Input HGNC Approved Gene Symbols, Refseq Gene Symbols, Entrez Gene IDs, Ensembl Gene IDs, Refseq Accession, OMIM, UniProt, CCDS, VEGA, or UCSC IDs
POLG, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-RNR1, MT-RNR2, MT-TA, MT-TC, MT-TD, MT-TE, MT-TF, MT-TG, MT-TH, MT-TI, MT-TK, MT-TL1, MT-TL2, MT-TM, MT-TN, MT-TP, MT-TQ, MT-TR, MT-TS1, MT-TS2, MT-TT, MT-TV, MT-TW, MT-TY
File name prefix:   

*Note: Input can be a mixture of IDs from different sources. This tool maps them to HGNC genes by searching against each of these sources: HGNC Approved Gene Symbols and IDs, Refseq Gene Symbols, Entrez Gene IDs, Ensembl Gene IDs, Refseq Accession, OMIM, UniProt, CCDS, VEGA, or UCSC IDs (HGNC version 2017-08-10).

*Note: HGNC Approved Gene Symbols and Ensembl Gene IDs are the only fully supported input due to complexity in mapping of different gene ID systems. It is recommended that the users first map own input to them using this tool iteratively, or 3rd party tool.

Please save the BED (GRCh37, p13) file for the genes at Samplename6.bed , full data at Samplename6.tab.txt

BED file preview:
M 576 647 MT-TF;ENSG00000210049 M 647 1601 MT-RNR1;ENSG00000211459 M 1601 1670 MT-TV;ENSG00000210077 M 1670 3229 MT-RNR2;ENSG00000210082 M 3229 3304 MT-TL1;ENSG00000209082 M 3306 4262 MT-ND1;ENSG00000198888 M 4262 4331 MT-TI;ENSG00000210100 M 4328 4400 MT-TQ;ENSG00000210107 M 4401 4469 MT-TM;ENSG00000210112 M 4469 5511 MT-ND2;ENSG00000198763 M 5511 5579 MT-TW;ENSG00000210117 M 5586 5655 MT-TA;ENSG00000210127 M 5656 5729 MT-TN;ENSG00000210135 M 5760 5826 MT-TC;ENSG00000210140 M 5825 5891 MT-TY;ENSG00000210144 M 5903 7445 MT-CO1;ENSG00000198804 M 7445 7514 MT-TS1;ENSG00000210151 M 7517 7585 MT-TD;ENSG00000210154 M 7585 8269 MT-CO2;ENSG00000198712 M 8294 8364 MT-TK;ENSG00000210156 M 8365 8572 MT-ATP8;ENSG00000228253 M 8526 9207 MT-ATP6;ENSG00000198899 M 9206 9990 MT-CO3;ENSG00000198938 M 9990 10058 MT-TG;ENSG00000210164 M 10058 10404 MT-ND3;ENSG00000198840 M 10404 10469 MT-TR;ENSG00000210174 M 10469 10766 MT-ND4L;ENSG00000212907 M 10759 12137 MT-ND4;ENSG00000198886 M 12137 12206 MT-TH;ENSG00000210176 M 12206 12265 MT-TS2;ENSG00000210184 M 12265 12336 MT-TL2;ENSG00000210191 M 12336 14148 MT-ND5;ENSG00000198786 M 14148 14673 MT-ND6;ENSG00000198695 M 14673 14742 MT-TE;ENSG00000210194 M 14746 15887 MT-CYB;ENSG00000198727 M 15887 15953 MT-TT;ENSG00000210195 M 15955 16023 MT-TP;ENSG00000210196 15 89859533 89878092 POLG;ENSG00000140521

Your input genes (38):
POLG, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-RNR1, MT-RNR2, MT-TA, MT-TC, MT-TD, MT-TE, MT-TF, MT-TG, MT-TH, MT-TI, MT-TK, MT-TL1, MT-TL2, MT-TM, MT-TN, MT-TP, MT-TQ, MT-TR, MT-TS1, MT-TS2, MT-TT, MT-TV, MT-TW, MT-TY

Genes matched to HGNC approved symbols (38):
MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-RNR1, MT-RNR2, MT-TA, MT-TC, MT-TD, MT-TE, MT-TF, MT-TG, MT-TH, MT-TI, MT-TK, MT-TL1, MT-TL2, MT-TM, MT-TN, MT-TP, MT-TQ, MT-TR, MT-TS1, MT-TS2, MT-TT, MT-TV, MT-TW, MT-TY, POLG
Genes without position information from Ensembl GRCh37_p13 or UCSC RefGene (hg19):

Input entries not matched in HGNC yet: .
