Summary
- Splice variants
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Comparative Genomics
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Gene: Ints12 ENSRNOG00000011844

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Description

integrator complex subunit 12 [Source:RGD Symbol;Acc:1359136]

Gene Synonyms

MGC94937, Phf22, int12

Location

Primary_assembly 2: 224,265,736-224,283,516 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants) and 209 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116296.2	Ints12-202	3142	467aa	ENSRNOP00000088831.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H2UHJ4	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000016066.8	Ints12-201	3027	461aa	ENSRNOP00000016066.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H2UHJ4 A6HVU5 Q68FR3	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

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