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2025-05-09 19:34:19, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_152447 3747 bp mRNA linear PRI 15-JUN-2013
DEFINITION Homo sapiens leucine rich repeat and fibronectin type III domain
containing 5 (LRFN5), mRNA.
ACCESSION NM_152447
VERSION NM_152447.3 GI:194733750
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 3747)
AUTHORS Avery,C.L., Sitlani,C.M., Arking,D.E., Arnett,D.K., Bis,J.C.,
Boerwinkle,E., Buckley,B.M., Ida Chen,Y.D., de Craen,A.J.,
Eijgelsheim,M., Enquobahrie,D., Evans,D.S., Ford,I., Garcia,M.E.,
Gudnason,V., Harris,T.B., Heckbert,S.R., Hochner,H., Hofman,A.,
Hsueh,W.C., Isaacs,A., Jukema,J.W., Knekt,P., Kors,J.A.,
Krijthe,B.P., Kristiansson,K., Laaksonen,M., Liu,Y., Li,X.,
Macfarlane,P.W., Newton-Cheh,C., Nieminen,M.S., Oostra,B.A.,
Peloso,G.M., Porthan,K., Rice,K., Rivadeneira,F.F., Rotter,J.I.,
Salomaa,V., Sattar,N., Siscovick,D.S., Slagboom,P.E., Smith,A.V.,
Sotoodehnia,N., Stott,D.J., Stricker,B.H., Sturmer,T., Trompet,S.,
Uitterlinden,A.G., van Duijn,C., Westendorp,R.G., Witteman,J.C.,
Whitsel,E.A. and Psaty,B.M.
TITLE Drug-gene interactions and the search for missing heritability: a
cross-sectional pharmacogenomics study of the QT interval
JOURNAL Pharmacogenomics J. (2013) In press
PUBMED 23459443
REMARK Publication Status: Available-Online prior to print
REFERENCE 2 (bases 1 to 3747)
AUTHORS Oudot-Mellakh,T., Cohen,W., Germain,M., Saut,N., Kallel,C.,
Zelenika,D., Lathrop,M., Tregouet,D.A. and Morange,P.E.
TITLE Genome wide association study for plasma levels of natural
anticoagulant inhibitors and protein C anticoagulant pathway: the
MARTHA project
JOURNAL Br. J. Haematol. 157 (2), 230-239 (2012)
PUBMED 22443383
REFERENCE 3 (bases 1 to 3747)
AUTHORS Nam,J., Mah,W. and Kim,E.
TITLE The SALM/Lrfn family of leucine-rich repeat-containing cell
adhesion molecules
JOURNAL Semin. Cell Dev. Biol. 22 (5), 492-498 (2011)
PUBMED 21736948
REMARK GeneRIF: SALM5/Lrfn5, has recently been implicated in severe
progressive autism and familial schizophrenia, pointing to the
clinical importance of SALMs.[review]
Review article
REFERENCE 4 (bases 1 to 3747)
AUTHORS Mah,W., Ko,J., Nam,J., Han,K., Chung,W.S. and Kim,E.
TITLE Selected SALM (synaptic adhesion-like molecule) family proteins
regulate synapse formation
JOURNAL J. Neurosci. 30 (16), 5559-5568 (2010)
PUBMED 20410109
REMARK GeneRIF: Expression of SALM family proteins SALM3 and SALM5 in
nonneural and neural cells induces both excitatory and inhibitory
presynaptic differentiation in contacting axons.
REFERENCE 5 (bases 1 to 3747)
AUTHORS Morimura,N., Inoue,T., Katayama,K. and Aruga,J.
TITLE Comparative analysis of structure, expression and PSD95-binding
capacity of Lrfn, a novel family of neuronal transmembrane proteins
JOURNAL Gene 380 (2), 72-83 (2006)
PUBMED 16828986
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DA096504.1, AK096627.1, BC043165.1, AL138498.5 and AW013887.1.
On Jul 31, 2008 this sequence version replaced gi:31542243.
