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OPA3

  • OPA3

    • Protein-coding gene in the species Homo sapiens

    encoded by the OPA3 gene. Costeff syndrome, or 3-methylglutaconic aciduria type III, is a genetic disorder caused by mutations in the OPA3 gene. In addition

    OPA3

    OPA3

    OPA3

  • Costeff syndrome

    • Medical condition

    3-methylglutaconic aciduria type III, is a genetic disorder caused by mutations in the OPA3 gene. It is typically associated with the onset of visual deterioration (optic

    Costeff syndrome

    Costeff syndrome

    Costeff_syndrome

  • 3-Methylglutaconic aciduria

    • Medical condition

    [citation needed] Type III 258501 OPA3 19q13.2-q13.3 3-Methylglutaconic aciduria type III or Costeff syndrome Mutations in the OPA3 gene cause 3-methylglutaconic

    3-Methylglutaconic aciduria

    3-Methylglutaconic aciduria

    3-Methylglutaconic_aciduria

  • Behr syndrome

    • Medical condition

    described. Some reported cases have been found to carry mutations in the OPA1, OPA3 or C12ORF65 genes which are known causes of pure optic atrophy or optic atrophy

    Behr syndrome

    Behr syndrome

    Behr_syndrome

  • Wolfram syndrome

    • Human disease

    tested negative for mutation in the common optic neuropathy genes OPA1, OPA3 and LHON were selected for further genetic testing for WS. The primary genetic

    Wolfram syndrome

    Wolfram syndrome

    Wolfram_syndrome

  • List of human protein-coding genes 5

    • A0A2R8YFL7 11063 OOSP4B HGNC:53905; A0A2R8Y4Y8 11064 OPA1 HGNC:8140; O60313 11065 OPA3 HGNC:8142; Q9H6K4 11066 OPALIN HGNC:20707; Q96PE5 11067 OPCML HGNC:8143;

    List of human protein-coding genes 5

    List_of_human_protein-coding_genes_5

  • CLPB

    • Protein found in humans

    This protein is known to interact with: HAX1 PARL HTRA2 SMAC/DIABLO OPA1 OPA3 PHB2 MICU1 MICU2 SLC25A25 SLC25A13 TIMM8A TIMM8B TIMM13 TIMM21 TIMM22 TIMM23

    CLPB

    CLPB

    CLPB

  • List of OMIM disorder codes

    • aciduria type I; 250950; AUH 3-Methylglutaconic aciduria type III; 258501; OPA3 3-Methylglutaconic aciduria type V; 610198; DNAJC19 46XX true hermaphroditism;

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

  • Kjer's optic neuropathy

    • Medical condition

    chromosomal genes are described as causing optic atrophy: OPA2 (x-linked), OPA3 (dominant), OPA4 (dominant), OPA5 (dominant) and OPA6 (recessive) (see OMIM

    Kjer's optic neuropathy

    Kjer's_optic_neuropathy

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Online names & meanings

  • Kaneshka | கநேஷ்கா

    • Girl/Female

    Tamil

    Kaneshka | கநேஷ்கா

    Small

  • Ceallachan

    • Boy/Male

    Australian, Irish

    Ceallachan

    Strife

  • Alesia

    • Girl/Female

    Greek American

    Alesia

    Helper.

  • Moulton

    • Surname or Lastname

    English

    Moulton

    English : habitational name from any of the various places with this name, as for example in Cheshire, Lincolnshire, Norfolk, Northamptonshire, Suffolk, and North Yorkshire. For the most part these were named in Old English as ‘Mūla’s settlement’, from the Old English personal name or byname Mūla ‘mule’ + tūn ‘enclosure’, ‘settlement’, but in some cases they may have been originally farms where mules were reared or kept. In the case of the Norfolk place name the first element was probably a personal name Mōda, a short form of the various compound names with a first element mōd ‘spirit’, ‘mind’, ‘courage’.

  • Proby

    • Surname or Lastname

    English

    Proby

    English : unexplained.French : habitational name from a place so named in Jura.

  • Jareer

    • Boy/Male

    Arabic, Muslim

    Jareer

    Corpulent; A Distinguished Companion

  • Shubham

    • Boy/Male

    Hindu

    Shubham

    Auspicious

  • Saatvik

    • Boy/Male

    Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Tamil

    Saatvik

    Pious

  • Nuwaira

    • Girl/Female

    Indian

    Nuwaira

    Petals of flowers

  • Tivra

    • Girl/Female

    Hindu, Indian

    Tivra

    Intense; Strong; Strength

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