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23040 MYT1L

23040

MYT1L

myelin transcription factor 1 like

protein-coding

Homo sapiens

基因描述

Type Description
Definition myelin transcription factor 1 like

研究结论

Date Results Publications
2021-03-27 14:41:00 Nine newly identified individuals refine the phenotype associated with MYT1L mutations. 32065501
2021-02-20 13:29:00 MYT1L: A systematic review of genetic variation encompassing schizophrenia and autism. 32267091
2020-09-05 13:53:00 The crucial role of DNA-dependent protein kinase and myelin transcription factor 1-like protein in the miR-141 tumor suppressor network. 31522595
2019-09-14 10:43:00 Our finding supports the association of MYT1L mutations with early-onset syndromic obesity. The identification of novel monogenic forms of childhood-onset obesity will provide insights to the involved genetic and biologic pathways. 30055078
2019-07-20 10:05:00 Myt1l was a critical mediator of induced neuron cell reprogramming. 29453933

名称对应

Type IDs
Synonymous MRD39, NZF1, ZC2H2C2, ZC2HC4B, myT1-L
Gene
UniProtKB-ID: MYT1L_HUMAN, A0A3B3IS14_HUMAN, A0A3B3IRM3_HUMAN, A0A3B3IS61_HUMAN, A0A3B3ISW5_HUMAN, A0A2R8YF72_HUMAN, A0A3B3IRX5_HUMAN
UniprotKB: Q9UL68, A0A3B3IS14, A0A3B3IRM3, A0A3B3IS61, A0A3B3ISW5, A0A2R8YF72, A0A3B3IRX5
UniParc: UPI0008141673, UPI0007DC59D8, UPI00003782FC, UPI0007DC60A8, UPI0003EAF271, UPI0000140B19, UPI00004E55EA, UPI0003EAF15D, UPI0008164DAF
EMBL: AF036943, AC009471, BC150281, AC106046, AB029029, AC009232, AC008276, BC137272, BC137273, AC093390, BC071612, AC011301
Ensembl: ENSG00000186487
KO: hsa:23040
Nucleutide sequences
EMBL-CDS: AAI50282.1, AAH71612.1, BAA83058.2, AAF14051.1, AAI37274.1, AAI37273.1
Ensembl_TRS: ENST00000647694, ENST00000647738, ENST00000407844, ENST00000648928, ENST00000428368, ENST00000649207, ENST00000399161, ENST00000648316, ENST00000650485, ENST00000648318, ENST00000648665, ENST00000649663, ENST00000648339, ENST00000644820, ENST00000647755
Protein sequencees
Ensembl_PRO: ENSP00000497722, ENSP00000382114, ENSP00000497017, ENSP00000497870, ENSP00000384219, ENSP00000396103, ENSP00000496986, ENSP00000497479, ENSP00000497068, ENSP00000496831, ENSP00000497115, ENSP00000497493, ENSP00000497273, ENSP00000496210, ENSP00000496922
RefSeq: NP_001316781.1, NP_001316776.1, XP_011508630.1, NP_001316774.1, XP_016859096.1, XP_011508625.1, XP_011508628.1, XP_016859093.1, XP_016859094.1, XP_011508622.1, XP_016859104.1, XP_016859111.1, XP_011508634.1, NP_001316777.1, XP_016859100.1, NP_001316778.1, NP_001289981.1, XP_011508633.1, NP_001316775.1, XP_016859105.1, XP_016859107.1, XP_016859101.1, XP_011508620.1, XP_011508626.1, XP_016859109.1, XP_016859110.1, NP_001316780.1, XP_011508629.1, XP_011508624.1, XP_011508621.1, XP_011508623.1, XP_016859095.1, XP_016859097.1, NP_001316773.1, NP_055840.2, XP_011508627.1
Others
UniRef100: UniRef100_A0A2R8YF72, UniRef100_A0A3B3IRM3, UniRef100_Q9UL68, UniRef100_A0A3B3IS61, UniRef100_A0A3B3IS14, UniRef100_A0A3B3ISW5, UniRef100_A0A3B3IRX5
UniRef90: UniRef90_A0A3B3IRM3, UniRef90_Q9UL68, UniRef90_A0A3B3IS14, UniRef90_A0A3B3IRX5, UniRef90_A0A3B3IS61
UniRef50: UniRef50_P97500, UniRef50_O60284
UniGene: Hs.434418, Hs.669852
CCDS: CCDS77378.1, CCDS46222.1

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