Homo sapiens (human): 146850
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Entry
146850 CDS
T01001
Symbol
PIK3R6, C17orf38, HsT41028, p84_PIKAP, p87(PIKAP), p87PIKAP
Name
(RefSeq) phosphoinositide-3-kinase regulatory subunit 6
KO
K21290
phosphoinositide-3-kinase regulatory subunit 5/6
Organism
hsa
Homo sapiens (human)
Pathway
hsa04022
cGMP-PKG signaling pathway
hsa04062
Chemokine signaling pathway
hsa04072
Phospholipase D signaling pathway
hsa04151
PI3K-Akt signaling pathway
hsa04261
Adrenergic signaling in cardiomyocytes
hsa04371
Apelin signaling pathway
hsa04611
Platelet activation
hsa04725
Cholinergic synapse
hsa04921
Oxytocin signaling pathway
hsa05145
Toxoplasmosis
hsa05167
Kaposi sarcoma-associated herpesvirus infection
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06167
Human cytomegalovirus (HCMV)
nt06224
CXCR signaling (cancer)
nt06530
PI3K signaling
nt06533
Chemokine signaling
Element
N00153
CCR/CXCR-GNB/G-PI3K-RAC signaling pathway
N00154
CXCR-GNB/G-PI3K-AKT signaling pathway
N01657
GPCR-PI3K signaling pathway
N01746
CCR/CXCR-GNB/G-PI3K signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04072 Phospholipase D signaling pathway
146850 (PIK3R6)
04022 cGMP-PKG signaling pathway
146850 (PIK3R6)
04151 PI3K-Akt signaling pathway
146850 (PIK3R6)
09150 Organismal Systems
09151 Immune system
04611 Platelet activation
146850 (PIK3R6)
04062 Chemokine signaling pathway
146850 (PIK3R6)
09152 Endocrine system
04921 Oxytocin signaling pathway
146850 (PIK3R6)
09156 Nervous system
04725 Cholinergic synapse
146850 (PIK3R6)
09160 Human Diseases
09172 Infectious disease: viral
05167 Kaposi sarcoma-associated herpesvirus infection
146850 (PIK3R6)
09174 Infectious disease: parasitic
05145 Toxoplasmosis
146850 (PIK3R6)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
146850 (PIK3R6)
Membrane trafficking [BR:
hsa04131
]
Endocytosis
Rab GTPases and associated proteins
Rab associated proteins
146850 (PIK3R6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PI3K_1B_p101
Motif
Other DBs
NCBI-GeneID:
146850
NCBI-ProteinID:
NP_001010855
OMIM:
611462
HGNC:
27101
Ensembl:
ENSG00000276231
UniProt:
Q5UE93
B3KRK9
LinkDB
All DBs
Position
17:complement(8802722..8867677)
Genome browser
AA seq
754 aa
AA seq
DB search
MESSDVELDLQRSVQAVLRELSTQAPALQSNQGMWRWSLHKKVERDPGKSPVLVRILLRE
LEKAESQDLRHVIIPLLHTVMYVLTKATGITEELYQRIYAFCTRLLTLPTPYCTVALDCA
IRLKTEMAVPGTLYQRMVIAEQNLTNELYPYQERVFLFVDPELVSASVCSALLLEIEAAQ
AQQTPETCMRHVVSHALQAALGEACHAGALHRKLQASPRRTLEHYFHAVVAALEQMASEA
SPSREGHVERLEEIYCSLLGPAAGRCGGDLVQERPPSIPLPSPYITFHLWTGEEQLWKEL
VLFLRPRSQLRLSADLEVLDLQGLRPDRELARVSVLSTDSGIERDLPTGADELPAPGSPE
MERAGLQRKGGIKKRAWPLDFLMPGSWDGPPGLHRRTGRPSGDGEMLPGVSRLHTARVLV
LGDDRMLGRLAQAYHRLRKRETQKFCLTPRLSLQLYYIPVLAPEKPAASRQPELGELATF
