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2024-04-20 04:01:05, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001127667 2747 bp mRNA linear PRI 16-JUN-2013
DEFINITION Homo sapiens gelsolin (GSN), transcript variant 8, mRNA.
ACCESSION NM_001127667
VERSION NM_001127667.1 GI:189083781
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 2747)
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 2747)
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 2747)
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 2747)
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 2747)
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 2747)
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 2747)
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 2747)
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 2747)
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 2747)
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 DA294394.1, DC316173.1,
AK096280.1 and BC017491.1.
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 (8) differs in the 5' UTR and
coding sequence compared to variant 1. The resulting isoform (c)
has a shorter and distinct N-terminus compared to isoform a.
Variants 7 and 8 both encode isoform c.
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##
CDS exon combination :: AK295572.1, AK307859.1 [ECO:0000331]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-39 DA294394.1 1-39
40-607 DC316173.1 1-568
608-2613 AK096280.1 519-2524
2614-2747 BC017491.1 996-1129
FEATURES Location/Qualifiers
source 1..2747
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="9"
/map="9q33"
gene 1..2747
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="gelsolin"
/db_xref="GeneID:2934"
/db_xref="HGNC:4620"
/db_xref="MIM:137350"
exon 1..118
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
exon 119..211
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 129
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:151083385"
variation 165
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:11550200"
exon 212..273
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
misc_feature 235..237
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="upstream in-frame stop codon"
variation 236
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:202184446"
variation 248
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:369491966"
CDS 250..2478
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="isoform c is encoded by transcript variant 8;
brevin; actin-depolymerizing factor"
/codon_start=1
/product="gelsolin isoform c"
/protein_id="NP_001121139.1"
/db_xref="GI:189083782"
/db_xref="CCDS:CCDS48011.1"
/db_xref="GeneID:2934"
/db_xref="HGNC:4620"
/db_xref="MIM:137350"
/translation="
MEKLFCCFPNSMVVEHPEFLKAGKEPGLQIWRVEKFDLVPVPTNLYGDFFTGDAYVILKTVQLRNGNLQYDLHYWLGNECSQDESGAAAIFTVQLDDYLNGRAVQHREVQGFESATFLGYFKSGLKYKKGGVASGFKHVVPNEVVVQRLFQVKGRRVVRATEVPVSWESFNNGDCFILDLGNNIHQWCGSNSNRYERLKATQVSKGIRDNERSGRARVHVSEEGTEPEAMLQVLGPKPALPAGTEDTAKEDAANRKLAKLYKVSNGAGTMSVSLVADENPFAQGALKSEDCFILDHGKDGKIFVWKGKQANTEERKAALKTASDFITKMDYPKQTQVSVLPEGGETPLFKQFFKNWRDPDQTDGLGLSYLSSHIANVERVPFDAATLHTSTAMAAQHGMDDDGTGQKQIWRIEGSNKVPVDPATYGQFYGGDSYIILYNYRHGGRQGQIIYNWQGAQSTQDEVAASAILTAQLDEELGGTPVQSRVVQGKEPAHLMSLFGGKPMIIYKGGTSREGGQTAPASTRLFQVRANSAGATRAVEVLPKAGALNSNDAFVLKTPSAAYLWVGTGASEAEKTGAQELLRVLRAQPVQVAEGSEPDGFWEALGGKAAYRTSPRLKDKKMDAHPPRLFACSNKIGRFVIEEVPGELMQEDLATDDVMLLDTWDQVFVWVGKDSQEEEKTEALTSAKRYIETDPANRDRRTPITVVKQGFEPPSFVGWFLGWDDDYWSVDPLDRAMAELAA
"
misc_feature 304..642
/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(355..360,475..477,493..498,502..510,514..522,
526..531,562..564,568..570)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative actin binding interface [polypeptide
binding]; other site"
/db_xref="CDD:200446"
misc_feature order(406..408,499..501)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200446"
misc_feature 535..537
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 1 Ca binding site [ion binding];
other site"
/db_xref="CDD:200446"
misc_feature 685..954
/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 order(769..771,835..837)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200445"
misc_feature 1012..1314
/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 order(1117..1119,1189..1191)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200448"
misc_feature order(1297..1299,1312..1314)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding site [chemical
binding]; other site"
/db_xref="CDD:200448"
misc_feature 1444..1746
/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(1492..1497,1609..1611,1627..1632,1636..1644,
1648..1656,1660..1665,1696..1698,1702..1704)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative actin binding interface [polypeptide
binding]; other site"
/db_xref="CDD:200449"
misc_feature order(1543..1545,1633..1635)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200449"
misc_feature 1669..1671
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 1 Ca binding site [ion binding];
other site"
/db_xref="CDD:200449"
misc_feature 1717..1719
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding residue [chemical
binding]; other site"
/db_xref="CDD:200449"
misc_feature 1810..2076
/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 1834..1836
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding residue [chemical
binding]; other site"
/db_xref="CDD:200444"
misc_feature order(1900..1905,1969..1971)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200444"
misc_feature 2125..2421
/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(2218..2220,2284..2286)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200447"
variation 258
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:201734352"
exon 274..478
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 276
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:150353588"
variation 289
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:138068754"
