Homo sapiens (human): 3092
Help
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ANTH
I_LWEQ
HIP1_clath_bdg
Filament
Motif
Other DBs
NCBI-GeneID:
3092
NCBI-ProteinID:
NP_005329
OMIM:
601767
HGNC:
4913
Ensembl:
ENSG00000127946
UniProt:
O00291
B4DK46
Structure
PDB
LinkDB
All DBs
Position
7:complement(75533298..75738941)
Genome browser
AA seq
1037 aa
AA seq
DB search
MDRMASSMKQVPNPLPKVLSRRGVGAGLEAAERESFERTQTVSINKAINTQEVAVKEKHA
RTCILGTHHEKGAQTFWSVVNRLPLSSNAVLCWKFCHVFHKLLRDGHPNVLKDSLRYRNE
LSDMSRMWGHLSEGYGQLCSIYLKLLRTKMEYHTKNPRFPGNLQMSDRQLDEAGESDVNN
FFQLTVEMFDYLECELNLFQTVFNSLDMSRSVSVTAAGQCRLAPLIQVILDCSHLYDYTV
KLLFKLHSCLPADTLQGHRDRFMEQFTKLKDLFYRSSNLQYFKRLIQIPQLPENPPNFLR
ASALSEHISPVVVIPAEASSPDSEPVLEKDDLMDMDASQQNLFDNKFDDIFGSSFSSDPF
NFNSQNGVNKDEKDHLIERLYREISGLKAQLENMKTESQRVVLQLKGHVSELEADLAEQQ
HLRQQAADDCEFLRAELDELRRQREDTEKAQRSLSEIERKAQANEQRYSKLKEKYSELVQ
NHADLLRKNAEVTKQVSMARQAQVDLEREKKELEDSLERISDQGQRKTQEQLEVLESLKQ
ELATSQRELQVLQGSLETSAQSEANWAAEFAELEKERDSLVSGAAHREEELSALRKELQD
TQLKLASTEESMCQLAKDQRKMLLVGSRKAAEQVIQDALNQLEEPPLISCAGSADHLLST
VTSISSCIEQLEKSWSQYLACPEDISGLLHSITLLAHLTSDAIAHGATTCLRAPPEPADS
LTEACKQYGRETLAYLASLEEEGSLENADSTAMRNCLSKIKAIGEELLPRGLDIKQEELG
DLVDKEMAATSAAIETATARIEEMLSKSRAGDTGVKLEVNERILGCCTSLMQAIQVLIVA
SKDLQREIVESGRGTASPKEFYAKNSRWTEGLISASKAVGWGATVMVDAADLVVQGRGKF
EELMVCSHEIAASTAQLVAASKVKADKDSPNLAQLQQASRGVNQATAGVVASTISGKSQI
EETDNMDFSSMTLTQIKRQEMDSQVRVLELENELQKERQKLGELRKKHYELAGVAEGWEE
GTEASPPTLQEVVTEKE
NT seq
3114 nt
NT seq
+upstream
nt +downstream
nt
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
Homo sapiens (human): 55081
Help
Entry
55081 CDS
T01001
Symbol
IFT57, ESRRBL1, HIPPI, MHS4R2, OFD18
Name
(RefSeq) intraflagellar transport 57
KO
K04638
intraflagellar transport protein 57
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
Disease
H00454
Oral-facial-digital syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09164 Neurodegenerative disease
05016 Huntington disease
55081 (IFT57)
05022 Pathways of neurodegeneration - multiple diseases
55081 (IFT57)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
55081 (IFT57)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Intraflagellar transport (IFT) complex B2
55081 (IFT57)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
IFT57
MCPsignal
Ribonuc_L-PSP
SpecificRecomb
COG3_N
Mod_r
Motif
Other DBs
NCBI-GeneID:
55081
NCBI-ProteinID:
NP_060480
OMIM:
606621
HGNC:
17367
Ensembl:
ENSG00000114446
UniProt:
Q9NWB7
LinkDB
All DBs
Position
3:complement(108160812..108222424)
Genome browser
AA seq
429 aa
AA seq
DB search
MTAALAVVTTSGLEDGVPRSRGEGTGEVVLERGPGAAYHMFVVMEDLVEKLKLLRYEEEF
LRKSNLKAPSRHYFALPTNPGEQFYMFCTLAAWLINKAGRPFEQPQEYDDPNATISNILS
ELRSFGRTADFPPSKLKSGYGEHVCYVLDCFAEEALKYIGFTWKRPIYPVEELEEESVAE
DDAELTLNKVDEEFVEEETDNEENFIDLNVLKAQTYHLDMNETAKQEDILESTTDAAEWS
LEVERVLPQLKVTIRTDNKDWRIHVDQMHQHRSGIESALKETKGFLDKLHNEITRTLEKI
SSREKYINNQLENLVQEYRAAQAQLSEAKERYQQGNGGVTERTRLLSEVMEELEKVKQEM
EEKGSSMTDGAPLVKIKQSLTKLKQETVEMDIRIGIVEHTLLQSKLKEKSNMTRNMHATV
IPEPATGFY
NT seq
1290 nt
NT seq
+upstream
nt +downstream
nt
atgactgctgctctggccgtcgtcacgacgtcgggtttggaagatggggtgcctaggtcc
cgtggcgaagggaccggggaagtggtcttggagcgggggcccggcgcggcctaccacatg
ttcgtggtgatggaggacttggtggagaagctgaagctgctccgctacgaggaggagttc
ctccggaagagcaacctgaaggccccgtccagacactattttgcactgcctaccaaccct
ggcgaacagttctacatgttttgtactcttgctgcttggttgattaataaagcgggacgt
ccctttgagcagcctcaagaatatgatgaccctaatgcaacaatatctaacatactatcc
gagcttcggtcatttggaagaactgcagattttcctccttcaaaattaaagtcaggttat
ggagaacatgtatgctatgttcttgattgcttcgctgaagaagcattgaaatatattggt
ttcacctggaaaaggccaatatacccagtagaagaattagaagaagaaagcgttgcagaa
gatgatgcagaattaacattaaataaagtggatgaagaatttgtggaagaagagacagat
aatgaagaaaactttattgatctcaacgttttaaaggcccagacatatcacttggatatg
aacgagactgccaaacaagaagatattttggaatccacaacagatgctgcagaatggagc
ctagaagtggaacgtgtactaccgcaactgaaagtcacgattaggactgacaataaggat
tggagaatccatgttgaccaaatgcaccagcacagaagtggaattgaatctgctctaaag
gagaccaagggatttttggacaaactccataatgaaattactaggactttggaaaagatc
agcagccgagaaaagtacatcaacaatcagcttgagaatttggttcaagaatatcgtgca
gctcaagcccagctgagtgaggcaaaggagcgataccagcagggaaatggaggagtgacg
gaaagaaccagactcctctctgaggttatggaagaattagaaaaggtaaaacaagaaatg
gaagaaaagggcagcagcatgactgatggtgctcctttggtgaagattaaacagagctta
acaaaactgaagcaagaaactgtagagatggacattagaattggcattgtggaacacaca
ctactccaatcaaagctgaaggagaagtccaacatgactaggaacatgcatgccacagtt
attccagaaccagcaacaggcttttattaa
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integrated database retrieval system
