Type | Description |
---|---|
Definition | myelin transcription factor 1 like |
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 |
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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Refseq |
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