OMIM: 208900Inheritance: Autosomal recessive
Classification: Diseases of the nervous system
Related informations: Orphanet   
Gene Tests   
Clinical Synopsis   
Clinical TrialsGene/Locus: |    ATM |
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Dna Change: |    c.103C>T |
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Protein Change: |    p.Arg35X |
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Mutation Type: |    |
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Mutation Effect: |    |
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Location: |    exon 3 |
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Transcript: |    NM_000051.3 |
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Population | Ethnic Group | Region | Mutation Frquency | Coalescence Time | Reference |
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Morocco | Jews | 12 widely separated locations in Morocco | 32/33 risk alleles in Jewish families of North African origin (Morocco and Tunisia)) | NA | Gilad S et al., 1996Gilad S, Bar-Shira A, Harnik R, Shkedy D, Ziv Y, Khosravi R, Brown K, Vanagaite L, Xu G, Frydman M, Lavin MF, Hill D, Tagle DA, Shiloh Y, . Ataxia-telangiectasia: founder effect among north African Jews.. Hum. Mol. Genet.. 1996; 5(12):2033-7 |
Tunisia | Jews | cities of Nabil and Tunis | 32/33 risk alleles in Jewish families of North African origin (Morocco and Tunisia)) | NA | Gilad S et al., 1996Gilad S, Bar-Shira A, Harnik R, Shkedy D, Ziv Y, Khosravi R, Brown K, Vanagaite L, Xu G, Frydman M, Lavin MF, Hill D, Tagle DA, Shiloh Y, . Ataxia-telangiectasia: founder effect among north African Jews.. Hum. Mol. Genet.. 1996; 5(12):2033-7 |
Gene/Locus: |    ATM |
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Dna Change: |    c.1339C>T |
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Protein Change: |    p.Arg447x |
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Mutation Type: |    Substitution |
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Mutation Effect: |    Missense |
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Location: |    exon 10 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.[6672_6673delGG;6677_6680delTACG] |
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Protein Change: |    p.Met2224_Arg2227del4insIleSer |
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Mutation Type: |    Deletion |
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Mutation Effect: |    Frameshift |
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Location: |    exon 48 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.717_720delCCTC |
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Protein Change: |    p.Phe239LeufsX15 |
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Mutation Type: |    Deletion |
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Mutation Effect: |    Frameshift |
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Location: |    exon 7 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.1607+1G>T |
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Protein Change: |    |
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Mutation Type: |    Substitution |
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Mutation Effect: |    Splice site |
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Location: |    intron 10 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.2250G>A |
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Protein Change: |    |
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Mutation Type: |    Substitution |
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Mutation Effect: |    |
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Location: |    exon 14 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.2502_2503insA |
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Protein Change: |    p.Val835SerfsX7 |
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Mutation Type: |    Insertion |
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Mutation Effect: |    Frameshift |
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Location: |    exon 17 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.2720_2723del |
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Protein Change: |    |
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Mutation Type: |    Deletion |
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Mutation Effect: |    Frameshift |
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Location: |    exon 18 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.3576G>A |
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Protein Change: |    |
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Mutation Type: |    Substitution |
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Mutation Effect: |    |
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Location: |    exon 24 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.3802delG |
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Protein Change: |    p.Val1268X |
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Mutation Type: |    Deletion |
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Mutation Effect: |    Nonsense |
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Location: |    exon 26 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.3894_3895insT |
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Protein Change: |    p.Ala1299CysfsX3 |
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Mutation Type: |    Insertion |
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Mutation Effect: |    Frameshift |
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Location: |    exon 26 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.4396C>T |
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Protein Change: |    p.Arg1466X |
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Mutation Type: |    Substitution |
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Mutation Effect: |    Missense |
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Location: |    exon 29 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.5979_5983delTAAAG |
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Protein Change: |    p.Ser1993ArgfsX23 |
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Mutation Type: |    Deletion |
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Mutation Effect: |    Frameshift |
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Location: |    exon 40 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.7408T>G |
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Protein Change: |    p.Tyr2470Asp |
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Mutation Type: |    Substitution |
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Mutation Effect: |    Missense |
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Location: |    exon 50 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.7517_7520delGAGA |
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Protein Change: |    p.Arg2506ThrfsX3 |
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Mutation Type: |    Deletion |
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Mutation Effect: |    Frameshift |
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Location: |    exon 51 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.8283_8284delTC |
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Protein Change: |    p.Gln2762AlafsX6 |
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Mutation Type: |    Deletion |
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Mutation Effect: |    Frameshift |
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Location: |    exon 57 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.8977C>T |
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Protein Change: |    p.Arg2993X |
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Mutation Type: |    Substitution |
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Mutation Effect: |    Nonsense |
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Location: |    exon 62 |
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Transcript: |    NM_000051.3 |
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Gene/Locus: |    ATM |
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Dna Change: |    c.9139C>T |
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Protein Change: |    p.Arg3047X |
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Mutation Type: |    Substitution |
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Mutation Effect: |    Nonsense |
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Location: |    exon 63 |
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Transcript: |    NM_000051.3 |
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References
Chessa L, Piane M, Magliozzi M, Torrente I, Savio C, Lulli P, De Luca A, Dallapiccola B, Founder effects for ATM gene mutations in Italian Ataxia Telangiectasia families.Ann. Hum. Genet.. 2009; 73(0):532-9
Fares F, Axelord Ran S, David M, Zelnik N, Hecht Y, Khairaldeen H, Lerner A, Identification of two mutations for ataxia telangiectasia among the Druze community.Prenat. Diagn.. 2004; 24(5):358-62
Gilad S, Bar-Shira A, Harnik R, Shkedy D, Ziv Y, Khosravi R, Brown K, Vanagaite L, Xu G, Frydman M, Lavin MF, Hill D, Tagle DA, Shiloh Y, Ataxia-telangiectasia: founder effect among north African Jews.Hum. Mol. Genet.. 1996; 5(12):2033-7