STS 296..476
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="GSN"
/db_xref="UniSTS:253982"
variation 301
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143781307"
variation 311
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:115224458"
STS 336..613
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="MARC_23632-23633:1027531903:1"
/db_xref="UniSTS:268728"
variation 343
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373791435"
variation 357
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:149415778"
variation 368
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:149556868"
variation 370
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376961112"
variation 372
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:201642174"
variation 381
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:370368742"
variation 392
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:144219139"
variation 399
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374052802"
variation 408
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200027070"
variation 409
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:148748121"
variation 414
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368210196"
variation 415
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142305374"
variation 438
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201102347"
variation 440
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="g"
/db_xref="dbSNP:368868605"
variation 444
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146365204"
variation 462
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:139689268"
variation 468
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144551136"
exon 479..633
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 483
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373229223"
variation 504
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376627635"
variation 505
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:369305328"
variation 507
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371165744"
variation 509
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:79630438"
variation 513
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:140734150"
variation 514
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:2230287"
variation 523
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:145441439"
variation 525
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:116956127"
variation 553
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146956976"
variation 554
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:138153246"
variation 567
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142155964"
variation 569
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201920706"
variation 585
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373779982"
variation 604
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:367933536"
exon 634..795
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 663
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:180689280"
variation 664
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:41305623"
variation 675
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:186654124"
variation 679
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368197143"
STS 685..794
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="GDB:597556"
/db_xref="UniSTS:158100"
variation 702
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143628574"
variation 712
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:138951454"
variation 713
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:144099356"
variation 716
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141314418"
variation 725
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:150617780"
variation 769
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:121909715"
exon 796..945
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 820
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:11550199"
variation 829
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371175865"
variation 830
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375589943"
variation 879
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146329975"
variation 898
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376060588"
variation 913
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:369788495"
variation 920
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371320840"
variation 941
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:374011467"
exon 946..1035
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 962
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:202067009"
variation 971
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:139723535"
variation 991
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376744130"
variation 1003
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:150568054"
variation 1004
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144375242"
variation 1005
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:377624593"
variation 1012
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:188214536"
variation 1018
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146112795"
variation 1034
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148800857"
exon 1036..1168
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1036
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:113759985"
variation 1062
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201395524"
variation 1123
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142435036"
variation 1137
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374571846"
variation 1138
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:151155909"
exon 1169..1257
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1210..1211
