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
---
Name

CLEC12B (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q2HXU8

CCDS

This gene is a member of the Human CCDS set: CCDS44830.1, CCDS8610.1

Ensembl version

ENSG00000256660.1

Other assemblies

This gene maps to 10,010,627-10,018,619 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000168397 (version 3)

Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Contigs

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