Details for: ATP9A

Gene ID: 10079

Symbol: ATP9A

Ensembl ID: ENSG00000054793

Description: ATPase phospholipid transporting 9A (putative)

Associated with

Other Information

Genular Protein ID: 69577485

Symbol: ATP9A_HUMAN

Name: Probable phospholipid-transporting ATPase IIA

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11780052

Title: The DNA sequence and comparative analysis of human chromosome 20.

PubMed ID: 11780052

DOI: 10.1038/414865a

PubMed ID: 9734811

Title: Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.

PubMed ID: 9734811

DOI: 10.1093/dnares/5.3.169

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 21914794

Title: ATP9B, a P4-ATPase (a putative aminophospholipid translocase), localizes to the trans-Golgi network in a CDC50 protein-independent manner.

PubMed ID: 21914794

DOI: 10.1074/jbc.m111.281006

PubMed ID: 22814378

Title: N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.

PubMed ID: 22814378

DOI: 10.1073/pnas.1210303109

PubMed ID: 27733620

Title: The phospholipid flippase ATP9A is required for the recycling pathway from the endosomes to the plasma membrane.

PubMed ID: 27733620

DOI: 10.1091/mbc.e16-08-0586

PubMed ID: 30213940

Title: SNX3-retromer requires an evolutionary conserved MON2:DOPEY2:ATP9A complex to mediate Wntless sorting and Wnt secretion.

PubMed ID: 30213940

DOI: 10.1038/s41467-018-06114-3

PubMed ID: 30947313

Title: The P4-ATPase ATP9A is a novel determinant of exosome release.

PubMed ID: 30947313

DOI: 10.1371/journal.pone.0213069

PubMed ID: 34764295

Title: Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder.

PubMed ID: 34764295

DOI: 10.1038/s41525-021-00255-z

PubMed ID: 34379057

Title: Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive.

PubMed ID: 34379057

DOI: 10.1136/jmedgenet-2021-107843

PubMed ID: 36604604

Title: ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity.

PubMed ID: 36604604

DOI: 10.1038/s41380-022-01940-w

Sequence Information:

  • Length: 1047
  • Mass: 118583
  • Checksum: 80C307CF5A396755
  • Sequence:
  • MTDNIPLQPV RQKKRMDSRP RAGCCEWLRC CGGGEARPRT VWLGHPEKRD QRYPRNVINN 
    QKYNFFTFLP GVLFNQFKYF FNLYFLLLAC SQFVPEMRLG ALYTYWVPLG FVLAVTVIRE 
    AVEEIRCYVR DKEVNSQVYS RLTARGTVKV KSSNIQVGDL IIVEKNQRVP ADMIFLRTSE 
    KNGSCFLRTD QLDGETDWKL RLPVACTQRL PTAADLLQIR SYVYAEEPNI DIHNFVGTFT 
    REDSDPPISE SLSIENTLWA GTVVASGTVV GVVLYTGREL RSVMNTSNPR SKIGLFDLEV 
    NCLTKILFGA LVVVSLVMVA LQHFAGRWYL QIIRFLLLFS NIIPISLRVN LDMGKIVYSW 
    VIRRDSKIPG TVVRSSTIPE QLGRISYLLT DKTGTLTQNE MIFKRLHLGT VAYGLDSMDE 
    VQSHIFSIYT QQSQDPPAQK GPTLTTKVRR TMSSRVHEAV KAIALCHNVT PVYESNGVTD 
    QAEAEKQYED SCRVYQASSP DEVALVQWTE SVGLTLVGRD QSSMQLRTPG DQILNFTILQ 
    IFPFTYESKR MGIIVRDEST GEITFYMKGA DVVMAGIVQY NDWLEEECGN MAREGLRVLV 
    VAKKSLAEEQ YQDFEARYVQ AKLSVHDRSL KVATVIESLE MEMELLCLTG VEDQLQADVR 
    PTLETLRNAG IKVWMLTGDK LETATCTAKN AHLVTRNQDI HVFRLVTNRG EAHLELNAFR 
    RKHDCALVIS GDSLEVCLKY YEYEFMELAC QCPAVVCCRC APTQKAQIVR LLQERTGKLT 
    CAVGDGGNDV SMIQESDCGV GVEGKEGKQA SLAADFSITQ FKHLGRLLMV HGRNSYKRSA 
    ALSQFVIHRS LCISTMQAVF SSVFYFASVP LYQGFLIIGY STIYTMFPVF SLVLDKDVKS 
    EVAMLYPELY KDLLKGRPLS YKTFLIWVLI SIYQGSTIMY GALLLFESEF VHIVAISFTS 
    LILTELLMVA LTIQTWHWLM TVAELLSLAC YIASLVFLHE FIDVYFIATL SFLWKVSVIT 
    LVSCLPLYVL KYLRRRFSPP SYSKLTS

Genular Protein ID: 882255386

Symbol: Q2NLD0_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

Sequence Information:

