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2024-04-26 09:13:38, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001127666 2756 bp mRNA linear PRI 16-JUN-2013
DEFINITION Homo sapiens gelsolin (GSN), transcript variant 7, mRNA.
ACCESSION NM_001127666
VERSION NM_001127666.1 GI:189083779
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 2756)
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 2756)
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 2756)
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 2756)
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 2756)
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 2756)
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 2756)
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 2756)
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 2756)
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 2756)
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, DC341948.1,
AK096280.1 and BC017491.1.
This sequence is a reference standard in the RefSeqGene project.
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 (7) 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##
Transcript exon combination :: AK295572.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025083 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-34 DA294394.1 1-34
35-608 DC341948.1 1-574
609-2622 AK096280.1 511-2524
2623-2756 BC017491.1 996-1129
FEATURES Location/Qualifiers
source 1..2756
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="9"
/map="9q33"
gene 1..2756
/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..282
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
misc_feature 244..246
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="upstream in-frame stop codon"
variation 245
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:202184446"
variation 257
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:369491966"
CDS 259..2487
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="isoform c is encoded by transcript variant 7;
brevin; actin-depolymerizing factor"
/codon_start=1
/product="gelsolin isoform c"
/protein_id="NP_001121138.1"
/db_xref="GI:189083780"
/db_xref="CCDS:CCDS48011.1"
/db_xref="GeneID:2934"
/db_xref="HGNC:4620"
/db_xref="MIM:137350"
/translation="
MEKLFCCFPNSMVVEHPEFLKAGKEPGLQIWRVEKFDLVPVPTNLYGDFFTGDAYVILKTVQLRNGNLQYDLHYWLGNECSQDESGAAAIFTVQLDDYLNGRAVQHREVQGFESATFLGYFKSGLKYKKGGVASGFKHVVPNEVVVQRLFQVKGRRVVRATEVPVSWESFNNGDCFILDLGNNIHQWCGSNSNRYERLKATQVSKGIRDNERSGRARVHVSEEGTEPEAMLQVLGPKPALPAGTEDTAKEDAANRKLAKLYKVSNGAGTMSVSLVADENPFAQGALKSEDCFILDHGKDGKIFVWKGKQANTEERKAALKTASDFITKMDYPKQTQVSVLPEGGETPLFKQFFKNWRDPDQTDGLGLSYLSSHIANVERVPFDAATLHTSTAMAAQHGMDDDGTGQKQIWRIEGSNKVPVDPATYGQFYGGDSYIILYNYRHGGRQGQIIYNWQGAQSTQDEVAASAILTAQLDEELGGTPVQSRVVQGKEPAHLMSLFGGKPMIIYKGGTSREGGQTAPASTRLFQVRANSAGATRAVEVLPKAGALNSNDAFVLKTPSAAYLWVGTGASEAEKTGAQELLRVLRAQPVQVAEGSEPDGFWEALGGKAAYRTSPRLKDKKMDAHPPRLFACSNKIGRFVIEEVPGELMQEDLATDDVMLLDTWDQVFVWVGKDSQEEEKTEALTSAKRYIETDPANRDRRTPITVVKQGFEPPSFVGWFLGWDDDYWSVDPLDRAMAELAA
"
misc_feature 313..651
/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(364..369,484..486,502..507,511..519,523..531,
535..540,571..573,577..579)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative actin binding interface [polypeptide
binding]; other site"
/db_xref="CDD:200446"
misc_feature order(415..417,508..510)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200446"
misc_feature 544..546
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 1 Ca binding site [ion binding];
other site"
/db_xref="CDD:200446"
misc_feature 694..963
/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(778..780,844..846)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200445"
misc_feature 1021..1323
/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(1126..1128,1198..1200)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200448"
misc_feature order(1306..1308,1321..1323)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding site [chemical
binding]; other site"
/db_xref="CDD:200448"
misc_feature 1453..1755
/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(1501..1506,1618..1620,1636..1641,1645..1653,
1657..1665,1669..1674,1705..1707,1711..1713)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative actin binding interface [polypeptide
binding]; other site"
/db_xref="CDD:200449"
misc_feature order(1552..1554,1642..1644)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200449"
misc_feature 1678..1680
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 1 Ca binding site [ion binding];
other site"
/db_xref="CDD:200449"
misc_feature 1726..1728
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding residue [chemical
binding]; other site"
/db_xref="CDD:200449"
misc_feature 1819..2085
/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 1843..1845
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative nucleotide binding residue [chemical
binding]; other site"
/db_xref="CDD:200444"
misc_feature order(1909..1914,1978..1980)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200444"
misc_feature 2134..2430
/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(2227..2229,2293..2295)
/gene="GSN"
/gene_synonym="ADF; AGEL"
/note="putative type 2 Ca binding site [ion binding];
other site"
/db_xref="CDD:200447"
variation 267
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:201734352"
exon 283..487
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 285
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:150353588"
variation 298
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:138068754"
STS 305..485
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="GSN"
/db_xref="UniSTS:253982"
variation 310
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143781307"
variation 320
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:115224458"
STS 345..622
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="MARC_23632-23633:1027531903:1"
