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2024-04-25 20:58:28, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_000177 2719 bp mRNA linear PRI 16-JUN-2013
DEFINITION Homo sapiens gelsolin (GSN), transcript variant 1, mRNA.
ACCESSION NM_000177
VERSION NM_000177.4 GI:89276753
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 2719)
AUTHORS DiNubile,M.J.
TITLE Plasma gelsolin levels in the diagnosis, prognosis, and treatment
of lung complications of prematurity
JOURNAL Am. J. Respir. Crit. Care Med. 186 (11), 1195-1196 (2012)
PUBMED 23204381
REMARK GeneRIF: Circulating gelsolin level is an important biomarker in
preterm infants, developing bronchopulmonary dysplasia.
REFERENCE 2 (bases 1 to 2719)
AUTHORS Li,G.H., Arora,P.D., Chen,Y., McCulloch,C.A. and Liu,P.
TITLE Multifunctional roles of gelsolin in health and diseases
JOURNAL Med Res Rev 32 (5), 999-1025 (2012)
PUBMED 22886630
REMARK GeneRIF: REVIEW: functions of the plasma and cytoplasmic forms of
gelsolin, and their manifold impacts on cancer, apoptosis,
infection and inflammation, cardiac injury, pulmonary diseases, and
aging
Review article
REFERENCE 3 (bases 1 to 2719)
AUTHORS Shirkoohi,R., Fujita,H., Darmanin,S. and Takimoto,M.
TITLE Gelsolin induces promonocytic leukemia differentiation accompanied
by upregulation of p21CIP1
JOURNAL Asian Pac. J. Cancer Prev. 13 (9), 4827-4834 (2012)
PUBMED 23167427
REMARK GeneRIF: Our work confirms that the cytoskeletal tumor suppressor,
gelsolin, can induce monocytic myeloid differentiation in addition
to growth retardation in the human monocytic cell line U937.
REFERENCE 4 (bases 1 to 2719)
AUTHORS Mazumdar,B., Meyer,K. and Ray,R.
TITLE N-terminal region of gelsolin induces apoptosis of activated
hepatic stellate cells by a caspase-dependent mechanism
JOURNAL PLoS ONE 7 (8), E44461 (2012)
PUBMED 22952982
REMARK GeneRIF: Gelsolin modulation of cell death involved upregulation of
TRAIL-R1 and TRAIL-R2, and involved caspase 3 activation by
extrinsic pathway.
REFERENCE 5 (bases 1 to 2719)
AUTHORS Zhuo,J., Tan,E.H., Yan,B., Tochhawng,L., Jayapal,M., Koh,S.,
Tay,H.K., Maciver,S.K., Hooi,S.C., Salto-Tellez,M., Kumar,A.P.,
Goh,Y.C., Lim,Y.C. and Yap,C.T.
TITLE Gelsolin induces colorectal tumor cell invasion via modulation of
the urokinase-type plasminogen activator cascade
JOURNAL PLoS ONE 7 (8), E43594 (2012)
PUBMED 22927998
REMARK GeneRIF: novel functions of gelsolin in colorectal tumor cell
invasion through its modulation of the uPA/uPAR cascade
REFERENCE 6 (bases 1 to 2719)
AUTHORS de la Chapelle,A., Tolvanen,R., Boysen,G., Santavy,J.,
Bleeker-Wagemakers,L., Maury,C.P. and Kere,J.
TITLE Gelsolin-derived familial amyloidosis caused by asparagine or
tyrosine substitution for aspartic acid at residue 187
JOURNAL Nat. Genet. 2 (2), 157-160 (1992)
PUBMED 1338910
REFERENCE 7 (bases 1 to 2719)
AUTHORS Yu,F.X., Sun,H.Q., Janmey,P.A. and Yin,H.L.
