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84889 SLC7A3

84889

SLC7A3

solute carrier family 7 member 3

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 7 member 3

研究结论

Date Results Publications
2016-10-08 10:19:00 rare hypomorphic variants of SLC7A3 exist in male individuals, SLC7A3 variants possibly contribute to the etiology of autism spectrum disorders in male subjects in association with other genetic factors 26215737
2015-02-14 12:17:00 knockdown impaired AMPK-PPAR-alpha signaling and resulted in lipid accumulation under glucose starvation in liver cells 25130427
2013-07-06 12:33:00 CAT1, CAT2, and CAT3 localized in adult brains but with uneven distribution. 22870827
2010-01-21 00:00:00 It is concluded that similar to hCAT-1, hCAT-3 activity is decreased by via reduction of transporter molecules in the plasma membrane. 16332251
2010-01-21 00:00:00 is concluded that hCAT-3 is a passive transport system that conducts monovalent cations including L-Arg. 15737334

名称对应

Type IDs
Synonymous ATRC3, CAT-3, CAT3
Gene
UniProtKB-ID: CTR3_HUMAN
UniprotKB: Q8WY07
UniParc: UPI0000049F96
EMBL: BC033816, AK074865, AL627071, AF320612, AK027447, AK075014, CH471132
Ensembl: ENSG00000165349
KO: hsa:84889
Nucleutide sequences
EMBL-CDS: EAX05329.1, BAB55118.1, AAH33816.1, EAX05330.1, AAL37184.1, BAC11253.1, BAC11353.1
Ensembl_TRS: ENST00000298085, ENST00000374299
Protein sequencees
Ensembl_PRO: ENSP00000363417, ENSP00000298085
RefSeq: NP_116192.4, NP_001041629.1
Others
UniRef100: UniRef100_Q8WY07
UniRef90: UniRef90_Q8WY07
UniRef50: UniRef50_Q8WY07
UniGene: Hs.175220
CCDS: CCDS14404.1

全选

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研究热度

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