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Results for the Protein: NP_001257377
394025725
37

very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 4 [Homo sapiens]

Known Diseases associated with this Protein:
  VLCAD DEFICIENCY
8
0
8
0
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 ↕
GCDcd011519.7e-291401
VLCADcd011611405
AidBcd011546.1e-092397
AXOcd011500.00024563
ACAD_fadE5cd011531.3e-1817397
IVDcd011561.3e-7217402
MCADcd011576.5e-6218404
IBDcd011629.4e-4718404
ACAD_fadE6_17_26cd011522.4e-1420399
SCAD_SBCADcd011581.5e-10220404
CaiACOG19602e-12021405
ACADcd005671e-12324398
ACAD_FadE2cd011556.9e-1224380
LCADcd011607e-4631401
DszCcd011637e-0535390
Acyl-CoA_dh_Npfam027711.9e-2319133
Acyl-CoA_dh_Mpfam027701e-20137191
Acyl-CoA_dh_1pfam004412.6e-48251401
Acyl-CoA_dh_2pfam080282e-05266390

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM609575.0013 Diseasep.ALA317THRVLCAD DEFICIENCY
OMIM609575.0010 Diseasep.ARG311HISVLCAD DEFICIENCY
OMIM609575.0014 Diseasep.ARG351HISVLCAD DEFICIENCY
OMIM609575.0003 Diseasep.ARG514TRPVLCAD DEFICIENCY
OMIM609575.0009 Diseasep.GLY302ASPVLCAD DEFICIENCY
OMIM609575.0011 Diseasep.LYS148GLNVLCAD DEFICIENCY
OMIM609575.0008 Diseasep.LYS283GLNVLCAD DEFICIENCY
OMIM609575.0012 Diseasep.PHE359LEUVLCAD DEFICIENCY



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