KEGG   Homo sapiens (human): 3092
Entry
3092              CDS       T01001                                 
Symbol
HIP1, HIP-I, ILWEQ, SHON, SHONbeta, SHONgamma
Name
(RefSeq) huntingtin interacting protein 1
  KO
K04559  huntingtin interacting protein 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa05016  Huntington disease
hsa05022  Pathways of neurodegeneration - multiple diseases
Network
nt06461  Huntington disease
  Element
N00983  Mutation-caused aberrant Htt to extrinsic apoptotic pathway
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09164 Neurodegenerative disease
   05016 Huntington disease
    3092 (HIP1)
   05022 Pathways of neurodegeneration - multiple diseases
    3092 (HIP1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    3092 (HIP1)
Membrane trafficking [BR:hsa04131]
 Endocytosis
  Clathrin-mediated endocytosis
   Others
    3092 (HIP1)
SSDB
Motif
Pfam: ANTH I_LWEQ HIP1_clath_bdg Filament
Other DBs
NCBI-GeneID: 3092
NCBI-ProteinID: NP_005329
OMIM: 601767
HGNC: 4913
Ensembl: ENSG00000127946
UniProt: O00291 B4DK46
Structure
Position
7:complement(75533298..75738941)
AA seq 1037 aa
MDRMASSMKQVPNPLPKVLSRRGVGAGLEAAERESFERTQTVSINKAINTQEVAVKEKHA
RTCILGTHHEKGAQTFWSVVNRLPLSSNAVLCWKFCHVFHKLLRDGHPNVLKDSLRYRNE
LSDMSRMWGHLSEGYGQLCSIYLKLLRTKMEYHTKNPRFPGNLQMSDRQLDEAGESDVNN
FFQLTVEMFDYLECELNLFQTVFNSLDMSRSVSVTAAGQCRLAPLIQVILDCSHLYDYTV
KLLFKLHSCLPADTLQGHRDRFMEQFTKLKDLFYRSSNLQYFKRLIQIPQLPENPPNFLR
ASALSEHISPVVVIPAEASSPDSEPVLEKDDLMDMDASQQNLFDNKFDDIFGSSFSSDPF
NFNSQNGVNKDEKDHLIERLYREISGLKAQLENMKTESQRVVLQLKGHVSELEADLAEQQ
HLRQQAADDCEFLRAELDELRRQREDTEKAQRSLSEIERKAQANEQRYSKLKEKYSELVQ
NHADLLRKNAEVTKQVSMARQAQVDLEREKKELEDSLERISDQGQRKTQEQLEVLESLKQ
ELATSQRELQVLQGSLETSAQSEANWAAEFAELEKERDSLVSGAAHREEELSALRKELQD
TQLKLASTEESMCQLAKDQRKMLLVGSRKAAEQVIQDALNQLEEPPLISCAGSADHLLST
VTSISSCIEQLEKSWSQYLACPEDISGLLHSITLLAHLTSDAIAHGATTCLRAPPEPADS
LTEACKQYGRETLAYLASLEEEGSLENADSTAMRNCLSKIKAIGEELLPRGLDIKQEELG
DLVDKEMAATSAAIETATARIEEMLSKSRAGDTGVKLEVNERILGCCTSLMQAIQVLIVA
SKDLQREIVESGRGTASPKEFYAKNSRWTEGLISASKAVGWGATVMVDAADLVVQGRGKF
EELMVCSHEIAASTAQLVAASKVKADKDSPNLAQLQQASRGVNQATAGVVASTISGKSQI
EETDNMDFSSMTLTQIKRQEMDSQVRVLELENELQKERQKLGELRKKHYELAGVAEGWEE
GTEASPPTLQEVVTEKE
NT seq 3114 nt   +upstreamnt  +downstreamnt
atggatcggatggccagctccatgaagcaggtgcccaacccactgcccaaggtgctgagc
cggcgcggggtcggcgctgggctggaggcggcggagcgcgagagcttcgagcggactcag
actgtcagcatcaataaggccattaatacgcaggaagtggctgtaaaggaaaaacacgcc
agaacgtgcatactgggcacccaccatgagaaaggggcacagaccttctggtctgttgtc
aaccgcctgcctctgtctagcaacgcagtgctctgctggaagttctgccatgtgttccac
aaactcctccgagatggacacccgaacgtcctgaaggactctctgagatacagaaatgaa
ttgagtgacatgagcaggatgtggggccacctgagcgaggggtatggccagctgtgcagc
atctacctgaaactgctaagaaccaagatggagtaccacaccaaaaatcccaggttccca
ggcaacctgcagatgagtgaccgccagctggacgaggctggagaaagtgacgtgaacaac
tttttccagttaacagtggagatgtttgactacctggagtgtgaactcaacctcttccaa
acagtattcaactccctggacatgtcccgctctgtgtccgtgacggcagcagggcagtgc
