Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Dysf ENSRNOG00000032788

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Description

dysferlin [Source:RGD Symbol;Acc:1311023]

Gene Synonyms

LOC312492

Location

Primary_assembly 4: 118,047,989-118,248,273 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 7 transcripts (splice variants), 192 orthologues, 5 paralogues and is associated with 21 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000085765.3	Dysf-202	6771	2134aa	ENSRNOP00000074138.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K7B6	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000117268.2	Dysf-206	7065	2112aa	ENSRNOP00000087285.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GEZ7	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,
ENSRNOT00000115270.2	Dysf-205	7035	2102aa	ENSRNOP00000082754.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZVI7	-
ENSRNOT00000120244.2	Dysf-207	7026	2099aa	ENSRNOP00000078253.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZKQ3	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000106282.2	Dysf-203	7009	2133aa	ENSRNOP00000097863.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GM91	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000108867.2	Dysf-204	6529	2128aa	ENSRNOP00000078213.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZKH0	-
ENSRNOT00000064536.4	Dysf-201	6319	2029aa	ENSRNOP00000061606.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IAQ5 D4A6X1	-

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Summary

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