KEGG   Homo sapiens (human): 51117
Entry
51117             CDS       T01001                                 
Symbol
COQ4, CGI-92, COQ10D7, SPAX10
Name
(RefSeq) coenzyme Q4
  KO
K18586  ubiquinone biosynthesis protein COQ4
Organism
hsa  Homo sapiens (human)
Disease
H00999  Coenzyme Q10 deficiency
H01351  Spastic ataxia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09191 Unclassified: metabolism
   99987 Cofactor metabolism
    51117 (COQ4)
SSDB
Motif
Pfam: Coq4
Other DBs
NCBI-GeneID: 51117
NCBI-ProteinID: NP_057119
OMIM: 612898
HGNC: 19693
Ensembl: ENSG00000167113
UniProt: Q9Y3A0
Position
9:128322839..128334072
AA seq 265 aa
MATLLRPVLRRLCGLPGLQRPAAEMPLRARSDGAGPLYSHHLPTSPLQKGLLAAGSAAMA
LYNPYRHDMVAVLGETTGHRTLKVLRDQMRRDPEGAQILQERPRISTSTLDLGKLQSLPE
GSLGREYLRFLDVNRVSPDTRAPTRFVDDEELAYVIQRYREVHDMLHTLLGMPTNILGEI
VVKWFEAVQTGLPMCILGAFFGPIRLGAQSLQVLVSELIPWAVQNGRRAPCVLNLYYERR
WEQSLRALREELGITAPPMHVQGLA
NT seq 798 nt   +upstreamnt  +downstreamnt
atggcgactctgctgcgccctgtcctccgtcggctctgcgggctcccgggcctacagcgg
cctgcggcagaaatgcccctccgggctaggagcgacggcgccggcccgctatactcgcac
cacctccccacctccccgctgcagaaagggctgttggccgccggctccgcggcgatggcg
ctctataacccctaccgccacgacatggtcgcagttctaggggagaccacaggacaccgc
accctgaaggtcctcagggaccagatgaggagggatccagagggtgcccagatcctgcag
gagcgtccccggatttcgacatccaccctcgacctgggcaagctccagagcctgccggaa
ggctccctcggtcgcgagtatctccgtttcctggatgtgaacagggtctccccagacacc
cgagcacccacccgcttcgtggatgatgaggagctagcgtatgtgattcagcggtaccgg
gaggtgcacgacatgcttcacaccctgctggggatgcccaccaacatcctgggggagatc
gtggtgaaatggtttgaggctgtccagactggcctgcccatgtgcatcctgggtgcattc
tttggaccgatccgacttggcgctcagagcctgcaagtgctggtctcggagttgatccca
tgggccgttcagaacgggcgcagagccccatgtgtcctcaacctgtactatgagcggcgc
tgggagcagtccctgagggctctgcgggaggagctgggcattacagcaccacccatgcac
gtccagggcttggcctga

DBGET integrated database retrieval system