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: Bsph1 ENSRNOG00000052287

.

Description

binder of sperm protein homolog 1 [Source:RGD Symbol;Acc:1594649]

Gene Synonyms

LOC100912137, LOC691820

Location

Primary_assembly 1: 83,546,660-83,586,707 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 68 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000083154.3	Bsph1-201	1529	132aa	ENSRNOP00000068799.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JTQ2	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,
ENSRNOT00000089836.3	Bsph1-202	1395	122aa	ENSRNOP00000074764.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K8W7	-

.

Summary

.

.