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    ATP8A2 ATPase phospholipid transporting 8A2 [ Homo sapiens (human) ]

    Gene ID: 51761, updated on 10-Dec-2024

    Summary

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    Official Symbol
    ATP8A2provided by HGNC
    Official Full Name
    ATPase phospholipid transporting 8A2provided by HGNC
    Primary source
    HGNC:HGNC:13533
    See related
    Ensembl:ENSG00000132932 MIM:605870; AllianceGenome:HGNC:13533
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    IB; ATP; ML-1; ATPIB; CAMRQ4
    Summary
    The protein encoded by this gene is a member of the P4 ATPase family of proteins, which are thought to be involved in a process called lipid flipping, whereby phospholipids are translocated inwards from the exoplasmic leaflet to the cytosolic leaflet of the cell membrane, which aids in generating and maintaining asymmetry in membrane lipids. This protein is predicted to contain an E1 E2 ATPase, a haloacid dehalogenase-like hydrolase (HAD) domain, and multiple transmembrane domains. Associations between this protein and cell cycle control protein 50A are important for translocation of phosphatidylserine across membranes. Mutations in this gene have been associated with a syndrome (CAMRQ4) characterized by cerebellar ataxia and cognitive disabilities. In addition, a translocation breakpoint within this gene was observed in an individual with neurological dysfunction. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]
    Expression
    Biased expression in brain (RPKM 6.4), testis (RPKM 2.7) and 2 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See ATP8A2 in Genome Data Viewer
    Location:
    13q12.13
    Exon count:
    47
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (25371974..26025851)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (24581610..25239722)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (25946112..26599989)

    Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7486 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7487 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_32788 Neighboring gene CRISPRi-validated cis-regulatory element chr13.188 Neighboring gene nucleoporin 58 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr13:25971441-25972042 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr13:25972043-25972644 Neighboring gene elongin B pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:26028835-26029335 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:26052317-26053192 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:26086829-26087701 Neighboring gene NANOG hESC enhancer GRCh37_chr13:26118592-26119123 Neighboring gene RNA, U6 small nuclear 78, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7488 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7489 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr13:26484777-26485332 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr13:26485333-26485887 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:26548551-26549090 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:26549091-26549629 Neighboring gene uncharacterized LOC105370122 Neighboring gene RNA, 7SL, cytoplasmic 741, pseudogene Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:26550993-26551936 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:26552889-26553440 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:26585998-26586498 Neighboring gene RNY1 pseudogene 3 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:26586499-26586999 Neighboring gene long intergenic non-protein coding RNA 415 Neighboring gene shisa family member 2

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. P4 ATPases: flippases in health and disease. van der Mark VA, et al. Int J Mol Sci, 2013 Apr 11. PMID 23579954, Free PMC Article
    2. Changes in levels of normal ML-1 gene transcripts associated with the conversion of human nontumorigenic to tumorigenic phenotypes. Sun XL, et al. Gene Expr, 1999. PMID 10551800, Free PMC Article
    3. Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. Onat OE, et al. Eur J Hum Genet, 2013 Mar. PMID 22892528, Free PMC Article
    4. Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases. Matsell E, et al. Dis Model Mech, 2024 Jun 1. PMID 38436085, Free PMC Article
    5. P4-ATPases: lipid flippases in cell membranes. Lopez-Marques RL, et al. Pflugers Arch, 2014 Jul. PMID 24077738, Free PMC Article

    See all (34) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases.
      Title: Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases.
    2. On the track of the lipid transport pathway of the phospholipid flippase ATP8A2 - Mutation analysis of residues of the transmembrane segments M1, M2, M3 and M4.
      Title: On the track of the lipid transport pathway of the phospholipid flippase ATP8A2 - Mutation analysis of residues of the transmembrane segments M1, M2, M3 and M4.
    3. Two Siblings with Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome 4 and a Novel Variant of ATP8A2.
      Title: Two Siblings with Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome 4 and a Novel Variant of ATP8A2.
    4. Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum.
      Title: Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum.
    5. Congenital ataxia due to novel variant in ATP8A2.
      Title: Congenital ataxia due to novel variant in ATP8A2.
    6. ATP8A2-related disorders as recessive cerebellar ataxia.
      Title: ATP8A2-related disorders as recessive cerebellar ataxia.
    7. Functional analysis of the effect of disease-associated missense mutations on ATP8A2 show that the p.Ile376Met and p.Lys429Met variants fold in a native-like conformation, but lack key amino acid residues required for ATP-dependent lipid transport. In contrast, the p.Lys429Asn, pAla544Pro, p.Arg625Trp, and p.Trp702Arg variants are highly misfolded and undergo rapid proteosomal degradation.
      Title: Expression and functional characterization of missense mutations in ATP8A2 linked to severe neurological disorders.
    8. Using an electrophysiological method based on solid supported membranes, we observed the generation of a transient electrical current by the mammalian P4-ATPase ATP8A2 in the presence of ATP and the negatively charged lipid substrate phosphatidylserine, whereas only a diminutive current was generated with the lipid substrate phosphatidylethanolamine, which carries no or little charge under the conditions of the measuremen
      Title: Phosphatidylserine flipping by the P4-ATPase ATP8A2 is electrogenic.
    9. Study describes a new ATP8A2 gene mutations associated with a novel syndrome that includes encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy. The data expand both the genetic and phenotypic spectrum associated with ATP8A2 gene mutations.
      Title: New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy.
    10. ATP8A2 is involved in the development of the cerebro-cerebellar structures required for posture and gait.
      Title: Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion.
    Submit: New GeneRIF Correction See all GeneRIFs (13)

