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DYSF dysferlin [ Falco peregrinus (peregrine falcon) ]

Gene ID: 101913443, updated on 3-Aug-2024

Summary

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Gene symbol
DYSF
Gene description
dysferlin
See related
EnsemblRapid:ENSFPEG00020010415
Gene type
protein coding
RefSeq status
MODEL
Organism
Falco peregrinus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Neoaves; Telluraves; Australaves; Falconiformes; Falconidae; Falco
Orthologs
human mouse all
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Genomic context

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See DYSF in Genome Data Viewer
Location:
chromosome: 2
Exon count:
58
Annotation release Status Assembly Chr Location
RS_2023_04 current bFalPer1.pri (GCF_023634155.1) 2 NC_073722.1 (38466629..38571006)
102 previous assembly F_peregrinus_v1.0 (GCF_000337955.1) Unplaced Scaffold NW_004930253.1 (1638850..1739613, complement)

Chromosome 2 - NC_073722.1Genomic Context describing neighboring genes Neighboring gene poly(A) binding protein interacting protein 2B Neighboring gene zinc finger protein 638 Neighboring gene cytochrome P450 26B1 Neighboring gene exocyst complex component 6B

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

General gene information

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Homology

Gene Ontology Provided by RefSeq

Function Evidence Code Pubs
enables calcium ion binding IEA
Inferred from Electronic Annotation
more info
 PubMed 
enables calcium-dependent phospholipid binding IEA
Inferred from Electronic Annotation
more info
 PubMed 
Process Evidence Code Pubs
involved_in T-tubule organization IEA
Inferred from Electronic Annotation
more info
 PubMed 
involved_in macrophage activation involved in immune response IEA
Inferred from Electronic Annotation
more info
 PubMed 
involved_in monocyte activation involved in immune response IEA
Inferred from Electronic Annotation
more info
 PubMed 
involved_in negative regulation of phagocytosis IEA
Inferred from Electronic Annotation
more info
 PubMed 
involved_in plasma membrane repair IEA
Inferred from Electronic Annotation
more info
 PubMed 
involved_in vesicle fusion IEA
Inferred from Electronic Annotation
more info
 PubMed 
Component Evidence Code Pubs
located_in T-tubule IEA
Inferred from Electronic Annotation
more info
 PubMed 
located_in cytoplasmic vesicle IEA
Inferred from Electronic Annotation
more info
 PubMed 
located_in membrane IEA
Inferred from Electronic Annotation
more info
 PubMed 

General protein information

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Preferred Names
dysferlin
Names
dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive)

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: GCF_023634155.1-RS_2023_04

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference bFalPer1.pri Primary Assembly

Genomic

  1. NC_073722.1 Reference bFalPer1.pri Primary Assembly

    Range
    38466629..38571006
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_055796232.1 → XP_055652207.1  dysferlin isoform X3

  2. XM_055796237.1 → XP_055652212.1  dysferlin isoform X12

  3. XM_055796238.1 → XP_055652213.1  dysferlin isoform X13

  4. XM_055796234.1 → XP_055652209.1  dysferlin isoform X6

    Related
    ENSFPEP00020015384.1, ENSFPET00020015860.1

  5. XM_055796239.1 → XP_055652214.1  dysferlin isoform X14

  6. XM_055796240.1 → XP_055652215.1  dysferlin isoform X15

    Related
    ENSFPEP00020015391.1, ENSFPET00020015867.1

  7. XM_027789732.2 → XP_027645533.2  dysferlin isoform X1

  8. XM_055796231.1 → XP_055652206.1  dysferlin isoform X2

  9. XM_027789735.2 → XP_027645536.2  dysferlin isoform X7

  10. XM_055796233.1 → XP_055652208.1  dysferlin isoform X4

  11. XM_027789737.2 → XP_027645538.2  dysferlin isoform X8

  12. XM_027789740.2 → XP_027645541.2  dysferlin isoform X5

  13. XM_027789738.2 → XP_027645539.2  dysferlin isoform X9

  14. XM_055796235.1 → XP_055652210.1  dysferlin isoform X10

  15. XM_055796236.1 → XP_055652211.1  dysferlin isoform X11

Nucleotide Protein
Heading Accession and Version

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