Gene: dysf ENSDARG00000007370

Description

dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive) [Source:NCBI gene (formerly Entrezgene);Acc:560924]

Location

GRCz11:CM002891.2

About this gene

This gene has 2 transcripts (splice variants), 190 orthologues, 6 paralogues and is associated with 16 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000082620.7	dysf-201	9223	2097aa	ENSDARP00000077055.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F4H1	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 P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,
ENSDART00000135415.5	dysf-202	9146	2088aa	ENSDARP00000114340.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QIS3	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,

Summary