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Results for the Protein: NP_001029031
76496475
37

very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 2 precursor [Homo sapiens]

Known Diseases associated with this Protein:
  VLCAD DEFICIENCY
9
2
9
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:

VLCAD - cd01161
GCD - cd01151
AidB - cd01154
AXO - cd01150
IVD - cd01156
ACAD_fadE5 - cd01153
MCAD - cd01157
IBD - cd01162
Acyl-CoA_dh_N - pfam02771
SCAD_SBCAD - cd01158
ACAD_fadE6_17_26 - cd01152
CaiA - COG1960
ACAD_FadE2 - cd01155
ACAD - cd00567
LCAD - cd01160
DszC - cd01163
Acyl-CoA_dh_M - pfam02770
Acyl-CoA_dh_1 - pfam00441
Acyl-CoA_dh_2 - pfam08028




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
VLCADcd0116150459
GCDcd011519.7e-2955455
AidBcd011546.1e-0956451
AXOcd011500.000258617
ACAD_fadE5cd011531.3e-1871451
IVDcd011561.3e-7271456
MCADcd011576.5e-6272458
IBDcd011629.4e-4772458
ACAD_fadE6_17_26cd011522.4e-1474453
SCAD_SBCADcd011581.5e-10274458
CaiACOG19602e-12075459
ACADcd005671e-12378452
ACAD_FadE2cd011556.9e-1278434
LCADcd011607e-4685455
DszCcd011637e-0589444
Acyl-CoA_dh_Npfam027711.9e-2373187
Acyl-CoA_dh_Mpfam027701e-20191245
Acyl-CoA_dh_1pfam004412.6e-48305455
Acyl-CoA_dh_2pfam080282e-05320444

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs2230178 Polymorphismp.GLY43ASPN/A
dbSNPrs2230179 Polymorphismp.LEU17PHEN/A
OMIM609575.0013 Diseasep.ALA371THRVLCAD DEFICIENCY
OMIM609575.0010 Diseasep.ARG365HISVLCAD DEFICIENCY
OMIM609575.0014 Diseasep.ARG405HISVLCAD DEFICIENCY
OMIM609575.0003 Diseasep.ARG568TRPVLCAD DEFICIENCY
OMIM609575.0009 Diseasep.GLY356ASPVLCAD DEFICIENCY
OMIM609575.0011 Diseasep.LYS202GLNVLCAD DEFICIENCY
OMIM609575.0008 Diseasep.LYS337GLNVLCAD DEFICIENCY
OMIM609575.0012 Diseasep.PHE413LEUVLCAD DEFICIENCY
OMIM609575.0011 Diseasep.PRO42LEUVLCAD DEFICIENCY



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