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  • SAMD9
  • Protein-coding gene in the species Homo sapiens

    domain-containing protein 9 is a 1,589-amino-acid protein encoded by the SAMD9 gene. This cytoplasmic protein is a tumor suppressor that has a role in

    SAMD9

    SAMD9

    SAMD9

  • Myelodysplastic syndrome
  • Diverse collection of blood-related cancers

    may be genetically inherited, it is extremely rare. GATA2 deficiency and SAMD9/9L syndromes each account for about 15% of MDS cases in children. Causes

    Myelodysplastic syndrome

    Myelodysplastic syndrome

    Myelodysplastic_syndrome

  • Yemenite Jews
  • Jewish ethnic group

    for large-scale conversion of local Yemeni". In medicine, the mutation SAMD9 (sterile alpha motif domain containing 9), which encodes a protein involved

    Yemenite Jews

    Yemenite Jews

    Yemenite_Jews

  • Sterile alpha motif
  • Protein domain

    PPFIBP2; SAMD1; SAMD13; SAMD14; SAMD3; SAMD4A; SAMD4B; SAMD5; SAMD7; SAMD8; SAMD9; SARM1; SCMH1; SCML1; SCML2; SEC23IP; SGMS1; SHANK1; SHANK2; SHANK3; STARD13;

    Sterile alpha motif

    Sterile alpha motif

    Sterile_alpha_motif

  • Clonal hematopoiesis
  • Expansion of blood cells

    particularly when there are germ line mutations in CEBPA, DDX41, GATA2, RUNX1, or SAMD9/9L. Examples include ribosomopathies such as Schwachman-Diamond syndrome

    Clonal hematopoiesis

    Clonal_hematopoiesis

  • List of genes mutated in cutaneous conditions
  • syndrome RecQL4 DNA helicase Rothmund–Thomson syndrome RET MEN2A, MEN2B SAMD9 Familial tumoral calcinosis SERPINA1 Alpha 1-antitrypsin Alpha-1 antitrypsin

    List of genes mutated in cutaneous conditions

    List_of_genes_mutated_in_cutaneous_conditions

  • List of human protein-coding genes 7
  • Q5TGI4 14266 SAMD7 HGNC:25394; Q7Z3H4 14267 SAMD8 HGNC:26320; Q96LT4 14268 SAMD9 HGNC:1348; Q5K651 14269 SAMD9L HGNC:1349; Q8IVG5 14270 SAMD10 HGNC:16129;

    List of human protein-coding genes 7

    List_of_human_protein-coding_genes_7

  • List of OMIM disorder codes
  • sclerosis-2; 191100; TSC2 Tumoral calcinosis, familial, normophosphatemic; 610455; SAMD9 Tumoral calcinosis, hyperphosphatemic; 211900; KL Tumoral calcinosis, hyperphosphatemic

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

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Online names & meanings

  • Theudas
  • Girl/Female

    Biblical

    Theudas

    Flowing with water.

  • Falconner
  • Boy/Male

    English

    Falconner

    Falconer; one who trains falcons.

  • Samara
  • Girl/Female

    Indian

    Samara

    Soft pleasant light, A narrator of Hadith

  • Raag
  • Boy/Male

    Hindu, Indian

    Raag

    Music; Tune; Voice

  • Durgaa
  • Girl/Female

    Indian

    Durgaa

    Goddess Parvati, Goddess Durga

  • NES-TAUTA-KHUT
  • Female

    Egyptian

    NES-TAUTA-KHUT

    , the wife of Prince Sheshonk.

  • Kapotakshi
  • Girl/Female

    Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi

    Kapotakshi

    Eyes Like a Pigeon's

  • Sabiq
  • Boy/Male

    Muslim

    Sabiq

    Antecedent. Preceding.

  • Likitha
  • Girl/Female

    Australian, Hindu, Indian, Kannada, Tamil, Telugu

    Likitha

    Writer; Writing; Goddess Sarswathi

  • Vatchala
  • Girl/Female

    Indian

    Vatchala

    Pure

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