AP1M2 (NM_005498.5) sequence variants
(mu2, MU1B, MU-1B, HSMU1B, AP1-mu2)

Editor(s): Qing ZHOU   

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ADA2ADAM17ALPK1AP1M2AP1S3CARD14CDC42CEBPECOPAELF4F12HCK
IKBKGIL1R1IL1RNIL36RNLACC1LPIN2LYN
MEFVMVKNCSTNNLRC4NLRP1NLRP12NLRP3NLRP7NOD2OTULIN
PLCG1PLCG2PLD4POMPPSMA3PSMB10PSMB4PSMB8PSMB9PSMG2PSTPIP1
RBCK1RELARIPK1SAMD9LSH3BP2SLC29A3STING1
TBXAS1TLR7TNFAIP3TNFRSF11ATNFRSF1ATRAP1TRNT1UBA1UNC93B1WDR1

 

General web sites
DNA NC_000019.10 GRCh38.p13 ENSG00000129354 GRCh38.p13
  NC_000019.9 GRCh37.p13 ENSG00000129354 GRCh37.p13
mRNA NM_005498.5 ENST00000250244.11
CCDS CCDS45964.1  
Protein NP_005489.2 ENSP00000250244.5
NCBI Gene 10053  
OMIM Gene 607309  
OMIM Disease _  
Nomenclature HGNC  
 

PubMed of the initial paper:

Other links: