Summary
- Splice variants
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Gene: Spmip5 ENSRNOG00000025953

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Description

sperm microtubule inner protein 5 [Source:RGD Symbol;Acc:1584737]

Gene Synonyms

LOC681006

Location

Primary_assembly 1: 267,910,932-267,920,557 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 103 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000126754.1	Spmip5-203	2303	322aa	ENSRNOP00000099861.1	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,
ENSRNOT00000140957.1	Spmip5-204	2128	300aa	ENSRNOP00000109385.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000039453.8	Spmip5-201	874	224aa	ENSRNOP00000035488.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A2P4	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,
ENSRNOT00000114359.2	Spmip5-202	785	232aa	ENSRNOP00000092106.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AEX2	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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