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
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: C1qtnf7 ENSRNOG00000005094

.

Description

C1q and TNF related 7 [Source:RGD Symbol;Acc:1306978]

Gene Synonyms

Adig, Ctrp7, LOC305423

Location

Primary_assembly 14: 71,680,479-71,792,865 reverse strand.

GRCr8:CM070404.1

About this gene

This gene has 1 transcript (splice variant), 197 orthologues and 20 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000064495.5	C1qtnf7-201	1660	296aa	ENSRNOP00000061160.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2QC08	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,

.

Summary

.

.