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2025-05-09 16:27:11, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_014598 7978 bp mRNA linear PRI 14-JUL-2013
DEFINITION Homo sapiens suppressor of cytokine signaling 7 (SOCS7), mRNA.
ACCESSION NM_014598 XM_371052
VERSION NM_014598.2 GI:313850979
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 7978)
AUTHORS Pharoah PD, Tsai YY, Ramus SJ, Phelan CM, Goode EL, Lawrenson K,
Buckley M, Fridley BL, Tyrer JP, Shen H, Weber R, Karevan R, Larson
MC, Song H, Tessier DC, Bacot F, Vincent D, Cunningham JM, Dennis
J, Dicks E, Aben KK, Anton-Culver H, Antonenkova N, Armasu SM,
Baglietto L, Bandera EV, Beckmann MW, Birrer MJ, Bloom G, Bogdanova
N, Brenton JD, Brinton LA, Brooks-Wilson A, Brown R, Butzow R,
Campbell I, Carney ME, Carvalho RS, Chang-Claude J, Chen YA, Chen
Z, Chow WH, Cicek MS, Coetzee G, Cook LS, Cramer DW, Cybulski C,
Dansonka-Mieszkowska A, Despierre E, Doherty JA, Dork T, du Bois A,
Durst M, Eccles D, Edwards R, Ekici AB, Fasching PA, Fenstermacher
D, Flanagan J, Gao YT, Garcia-Closas M, Gentry-Maharaj A, Giles G,
Gjyshi A, Gore M, Gronwald J, Guo Q, Halle MK, Harter P, Hein A,
Heitz F, Hillemanns P, Hoatlin M, Hogdall E, Hogdall CK, Hosono S,
Jakubowska A, Jensen A, Kalli KR, Karlan BY, Kelemen LE, Kiemeney
LA, Kjaer SK, Konecny GE, Krakstad C, Kupryjanczyk J, Lambrechts D,
Lambrechts S, Le ND, Lee N, Lee J, Leminen A, Lim BK, Lissowska J,
Lubinski J, Lundvall L, Lurie G, Massuger LF, Matsuo K, McGuire V,
McLaughlin JR, Menon U, Modugno F, Moysich KB, Nakanishi T, Narod
SA, Ness RB, Nevanlinna H, Nickels S, Noushmehr H, Odunsi K, Olson
S, Orlow I, Paul J, Pejovic T, Pelttari LM, Permuth-Wey J, Pike MC,
Poole EM, Qu X, Risch HA, Rodriguez-Rodriguez L, Rossing MA,
Rudolph A, Runnebaum I, Rzepecka IK, Salvesen HB, Schwaab I, Severi
G, Shen H, Shridhar V, Shu XO, Sieh W, Southey MC, Spellman P,
Tajima K, Teo SH, Terry KL, Thompson PJ, Timorek A, Tworoger SS,
van Altena AM, van den Berg D, Vergote I, Vierkant RA, Vitonis AF,
Wang-Gohrke S, Wentzensen N, Whittemore AS, Wik E, Winterhoff B,
Woo YL, Wu AH, Yang HP, Zheng W, Ziogas A, Zulkifli F, Goodman MT,
Hall P, Easton DF, Pearce CL, Berchuck A, Chenevix-Trench G,
Iversen E, Monteiro AN, Gayther SA, Schildkraut JM and Sellers TA.
CONSRTM Australian Cancer Study; Australian Ovarian Cancer Study Group
TITLE GWAS meta-analysis and replication identifies three new
susceptibility loci for ovarian cancer
JOURNAL Nat. Genet. 45 (4), 362-370 (2013)
PUBMED 23535730
REFERENCE 2 (bases 1 to 7978)
AUTHORS Noguchi,S., Yamada,N., Kumazaki,M., Yasui,Y., Iwasaki,J., Naito,S.
and Akao,Y.
TITLE socs7, a target gene of microRNA-145, regulates interferon-beta
induction through STAT3 nuclear translocation in bladder cancer
cells
JOURNAL Cell Death Dis 4, E482 (2013)
PUBMED 23392170
REMARK GeneRIF: SOCS7 functioned as an oncogene, the finding that revealed
a novel mechanism of carcinogenesis in bladder cancer cells.
