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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Cblc ENSRNOG00000018953

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Description

Cbl proto-oncogene C [Source:RGD Symbol;Acc:1307651]

Gene Synonyms

LOC292699, MGC124804

Location

Primary_assembly 1: 88,567,932-88,584,709 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 96 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025829.9	Cblc-201	1657	497aa	ENSRNOP00000025829.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V8H4	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 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,
ENSRNOT00000110504.2	Cblc-203	1525	453aa	ENSRNOP00000095345.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AL90 A6J8V0	-
ENSRNOT00000092048.3	Cblc-202	1502	476aa	ENSRNOP00000070090.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R3L5	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,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data