cgcctcgccccgctgatccaggtcatcttggactgcagccacctttatgactacactgtc
aagcttctcttcaaactccactcctgcctcccagctgacaccctgcaaggccaccgggac
cgcttcatggagcagtttacaaagttgaaagatctgttctaccgctccagcaacctgcag
tacttcaagcggctcattcagatcccccagctgcctgagaacccacccaacttcctgcga
gcctcagccctgtcagaacatatcagccctgtggtggtgatccctgcagaggcctcatcc
cccgacagcgagccagtcctagagaaggatgacctcatggacatggatgcctctcagcag
aatttatttgacaacaagtttgatgacatctttggcagttcattcagcagtgatcccttc
aatttcaacagtcaaaatggtgtgaacaaggatgagaaggaccacttaattgagcgacta
tacagagagatcagtggattgaaggcacagctagaaaacatgaagactgagagccagcgg
gttgtgctgcagctgaagggccacgtcagcgagctggaagcagatctggccgagcagcag
cacctgcggcagcaggcggccgacgactgtgaattcctgcgggcagaactggacgagctc
aggaggcagcgggaggacaccgagaaggctcagcggagcctgtctgagatagaaaggaaa
gctcaagccaatgaacagcgatatagcaagctaaaggagaagtacagcgagctggttcag
aaccacgctgacctgctgcggaagaatgcagaggtgaccaaacaggtgtccatggccaga
caagcccaggtagatttggaacgagagaaaaaagagctggaggattcgttggagcgcatc
agtgaccagggccagcggaagactcaagaacagctggaagttctagagagcttgaagcag
gaacttgccacaagccaacgggagcttcaggttctgcaaggcagcctggaaacttctgcc
cagtcagaagcaaactgggcagccgagttcgccgagctagagaaggagcgggacagcctg
gtgagtggcgcagctcatagggaggaggaattatctgctcttcggaaagaactgcaggac
actcagctcaaactggccagcacagaggaatctatgtgccagcttgccaaagaccaacga
aaaatgcttctggtggggtccaggaaggctgcggagcaggtgatacaagacgccctgaac
cagcttgaagaacctcctctcatcagctgcgctgggtctgcagatcacctcctctccacg
gtcacatccatttccagctgcatcgagcaactggagaaaagctggagccagtatctggcc
tgcccagaagacatcagtggacttctccattccataaccctgctggcccacttgaccagc
gacgccattgctcatggtgccaccacctgcctcagagccccacctgagcctgccgactca
ctgaccgaggcctgtaagcagtatggcagggaaaccctcgcctacctggcctccctggag
gaagagggaagccttgagaatgccgacagcacagccatgaggaactgcctgagcaagatc
aaggccatcggcgaggagctcctgcccaggggactggacatcaagcaggaggagctgggg
gacctggtggacaaggagatggcggccacttcagctgctattgaaactgccacggccaga
atagaggagatgctcagcaaatcccgagcaggagacacaggagtcaaattggaggtgaat
gaaaggatccttggttgctgtaccagcctcatgcaagctattcaggtgctcatcgtggcc
tctaaggacctccagagagagattgtggagagcggcaggggtacagcatcccctaaagag
ttttatgccaagaactctcgatggacagaaggacttatctcagcctccaaggctgtgggc
tggggagccactgtcatggtggatgcagctgatctggtggtacaaggcagagggaaattt
gaggagctaatggtgtgttctcatgaaattgctgctagcacagcccagcttgtggctgca
tccaaggtgaaagctgataaggacagccccaacctagcccagctgcagcaggcctctcgg
ggagtgaaccaggccactgccggcgttgtggcctcaaccatttccggcaaatcacagatc
gaagagacagacaacatggacttctcaagcatgacgctgacacagatcaaacgccaagag
atggattctcaggttagggtgctagagctagaaaatgaattgcagaaggagcgtcaaaaa
ctgggagagcttcggaaaaagcactacgagcttgctggtgttgctgagggctgggaagaa
ggaacagaggcatctccacctacactgcaagaagtggtaaccgaaaaagaatag

  All links  
Disease (1)   
   OMIM (1)   
Gene (16)   
   RefGene (10)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (15)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (12)   
DNA sequence (64)   
   RefSeq(nuc) (12)   
   GenBank (26)   
   EMBL (26)   
3D Structure (3)   
   PDB (3)   
Protein domain (4)   
   Pfam (4)   
All databases (103)   

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