Homo sapiens (human): 118813
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Entry
118813 CDS
T01001
Symbol
ZFYVE27, PROTRUDIN, SPG33
Name
(RefSeq) zinc finger FYVE-type containing 27
KO
K19368
protrudin
Organism
hsa
Homo sapiens (human)
Pathway
hsa04144
Endocytosis
Disease
H00266
Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04144 Endocytosis
118813 (ZFYVE27)
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Gene cluster
GFIT
Motif
Pfam:
FYVE
FYVE_2
Motif
Other DBs
NCBI-GeneID:
118813
NCBI-ProteinID:
NP_653189
OMIM:
610243
HGNC:
26559
Ensembl:
ENSG00000155256
Pharos:
Q5T4F4
(Tbio)
UniProt:
Q5T4F4
Structure
PDB
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All DBs
Position
10:97737128..97760895
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AA seq
411 aa
AA seq
DB search
MQTSEREGSGPELSPSVMPEAPLESPPFPTKSPAFDLFNLVLSYKRLEIYLEPLKDAGDG
VRYLLRWQMPLCSLLTCLGLNVLFLTLNEGAWYSVGALMISVPALLGYLQEVCRARLPDS
ELMRRKYHSVRQEDLQRGRLSRPEAVAEVKSFLIQLEAFLSRLCCTCEAAYRVLHWENPV
VSSQFYGALLGTVCMLYLLPLCWVLTLLNSTLFLGNVEFFRVVSEYRASLQQRMNPKQEE
HAFESPPPPDVGGKDGLMDSTPALTPTEDLTPGSVEEAEEAEPDEEFKDAIEETHLVVLE
DDEGAPCPAEDELALQDNGFLSKNEVLRSKVSRLTERLRKRYPTNNFGNCTGCSATFSVL
KKRRSCSNCGNSFCSRCCSFKVPKSSMGATAPEAQRETVFVCASCNQTLSK
NT seq
1236 nt
NT seq
+upstream
nt +downstream
nt
atgcagacatcagaacgtgaggggagtgggccggagctgagccccagcgtgatgcccgag
gctcccctggagtctccaccttttcctaccaagtccccagcgtttgaccttttcaacttg
gttctctcctacaagaggctggagatctacctggaacccttgaaggatgcaggtgatggt
gttcgatacttgctcaggtggcagatgcctttgtgttccttgctgacctgcctgggcctc
aacgtcttgttcctcactttgaatgagggtgcatggtactcagtaggtgccctgatgatt
tcagtgcccgccctgctgggctaccttcaggaggtttgccgggcacggctgcctgattcc
gagctgatgcggaggaagtatcatagcgtgaggcaggaggacctgcagagaggtcgcctg
tctcgtcccgaggccgtggctgaggtgaagagcttcttgatccagctggaggccttcctg
agccgcctgtgctgcacatgtgaagccgcctaccgcgtgctgcactgggagaaccccgtc
gtgtcctcacagttctatggggctcttctgggcacagtctgcatgctgtatttgctgcca
ctctgctgggttctcacccttttaaacagcacgctctttctggggaatgtggagttcttc
cgagttgtgtctgagtacagggcatctctgcagcagaggatgaacccaaagcaggaagag
catgcctttgagagtcctccaccaccagatgttggggggaaggatggtctgatggacagc
acgcctgccctcacacccacggaggacctcacaccgggcagcgtggaggaggctgaggag
gctgagccagatgaagagtttaaagatgcgattgaggagacccacttggtggtgctggag
gatgatgagggcgccccgtgcccagcagaggatgagctggccctgcaggacaacgggttc
ctgagcaagaatgaggtgctgcgcagcaaggtgtctcggctcacggagcggctccgcaag
cgctaccccaccaacaacttcgggaactgcacgggctgctcggccaccttctcagtgctg
aagaagaggcggagctgcagtaattgtggaaacagcttctgctctcgatgctgctccttc
aaggtgcccaagtcctccatgggggccacagcccctgaagcccagagggagactgtgttt
gtgtgtgcctcgtgtaaccagaccttgagcaagtga
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