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

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Gene: HNF1B ENSSSCG00000022417

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Description

HNF1 homeobox B [Source:NCBI gene (formerly Entrezgene);Acc:397002]

Location

Primary_assembly 12: 39,143,121-39,201,631 reverse strand.

Sscrofa11.1:CM000823.5

About this gene

This gene has 4 transcripts (splice variants), 220 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000067450.2	HNF1B-201	2102	577aa	ENSSSCP00000069206.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QWH0	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,
ENSSSCT00000023424.2	HNF1B-204	3072	557aa	ENSSSCP00000028034.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1T5E6 I3LV82	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,
ENSSSCT00000077806.2	HNF1B-202	2068	548aa	ENSSSCP00000066526.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1T5F5 A0A5G2R7E8	-
ENSSSCT00000090025.1	HNF1B-203	1825	457aa	ENSSSCP00000072714.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1T4P3 A0A5G2R6K9	-

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Summary

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