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    Associated conditions

    Description Tests
    Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4
    MedGen: C3808977 OMIM: 615268 GeneReviews: Not available
    		Compare labs

    EBI GWAS Catalog

    Description
    A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
    EBI GWAS Catalog
    Genetic variants associated with disordered eating.
    EBI GWAS Catalog

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • DKFZp434B1913

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables ATP binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables ATP hydrolysis activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables ATPase-coupled intramembrane lipid transporter activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables magnesium ion binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables phosphatidylethanolamine flippase activity ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    enables phosphatidylserine flippase activity ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    enables phosphatidylserine floppase activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in aminophospholipid translocation ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    involved_in axonogenesis IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in detection of light stimulus involved in visual perception IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in determination of adult lifespan IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in eating behavior IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in inner ear morphogenesis IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in involuntary skeletal muscle contraction IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in negative regulation of cell population proliferation TAS
    Traceable Author Statement
    more info
    		 PubMed 
    involved_in neurofilament cytoskeleton organization IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in neuromuscular process controlling posture IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in neuron development IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in phospholipid translocation IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in positive regulation of multicellular organism growth IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in positive regulation of neuron projection development IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in positive regulation of phospholipid translocation IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in response to auditory stimulus IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in retina layer formation IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in skin development IEA
    Inferred from Electronic Annotation
    more info
    		  
    Component Evidence Code Pubs
    located_in Golgi apparatus IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in Golgi membrane IEA
    Inferred from Electronic Annotation
    more info
    		  
    located_in cell projection IEA
    Inferred from Electronic Annotation
    more info
    		  
    located_in endosome membrane IEA
    Inferred from Electronic Annotation
    more info
    		  
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
    		  
    part_of phospholipid-translocating ATPase complex IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in plasma membrane IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    is_active_in trans-Golgi network IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  

    General protein information

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    Preferred Names
    phospholipid-transporting ATPase IB
    Names
    ATPase, aminophospholipid transporter, class I, type 8A, member 2
    ATPase, aminophospholipid transporter-like, class I, type 8A, member 2
    P4-ATPase flippase complex alpha subunit ATP8A2
    probable phospholipid-transporting ATPase IB
    NP_001300670.1
    NP_001397934.1
    NP_001397935.1
    NP_057613.4
    XP_005266476.1
    XP_011533406.1
    XP_011533409.1
    XP_011533411.1
    XP_011533415.1
    XP_016876114.1
    XP_016876115.1
    XP_024305137.1
    XP_047286339.1
    XP_054230574.1
    XP_054230575.1
    XP_054230576.1
    XP_054230577.1
    XP_054230578.1
    XP_054230579.1
    XP_054230580.1
    XP_054230581.1
    XP_054230582.1
    XP_054230583.1

    NCBI Reference Sequences (RefSeq)

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    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_042855.1 RefSeqGene

