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 ENSPTRG00000009059

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Description

HNF1 homeobox B [Source:VGNC Symbol;Acc:VGNC:12273]

Location

Chromosome 17: 19,710,172-19,773,288 forward strand.

Pan_tro_3.0:CM000331.3

About this gene

This gene has 4 transcripts (splice variants), 218 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000107340.1	HNF1B-201	7198	557aa	ENSPTRP00000082398.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T0L8 A0A6D2WEW2	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSPTRT00000101484.1	HNF1B-202	7079	548aa	ENSPTRP00000080087.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3ST24 A0A6D2X792	-
ENSPTRT00000016691.3	HNF1B-203	1374	457aa	ENSPTRP00000015442.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WGG0 H2QCS4	-
ENSPTRT00000104520.1	HNF1B-204	861	286aa	ENSPTRP00000089075.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TJK7	-

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Summary

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