Type | Description |
---|---|
Definition | adaptor related protein complex 3 subunit mu 2 |
Date | Results | Publications |
---|---|---|
2010-01-21 00:00:00 | some AP3M2 mutations still remain candidates for unmapped disorders including epilepsy, febrile seizure, and other neuronal developmental disorders associated with functional abnormalities of GABAergic transmission | 17293072 |
2009-06-24 21:33:00 | Observational study of gene-disease association. (HuGE Navigator) | 19481122 |
2008-03-13 09:08:00 | Observational study of genotype prevalence. (HuGE Navigator) | 17293072 |
Type | IDs |
---|---|
Synonymous | AP47B, CLA20, P47B |
Gene |
UniProtKB-ID:
AP3M2_HUMAN,
A0A384NYL6_HUMAN
UniprotKB:
P53677,
A0A384NYL6
UniParc:
UPI0000125033,
UPI00001BB2AC
EMBL:
GQ891535,
D38293,
BC056398,
CH471080,
AC103724,
AK315228,
BC056257
Ensembl:
ENSG00000070718
KO:
hsa:10947
|
Nucleutide sequences |
EMBL-CDS:
AAH56398.1,
BAG37657.1,
BAA07415.1,
EAW63236.1,
AAH56257.1,
EAW63237.1,
EAW63238.1,
ADO22397.1
Ensembl_TRS:
ENST00000174653,
ENST00000396926,
ENST00000518421,
ENST00000530375
|
Protein sequencees |
Ensembl_PRO:
ENSP00000174653,
ENSP00000431918,
ENSP00000380132,
ENSP00000428787
RefSeq:
NP_001127768.1,
XP_016868466.1,
NP_006794.1
|
Others |
UniRef100:
UniRef100_P53677
UniRef90:
UniRef90_P53677
UniRef50:
UniRef50_P53677
UniGene:
Hs.654529
CCDS:
CCDS6125.1
|
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Refseq |
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