Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Molecular interactions
Regulation
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ID History
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Gene: ITPK1 ENSBTAG00000009845

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Description

inositol-tetrakisphosphate 1-kinase [Source:VGNC Symbol;Acc:VGNC:30343]

Location

Primary_assembly 21: 57,590,662-57,754,711 reverse strand.

ARS-UCD2.0:CM008188.2

About this gene

This gene has 4 transcripts (splice variants) and 226 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000072598.2	ITPK1-204	2075	474aa	ENSBTAP00000066033.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF7ABH7	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000098774.1	ITPK1-201	1951	428aa	ENSBTAP00000102385.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TUS9	-
ENSBTAT00000117143.1	ITPK1-203	1923	461aa	ENSBTAP00000087416.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SW26	-
ENSBTAT00000045234.5	ITPK1-202	1714	420aa	ENSBTAP00000042643.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DKA8	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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