/db_xref="UniSTS:268728"
variation 352
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373791435"
variation 366
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:149415778"
variation 377
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:149556868"
variation 379
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376961112"
variation 381
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:201642174"
variation 390
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:370368742"
variation 401
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:144219139"
variation 408
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374052802"
variation 417
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200027070"
variation 418
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:148748121"
variation 423
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368210196"
variation 424
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142305374"
variation 447
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201102347"
variation 449
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="g"
/db_xref="dbSNP:368868605"
variation 453
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146365204"
variation 471
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:139689268"
variation 477
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144551136"
exon 488..642
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 492
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373229223"
variation 513
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376627635"
variation 514
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:369305328"
variation 516
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371165744"
variation 518
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:79630438"
variation 522
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:140734150"
variation 523
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:2230287"
variation 532
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:145441439"
variation 534
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:116956127"
variation 562
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146956976"
variation 563
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:138153246"
variation 576
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142155964"
variation 578
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201920706"
variation 594
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:373779982"
variation 613
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:367933536"
exon 643..804
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 672
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:180689280"
variation 673
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:41305623"
variation 684
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:186654124"
variation 688
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368197143"
STS 694..803
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="GDB:597556"
/db_xref="UniSTS:158100"
variation 711
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143628574"
variation 721
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:138951454"
variation 722
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:144099356"
variation 725
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141314418"
variation 734
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:150617780"
variation 778
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:121909715"
exon 805..954
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 829
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:11550199"
variation 838
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371175865"
variation 839
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375589943"
variation 888
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146329975"
variation 907
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376060588"
variation 922
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:369788495"
variation 929
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371320840"
variation 950
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:374011467"
exon 955..1044
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 971
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:202067009"
variation 980
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:139723535"
variation 1000
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376744130"
variation 1012
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:150568054"
variation 1013
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144375242"
variation 1014
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:377624593"
variation 1021
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:188214536"
variation 1027
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:146112795"
variation 1043
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148800857"
exon 1045..1177
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1045
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:113759985"
variation 1071
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201395524"
variation 1132
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142435036"
variation 1146
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374571846"
variation 1147
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:151155909"
exon 1178..1266
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1219..1220
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ac"
/replace="c"
/db_xref="dbSNP:148582809"
variation 1238
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:139028645"
exon 1267..1482
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1272
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:145170518"
variation 1328
