Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: HNF1B ENSOCUG00000003682

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Description

HNF1 homeobox B [Source:UniProtKB Gene Name;Acc:A0A5F9CS50]

Location

Chromosome 19: 25,217,906-25,271,343 forward strand.

OryCun2.0:CM000808.1

About this gene

This gene has 3 transcripts (splice variants), 219 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000003681.4	HNF1B-203	1710	569aa	ENSOCUP00000003191.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1SK71	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,
ENSOCUT00000054671.1	HNF1B-201	1665	554aa	ENSOCUP00000036463.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F9CS50	-
ENSOCUT00000057896.1	HNF1B-202	1392	463aa	ENSOCUP00000043803.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F9DD96	-

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Summary

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