Further COMPARE with your original gene list to find any not matched.

Per gene details

1. MT-TF Exome E ENSG00000210049 G GTR H N Variants: 18(18) , HGMD: , ClinVar: 7 Gene region M:577..647 HGNC Gene: MT-TF, mitochondrially encoded tRNA phenylalanine; Alias_symbol: trnF; Previous_Symbols: MTTF; ensembl_gene_id; ENSG00000210049; Refseq accession: ; OMIM ID: 590070; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: MELAS SYNDROME, MERRF	2. MT-RNR1 Exome E ENSG00000211459 G GTR H N Variants: 108(108) , HGMD: , ClinVar: 49 Gene region M:648..1601 HGNC Gene: MT-RNR1, mitochondrially encoded 12S RNA; Alias_symbol: 12S; Previous_Symbols: MTRNR1; ensembl_gene_id; ENSG00000211459; Refseq accession: ; OMIM ID: 561000; CCDS_ids: ; VEGA_ids: ; uniprot_ids: A0A0C5B5G6 Mitochondrial Disease: 500008, 580000	3. MT-TV Exome E ENSG00000210077 G GTR H N Variants: 12(12) , HGMD: , ClinVar: 5 Gene region M:1602..1670 HGNC Gene: MT-TV, mitochondrially encoded tRNA valine; Alias_symbol: trnV; Previous_Symbols: MTTV; ensembl_gene_id; ENSG00000210077; Refseq accession: ; OMIM ID: 590105; CCDS_ids: ; VEGA_ids: ; uniprot_ids:
4. MT-RNR2 Exome E ENSG00000210082 G GTR H N Variants: 104(104) , HGMD: , ClinVar: 6 Gene region M:1671..3229 HGNC Gene: MT-RNR2, mitochondrially encoded 16S RNA; Alias_symbol: HN|16S; Previous_Symbols: MTRNR2; ensembl_gene_id; ENSG00000210082; Refseq accession: NC_012920; OMIM ID: 561010; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Q8IVG9 Mitochondrial Disease: 515000	5. MT-TL1 Exome E ENSG00000209082 G GTR H N Variants: 34(34) , HGMD: , ClinVar: 14 Gene region M:3230..3304 HGNC Gene: MT-TL1, mitochondrially encoded tRNA leucine 1 (UUA/G); Alias_symbol: TRNL1; Previous_Symbols: MTTL1; ensembl_gene_id; ENSG00000209082; Refseq accession: ; OMIM ID: 590050; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: 220110, CVS, KSS, MELAS SYNDROME, MERRF, MIDD	6. MT-ND1 Exome E ENSG00000198888 G GTR H N Variants: 87(87) , HGMD: , ClinVar: 41 Gene region M:3307..4262 HGNC Gene: MT-ND1, mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1; Alias_symbol: ND1|NAD1; Previous_Symbols: MTND1; ensembl_gene_id; ENSG00000198888; Refseq accession: YP_003024026; OMIM ID: 516000; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P03886 Mitochondrial Disease: 252010, 500008, LDYT, LHON, MELAS SYNDROME
7. MT-TI Exome E ENSG00000210100 G GTR H N Variants: 22(22) , HGMD: , ClinVar: 12 Gene region M:4263..4331 HGNC Gene: MT-TI, mitochondrially encoded tRNA isoleucine; Alias_symbol: trnI; Previous_Symbols: MTTI; ensembl_gene_id; ENSG00000210100; Refseq accession: ; OMIM ID: 590045; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: 500005, 500008	8. MT-TQ Exome E ENSG00000210107 G GTR H N Variants: 16(16) , HGMD: , ClinVar: 5 Gene region M:4329..4400 HGNC Gene: MT-TQ, mitochondrially encoded tRNA glutamine; Alias_symbol: trnQ; Previous_Symbols: MTTQ; ensembl_gene_id; ENSG00000210107; Refseq accession: ; OMIM ID: 590030; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: MELAS SYNDROME	9. MT-TM Exome E ENSG00000210112 G GTR H N Variants: 8(8) , HGMD: , ClinVar: 1 Gene region M:4402..4469 HGNC Gene: MT-TM, mitochondrially encoded tRNA methionine; Alias_symbol: trnM; Previous_Symbols: MTTM; ensembl_gene_id; ENSG00000210112; Refseq accession: ; OMIM ID: 590065; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: CPEO,CPEO Plus
