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: Molecular function
- GO: Cellular component
- GO: Biological process
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: Ints13 ENSRNOG00000001808

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Description

integrator complex subunit 13 [Source:RGD Symbol;Acc:1592236]

Gene Synonyms

Asun, LOC690728

Location

Primary_assembly 4: 181,189,765-181,222,235 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000118399.2	Ints13-202	3747	732aa	ENSRNOP00000083691.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZWB2 A6IN18	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,
ENSRNOT00000065730.3	Ints13-201	2996	706aa	ENSRNOP00000061847.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A6N9	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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