Human (GRCh37.p13)
Description

multiple C2 domains, transmembrane 2 [Source:HGNC Symbol;Acc:25636]

Gene Synonyms

FLJ11175, FLJ33303, RP11-4F5.2

Location

Chromosome 15: 94,774,767-95,023,632 forward strand.

GRCh37:CM000677.1

About this gene

This gene has 10 transcripts (splice variants), 4 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000357742.4MCTP2-0023965878aaENSP00000350377.4
 
Protein coding
CCDS32338Q6DN12 Q9NPN6 NM_018349.3GENCODE basic
ENST00000451018.3MCTP2-0092472823aaENSP00000395109.3
 
Protein coding
CCDS53975Q6DN12 Q9NPN6 NM_001159643.1GENCODE basic
ENST00000331706.4MCTP2-2012222306aaENSP00000329646.4
 
Protein coding
CCDS53976Q6DN12 -GENCODE basic
ENST00000557742.1MCTP2-0031957306aaENSP00000454847.1
 
Protein coding
CCDS53976Q6DN12 NM_001159644.1GENCODE basic
ENST00000543482.1MCTP2-0011422396aaENSP00000438521.1
 
Protein coding
F5H415 -GENCODE basic
ENST00000456504.1MCTP2-0044493199aaENSP00000388887.1
 
Nonsense mediated decay
Q6DN12 --
ENST00000449432.3MCTP2-006836No protein-
 
Processed transcript
---
ENST00000561608.1MCTP2-010796No protein-
 
Processed transcript
---
ENST00000556363.1MCTP2-0054374No protein-
 
Retained intron
---
ENST00000557505.1MCTP2-008585No protein-
 
Retained intron
---