10. MT-ND2 Exome E ENSG00000198763 G GTR H N Variants: 49(49) , HGMD: , ClinVar: 16 Gene region M:4470..5511 HGNC Gene: MT-ND2, mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2; Alias_symbol: ND2|NAD2; Previous_Symbols: MTND2; ensembl_gene_id; ENSG00000198763; Refseq accession: YP_003024027; OMIM ID: 516001; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P03891 Mitochondrial Disease: 252010, LHON	11. MT-TW Exome E ENSG00000210117 G GTR H N Variants: 16(16) , HGMD: , ClinVar: 9 Gene region M:5512..5579 HGNC Gene: MT-TW, mitochondrially encoded tRNA tryptophan; Alias_symbol: trnW; Previous_Symbols: MTTW; ensembl_gene_id; ENSG00000210117; Refseq accession: ; OMIM ID: 590095; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: CPEO,CPEO Plus	12. MT-TA Exome E ENSG00000210127 G GTR H N Variants: 6(6) , HGMD: , ClinVar: 4 Gene region M:5587..5655 HGNC Gene: MT-TA, mitochondrially encoded tRNA alanine; Alias_symbol: trnA; Previous_Symbols: MTTA; ensembl_gene_id; ENSG00000210127; Refseq accession: ; OMIM ID: 590000; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: CPEO,CPEO Plus
13. MT-TN Exome E ENSG00000210135 G GTR H N Variants: 7(7) , HGMD: , ClinVar: 3 Gene region M:5657..5729 HGNC Gene: MT-TN, mitochondrially encoded tRNA asparagine; Alias_symbol: trnN; Previous_Symbols: MTTN; ensembl_gene_id; ENSG00000210135; Refseq accession: ; OMIM ID: 590010; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: 220110, 252010	14. MT-TC Exome E ENSG00000210140 G GTR H N Variants: 10(10) , HGMD: , ClinVar: 2 Gene region M:5761..5826 HGNC Gene: MT-TC, mitochondrially encoded tRNA cysteine; Alias_symbol: trnC; Previous_Symbols: MTTC; ensembl_gene_id; ENSG00000210140; Refseq accession: ; OMIM ID: 590020; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: MELAS SYNDROME	15. MT-TY Exome E ENSG00000210144 G GTR H N Variants: 5(5) , HGMD: , ClinVar: 4 Gene region M:5826..5891 HGNC Gene: MT-TY, mitochondrially encoded tRNA tyrosine; Alias_symbol: trnY; Previous_Symbols: MTTY; ensembl_gene_id; ENSG00000210144; Refseq accession: ; OMIM ID: 590100; CCDS_ids: ; VEGA_ids: ; uniprot_ids:
16. MT-CO1 Exome E ENSG00000198804 G GTR H N Variants: 82(82) , HGMD: , ClinVar: 22 Gene region M:5904..7445 HGNC Gene: MT-CO1, mitochondrially encoded cytochrome c oxidase I; Alias_symbol: COX1|COI; Previous_Symbols: MTCO1; ensembl_gene_id; ENSG00000198804; Refseq accession: YP_003024028; OMIM ID: 516030; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P00395 Mitochondrial Disease: 220110, 550500, 580000	17. MT-TS1 Exome E ENSG00000210151 G GTR H