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

Configure this page

Share this page

Bookmark this page

.

Gene: Rhoxf12 ENSRNOG00000040033

.

Description

Rhox homeobox family member 12 [Source:RGD Symbol;Acc:1563789]

Gene Synonyms

LOC363437, Rhox12

Location

Primary_assembly X: 121,756,211-121,761,534 reverse strand.

GRCr8:CM070411.1

About this gene

This gene has 2 transcripts (splice variants) and 11 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000061546.5	Rhoxf12-201	628	175aa	ENSRNOP00000058263.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JMJ3 F7F8E5	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,
ENSRNOT00000104732.2	Rhoxf12-202	470	154aa	ENSRNOP00000087640.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AGY0	-

.

Summary

.

.