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79648 MCPH1

79648

MCPH1

microcephalin 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition microcephalin 1

研究结论

Date Results Publications
2021-03-13 13:27:00 MCPH1 Lack of Function Enhances Mitotic Cell Sensitivity Caused by Catalytic Inhibitors of Topo II. 32276518
2020-12-19 13:45:00 Microcephalin 1/BRIT1-TRF2 interaction promotes telomere replication and repair, linking telomere dysfunction to primary microcephaly. 33203878
2020-12-12 13:23:00 Analysis of the ""centrosome-ome"" identifies MCPH1 deletion as a cause of centrosome amplification in human cancer. 32681070
2020-10-31 13:17:00 Microcephaly family protein MCPH1 stabilizes RAD51 filaments. 32735676
2020-05-23 11:55:00 results demonstrate that, although MCPH1 function is dispensable for activation and maintenance of the decatenation checkpoint, it is required for the adaptive response that bypasses the topoisomerase II inhibition----mediated G2 arrest. 30964711

名称对应

Type IDs
Synonymous BRIT1, MCT
Gene
UniProtKB-ID: MCPH1_HUMAN
UniprotKB: Q8NEM0
UniParc: UPI000020FF7E, UPI0001C4E0EF, UPI000020FF7B
EMBL: AF287957, KC877206, AC016065, BC030702, KC877207, AK301702, AX087870, BK004076, AC018398, AK022909
Ensembl: ENSG00000147316, ENSG00000285262
KO: hsa:79648
Nucleutide sequences
EMBL-CDS: AAH30702.2, CAC34661.1, BAG63174.1, BAB14304.1, DAA04567.1
Ensembl_TRS: ENST00000646478, ENST00000519480, ENST00000647051, ENST00000522905, ENST00000344683, ENST00000643429
Protein sequencees
Ensembl_PRO: ENSP00000496505, ENSP00000430768, ENSP00000493874, ENSP00000430962, ENSP00000342924, ENSP00000494584
RefSeq: XP_011533062.1, XP_011533060.1, XP_016869321.1, NP_001308972.2, XP_011533058.1, XP_016869318.1, NP_001308974.2, NP_001166045.2, NP_001350909.1, XP_011533057.1, XP_016869320.1, XP_011533059.1, NP_001350908.1, NP_001308971.2, XP_016869322.1, NP_078872.3, NP_001166046.1, XP_011533061.1
Others
UniRef100: UniRef100_Q8NEM0
UniRef90: UniRef90_Q8NEM0
UniRef50: UniRef50_Q8NEM0
UniGene: Hs.656769, Hs.708770
CCDS: CCDS43689.1, CCDS55191.1

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