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2038 EPB42

2038

EPB42

erythrocyte membrane protein band 4.2

protein-coding

Homo sapiens

基因描述

Type Description
Definition erythrocyte membrane protein band 4.2

研究结论

Date Results Publications
2011-01-29 10:36:00 study shows that cytoplasmic hereditary spherocytosis mutants cause impaired binding of protein 4.2 to AE1, leaving protein 4.2 susceptible to loss during erythrocyte development 21039340
2010-05-31 11:05:00 Data suggest that one or both of proteins 4.1 and 4.2 cause a portion of band 3 to localize near the spectrin-actin junctions and provide another point of attachment between the membrane skeleton and the lipid bilayer. 20007969
2010-01-21 00:00:00 protein 4.2 strongly influences CD47 levels as well as the extent of membrane skeleton attachment in erythrocytes 14551146
2010-01-21 00:00:00 Evidence protein 4.2 interacts with the Rh membrane complex member CD47 obtained from red cells of patients with hereditary spherocytosis associated with complete protein 4.2 deficiency 12393467
2010-01-21 00:00:00 spectrin binding domain 12049649

名称对应

Type IDs
Synonymous PA, SPH5
Gene
UniProtKB-ID: EPB42_HUMAN
UniprotKB: P16452
UniParc: UPI000050ED3D, UPI0000551B79, UPI000013E639
EMBL: L06513, L06512, L06448, M30647, M30646, L06515, L06449, CH471125, BC099627, AC068724, M29399, L06518, L06516, L06511, M60298, L06450, L06447, L06517, BC096093, L06519, BC096094
Ensembl: ENSG00000166947
KO: hsa:2038
Nucleutide sequences
EMBL-CDS: EAW92591.1, AAH99627.1, AAA35798.1, AAA36402.1, AAA52385.1, AAH96094.1, AAA36401.1, AAA74589.1, AAH96093.1
Ensembl_TRS: ENST00000622454, ENST00000441366, ENST00000648595
Protein sequencees
Ensembl_PRO: ENSP00000497777, ENSP00000481226, ENSP00000396616
RefSeq: XP_011519652.1, XP_011519653.1, XP_011519656.1, XP_011519655.1, NP_000110.2, XP_011519651.1, XP_005254282.1, NP_001107606.1, XP_011519654.1
Others
UniRef100: UniRef100_P16452
UniRef90: UniRef90_P16452
UniRef50: UniRef50_P16452
UniGene: Hs.368642
CCDS: CCDS10093.1, CCDS45249.1

全选

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