KEGG   Homo sapiens (human): 10525
Entry
10525             CDS       T01001                                 
Symbol
HYOU1, GRP-170, Grp170, HSP12A, IMD59, ORP-150, ORP150
Name
(RefSeq) hypoxia up-regulated 1
  KO
K09486  hypoxia up-regulated 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04141  Protein processing in endoplasmic reticulum
Disease
H00093  Combined immunodeficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   04141 Protein processing in endoplasmic reticulum
    10525 (HYOU1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03110 Chaperones and folding catalysts [BR:hsa03110]
    10525 (HYOU1)
Chaperones and folding catalysts [BR:hsa03110]
 Heat shock proteins
  HSP110
   10525 (HYOU1)
SSDB
Motif
Pfam: HSP70 HYOU1_C MreB_Mbl AbiEi_3_N
Other DBs
NCBI-GeneID: 10525
NCBI-ProteinID: NP_001124463
OMIM: 601746
HGNC: 16931
Ensembl: ENSG00000149428
UniProt: Q9Y4L1 A0A384P5T6 Q6IN67 B3KXH0 B7Z766 B7Z602
Position
11:complement(119044188..119057205)
AA seq 999 aa
MADKVRRQRPRRRVCWALVAVLLADLLALSDTLAVMSVDLGSESMKVAIVKPGVPMEIVL
NKESRRKTPVIVTLKENERFFGDSAASMAIKNPKATLRYFQHLLGKQADNPHVALYQARF
PEHELTFDPQRQTVHFQISSQLQFSPEEVLGMVLNYSRSLAEDFAEQPIKDAVITVPVFF
NQAERRAVLQAARMAGLKVLQLINDNTATALSYGVFRRKDINTTAQNIMFYDMGSGSTVC
TIVTYQMVKTKEAGMQPQLQIRGVGFDRTLGGLEMELRLRERLAGLFNEQRKGQRAKDVR
ENPRAMAKLLREANRLKTVLSANADHMAQIEGLMDDVDFKAKVTRVEFEELCADLFERVP
GPVQQALQSAEMSLDEIEQVILVGGATRVPRVQEVLLKAVGKEELGKNINADEAAAMGAV
YQAAALSKAFKVKPFVVRDAVVYPILVEFTREVEEEPGIHSLKHNKRVLFSRMGPYPQRK
VITFNRYSHDFNFHINYGDLGFLGPEDLRVFGSQNLTTVKLKGVGDSFKKYPDYESKGIK
AHFNLDESGVLSLDRVESVFETLVEDSAEEESTLTKLGNTISSLFGGGTTPDAKENGTDT
VQEEEESPAEGSKDEPGEQVELKEEAEAPVEDGSQPPPPEPKGDATPEGEKATEKENGDK
SEAQKPSEKAEAGPEGVAPAPEGEKKQKPARKRRMVEEIGVELVVLDLPDLPEDKLAQSV
QKLQDLTLRDLEKQEREKAANSLEAFIFETQDKLYQPEYQEVSTEEQREEISGKLSAAST
WLEDEGVGATTVMLKEKLAELRKLCQGLFFRVEERKKWPERLSALDNLLNHSSMFLKGAR
LIPEMDQIFTEVEMTTLEKVINETWAWKNATLAEQAKLPATEKPVLLSKDIEAKMMALDR
EVQYLLNKAKFTKPRPRPKDKNGTRAEPPLNASASDQGEKVIPPAGQTEDAEPISEPEKV
ETGSEPGDTEPLELGGPGAEPEQKEQSTGQKRPLKNDEL
NT seq 3000 nt   +upstreamnt  +downstreamnt
atggcagacaaagttaggaggcagaggccgaggaggcgagtctgttgggccttggtggct
gtgctcttggcagacctgttggcactgagtgatacactggcagtgatgtctgtggacctg
ggcagtgagtccatgaaggtggccattgtcaaacctggagtgcccatggaaattgtcttg
aataaggaatctcggaggaaaacaccggtgatcgtgaccctgaaagaaaatgaaagattc
tttggagacagtgcagcaagcatggcgattaagaatccaaaggctacgctacgttacttc
cagcacctcctggggaagcaggcagataacccccatgtagctctttaccaggcccgcttc
ccggagcacgagctgactttcgacccacagaggcagactgtgcactttcagatcagctcg
cagctgcagttctcacctgaggaagtgttgggcatggttctcaattattctcgttctcta
gctgaagattttgcagagcagcccatcaaggatgcagtgatcaccgtgccagtcttcttc
aaccaggccgagcgccgagctgtgctgcaggctgctcgtatggctggcctcaaagtgctg
cagctcatcaatgacaacaccgccactgccctcagctatggtgtcttccgccggaaagat
