignment:Splign:1.39.8"
variation 4375
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:61736805"
variation 4387
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:200871316"
variation 4389
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:113315760"
variation 4403
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:202049650"
variation 4413
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372279165"
variation 4414
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370953127"
variation 4452
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:375390952"
variation 4456
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:370518474"
variation 4457
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:373708039"
variation 4472
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:61735035"
variation 4480
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:374822514"
variation 4492
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:372436243"
variation 4508
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:375488894"
variation 4517
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:201489582"
variation 4523
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:371861582"
variation 4524
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:375109205"
variation 4578
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:138930698"
variation 4587
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:149459132"
variation 4588
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:7499"
variation 4596
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:369152864"
variation 4601
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:371710532"
variation 4602
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:373537387"
variation 4605
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:376696662"
variation 4614
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:369684141"
variation 4643
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:8199"
variation 4699
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:369628824"
STS 4761..4992
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/standard_name="SHGC-8080"
/db_xref="UniSTS:7730"
variation 4785
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:143852653"
variation 4849
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:17004784"
variation 4863
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:148610040"
variation 4871
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:183949177"
variation 4874
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:17255281"
variation 4878
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:17004785"
variation 4912
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:7867"
variation 4920
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:146206934"
variation 5003
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:368394587"
variation 5011
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:371166816"
variation 5014
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:11544972"
variation 5346
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:370216895"
variation 5421
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="t"
/db_xref="dbSNP:17255379"
variation 5424
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:17004786"
variation 5436
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:186538749"
variation 5477
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:367569832"
variation 5490
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:117981301"
STS 5532..5873
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/standard_name="SHGC-12530"
/db_xref="UniSTS:98863"
variation 5615
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:377445664"
variation 5618
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1063505"
STS 5650..5876
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/standard_name="SHGC-87711"
/db_xref="UniSTS:81506"
variation 5719..5720
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="ca"
/db_xref="dbSNP:143456926"
variation 5720..5721
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="ca"
/db_xref="dbSNP:78063943"
variation 5720
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="c"
/db_xref="dbSNP:201512613"
variation 5721..5722
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace=""
/replace="ca"
/db_xref="dbSNP:71868999"
