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113235 SLC46A1

113235

SLC46A1

solute carrier family 46 member 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 46 member 1

研究结论

Date Results Publications
2021-03-13 13:17:00 A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformation. 32893190
2021-02-27 13:53:00 Impact of hypoxia on chemoresistance of mesothelioma mediated by the proton-coupled folate transporter, and preclinical activity of new anti-LDH-A compounds. 32493992
2021-02-27 13:45:00 Decreased placental folate transporter expression and activity in first and second trimester in obese mothers. 31926453
2020-10-10 13:01:00 SLC46A1 contributes to hepatic iron metabolism by importing heme in hepatocytes. 32621820
2020-05-23 12:05:00 we report the same deep intronic mutation of c.1166-285T>G shared by four unrelated Japanese patients with hereditary folate malabsorption 31494288

名称对应

Type IDs
Synonymous G21, HCP1, PCFT
Gene
UniProtKB-ID: PCFT_HUMAN, A0A024QZ44_HUMAN, A0A024QZ15_HUMAN
UniprotKB: Q96NT5, A0A024QZ44, A0A024QZ15
UniParc: UPI0000050394, UPI00000728A8
EMBL: AL832613, AK074161, AK054669, DQ496103, BC010691, CH471159
Ensembl: ENSG00000076351
KO: hsa:113235
Nucleutide sequences
EMBL-CDS: BAB70789.1, BAB84987.1, AAH10691.1, CAD89945.1, ABF47092.1, EAW51086.1, EAW51089.1, EAW51085.1, EAW51087.1
Gene_ORFName: hCG_31812, hCG_31812
Ensembl_TRS: ENST00000618626, ENST00000612814
Protein sequencees
Ensembl_PRO: ENSP00000480703, ENSP00000483652
RefSeq: XP_005277843.1, XP_016879599.1, NP_001229295.1, NP_542400.2
Others
UniRef100: UniRef100_Q96NT5, UniRef100_A0A024QZ44
UniRef90: UniRef90_A0A1U7U832, UniRef90_Q96NT5
UniRef50: UniRef50_Q96NT5
UniGene: Hs.446689
CCDS: CCDS74020.1, CCDS74019.1

全选

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