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Results for the Protein: NP_001070654
116284396

myosin-14 isoform 1 [Homo sapiens]

Known Diseases associated with this Protein:
  DEAFNESS, AUTOSOMAL DOMINANT 4
  PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
6
2
6
2
0
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
Myosin_N - pfam02736
MYSc_type_IX - cd01385
MYSc - smart00242
MYSc_type_VIII - cd01383
MYSc_type_II - cd01377
MYSc_type_VI - cd01382
MYSc_type_XI - cd01384
MYSc_type_XV - cd01387
MYSc_type_XVIII - cd01386
MYSc_type_III - cd01379
MYSc_type_V - cd01380
MYSc - cd00124
MYSc_type_VII - cd01381
Myosin_head - pfam00063
MYSc_type_I - cd01378
Motor_domain - cd01363
IQ - smart00015
IQ - pfam00612
Myosin_tail_1 - pfam01576




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
MYSc_type_IXcd013852.6e-7199811
MYSc_type_VIIIcd013835.7e-157100807
MYSc_type_IIcd01377101807
MYSc_type_VIcd013821.2e-95102810
MYSc_type_XIcd013841.3e-195105812
MYSc_type_XVcd013871e-154105807
MYSccd001242e-281106807
MYSc_type_VIIcd013816.1e-186106807
MYSc_type_Vcd013801e-209106807
MYSc_type_IIIcd013791.4e-68106830
MYSc_type_XVIIIcd013861.6e-36106807
MYSc_type_Icd013783.6e-184108807
Motor_domaincd013634.9e-104141706
COG5022COG50221.5e-303351606
Myosin_Npfam027361.4e-065395
Myosin_headpfam00063107796
IQpfam006120.0002812832
Myosin_tail_1pfam015761.9e-18110981955
MYScsmart00242100808
IQsmart000151.8e-05810832

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs11669191 Polymorphismp.ALA1217GLUN/A
dbSNPrs34498817 Polymorphismp.PRO342ALAN/A
OMIM608568.0006 Diseasep.ARG908LEUPERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
OMIM608568.0003 Diseasep.ARG693SERDEAFNESS, AUTOSOMAL DOMINANT 4
OMIM608568.0004 Diseasep.GLY376CYSDEAFNESS, AUTOSOMAL DOMINANT 4
OMIM608568.0002 Diseasep.LEU943PHEDEAFNESS, AUTOSOMAL DOMINANT 4
OMIM608568.0005 Diseasep.SER120LEUDEAFNESS, AUTOSOMAL DOMINANT 4
OMIM608568.0001 Diseasep.SER7TERDEAFNESS, AUTOSOMAL DOMINANT 4



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