KEGG   Homo sapiens (human): 10079
Entry
10079             CDS       T01001                                 
Symbol
ATP9A, ATPIIA, NEDGBA
Name
(RefSeq) ATPase phospholipid transporting 9A (putative)
  KO
K26679  phospholipid-transporting ATPase IIA [EC:7.6.2.1]
Organism
hsa  Homo sapiens (human)
Disease
H02459  Syndromic neurodevelopmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    10079 (ATP9A)
Enzymes [BR:hsa01000]
 7. Translocases
  7.6  Catalysing the translocation of other compounds
   7.6.2  Linked to the hydrolysis of a nucleoside triphosphate
    7.6.2.1  P-type phospholipid transporter
     10079 (ATP9A)
Membrane trafficking [BR:hsa04131]
 Endosome - Golgi transport
  Others
   Others
    10079 (ATP9A)
SSDB
Motif
Pfam: PhoLip_ATPase_C PhoLip_ATPase_N Hydrolase E1-E2_ATPase Cation_ATPase Hydrolase_3
Other DBs
NCBI-GeneID: 10079
NCBI-ProteinID: NP_006036
OMIM: 609126
HGNC: 13540
Ensembl: ENSG00000054793
Pharos: O75110(Tdark)
UniProt: O75110 Q2NLD0 B4DR18
Position
20:complement(51596514..51768390)
AA seq 1047 aa
MTDNIPLQPVRQKKRMDSRPRAGCCEWLRCCGGGEARPRTVWLGHPEKRDQRYPRNVINN
QKYNFFTFLPGVLFNQFKYFFNLYFLLLACSQFVPEMRLGALYTYWVPLGFVLAVTVIRE
AVEEIRCYVRDKEVNSQVYSRLTARGTVKVKSSNIQVGDLIIVEKNQRVPADMIFLRTSE
KNGSCFLRTDQLDGETDWKLRLPVACTQRLPTAADLLQIRSYVYAEEPNIDIHNFVGTFT
REDSDPPISESLSIENTLWAGTVVASGTVVGVVLYTGRELRSVMNTSNPRSKIGLFDLEV
NCLTKILFGALVVVSLVMVALQHFAGRWYLQIIRFLLLFSNIIPISLRVNLDMGKIVYSW
VIRRDSKIPGTVVRSSTIPEQLGRISYLLTDKTGTLTQNEMIFKRLHLGTVAYGLDSMDE
VQSHIFSIYTQQSQDPPAQKGPTLTTKVRRTMSSRVHEAVKAIALCHNVTPVYESNGVTD
QAEAEKQYEDSCRVYQASSPDEVALVQWTESVGLTLVGRDQSSMQLRTPGDQILNFTILQ
IFPFTYESKRMGIIVRDESTGEITFYMKGADVVMAGIVQYNDWLEEECGNMAREGLRVLV
VAKKSLAEEQYQDFEARYVQAKLSVHDRSLKVATVIESLEMEMELLCLTGVEDQLQADVR
PTLETLRNAGIKVWMLTGDKLETATCTAKNAHLVTRNQDIHVFRLVTNRGEAHLELNAFR
RKHDCALVISGDSLEVCLKYYEYEFMELACQCPAVVCCRCAPTQKAQIVRLLQERTGKLT
CAVGDGGNDVSMIQESDCGVGVEGKEGKQASLAADFSITQFKHLGRLLMVHGRNSYKRSA
ALSQFVIHRSLCISTMQAVFSSVFYFASVPLYQGFLIIGYSTIYTMFPVFSLVLDKDVKS
EVAMLYPELYKDLLKGRPLSYKTFLIWVLISIYQGSTIMYGALLLFESEFVHIVAISFTS
LILTELLMVALTIQTWHWLMTVAELLSLACYIASLVFLHEFIDVYFIATLSFLWKVSVIT
LVSCLPLYVLKYLRRRFSPPSYSKLTS
NT seq 3144 nt   +upstreamnt  +downstreamnt
atgacggacaacatcccgctgcagccggtgcgccagaagaagcggatggacagcaggccc
cgcgccgggtgctgcgagtggctgagatgctgcggtggaggggaggccaggccccgcact
gtctggctggggcaccccgagaagagagaccagaggtatcctcggaatgtcatcaacaat
cagaagtacaatttcttcacctttcttcctggggtgctgttcaaccagttcaaatacttt
ttcaacctctatttcttacttcttgcctgctctcagtttgttcccgaaatgagacttggt
gcactctatacctactgggttcccctgggcttcgtgctggccgtcactgtcatccgtgag
gcggtggaggagatccgatgctacgtgcgggacaaggaagtcaactcccaggtctacagc
cggctcacagcacgaggcacagtgaaggtgaagagttctaacatccaagttggagacctt
atcatcgttgaaaagaaccagcgggtccctgccgacatgatcttcctgaggacatcagaa
aaaaacgggtcatgcttcttgcggacggatcagctggatggggagacggactggaagctg
cggcttcccgtggcctgcacgcagaggctccccacggccgccgaccttcttcagattcga
tcgtatgtgtacgcagaagagccaaatattgacattcacaacttcgtgggaacttttacc
cgagaagacagcgaccccccgatcagcgagagcctgagcatagagaacacgctgtgggct
