Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: RBKS ENSGALG00010020057

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Description

ribokinase [Source:HGNC Symbol;Acc:HGNC:30325]

Location

Primary_assembly 3: 27,268,334-27,333,283 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028484.1

About this gene

This gene has 4 transcripts (splice variants), 197 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010048460.1	RBKS-202	1899	331aa	ENSGALP00010028572.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSGALT00010048451.1	RBKS-204	1994	303aa	ENSGALP00010028565.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N8A7	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,
ENSGALT00010048464.1	RBKS-201	1951	315aa	ENSGALP00010028575.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSGALT00010048455.1	RBKS-203	1892	305aa	ENSGALP00010028568.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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