Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Molecular interactions
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Gene: Iqcg ENSRNOG00000026420

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Description

IQ motif containing G [Source:RGD Symbol;Acc:1311606]

Gene Synonyms

LOC363796, RGD1311606

Location

Primary_assembly 11: 81,235,090-81,276,249 forward strand.

GRCr8:CM070401.1

About this gene

This gene has 2 transcripts (splice variants), 153 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000087633.3	Iqcg-202	1541	421aa	ENSRNOP00000071586.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K0U5	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,
ENSRNOT00000032518.6	Iqcg-201	1846	419aa	ENSRNOP00000037862.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IRM7 G3V973	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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Summary

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