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Results for Proteins associated with the Gene: TBC1D24
TBC1D24
57465


Known Diseases associated with this Protein:
  DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND
  EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16
  EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16 (EIEE16)
  FAMILIAL INFANTILE MYOCLONIC EPILEPSY (FIME)
  MYOCLONIC EPILEPSY, INFANTILE, FAMILIAL
  SEIZURES SYNDROME
12
0
8
0
4
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:

TBC - smart00164
RabGAP-TBC - pfam00566
OXR1 - COG5142
TLDc - smart00584
TLD - pfam07534


Swiss-Prot Protein: Q9ULP9
Identical to: NP_001186036
   Default View:




Default View:

TBC - smart00164
RabGAP-TBC - pfam00566
OXR1 - COG5142
TLDc - smart00584
TLD - pfam07534



Default View:

TBC - smart00164
RabGAP-TBC - pfam00566
OXR1 - COG5142
TLDc - smart00584
TLD - pfam07534


RefSeq Protein: NP_065756
   Default View:





Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
Q9ULP9RabGAP-TBCpfam00566482601.2e-24
Q9ULP9OXR1COG51423095540.00099
Q9ULP9TBCsmart00164422380.0006
Q9ULP9TLDcsmart005843425543.8e-121
Q9ULP9TLDpfam075343685549.3e-21
NP_001186036RabGAP-TBCpfam00566482601.2e-24
NP_001186036OXR1COG51423095540.00099
NP_001186036TBCsmart00164422380.0006
NP_001186036TLDcsmart005843425543.8e-121
NP_001186036TLDpfam075343685549.3e-21
NP_065756RabGAP-TBCpfam00566482601.2e-24
NP_065756OXR1COG51423035480.0005
NP_065756TBCsmart00164422380.0006
NP_065756TLDcsmart005843365483.8e-121
NP_065756TLDpfam075343625489.3e-21



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