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

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Gene: Ctsf ENSRNOG00000019708

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Description

cathepsin F [Source:RGD Symbol;Acc:1308181]

Gene Synonyms

LOC361704, MGC124702

Location

Primary_assembly 1: 211,582,098-211,587,916 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant), 530 orthologues, 27 paralogues and is associated with 8 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000026718.8	Ctsf-201	1933	462aa	ENSRNOP00000026718.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A9LRS7 Q499S6	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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