      Range
      4964..658841
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001313741.1 → NP_001300670.1  phospholipid-transporting ATPase IB isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR, lacks a portion of the 5' coding region, and lacks an alternate in-frame exon in the central coding region. These differences cause translation initiation at a downstream start codon and result in an isoform (2) with a shorter N-terminus, and lacking an internal segment, compared to isoform 1.
      Source sequence(s)
      AK094653, AK126031, AK127263, AK302980, AL136438, AL138815, AL139004, AL390129, AL669971, BP396213, HY026915
      UniProtKB/TrEMBL
      B7Z880, Q6ZU25
      Conserved Domains (6) summary
      TIGR01652
      Location:28 → 1041
      ATPase-Plipid; phospholipid-translocating P-type ATPase, flippase
      pfam00122
      Location:85 → 304
      E1-E2_ATPase; E1-E2 ATPase
      pfam13246
      Location:466 → 564
      Cation_ATPase; Cation transport ATPase (P-type)
      pfam16209
      Location:17 → 79
      PhoLip_ATPase_N; Phospholipid-translocating ATPase N-terminal
      pfam16212
      Location:808 → 1034
      PhoLip_ATPase_C; Phospholipid-translocating P-type ATPase C-terminal
      cl21460
      Location:776 → 805
      HAD_like; Haloacid Dehalogenase-like Hydrolases

    2. NM_001411005.1 → NP_001397934.1  phospholipid-transporting ATPase IB isoform 3

      Status: REVIEWED

      Source sequence(s)
      AL136438, AL138815, AL138958, AL139004, AL157366, AL356316, AL669971
      Consensus CDS
      CCDS91793.1
      UniProtKB/TrEMBL
      A0A804HKW9, A0A804HLG3
      Related
      ENSP00000508103.1, ENST00000682472.1

    3. NM_001411006.1 → NP_001397935.1  phospholipid-transporting ATPase IB isoform 4

      Status: REVIEWED

      Source sequence(s)
      AL136438, AL138815, AL138958, AL157366, AL356316, AL669971
      Consensus CDS
      CCDS91792.1
      UniProtKB/TrEMBL
      A0A804HI09, A0A804HLG3
      Related
      ENSP00000506846.1, ENST00000683960.1

    4. NM_016529.6 → NP_057613.4  phospholipid-transporting ATPase IB isoform 1

      See identical proteins and their annotated locations for NP_057613.4

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1).
      Source sequence(s)
      AF236871, AK094653, AK126031, AK127263, AL136438, AL138815, AL138958, AL139004, AL390129, AL669971, BP396213, DA326706
      Consensus CDS
      CCDS41873.1
      UniProtKB/Swiss-Prot
      Q6ZSP3, Q9H527, Q9NPU6, Q9NTI2, Q9NTL2, Q9NYM3
      UniProtKB/TrEMBL
      A0A804HLG3
      Related
      ENSP00000371070.2, ENST00000381655.7
      Conserved Domains (1) summary
      TIGR01652
      Location:68 → 1106
      ATPase-Plipid; phospholipid-translocating P-type ATPase, flippase

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000013.11 Reference GRCh38.p14 Primary Assembly

      Range
      25371974..26025851
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_011535107.4 → XP_011533409.1  phospholipid-transporting ATPase IB isoform X8

      UniProtKB/TrEMBL
      A0A804HLG3
      Related
      ENSP00000508339.1, ENST00000683303.1
      Conserved Domains (6) summary
      TIGR01652
      Location:68 → 1051
      ATPase-Plipid; phospholipid-translocating P-type ATPase, flippase
      pfam00122
      Location:125 → 344
      E1-E2_ATPase; E1-E2 ATPase
      pfam13246
      Location:506 → 604
      Cation_ATPase; Cation transport ATPase (P-type)
      pfam16209
      Location:57 → 119
      PhoLip_ATPase_N; Phospholipid-translocating ATPase N-terminal
      pfam16212
      Location:848 → 1054
      PhoLip_ATPase_C; Phospholipid-translocating P-type ATPase C-terminal
      cl21460
      Location:816 → 845
      HAD_like; Haloacid Dehalogenase-like Hydrolases

    2. XM_011535113.3 → XP_011533415.1  phospholipid-transporting ATPase IB isoform X5

      UniProtKB/TrEMBL
      A0A804HKN1
      Conserved Domains (3) summary
      pfam00122
      Location:125 → 344
      E1-E2_ATPase; E1-E2 ATPase
      pfam13246
      Location:506 → 604
      Cation_ATPase; Cation transport ATPase (P-type)
      pfam16209
      Location:57 → 119
      PhoLip_ATPase_N; Phospholipid-translocating ATPase N-terminal