Sequence Note: The RefSeq transcript and protein were derived from
transcript and genomic sequence to make the sequence consistent
with the reference genome assembly. The genomic coordinates used
for the transcript record were based on alignments.
##Evidence-Data-START##
Transcript exon combination :: AK096627.1, BC043165.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025088, ERS025090 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-148 DA096504.1 1-148
149-701 AK096627.1 122-674
702-1920 BC043165.1 127-1345
1921-2583 AK096627.1 1894-2556
2584-3296 AL138498.5 69378-70090 c
3297-3481 AK096627.1 3270-3454
3482-3747 AW013887.1 1-266 c
FEATURES Location/Qualifiers
source 1..3747
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q21.1"
gene 1..3747
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="leucine rich repeat and fibronectin type III domain
containing 5"
/db_xref="GeneID:145581"
/db_xref="HGNC:20360"
/db_xref="HPRD:17445"
/db_xref="MIM:612811"
exon 1..1002
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/inference="alignment:Splign:1.39.8"
variation 59
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:80337487"
variation 119
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="g"
/db_xref="dbSNP:143707970"
variation 126
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376386142"
variation 229
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:186264704"
variation 339
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:192016172"
variation 440
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:78328447"
variation 468
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:183383430"
variation 525
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1137567"
variation 606
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="g"
/db_xref="dbSNP:141251236"
variation 613
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373551302"
variation 622..623
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace=""
/replace="c"
/db_xref="dbSNP:34520734"
variation 634
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:76767345"
variation 851
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:11620636"
exon 1003..1178
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/inference="alignment:Splign:1.39.8"
variation 1071
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:183079892"
exon 1179..2583
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/inference="alignment:Splign:1.39.8"
variation 1181
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="g"
/replace="t"
/db_xref="dbSNP:77016987"
misc_feature 1190..1192
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="upstream in-frame stop codon"
CDS 1199..3358
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="fibronectin type III, immunoglobulin and leucine
rich repeat domains 8; leucine-rich repeat and fibronectin
type-III domain-containing protein 5"
/codon_start=1
/product="leucine-rich repeat and fibronectin type-III
domain-containing protein 5 precursor"
/protein_id="NP_689660.2"
/db_xref="GI:31542244"
/db_xref="CCDS:CCDS9678.1"
/db_xref="GeneID:145581"
/db_xref="HGNC:20360"
/db_xref="HPRD:17445"
/db_xref="MIM:612811"
/translation="
MEKILFYLFLIGIAVKAQICPKRCVCQILSPNLATLCAKKGLLFVPPNIDRRTVELRLADNFVTNIKRKDFANMTSLVDLTLSRNTISFITPHAFADLRNLRALHLNSNRLTKITNDMFSGLSNLHHLILNNNQLTLISSTAFDDVFALEELDLSYNNLETIPWDAVEKMVSLHTLSLDHNMIDNIPKGTFSHLHKMTRLDVTSNKLQKLPPDPLFQRAQVLATSGIISPSTFALSFGGNPLHCNCELLWLRRLSREDDLETCASPPLLTGRYFWSIPEEEFLCEPPLITRHTHEMRVLEGQRATLRCKARGDPEPAIHWISPEGKLISNATRSLVYDNGTLDILITTVKDTGAFTCIASNPAGEATQIVDLHIIKLPHLLNSTNHIHEPDPGSSDISTSTKSGSNTSSSNGDTKLSQDKIVVAEATSSTALLKFNFQRNIPGIRMFQIQYNGTYDDTLVYRMIPPTSKTFLVNNLAAGTMYDLCVLAIYDDGITSLTATRVVGCIQFTTEQDYVRCHFMQSQFLGGTMIIIIGGIIVASVLVFIIILMIRYKVCNNNGQHKVTKVSNVYSQTNGAQIQGCSVTLPQSVSKQAVGHEENAQCCKATSDNVIQSSETCSSQDSSTTTSALPPSWTSSTSVSQKQKRKTGTKPSTEPQNEAVTNVESQNTNRNNSTALQLASRPPDSVTEGPTSKRAHIKPNALLTNVDQIVQETQRLELI
"
sig_peptide 1199..1249
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 1250..3355
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/product="Leucine-rich repeat and fibronectin type-III
domain-containing protein 5"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2)"
misc_feature 1352..1417
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2);
Region: LRR 1"
misc_feature 1361..1531
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="Leucine rich repeat; Region: LRR_8; pfam13855"
/db_xref="CDD:206026"
