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

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Gene: LOC100911229 ENSRNOG00000055604

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Description

sperm motility kinase-like [Source:RGD Symbol;Acc:6494469]

Location

Primary_assembly 16: 71,071,845-71,176,054 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 6 transcripts (splice variants), 106 orthologues and 69 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000131677.1	LOC100911229-203	13353	654aa	ENSRNOP00000101460.1	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,
ENSRNOT00000157443.1	LOC100911229-204	12622	654aa	ENSRNOP00000104742.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000163580.1	LOC100911229-206	11684	654aa	ENSRNOP00000101968.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000160131.1	LOC100911229-205	11336	654aa	ENSRNOP00000109031.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000039592.7	LOC100911229-201	9504	654aa	ENSRNOP00000033067.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1A5Q6	-
ENSRNOT00000081838.3	LOC100911229-202	9480	654aa	ENSRNOP00000070378.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JXR8	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data