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55295 KLHL26

55295

KLHL26

kelch like family member 26

protein-coding

Homo sapiens

基因描述

Type Description
Definition kelch like family member 26

研究结论

Date Results Publications
2021-04-03 13:32:00 Novel KLHL26 variant associated with a familial case of Ebstein's anomaly and left ventricular noncompaction. 31985165

名称对应

Type IDs
Gene
UniProtKB-ID: KLH26_HUMAN, M0R1N0_HUMAN, M0R1P3_HUMAN, A0A024R7N5_HUMAN
UniprotKB: Q53HC5, M0R1N0, M0R1P3, A0A024R7N5
UniParc: UPI0002A475AC, UPI0002A471FE, UPI0000071AC2
EMBL: CH471106, AC008998, AK001940, AK222656, BC026319, AC004476
Ensembl: ENSG00000167487
KO: hsa:55295
Nucleutide sequences
EMBL-CDS: BAA91990.1, BAD96376.1, AAH26319.1, EAW84729.1, EAW84728.1
Gene_ORFName: hCG_37049
Ensembl_TRS: ENST00000300976, ENST00000599006, ENST00000595182
Protein sequencees
Ensembl_PRO: ENSP00000300976, ENSP00000472001, ENSP00000472032
RefSeq: NP_001332912.1, NP_001332910.1, NP_001332913.1, NP_001332911.1, NP_060786.1, NP_001332914.1
Others
UniRef100: UniRef100_M0R1N0, UniRef100_M0R1P3, UniRef100_Q53HC5
UniRef90: UniRef90_A0A2K5VJQ5, UniRef90_Q53HC5, UniRef90_A0A2I3NG27
UniRef50: UniRef50_A0A2I3NG27, UniRef50_A0A2K5VJQ5, UniRef50_Q53HC5
UniGene: Hs.250632
CCDS: CCDS12384.1

全选

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