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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.

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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 ↕
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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