Gene: Ahi1 ENSRNOG00000013969

Description

Abelson helper integration site 1 [Source:RGD Symbol;Acc:1303040]

Gene Synonyms

Ahi-1, LOC103690149

Location

Primary_assembly 1: 17,582,006-17,711,774 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 190 orthologues, 25 paralogues and is associated with 24 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000097444.2	Ahi1-203	4961	1048aa	ENSRNOP00000080424.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZQ93	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 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,
ENSRNOT00000095156.2	Ahi1-202	4959	1011aa	ENSRNOP00000086069.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A5B3	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,
ENSRNOT00000019076.8	Ahi1-201	4934	1039aa	ENSRNOP00000019077.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M9F9	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,