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1,972 Possible Causes for Prot

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  • Influenza

    Entry status i Reviewed (UniProtKB/Swiss-Prot) Annotation program Viral Protein Annotation Program[uniprot.org] Influenza A (HA /California (H1N1)) Product Code: PM-INFA-HACal Pool of 139 peptides derived from a peptide scan (15mers with 11 aa overlap) through Hemagglutinin (Swiss-Prot[shop.jpt.com] PA_I34A1 Accession i P03433 Primary (citable) accession number: P03433 Secondary accession number(s): A4GXH3, Q20N31, Q8JUU6 Entry history i Integrated into UniProtKB/Swiss-Prot[uniprot.org]

  • Appendicitis

    J Food Prot 70:11–16 PubMed Google Scholar 16.[doi.org] J Food Prot 69:2107–2112 PubMed Google Scholar 17.[doi.org] J Food Prot 67:1123–1127 PubMed Google Scholar 30. Fredriksson-Ahomaa M, Stolle A, Korkeala H (2006) Molecular epidemiology of Yersinia enterocolitica infections.[doi.org]

  • Bardet-Biedl Syndrome 10

    Entry status i Reviewed (UniProtKB/Swiss-Prot) Annotation program Chordata Protein Annotation Program[uniprot.org] Entry name i BBS10_PONAB Accession i Q5R8P3 Primary (citable) accession number: Q5R8P3 Secondary accession number(s): Q5RFC0 Entry history i Integrated into UniProtKB/Swiss-Prot[uniprot.org] […] annotation databases Entry information i Entry name i BBS10_MOUSE Accession i Q9DBI2 Primary (citable) accession number: Q9DBI2 Entry history i Integrated into UniProtKB/Swiss-Prot[uniprot.org]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    UniProtKB/Swiss-Prot : 75 Microcephaly 10, primary, autosomal recessive: A form of microcephaly, a disease defined as a head circumference more than 3 standard deviations[malacards.org] Mutation Database (HGMD) ZNF335 SNPedia medical, phenotypic, and genealogical associations of SNPs for ZNF335 No data available for Polymorphic Variants from UniProtKB/Swiss-Prot[genecards.org] Entry status i Reviewed (UniProtKB/Swiss-Prot) Annotation program Chordata Protein Annotation Program Disclaimer Any medical or genetic information present in this entry is[uniprot.org]

  • Amelogenesis Imperfecta Hypomaturation Type IIA5

    Related phenotypes are carious teeth and amelogenesis imperfecta UniProtKB/Swiss-Prot : 75 Amelogenesis imperfecta, hypomaturation type, 2A5: A defect of enamel formation.[malacards.org] Polymorphic Variants from UniProtKB/Swiss-Prot for SLC24A4 Gene NCKX4_HUMAN-Q8NFF2 Genetic variants in SLC24A4 define the skin/hair/eye pigmentation variation locus 6 (SHEP6[genecards.org]

  • Amelogenesis Imperfecta Type 1G with Nephrocalcinosis

    UniProtKB/Swiss-Prot : 75 Amelogenesis imperfecta 1G: A disorder characterized by dental anomalies, gingival overgrowth, and nephrocalcinosis.[malacards.org] […] phenotypic, and genealogical associations of SNPs for FAM20A SNP Genotyping and Copy Number Assay Products No data available for Polymorphic Variants from UniProtKB/Swiss-Prot[genecards.org]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2G

    UniProtKB/Swiss-Prot : 75 Limb-girdle muscular dystrophy 2G: An autosomal recessive degenerative myopathy characterized by proximal and distal muscle weakness and atrophy[malacards.org] Entry status i Reviewed (UniProtKB/Swiss-Prot) Annotation program Chordata Protein Annotation Program Disclaimer Any medical or genetic information present in this entry is[uniprot.org] Mutation Database (HGMD) TCAP SNPedia medical, phenotypic, and genealogical associations of SNPs for TCAP No data available for Polymorphic Variants from UniProtKB/Swiss-Prot[genecards.org]

  • Trichomegaly-Retina Pigmentary Degeneration-Dwarfism Syndrome

    Affiliated tissues include retina , pituitary and thyroid , and related phenotypes are cryptorchidism and hypogonadotrophic hypogonadism UniProtKB/Swiss-Prot : 75 Oliver-McFarlane[malacards.org] Mutation Database (HGMD) PNPLA6 SNPedia medical, phenotypic, and genealogical associations of SNPs for PNPLA6 No data available for Polymorphic Variants from UniProtKB/Swiss-Prot[genecards.org]

  • Isolated CoQ-Cytochrome C Reductase Deficiency

    Entry status i Reviewed (UniProtKB/Swiss-Prot) Annotation program Chordata Protein Annotation Program Disclaimer Any medical or genetic information present in this entry is[uniprot.org] HUMAN Accession i O14949 Primary (citable) accession number: O14949 Secondary accession number(s): Q5FVE2, Q9BV88, Q9T2V7 Entry history i Integrated into UniProtKB/Swiss-Prot[uniprot.org] […] i QCR7_HUMAN Accession i P14927 Primary (citable) accession number: P14927 Secondary accession number(s): E5RJU0, Q6FGD1 Entry history i Integrated into UniProtKB/Swiss-Prot[uniprot.org]

  • Autosomal Recessive Hypohidrotic Ectodermal Dysplasia Type 10B

    AC Q9UNE0; B2R9H2; B4DLC5; D3DX74; E9PC98; Q52LL5; Q9UND9; DT 27-MAY-2002, integrated into UniProtKB/Swiss-Prot. DT 01-MAY-2000, sequence version 1.[genome.jp] Affiliated tissues include skin , eye and breast , and related phenotypes are xerostomia and everted lower lip vermilion UniProtKB/Swiss-Prot : 75 Ectodermal dysplasia 11B[malacards.org] […] available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for EDAR Gene Polymorphic Variants from UniProtKB/Swiss-Prot[genecards.org]

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