Human (GRCh37.p13)
Description

C-type lectin domain family 12, member B [Source:HGNC Symbol;Acc:31966]

Gene Synonyms

UNQ5782

Location

Chromosome 12: 10,163,226-10,171,218 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 5 transcripts (splice variants) and 6 paralogues.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000338896.5CLEC12B-0011097276aa
 
Protein coding
CCDS44830Q2HXU8 NM_001129998.1Ensembl CanonicalGENCODE Basic
ENST00000396502.1CLEC12B-0033029232aa
 
Protein coding
CCDS8610Q2HXU8 NM_205852.2GENCODE Basic
ENST00000539155.1CLEC12B-004289865aa
 
Nonsense mediated decay
F5H4H7 --
ENST00000544853.1CLEC12B-0021193232aa
 
Nonsense mediated decay
CCDS8610Q2HXU8 --
ENST00000535903.1CLEC12B-005531No protein
 
Retained intron
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As of the latest update in March 2020 we are not supporting data for species other than human on this GRCh37 site and the view you wish to use is disabled.

You can read more about why we have done this on our blog.

You can still view this page on the following archive resources:

1. The Ensembl 75 archive represents a code and data freeze taken in February 2014.

2. The GRCh37 archive represents a code and data freeze taken in January 2019.