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Results for Proteins associated with the Gene: SCN9A
SCN9A
6335


Known Diseases associated with this Protein:
  CONGENITAL INDIFFERENCE TO PAIN AUTOSOMAL RECESSIVE (CIPAR)
  FEBRILE SEIZURES, FAMILIAL, 3B (FEB3B)
  GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS 7 (GEFS+7)
  PAROXYSMAL EXTREME PAIN DISORDER (PEPD)
  PRIMARY ERYTHERMALGIA (PERYTHM)
22
13
0
0
35
Tips:
 The Domains on the Default View are decided by HMMER's search E-Value of the Protein against the Domain model.
 Clicking a check box on the left will display or hide the corresponding domain(s).
 To view the Protein page, either click on the protein links in the box to the left or the blue bar above the Protein's graphic.


Default View:

Ion_trans - pfam00520
DUF3451 - pfam11933
Na_trans_assoc - pfam06512
IQ - smart00015


Swiss-Prot Protein: Q15858
   Default View:


Default View:

Ion_trans - pfam00520
DUF3451 - pfam11933
Na_trans_assoc - pfam06512
IQ - smart00015


RefSeq Protein: NP_002968
   Default View:



Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
NP_002968Ion_transpfam005207679561.3e-58
NP_002968Ion_transpfam00520121714456.6e-72
NP_002968Ion_transpfam00520153817488.6e-69
NP_002968DUF3451pfam119334636843.4e-99
NP_002968Na_trans_assocpfam0651297111912.8e-107
NP_002968IQsmart00015187718995.4e-05



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