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
External references
Supporting evidence
ID History
- Gene history

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Gene: HNF1B ENSMODG00000019108

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Description

HNF1 homeobox B [Source:UniProtKB Gene Name;Acc:A0A5F8H289]

Location

Primary_assembly 2: 498,527,797-498,617,059 reverse strand.

ASM229v1:CM000369.1

About this gene

This gene has 3 transcripts (splice variants), 219 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMODT00000024274.3	HNF1B-203	1677	558aa	ENSMODP00000023850.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7F998	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,
ENSMODT00000074222.1	HNF1B-201	1644	548aa	ENSMODP00000053506.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F8H289	-
ENSMODT00000068747.1	HNF1B-202	1371	457aa	ENSMODP00000048587.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F8GMB6	-

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Summary

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