Human (GRCh38.p14)
Description

C2 calcium dependent domain containing 2 [Source:HGNC Symbol;Acc:HGNC:1266]

Gene Synonyms

C21ORF25, C21ORF258, DKFZP586F0422, TMEM24L

Location

Chromosome 21: 41,885,112-41,954,018 reverse strand.

GRCh38:CM000683.2

About this gene

This gene has 8 transcripts (splice variants), 194 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000380486.4C2CD2-2026473696aaENSP00000369853.3
 
Protein coding
CCDS42933Q9Y426-1 NM_015500.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000329623.11C2CD2-2015844541aaENSP00000329302.7
 
Protein coding
CCDS13677Q9Y426-2 -GENCODE basicTSL:1
ENST00000449165.5C2CD2-2034559182aaENSP00000388704.1
 
Protein coding
H7BZB0 -TSL:1CDS 5' incomplete
ENST00000478372.1C2CD2-205356No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000482186.5C2CD2-2074542No protein-
 
Retained intron
--TSL:1
ENST00000482084.5C2CD2-2064123No protein-
 
Retained intron
--TSL:2
ENST00000467074.6C2CD2-2041952No protein-
 
Retained intron
--TSL:5
ENST00000490479.1C2CD2-208761No protein-
 
Retained intron
--TSL:3