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ac"
/replace="c"
/db_xref="dbSNP:148582809"
variation 1229
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:139028645"
exon 1258..1473
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1263
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:145170518"
variation 1319
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:372681751"
variation 1326
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:377247829"
variation 1329
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:367632035"
variation 1360
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:75508371"
variation 1364
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:370764119"
variation 1378
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375323203"
variation 1380
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201325199"
variation 1383
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371171301"
variation 1395
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200399610"
variation 1396
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:200018246"
variation 1426
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376180600"
variation 1440
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201365952"
variation 1441
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:372218880"
variation 1452
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:147583697"
variation 1453
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142034230"
variation 1462
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376488491"
variation 1472
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368537807"
exon 1474..1607
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1482
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371836872"
variation 1485
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:202240818"
variation 1486
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368079865"
variation 1503
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:111273576"
variation 1507
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:140042418"
variation 1521
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:149375418"
variation 1535
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375227932"
variation 1542
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:2304393"
variation 1570
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:116185403"
variation 1577
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148309276"
variation 1582
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368923816"
exon 1608..1698
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1632
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:141406100"
variation 1681
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:145721476"
exon 1699..1869
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1699
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:370997492"
variation 1702
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:138341672"
variation 1703
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142828669"
variation 1725
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200156774"
variation 1726
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375902120"
variation 1747
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:146125870"
variation 1767
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374982895"
variation 1769
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139832048"
variation 1788
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:199681748"
variation 1795
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:58750568"
variation 1817
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:77681311"
variation 1820
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148410442"
variation 1836
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:145051977"
variation 1837
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:147554026"
variation 1845
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:140414249"
exon 1870..2044
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1876
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:371993530"
variation 1919
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:184844415"
variation 1922
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376326631"
variation 1928
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201307081"
variation 1944
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:144259173"
variation 1945
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:151208452"
variation 1947
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:374022157"
variation 1962
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:73660439"
variation 1972
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368207411"
variation 1976
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:76463933"
variation 1983
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:369846947"
exon 2045..2169
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2064
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139239940"
variation 2067
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:145066574"
variation 2068
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141082919"
variation 2096
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:200319453"
variation 2132
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:9696578"
variation 2161
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371328761"
exon 2170..2247
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2213
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144434647"
variation 2239
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:186351262"
variation 2242
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:377710586"
exon 2248..2308
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2259
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:201752493"
exon 2309..2717
