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57466 SCAF4

57466

SCAF4

SR-related CTD associated factor 4

protein-coding

Homo sapiens

基因描述

Type Description
Definition SR-related CTD associated factor 4

研究结论

Date Results Publications
2020-10-24 14:11:00 Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired 32730804
2020-03-14 11:57:00 Together, SCAF4 and SCAF8 coordinate the transition between elongation and termination, ensuring correct polyA site selection and RNAPII transcriptional termination in human cells. 31104839
2014-07-12 10:47:00 Report frequency of SFRS15 SNPs in diabetic nephropathy. 24821155
2010-09-15 22:07:00 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20628086
2010-09-15 22:07:00 Observational study of gene-disease association. (HuGE Navigator) 19913121

名称对应

Type IDs
Synonymous SFRS15, SRA4
Gene
UniProtKB-ID: SCAF4_HUMAN
UniprotKB: O95104
UniParc: UPI00001C2045, UPI0000206D66, UPI000194EC28
EMBL: AL117417, AF023142, AP001711, BC064990, BC052286, AK308406, AL834304, AB032998, BC014921
Ensembl: ENSG00000156304
KO: hsa:57466
Nucleutide sequences
EMBL-CDS: AAH14921.1, CAD38974.2, AAD09327.1, AAH64990.1, BAA86486.1, AAH52286.1, CAB55911.1
Ensembl_TRS: ENST00000286835, ENST00000434667, ENST00000399804
Protein sequencees
Ensembl_PRO: ENSP00000402377, ENSP00000286835, ENSP00000382703
RefSeq: NP_001138916.1, XP_016883906.1, XP_006724098.1, XP_016883905.1, XP_005261074.1, XP_006724099.1, NP_065757.1, XP_016883904.1, NP_001138917.1
Others
UniRef100: UniRef100_O95104
UniRef90: UniRef90_O95104
UniRef50: UniRef50_O95104
UniGene: Hs.17255
CCDS: CCDS33537.1, CCDS54482.1, CCDS46644.1

全选

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