Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Phenotypes
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Gene: Akap14 ENSRNOG00000006899

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Description

A-kinase anchoring protein 14 [Source:RGD Symbol;Acc:708510]

Gene Synonyms

LOC60332

Location

Primary_assembly X: 121,259,899-121,276,376 reverse strand.

GRCr8:CM070411.1

About this gene

This gene has 2 transcripts (splice variants), 143 orthologues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000009123.7	Akap14-201	1848	502aa	ENSRNOP00000009123.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JMH8 O35817	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,
ENSRNOT00000105076.2	Akap14-202	2696	484aa	ENSRNOP00000095169.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ANA3	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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