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9197 SLC33A1

9197

SLC33A1

solute carrier family 33 member 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 33 member 1

研究结论

Date Results Publications
2017-07-29 12:03:00 results indicate that increased expression of AT-1 can cause an autistic-like phenotype by affecting key neuronal metabolic pathways. 27242167
2015-10-03 11:19:00 SLC33A1 can negatively regulate BMP signaling. 25402622
2012-11-24 11:01:00 IRE1/XBP1 controls the induction of autophagy/ERAD(II) during the unfolded protein response by activating the ER membrane transporter SLC33A1/AT-1 22787145
2012-03-17 11:44:00 Homozygosity mapping displayed a region of commonality among three families at chromosome 3q25. Deep sequencing and conventional sequencing disclosed homozygous or compound heterozygous mutations for all affected subjects in SLC33A1. 22243965
2011-05-14 10:12:00 translocates acetyl-CoA into the ER lumen and is essential for cell viability 20826464

名称对应

Type IDs
Synonymous ACATN, AT-1, AT1, CCHLND, SPG42
Gene
UniProtKB-ID: ACATN_HUMAN
UniprotKB: O00400
UniParc: UPI000006E3FD
EMBL: D88152, BC014416, AK312268, CH471052
Ensembl: ENSG00000169359
KO: hsa:9197
Nucleutide sequences
EMBL-CDS: AAH14416.1, BAA20072.1, EAW78744.1, EAW78743.1, BAG35199.1
Ensembl_TRS: ENST00000359479, ENST00000643144
Protein sequencees
Ensembl_PRO: ENSP00000352456, ENSP00000496241
RefSeq: NP_001177921.1, NP_004724.1, XP_016862952.1, NP_001350812.1, XP_016862953.1, XP_011511613.1
Others
UniRef100: UniRef100_O00400
UniRef90: UniRef90_O00400
UniRef50: UniRef50_O00400
UniGene: Hs.478031
CCDS: CCDS3173.1

全选

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研究热度

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