Human (GRCh37.p13)
Description

C-type lectin domain family 1, member B [Source:HGNC Symbol;Acc:24356]

Gene Synonyms

1810061I13Rik, CLEC2, CLEC2B, PRO1384, QDED721

Location

Chromosome 12: 10,138,241-10,166,023 reverse strand.

GRCh37:CM000674.1

About this gene

This gene has 4 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
ENST00000298527.6CLEC1B-005952229aa
 
Protein coding
CCDS41752Q9P126 NM_016509.3Ensembl CanonicalGENCODE Basic
ENST00000428126.2CLEC1B-0013054196aa
 
Protein coding
CCDS41751Q9P126 -GENCODE Basic
ENST00000348658.4CLEC1B-201869196aa
 
Protein coding
CCDS41751Q9P126 NM_001099431.1GENCODE Basic
ENST00000398937.2CLEC1B-00678396aa
 
Protein coding
H7BYT7 -CDS 5' incomplete
Name

CLEC1B (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q9P126

CCDS

This gene is a member of the Human CCDS set: CCDS41751.1, CCDS41752.1

Ensembl version

ENSG00000165682.10

Other assemblies

This gene maps to 9,985,642-10,013,424 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:
OTTHUMG00000168502 (version 1)

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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