LGRVDPWYQSNVNTLCPAIHKLAEMPPSLDTSRTVDPFILDVITYYIRMGTQPIYFQIYT
VKIFFSDLSQDPTEDIFLIELKVKIQDSKFPKDGFSPRRRGVAEGPGAELSLCYQKALLS
HRPREVTVSLRATGLILKAIPASDTEVSGSSHCPLPAAPVTDHTCLNVNVTEVVKSSNLA
GKSFSTVTNTFRTNNIQIQSRDQRLLTLSLDKDDQRTFRDVVRFEVAPCPEPCSGAQKSK
APWLNLHGQQEVEAIKAKPKPLLMPINTFSGIVQ
NT seq
2265 nt
NT seq
+upstream
nt +downstream
nt
atggagagctcagatgtggagctggacctccagaggagcgtgcaggctgtgctccgggag
ctcagcacccaggcccctgccctgcagagcaaccaaggcatgtggaggtggtccctgcac
aagaaggtcgagcgagatcccggtaagagcccagtgctggtccgcattcttctcagagaa
ctggagaaggcggaaagccaggacctccggcatgtcatcattcccttgctgcacactgta
atgtacgtgctcaccaaggccacaggaatcacagaagagctctaccagagaatctatgcc
ttttgcacaaggttactgaccctgcccaccccctactgcacagtcgccttggactgcgcg
ataaggctgaaaacggagatggctgtcccagggacactgtaccaaaggatggtcattgcc
gaacagaacttgacgaatgagctgtatccctaccaggagagagtgttcctcttcgtggat
cctgagctggtgtctgcgtctgtgtgcagtgctctgctactggagatcgaggcggcccag
gcgcagcagacaccagagacctgcatgcgccacgtggtctcccacgccctgcaggcggct
ctgggggaggcctgtcacgcaggcgctctgcacaggaagctgcaggccagccctcgccgc
accctggagcactatttccacgccgtggtggccgccttggagcagatggccagcgaggcc
agcccgagccgggagggacacgtagagaggctggaggagatttactgctcgctgctgggt
cccgcggcggggcgctgcggtggtgaccttgtccaagagcggccaccaagcattcccctg
cccagcccctacatcaccttccacttgtggaccggtgaggagcagctctggaaggaactg
gtgctcttcctccgcccaagatcccagctgcgcctcagtgctgacttggaggtcttggat
ctgcagggcctccggccggaccgggagttggcccgggtttctgtgctgtccactgacagc
ggcattgagcgggaccttcccacgggggctgatgagctgcctgcacccggcagccctgag
atggagcgagccgggctgcagcgcaaagggggcatcaagaagcgtgcatggcccctggac
ttcttgatgcctggcagctgggacgggcccccagggctgcaccggaggacaggccggccc
agtggggatggggaaatgctgcccggcgtgtcccggctgcacacagcccgggtacttgtg
ctcggagatgacaggatgctggggcgcctggcccaggcctaccacagactcaggaaacgg
gagacccagaagttctgcctcactcccagactcagcctgcagctctactacatccccgtg
ctggcgcctgagaagcctgcagcatccaggcagccggagctgggagagctggctacgttc
ctgggccgcgtagacccgtggtaccagagcaacgtcaacacgctgtgccccgccatccac
aagctggctgagatgcctccttccctggacacatcccggactgtggaccccttcatccta
gacgtcatcacctactacatccgcatgggcacccaacccatctatttccagatctacaca
gtcaagatctttttcagtgacctgagccaagaccctactgaggacattttcctcattgaa
ctgaaggtgaagatccaagattctaaattccccaaagatggcttttcacccaggaggaga
ggcgtggctgagggcccaggggcagagctctccctatgctaccagaaggccttgcttagc
caccggccccgagaggtcaccgtttccctgcgggccactgggctgatcctgaaggccatt
ccagccagcgacacagaagtttcagggtctagccattgccccctgcctgctgctcctgtc
acagaccacacatgtctgaatgtcaacgtgacagaggttgtcaagtcctccaacttggcg
ggaaagtccttctctacagtgaccaacaccttcaggacgaacaatatccagatccagagc
cgggaccagaggctgctgacactgtcgctggacaaggacgatcaacgcactttcagggat
gtggtcagattcgaggttgctccctgcccagaaccatgttctggggcccagaagtccaag
gcaccgtggctcaatttgcatgggcaacaggaggtggaagcaatcaaagccaagcccaag
ccccttctgatgcccatcaacacattctctggtattgtccagtga
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