Details for: ATP9A
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
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
PubMed ID: 22814378
Title: N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.
PubMed ID: 22814378
PubMed ID: 27733620
Title: The phospholipid flippase ATP9A is required for the recycling pathway from the endosomes to the plasma membrane.
PubMed ID: 27733620
PubMed ID: 30213940
Title: SNX3-retromer requires an evolutionary conserved MON2:DOPEY2:ATP9A complex to mediate Wntless sorting and Wnt secretion.
PubMed ID: 30213940
PubMed ID: 30947313
Title: The P4-ATPase ATP9A is a novel determinant of exosome release.
PubMed ID: 30947313
PubMed ID: 34764295
Title: Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder.
PubMed ID: 34764295
PubMed ID: 34379057
Title: Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive.
PubMed ID: 34379057
PubMed ID: 36604604
Title: ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity.
PubMed ID: 36604604
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.