attaacaccactgcccagaatatcatgttctatgacatgggctcaggcagcaccgtatgc
accattgtgacctaccagatggtgaagactaaggaagctgggatgcagccacagctgcag
atccggggagtaggatttgaccgtaccctggggggcctggagatggagctccggcttcga
gaacgcctggctgggcttttcaatgagcagcgcaagggtcagagagcaaaggatgtgcgg
gagaacccgcgtgccatggccaagctgctgcgtgaggctaatcggctcaaaaccgtcctc
agtgccaacgctgaccacatggcacagattgaaggcctgatggatgatgtggacttcaag
gcaaaagtgactcgtgtggaatttgaggagttgtgtgcagacttgtttgagcgggtgcct
gggcctgtacagcaggccctccagagtgccgaaatgagtctggatgagattgagcaggtg
atcctggtgggtggggccactcgggtccccagagttcaggaggtgctgctgaaggccgtg
ggcaaggaggagctggggaagaacatcaatgcagatgaagcagccgccatgggggcagtg
taccaggcagctgcgctcagcaaagcctttaaagtgaagccatttgtcgtccgagatgca
gtggtctaccccatcctggtggagttcacgagggaggtggaggaggagcctgggattcac
agcctgaagcacaataaacgggtactcttctctcggatggggccctaccctcaacgcaaa
gtcatcacctttaaccgctacagccatgatttcaacttccacatcaactacggcgacctg
ggcttcctggggcctgaagatcttcgggtatttggctcccagaatctgaccacagtgaag
ctaaaaggggtgggtgacagcttcaagaagtatcctgactacgagtccaagggcatcaag
gctcacttcaacctggatgagagtggcgtgctcagtctagacagggtggagtctgtattt
gagacactggtagaggacagcgcagaagaggaatctactctcaccaaacttggcaacacc
atttccagcctgtttggaggcggtaccacaccagatgccaaggagaatggtactgatact
gtccaggaggaagaggagagccctgcagaggggagcaaggacgagcctggggagcaggtg
gagctcaaggaggaagctgaggccccagtggaggatggctctcagcccccaccccctgaa
cctaagggagatgcaacccctgagggagaaaaggccacagaaaaagaaaatggggacaag
tctgaggcccagaaaccaagtgagaaggcagaggcagggcctgagggcgtcgctccagcc
ccagagggagagaagaagcagaagcccgccaggaagcggcgaatggtagaggagatcggg
gtggagctggttgttctggacctgcctgacttgccagaggataagctggctcagtcggtg
cagaaacttcaggacttgacactccgagacctggagaagcaggaacgggaaaaagctgcc
aacagcttggaagcattcatatttgagacccaggacaagctgtaccagcccgagtaccag
gaagtgtccacagaggagcagcgtgaggagatctctgggaagctcagcgccgcatccacc
tggctggaggatgagggtgttggagccaccacagtgatgttgaaggagaagctggctgag
ctgaggaagctgtgccaagggctgttttttcgggtagaggagcgcaagaagtggcccgaa
cggctgtctgccctcgataatctcctcaaccattccagcatgttcctcaagggggcccgg
ctcatcccagagatggaccagatcttcactgaggtggagatgacaacgttagagaaagtc
atcaatgagacctgggcctggaagaatgcaactctggccgagcaggctaagctgcccgcc
acagagaagcctgtgttgctctcaaaagacattgaagctaagatgatggccctggaccga
gaggtgcagtatctgctcaataaggccaagtttaccaagccccggccccggcctaaggac
aagaatgggacccgggcagagccacccctcaatgccagtgccagtgaccagggggagaag
gtcatccctccagcaggccagactgaagatgcagagcccatttcagaacctgagaaagta
gagactggatccgagccaggagacactgagcctttggagttaggaggtcctggagcagaa
cctgaacagaaagaacaatcgacaggacagaagcggcctttgaagaacgacgaactataa

  All links  
Disease (2)   
   OMIM (2)   
Gene (14)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (28)   
   UniProt (6)   
   SWISS-PROT (1)   
   RefSeq(pep) (21)   
DNA sequence (71)   
   RefSeq(nuc) (21)   
   GenBank (25)   
   EMBL (25)   
Protein domain (3)   
   Pfam (3)   
All databases (118)   

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