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: Mospd1 ENSRNOG00000066239

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Description

motile sperm domain containing 1 [Source:RGD Symbol;Acc:1359486]

Gene Synonyms

LOC317312

Location

Primary_assembly X: 138,020,115-138,047,603 reverse strand.

GRCr8:CM070411.1

About this gene

This gene has 3 transcripts (splice variants), 214 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000161890.1	Mospd1-204	846	215aa	ENSRNOP00000112498.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000003192.8	Mospd1-202	2034	213aa	ENSRNOP00000003192.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q064 A6KUJ2 Q5RJS6	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000102965.2	Mospd1-203	1870	214aa	ENSRNOP00000076964.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y568	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,

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Summary

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