Gene: Pex11g ENSRNOG00000028100

Description

peroxisomal biogenesis factor 11 gamma [Source:RGD Symbol;Acc:1307070]

Gene Synonyms

LOC288369, Pex11c

Location

Primary_assembly 12: 6,277,664-6,318,919 reverse strand.

GRCr8:CM070402.1

About this gene

This gene has 5 transcripts (splice variants), 187 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000037564.6	Pex11g-201	1491	304aa	ENSRNOP00000033197.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4AEJ6	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,
ENSRNOT00000161162.1	Pex11g-205	1245	222aa	ENSRNOP00000105952.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000132382.1	Pex11g-204	825	218aa	ENSRNOP00000104074.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000095285.2	Pex11g-202	531	176aa	ENSRNOP00000087462.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A5W5	-
ENSRNOT00000110489.2	Pex11g-203	531	176aa	ENSRNOP00000089073.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A7E4	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,