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 7978)
AUTHORS Ge,D., Gao,A.C., Zhang,Q., Liu,S., Xue,Y. and You,Z.
TITLE LNCaP prostate cancer cells with autocrine interleukin-6 expression
are resistant to IL-6-induced neuroendocrine differentiation due to
increased expression of suppressors of cytokine signaling
JOURNAL Prostate 72 (12), 1306-1316 (2012)
PUBMED 22213096
REMARK GeneRIF: LNCaP-S17 cells are resistant to exogenous IL-6-induced
neuroendocrine differentiation due to increased levels of CIS/SOCS7
that block activation of JAK2-STAT3 pathways.
REFERENCE 4 (bases 1 to 7978)
AUTHORS Pazienza,V., Vinciguerra,M., Andriulli,A. and Mangia,A.
TITLE Hepatitis C virus core protein genotype 3a increases SOCS-7
expression through PPAR-{gamma} in Huh-7 cells
JOURNAL J. Gen. Virol. 91 (PT 7), 1678-1686 (2010)
PUBMED 20357037
REMARK GeneRIF: findings show that PPAR-gamma is involved in the
regulation of SOCS-7 expression by hepatitis C virus core protein
genotype 3a
REFERENCE 5 (bases 1 to 7978)
AUTHORS Sasi,W., Jiang,W.G., Sharma,A. and Mokbel,K.
TITLE Higher expression levels of SOCS 1,3,4,7 are associated with
earlier tumour stage and better clinical outcome in human breast
cancer
JOURNAL BMC Cancer 10, 178 (2010)
PUBMED 20433750
REMARK GeneRIF: Higher mRNA expression levels of SOCS1, 3, 4 and 7 are
significantly associated with earlier tumour stage and better
clinical outcome in human breast cancer.
Publication Status: Online-Only
REFERENCE 6 (bases 1 to 7978)
AUTHORS Krebs,D.L., Uren,R.T., Metcalf,D., Rakar,S., Zhang,J.G., Starr,R.,
De Souza,D.P., Hanzinikolas,K., Eyles,J., Connolly,L.M.,
Simpson,R.J., Nicola,N.A., Nicholson,S.E., Baca,M., Hilton,D.J. and
Alexander,W.S.
TITLE SOCS-6 binds to insulin receptor substrate 4, and mice lacking the
SOCS-6 gene exhibit mild growth retardation
JOURNAL Mol. Cell. Biol. 22 (13), 4567-4578 (2002)
PUBMED 12052866
REFERENCE 7 (bases 1 to 7978)
AUTHORS Cooney,R.N.
TITLE Suppressors of cytokine signaling (SOCS): inhibitors of the
JAK/STAT pathway
JOURNAL Shock 17 (2), 83-90 (2002)
PUBMED 11837794
REMARK Review article
REFERENCE 8 (bases 1 to 7978)
AUTHORS Dogusan,Z., Hooghe-Peters,E.L., Berus,D., Velkeniers,B. and
Hooghe,R.
TITLE Expression of SOCS genes in normal and leukemic human leukocytes
stimulated by prolactin, growth hormone and cytokines
JOURNAL J. Neuroimmunol. 109 (1), 34-39 (2000)
PUBMED 10969179
REFERENCE 9 (bases 1 to 7978)
AUTHORS Hilton,D.J., Richardson,R.T., Alexander,W.S., Viney,E.M.,
Willson,T.A., Sprigg,N.S., Starr,R., Nicholson,S.E., Metcalf,D. and
Nicola,N.A.
TITLE Twenty proteins containing a C-terminal SOCS box form five
structural classes
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 95 (1), 114-119 (1998)
PUBMED 9419338
REFERENCE 10 (bases 1 to 7978)
AUTHORS Matuoka,K., Miki,H., Takahashi,K. and Takenawa,T.
TITLE A novel ligand for an SH3 domain of the adaptor protein Nck bears
an SH2 domain and nuclear signaling motifs
JOURNAL Biochem. Biophys. Res. Commun. 239 (2), 488-492 (1997)
PUBMED 9344857
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AC183084.2, BC128607.1, AB005216.1 and AC124789.12.
