Homo sapiens (human): 51062
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Entry
51062 CDS
T01001
Symbol
ATL1, AD-FSP, FSP1, GBP3, HSN1D, SPG3, SPG3A, atlastin1
Name
(RefSeq) atlastin GTPase 1
KO
K17339
atlastin [EC:3.6.5.-]
Organism
hsa
Homo sapiens (human)
Disease
H00265
Hereditary sensory and autonomic neuropathy
H00266
Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
51062 (ATL1)
Membrane trafficking [BR:
hsa04131
]
Endoplasmic reticulum (ER) - Golgi transport
Others
Others
51062 (ATL1)
Autophagy
ER-phagy
ER-phagy recepters
51062 (ATL1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
GBP
GBP_C
DUF2207_C
Motif
Other DBs
NCBI-GeneID:
51062
NCBI-ProteinID:
NP_056999
OMIM:
606439
HGNC:
11231
Ensembl:
ENSG00000198513
UniProt:
Q8WXF7
A0A0S2Z5B0
Q53F53
Structure
PDB
PDBj
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All DBs
Position
14:50533082..50633068
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AA seq
558 aa
AA seq
DB search
MAKNRRDRNSWGGFSEKTYEWSSEEEEPVKKAGPVQVLIVKDDHSFELDETALNRILLSE
AVRDKEVVAVSVAGAFRKGKSFLMDFMLRYMYNQESVDWVGDYNEPLTGFSWRGGSERET
TGIQIWSEIFLINKPDGKKVAVLLMDTQGTFDSQSTLRDSATVFALSTMISSIQVYNLSQ
NVQEDDLQHLQLFTEYGRLAMEETFLKPFQSLIFLVRDWSFPYEFSYGADGGAKFLEKRL
KVSGNQHEELQNVRKHIHSCFTNISCFLLPHPGLKVATNPNFDGKLKEIDDEFIKNLKIL
IPWLLSPESLDIKEINGNKITCRGLVEYFKAYIKIYQGEELPHPKSMLQATAEANNLAAV
ATAKDTYNKKMEEICGGDKPFLAPNDLQTKHLQLKEESVKLFRGVKKMGGEEFSRRYLQQ
LESEIDELYIQYIKHNDSKNIFHAARTPATLFVVIFITYVIAGVTGFIGLDIIASLCNMI
MGLTLITLCTWAYIRYSGEYRELGAVIDQVAAALWDQGSTNEALYKLYSAAATHRHLYHQ
AFPTPKSESTEQSEKKKM
NT seq
1677 nt
NT seq
+upstream
nt +downstream
nt
atggccaagaaccgcagggacagaaacagttggggtggattttcggaaaagacatatgaa
tggagctcagaagaggaggagccagtgaaaaaggcaggaccagtccaagtcctcattgtc
aaagatgaccattcctttgagttagatgaaactgcattaaatcggatccttctctcggag
gctgtcagagacaaggaggttgttgctgtatctgttgctggagcatttagaaaaggaaaa
tcattcctgatggacttcatgttgagatacatgtacaaccaggaatcagttgattgggtt
ggagactacaatgaaccattgactggtttttcatggagaggtggatctgagcgagagacc
acaggaattcagatatggagtgaaatcttccttatcaataaacctgatggtaaaaaggtt
gcagtgttattgatggatactcagggaacctttgatagtcagtcaactttgagagattca
gccacagtatttgcccttagcacaatgatcagctcaatacaggtatataacttatcccaa
aatgtccaggaggatgatcttcagcacctccagcttttcactgagtatggcagactggca
atggaggaaacattcctgaagccatttcagagtctgatatttcttgttcgagactggagt
ttcccatacgaattttcatatggagccgatggtggtgccaaattcttggaaaaacgcctc
aaggtctcagggaaccagcatgaagaactacagaacgtcagaaaacacatccattcctgt
ttcaccaacatttcctgttttctgctacctcatcctggcttaaaagtagctaccaatcca
aactttgatggaaaattgaaagaaatagatgatgaattcatcaaaaacttgaaaatactg
attccttggctacttagtcccgagagcctagatattaaagagatcaatgggaataaaatc
acctgccggggtctggtggagtacttcaaggcttatataaagatctatcaaggtgaagaa
ttaccacatcccaaatccatgttacaggccacagcagaagctaacaatttagcagccgtg
gcaactgccaaggacacatacaacaaaaaaatggaagagatttgtggtggtgacaaacca
tttctggccccaaatgacttgcagaccaaacacctgcaacttaaggaagaatctgtgaag
ctattccgaggggtgaagaagatgggtggggaagaatttagccggcgttacctgcagcag
ttggagagtgaaatagatgaactttacatccaatatatcaagcacaatgatagcaaaaat
atcttccatgcagctcgtaccccagccacactgtttgtagtcatctttatcacatatgtg
attgctggtgtgactggattcattggtttggacatcatagctagcctatgcaatatgata
atgggactgacccttatcaccctgtgcacttgggcatatatccggtactctggagaatac
cgagagctgggagctgtaatagaccaggtggctgcagctctgtgggaccagggaagtaca
aatgaggctttgtacaagctttacagtgcagcagcaacccacagacatctgtatcatcaa
gctttccctacaccaaagtcggaatctactgaacaatcagaaaagaaaaaaatgtaa
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