Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- 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

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Gene: Mex3d ENSRNOG00000030830

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Description

mex-3 RNA binding family member D [Source:RGD Symbol;Acc:1310576]

Gene Synonyms

LOC299613, Rkhd1

Location

Primary_assembly 7: 9,976,253-9,983,383 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 167 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000040170.8	Mex3d-201	2366	732aa	ENSRNOP00000047111.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M5V7	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 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,
ENSRNOT00000109301.2	Mex3d-202	3199	719aa	ENSRNOP00000081736.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZUR2	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,

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Summary

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