| Entry |
|
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| Symbol |
HAP1
|
|---|
| Name |
(RefSeq) huntingtin-associated protein 1 isoform X1
|
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| KO |
| K04647 | huntingtin-associated protein 1 |
|
|---|
| Organism |
mmur Microcebus murinus (gray mouse lemur)
|
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| Pathway |
| mmur05022 | Pathways of neurodegeneration - multiple diseases |
|
|---|
| Brite |
KEGG Orthology (KO) [BR:mmur00001]
09150 Organismal Systems
09156 Nervous system
04727 GABAergic synapse
105872029 (HAP1)
09160 Human Diseases
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
105872029 (HAP1)
05016 Huntington disease
105872029 (HAP1)
05022 Pathways of neurodegeneration - multiple diseases
105872029 (HAP1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:mmur04131]
105872029 (HAP1)
Membrane trafficking [BR:mmur04131]
Exocytosis
Calcium ion-dependent exocytosis
Others
105872029 (HAP1)
|
|---|
| SSDB |
|
|---|
| Motif |
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| Other DBs |
|
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| LinkDB |
|
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| Position |
16:complement(30325327..30335079)
|
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| AA seq |
640 aa
MRPKELGQSCAGDRPGPGRGPGDPAAVTPAPPPAASPAPEPSAEPGPAPAQAPRVGQGAG
SRAASGSQSASEAPAGARPASEAGAKRNAQSVPDNSDAPWTRFVFQGPFGPRATGLGTGK
AAGIWKTPAAYIGRRPGVSGPERAAFIRELEEALCPNLPPPSKKITPDDIKVMLYLLEER
ERDLNTAARIGQSLVKQNSVLMEENSKLEAMLGSAREEILHLRHQVNLRDDLLQLYSDSD
EDEDEEEEEEEEEEKQEQQQEEQQRDHAYDAPKPTPRKGKGKVKHRCPQLEAMQRRLKLL
EQENDQLREEASQLDTMEDEEQMLILECVEQFSEASQQMAELSEVLVLRLENYERQQKEV
SQLQAQVSKLQQRCQSYGMETEKLQKQLASEKEIQMQLQEELQDLREKHTDGGSMLIETQ
EKAKTLRQQPRVSTGSVTHYAYGVPLQALPSFQQTLAEELRTSLRRIISDPVYYTERNYG
RPRGDTPKPRYDLRYSEEKKQKQRFQAKEGSIAAKDVEPVEDFEPAEELVPEEELGATEE
VLAEEGVTDEGELVSEETEAWEEVEPEVDEATRMNVVTSALEASGLGPSRLDMKCVLQQL
ADWQDAHYRRQLKQKVPQKGECSRRGLPPASQPSCRSSSR |
|---|
| NT seq |
1923 nt +upstreamnt +downstreamnt
atgcgcccgaaggagcttgggcagagctgcgccggggaccggccgggccccggacgcgga
cccggggaccccgcagcggtcacccctgctcccccgcccgcagccagtccggctccagag
ccctcggccgagcccggacccgctcccgcgcaggcaccgcgggttggacagggagcagga
tccagagcagcctccggatcccaatccgcctcggaagcccctgccggagctcgcccggcc
tccgaggctggagccaagcggaatgcgcagtccgtgcccgacaactcggacgcgccgtgg
actcgcttcgtattccaagggccctttggtccccgggccactggcctggggactggaaag
gcagcgggcatctggaagacgccagccgcctacattggccggcggccgggggtgtcgggt
cctgagcgcgccgcctttattcgggagctggaggaagcgctgtgccctaacctacctccg
ccctccaagaagatcactccagatgatatcaaagtgatgttatatttgctggaggagaga
gagcgggacctgaacacagcagctcgcattggccagtccctggtgaaacagaacagcgtt
ttgatggaggagaacagcaagctggaagccatgctgggctcagcccgggaggagatttta
cacctcagacaccaggtgaaccttcgagatgacctccttcagctctactcagactctgat
gaggatgaggatgaagaagaggaggaggaagaggaagaggagaaacaggagcagcagcag
gaggaacagcagcgtgatcacgcctatgatgcccctaagccgactcccaggaaggggaag
gggaaggtgaagcaccgctgcccacagctggaagccatgcaacggaggctcaagctgctg
gagcaggagaacgaccagctgagagaggaggcctctcaactcgacaccatggaggatgag
gagcagatgctcattctggaatgtgtggagcagttttcggaggccagccagcagatggcc
gagctgtcggaggtgctggtgctcaggctggaaaactatgaacgtcagcagaaggaggtc
tctcagctgcaggcccaggtctcaaagctgcagcagcgctgccagtcgtatgggatggag
actgagaagttgcagaagcagctggcttcggagaaagaaatccagatgcagctccaagaa
gagctgcaggacctgcgggagaagcacacggatggtgggagcatgctgattgagacacag
gagaaggcgaagaccctccgccagcaaccccgggtgtccactgggtctgtcacccactac
gcgtacggcgtgcctctgcaggcacttcctagtttccagcagaccctggctgaggagctc
aggacgtcgctgcggaggatcatctcagaccctgtgtactacaccgagaggaattatggg
aggcccagaggggacacgccaaagccgagatacgatcttcgctacagtgaggagaagaag
cagaaacagaggttccaggccaaggaggggtcgatagcggcaaaggatgttgagccggtg
gaagatttcgagcctgcggaggagctggtgcccgaggaagagctgggggccacagaagag
gtgctggctgaagaaggggtaacggacgagggagagctggtgtccgaggagacagaggcc
tgggaagaggtggagccagaagtggatgaggccactcggatgaacgtggtgacctcagcc
ctggaggccagcggcttgggcccttcgcgcctcgacatgaagtgtgtgctccagcaactg
gccgactggcaggatgcccactacaggaggcagctaaagcagaaggtgccccagaaaggt
gagtgctcccgcaggggcctccctccagccagccagccaagctgcagatcgtcaagccga
tga |
|---|