  • Length: 891
  • Mass: 100275
  • Checksum: 73A6754D8103AFC9
  • Sequence:
  • VGDLIIVEKN QRVPADMIFL RTSEKNGSCF LRTDQLDGET DWKLRLPVAC TQRLPTAADL 
    LQIRSYVYAE EPNIDIHNFV GTFTREDSDP PISESLSIEN TLWAGTVVAS GTVVGVVLYT 
    GRELRSVMNT SNPRSKIGLF DLEVNCLTKI LFGALVVVSL VMVALQHFAG RWYLQIIRFL 
    LLFSNIIPIS LRVNLDMGKI VYSWVIRRDS KIPGTVVRSS TIPEQLGRIS YLLTDKTGTL 
    TQNEMIFKRL HLGTVAYGLD SMDEVQSHIF SIYTQQSQDP PAQKGPTLTT KVRRTMSSRV 
    HEAVKAIALC HNVTPVYESN GVTDQAEAEK QYEDSCRVYQ ASSPDEVALV QWTESVGLTL 
    VGRDQSSMQL RTPGDQILNF TILQIFPFTY ESKRMGIIVR DESTGEITFY MKGADVVMAG 
    IVQYNDWLEE ECGNMAREGL RVLVVAKKSL AEEQYQDFEA RYVQAKLSVH DRSLKVATVI 
    ESLEMEMELL CLTGVEDQLQ ADVRPTLETL RNAGIKVWML TGDKLETATC TAKNAHLVTR 
    NQDIHVFRLV TNRGEAHLEL NAFRRKHDCA LVISGDSLEV CLKYYEYEFM ELACQCPAVV 
    CCRCAPTQKA QIVRLLQERT GKLTCAVGDG GNDVSMIQES DCGVGVEGKE GKQASLAADF 
    SITQFKHLGR LLMVHGRNSY KRSAALSQFV IHRSLCISTM QAVFSSVFYF ASVPLYQGFL 
    IIGYSTIYTM FPVFSLVLDK DVKSEVAMLY PELYKDLLKG RPLSYKTFLI WVLISIYQGS 
    TIMYGALLLF ESEFVHIVAI SFTSLILTEL LMVALTIQTW HWLMTVAELL SLACYIASLV 
    FLHEFIDVYF IATLSFLWKV SVITLVSCLP LYVLKYLRRR FSPPSYSKLT S

Genular Protein ID: 591639739

Symbol: B4DR18_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 1032
  • Mass: 116776
  • Checksum: 9273C97989FD0C33
  • Sequence:
  • MDSRPRAGCC EWLRCCGGGE ARPRTVWLGH PEKRDQRYPR NVINNQKYNF FTFLPGVLFN 
    QFKYFFNLYF LLLACSQFVP EMRLGALYTY WVPLGFVLAV TVIREAVEEI RCYVRDKEVN 
    SQVYSRLTAR GTVKVKSSNI QVGDLIIVEK NQRVPADMIF LRTSEKNGSC FLRTDQLDGE 
    TDWKLRLPVA CTQRLPTAAD LLQIRSYVYA EEPNIDIHNF VGTFTREDSD PPISESLSIE 
    NTLWAGTVVA SGTVVGVVLY TGRELRSVMN TSNPRSKIGL FDLEVNCLTK ILFGALVVVS 
    LVMVALQHFA GRWYLQIIRF LLLFSNIIPI SLRVNLDMGK IVYSWVIRRD SKIPGTVVRS 
    STIPEQLGRI SYLLTDKTGT LTQNEMIFKR LHLGTVAYGL DSMDEVQSHI FSIYTQQSQD 
    PPAQKGPTLT TKVRRTMSSR VHEAVKAIAL CHNVTPVYES NGVTDQAEAE KQYEDSCRVY 
    QASSPDEVAL VQWTESVGLT LVGRDQSSMQ LRTPGDQILN FTILQIFPFT YESKRMGIIV 
    RDESTGEITF YMKGADVVMA GIVQYNDWLE EECGNMAREG LRVLVVAKKS LAEEQYQDFE 
    ARYVQAKLSV HDRSLKVATV IESLEMEMEL LCLTGVEDQL QADVRPTLET LRNAGIKVWM 
    LTGDKLETAT CTAKNAHLVT RNQDIHVFRL VTNRGEAHLE LNAFRRKHDC ALVISGDSLE 
    VCLKYYEYEF MELACQCPAV VCCRCAPTQK AQIVRLLQER TGKLTCAVGD GGNDVSMIQE 
    SDCGVGVEGK EGKQASLAAD FSITQFKHLG RLLMVHGRNS YKRSAALSQF VIHRSLCIST 
    MQAVFSSVFY FASVPLYQGF LIIGYSTIYT MFPVFSLVLD KDVKSEVAML YPELYKDLLK 
    GRPLSYKTFL IWVLISIYQG STIMYGALLL FESEFVHIVA ISFTSLILTE LLMVALTIQT 
    WHWLMTVAEL LSLACYIASL VFLHEFIDVY FIATLSFLWK VSVITLVSCL PLYVLKYLRR 
    RFSPPSYSKL TS

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.