Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
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Gene: Spem1 ENSRNOG00000015419

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Description

spermatid maturation 1 [Source:RGD Symbol;Acc:1593311]

Gene Synonyms

LOC691981

Location

Primary_assembly 10: 55,040,195-55,041,479 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 77 orthologues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000020675.7	Spem1-201	1025	312aa	ENSRNOP00000020676.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HFU1 D3ZZ79	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,

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Summary

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