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:372681751"
variation 1335
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:377247829"
variation 1338
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:367632035"
variation 1369
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:75508371"
variation 1373
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:370764119"
variation 1387
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375323203"
variation 1389
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:201325199"
variation 1392
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371171301"
variation 1404
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200399610"
variation 1405
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:200018246"
variation 1435
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376180600"
variation 1449
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201365952"
variation 1450
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:372218880"
variation 1461
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:147583697"
variation 1462
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142034230"
variation 1471
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376488491"
variation 1481
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368537807"
exon 1483..1616
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1491
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:371836872"
variation 1494
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:202240818"
variation 1495
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368079865"
variation 1512
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:111273576"
variation 1516
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:140042418"
variation 1530
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:149375418"
variation 1544
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375227932"
variation 1551
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:2304393"
variation 1579
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:116185403"
variation 1586
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148309276"
variation 1591
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368923816"
exon 1617..1707
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1641
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:141406100"
variation 1690
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:145721476"
exon 1708..1878
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1708
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:370997492"
variation 1711
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:138341672"
variation 1712
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:142828669"
variation 1734
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:200156774"
variation 1735
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375902120"
variation 1756
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:146125870"
variation 1776
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:374982895"
variation 1778
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139832048"
variation 1797
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:199681748"
variation 1804
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:58750568"
variation 1826
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:77681311"
variation 1829
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:148410442"
variation 1845
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:145051977"
variation 1846
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:147554026"
variation 1854
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:140414249"
exon 1879..2053
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 1885
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="c"
/db_xref="dbSNP:371993530"
variation 1928
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:184844415"
variation 1931
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:376326631"
variation 1937
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:201307081"
variation 1953
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:144259173"
variation 1954
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:151208452"
variation 1956
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:374022157"
variation 1971
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:73660439"
variation 1981
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:368207411"
variation 1985
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:76463933"
variation 1992
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:369846947"
exon 2054..2178
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2073
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139239940"
variation 2076
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:145066574"
variation 2077
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141082919"
variation 2105
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:200319453"
variation 2141
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:9696578"
variation 2170
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371328761"
exon 2179..2256
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2222
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:144434647"
variation 2248
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:186351262"
variation 2251
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:377710586"
exon 2257..2317
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2268
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:201752493"
exon 2318..2726
/gene="GSN"
/gene_synonym="ADF; AGEL"
/inference="alignment:Splign:1.39.8"
variation 2336
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:142854368"
variation 2347
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:375881478"
variation 2348
