Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Fhdc1 ENSRNOG00000024594

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Description

FH2 domain containing 1 [Source:RGD Symbol;Acc:1311955]

Gene Synonyms

LOC295161, RGD1311955

Location

Primary_assembly 2: 172,089,010-172,125,956 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 1 transcript (splice variant), 274 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000066477.5	Fhdc1-201	4106	1148aa	ENSRNOP00000060810.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J5W7 D3ZL83	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,

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Summary

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