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Results for the Protein: NP_001257376
394025723
37

very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 3 [Homo sapiens]

Known Diseases associated with this Protein:
  VLCAD DEFICIENCY
9
0
9
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
ACAD_fadE5 - cd01153
IVD - cd01156
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 ↕
VLCADcd0116195504
GCDcd011519.7e-29100500
AidBcd011546.1e-09101496
AXOcd011500.0002103662
IVDcd011561.3e-72116501
ACAD_fadE5cd011531.3e-18116496
MCADcd011576.5e-62117503
IBDcd011629.4e-47117503
ACAD_fadE6_17_26cd011522.4e-14119498
SCAD_SBCADcd011581.5e-102119503
CaiACOG19602e-120120504
ACADcd005671e-123123497
ACAD_FadE2cd011556.9e-12123479
LCADcd011607e-46130500
DszCcd011637e-05134489
Acyl-CoA_dh_Npfam027711.9e-23118232
Acyl-CoA_dh_Mpfam027701e-20236290
Acyl-CoA_dh_1pfam004412.6e-48350500
Acyl-CoA_dh_2pfam080282e-05365489

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM609575.0013 Diseasep.ALA416THRVLCAD DEFICIENCY
OMIM609575.0010 Diseasep.ARG410HISVLCAD DEFICIENCY
OMIM609575.0014 Diseasep.ARG450HISVLCAD DEFICIENCY
OMIM609575.0003 Diseasep.ARG613TRPVLCAD DEFICIENCY
OMIM609575.0009 Diseasep.GLY401ASPVLCAD DEFICIENCY
OMIM609575.0011 Diseasep.LYS247GLNVLCAD DEFICIENCY
OMIM609575.0008 Diseasep.LYS382GLNVLCAD DEFICIENCY
OMIM609575.0012 Diseasep.PHE458LEUVLCAD DEFICIENCY
OMIM609575.0011 Diseasep.PRO65LEUVLCAD DEFICIENCY



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