Create issue ticket

4 Possible Causes for Mutation in the TARS2 Gene

  • Combined Oxidative Phosphorylation Defect Type 13

    […] in the LYRM4 gene ({613311}) on 6p25; COXPD20 ({615917}), caused by mutation in the VARS2 gene ({612802}) on 6p21; COXPD21 ({615918}), caused by mutation in the TARS2 gene[diseaseinfosearch.org] […] in the LYRM4 gene (613311) on 6p25; COXPD20 (615917), caused by mutation in the VARS2 gene (612802) on 6p21; COXPD21 (615918), caused by mutation in the TARS2 gene (612805[ncbi.nlm.nih.gov] ({612805}) on 1q21; COXPD22 ({616045}), caused by mutation in the ATP5A1 gene ({164360}) on 18q12; COXPD23 ({616198}), caused by mutation in the GTPBP3 ({608536}) gene on[diseaseinfosearch.org]

  • Combined Oxidative Phosphorylation Deficiency Type 24

    […] in the LYRM4 gene (613311) on 6p25; COXPD20 (615917), caused by mutation in the VARS2 gene (612802) on 6p21; COXPD21 (615918), caused by mutation in the TARS2 gene (612805[ncbi.nlm.nih.gov] […] in the LYRM4 gene ({613311}) on 6p25; COXPD20 ({615917}), caused by mutation in the VARS2 gene ({612802}) on 6p21; COXPD21 ({615918}), caused by mutation in the TARS2 gene[diseaseinfosearch.org] ) on 1q21; COXPD22 (616045), caused by mutation in the ATP5A1 gene (164360) on 18q12; COXPD23 (616198), caused by mutation in the GTPBP3 (608536) gene on 19p13; COXPD24 (616239[ncbi.nlm.nih.gov]

  • Combined Oxidative Phosphorylation Deficiency 22

    […] in the LYRM4 gene (613311) on 6p25; COXPD20 (615917), caused by mutation in the VARS2 gene (612802) on 6p21; COXPD21 (615918), caused by mutation in the TARS2 gene (612805[ncbi.nlm.nih.gov] ) on 1q21; COXPD22 (616045), caused by mutation in the ATP5A1 gene (164360) on 18q12; COXPD23 (616198), caused by mutation in the GTPBP3 (608536) gene on 19p13; COXPD24 (616239[ncbi.nlm.nih.gov] COXPD17 (615440), caused by mutation in the ELAC2 gene (605367) on 17p11; COXPD18 (615578), caused by mutation in the SFXN4 gene (615564) on 10q26; COXPD19 (615595), caused by mutation[ncbi.nlm.nih.gov]

  • Combined Oxidative Phosphorylation Deficiency 15

    […] in the LYRM4 gene ({613311}) on 6p25; COXPD20 ({615917}), caused by mutation in the VARS2 gene ({612802}) on 6p21; COXPD21 ({615918}), caused by mutation in the TARS2 gene[diseaseinfosearch.org] ({612805}) on 1q21; COXPD22 ({616045}), caused by mutation in the ATP5A1 gene ({164360}) on 18q12; COXPD23 ({616198}), caused by mutation in the GTPBP3 ({608536}) gene on[diseaseinfosearch.org] }), caused by mutation in the ELAC2 gene ({605367}) on 17p11; COXPD18 ({615578}), caused by mutation in the SFXN4 gene ({615564}) on 10q26; COXPD19 ({615595}), caused by mutation[diseaseinfosearch.org]

Further symptoms