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

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Gene: Mak16 ENSRNOG00000010783

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Description

MAK16 homolog [Source:RGD Symbol;Acc:1311297]

Gene Synonyms

LOC306526, MGC109625, RGD1311297, Rbm13

Location

Primary_assembly 16: 67,675,735-67,684,836 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 2 transcripts (splice variants) and 202 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000108793.2	Mak16-202	2325	298aa	ENSRNOP00000086313.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A0Z5	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,
ENSRNOT00000015297.8	Mak16-201	2377	293aa	ENSRNOP00000015297.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IVV8 F7F652	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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