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: Rbm10 ENSRNOG00000008472

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Description

RNA binding motif protein 10 [Source:RGD Symbol;Acc:631366]

Location

Primary_assembly X: 4,093,914-4,126,060 reverse strand.

GRCr8:CM070411.1

About this gene

This gene has 3 transcripts (splice variants), 180 orthologues, 2 paralogues and is associated with 18 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000096592.2	Rbm10-203	3371	929aa	ENSRNOP00000084552.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A0D6	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,
ENSRNOT00000011317.8	Rbm10-201	3137	851aa	ENSRNOP00000011317.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ACC8 P70501	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,
ENSRNOT00000077453.3	Rbm10-202	2953	910aa	ENSRNOP00000072756.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K3S6	-

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Summary

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