KEGG   Homo sapiens (human): 84552Help
Entry
84552             CDS       T01001                                 

Gene name
PARD6G, PAR-6G, PAR6gamma
Definition
(RefSeq) par-6 family cell polarity regulator gamma
  KO
K06093  partitioning defective protein 6
Organism
hsa  Homo sapiens (human)
Pathway
hsa04015  Rap1 signaling pathway
hsa04144  Endocytosis
hsa04360  Axon guidance
hsa04390  Hippo signaling pathway
hsa04530  Tight junction
hsa05165  Human papillomavirus infection
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04015 Rap1 signaling pathway
    84552 (PARD6G)
   04390 Hippo signaling pathway
    84552 (PARD6G)
 09140 Cellular Processes
  09141 Transport and catabolism
   04144 Endocytosis
    84552 (PARD6G)
  09144 Cellular community - eukaryotes
   04530 Tight junction
    84552 (PARD6G)
 09150 Organismal Systems
  09158 Development
   04360 Axon guidance
    84552 (PARD6G)
 09160 Human Diseases
  09167 Infectious diseases
   05165 Human papillomavirus infection
    84552 (PARD6G)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    84552 (PARD6G)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic Type
  Centrosome formation and ciliogenesis proteins
   Pericentriolar materials (PCM)
    Centriolar satellite
     84552 (PARD6G)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif
Pfam: PB1 PDZ PDZ_2
Motif
Other DBs
NCBI-GeneID: 84552
NCBI-ProteinID: NP_115899
OMIM: 608976
HGNC: 16076
Ensembl: ENSG00000178184
Vega: OTTHUMG00000132922
Pharos: Q9BYG4(Tdark)
UniProt: Q9BYG4
Position
18q23
AA seq 376 aa AA seqDB search
MNRSFHKSQTLRFYDCSAVEVKSKFGAEFRRFSLDRHKPGKFEDFYKLVVHTHHISNSDV
TIGYADVHGDLLPINNDDNFCKAVSSANPLLRVFIQKREEAERGSLGAGSLCRRRRALGA
LRDEGPRRRAHLDIGLPRDFRPVSSIIDVDLVPETHRRVRLHRHGCEKPLGFYIRDGASV
RVTPHGLEKVPGIFISRMVPGGLAESTGLLAVNDEVLEVNGIEVAGKTLDQVTDMMIANS
HNLIVTVKPANQRNNVVRGGRALGSSGPPSDGTAGFVGPPAPRVLQNFHPDEAESDEDND
VVIEGTLEPARPPQTPGAPAGSLSRVNGAGLAQRLQRDLALDGGLQRLLSSLRADPRHSL
ALPPGGVEEHGPAVTL
NT seq 1131 nt NT seq  +upstreamnt  +downstreamnt
atgaaccgaagttttcacaagtctcagaccttgcgattctacgattgcagcgcagtggaa
gtcaagagcaagtttggggcggaattccgaaggttctctctggaccgtcataagcctggg
aagtttgaagatttctacaagctggttgtgcacacccaccatatctccaacagtgatgta
actattggctatgcagatgtgcacggagacctgctgcccatcaacaatgatgacaacttc
tgcaaggcggtttctagtgcaaatcccctgctcagggtcttcatccagaaacgagaggag
gccgagcgtggcagcctcggcgcgggctcgctgtgcaggcggaggcgggcgctgggcgcg
ctgcgtgatgaaggaccccggcggcgtgcacacctggacatcggcctcccgcgcgacttc
cgccccgtatcatccatcatcgatgtggacctggtccccgagacgcaccggcgagtgcgg
ctgcaccggcacggctgcgagaagccgctgggcttctacatccgcgatggcgccagcgtg
cgcgtgaccccgcacgggctggagaaggtgcccggcatcttcatctcgcgcatggtaccc
gggggcctggcggagagcaccgggctgctggctgtgaatgacgaggtcctggaggtgaac
ggcattgaggtggccgggaagacgctggaccaggtcacggacatgatgatcgccaacagc
cacaacctcatcgtcaccgtcaagcccgccaaccagcgcaacaacgtggtgcgcggcggc
cgcgcgttgggcagctcgggaccgccctcggacggcaccgcgggcttcgtgggtcccccc
gccccgcgcgtcctgcagaacttccaccccgacgaggcggagagcgatgaggacaacgac
gtcgtcatcgagggcacactggagcctgcacgtcccccccagaccccgggcgcgcccgca
ggcagcctctcccgggtcaatggcgcgggcctggcgcagcggctgcagcgggacctggcc
ctggacggcggcctccagcggctgctcagctccctgcgggccgacccccgtcacagcctg
gcgctgccgccaggcggcgtggaggagcacgggcccgcggtcacgctctag

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