TITLE Identification of a polyphosphoinositide-binding sequence in an
actin monomer-binding domain of gelsolin
JOURNAL J. Biol. Chem. 267 (21), 14616-14621 (1992)
PUBMED 1321812
REFERENCE 8 (bases 1 to 2719)
AUTHORS de la Chapelle,A., Kere,J., Sack,G.H. Jr., Tolvanen,R. and
Maury,C.P.
TITLE Familial amyloidosis, Finnish type: G654----a mutation of the
gelsolin gene in Finnish families and an unrelated American family
JOURNAL Genomics 13 (3), 898-901 (1992)
PUBMED 1322359
REFERENCE 9 (bases 1 to 2719)
AUTHORS Paunio,T., Kiuru,S., Hongell,V., Mustonen,E., Syvanen,A.C.,
Bengstrom,M., Palo,J. and Peltonen,L.
TITLE Solid-phase minisequencing test reveals Asp187----Asn (G654----A)
mutation of gelsolin in all affected individuals with Finnish type
of familial amyloidosis
JOURNAL Genomics 13 (1), 237-239 (1992)
PUBMED 1315718
REFERENCE 10 (bases 1 to 2719)
AUTHORS Haltia,M., Levy,E., Meretoja,J., Fernandez-Madrid,I., Koivunen,O.
and Frangione,B.
TITLE Gelsolin gene mutation--at codon 187--in familial amyloidosis,
Finnish: DNA-diagnostic assay
JOURNAL Am. J. Med. Genet. 42 (3), 357-359 (1992)
PUBMED 1311149
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DB250757.1 and BC026033.1.
On Mar 9, 2006 this sequence version replaced gi:38016941.
Summary: The protein encoded by this gene binds to the 'plus' ends
of actin monomers and filaments to prevent monomer exchange. The
encoded calcium-regulated protein functions in both assembly and
disassembly of actin filaments. Defects in this gene are a cause of
familial amyloidosis Finnish type (FAF). Multiple transcript
variants encoding several different isoforms have been found for
this gene. [provided by RefSeq, Jul 2008].
Transcript Variant: This variant (1) represents the longest isoform
(a).
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 :: BC026033.1, AK315494.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-56 DB250757.1 1-56
57-2719 BC026033.1 1-2663
FEATURES Location/Qualifiers
source 1..2719
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="9"
/map="9q33"
gene 1..2719
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="gelsolin"
/db_xref="GeneID:2934"
/db_xref="HGNC:4620"
/db_xref="HPRD:00674"
/db_xref="MIM:137350"
exon 1..205
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
CDS 62..2410
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="isoform a precursor is encoded by transcript
variant 1; brevin; actin-depolymerizing factor"
/codon_start=1
/product="gelsolin isoform a precursor"
/protein_id="NP_000168.1"
/db_xref="GI:4504165"
/db_xref="CCDS:CCDS6828.1"
/db_xref="GeneID:2934"
/db_xref="HGNC:4620"
/db_xref="HPRD:00674"
/db_xref="MIM:137350"
/translation="
MAPHRPAPALLCALSLALCALSLPVRAATASRGASQAGAPQGRVPEARPNSMVVEHPEFLKAGKEPGLQIWRVEKFDLVPVPTNLYGDFFTGDAYVILKTVQLRNGNLQYDLHYWLGNECSQDESGAAAIFTVQLDDYLNGRAVQHREVQGFESATFLGYFKSGLKYKKGGVASGFKHVVPNEVVVQRLFQVKGRRVVRATEVPVSWESFNNGDCFILDLGNNIHQWCGSNSNRYERLKATQVSKGIRDNERSGRARVHVSEEGTEPEAMLQVLGPKPALPAGTEDTAKEDAANRKLAKLYKVSNGAGTMSVSLVADENPFAQGALKSEDCFILDHGKDGKIFVWKGKQANTEERKAALKTASDFITKMDYPKQTQVSVLPEGGETPLFKQFFKNWRDPDQTDGLGLSYLSSHIANVERVPFDAATLHTSTAMAAQHGMDDDGTGQKQIWRIEGSNKVPVDPATYGQFYGGDSYIILYNYRHGGRQGQIIYNWQGAQSTQDEVAASAILTAQLDEELGGTPVQSRVVQGKEPAHLMSLFGGKPMIIYKGGTSREGGQTAPASTRLFQVRANSAGATRAVEVLPKAGALNSNDAFVLKTPSAAYLWVGTGASEAEKTGAQELLRVLRAQPVQVAEGSEPDGFWEALGGKAAYRTSPRLKDKKMDAHPPRLFACSNKIGRFVIEEVPGELMQEDLATDDVMLLDTWDQVFVWVGKDSQEEEKTEALTSAKRYIETDPANRDRRTPITVVKQGFEPPSFVGWFLGWDDDYWSVDPLDRAMAELAA
"
sig_peptide 62..142
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 143..2407
/gene="GSN"
/gene_synonym="ADF; AGEL"
/product="gelsolin isoform a"
misc_feature 218..589
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P06396.1);
Region: Actin-severing (Potential)"
misc_feature 236..574
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="Gelsolin sub-domain 1-like domain found in
gelsolin, severin, villin, and related proteins; Region:
gelsolin_S1_like; cd11290"
/db_xref="CDD:200446"
misc_feature order(287..292,407..409,425..430,434..442,446..454,
458..463,494..496,500..502)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative actin binding interface [polypeptide
binding]; other site"
/db_xref="CDD:200446"
misc_feature 317..319
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphotyrosine, by SRC, in vitro; propagated from
UniProtKB/Swiss-Prot (P06396.1); phosphorylation site"
misc_feature order(338..340,431..433)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200446"
misc_feature 428..439
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P06396.1);
Region: Actin-actin interfilament contact point"
misc_feature 467..469
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 1 Ca binding site [ion binding];
other site"
/db_xref="CDD:200446"
misc_feature 545..568
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P06396.1);
Region: Polyphosphoinositide binding (By similarity)"
misc_feature 617..886
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="Gelsolin sub-domain 2-like domain found in
