Gene: Diaph1 ENSRNOG00000019688

Description

diaphanous-related formin 1 [Source:RGD Symbol;Acc:1310707]

Gene Synonyms

DRF1, Diap1, LOC307483, mDIA1

Location

Primary_assembly 18: 29,920,889-30,020,280 reverse strand.

GRCr8:CM070408.1

About this gene

This gene has 3 transcripts (splice variants), 208 orthologues, 15 paralogues and is associated with 18 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000060432.7	Diaph1-201	5617	1266aa	ENSRNOP00000057176.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QTN9	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,
ENSRNOT00000147673.1	Diaph1-203	5608	1263aa	ENSRNOP00000108105.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000102970.2	Diaph1-202	5590	1257aa	ENSRNOP00000088426.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A828	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,