On Dec 10, 2010 this sequence version replaced gi:53831996.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
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 :: AB005216.1, BC128607.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025085 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-559 AC183084.2 1701-2259 c
560-1189 BC128607.1 16-645
1190-1190 AB005216.1 701-701
1191-2018 BC128607.1 647-1474
2019-7978 AC124789.12 3601-9560 c
FEATURES Location/Qualifiers
source 1..7978
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="17"
/map="17q12"
gene 1..7978
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/note="suppressor of cytokine signaling 7"
/db_xref="GeneID:30837"
/db_xref="HGNC:29846"
/db_xref="HPRD:12299"
/db_xref="MIM:608788"
exon 1..909
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
CDS 122..1867
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/note="NCK-associated protein 4; Nck, Ash and
phospholipase C binding protein; NAP-4; SOCS-7; nck, Ash
and phospholipase C gamma-binding protein"
/codon_start=1
/product="suppressor of cytokine signaling 7"
/protein_id="NP_055413.1"
/db_xref="GI:53831997"
/db_xref="CCDS:CCDS32637.1"
/db_xref="GeneID:30837"
/db_xref="HGNC:29846"
/db_xref="HPRD:12299"
/db_xref="MIM:608788"
/translation="
MVFRNVGRPPEEEDVEAAPEPGPSELLCPRHRCALDPKALPPGLALERTWGPAAGLEAQLAALGLGQPAGPGVKTVGGGCCPCPCPPQPPPPQPQPPAAAPQAGEDPTETSDALLVLEGLESEAESLETNSCSEEELSSPGRGGGGGGRLLLQPPGPELPPVPFPLQDLVPLGRLSRGEQQQQQQQQPPPPPPPPGPLRPLAGPSRKGSFKIRLSRLFRTKSCNGGSGGGDGTGKRPSGELAASAASLTDMGGSAGRELDAGRKPKLTRTQSAFSPVSFSPLFTGETVSLVDVDISQRGLTSPHPPTPPPPPRRSLSLLDDISGTLPTSVLVAPMGSSLQSFPLPPPPPPHAPDAFPRIAPIRAAESLHSQPPQHLQCPLYRPDSSSFAASLRELEKCGWYWGPMNWEDAEMKLKGKPDGSFLVRDSSDPRYILSLSFRSQGITHHTRMEHYRGTFSLWCHPKFEDRCQSVVEFIKRAIMHSKNGKFLYFLRSRVPGLPPTPVQLLYPVSRFSNVKSLQHLCRFRIRQLVRIDHIPDLPLPKPLISYIRKFYYYDPQEEVYLSLKEAQLISKQKQEVEPST
"
misc_feature 491..1603
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (O14512.2);
Region: Mediates interaction with SORBS3"
misc_feature 1286..1588
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/note="Src homology 2 (SH2) domain found in suppressor of
cytokine signaling (SOCS) proteins; Region: SH2_SOCS7;
cd10388"
/db_xref="CDD:198251"
misc_feature order(1340..1342,1394..1396,1400..1402,1424..1426,
1463..1465)
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/note="phosphotyrosine binding pocket [polypeptide
binding]; other site"
/db_xref="CDD:198251"
misc_feature order(1493..1495,1499..1501,1553..1555)
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/note="hydrophobic binding pocket [polypeptide binding];
other site"
/db_xref="CDD:198251"
misc_feature 1658..1804
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/note="SOCS (suppressors of cytokine signaling) box of
SOCS7-like proteins. Together with CIS1, the CIS/SOCS
family of proteins is characterized by the presence of a
C-terminal SOCS box and a central SH2 domain. SOCS7 is
important in the functioning of neuronal...; Region:
SOCS_SOCS7; cd03741"
/db_xref="CDD:58145"
misc_feature order(1661..1678,1694..1696,1715..1717,1733..1735,
1748..1750)
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/note="putative elongin B/C interaction [polypeptide
binding]; other site"
/db_xref="CDD:58145"
variation 255
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:182736053"
variation 257
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:113299524"
variation 379
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:41377745"
variation 414
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:201577908"
variation 499
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:41351844"
variation 542
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:372829995"
variation 608
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:201639550"
variation 644
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="c"
/db_xref="dbSNP:56279143"
variation 657..658
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="gca"
/db_xref="dbSNP:55849419"
variation 681..682
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="gca"
/db_xref="dbSNP:60453610"
variation 682
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="gca"
/db_xref="dbSNP:41492748"
variation 730
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="t"
/db_xref="dbSNP:376084903"
variation 783
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200638330"
variation 794
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368529614"
variation 802
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:370980742"
