KEGG   Gorilla gorilla gorilla (western lowland gorilla): 101131809
Entry
101131809         CDS       T02442                                 
Symbol
HAP1
Name
(RefSeq) huntingtin-associated protein 1 isoform X3
  KO
K04647  huntingtin-associated protein 1
Organism
ggo  Gorilla gorilla gorilla (western lowland gorilla)
Pathway
ggo04727  GABAergic synapse
ggo05014  Amyotrophic lateral sclerosis
ggo05016  Huntington disease
ggo05022  Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:ggo00001]
 09150 Organismal Systems
  09156 Nervous system
   04727 GABAergic synapse
    101131809 (HAP1)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    101131809 (HAP1)
   05016 Huntington disease
    101131809 (HAP1)
   05022 Pathways of neurodegeneration - multiple diseases
    101131809 (HAP1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:ggo04131]
    101131809 (HAP1)
Membrane trafficking [BR:ggo04131]
 Exocytosis
  Calcium ion-dependent exocytosis
   Others
    101131809 (HAP1)
SSDB
Motif
Pfam: HAP1_N bZIP_1
Other DBs
NCBI-GeneID: 101131809
NCBI-ProteinID: XP_030867604
LinkDB
Position
4:join(50732640..50733108,50734444..50734523,50734848..50735015,50735127..50735269,50735463..50735568,50735647..50735713,50738446..50738576,50738941..50739015,50739633..50739724,50740878..50740916,50741621..50742074)
AA seq 607 aa
MRPKRSGQCFAGSRLGPGEPAALTCAPSPSASPAPEPSAQPQARGTGQRAGSRAASGSQF
LSEARTGARPASEAGAKAGARRPSAFSAIQGDVRSMPDNSDAPWTRFVFQGPFGSRATGR
RTGKAAGIWKTPAAYVGRRPGVSGPERAAFIRELEEALCPNLPPPVKKITQEDVKVMLYL
LEELLPPVWESVTYGMVLLQRERDLNTAARIGQSLVKQNSVLMEENSKLEALLGSAKEEI
LHLRHQVNLRDELLQLYSDSDEEDEEEEEEEAEEDQQCAHPCDAPKLISQEALLHQHHCP
QLEALQEKLRLLEEENHQLREEASQLDTLEDEEQMLILECVEQFSEASQQMAELSEVLVL
RLENYERQQQEVARLQARVLKLQQRCRTYGAETEKLQKQLASEKEIQMQLQEEETLPGFQ
ETLAEERRTSLRRRISDPVYFMERNYEMPRGDTSSLRYDFRYSEDREQVQGFEAEEGLML
AADIMRGEDFTPAEELVPEEELGAAKKVPAEEGVMEEAELVSEETEGWEEVELELDEATR
MNVVTSALEASGLGPSHLDMNYVLQQLANWQDAHYRRQLRWKMLQKGECPHGALPAASRT
SCRSSCR
NT seq 1824 nt   +upstreamnt  +downstreamnt
atgcgcccgaagaggtcgggccagtgcttcgcggggagccggctcggacccggggaacca
gcggcactcacctgtgcaccttcgccctcagccagtcccgctccggagccctctgcgcag
ccgcaggcacggggcactggacagagagcaggatcccgagccgcctctggatcccagttc
ctctcggaagcccgcactggagctcgcccggcctccgaggctggagccaaggcaggagcc
cggcgcccgtccgcattctcggccatccaaggggatgtccggtctatgcccgacaattcg
gacgcgccgtggacccgcttcgtattccaagggccgtttggttcccgggccactggccgg
aggactggaaaggcagcgggcatctggaagacgccagccgcctacgttggccggcgaccc
ggggtgtccggccctgagcgcgccgcctttattcgggagctggaggaagcactgtgtcct
aacctacctccgccagtcaaaaagatcacccaggaagacgtcaaagtgatgttatatttg
ctggaggagcttctcccacctgtctgggagagcgttacctatgggatggtccttctgcag
agagagagggacctgaacactgcagctcgcatcggccagtccctggtgaaacagaacagt
gttttgatggaggagaacagcaagctggaagccttgctgggctcagccaaggaggagatt
ttacacctcagacaccaggtgaacttgagggatgagctcctccagctctactcagattct
gatgaggaggatgaggaggaagaagaagaggaagcagaggaagaccagcagtgtgctcat
ccctgtgatgcccctaagctgatttcgcaggaggcattgctgcaccagcaccactgccca
cagctggaagccttgcaggagaagctgaggctgctggaggaggagaatcatcagctgaga
gaagaggcctctcaactcgacactcttgaggatgaggaacagatgctcattctggagtgt
gtggagcagttttcggaggccagccaacagatggctgagctgtcagaggtgctggtgctc
aggctggaaaactatgaacggcagcagcaggaggttgctcggctgcaggcccgggtgctg
aagctgcagcagcgctgccggacgtatggggctgagactgaaaagttgcagaagcagctg
gcttcggagaaggaaatccagatgcagctccaggaagaggagactcttcctggtttccag
gagacgctggctgaggagcgcagaacgtctctaaggaggaggatctcagaccctgtgtat
tttatggagaggaattatgagatgcccagaggggacacatccagcctaaggtatgatttt
cgctacagtgaggatcgagagcaggtgcaggggtttgaggctgaggaagggttgatgctg
gcagcggatattatgcggggggaagatttcacgcctgcggaggagttggtgcccgaggag
gagctgggggctgccaagaaggtgccggctgaggaaggggtgatggaagaggcagagctg
gtgtcagaggagaccgagggctgggaggaggtggaactggagctggatgaggcaacgcgg
atgaacgtggtgacatcagccctggaggccagcggcttgggcccttcacacctggacatg
aattatgtcctccagcagctggccaactggcaagatgcccattacaggcggcagctgagg
tggaagatgctccagaaaggtgagtgcccccacggggccctccctgccgccagccggaca
agctgcagatcgtcgtgccgatga

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