variation 5721
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="g"
/db_xref="dbSNP:1063507"
variation 5763
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:190947105"
variation 5790
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:144079697"
variation 5809
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="c"
/replace="t"
/db_xref="dbSNP:115900328"
variation 5819
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="a"
/replace="g"
/db_xref="dbSNP:182474443"
variation 5833
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
/replace="g"
/replace="t"
/db_xref="dbSNP:78156175"
polyA_signal 5871..5876
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
polyA_site 5894
/gene="COL18A1"
/gene_synonym="KNO; KNO1; KS"
ORIGIN
agctccagccgcactgccccgatggctccctacccctgtggctgccacatcctgctgctgctcttctgctgcctggcggctgcccgggccaacctgctgaacctgaactggctttggttcaataatgaggacaccagccatgcagctaccacgatccctgagccccaggggcccctgcctgtgcagcccacagcagataccaccacacacgtgaccccccggaatggttccacagagccagcgacagcccctggcagccctgagccaccctcagagctgctggaagatggccaggacacccccacttctgccgagagcccggacgcgccagaggagaacattgccggtgtcggagccgagatcctgaacgtggccaaaggcatccggagcttcgtccagctgtggaatgacactgtccccactgagagcttggccagggcggaaaccctggtcctggagactcctgtgggcccccttgccctcgctgggccttccagcaccccccaggagaatgggaccactctctggcccagccgtggcattcctagctctccgggcgcccacacaaccgaggctggcaccttgcctgcacccaccccatcgcctccctccctgggcaggccctgggcaccactcacggggccctcagtgccaccaccatcttcagagcgcatcagcgaggaggtggggctgctgcagctccttggggaccccccgccccagcaggtcacccagacggatgaccccgacgtcgggctggcctacgtctttgggccagatgccaacagtggccaagtggcccggtaccacttccccagcctcttcttccgtgacttctcactgctgttccacatccggccagccacagagggcccaggggtgctgttcgccatcacggactcggcgcaggccatggtcttgctgggcgtgaagctctctggggtgcaggacgggcaccaggacatctccctgctctacacagaaccaggtgcaggccagacccacacagccgccagcttccggctccccgccttcgtcggccagtggacacacttagccctcagtgtggcaggtggctttgtggccctctacgtggactgtgaggagttccagagaatgccgcttgctcggtcctcacggggcctggagctggagcctggcgccgggctcttcgtggctcaggcggggggagcggaccctgacaagttccagggggtgatcgctgagctgaaggtgcgcagggacccccaggtgagccccatgcactgcctggacgaggaaggcgatgactcagatggggcatccggagactctggcagcgggctcggggacgcccgggagcttctcagggaggagacgggcgcggccctaaaacccaggctccccgcgccaccccccgtcaccacgccacccttggctggaggcagcagcacggaagattccagaagtgaagaagtcgaggagcagaccacggtggcttcgttaggagctcagacacttcctggctcagattctgtctccacgtgggacgggagtgtccggacccctgggggccgcgtgaaagagggcggcctgaaggggcagaaaggggagccaggtgttccgggcccacctggccgggcaggccccccaggatccccatgcctacctggtcccccgggtctcccgtgcccagtgagtcccctgggtcctgcaggcccagcgttgcaaactgtccccggaccacaaggacccccagggcctccggggagggacggcacccctggaagggacggcgagccgggcgaccccggtgaagacggaaagccgggcgacaccgggccacaaggcttccccgggactccaggggacgtaggtcccaagggcgacaagggagaccctggggttggagagagagggcccccaggaccccaagggcctccagggcccccaggaccctccttcagacacgacaagctgaccttcattgacatggagggatctggcttcgggggcgatctggaggccctgcggggtcctcgaggcttccctggacctcccggaccccccggtgtcccaggcctgcccggcgagccaggccgctttggggtgaacagctccgacgtcccaggacccgccggccttcctggtgtgcctgggcgcgagggtccccccgggtttcctggcctcccgggacccccaggccctccgggaagagaggggcccccaggaaggactgggcagaaaggcagcctgggtgaagcaggcgccccaggacataaggggagcaagggagcccccggtcctgctggtgctcgtggggagagcggcctggcaggagcccccggacctgctggaccaccaggcccccctgggccccctgggcccccaggaccaggactccccgctggatttgatgacatggaaggctccggggggcccttctggtcaacagcccgaagcgctgatgggccacagggacctcccggcctgccgggacttaagggggatcctggcgtgcctgggctgccgggggcgaagggagaagttggagcagatggagtccccgggttccccggcctccctggcagagagggcattgctgggccccaggggccaaagggagacagaggcagccggggagaaaagggagatccagggaaggacggagtcgggcagccgggcctccctggcccccccggacccccgggacctgtggtctacgtgtcggagcaggacggatccgtcctgagcgtgccgggacctgagggccggccgggtttcgcaggctttcccggacctgcaggacccaagggcaacctgggctctaagggcgaacgaggctccccgggacccaagggtgagaagggtgaaccgggcagcatcttcagccccgacggcggtgccctgggccctgcccagaaaggagccaagggagagccgggcttccgaggacccccgggtccatacggacggccggggtacaagggagagattggctttcctggacggccgggtcgccccgggatgaacggattgaaaggagagaaaggggagccgggagatgccagccttggatttggcatgaggggaatgcccggccccccaggacctccagggcccccaggccctccagggactcctgtttacgacagcaatgtgtttgctgagtccagccgccccgggcctccaggattgccagggaatcagggccctccaggacccaagggcgccaaaggagaagtgggcccccccggaccaccagggcagtttccgtttgactttcttcagttggaggctgaaatgaagggggagaagggagaccgaggtgatgcaggacagaaaggcgaaaggggggagcccgggggcggcggtttcttcggctccagcctgcccggcccccccggccccccaggcccacgtggctaccctgggattccaggtcccaagggagagagcatccggggccagcccggcccacctggacctcagggaccccccggcatcggctacgaggggcgccagggccctcccggccccccaggccccccagggcccccttcatttcctggccctcacaggcagactatcagcgttcccggccctccgggcccccctgggccccctgggccccctggaaccatgggcgcctcctcaggggtgaggctctgggctacacgccaggccatgctgggccaggtgcacgaggttcccgagggctggctcatcttcgtggccgagcaggaggagctctacgtccgcgtgcagaacgggttccggaaggtccagctggaggcccggacaccactcccacgagggacggacaatgaagtggccgccttgcagccccccgtggtgcagctgcacgacagcaacccctacccgcggcgggagcacccccaccccaccgcgcggccctggcgggcagatgacatcctggccagcccccctcgcctgcccgagccccagccctaccccggagccccgcaccacagctcctacgtgcacctgcggccggcgcgacccacaagcccacccgcccacagccaccgcgacttccagccggtgctccacctggttgcgctcaacagccccctgtcaggcggcatgcggggcatccgcggggccgacttccagtgcttccagcaggcgcgggccgtggggctggcgggcaccttccgcgccttcctgtcctcgcgcctgcaggacctgtacagcatcgtgcgccgtgccgaccgcgcagccgtgcccatcgtcaacctcaaggacgagctgctgtttcccagctgggaggctctgttctcaggctctgagggtccgctgaagcccggggcacgcatcttctcctttgacggcaaggacgtcctgaggcaccccacctggccccagaagagcgtgtggcatggctcggaccccaacgggcgcaggctgaccgagagctactgtgagacgtggcggacggaggctccctcggccacgggccaggcctcctcgctgctggggggcaggctcctggggcagagtgccgcgagctgccatcacgcctacatcgtgctctgcattgagaacagcttcatgactgcctccaagtagccaccgcctggatgcggatggccggagaggaccggcggctcggaggaagcccccaccgtgggcagggagcggccggccagcccctggccccaggacctggctgccatactttcctgtatagttcacgtttcatgtaatcctcaagaaataaaaggaagccaaagagtgtatttttttaaaagtttaaaacagaagcctgatgctgacattcacctgccccaactctcccctgacctgtgagcccagctgggtcaggcagggtgcagtatcatgccctgtgcaacctcttggcctgatcagaccacggctcgatttctccaggatttcctgctttgggaagccgtgctcgccccagcaggtgctgacttcatctcccacctagcagcaccgttctgtgcacaaaacccagacctgttagcagacaggccccgtgaggcaatgggagctgaggccacactcagcacaaggccatctgggctcctccagggtgtgtgctcgccctgcggtagatgggagggaggctcaggtccctggggctagggggagccccttctgctcagctctgggccattctccacagcaaccccaggctgaagcaggttcccaagctcagaggcgcactgtgacccccagctccggcctgtcctccaacaccaagcacagcagcctggggctggcctcccaaatgagccatgagatgatacatccaaagcagacagctccaccctggccgagtccaagctgggagattcaagggacccatgagttggggtctggcagcctcccatccagggcccccatctcatgcccctggctgggacgtggctcagccagcacttgtccagctgagcgccaggatggaacacggccacatcaaagaggctgaggctggcacaggacatgcggtagccagcacacagggcagtgagggagggctgtcatctgtgcactgcccatggacaggctggctccagatgcagggcagtcattggctgtctcctaggaaacccatatccttaccctccttgggactgaaggggaaccccggggtgcccacaggccgccctgcgggtgaacaaagcagccacgaggtgcaacaaggtcctctgtcagtcacagccacccctgagatccggcaacatcaacccgagtcattcgttctgtggagggacaagtggactcagggcagcgccaggctgaccacagcacagccaacacgcacctgcctcaggactgcgacgaaaccggtggggctggttctgtaattgtgtgtgatgtgaagccaattcagacaggcaaataaaagtgaccttttacactgaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:80781 -> Molecular function: GO:0005198 [structural molecule activity] evidence: IEA
GeneID:80781 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:80781 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI
GeneID:80781 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
GeneID:80781 -> Biological process: GO:0001525 [angiogenesis] evidence: IEA
GeneID:80781 -> Biological process: GO:0001886 [endothelial cell morphogenesis] evidence: IEA
GeneID:80781 -> Biological process: GO:0007155 [cell adhesion] evidence: IEA
GeneID:80781 -> Biological process: GO:0007601 [visual perception] evidence: TAS
GeneID:80781 -> Biological process: GO:0008284 [positive regulation of cell proliferation] evidence: IEA
GeneID:80781 -> Biological process: GO:0008285 [negative regulation of cell proliferation] evidence: TAS
GeneID:80781 -> Biological process: GO:0009887 [organ morphogenesis] evidence: TAS
GeneID:80781 -> Biological process: GO:0022617 [extracellular matrix disassembly] evidence: TAS
GeneID:80781 -> Biological process: GO:0030198 [extracellular matrix organization] evidence: TAS
GeneID:80781 -> Biological process: GO:0030335 [positive regulation of cell migration] evidence: IEA
GeneID:80781 -> Biological process: GO:0030574 [collagen catabolic process] evidence: TAS
GeneID:80781 -> Biological process: GO:0043065 [positive regulation of apoptotic process] evidence: IEA
GeneID:80781 -> Cellular component: GO:0005576 [extracellular region] evidence: TAS
GeneID:80781 -> Cellular component: GO:0005581 [collagen] evidence: IEA
GeneID:80781 -> Cellular component: GO:0005604 [basement membrane] evidence: IEA
GeneID:80781 -> Cellular component: GO:0005615 [extracellular space] evidence: IDA
GeneID:80781 -> Cellular component: GO:0005788 [endoplasmic reticulum lumen] evidence: TAS
GeneID:80781 -> Cellular component: GO:0031012 [extracellular matrix] evidence: IDA
GeneID:80781 -> Cellular component: GO:0031012 [extracellular matrix] evidence: TAS
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@meso_cacase at
DBCLS
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