variation 904
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375541134"
exon 910..974
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 929
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:75445121"
variation 930
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="c"
/db_xref="dbSNP:76549267"
variation 947
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:139493404"
variation 949
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368047299"
exon 975..1079
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 990
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:368507568"
variation 1008
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:77546775"
variation 1037
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:199883782"
variation 1057
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:146657304"
variation 1067
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:140733557"
exon 1080..1181
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 1084
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:144493134"
variation 1147
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:142786789"
variation 1158
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:145376452"
variation 1159
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:149190855"
variation 1162
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:371505316"
exon 1182..1312
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 1193
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:199820589"
variation 1194
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201354583"
variation 1221
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:369677064"
variation 1239
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:373112910"
variation 1249
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:200305110"
variation 1266
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:370033423"
variation 1269
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:372664557"
exon 1313..1481
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 1382
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:143317326"
variation 1478
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:148327709"
exon 1482..1610
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 1522
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:140480789"
variation 1555
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:147043285"
exon 1611..1746
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 1633
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:138279795"
variation 1636
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:61744884"
variation 1675
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:201020366"
exon 1747..1897
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 1762
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:147429718"
variation 1813
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:200707695"
variation 1822
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:138060923"
variation 1824
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="c"
/db_xref="dbSNP:369848227"
variation 1836
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:55687042"
exon 1898..7978
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/inference="alignment:Splign:1.39.8"
variation 1954..1955
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="ag"
/db_xref="dbSNP:370878759"
variation 1957..1958
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="ag"
/db_xref="dbSNP:56126906"
variation 2015
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:3748728"
variation 2046
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="c"
/db_xref="dbSNP:145907745"
variation 2047
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:138717560"
variation 2052
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:3193291"
variation 2195
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:3748727"
variation 2250
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="caggt"
/db_xref="dbSNP:41502245"
variation 2255
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:56259056"
variation 2385
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:7221139"
variation 2562
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:185290596"
variation 2607
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:191417154"
variation 2632
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:41421647"
variation 2717
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:183194230"
variation 2994
