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401145 CCSER1

401145

CCSER1

coiled-coil serine rich protein 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition coiled-coil serine rich protein 1

研究结论

Date Results Publications
2013-10-26 12:37:00 FAM190A is a regulator or structural component required for normal mitosis and that both the rare truncating mutations and common in-frame deletion alteration of FAM190A may contribute to the chromosomal instability of cancer. 23665203
2010-12-11 10:50:00 Two SNPs located in genes coding for as yet uncharacterized proteins expressed in the cerebellum, XKR4 in 8q12.1, and FAM190A in 4q22.1 suggest association with association with attention deficit hyperactivity disorder. [FAM190A] 20607790
2010-06-30 22:05:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614

名称对应

Type IDs
Synonymous FAM190A
Gene
UniProtKB-ID: CCSE1_HUMAN
UniprotKB: Q9C0I3
UniParc: UPI00005A6104, UPI0000192716
EMBL: AC004054, AC098593, AC074124, AC097524, AC110796, AC093793, AC019188, AC093781, AC093729, BC051694, AC114787, AC096897, AC107049, AC079301, AC110774, AB051467
Ensembl: ENSG00000184305
KO: hsa:401145
Nucleutide sequences
EMBL-CDS: AAH51694.1, BAB21771.1, AAY41009.1
Ensembl_TRS: ENST00000432775, ENST00000509176
Protein sequencees
Ensembl_PRO: ENSP00000389283, ENSP00000425040
RefSeq: XP_011530258.1, XP_011530239.1, XP_016863687.1, XP_016863685.1, XP_016863684.1, NP_001364916.1, NP_997374.1, XP_011530238.1, XP_016863683.1, XP_011530260.1, XP_016863688.1, XP_011530253.1, XP_011530240.1, XP_011530251.1, XP_011530244.1, XP_011530250.1, NP_001138537.1, XP_011530252.1, XP_016863689.1, XP_011530245.1, XP_011530241.1, XP_011530249.1, XP_016863690.1, XP_011530243.1, XP_011530248.1, XP_011530259.1, XP_011530257.1, XP_011530247.1
Others
UniRef100: UniRef100_Q9C0I3
UniRef90: UniRef90_Q9C0I3
UniRef50: UniRef50_Q9C0I3
UniGene: Hs.654735
CCDS: CCDS47099.1, CCDS47100.1

全选

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