AP1S3 (NM_001039569.2) sequence variants

Editor(s): Francesca CAPON   

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ADA2ADAM17ALPK1AP1S3CARD14CDC42CEBPECOPAELF4F12HCK
IKBKGIL1R1IL1RNIL36RNLACC1LPIN2LYN
MEFVMVKNCSTNNLRC4NLRP1NLRP12NLRP3NLRP7NOD2OTULIN
PLCG1PLCG2POMPPSMA3PSMB10PSMB4PSMB8PSMB9PSMG2PSTPIP1
RBCK1RELARIPK1SAMD9LSH3BP2SLC29A3STING1
TNFAIP3TNFRSF11ATNFRSF1ATRAP1TRNT1UBA1WDR1

 

General web sites
DNA NC_000002.12 GRCh38.p13 ENSG00000152056 GRCh38.p13
  NC_000002.11 GRCh37.p13 ENSG00000152056 GRCh37.p13
  NG_034017.1  
mRNA NM_001039569.2 ENST00000396654.7
CCDS CCDS42827.1  
Protein NP_001034658.1 ENSP00000379891.2
NCBI Gene 130340  
OMIM Gene 615781  
OMIM Disease 616106  
Nomenclature HGNC  
     

PubMed of the initial paper:

Other links: