Homo sapiens (human): 9001
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Entry
9001 CDS
T01001
Symbol
HAP1, HAP2, HIP5, HLP, hHLP1
Name
(RefSeq) huntingtin associated protein 1
KO
K04647
huntingtin-associated protein 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04727
GABAergic synapse
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05022
Pathways of neurodegeneration - multiple diseases
Network
nt06461
Huntington disease
nt06466
Pathways of neurodegeneration
Element
N00977
Mutation-caused aberrant Htt to retrograde axonal transport
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09156 Nervous system
04727 GABAergic synapse
9001 (HAP1)
09160 Human Diseases
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
9001 (HAP1)
05016 Huntington disease
9001 (HAP1)
05022 Pathways of neurodegeneration - multiple diseases
9001 (HAP1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
9001 (HAP1)
Membrane trafficking [BR:
hsa04131
]
Exocytosis
Calcium ion-dependent exocytosis
Others
9001 (HAP1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
HAP1_N
NOA36
bZIP_1
Motif
Other DBs
NCBI-GeneID:
9001
NCBI-ProteinID:
NP_817084
OMIM:
600947
HGNC:
4812
Ensembl:
ENSG00000173805
Pharos:
P54257
(Tbio)
UniProt:
P54257
LinkDB
All DBs
Position
17:complement(41717739..41734646)
Genome browser
AA seq
619 aa
AA seq
DB search
MRPKRLGRCCAGSRLGPGDPAALTCAPSPSASPAPEPSAQPQARGTGQRVGSRATSGSQF
LSEARTGARPASEAGAKAGARRPSAFSAIQGDVRSMPDNSDAPWTRFVFQGPFGSRATGR
GTGKAAGIWKTPAAYVGRRPGVSGPERAAFIRELEEALCPNLPPPVKKITQEDVKVMLYL
LEELLPPVWESVTYGMVLQRERDLNTAARIGQSLVKQNSVLMEENSKLEALLGSAKEEIL
YLRHQVNLRDELLQLYSDSDEEDEDEEEEEEEKEAEEEQEEEEAEEDLQCAHPCDAPKLI
SQEALLHQHHCPQLEALQEKLRLLEEENHQLREEASQLDTLEDEEQMLILECVEQFSEAS
QQMAELSEVLVLRLENYERQQQEVARLQAQVLKLQQRCRMYGAETEKLQKQLASEKEIQM
QLQEEETLPGFQETLAEELRTSLRRMISDPVYFMERNYEMPRGDTSSLRYDFRYSEDREQ
VRGFEAEEGLMLAADIMRGEDFTPAEEFVPQEELGAAKKVPAEEGVMEEAELVSEETEGW
EEVELELDEATRMNVVTSALEASGLGPSHLDMNYVLQQLANWQDAHYRRQLRWKMLQKGE
CPHGALPAASRTSCRSSCR
NT seq
1860 nt
NT seq
+upstream
nt +downstream
nt
atgcgcccgaagaggttgggccggtgctgcgcggggagccggctcggacccggggaccca
gcagcactcacctgtgcaccttcgccctcagccagtcccgctccggagccctctgcgcag
ccgcaggcacggggcactggacagagagtaggatcccgagccacctctggatcccagttc
ctctcggaagcccgcaccggagctcgcccggcctcggaggctggagccaaggcaggagcc
cggcgcccgtccgcattctcggccatccaaggggatgtccggtctatgcccgacaattcg
gacgcgccgtggacccgcttcgtattccaagggccgtttggttcccgggccactggccgg
gggactggaaaggcagcgggcatctggaagacgccagccgcctacgttggccggcgaccc
ggggtgtccggccctgagcgcgccgcctttattcgggagctggaggaagcactgtgtcct
aacctacctccgccagtcaaaaagatcacccaggaagacgtcaaagtgatgttatatttg
ctggaggagcttctcccacctgtctgggagagcgttacctatgggatggtcctgcagaga
gagagggacctgaacactgcagctcgcatcggccagtccctggtgaaacagaacagtgtt
ttgatggaggagaacagcaagctggaagccctgctgggctcagccaaggaggagatttta
tacctcagacaccaggtgaacttgcgggatgagctcctccagctctactcagattctgat
gaggaggatgaggatgaagaagaggaggaggaagaaaaggaggcagaagaggaacaggaa
gaagaagaagcagaggaagacctgcagtgtgctcatccctgtgatgcccctaagctgatt
tcgcaggaggcattgctgcaccagcaccactgcccacagctggaagccttgcaggagaag
ctgaggctgctggaggaggagaatcatcagctgagagaagaggcctctcaactcgacact
cttgaggatgaggaacagatgctcattctggagtgtgtggagcagttttcggaggccagc
caacagatggctgagctgtcggaggtgctggtgctcaggctggaaaactatgaacggcag
cagcaggaggtcgctcggctgcaggcccaggtgctgaagctgcagcagcgctgccggatg
tatggggctgagactgaaaagttgcagaagcagctggcttcggagaaggaaatccagatg
cagctccaggaagaggagactcttcctggtttccaggagacgctggctgaggagctcaga
acgtctctaaggaggatgatctcagaccctgtgtattttatggagaggaattatgagatg
cccagaggggacacatccagcctaaggtatgattttcgctacagtgaggatcgagagcag
gtgcgggggtttgaggctgaggaagggttgatgctggcagcggatatcatgcggggggaa
gatttcacgcctgcggaggagttcgtgccccaggaggagctgggggctgccaagaaggtg
ccggctgaggaaggggtgatggaagaggcagagctggtgtcagaggagaccgagggctgg
gaggaggtggaactggagctggatgaggcaacgcggatgaacgtggtgacatcagccctg
gaggccagcggcttgggcccttcacacctggacatgaattatgtcctccagcagctggcc
aactggcaagatgcccattacaggcggcagctgaggtggaagatgctccagaaaggtgag
tgcccccacggggccctccctgccgccagccggacaagctgcagatcgtcgtgccgatga
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