Home News About DMDM Database Statistics Research Publications Contact  

Results for the Protein: Q9ULV0
296439293

MYO5B_HUMAN RecName: Full=Unconventional myosin-Vb

Known Diseases associated with this Protein:
  DIARRHEA 2, WITH MICROVILLUS ATROPHY (DIAR2)
  MICROVILLUS INCLUSION DISEASE
7
6
4
5
4
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

 Clicking a check box will display or hide the correlated domain.

 To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic.



Default View:

COG5022 - COG5022
MYSc - smart00242
MYSc_type_VIII - cd01383
MYSc_type_VI - cd01382
MYSc_type_IX - cd01385
MYSc_type_XV - cd01387
MYSc_type_XI - cd01384
MYSc_type_III - cd01379
MYSc_type_V - cd01380
MYSc_type_II - cd01377
MYSc - cd00124
MYSc_type_VII - cd01381
MYSc_type_I - cd01378
Myosin_head - pfam00063
MYSc_type_XVIII - cd01386
Motor_domain - cd01363
IQ - pfam00612
IQ - smart00015
DIL - pfam01843


Swiss-Prot Protein: Q9ULV0
Identical to: NP_001073936
   Default View:


















Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
MYSc_type_VIcd013827.8e-12666761
MYSc_type_IXcd013852.1e-12367769
MYSc_type_XVcd013871.3e-19169760
MYSc_type_XIcd013841e-30069764
MYSccd0012470760
MYSc_type_IIcd013772.1e-25070760
MYSc_type_Icd013785.6e-21970760
MYSc_type_VIIcd013811.3e-25170760
MYSc_type_IIIcd013791.9e-8570806
MYSc_type_Vcd0138070760
MYSc_type_XVIIIcd013867.4e-1373760
Motor_domaincd013637.4e-54106660
COG5022COG502211496
Myosin_headpfam0006371749
IQpfam006120.00094836856
IQpfam006128.2e-07861881
IQpfam006121.4e-05884904
DILpfam018431.1e-5416801785
MYScsmart0024264761
IQsmart000151.4e-07859881
IQsmart000156e-05882904

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
Swiss-ProtVAR_054995Diseasep.ARG656CYSDiarrhea 2, with microvillus atrophy (DIAR2)
Swiss-ProtVAR_054994Diseasep.ARG219HISDiarrhea 2, with microvillus atrophy (DIAR2)
dbSNPrs2298624 Polymorphismp.ARG918HISN/A
dbSNPrs16951438 Polymorphismp.CYS10GLYN/A
dbSNPrs1942418 Polymorphismp.GLY1321GLUN/A
Swiss-ProtVAR_056185Polymorphismp.LYS942ARGN/A
dbSNPrs17659179 Polymorphismp.LYS307ASNN/A
dbSNPrs1815930 Polymorphismp.THR126ALAN/A
Swiss-ProtVAR_054993Diseasep.VAL108GLYDiarrhea 2, with microvillus atrophy (DIAR2)
OMIM606540.0005 Diseasep.ARG656CYSMICROVILLUS INCLUSION DISEASE
OMIM606540.0006 Diseasep.PRO660LEUMICROVILLUS INCLUSION DISEASE
OMIM606540.0004 Diseasep.TRP375TERMICROVILLUS INCLUSION DISEASE
OMIM606540.0003 Diseasep.VAL108GLYMICROVILLUS INCLUSION DISEASE



   |   1000 Hilltop Circle, Baltimore, MD 21250   |   Department of Biological Sciences   |   Phone: 410-455-2258