gelsolin, severin, villin, and related proteins; Region:
gelsolin_S2_like; cd11289"
/db_xref="CDD:200445"
misc_feature 623..649
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P06396.1);
Region: Polyphosphoinositide binding (By similarity)"
misc_feature 653..775
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P06396.1);
Region: Gelsolin-like 2"
misc_feature order(701..703,767..769)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200445"
misc_feature order(704..706,743..745)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="disulfide bridge bond"
misc_feature 944..1246
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="Gelsolin sub-domain 3-like domain found in
gelsolin, severin, villin, and related proteins; Region:
gelsolin_S3_like; cd11292"
/db_xref="CDD:200448"
misc_feature 1001..1129
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P06396.1);
Region: Gelsolin-like 3"
misc_feature order(1049..1051,1121..1123)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200448"
misc_feature order(1229..1231,1244..1246)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding site [chemical
binding]; other site"
/db_xref="CDD:200448"
misc_feature 1268..1270
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="proteolytic cleavage site; modified site"
/db_xref="HPRD:02799"
misc_feature 1271..1273
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="myristoylation site"
misc_feature 1286..1288
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphotyrosine, by SRC, in vitro; propagated from
UniProtKB/Swiss-Prot (P06396.1); phosphorylation site"
misc_feature 1361..2407
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P06396.1);
Region: Actin-binding, Ca-sensitive (Potential)"
misc_feature 1376..1678
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="Gelsolin sub-domain 4-like domain found in
gelsolin, severin, villin, and related proteins; Region:
gelsolin_S4_like; cd11293"
/db_xref="CDD:200449"
misc_feature order(1424..1429,1541..1543,1559..1564,1568..1576,
1580..1588,1592..1597,1628..1630,1634..1636)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative actin binding interface [polypeptide
binding]; other site"
/db_xref="CDD:200449"
misc_feature 1454..1456
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphotyrosine, by SRC; propagated from
UniProtKB/Swiss-Prot (P06396.1); phosphorylation site"
misc_feature order(1475..1477,1565..1567)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200449"
misc_feature 1601..1603
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 1 Ca binding site [ion binding];
other site"
/db_xref="CDD:200449"
misc_feature 1649..1651
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding residue [chemical
binding]; other site"
/db_xref="CDD:200449"
misc_feature 1742..2008
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="Gelsolin sub-domain 5-like domain found in
gelsolin, severin, villin, and related proteins; Region:
gelsolin_S5_like; cd11288"
/db_xref="CDD:200444"
misc_feature 1766..1768
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding residue [chemical
binding]; other site"
/db_xref="CDD:200444"
misc_feature order(1832..1837,1901..1903)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200444"
misc_feature 1868..1870
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphotyrosine, by SRC, in vitro; propagated from
UniProtKB/Swiss-Prot (P06396.1); phosphorylation site"
misc_feature 2012..2014
/gene="GSN"
/gene_synonym="ADF; AGEL"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphotyrosine, by SRC, in vitro; propagated from
UniProtKB/Swiss-Prot (P06396.1); phosphorylation site"
misc_feature 2057..2353
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="Gelsolin sub-domain 6-like domain found in
gelsolin, severin, villin, and related proteins; Region:
gelsolin_S6_like; cd11291"
/db_xref="CDD:200447"
misc_feature order(2150..2152,2216..2218)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200447"
variation 163
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:369326886"
variation 196
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:372837702"
variation 201
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376281622"
exon 206..410
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 208
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:150353588"
variation 221
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:138068754"
STS 228..408
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="GSN"
/db_xref="UniSTS:253982"
variation 233
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143781307"
variation 243
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:115224458"
STS 268..545
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="MARC_23632-23633:1027531903:1"
/db_xref="UniSTS:268728"
variation 275
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373791435"
variation 289
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:149415778"
variation 300
