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: Ccdc9b ENSRNOG00000028910

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Description

coiled-coil domain containing 9B [Source:RGD Symbol;Acc:1565536]

Gene Synonyms

LOC311323, RGD1565536

Location

Primary_assembly 3: 126,192,232-126,199,580 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 2 transcripts (splice variants), 174 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000045362.6	Ccdc9b-201	1554	517aa	ENSRNOP00000046560.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZKN0	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,
ENSRNOT00000092158.3	Ccdc9b-202	2674	499aa	ENSRNOP00000070443.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JXY0	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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