Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
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ID History
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Gene: Ccdc137 ENSRNOG00000048712

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Description

coiled-coil domain containing 137 [Source:RGD Symbol;Acc:1591129]

Gene Synonyms

LOC688298

Location

Primary_assembly 10: 106,229,099-106,235,502 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000118258.2	Ccdc137-202	1774	310aa	ENSRNOP00000076646.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y5F8	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,
ENSRNOT00000072099.3	Ccdc137-201	3056	289aa	ENSRNOP00000066630.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HLD2 M0RAS3	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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