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:149556868"
variation 302
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376961112"
variation 304
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:201642174"
variation 313
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:370368742"
variation 324
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:144219139"
variation 331
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374052802"
variation 340
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200027070"
variation 341
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:148748121"
variation 346
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368210196"
variation 347
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142305374"
variation 370
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201102347"
variation 372
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="g"
/db_xref="dbSNP:368868605"
variation 376
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146365204"
variation 394
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:139689268"
variation 400
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144551136"
exon 411..565
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 415
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373229223"
variation 436
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376627635"
variation 437
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:369305328"
variation 439
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371165744"
variation 441
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:79630438"
variation 445
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:140734150"
variation 446
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:2230287"
variation 455
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:145441439"
variation 457
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:116956127"
variation 485
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146956976"
variation 486
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:138153246"
variation 499
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142155964"
variation 501
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201920706"
variation 517
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373779982"
variation 536
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:367933536"
exon 566..727
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 595
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:180689280"
variation 596
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:41305623"
variation 607
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:186654124"
variation 611
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368197143"
STS 617..726
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="GDB:597556"
/db_xref="UniSTS:158100"
variation 634
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143628574"
variation 644
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:138951454"
variation 645
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:144099356"
variation 648
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141314418"
variation 657
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:150617780"
variation 701
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:121909715"
exon 728..877
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 752
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:11550199"
variation 761
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371175865"
variation 762
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375589943"
variation 811
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146329975"
variation 830
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376060588"
variation 845
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:369788495"
variation 852
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371320840"
variation 873
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:374011467"
exon 878..967
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 894
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:202067009"
variation 903
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:139723535"
variation 923
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376744130"
variation 935
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:150568054"
variation 936
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144375242"
variation 937
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:377624593"
variation 944
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:188214536"
variation 950
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146112795"
variation 966
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148800857"
exon 968..1100
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 968
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:113759985"
variation 994
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201395524"