misc_feature 1424..1489
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2);
Region: LRR 2"
misc_feature 1496..1561
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2);
Region: LRR 3"
misc_feature 1568..1633
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2);
Region: LRR 4"
misc_feature 1640..1705
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2);
Region: LRR 5"
misc_feature 1643..1819
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="Leucine rich repeat; Region: LRR_8; pfam13855"
/db_xref="CDD:206026"
misc_feature 1712..1777
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2);
Region: LRR 6"
misc_feature 1784..1849
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2);
Region: LRR 7"
misc_feature 1916..>2014
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="Leucine rich repeat C-terminal domain; Region:
LRRCT; smart00082"
/db_xref="CDD:197506"
misc_feature 2057..2320
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 2099..2320
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="Subgroup of the immunoglobulin (Ig) superfamily;
Region: Ig_2; cd05764"
/db_xref="CDD:143241"
misc_feature 2459..2680
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/note="Fibronectin type 3 domain; One of three types of
internal repeats found in the plasma protein fibronectin.
Its tenth fibronectin type III repeat contains an RGD cell
recognition sequence in a flexible loop between 2 strands.
Approximately 2% of all...; Region: FN3; cl00065"
/db_xref="CDD:206813"
misc_feature 2786..2848
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96NI6.2);
transmembrane region"
variation 1203
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:199536784"
variation 1214
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141649332"
variation 1217
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="t"
/db_xref="dbSNP:77336898"
variation 1222
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146169929"
variation 1267
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:374199959"
variation 1310
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199855789"
variation 1314
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace=""
/replace="a"
/db_xref="dbSNP:35910183"
variation 1375
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="g"
/replace="t"
/db_xref="dbSNP:1886164"
variation 1388
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:185649544"
variation 1396
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144132966"
variation 1439
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="t"
/db_xref="dbSNP:200283889"
variation 1441
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370921286"
variation 1456
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:151006633"
variation 1484
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:190113136"
variation 1519
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:181581182"
variation 1533
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:76592962"
variation 1548
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:111434182"
variation 1550
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139662562"
variation 1639
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:117966123"
variation 1713
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145569146"
variation 1793
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:140770648"
variation 1824
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="t"
/db_xref="dbSNP:188537104"
variation 1885
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141598594"
variation 1886
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="g"
/db_xref="dbSNP:375396897"
variation 1911
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="g"
/replace="t"
/db_xref="dbSNP:147067718"
variation 1912
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:61742049"
variation 1921
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:17854265"
variation 1955
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:147658218"
variation 1972
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:367997664"
variation 2067
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:370216412"
variation 2143
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150248310"
variation 2167
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200743284"
variation 2216
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201273688"
variation 2257
