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Results for the Protein: NP_001124450
195976758

dysferlin isoform 11 [Homo sapiens]

Known Diseases associated with this Protein:
  MIYOSHI MYOPATHY
  MIYOSHI MYOPATHY, INCLUDED
  MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
  MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B, IN
  MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B, INCLUDED
  MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET, INCLUDED;;
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Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

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Default View:

C2 - smart00239
C2A_MCTP_PRT_plant - cd04022
C2A_SLP - cd08521
C2B_Synaptotagmin-7 - cd08405
C2C_Tricalbin-like - cd04045
C2_Smurf-like - cd08382
C2 - pfam00168
C2C_KIAA1228 - cd04030
C2A_Rabphilin_Doc2 - cd04035
C2B_Synaptotagmin - cd00276
C2_plant_PLD - cd04015
C2B_Munc13-like - cd04009
C2 - cd00030
C2A_Ferlin - cd08373
C2B_Ferlin - cd04011
FerI - pfam08151
C2C_Ferlin - cd04018
C2A_fungal - cd04041
C2D_Tricalbin-like - cd04040
FerA - pfam08165
FerB - pfam08150
DysFN - smart00693
DysFC - smart00694
C2A_Synaptotagmin-8 - cd08387
C2_PKC_alpha_gamma - cd04026
C2A_RIM1alpha - cd04031
C2D_Ferlin - cd04017
C2C_MCTP_PRT - cd08377
C2B_RasA1_RasA4 - cd04025
C2A_MCTP_PRT - cd04042
C2_ArfGAP - cd04038
C2B_RasGAP - cd08675
C2A_C2C_Synaptotagmi - cd08391
C2A_Synaptotagmin-li - cd04024
C2_KIAA0528-like - cd08688
C2_Calpain - cd04046
C2B_Synaptotagmin-1 - cd08402
C2B_MCTP_PRT - cd08376
C2E_Ferlin - cd04037
C2F_Ferlin - cd08374




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
C2C_Tricalbin-likecd040459.4e-061114
C2_Smurf-likecd083824.9e-051122
C2B_Synaptotagmin-7cd084050.000141120
C2A_SLPcd085210.000111103
C2cd000306.2e-212105
C2B_Synaptotagmincd002760.00035297
C2B_Munc13-likecd040096.8e-072107
C2_plant_PLDcd040150.000412124
C2C_KIAA1228cd040302.7e-062104
C2A_Rabphilin_Doc2cd040358.8e-072105
C2A_Ferlincd083731.6e-5010135
C2B_Ferlincd040116.3e-68217326
C2cd000304.7e-11222323
C2C_Ferlincd040181.3e-107380554
C2cd000301.1e-12381498
C2D_Tricalbin-likecd040400.00025381516
C2A_fungalcd040410.00023381497
C2A_Synaptotagmin-8cd083870.0005511381266
C2_PKC_alpha_gammacd040269.4e-0611391274
C2A_RIM1alphacd040313e-0511411261
C2D_Ferlincd040177.3e-8011521280
C2C_MCTP_PRTcd083770.0003811521277
C2B_RasA1_RasA4cd040252e-0911531279
C2A_MCTP_PRTcd040420.0003111531278
C2cd000303.9e-2411541260
C2A_Synaptotagmin-licd040244.3e-0711541276
C2_ArfGAPcd040387.9e-0611541305
C2A_C2C_Synaptotagmicd083915e-0711541276
C2B_RasGAPcd086752e-0711541274
C2_KIAA0528-likecd086881.3e-0511541261
C2_Calpaincd040460.0003111571283
C2B_Synaptotagmin-1cd084020.0003815961718
C2E_Ferlincd040373.6e-8416001723
C2B_MCTP_PRTcd083764.8e-0516001709
C2cd000303.9e-1816011707
C2F_Ferlincd083747.4e-8518331965
C2cd000302.5e-1118341965
C2pfam001689.2e-23285
C2pfam001681.5e-12222302
C2pfam001681.5e-19381479
C2pfam001687.5e-2311541244
C2pfam001683.8e-2016011684
C2smart002392.2e-221100
C2smart002392.6e-16221317
FerIpfam081519.1e-45303374
C2smart002391.4e-19380494
FerApfam081653e-25694759
FerBpfam081507.3e-56786861
DysFNsmart006932.6e-22874933
DysFNsmart006931.5e-219461002
DysFCsmart006942.8e-1510111049
DysFCsmart006942.4e-1210681101
C2smart002391.4e-2311531258
C2smart002393.1e-2016001699
C2smart002395e-2318331962

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs34660230 Polymorphismp.ALA1072PRON/A
dbSNPrs115279465 Polymorphismp.ALA350VALN/A
dbSNPrs34211915 Polymorphismp.ARG1022GLNN/A
dbSNPrs61738567 Polymorphismp.ASP1459GLYN/A
dbSNPrs34671418 Polymorphismp.ILE834VALN/A
dbSNPrs13407355 Polymorphismp.LEU189VALN/A
OMIM603009.0004 Diseasep.ARG2024CYSMIYOSHI MYOPATHY||MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B, INCLUDED
OMIM603009.0011 Diseasep.ARG1028HISMIYOSHI MYOPATHY
OMIM603009.0012 Diseasep.ARG1887TERMIYOSHI MYOPATHY||MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET, INCLUDED;;||MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B, IN
OMIM603009.0013 Diseasep.ASP607TYRMUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
OMIM603009.0001 Diseasep.GLN587TERMIYOSHI MYOPATHY
OMIM603009.0014 Diseasep.GLU1716GLYMUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
OMIM603009.0017 Diseasep.GLY267ARGMUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
OMIM603009.0015 Diseasep.GLY487ARGMIYOSHI MYOPATHY
OMIM603009.0018 Diseasep.GLY267TRPMIYOSHI MYOPATHY
OMIM603009.0003 Diseasep.ILE1280VALMIYOSHI MYOPATHY||MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B, INCLUDED
OMIM603009.0007 Diseasep.PRO773ARGMUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B||MIYOSHI MYOPATHY, INCLUDED
OMIM603009.0010 Diseasep.TRP981CYSMIYOSHI MYOPATHY
OMIM603009.0009 Diseasep.VAL66ASPMUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B



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