ggcactgtggtcgcatcaggtactgttgtgggtgttgttctttacactggcagagaactc
cggagtgtcatgaatacctcaaatccccgaagtaagatcggcctgttcgacttggaagtg
aactgcctcaccaagatcctctttggtgccctggtggtggtctcgctggtcatggttgcc
cttcagcactttgcaggccgttggtacctgcagatcatccgcttcctcctcttgttttcc
aacatcatccccattagtttgcgtgtgaacctggacatgggcaagatcgtgtacagctgg
gtgattcgaagggactcgaaaatccccgggaccgtggttcgctccagcacgattcctgag
cagctgggcaggatttcgtacttactcacagacaagacaggcactcttacccagaacgag
atgattttcaaacggctccatctcggaacagtagcctacggcctcgactcaatggacgaa
gtacaaagccacattttcagcatttacacccagcaatcccaggacccaccggctcagaag
ggcccaacgctcaccactaaggtccggcggaccatgagcagccgcgtgcacgaagccgtg
aaggccatcgcgctctgccacaacgtgactcccgtgtatgagtccaacggtgtgactgat
caggctgaggccgagaagcagtacgaagactcctgccgcgtataccaggcatccagcccc
gatgaggtggccctggtacagtggacggaaagtgtgggcttaaccctggtgggccgagac
cagtcttccatgcagctgaggacccctggcgaccagatcctgaacttcaccatcctacag
atcttccctttcacctatgaaagcaaacgtatgggcatcatcgtgcgggatgaatcaact
ggagaaattacgttttacatgaagggagcagatgtggtcatggctggcattgtgcagtac
aatgactggttggaggaagagtgtggcaacatggcccgagaagggctgcgggtgctcgtg
gtggcaaagaagtctcttgcagaggagcagtatcaggactttgaagcccgctacgtccag
gccaagctgagtgtgcacgaccgctccctcaaagtggccacggtgatcgagagcctggag
atggagatggaactgctgtgcctgacgggcgtggaggaccagctgcaggcagatgtgcgg
cccacgctggagaccctgaggaatgctggcatcaaggtttggatgctgacaggggacaag
ctggagacagctacgtgcacagcgaagaatgcacatctggtgaccagaaaccaagacatc
cacgtttttcggctggtgaccaaccgcggggaggctcacctcgagctgaacgccttccgc
aggaagcatgattgtgccctggtcatctcgggagactccctggaggtttgcctcaagtac
tatgagtacgagttcatggagctggcctgccagtgcccggccgtagtctgctgccgatgt
gcccccacccagaaggcccagatcgtgcgcctgcttcaggagcgcacgggcaagctcacc
tgtgcagtaggggacggaggcaatgacgtcagcatgattcaggaatctgactgcggcgtg
ggagtggaaggaaaggaaggaaaacaggcttcgttggctgcagacttctccatcactcaa
tttaagcatcttggccggttgcttatggtgcatggccggaacagctacaagcggtcagcc
gccctcagccagttcgtgattcacaggagcctctgtatcagcaccatgcaggctgtcttt
tcctccgtgttttactttgcctccgtccctctctatcaaggattcctcatcattgggtac
tccacaatttacaccatgtttcctgtgttttctctggtcctggacaaagatgtcaaatcg
gaagttgccatgctgtatcctgagctctacaaggatcttctcaagggacggccgttgtcc
tacaagacattcttaatatgggttttgattagcatctatcaagggagcaccatcatgtac
ggggcgctgctgctgtttgagtcggagttcgtgcacatcgtggccatctccttcacctcg
ctgatcctcaccgagctgctcatggtggcgctgaccatccagacctggcactggctcatg
acagtggcggagctgctcagcctggcctgctacatcgcctccctggtgttcttacacgag
ttcatcgatgtgtacttcatcgccaccttgtcattcttgtggaaagtctccgtcatcact
ctggtcagctgcctccccctctatgtcctcaagtacctgcgaagacggttctctcccccc
agctactcaaagctcacatcatag

  All links  
Ontology (3)   
   KEGG BRITE (3)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Chemical reaction (1)   
   KEGG ENZYME (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (23)   
   KEGG ORTHOLOGY (1)   
   RefGene (14)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
   PHAROS (1)   
Protein sequence (5)   
   UniProt (3)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (29)   
   RefSeq(nuc) (1)   
   GenBank (14)   
   EMBL (14)   
Protein domain (6)   
   Pfam (6)   
All databases (71)   

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