Human (GRCh38.p14)
Description

mutS homolog 2 [Source:HGNC Symbol;Acc:HGNC:7325]

Gene Synonyms

COCA1, HNPCC, HNPCC1, MSH-2

Location

Chromosome 2: 47,403,067-47,663,146 forward strand.

GRCh38:CM000664.2

About this gene

This gene has 9 transcripts (splice variants), 215 orthologues, 4 paralogues and is associated with 88 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000233146.7MSH2-2013115934aaENSP00000233146.2
 
Protein coding
CCDS1834P43246-1 NM_000251.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000645506.1MSH2-2087893924aaENSP00000495455.1
 
Protein coding
CCDS92750A0A2R8Y6P0 -GENCODE basic
ENST00000406134.5MSH2-2023628921aaENSP00000384199.1
 
Protein coding
E9PHA6 -GENCODE basicTSL:1
ENST00000543555.6MSH2-2043018868aaENSP00000442697.1
 
Protein coding
CCDS58709P43246-2 -GENCODE basicTSL:2
ENST00000644092.1MSH2-2055343558aaENSP00000496351.1
 
Nonsense mediated decay
A0A2R8Y7S8 --
ENST00000646415.1MSH2-2094523938aaENSP00000495543.1
 
Nonsense mediated decay
A0A2R8YG02 --
ENST00000644900.2MSH2-2063846883aaENSP00000495641.2
 
Nonsense mediated decay
A0A2R8Y713 --
ENST00000645339.1MSH2-2073113918aaENSP00000496441.1
 
Nonsense mediated decay
A0A2R8YFH0 --
ENST00000467323.1MSH2-203313No protein-
 
Protein coding CDS not defined
--TSL:3