N Variants: 23(23) , HGMD: , ClinVar: 17 Gene region M:7446..7514 HGNC Gene: MT-TS1, mitochondrially encoded tRNA serine 1 (UCN); Alias_symbol: TRNS1; Previous_Symbols: MTTS1; ensembl_gene_id; ENSG00000210151; Refseq accession: ; OMIM ID: 590080; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: 500008, MELAS SYNDROME, MERRF	18. MT-TD Exome E ENSG00000210154 G GTR H N Variants: 8(8) , HGMD: , ClinVar: 1 Gene region M:7518..7585 HGNC Gene: MT-TD, mitochondrially encoded tRNA aspartic acid; Alias_symbol: trnD; Previous_Symbols: MTTD; ensembl_gene_id; ENSG00000210154; Refseq accession: ; OMIM ID: 590015; CCDS_ids: ; VEGA_ids: ; uniprot_ids:
19. MT-CO2 Exome E ENSG00000198712 G GTR H N Variants: 36(36) , HGMD: , ClinVar: 13 Gene region M:7586..8269 HGNC Gene: MT-CO2, mitochondrially encoded cytochrome c oxidase II; Alias_symbol: COX2|CO2; Previous_Symbols: MTCO2; ensembl_gene_id; ENSG00000198712; Refseq accession: YP_003024029; OMIM ID: 516040; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P00403 Mitochondrial Disease: 220110	20. MT-TK Exome E ENSG00000210156 G GTR H N Variants: 23(23) , HGMD: , ClinVar: 7 Gene region M:8295..8364 HGNC Gene: MT-TK, mitochondrially encoded tRNA lysine; Alias_symbol: trnK; Previous_Symbols: MERRF|MTTK; ensembl_gene_id; ENSG00000210156; Refseq accession: ; OMIM ID: 590060; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: 556500, MELAS SYNDROME, MERRF, MIDD, MTDPS1	21. MT-ATP8 Exome E ENSG00000228253 G GTR H N Variants: 12(12) , HGMD: , ClinVar: 5 Gene region M:8366..8572 HGNC Gene: MT-ATP8, mitochondrially encoded ATP synthase 8; Alias_symbol: ATP8|A6L; Previous_Symbols: MTATP8; ensembl_gene_id; ENSG00000228253; Refseq accession: YP_003024030; OMIM ID: 516070; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P03928 Mitochondrial Disease: 500006
22. MT-ATP6 Exome E ENSG00000198899 G GTR H N Variants: 66(66) , HGMD: , ClinVar: 29 Gene region M:8527..9207 HGNC Gene: MT-ATP6, mitochondrially encoded ATP synthase 6; Alias_symbol: ATP6|ATPase-6|Su6m; Previous_Symbols: MTATP6|RP; ensembl_gene_id; ENSG00000198899; Refseq accession: YP_003024031; OMIM ID: 516060; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P00846 Mitochondrial Disease: 500003, 500006, 500010, 500015, LHON, MLASA3, MTATP6, NARP SYNDROME	23. MT-CO3 Exome E ENSG00000198938 G GTR H N Variants: 54(54) , HGMD: , ClinVar: 17 Gene region M:9207..9990 HGNC Gene: MT-CO3, mitochondrially encoded cytochrome c oxidase III; Alias_symbol: COX3|COIII|CO3; Previous_Symbols: MTCO3; ensembl_gene_id; ENSG00000198938; Refseq accession: YP_003024032; OMIM ID: 516050; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P00414 Mitochondrial Disease: 220110, LHON	24. MT-TG Exome E ENSG00000210164 G GTR H N Variants: 10(10) , HGMD: , ClinVar: 4 Gene region M:9991..10058 HGNC Gene: MT-TG, mitochondrially encoded tRNA glycine; Alias_symbol: trnG; Previous_Symbols: MTTG; ensembl_gene_id; ENSG00000210164; Refseq accession: ; OMIM ID: 590035; CCDS_ids: ; VEGA_ids: ; uniprot_ids:
25. MT-ND3 Exome E ENSG00000198840 G GTR H N Variants: 24(24) , HGMD: , ClinVar: 10 Gene region M:10059..10404 HGNC Gene: MT-ND3, mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3; Alias_symbol: ND3|NAD3; Previous_Symbols: MTND3; ensembl_gene_id; ENSG00000198840; Refseq accession: YP_003024033; OMIM ID: 516002; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P03897 Mitochondrial Disease: 252010, 500014, LDYT	26. MT-TR Exome E ENSG00000210174 G GTR H N Variants: 7(7) , HGMD: , ClinVar: 2 Gene region M:10405..10469 HGNC Gene: MT-TR, mitochondrially encoded tRNA arginine; Alias_symbol: trnR; Previous_Symbols: MTTR; ensembl_gene_id; ENSG00000210174; Refseq accession: ; OMIM ID: 590005; CCDS_ids: ; VEGA_ids: ; uniprot_ids:	27. MT-ND4L Exome E ENSG00000212907 G GTR H N Variants: 22(22) , HGMD: , ClinVar: 4 Gene region M:10470..10766 HGNC Gene: MT-ND4L, mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L; Alias_symbol: ND4L|NAD4L; Previous_Symbols: MTND4L; ensembl_gene_id; ENSG00000212907; Refseq accession: YP_003024034; OMIM ID: 516004; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P03901
28. MT-ND4 Exome E ENSG00000198886 G GTR H N Variants: 73(73) , HGMD: , ClinVar: 16 Gene region M:10760..12137 HGNC Gene: MT-ND4, mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4; Alias_symbol: ND4|NAD4; Previous_Symbols: MTND4|LHON; ensembl_gene_id; ENSG00000198886; Refseq accession: YP_003024035; OMIM ID: 516003; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P03905 Mitochondrial Disease: 252010, LDYT, LHON, MELAS SYNDROME	29. MT-TH Exome E ENSG00000210176 G GTR H N Variants: 9(9) , HGMD: , ClinVar: 6 Gene region M:12138..12206 HGNC Gene: MT-TH, mitochondrially encoded tRNA histidine; Alias_symbol: trnH; Previous_Symbols: MTTH; ensembl_gene_id; ENSG00000210176; Refseq accession: ; OMIM ID: 590040; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: 500008, MELAS SYNDROME, MERRF	30. MT-TS2 Exome E ENSG00000210184 G GTR H N Variants: 11(11) , HGMD: , ClinVar: 3 Gene region M:12207..12265 HGNC Gene: MT-TS2, mitochondrially encoded tRNA serine 2 (AGU/C); Alias_symbol: TRNS2|RP8; Previous_Symbols: MTTS2; ensembl_gene_id; ENSG00000210184; Refseq accession: ; OMIM ID: 590085; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: 500004, MELAS SYNDROME, MERRF
31. MT-TL2 Exome E ENSG00000210191 G GTR H N Variants: 14(14) , HGMD: , ClinVar: 5 Gene region M:12266..12336 HGNC Gene: MT-TL2, mitochondrially encoded tRNA leucine 2 (CUN); Alias_symbol: TRNL2; Previous_Symbols: MTTL2; ensembl_gene_id; ENSG00000210191; Refseq accession: ; OMIM ID: 590055; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: CPEO,CPEO Plus	32. MT-ND5 Exome E ENSG00000198786 G GTR H N Variants: 135(135) , HGMD: , ClinVar: 28 Gene region M:12337..14148 HGNC Gene: MT-ND5, mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5; Alias_symbol: ND5|NAD5; Previous_Symbols: MTND5; ensembl_gene_id; ENSG00000198786; Refseq