KEGG   Homo sapiens (human): 50855Help
Entry
50855             CDS       T01001                                 

Gene name
PARD6A, PAR-6A, PAR6, PAR6C, PAR6alpha, TAX40, TIP-40
Definition
(RefSeq) par-6 family cell polarity regulator alpha
  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
    50855 (PARD6A)
   04390 Hippo signaling pathway
    50855 (PARD6A)
 09140 Cellular Processes
  09141 Transport and catabolism
   04144 Endocytosis
    50855 (PARD6A)
  09144 Cellular community - eukaryotes
   04530 Tight junction
    50855 (PARD6A)
 09150 Organismal Systems
  09158 Development
   04360 Axon guidance
    50855 (PARD6A)
 09160 Human Diseases
  09172 Infectious diseases: Viral
   05165 Human papillomavirus infection
    50855 (PARD6A)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    50855 (PARD6A)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic Type
  Centrosome formation and ciliogenesis proteins
   Pericentriolar materials (PCM)
    Centriolar satellite
     50855 (PARD6A)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif
Pfam: PB1 PDZ PDZ_6
Motif
Other DBs
NCBI-GeneID: 50855
NCBI-ProteinID: NP_058644
OMIM: 607484
HGNC: 15943
Ensembl: ENSG00000102981
Vega: OTTHUMG00000137534
Pharos: Q9NPB6(Tbio)
UniProt: Q9NPB6
Structure
PDB: 

Position
16q22.1
AA seq 346 aa AA seqDB search
MARPQRTPARSPDSIVEVKSKFDAEFRRFALPRASVSGFQEFSRLLRAVHQIPGLDVLLG
YTDAHGDLLPLTNDDSLHRALASGPPPLRLLVQKRAEADSSGLAFASNSLQRRKKGLLLR
PVAPLRTRPPLLISLPQDFRQVSSVIDVDLLPETHRRVRLHKHGSDRPLGFYIRDGMSVR
VAPQGLERVPGIFISRLVRGGLAESTGLLAVSDEILEVNGIEVAGKTLDQVTDMMVANSH
NLIVTVKPANQRNNVVRGASGRLTGPPSAGPGPAEPDSDDDSSDLVIENRQPPSSNGLSQ
GPPCWDLHPGCRHPGTRSSLPSLDDQEQASSGWGSRIRGDGSGFSL
NT seq 1041 nt NT seq  +upstreamnt  +downstreamnt
atggcccggccgcagaggactccggcgcgcagtcccgatagcatcgtcgaggtgaagagc
aaatttgacgccgagttccgacgcttcgcgctgcctcgcgcttcggtgagcggcttccag
gagttctcgcggttgctgcgggcggtgcaccagatcccgggcctggacgtgctacttggc
tatacggatgctcatggcgacctgctgcccctcaccaacgacgacagcctgcaccgggcc
ctggccagcgggcccccgccactgcgcctactggtgcagaagcgggcagaagctgactcc
agcggcctggcttttgcctccaactctctgcagcggcgcaagaaagggctcttgctgcgg
ccagtggcacccctgcgcacccggccacccttgctaatcagcctgccccaagatttccgc
caggtttcctcagtcatagacgtggacctactgcctgagacccaccgacgggtgcggctg
cacaagcatggttcagaccgccccctgggcttctacatccgagatggcatgagcgtgcgt
gtggctccccagggcctggagcgggttccaggaatcttcatctcccgcctggtacgtggg
ggtctggctgagagtacagggctgctggcggtcagtgatgagatcctcgaggtcaatggc
attgaagtagccgggaagaccttggaccaagtgacggacatgatggttgccaacagccat
aacctcattgtcactgtcaagcccgccaaccagcgcaataacgtggtgcgaggggcatct
gggcgtttgacaggtcctccctctgcagggcctgggcctgctgagcctgatagtgacgat
gacagcagtgacctggtcattgagaaccgccagcctcccagttccaatgggctgtctcag
gggcccccgtgctgggacctgcaccctggctgccgacatcctggtacccgcagctctctg
ccctccctggatgaccaggagcaggccagttctggctgggggagtcgcattcgaggagat
ggtagtggcttcagcctctga

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