variation 1055
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142435036"
variation 1069
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374571846"
variation 1070
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:151155909"
exon 1101..1189
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1142..1143
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ac"
/replace="c"
/db_xref="dbSNP:148582809"
variation 1161
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:139028645"
exon 1190..1405
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1195
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:145170518"
variation 1251
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:372681751"
variation 1258
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:377247829"
variation 1261
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:367632035"
variation 1292
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:75508371"
variation 1296
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:370764119"
variation 1310
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375323203"
variation 1312
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201325199"
variation 1315
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371171301"
variation 1327
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200399610"
variation 1328
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:200018246"
variation 1358
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376180600"
variation 1372
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201365952"
variation 1373
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:372218880"
variation 1384
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:147583697"
variation 1385
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142034230"
variation 1394
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376488491"
variation 1404
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368537807"
exon 1406..1539
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1414
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371836872"
variation 1417
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:202240818"
variation 1418
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368079865"
variation 1435
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:111273576"
variation 1439
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:140042418"
variation 1453
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:149375418"
variation 1467
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375227932"
variation 1474
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:2304393"
variation 1502
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:116185403"
variation 1509
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148309276"
variation 1514
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368923816"
exon 1540..1630
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1564
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:141406100"
variation 1613
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:145721476"
exon 1631..1801
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1631
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:370997492"
variation 1634
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:138341672"
variation 1635
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142828669"
variation 1657
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200156774"
variation 1658
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375902120"
variation 1679
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:146125870"
variation 1699
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374982895"
variation 1701
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139832048"
variation 1720
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:199681748"
variation 1727
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:58750568"
variation 1749
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:77681311"
variation 1752
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148410442"
variation 1768
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:145051977"
variation 1769
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:147554026"
variation 1777
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:140414249"
exon 1802..1976
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1808
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:371993530"
variation 1851
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:184844415"
variation 1854
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376326631"
variation 1860
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201307081"
variation 1876
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:144259173"
variation 1877
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:151208452"
variation 1879
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:374022157"