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="g"
/replace="t"
/db_xref="dbSNP:61744159"
variation 2300
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="g"
/db_xref="dbSNP:143251931"
variation 2376
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="g"
/replace="t"
/db_xref="dbSNP:368716591"
variation 2383
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:201771170"
variation 2419
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372315722"
variation 2422
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:148376105"
variation 2491
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="t"
/db_xref="dbSNP:375380713"
variation 2532
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200029150"
exon 2584..3296
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/inference="alignment:Splign:1.39.8"
variation 2598
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369343795"
variation 2646
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142301191"
variation 2647
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141598076"
variation 2727
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:150445484"
variation 2728
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:181411518"
variation 2744
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:138417169"
variation 2764
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:6572117"
variation 2790
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146218561"
variation 2812
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375382591"
variation 2868
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:184300558"
variation 2884
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="g"
/db_xref="dbSNP:139239177"
variation 2889
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:150568237"
variation 2896
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149456109"
variation 2954
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373989159"
variation 2959
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="g"
/db_xref="dbSNP:189076635"
variation 3051
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:143897378"
variation 3057
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148679546"
variation 3063
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142220815"
variation 3095
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="g"
/replace="t"
/db_xref="dbSNP:376533514"
variation 3135
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370624158"
variation 3140
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150763995"
variation 3153
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373913705"
variation 3238
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377068056"
variation 3239
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:139679791"
variation 3241
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="t"
/db_xref="dbSNP:112647558"
variation 3253
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:34676437"
variation 3265
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="g"
/replace="t"
/db_xref="dbSNP:143357119"
variation 3270
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:369488450"
exon 3297..3340
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/inference="alignment:Splign:1.39.8"
exon 3341..3732
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/inference="alignment:Splign:1.39.8"
variation 3349
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:116217484"
variation 3371..3373
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace=""
/replace="ctc"
/db_xref="dbSNP:150172548"
variation 3372
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200428617"
variation 3381
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375213734"
variation 3389
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="c"
/db_xref="dbSNP:201953168"
variation 3393
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="g"
/replace="t"
/db_xref="dbSNP:201250483"
variation 3466
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:193174264"
variation 3467
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:182543688"
variation 3470
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:187190762"
variation 3480
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:191949312"
STS 3495..3662
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/standard_name="RH48353"
/db_xref="UniSTS:19790"
variation 3516
