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: Rab35 ENSRNOG00000022014

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Description

RAB35, member RAS oncogene family [Source:RGD Symbol;Acc:1306362]

Gene Synonyms

LOC288700

Location

Primary_assembly 12: 40,967,103-40,991,195 reverse strand.

mRatBN7.2:CM026985.1

About this gene

This gene has 5 transcripts (splice variants), 212 orthologues and 71 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000030031.5	Rab35-201	2211	272aa	ENSRNOP00000029070.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QFM9	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,
ENSRNOT00000113162.1	Rab35-204	2197	198aa	ENSRNOP00000081478.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZT09	-
ENSRNOT00000106644.1	Rab35-203	2070	203aa	ENSRNOP00000085013.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A0E0	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,
ENSRNOT00000114049.1	Rab35-205	2044	221aa	ENSRNOP00000092476.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ADQ8	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,
ENSRNOT00000103324.1	Rab35-202	1931	183aa	ENSRNOP00000088611.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A5F7	-

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Summary

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