UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
M M0 M1 M2 M4 M5 M7 M8 M9 MA MB MC MD ME MF MG MH MI MK ML MM MN MO MP MR MS MT MU MV MY
MM MM2 MMD MMF MMI MMM MMR MMS MMV

MMSET Protein

[Encoded by human oncogene WHSC1 Gene, 1365-amino acid 152 kD Wolf-Hirschhorn Syndrome Candidate 1 Protein contains a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. WHSC1 is preferentially expressed in rapidly growing embryonic tissues, in a pattern corresponding to affected organs in WHS patients. The nature of the protein motifs and expression pattern suggest that WHSC1 is a good candidate responsible for many of the phenotypic features of WHS; a malformation syndrome associated with hemizygous deletion of the chromosome 4 distal short arm. (OMIM, Swiss-Prot, LocusLink, and NCI) ( NCI )]
UMLS (NCI) C1309784
Multiple Myeloma Set Domain Protein
NSD2 Protein
Nuclear Set Domain-Containing 2 Protein
WHSC1
WHSC1 Protein
Wolf-Hirschhorn Syndrome Candidate 1 Protein
 
Amino Acid, Peptide, or Protein
Biologically Active Substance

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