Gene: Yap1 ENSRNOG00000005933

Description

Yes1 associated transcriptional regulator [Source:RGD Symbol;Acc:1306035]

Gene Synonyms

LOC363014, YAP65, Yap

Location

Primary_assembly 8: 13,380,551-13,451,437 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 3 transcripts (splice variants), 263 orthologues, 1 paralogue and is associated with 23 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000007866.8	Yap1-201	4217	491aa	ENSRNOP00000007866.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	R9PXS9	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,
ENSRNOT00000085285.3	Yap1-203	4169	475aa	ENSRNOP00000074302.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R8L7	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,
ENSRNOT00000031189.9	Yap1-202	4085	447aa	ENSRNOP00000034369.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QHR7	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,