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:148066376"
variation 3064
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:141768666"
variation 3072
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="c"
/db_xref="dbSNP:146025537"
variation 3120
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:41465244"
variation 3142
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="t"
/db_xref="dbSNP:370479771"
variation 3168
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:41350045"
variation 3192
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:41470153"
variation 3221
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:3748726"
variation 3269..3270
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="g"
/db_xref="dbSNP:35011456"
variation 3300..3301
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="g"
/db_xref="dbSNP:34408289"
variation 3321
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:41476051"
variation 3505
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:143371485"
variation 3600
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:191704465"
variation 3670
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045638"
variation 3739
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:183283986"
variation 3740
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369866206"
variation 3837..3838
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="t"
/db_xref="dbSNP:111228668"
variation 3840..3841
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="t"
/db_xref="dbSNP:377182110"
variation 3848..3849
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="t"
/db_xref="dbSNP:372764632"
variation 3946
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:146103054"
variation 4079
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374527613"
variation 4085
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:187955988"
variation 4116
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="c"
/db_xref="dbSNP:78913515"
variation 4170
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="t"
/db_xref="dbSNP:191262759"
variation 4221
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:377293884"
variation 4234
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:368417658"
variation 4269
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:3748725"
variation 4308
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:72834024"
variation 4321
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:73298678"
variation 4383
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:3748724"
variation 4414
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:183782815"
variation 4501
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:187767364"
variation 4546
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:376495923"
variation 4586
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:371819588"
variation 4591
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:139731078"
variation 4724
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:375072810"
variation 4741
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:3748723"
variation 4784
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:149772292"
variation 4833
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="c"
/db_xref="dbSNP:116439453"
variation 4844
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:115900316"
variation 4847
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:145693495"
STS 4859..5036
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/standard_name="D10S2448"
/db_xref="UniSTS:474444"
variation 4906
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:192891373"
STS 4936..5037
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/standard_name="D8S2282"
/db_xref="UniSTS:473910"
STS 4963..5041
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/standard_name="RH36905"
/db_xref="UniSTS:87932"
variation 5175
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:148925419"
variation 5218
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="t"
/db_xref="dbSNP:117177630"
variation 5219
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:184902717"
variation 5239
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:145694149"
variation 5332
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:369632145"
variation 5379
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:147745237"
variation 5383
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374068854"
variation 5420
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:142580652"
variation 5422
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:190143631"
variation 5434
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="c"
/db_xref="dbSNP:181796130"
variation 5503
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:116178054"
variation 5557
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:113484307"
variation 5632
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:118104419"
variation 5673
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:138728763"
variation 5742
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:140166851"
variation 5757
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:184560147"
variation 5767
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:150300962"
variation 5785
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:137941819"
variation 5806
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:367744908"
variation 5987
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:114743406"
variation 5996..5997
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="tg"
/db_xref="dbSNP:143774148"
variation 6014..6015
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="gt"
/db_xref="dbSNP:58800510"
variation 6020
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:146044214"
STS 6206..6317
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/standard_name="A005S24"
/db_xref="UniSTS:29024"
STS 6206..6317
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/standard_name="G20462"
/db_xref="UniSTS:29023"
variation 6219
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:138752854"
variation 6269
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:141753196"
variation 6281
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="t"
/db_xref="dbSNP:372136066"
variation 6408
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:146228532"
variation 6450
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:16968693"
variation 6451
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:60045196"
variation 6468
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:148748932"
variation 6685
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:141487587"
variation 6697
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:114719036"
variation 6728
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:150845815"
variation 6799
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="t"
/db_xref="dbSNP:368418407"
variation 6815
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:189344139"
variation 6923
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="t"
/db_xref="dbSNP:139279824"
variation 6980
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:112667628"
variation 7011
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:145346717"
variation 7131
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:73298684"
variation 7161
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374642319"
variation 7174
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:182035720"
variation 7222
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:147747951"
variation 7244
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:111278870"
variation 7255
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:199532320"
variation 7260
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:367839698"
variation 7282
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:371506757"
variation 7361
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:12943094"
variation 7419..7420
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="c"
/db_xref="dbSNP:111645811"
variation 7425
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="g"
/db_xref="dbSNP:190919838"
variation 7426..7427
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace=""
/replace="c"
/db_xref="dbSNP:376534978"
variation 7442
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:181219128"
variation 7503
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:186461091"
variation 7516
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:74892863"
variation 7529
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:12941155"
variation 7581
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="c"
/replace="t"
/db_xref="dbSNP:61377194"
variation 7601
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="g"
/replace="t"
/db_xref="dbSNP:140974966"
variation 7855
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="t"
/db_xref="dbSNP:79240905"
variation 7939
/gene="SOCS7"
/gene_synonym="NAP4; NCKAP4"
/replace="a"
/replace="g"
/db_xref="dbSNP:376610237"
ORIGIN
ccttggctatggagaggcggcccccgagccaggccctccgccaccgcccccgggccatggccccccgccgccacccttcctcgcgcggcccggcccgcggggctcccggccgccgcagctgatggtgttccgcaacgtgggtcggccgccggaggaggaggacgtggaggcggccccggagccgggaccctcggaactgctgtgtccccggcaccgctgtgccctggaccccaaggccctgccgccgggcttggcgctcgagcggacctggggcccggcggctggactagaggcgcagttggcggctctggggctcgggcagccggcggggccgggggtcaagacagtcggtgggggttgctgcccgtgtccgtgtcctcctcagccgccccctccgcagccccagccgcctgctgccgccccgcaggccggggaggaccccacggaaacgagcgacgcgctgctggtcctggagggcttggaatcggaggccgagagcctggagactaacagctgctcggaagaggagctcagcagcccgggtcgcggaggaggagggggcggccggcttctgctgcagcccccaggccctgaattacctccggtgcccttcccgctgcaggacttggtccctctggggcgcctgagtagaggggagcagcagcagcagcagcagcagcaacctcccccgcccccgcctcctcccgggcccctccggccactcgcgggtccttctcggaagggctccttcaaaatccgcctcagtcgcctctttcgcaccaagagctgcaacggtggctccggcggtggggatgggaccggcaagaggccttctggagagctggctgcttcagctgcgagcctgacagacatgggaggctctgcgggccgggagctggacgcggggaggaaacccaagttgacaagaactcaaagtgccttttctccggtctccttcagccccctgttcacaggtgaaactgtgtcgcttgtggatgtggacatttctcagcggggcctgacctctccacaccctccaactccccctcctcctccgagaagaagcctcagcctcctagatgatatcagtgggacgctgcctacatctgtccttgtggctccgatggggtcttccttgcagtctttccccctacctccgcctcctccaccccatgccccagatgcatttccccggattgctcccatccgagcagctgaatccctgcacagccaacccccacagcacctccagtgtcccctctaccggcctgactcgagcagctttgcagccagccttcgagagttggagaagtgtggttggtattgggggccaatgaattgggaagatgcagagatgaagctgaaagggaaaccagatggttctttcctggtacgagacagttctgatcctcgttacatcctgagcctcagtttccgatcacagggtatcacccaccacactagaatggagcactacagaggaaccttcagcctgtggtgtcatcccaagtttgaggaccgctgtcaatctgttgtagagtttattaagagagccattatgcactccaagaatggaaagtttctctatttcttaagatccagggttccaggactgccaccaactcctgtccagctgctctatccagtgtcccgattcagcaatgtcaaatccctccagcacctttgcagattccggatacgacagctcgtcaggatagatcacatcccagatctcccactgcctaaacctctgatctcttatatccgaaagttctactactatgatcctcaggaagaggtatacctgtctctaaaggaagcgcagctcatttccaaacagaagcaagaggtggaaccctccacgtagcgaggggctccctgctggtcaccaccaagggcatttggttgccaagctccagctttgaagaaccaaattaagctaccatgaaaagaagaggaaaagtgagggaacaggaaggttgggattctctgtgcagagactttggttccccacgcagccctggggcttggaagaagcacatgaccgtactctgcgtggggctccacctcacacccacccctgggcatcttaggactggaggggctccttggaaaactggaagaagtctcaacactgtttctttttcagaagttttgtttttgatatttatattacttggtatggaaaactcaccttgaaggcagttggggtttgtgcccgttggattgaaagtggtgcgaagggtgagcaggtccaaagaaggggtgggaggagggaacaggggacggccattcagctggtgccaaaggcagagttagagtctgtgctgtgggcctggaagatgggaggaggggcttgaggtttgcaaaggactgggagttcctgaggaagggggaatctgcctcttgttgccatgggcagctgttgtaggagcaggagagaaaggagggtgggtggtctcgaaaagaatattgggcaaaacctagccaattggccttagctgggagaagtagtgactcctgcatccttttttaaggtttaggaacctgagttcagaaacacctctcatggaagctgtactagttgtgatttacttaattccttaagttccatgacctgaagttaaccccgttcttcctctgctctcaacccattgccccttgagataactgtacatgtcactctgatcatggtaacagcatccctattgcttctgccagctgtcatggcaatcgtgtttcccatcacctgggcggttcagagccagtcatgggctgctgaatttaatggagcatgtttccaggttcttcatggcaaactgtactcatgacttaggagtgagtgttacttccatgtgcctgtcagcttgtgagggggaatgtggaggaaggtgagaaatacagctcccacagttgtgctcttcctagaggaagctctcagaacgcagccctcacgggatttccttaggtcagaggagagcatcgcatctcacgtttttaggtttatcactgccatcccacttctgggatgggaggtagcaagggcttctgtattttcttgtgttcattctagcaacccagacatttccggatcagatcctgctggtctccactcactggaaagtctgccagatgccgatttgagagctgcctgtccctgctttcaggaggagcggggagaaaaactccaatggtctttaatggtttctgcagctggccatggccaattcatatgacattgtgagtttgctttcttatagagctgctctggggagaggtttgctattgagatgtaacagtggagctgttgggtcttcatgactcctttgcgtgtgttccatgggactctctttctgggttccccatgcttatagttgcctcgtgtcacaagacagatactaatgtcaggtttgtggcttcctgatggtttgggtggggccccagtgtcctggtaatttataggactgcctcatctgggagcattgccttcttccttagtcccacgtggagtgaccagtcttcctccttgtagctgaacagggaggaaacttgcaccattacctgactgtggaagggtggcccacaagatgagctgtgcaccataaacacagcccacctctgatttgtcatgtggtacctcttctttccttggcttccatggtagtattaccaactaagcaagattgtgatcccagaaattggcttagcatgtgagtgttgcctcgtgagagtacaagtaatataactcgccatcttgcaggaagtgccaccccaatatagagcctgaagttggaatctgttgagatccttgggtggctgatatacagcctgggatctttcttttttttgttccttttcaaccacccataattttaatattattttttagtgtgtgtgtgcctggctttgcgctagatattgtagaaaacaaaaaaggtaaaagacgtaatatgtggcctaagggagcttttaggtgactgctgcacatcaagcagaaaatcaaggactatctaaagacgtttatagtagataagatcagggtagaccagatggtctgggaaagttctgtgcctctgaggctttgggttgtagtcaatggcaggacagacagtgagatgaaaaacacatgagcaaaagcaaggaagcagaaatctgcatggcatgtactgaacagtgcacagccctgttagagcaacatggttaaagaatcctttccagtgcggttttctagatggaagcttcccagccaccaggcagacctgagtgccgaggggttatgatggtgaggtggagcccaaagcccaaaggagtcagcaaggctcctgcccattgccagggcctcactatggtcagctcaggccatgtgagggaggcagagcctccgcaccccctgtgttactggggtttcttctggagaactcatacattcaggtacaaaacaaaccaactgaggaggtgtgacccaacctcaccacccacctttctcctcctggggagtgtcgtgttgaactgtgtctgtgtcagtgcactggtcccagccctggccgcagcctagtcctttctctgtggagtgggctgcaaaacagcagcgcaagaggagacagtcttcgtcaggtgtgggtgtttggtgcctgcatgggtggccttgcacagagcagttaggggaagatgagggggaggcatggggctgggccagctctctgggatacagcctggtcagagagtaaatggagcagaggaacaggtgtggcagcacctgcccttcacctccctgaccaggcccgtccctccttcgccagtgctgtgcagagctcatttaaatgtattcctttctaggtctgggcgcggtggctcacgcctgtaatcccagcactttgggaggctgaggtgggtggatcatgaggtcgggagttcaagaccagcttggccaaacagtgaaaccctatctctactaaaatacaaaaattagctgggcatggtggcatgcgcctgtagtcccagctacttgggaggctgagacaggagaattgcttgaacccaggaggcggaggttgcactgagccgagattgcgccactgccctctagcctagacgacagagtgagactccatctcaaaaaaaataaataatttctttctggttgtattttcaagtcacaaattggaaaaggcttacatctagggacccactgttgattcctaagttgtgggtgggtgatatcagtggcctcagtgcctgcataaccctcacctgtttatgactgatctactgtaaccttcctcaggttgagagtgagctgctgtgagccagtgacaactactgctacaacttgctgttacttgaaattcgtgtgctatgttggtagcacaggagtaggcgggcgggggttttggtgtgggcactaggtaagtgggtggcaaccggctctttgggaccattggtgctgacctttgcctggtcacctgcctgtgcctaggccaagtgaatgttacatcttggaacctgagccatggaggtggcgccacctccctgaggagaaaggtgtggccaaaggaaactcctgcatggctcctgctccttccccttccctacatttcacttgggctaatgatgtaagccccccttgaggttggggatggtgtggagatagctgcagacacccctgtaacagacatccaggaagaattagggagtgggggtaattatagttcctaggtctaggggtgagaggtgggagtagaaccagaagtgccctggaatccagccgtgtcagccctcaccccagggcccccaggaaagcatggcctgcttgaagccctctgctccctgcagaaactggggcgaggaggagctttttccttcagttagatctttcccttccctgctgcctcgctcccttagctttggagccctaaagttagtggacaagacactgggataaagctctatggctgctggaaggaggtctgagtctgtgtgtgtgcatatgcatgcatgtgtgtgtgtgtgtgtgtcctcatttgcagaagtcttgctaccagttagggtgttaagagcatctccactgggcggagacctggcatttgttttccactgttaagagaatgacacaccccctgtcatgtaagggaggagctattgagttagacattttccctatgggaatcctcggtttggtttgtgggaaaggagggaatggataagtgatttttatctctaatcgtcaacacagctgttcttccactgaatttgtgctattgcatacatgtagccatctttcttttcactgcagcagtgtttatcagtagttcaaaatgatttatttgctcctggggagtaaaaccttttttattaaaaaaagaaaaagaaaaaaaaaagaaagaaaagtgtgcccccctcctatgctgcgatagctataaaatgattgggtcacaaaggtcaagtctgcacgtccctgtggtagaccctgctttcacattggagccttcacactcagcacaaaatgattggaggccttgataaaatggagagcaaagtcttgggagcagtgaaatgggggttggatcatagagacaggcgctggggactcgggtactgcagttaggaaagtagcgttatgagttgtactgaaaatgttgattctctaatctgccagaaaaggacctgtcttttcatgcagatttcatattgtctttgtccttttcattgcttcttgaccttcctggcaggtgtcgctcagtttcttcctgtttcccttcctgtcctctccacacctgctatcccgtcccactcccatctacctcccgggaagccagccctgcatgctgagtttgtgacctgcttcattcccatttcatttctagagggtttagaggtgacctggaaccgttccctttccctctcctaccccctcctctgcaacaccaagaggcctggaggggcagacagaaagcagccagccacggcgggaagacatgcatgtttggttgcagctggactgcgatcgtagttcctcctggagatagagtgtgaggaacttaggacactcttcctcagactctgggatcatcacataccacactgccccgctcagagtttcgtcctgagctccctaaccagctcaggtggagcagaagcctgctctcactcctccatctctggtgctcccttgggcggggacctgtccctcactcttaggcccagaacctgtccaagggacaggtagggtccaggtgccactttgggtagctggctgttggaatgcccacactggtgctgcctgtggcatagccactgctgtacgtttttggttgtttttaagaaactcgatgaagaggggtgtcattctgggctcggggtggttgccaatttttcaccagaaagggagccaccccttgcaaccacttctgtctccgttagccccccctctgccctcctccaagccaaagcgtggcctggcttttgtcttcccatttagttttcctcttttacccttccttttgtgcttaatttattaaaatagttgctgtataatttattttcataaactataaaaaaatactaaatggttaaaatagacttgcaggccaatcttaaatggggtgggaggggtctgagggtgggatggggaaagggaaagaggttttgatataaacaaaacaaatgcactttgggtgtgttttggtatttttctggggatagagggggtggggttagggatgtccctgtagattagttccagaatggggtgtctgtatatactgtattaataggcatgtttgactctcgtaaagggacgttagtagctgctgcaggtcctgtttggaaaccccatgtacaattcccagttttttgtaagtgtcagtgcgagagacatttgactcttgtgtttgtatctcctttttatgattgctgtacctacccatgtctttttggggaggggtgaaaagagatttgaaataaaaatgtttagaaatta
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:30837 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:30837 -> Molecular function: GO:0017124 [SH3 domain binding] evidence: NAS
GeneID:30837 -> Biological process: GO:0008150 [biological_process] evidence: ND
GeneID:30837 -> Biological process: GO:0008286 [insulin receptor signaling pathway] evidence: IEA
GeneID:30837 -> Biological process: GO:0009968 [negative regulation of signal transduction] evidence: IEA
GeneID:30837 -> Biological process: GO:0016567 [protein ubiquitination] evidence: IEA
GeneID:30837 -> Biological process: GO:0035556 [intracellular signal transduction] evidence: IEA
GeneID:30837 -> Biological process: GO:0040008 [regulation of growth] evidence: IEA
GeneID:30837 -> Biological process: GO:0045444 [fat cell differentiation] evidence: IEA
GeneID:30837 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
GeneID:30837 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:30837 -> Cellular component: GO:0005886 [plasma membrane] evidence: IEA
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