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
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Ccdc184 ENSRNOG00000021945

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Description

coiled-coil domain containing 184 [Source:RGD Symbol;Acc:1593153]

Gene Synonyms

MGC114464

Location

Primary_assembly 7: 131,176,373-131,183,680 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 3 transcripts (splice variants) and 85 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000151677.1	Ccdc184-203	3058	193aa	ENSRNOP00000109967.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KC62	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,
ENSRNOT00000131926.1	Ccdc184-202	2036	193aa	ENSRNOP00000110778.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KC62	-
ENSRNOT00000031157.5	Ccdc184-201	1918	193aa	ENSRNOP00000038126.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KC62 Q4V8F1	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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Gene tree

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