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: 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: Atp5f1c ENSRNOG00000019223

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Description

ATP synthase F1 subunit gamma [Source:RGD Symbol;Acc:620011]

Gene Synonyms

Atp5c1

Location

Primary_assembly 17: 73,333,588-73,383,073 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 5 transcripts (splice variants), 254 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000041346.6	Atp5f1c-201	1806	601aa	ENSRNOP00000049879.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6QI09	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,
ENSRNOT00000064802.5	Atp5f1c-202	1150	297aa	ENSRNOP00000061946.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8J8YGG0	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSRNOT00000098367.2	Atp5f1c-203	982	280aa	ENSRNOP00000076528.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5YBP6	-
ENSRNOT00000104116.2	Atp5f1c-204	965	298aa	ENSRNOP00000090262.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GIR3 Q6PCU0	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,
ENSRNOT00000116066.2	Atp5f1c-205	838	278aa	ENSRNOP00000097532.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8J8YGG0	-

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Summary

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