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221037 JMJD1C

221037

JMJD1C

jumonji domain containing 1C

protein-coding

Homo sapiens

基因描述

Type Description
Definition jumonji domain containing 1C

研究结论

Date Results Publications
2021-01-02 12:48:00 Jumonji domain containing 1C (JMJD1C) sequence variants in seven patients with autism spectrum disorder, intellectual disability and seizures. 31954878
2020-05-23 10:54:00 JMJD1C activates lipogenic gene transcription in liver.JMJD1C demethylates histone H3 K9 lysine at lipogenic promoters.JMJD1C is phosphorylated at the threonine T505 by mTOR. 32034158
2019-09-07 10:58:00 High JMJD1C expression is associated with increased metabolic dysregulation and leukemogenesis. 30622285
2019-07-13 12:25:00 Polymorphisms in JMJD1C are associated with pubertal onset in boys and reproductive function in men 29222425
2019-02-02 11:32:00 JMJD1C is the autosomal gene where variants have been demonstrated to be associated with Testosterone (one of Cardiovascular disease risk factors) at genome-wide significance. 29804699

名称对应

Type IDs
Synonymous KDM3C, TRIP-8, TRIP8
Gene
UniProtKB-ID: JHD2C_HUMAN, B7ZLC8_HUMAN
UniprotKB: Q15652, B7ZLC8
UniParc: UPI0000487D9C, UPI0000198BEF, UPI00001A7D59, UPI000189A73C
EMBL: BX537954, AC022022, AL590502, BC143722, AK027280, EF068222, AB037801, AL713895, L40411, AL831917, AL607128
Ensembl: ENSG00000171988
KO: hsa:221037
Nucleutide sequences
EMBL-CDS: BAA92618.1, AAC41741.1, CAD97921.1, ABK64187.1, CAD38578.1, AAI43723.1
Ensembl_TRS: ENST00000542921, ENST00000399262
Protein sequencees
Ensembl_PRO: ENSP00000382204, ENSP00000444682
RefSeq: NP_001309183.1, XP_016871386.1, NP_001269877.1, XP_011537810.1, XP_024303651.1, XP_024303650.1, XP_016871389.1, XP_011537805.1, NP_116165.1, XP_016871387.1, XP_016871391.1, NP_001309187.1, NP_001305082.1, XP_016871390.1, NP_001305083.1, NP_001309181.1, XP_016871388.1, XP_016871392.1
Others
UniRef100: UniRef100_Q15652, UniRef100_B7ZLC8
UniRef90: UniRef90_Q15652
UniRef50: UniRef50_Q15652
UniGene: Hs.413416
CCDS: CCDS60538.1, CCDS41532.1

全选

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