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:143285592"
variation 2356
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:148360076"
variation 2360
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:141510612"
variation 2373
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:368986042"
variation 2406
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:9102"
variation 2407
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:139420096"
STS 2418..2574
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="RH17399"
/db_xref="UniSTS:34031"
variation 2514
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:371549019"
variation 2515
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:376801564"
STS 2516..2681
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="G10520"
/db_xref="UniSTS:56986"
STS 2517..2707
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="SHGC-132035"
/db_xref="UniSTS:173882"
STS 2519..2646
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="STS-X04412"
/db_xref="UniSTS:16463"
STS 2532..2692
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="D9S1050E"
/db_xref="UniSTS:29132"
STS 2544..2650
/gene="GSN"
/gene_synonym="ADF; AGEL"
/standard_name="D9S1953"
/db_xref="UniSTS:63945"
variation 2549
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051142"
variation 2560
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="g"
/db_xref="dbSNP:374518331"
variation 2561
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:143181937"
variation 2575
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051174"
variation 2583..2584
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:147410423"
variation 2584..2585
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:372955427"
variation 2604..2605
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:71694034"
variation 2609..2610
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:377469209"
variation 2609
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="g"
/db_xref="dbSNP:15034"
variation 2612
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:66991108"
variation 2615..2616
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ttt"
/db_xref="dbSNP:369363704"
variation 2615
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:71663525"
variation 2616..2617
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/db_xref="dbSNP:376569726"
variation 2622..2623
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:71680051"
variation 2624..2625
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="tttt"
/db_xref="dbSNP:71659520"
variation 2627
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="g"
/replace="t"
/db_xref="dbSNP:73660440"
variation 2629
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="a"
/replace="t"
/db_xref="dbSNP:11550202"
variation 2655..2656
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace=""
/replace="ag"
/db_xref="dbSNP:71695753"
variation 2674
/gene="GSN"
/gene_synonym="ADF; AGEL"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051286"
ORIGIN
tcccgcccgcgccctgcccaccccggccgcgcgcaccacaacgcccccgccccgccgcccggaaccagctgagcgcagctggacccagcagccgctgtctccagtgccgcagcagcaggtagtgctcatagctctctttgtccagtgcttcggccttggtcccagcgccttcccacggagcagcactcttcaccctgcacagccttgttagttcttgcagatacagcgctaggaaaaggggagtaattcaggtctagaatggaaaaactgttttgttgctttcccaacagcatggtggtggaacaccccgagttcctcaaggcagggaaggagcctggcctgcagatctggcgtgtggagaagttcgatctggtgcccgtgcccaccaacctttatggagacttcttcacgggcgacgcctacgtcatcctgaagacagtgcagctgaggaacggaaatctgcagtatgacctccactactggctgggcaatgagtgcagccaggatgagagcggggcggccgccatctttaccgtgcagctggatgactacctgaacggccgggccgtgcagcaccgtgaggtccagggcttcgagtcggccaccttcctaggctacttcaagtctggcctgaagtacaagaaaggaggtgtggcatcaggattcaagcacgtggtacccaacgaggtggtggtgcagagactcttccaggtcaaagggcggcgtgtggtccgtgccaccgaggtacctgtgtcctgggagagcttcaacaatggcgactgcttcatcctggacctgggcaacaacatccaccagtggtgtggttccaacagcaatcggtatgaaagactgaaggccacacaggtgtccaagggcatccgggacaacgagcggagtggccgggcccgagtgcacgtgtctgaggagggcactgagcccgaggcgatgctccaggtgctgggccccaagccggctctgcctgcaggtaccgaggacaccgccaaggaggatgcggccaaccgcaagctggccaagctctacaaggtctccaatggtgcagggaccatgtccgtctccctcgtggctgatgagaaccccttcgcccagggggccctgaagtcagaggactgcttcatcctggaccacggcaaagatgggaaaatctttgtctggaaaggcaagcaggcaaacacggaggagaggaaggctgccctcaaaacagcctctgacttcatcaccaagatggactaccccaagcagactcaggtctcggtccttcctgagggcggtgagaccccactgttcaagcagttcttcaagaactggcgggacccagaccagacagatggcctgggcttgtcctacctttccagccatatcgccaacgtggagcgggtgcccttcgacgccgccaccctgcacacctccactgccatggccgcccagcacggcatggatgacgatggcacaggccagaaacagatctggagaatcgaaggttccaacaaggtgcccgtggaccctgccacatatggacagttctatggaggcgacagctacatcattctgtacaactaccgccatggtggccgccaggggcagataatctataactggcagggtgcccagtctacccaggatgaggtcgctgcatctgccatcctgactgctcagctggatgaggagctgggaggtacccctgtccagagccgtgtggtccaaggcaaggagcccgcccacctcatgagcctgtttggtgggaagcccatgatcatctacaagggcggcacctcccgcgagggcgggcagacagcccctgccagcacccgcctcttccaggtccgcgccaacagcgctggagccacccgggctgttgaggtattgcctaaggctggtgcactgaactccaacgatgcctttgttctgaaaaccccctcagccgcctacctgtgggtgggtacaggagccagcgaggcagagaagacgggggcccaggagctgctcagggtgctgcgggcccaacctgtgcaggtggcagaaggcagcgagccagatggcttctgggaggccctgggcgggaaggctgcctaccgcacatccccacggctgaaggacaagaagatggatgcccatcctcctcgcctctttgcctgctccaacaagattggacgttttgtgatcgaagaggttcctggtgagctcatgcaggaagacctggcaacggatgacgtcatgcttctggacacctgggaccaggtctttgtctgggttggaaaggattctcaagaagaagaaaagacagaagccttgacttctgctaagcggtacatcgagacggacccagccaatcgggatcggcggacgcccatcaccgtggtgaagcaaggctttgagcctccctcctttgtgggctggttccttggctgggatgatgattactggtctgtggaccccttggacagggccatggctgagctggctgcctgaggaggggcagggcccacccatgtcaccggtcagtgccttttggaactgtccttccctcaaagaggccttagagcgagcagagcagctctgctatgagtgtgtgtgtgtgtgtgtgttgtttcttttttttttttttacagtatccaaaaatagccctgcaaaaattcagagtccttgcaaaattgtctaaaatgtcagtgtttgggaaattaaatccaataaaaacattttgaagtgtgaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
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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