KEGG   Homo sapiens (human): 84842
Entry
84842             CDS       T01001                                 
Symbol
HPDL, 4-HPPD-L, GLOXD1, NEDSWMA, SPG83
Name
(RefSeq) 4-hydroxyphenylpyruvate dioxygenase like
  KO
K24788  4-hydroxyphenylpyruvate dioxygenase-like protein [EC:1.13.-.-]
Organism
hsa  Homo sapiens (human)
Disease
H00266  Hereditary spastic paraplegia
H02470  Neurodevelopmental disorder with structural brain abnormalities
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09191 Unclassified: metabolism
   99980 Enzymes with EC numbers
    84842 (HPDL)
SSDB
Motif
Pfam: Glyoxalase Glyoxalase_4
Other DBs
NCBI-GeneID: 84842
NCBI-ProteinID: NP_116145
OMIM: 618994
HGNC: 28242
Ensembl: ENSG00000186603
UniProt: Q96IR7
Position
1:45326895..45328710
AA seq 371 aa
MAAPALRLCHIAFHVPAGQPLARNLQRLFGFQPLASREVDGWRQLALRSGDAVFLVNEGA
GSGEPLYGLDPRHAVPSATNLCFDVADAGAATRELAALGCSVPVPPVRVRDAQGAATYAV
VSSPAGILSLTLLERAGYRGPFLPGFRPVSSAPGPGWVSRVDHLTLACTPGSSPTLLRWF
HDCLGFCHLPLSPGEDPELGLEMTAGFGLGGLRLTALQAQPGSIVPTLVLAESLPGATTR
QDQVEQFLARHKGPGLQHVGLYTPNIVEATEGVATAGGQFLAPPGAYYQQPGKERQIRAA
GHEPHLLARQGILLDGDKGKFLLQVFTKSLFTEDTFFLELIQRQGATGFGQGNIRALWQS
VQEQSARSQEA
NT seq 1116 nt   +upstreamnt  +downstreamnt
atggccgcgcccgcccttcgtttgtgccacatcgccttccacgtgcccgccgggcagccc
ctagcccggaacctgcagcgcctcttcggcttccagcccctggcttcgcgggaggtggac
ggctggcggcagctagccctgcgcagcggcgacgcggtctttttggtgaacgagggcgca
gggtctggagagccgctgtacggcctggatccgcgtcacgccgtgcccagcgccacaaac
ctgtgcttcgacgtggcggacgccggcgctgcaacccgggagctggcagcgctgggctgc
agcgtgcctgtccctcccgttcgcgtgcgggacgcgcagggtgccgccacttacgccgtg
gtcagctcgcctgccggcatcctcagcctgaccttgctggagcgcgctggctaccgcgga
cccttcctacccggcttcaggcccgtgtcctctgcgcctggccccgggtgggtcagccgc
gtggaccacctgaccttggcctgcacccccggcagctcccccacacttttgcgctggttc
cacgactgcctgggcttttgccacttgccgctgagcccaggtgaggatcccgagctgggc
ctcgaaatgacagcagggtttgggcttgggggactgaggcttacagccctgcaggcccag
ccgggcagcattgtccccactcttgttctggctgagtcccttccgggggcgacgacacga
caggaccaggtggagcagttcctggcccggcacaaggggccaggcctgcagcacgtgggg
ctgtatacgcctaacattgtggaggccactgagggggtggcaactgctggaggccagttc
ctggctccccctggggcatactaccagcagccaggaaaggagaggcagatccgagctgca
gggcacgagcctcatctgcttgctcgacaggggatcctgctagatggtgataaaggcaag
tttctgcttcaggtcttcaccaagtccctttttactgaggacactttcttcctggagctg
attcagaggcagggggccactggctttggtcagggcaacatcagagctctgtggcagtcc
gtacaggagcaatctgccaggagccaggaagcctaa

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Ontology (1)   
   KEGG BRITE (1)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (9)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (9)   
   RefSeq(nuc) (1)   
   GenBank (4)   
   EMBL (4)   
Protein domain (2)   
   Pfam (2)   
All databases (30)   

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