    3. XM_017020626.2 → XP_016876115.1  phospholipid-transporting ATPase IB isoform X7

      UniProtKB/TrEMBL
      A0A804HKN1

    4. XM_017020625.3 → XP_016876114.1  phospholipid-transporting ATPase IB isoform X6

      UniProtKB/TrEMBL
      A0A804HKN1

    5. XM_047430383.1 → XP_047286339.1  phospholipid-transporting ATPase IB isoform X1

      UniProtKB/TrEMBL
      Q6ZU25

    6. XM_005266419.2 → XP_005266476.1  phospholipid-transporting ATPase IB isoform X1

      See identical proteins and their annotated locations for XP_005266476.1

      UniProtKB/TrEMBL
      Q6ZU25
      Related
      ENSP00000507489.1, ENST00000684424.1
      Conserved Domains (1) summary
      TIGR01652
      Location:28 → 1066
      ATPase-Plipid; phospholipid-translocating P-type ATPase, flippase

    7. XM_011535104.3 → XP_011533406.1  phospholipid-transporting ATPase IB isoform X2

      UniProtKB/TrEMBL
      Q6ZU25
      Related
      ENST00000683945.1
      Conserved Domains (6) summary
      TIGR01652
      Location:34 → 1066
      ATPase-Plipid; phospholipid-translocating P-type ATPase, flippase
      pfam00122
      Location:85 → 304
      E1-E2_ATPase; E1-E2 ATPase
      pfam13246
      Location:466 → 564
      Cation_ATPase; Cation transport ATPase (P-type)
      pfam16209
      Location:34 → 79
      PhoLip_ATPase_N; Phospholipid-translocating ATPase N-terminal
      pfam16212
      Location:808 → 1059
      PhoLip_ATPase_C; Phospholipid-translocating P-type ATPase C-terminal
      cl21460
      Location:776 → 805
      HAD_like; Haloacid Dehalogenase-like Hydrolases

    8. XM_011535109.4 → XP_011533411.1  phospholipid-transporting ATPase IB isoform X3

      See identical proteins and their annotated locations for XP_011533411.1

      UniProtKB/TrEMBL
      Q6ZU25
      Conserved Domains (5) summary
      TIGR01652
      Location:1 → 946
      ATPase-Plipid; phospholipid-translocating P-type ATPase, flippase
      pfam00122
      Location:2 → 184
      E1-E2_ATPase; E1-E2 ATPase
      pfam13246
      Location:346 → 444
      Cation_ATPase; Cation transport ATPase (P-type)
      pfam16212
      Location:688 → 939
      PhoLip_ATPase_C; Phospholipid-translocating P-type ATPase C-terminal
      cl21460
      Location:656 → 685
      HAD_like; Haloacid Dehalogenase-like Hydrolases

    9. XM_024449369.1 → XP_024305137.1  phospholipid-transporting ATPase IB isoform X4

      UniProtKB/TrEMBL
      Q6ZU25
      Conserved Domains (1) summary
      TIGR01652
      Location:1 → 908
      ATPase-Plipid; phospholipid-translocating P-type ATPase, flippase

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_187593.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      489..133501 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060937.1 Alternate T2T-CHM13v2.0

      Range
      24581610..25239722
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054374602.1 → XP_054230577.1  phospholipid-transporting ATPase IB isoform X9

      UniProtKB/TrEMBL
      A0A804HLG3

    2. XM_054374605.1 → XP_054230580.1  phospholipid-transporting ATPase IB isoform X10

      UniProtKB/TrEMBL
      A0A804HKN1

    3. XM_054374606.1 → XP_054230581.1  phospholipid-transporting ATPase IB isoform X5

      UniProtKB/TrEMBL
      A0A804HKN1

    4. XM_054374608.1 → XP_054230583.1  phospholipid-transporting ATPase IB isoform X7

      UniProtKB/TrEMBL
      A0A804HKN1

    5. XM_054374607.1 → XP_054230582.1  phospholipid-transporting ATPase IB isoform X6

      UniProtKB/TrEMBL
      A0A804HKN1

    6. XM_054374601.1 → XP_054230576.1  phospholipid-transporting ATPase IB isoform X1

      UniProtKB/TrEMBL
      Q6ZU25

    7. XM_054374599.1 → XP_054230574.1  phospholipid-transporting ATPase IB isoform X1

      UniProtKB/TrEMBL
      Q6ZU25

    8. XM_054374600.1 → XP_054230575.1  phospholipid-transporting ATPase IB isoform X2

      UniProtKB/TrEMBL
      Q6ZU25

    9. XM_054374603.1 → XP_054230578.1  phospholipid-transporting ATPase IB isoform X3

      UniProtKB/TrEMBL
      Q6ZU25

    10. XM_054374604.1 → XP_054230579.1  phospholipid-transporting ATPase IB isoform X4

      UniProtKB/TrEMBL
      Q6ZU25
    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q9NTI2.3 GenPept UniProtKB/Swiss-Prot:Q9NTI2

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