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: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Gene: Sinhcaf ENSRNOG00000049943

Description

SIN3-HDAC complex associated factor [Source:RGD Symbol;Acc:1595037]

Gene Synonyms

Fam60a, LOC100909791, LOC686611, MGC187734

Location

GRCr8:CM070394.1

About this gene

This gene has 1 transcript (splice variant), 265 orthologues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000071930.4	Sinhcaf-201	2753	221aa	ENSRNOP00000067114.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A9K3Y7U5 B4F781	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,

Upcoming Ensembl Platform Transition