Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: C1QTNF7 ENSSSCG00000008737

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Description

C1q and TNF related 7 [Source:VGNC Symbol;Acc:VGNC:85986]

Location

Primary_assembly 8: 10,738,389-10,756,411 forward strand.

Sscrofa11.1:CM000819.5

About this gene

This gene has 2 transcripts (splice variants), 197 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000070634.2	C1QTNF7-202	1249	311aa	ENSSSCP00000069292.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2REI7	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,
ENSSSCT00000065130.2	C1QTNF7-201	2216	289aa	ENSSSCP00000037528.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A0U0 A0A8D0X729	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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