accession: YP_003024036; OMIM ID: 516005; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P03915 Mitochondrial Disease: LHON, MELAS SYNDROME, MERRF	33. MT-ND6 Exome E ENSG00000198695 G GTR H N Variants: 43(43) , HGMD: , ClinVar: 21 Gene region M:14149..14673 HGNC Gene: MT-ND6, mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6; Alias_symbol: NAD6|ND6; Previous_Symbols: MTND6; ensembl_gene_id; ENSG00000198695; Refseq accession: YP_003024037; OMIM ID: 516006; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P03923 Mitochondrial Disease: 553000, LDYT, LHON, MELAS SYNDROME
34. MT-TE Exome E ENSG00000210194 G GTR H N Variants: 12(12) , HGMD: , ClinVar: 6 Gene region M:14674..14742 HGNC Gene: MT-TE, mitochondrially encoded tRNA glutamic acid; Alias_symbol: trnE; Previous_Symbols: MTTE; ensembl_gene_id; ENSG00000210194; Refseq accession: ; OMIM ID: 590025; CCDS_ids: ; VEGA_ids: ; uniprot_ids: Mitochondrial Disease: 500002, MIDD, MMIT	35. MT-CYB Exome E ENSG00000198727 G GTR H N Variants: 90(90) , HGMD: , ClinVar: 84 Gene region M:14747..15887 HGNC Gene: MT-CYB, mitochondrially encoded cytochrome b; Alias_symbol: COB|CYTB|UQCR3; Previous_Symbols: MTCYB; ensembl_gene_id; ENSG00000198727; Refseq accession: YP_003024038; OMIM ID: 516020; CCDS_ids: ; VEGA_ids: ; uniprot_ids: P00156 Mitochondrial Disease: 500000, 601665, LHON, MTCYB	36. MT-TT Exome E ENSG00000210195 G GTR H N Variants: 21(21) , HGMD: , ClinVar: 6 Gene region M:15888..15953 HGNC Gene: MT-TT, mitochondrially encoded tRNA threonine; Alias_symbol: trnT; Previous_Symbols: MTTT|LIMM; ensembl_gene_id; ENSG00000210195; Refseq accession: ; OMIM ID: 590090; CCDS_ids: ; VEGA_ids: ; uniprot_ids:
37. MT-TP Exome E ENSG00000210196 G GTR H N Variants: 9(9) , HGMD: , ClinVar: 3 Gene region M:15956..16023 HGNC Gene: MT-TP, mitochondrially encoded tRNA proline; Alias_symbol: trnP; Previous_Symbols: MTTP; ensembl_gene_id; ENSG00000210196; Refseq accession: ; OMIM ID: 590075; CCDS_ids: ; VEGA_ids: ; uniprot_ids:	38. POLG Exome E ENSG00000140521 G GTR H N Variants: 772(651) , HGMD: 277, ClinVar: 464 Gene region 15:89859534..89878092 HGNC Gene: POLG, DNA polymerase gamma, catalytic subunit; Alias_symbol: POLG1|POLGA; Previous_Symbols: ; ensembl_gene_id; ENSG00000140521; Refseq accession: NM_002693; OMIM ID: 174763; CCDS_ids: CCDS10350; VEGA_ids: OTTHUMG00000149646; uniprot_ids: P54098 Mitochondrial Disease: 258450, MTDPS1, MTDPS4A, MTDPS4B, PEOA1, SANDO 157640; MeSH: C1834846; Progressive external ophthalmoplegia, autosomal dominant, 157640; PEOA1 203700; MeSH: C0205710; Mitochondrial DNA depletion syndrome 4A (Alpers type), 203700; MTDPS4A 258450; MeSH: C1850303; Progressive external ophthalmoplegia, autosomal recessive, 258450 607459; MeSH: C1843851; Mitochondrial recessive ataxia syndrome (includes SANDO and SCAE), 607459; SANDO 613662; MeSH: C3150914; Mitochondrial DNA depletion syndrome 4B (MNGIE type), 613662; MTDPS4B

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