Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - 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
External references
Supporting evidence
ID History
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Gene: Ccdc103 ENSRNOG00000002905

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Description

coiled-coil domain containing 103 [Source:RGD Symbol;Acc:1562370]

Gene Synonyms

LOC498006, RGD1562370

Location

Primary_assembly 10: 88,346,453-88,349,853 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant) and 146 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000003890.6	Ccdc103-201	956	237aa	ENSRNOP00000003890.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HJN3 D3Z8H9	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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