Human (GRCh38.p14)
Description

multiple C2 and transmembrane domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25636]

Gene Synonyms

FLJ11175, FLJ33303

Location

Chromosome 15: 94,231,538-94,483,952 forward strand.

GRCh38:CM000677.2

About this gene

This gene has 9 transcripts (splice variants), 270 orthologues, 1 paralogue and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000357742.10MCTP2-2017724878aaENSP00000350377.4
 
Protein coding
CCDS32338Q6DN12-1 NM_001385001.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000451018.7MCTP2-2032472823aaENSP00000395109.3
 
Protein coding
CCDS53975Q6DN12-2 -GENCODE basicTSL:1
ENST00000557742.1MCTP2-2081957306aaENSP00000454847.1
 
Protein coding
CCDS53976Q6DN12-4 -GENCODE basicTSL:1
ENST00000543482.5MCTP2-2051422396aaENSP00000438521.1
 
Protein coding
F5H415 -GENCODE basicTSL:2
ENST00000456504.5MCTP2-2044493199aaENSP00000388887.1
 
Nonsense mediated decay
Q6DN12-6 -TSL:1
ENST00000449432.3MCTP2-202836No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000561608.5MCTP2-209796No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000556363.5MCTP2-2064374No protein-
 
Retained intron
--TSL:5
ENST00000557505.1MCTP2-207585No protein-
 
Retained intron
--TSL:4