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197320 ZNF778

197320

ZNF778

zinc finger protein 778

protein-coding

Homo sapiens

基因描述

Type Description
Definition zinc finger protein 778

研究结论

Date Results Publications
2010-07-05 11:30:00 ZNF778 is a candidate gene for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome. 19920853

名称对应

Type IDs
Gene
UniProtKB-ID: ZN778_HUMAN, A0A0A0MSW5_HUMAN
UniprotKB: Q96MU6, A0A0A0MSW5
UniParc: UPI00001B6521, UPI0001AE6853, UPI0000E02EC4
EMBL: KF456218, BC125192, AK056437, AC009113
Ensembl: ENSG00000170100
KO: hsa:197320
Nucleutide sequences
EMBL-CDS: AAI25193.3, BAB71183.1
Ensembl_TRS: ENST00000306502, ENST00000620195, ENST00000433976
Protein sequencees
Ensembl_PRO: ENSP00000305203, ENSP00000481538, ENSP00000405289
RefSeq: XP_024305952.1, NP_001188336.1, XP_016878505.1, XP_024305951.1, XP_024305950.1, XP_016878504.1, NP_872337.2, XP_011521242.1, NP_001365810.1, XP_024305953.1, XP_016878506.1
Others
UniRef100: UniRef100_Q96MU6, UniRef100_A0A0A0MSW5
UniRef90: UniRef90_Q96MU6
UniRef50: UniRef50_Q96MU6
UniGene: Hs.647385
CCDS: CCDS45550.1

全选

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研究热度

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