variation 1894
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:73660439"
variation 1904
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368207411"
variation 1908
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:76463933"
variation 1915
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:369846947"
exon 1977..2101
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1996
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139239940"
variation 1999
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:145066574"
variation 2000
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141082919"
variation 2028
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:200319453"
variation 2064
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:9696578"
variation 2093
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371328761"
exon 2102..2179
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2145
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144434647"
variation 2171
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:186351262"
variation 2174
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:377710586"
exon 2180..2240
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2191
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:201752493"
exon 2241..2649
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2259
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142854368"
variation 2270
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375881478"
variation 2271
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143285592"
variation 2279
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:148360076"
variation 2283
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141510612"
variation 2296
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368986042"
variation 2329
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:9102"
variation 2330
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139420096"
STS 2341..2497
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="RH17399"
/db_xref="UniSTS:34031"
variation 2437
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371549019"
variation 2438
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376801564"
STS 2439..2604
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="G10520"
/db_xref="UniSTS:56986"
STS 2440..2630
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="SHGC-132035"
/db_xref="UniSTS:173882"
STS 2442..2569
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="STS-X04412"
/db_xref="UniSTS:16463"
STS 2455..2615
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="D9S1050E"
/db_xref="UniSTS:29132"
STS 2467..2573
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="D9S1953"
/db_xref="UniSTS:63945"
variation 2472
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051142"
variation 2483
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:374518331"
variation 2484
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:143181937"
variation 2498
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051174"
variation 2506..2507
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:147410423"
variation 2507..2508
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:372955427"
variation 2527..2528
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:71694034"
variation 2532..2533
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:377469209"
variation 2532
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:15034"
variation 2535
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:66991108"
variation 2538..2539
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ttt"
/db_xref="dbSNP:369363704"
variation 2538
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:71663525"
variation 2539..2540
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:376569726"
variation 2545..2546
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:71680051"
variation 2547..2548
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="tttt"
/db_xref="dbSNP:71659520"
variation 2550
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:73660440"
variation 2552
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:11550202"
variation 2578..2579
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ag"
/db_xref="dbSNP:71695753"
variation 2597
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051286"
ORIGIN