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2327
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142854368"
variation 2338
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375881478"
variation 2339
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143285592"
variation 2347
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:148360076"
variation 2351
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141510612"
variation 2364
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368986042"
variation 2397
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:9102"
variation 2398
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139420096"
STS 2409..2565
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="RH17399"
/db_xref="UniSTS:34031"
variation 2505
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371549019"
variation 2506
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376801564"
STS 2507..2672
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="G10520"
/db_xref="UniSTS:56986"
STS 2508..2698
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="SHGC-132035"
/db_xref="UniSTS:173882"
STS 2510..2637
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="STS-X04412"
/db_xref="UniSTS:16463"
STS 2523..2683
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="D9S1050E"
/db_xref="UniSTS:29132"
STS 2535..2641
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="D9S1953"
/db_xref="UniSTS:63945"
variation 2540
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051142"
variation 2551
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:374518331"
variation 2552
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:143181937"
variation 2566
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051174"
variation 2574..2575
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:147410423"
variation 2575..2576
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:372955427"
variation 2595..2596
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:71694034"
variation 2600..2601
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:377469209"
variation 2600
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:15034"
variation 2603
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:66991108"
variation 2606..2607
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ttt"
/db_xref="dbSNP:369363704"
variation 2606
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:71663525"
variation 2607..2608
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:376569726"
variation 2613..2614
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:71680051"
variation 2615..2616
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="tttt"
/db_xref="dbSNP:71659520"
variation 2618
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:73660440"
variation 2620
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:11550202"
variation 2646..2647
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ag"
/db_xref="dbSNP:71695753"
variation 2665
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051286"
ORIGIN
tcccgcccgcgccctgcccaccccggccgcgcgcaccacaacgcccccgccccgccgcccggaaccagctgagcgcagctggacccagcagccgctgtctccagtgccgcagcagcaggtagtgctcatagctctctttgtccagtgcttcggccttggtcccagcgccttcccacggagcagcactcttcaccctgcacagccttgttagatacagcgctaggaaaaggggagtaattcaggtctagaatggaaaaactgttttgttgctttcccaacagcatggtggtggaacaccccgagttcctcaaggcagggaaggagcctggcctgcagatctggcgtgtggagaagttcgatctggtgcccgtgcccaccaacctttatggagacttcttcacgggcgacgcctacgtcatcctgaagacagtgcagctgaggaacggaaatctgcagtatgacctccactactggctgggcaatgagtgcagccaggatgagagcggggcggccgccatctttaccgtgcagctggatgactacctgaacggccgggccgtgcagcaccgtgaggtccagggcttcgagtcggccaccttcctaggctacttcaagtctggcctgaagtacaagaaaggaggtgtggcatcaggattcaagcacgtggtacccaacgaggtggtggtgcagagactcttccaggtcaaagggcggcgtgtggtccgtgccaccgaggtacctgtgtcctgggagagcttcaacaatggcgactgcttcatcctggacctgggcaacaacatccaccagtggtgtggttccaacagcaatcggtatgaaagactgaaggccacacaggtgtccaagggcatccgggacaacgagcggagtggccgggcccgagtgcacgtgtctgaggagggcactgagcccgaggcgatgctccaggtgctgggccccaagccggctctgcctgcaggtaccgaggacaccgccaaggaggatgcggccaaccgcaagctggccaagctctacaaggtctccaatggtgcagggaccatgtccgtctccctcgtggctgatgagaaccccttcgcccagggggccctgaagtcagaggactgcttcatcctggaccacggcaaagatgggaaaatctttgtctggaaaggcaagcaggcaaacacggaggagaggaaggctgccctcaaaacagcctctgacttcatcaccaagatggactaccccaagcagactcaggtctcggtccttcctgagggcggtgagaccccactgttcaagcagttcttcaagaactggcgggacccagaccagacagatggcctgggcttgtcctacctttccagccatatcgccaacgtggagcgggtgcccttcgacgccgccaccctgcacacctccactgccatggccgcccagcacggcatggatgacgatggcacaggccagaaacagatctggagaatcgaaggttccaacaaggtgcccgtggaccctgccacatatggacagttctatggaggcgacagctacatcattctgtacaactaccgccatggtggccgccaggggcagataatctataactggcagggtgcccagtctacccaggatgaggtcgctgcatctgccatcctgactgctcagctggatgaggagctgggaggtacccctgtccagagccgtgtggtccaaggcaaggagcccgcccacctcatgagcctgtttggtgggaagcccatgatcatctacaagggcggcacctcccgcgagggcgggcagacagcccctgccagcacccgcctcttccaggtccgcgccaacagcgctggagccacccgggctgttgaggtattgcctaaggctggtgcactgaactccaacgatgcctttgttctgaaaaccccctcagccgcctacctgtgggtgggtacaggagccagcgaggcagagaagacgggggcccaggagctgctcagggtgctgcgggcccaacctgtgcaggtggcagaaggcagcgagccagatggcttctgggaggccctgggcgggaaggctgcctaccgcacatccccacggctgaaggacaagaagatggatgcccatcctcctcgcctctttgcctgctccaacaagattggacgttttgtgatcgaagaggttcctggtgagctcatgcaggaagacctggcaacggatgacgtcatgcttctggacacctgggaccaggtctttgtctgggttggaaaggattctcaagaagaagaaaagacagaagccttgacttctgctaagcggtacatcgagacggacccagccaatcgggatcggcggacgcccatcaccgtggtgaagcaaggctttgagcctccctcctttgtgggctggttccttggctgggatgatgattactggtctgtggaccccttggacagggccatggctgagctggctgcctgaggaggggcagggcccacccatgtcaccggtcagtgccttttggaactgtccttccctcaaagaggccttagagcgagcagagcagctctgctatgagtgtgtgtgtgtgtgtgtgttgtttcttttttttttttttacagtatccaaaaatagccctgcaaaaattcagagtccttgcaaaattgtctaaaatgtcagtgtttgggaaattaaatccaataaaaacattttgaagtgtgaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
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
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