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: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Hddc3 ENSRNOG00000012236

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Description

HD domain containing 3 [Source:RGD Symbol;Acc:1311839]

Gene Synonyms

LOC308758, RGD1311839

Location

Primary_assembly 1: 143,705,320-143,711,010 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 187 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000099679.2	Hddc3-202	1774	183aa	ENSRNOP00000080516.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZQC5	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,
ENSRNOT00000016445.7	Hddc3-201	1723	166aa	ENSRNOP00000016445.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A500	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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