acttaaggtcggcgacccgaggccgcggctgccgactgggtcccctgccgctgtcgccaccatggctccgcaccgccccgcgcccgcgctgctttgcgcgctgtccctggcgctgtgcgcgctgtcgctgcccgtccgcgcggccactgcgtcgcggggggcgtcccaggcgggggcgccccaggggcgggtgcccgaggcgcggcccaacagcatggtggtggaacaccccgagttcctcaaggcagggaaggagcctggcctgcagatctggcgtgtggagaagttcgatctggtgcccgtgcccaccaacctttatggagacttcttcacgggcgacgcctacgtcatcctgaagacagtgcagctgaggaacggaaatctgcagtatgacctccactactggctgggcaatgagtgcagccaggatgagagcggggcggccgccatctttaccgtgcagctggatgactacctgaacggccgggccgtgcagcaccgtgaggtccagggcttcgagtcggccaccttcctaggctacttcaagtctggcctgaagtacaagaaaggaggtgtggcatcaggattcaagcacgtggtacccaacgaggtggtggtgcagagactcttccaggtcaaagggcggcgtgtggtccgtgccaccgaggtacctgtgtcctgggagagcttcaacaatggcgactgcttcatcctggacctgggcaacaacatccaccagtggtgtggttccaacagcaatcggtatgaaagactgaaggccacacaggtgtccaagggcatccgggacaacgagcggagtggccgggcccgagtgcacgtgtctgaggagggcactgagcccgaggcgatgctccaggtgctgggccccaagccggctctgcctgcaggtaccgaggacaccgccaaggaggatgcggccaaccgcaagctggccaagctctacaaggtctccaatggtgcagggaccatgtccgtctccctcgtggctgatgagaaccccttcgcccagggggccctgaagtcagaggactgcttcatcctggaccacggcaaagatgggaaaatctttgtctggaaaggcaagcaggcaaacacggaggagaggaaggctgccctcaaaacagcctctgacttcatcaccaagatggactaccccaagcagactcaggtctcggtccttcctgagggcggtgagaccccactgttcaagcagttcttcaagaactggcgggacccagaccagacagatggcctgggcttgtcctacctttccagccatatcgccaacgtggagcgggtgcccttcgacgccgccaccctgcacacctccactgccatggccgcccagcacggcatggatgacgatggcacaggccagaaacagatctggagaatcgaaggttccaacaaggtgcccgtggaccctgccacatatggacagttctatggaggcgacagctacatcattctgtacaactaccgccatggtggccgccaggggcagataatctataactggcagggtgcccagtctacccaggatgaggtcgctgcatctgccatcctgactgctcagctggatgaggagctgggaggtacccctgtccagagccgtgtggtccaaggcaaggagcccgcccacctcatgagcctgtttggtgggaagcccatgatcatctacaagggcggcacctcccgcgagggcgggcagacagcccctgccagcacccgcctcttccaggtccgcgccaacagcgctggagccacccgggctgttgaggtattgcctaaggctggtgcactgaactccaacgatgcctttgttctgaaaaccccctcagccgcctacctgtgggtgggtacaggagccagcgaggcagagaagacgggggcccaggagctgctcagggtgctgcgggcccaacctgtgcaggtggcagaaggcagcgagccagatggcttctgggaggccctgggcgggaaggctgcctaccgcacatccccacggctgaaggacaagaagatggatgcccatcctcctcgcctctttgcctgctccaacaagattggacgttttgtgatcgaagaggttcctggtgagctcatgcaggaagacctggcaacggatgacgtcatgcttctggacacctgggaccaggtctttgtctgggttggaaaggattctcaagaagaagaaaagacagaagccttgacttctgctaagcggtacatcgagacggacccagccaatcgggatcggcggacgcccatcaccgtggtgaagcaaggctttgagcctccctcctttgtgggctggttccttggctgggatgatgattactggtctgtggaccccttggacagggccatggctgagctggctgcctgaggaggggcagggcccacccatgtcaccggtcagtgccttttggaactgtccttccctcaaagaggccttagagcgagcagagcagctctgctatgagtgtgtgtgtgtgtgtgtgttgtttcttttttttttttttacagtatccaaaaatagccctgcaaaaattcagagtccttgcaaaattgtctaaaatgtcagtgtttgggaaattaaatccaataaaaacattttgaagtgtgaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:2934 -> Molecular function: GO:0003779 [actin binding] evidence: IEA
GeneID:2934 -> Molecular function: GO:0005509 [calcium ion binding] evidence: TAS
GeneID:2934 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:2934 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
GeneID:2934 -> Biological process: GO:0006921 [cellular component disassembly involved in execution phase of apoptosis] evidence: TAS
GeneID:2934 -> Biological process: GO:0007568 [aging] evidence: IEA
GeneID:2934 -> Biological process: GO:0014003 [oligodendrocyte development] evidence: IEA
GeneID:2934 -> Biological process: GO:0016192 [vesicle-mediated transport] evidence: IEA
GeneID:2934 -> Biological process: GO:0030041 [actin filament polymerization] evidence: IDA
GeneID:2934 -> Biological process: GO:0030041 [actin filament polymerization] evidence: ISS
GeneID:2934 -> Biological process: GO:0030155 [regulation of cell adhesion] evidence: IEA
GeneID:2934 -> Biological process: GO:0042246 [tissue regeneration] evidence: IEA
GeneID:2934 -> Biological process: GO:0045471 [response to ethanol] evidence: IEA
GeneID:2934 -> Biological process: GO:0048015 [phosphatidylinositol-mediated signaling] evidence: IEA
GeneID:2934 -> Biological process: GO:0051014 [actin filament severing] evidence: IDA
GeneID:2934 -> Biological process: GO:0051014 [actin filament severing] evidence: ISS
GeneID:2934 -> Biological process: GO:0051016 [barbed-end actin filament capping] evidence: TAS
GeneID:2934 -> Biological process: GO:0051593 [response to folic acid] evidence: IEA
GeneID:2934 -> Biological process: GO:0060271 [cilium morphogenesis] evidence: IMP
GeneID:2934 -> Biological process: GO:0071276 [cellular response to cadmium ion] evidence: IEA
GeneID:2934 -> Cellular component: GO:0001726 [ruffle] evidence: IEA
GeneID:2934 -> Cellular component: GO:0005576 [extracellular region] evidence: IDA
GeneID:2934 -> Cellular component: GO:0005576 [extracellular region] evidence: ISS
GeneID:2934 -> Cellular component: GO:0005576 [extracellular region] evidence: NAS
GeneID:2934 -> Cellular component: GO:0005576 [extracellular region] evidence: TAS
GeneID:2934 -> Cellular component: GO:0005615 [extracellular space] evidence: IEA
GeneID:2934 -> Cellular component: GO:0005829 [cytosol] evidence: IDA
GeneID:2934 -> Cellular component: GO:0005829 [cytosol] evidence: ISS
GeneID:2934 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:2934 -> Cellular component: GO:0015629 [actin cytoskeleton] evidence: IEA
GeneID:2934 -> Cellular component: GO:0030027 [lamellipodium] evidence: IEA
GeneID:2934 -> Cellular component: GO:0043234 [protein complex] evidence: IEA
GeneID:2934 -> Cellular component: GO:0048471 [perinuclear region of cytoplasm] evidence: IEA
GeneID:2934 -> Cellular component: GO:0070062 [extracellular vesicular exosome] evidence: IDA
by
@meso_cacase at
DBCLS
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