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84187 TMEM164

84187

TMEM164

transmembrane protein 164

protein-coding

Homo sapiens

基因描述

Type Description
Definition transmembrane protein 164

研究结论

Date Results Publications
2020-04-25 12:30:00 Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes are associated with Alport syndrome, intellectual disability, midface hypoplasia, and elliptocytosis. 30737907

名称对应

Type IDs
Synonymous bB360B22.3
Gene
UniProtKB-ID: TM164_HUMAN
UniprotKB: Q5U3C3
UniParc: UPI0000211C26, UPI00004560FF
EMBL: AK094127, BC085605, AL360224, AL359079
Ensembl: ENSG00000157600
KO: hsa:84187
Nucleutide sequences
EMBL-CDS: AAH85605.1, BAG52820.1
Ensembl_TRS: ENST00000372068, ENST00000372072, ENST00000372073
Protein sequencees
Ensembl_PRO: ENSP00000361143, ENSP00000361138, ENSP00000384075
RefSeq: XP_016885387.1, XP_011529357.1, NP_001340780.1, XP_016885389.1, XP_016885383.1, XP_005262262.1, NP_060168.2, NP_115603.2, XP_016885384.1, XP_016885386.1, XP_005262265.1, NP_001340778.1, XP_016885388.1, XP_011529356.1, NP_001340779.1
Others
UniRef100: UniRef100_Q5U3C3
UniRef90: UniRef90_Q5U3C3
UniRef50: UniRef50_Q5U3C3
UniGene: Hs.496572
CCDS: CCDS14550.2, CCDS55475.1

全选

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研究热度

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