Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Ripor1 ENSRNOG00000017604

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Description

RHO family interacting cell polarization regulator 1 [Source:RGD Symbol;Acc:1307772]

Gene Synonyms

Fam65a, LOC291974, RGD1307772

Location

Primary_assembly 19: 50,387,523-50,416,319 forward strand.

GRCr8:CM070409.1

About this gene

This gene has 4 transcripts (splice variants), 248 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000139880.1	Ripor1-204	3714	1237aa	ENSRNOP00000102696.1	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,
ENSRNOT00000023710.8	Ripor1-201	4327	1231aa	ENSRNOP00000023710.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IYQ6 Q4FZU8	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,
ENSRNOT00000089022.3	Ripor1-202	4145	1231aa	ENSRNOP00000069592.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JVR9	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,
ENSRNOT00000116738.2	Ripor1-203	3949	1183aa	ENSRNOP00000096363.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6B430	-

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Summary

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