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373916061"
variation 3548
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="g"
/db_xref="dbSNP:112048047"
variation 3582
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="c"
/replace="t"
/db_xref="dbSNP:112965685"
variation 3587..3588
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace=""
/replace="t"
/db_xref="dbSNP:201977258"
variation 3598
/gene="LRFN5"
/gene_synonym="C14orf146; FIGLER8; SALM5"
/replace="a"
/replace="t"
/db_xref="dbSNP:11539099"
ORIGIN
atctgatgcatttgactgtcttttatccaactgcccagaagcaaatgtgttaactcggcgatgccccttcatgcccgggttcttgcagagctctgaggacgcccagacccattttcctggctggatttggagcggctgctgggctgtggacccaggtgtgtggatcgctttacccagaagcttggaaagcgccaatattaacctgcttccaggtacatcacaaggtcaagagagtgtcttgcagccctcttgtttccgtgtatctacaccttcttctcttggccagaaggatatttacgttttggttcacagcatttgaagccaaaagttcagcccttcgaactggtttgctatacaaaacaaaacaaaacaaataaggtaatgaggattgcttattaaactgcttaacaaaatccccgactcttcctcagccctttctcggctccctcctccccaccaaaatgtcaccagctcttgaattacgtggattcgggttggaggagaacttgaaggaaacgtgattaaagggctatgcgagaacgctctctttgctgcccgcggtccggtgggcttcgaagccaatcgtgagaaggaccggttccctccgtgctgcttcctccccgtgcagtgctgggtgtgcgtgtgcgagtgtgagtgcaagtgcgcgcgcgcccgggtgcgagtgtgtgtgagtgtgagcgtgtgtctgtgtgtgcgtgcgcggccgccctgcctctgcccgctccccgggcgcggagccgcgggtttcatggggcgattgcagcgattcccccacccagagcgacctgcgggcagcggcggcagtggcaggagccgcctttccgattccctacgatgcgggtgctgagctatggcaaagggcagcgaagtgacgagcgagacccgcgtacgactgtgaaagccacctggagccaccttgccgggattgtacctgcaggcagaaagtcttcctacgaccgtcttttcccttagaggcaccagaatccctgtaaccattcatccaggtgttgagaagatatgtagcagccgagcacccatcttttgacaccgtcctctgaaatcagctttggagatgctttcactctgtccgtcttctgcagcagccaggcagagtgccgactccttcacagccgtgaggaactcttcaggctccagaagctcttaaacctgatctacaatggaaaaaattcttttttatctgtttctcattggcatagcagtgaaagctcagatctgtccaaagcgttgtgtctgtcagattttgtctcctaatcttgcaaccctttgtgccaagaaagggcttttatttgttccaccaaacattgacagaagaactgtggaactgcggttggcagacaattttgttacaaatattaaaaggaaagattttgccaatatgaccagcttggtggacctgactctatccaggaatacaataagttttattacacctcatgctttcgctgacctacgaaatttgagggctttgcatttgaatagcaacagattgactaaaattacaaatgatatgttcagtggtctttccaatcttcatcatttgatactgaacaacaatcagctgactttaatttcctctacagcgtttgatgatgtcttcgcccttgaggagctggatctgtcctataataatctagaaaccattccttgggatgctgttgagaagatggttagcttgcatacccttagtttggatcacaatatgattgataacattcctaaggggaccttctcccatttgcacaagatgactcggttagatgtgacatcaaataaattgcagaagctaccacctgaccctctctttcagcgagctcaggtactagcaacctcaggaatcataagcccatctacttttgcattaagttttggtggaaaccccttgcattgcaattgtgaattgttgtggttgaggcgtctgtccagagaagatgacttagagacctgtgcttctcctccacttttaactggccgctacttttggtcaattcctgaagaagagtttttgtgtgagcctcctctcattactcgtcatacacatgagatgagagtcctggagggacaaagggcaacactgaggtgcaaagccaggggagaccctgagcctgcaattcactggatttctcctgaagggaagcttatttcaaatgcaacaagatctctggtgtatgataacggaacacttgacattcttatcacaactgtaaaggatacaggtgcttttacctgcattgcttccaatcctgctggggaagcaacacaaatagtggatcttcatataattaagctccctcacttactaaatagtacaaaccatatccatgagcctgatcctggttcttcagatatctcaacttctaccaagtcaggttctaatacaagcagtagtaatggtgatactaaattgagtcaagataaaattgtggtggcagaagctacatcatcaacggcactacttaaatttaattttcaaagaaatatccctggaatacgtatgtttcaaatccagtacaatggtacttatgatgacacccttgtttacagaatgatacctcctacgagcaaaacttttctggtcaataatctggctgctggaactatgtatgacttgtgtgtcttggccatatatgatgatggcatcacttccctcactgccacaagagtcgtgggttgcatccagtttactacggaacaggattatgtgcgttgccatttcatgcagtctcagtttttgggaggcaccatgattattattattggtggaatcattgtagcatctgtgctggtattcatcattattctgatgatccggtataaggtttgcaacaataatgggcaacacaaggtcaccaaggttagcaatgtttattcccaaactaacggggctcaaatacaaggctgtagtgtaacgctgccccagtccgtgtccaaacaagctgtgggacacgaagagaatgcccagtgttgtaaagctaccagtgacaatgtgattcaatcttcagaaacttgttcgagtcaggactcctctaccactacctctgctttgcctccttcctggacttcaagcacttctgtgtcccaaaagcagaaaagaaagactggcacaaagccaagtacagaaccacagaatgaagccgtcacaaatgttgaatcccaaaacactaacaggaacaactcaactgccttgcagttagctagccgtcctcccgattctgtcacagaggggcccacgtctaaaagagcacatataaagccaaatgctttgctgactaatgttgaccagattgtccaggaaacacagaggctggagttaatctgaagagcaccacttctcctctctctcctgaaaaaatttgccactgatatttttactggataaaattcaaaaatgtttcaattcacaaaggctaattgttgaactggtgtcgtagaagaaattgtctacaggagccaaggtgaaagtctctgatgacggcggaactggctccattagaccatggttcatcctcttttaaaaccaaatttttttttcttctggcctacaagtattttttttttaaaaaagaaaaaaagcctacattggcatcaagttctgtatcaatccatcttacattgccatccatgatttaacagactgtagaatcttgaataatctatatcactttaacaaataaatgttttactatgacagaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:145581 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
by
@meso_cacase at
DBCLS
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