Homo sapiens (human): 27128
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Entry
27128 CDS
T01001
Symbol
CYTH4, CYT4, DJ63G5.1, PSCD4, cytohesin-4
Name
(RefSeq) cytohesin 4
KO
K18441
cytohesin
Organism
hsa
Homo sapiens (human)
Pathway
hsa04072
Phospholipase D signaling pathway
hsa04144
Endocytosis
hsa05130
Pathogenic Escherichia coli infection
hsa05131
Shigellosis
hsa05132
Salmonella infection
Network
nt06180
Pathogenic Escherichia coli
nt06181
Salmonella
nt06182
Shigella
Element
N01066
ARNO-ARF-ACTB_G signaling pathway
N01067
Shigella IpgD to ARNO-ARF-ACTB_G signaling pathway
N01129
Salmonella SopB to ARNO-ARF-ACTB/G signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04072 Phospholipase D signaling pathway
27128 (CYTH4)
09140 Cellular Processes
09141 Transport and catabolism
04144 Endocytosis
27128 (CYTH4)
09160 Human Diseases
09171 Infectious disease: bacterial
05130 Pathogenic Escherichia coli infection
27128 (CYTH4)
05131 Shigellosis
27128 (CYTH4)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
27128 (CYTH4)
Membrane trafficking [BR:
hsa04131
]
Endocytosis
Arf GTPases and associated proteins
Arf associated proteins
27128 (CYTH4)
Endosome - Golgi transport
Arf GTPase associated proteins
27128 (CYTH4)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Sec7
PH
PH_11
STX6_10_61_N
PH_20
PH_3
PH_8
Motif
Other DBs
NCBI-GeneID:
27128
NCBI-ProteinID:
NP_037517
OMIM:
606514
HGNC:
9505
Ensembl:
ENSG00000100055
UniProt:
Q9UIA0
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All DBs
Position
22:37282508..37315341
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AA seq
394 aa
AA seq
DB search
MDLCHPEPAELSSGETEELQRIKWHRKQLLEDIQKLKDEIADVFAQIDCFESAEESRMAQ
KEKELCIGRKKFNMDPAKGIQYFIEHKLLTPDVQDIARFLYKGEGLNKTAIGTYLGERDP
INLQVLQAFVDCHEFANLNLVQALRQFLWSFRLPGEAQKIDRMMEAFATRYCLCNPGVFQ
STDTCYVLSFSIIMLNTSLHNPNVRDRPPFERFVSMNRGINNGSDLPEDQLRNLFDSIKS
EPFSIPEDDGNDLTHTFFNPDREGWLLKLGGRVKTWKRRWFILTDNCLYYFEFTTDKEPR
GIIPLENLSVQKVDDPKKPFCLELYNPSCRGQKIKACKTDGDGRVVEGKHESYRISATSA
EERDQWIESIRASITRVPFYDLVSTRKKKIASKQ
NT seq
1185 nt
NT seq
+upstream
nt +downstream
nt
atggacctgtgccacccagagcccgcggagctgagcagcggggagacggaagagttacag
aggatcaagtggcaccgaaagcagctcctggaggacatccagaagctgaaggatgagatt
gcagatgtgtttgcccaaatcgactgcttcgagagtgcggaggagagccggatggcccag
aaggagaaggagctgtgtattgggcgcaagaagttcaacatggaccccgccaagggtatc
cagtatttcattgagcacaagctgctgacccctgacgtccaggacattgcacggttcctg
tataaaggcgagggcctcaacaagacagccattggtacctacctgggggagagggatccc
atcaacctgcaggtcctccaggccttcgtggactgccacgagttcgccaacctcaacctc
gtccaggccctcaggcagttcctgtggagcttccggctgccgggcgaggcccagaagata
gaccggatgatggaggcctttgccactcgatactgcctctgcaacccaggcgtcttccag
tccacagacacctgctacgtgttgtccttctccatcatcatgctcaacaccagcctccac
aatcccaacgtccgggacaggccgccttttgagcgctttgtgtccatgaaccgcggcatc
aacaatggtagcgacctgcccgaggaccagctgcggaacctcttcgacagcatcaagagt
gagccattctccatccctgaggacgacggcaatgacctcactcacaccttcttcaatcca
gaccgggagggttggctgctcaagctagggggccgcgtgaagacgtggaaacggcgctgg
ttcatcctgaccgacaactgcctctactacttcgagttcaccactgacaaggagccacgg
ggaattatacctcttgagaacctctcggtgcagaaggtggatgaccccaagaagccattc
tgcctggagctctacaaccctagctgccgaggccagaaaatcaaggcctgcaagaccgat
ggcgacggcagggtggtggagggcaagcacgaatcgtaccgcatctcagccaccagtgcc
gaggaacgtgaccagtggatcgagtccatccgagccagcatcacccgtgtccccttctac
gacctggtctctactcggaagaagaagattgccagcaagcagtga
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