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11022 TDRKH

11022

TDRKH

tudor and KH domain containing

protein-coding

Homo sapiens

基因描述

Type Description
Definition tudor and KH domain containing

研究结论

Date Results Publications
2020-03-14 11:57:00 TDRKH missense mutation segregates with dominant distal hereditary motor neuropathy in a four generation pedigree. 30503856
2018-06-23 11:44:00 Unlike most other Tudor domains TDRD2 preferentially recognizes an unmethylated arginine-rich sequence from PIWIL1. 29118143
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20877624
2010-01-21 00:00:00 Tudor domain proteins interact with arginine-glycine-rich motifs in a methylarginine-dependent manner. 15955813

名称对应

Type IDs
Synonymous TDRD2
Gene
UniProtKB-ID: TDRKH_HUMAN, B4DJ68_HUMAN
UniprotKB: Q9Y2W6, B4DJ68
UniParc: UPI0001638968, UPI000020426A, UPI0000204267
EMBL: BC022467, AL589765, AK295948, AF119121, AF227192, CH471121
Ensembl: ENSG00000182134
KO: hsa:11022
Nucleutide sequences
EMBL-CDS: EAW53411.1, EAW53409.1, EAW53410.1, AAF36701.1, AAD30971.1, BAG58730.1
Ensembl_TRS: ENST00000368827, ENST00000368825, ENST00000368822, ENST00000368824, ENST00000458431
Protein sequencees
Ensembl_PRO: ENSP00000357815, ENSP00000357819, ENSP00000395718, ENSP00000357812, ENSP00000357817
RefSeq: NP_001077433.1, XP_016855616.1, XP_016855611.1, XP_016855619.1, XP_016855617.1, XP_016855615.1, XP_016855614.1, XP_016855618.1, XP_016855612.1, XP_016855613.1, XP_005244913.1, NP_001077432.1, NP_001077434.1, NP_006853.2
Others
UniRef100: UniRef100_Q9Y2W6
UniRef90: UniRef90_Q9Y2W6
UniRef50: UniRef50_Q80VL1
UniGene: Hs.144439
CCDS: CCDS41394.1, CCDS41395.1

全选

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