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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: F13B ENSG00000143278

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Description

coagulation factor XIII, B polypeptide [Source:HGNC Symbol;Acc:3534]

Gene Synonyms

FXIIIB

Location

Chromosome 1: 197,008,321-197,036,397 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 2 transcripts (splice variants), 6 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000367412.1	F13B-001	2217	661aa	ENSP00000356382.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS1388	P05160	NM_001994.2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000490002.1	F13B-002	596	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

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Summary

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