MYG1 - MYG1 exonuclease Gene

Also Known as MYG; Gamm1; MST024; MSTP024; C12orf10

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 60314

About MYG1

Cytogenetic location: 12q13.13 Genomic coordinates (GRCh38): 12:53,299,695-53,307,177 (from NCBI)

This gene has 10 transcripts (splice variants) and 204 orthologues. Broad expression in testis (RPKM 46.7), ovary (RPKM 22.5) and 25 other tissues.

Summary

Predicted to enable nuclease activity. Predicted to be involved in nucleic acid phosphodiester bond hydrolysis. Predicted to act upstream of or within locomotory exploration behavior. Located in mitochondrion and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

MYG1 Products (1)

mRNA Protein Name
NM_021640.4 NP_067653.4 MYG1 exonuclease precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Cellular Component GO Annotation Evidence References Source
located in mitochondrion IDA
IDA: Inferred from direct assay
19014353 GOA
located in nucleus IDA
IDA: Inferred from direct assay
19014353 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

MYG1 Protein Structure

UPF0160

UPF0160: Uncharacterised protein family (UPF0160) (46 - 366)

  • 0
  • 100
  • 200
  • 300
  • 376 a.a.
Protein Preferred Names Protein Names

MYG1 exonuclease

  • UPF0160 protein MYG1, mitochondrial

MYG1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
MYG1 Q9HB07 FAM9B Homo sapiens Q8IZU0 31515488
Intra
MYG1 Q9HB07 FAM9B Homo sapiens Q8IZU0 25416956
Intra
MYG1 Q9HB07 DCDC2 Homo sapiens Q9UHG0 32296183
Intra
MYG1 Q9HB07 DCDC2 Homo sapiens Q9UHG0 32296183
Intra
MYG1 Q9HB07 DCDC2 Homo sapiens Q9UHG0 32296183
Intra
MYG1 Q9HB07 PELO Homo sapiens Q9BRX2 32814053
Intra
MYG1 Q9HB07 PELO Homo sapiens Q9BRX2 32814053
Intra
MYG1 Q9HB07 PELO Homo sapiens Q9BRX2 32814053
Intra
MYG1 Q9HB07 AGTRAP Homo sapiens Q6RW13-2 32296183
Intra
MYG1 Q9HB07 AGTRAP Homo sapiens Q6RW13-2 32296183
Intra
MYG1 Q9HB07 CMTM5 Homo sapiens Q96DZ9-2 32296183
Intra
MYG1 Q9HB07 CMTM5 Homo sapiens Q96DZ9-2 32296183
Intra
MYG1 Q9HB07 AP1B1 Homo sapiens Q10567-3 32296183
Intra
MYG1 Q9HB07 AP1B1 Homo sapiens Q10567-3 32296183
Intra
MYG1 Q9HB07 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
MYG1 Q9HB07 SYNGR1 Homo sapiens O43759-2 32296183
Intra
MYG1 Q9HB07 SYNGR1 Homo sapiens O43759-2 32296183
Intra
MYG1 Q9HB07 SYNGR1 Homo sapiens O43759-2 32296183
Intra
MYG1 Q9HB07 DGAT2L6 Homo sapiens Q6ZPD8 32296183
Intra
MYG1 Q9HB07 DGAT2L6 Homo sapiens Q6ZPD8 32296183
Intra
MYG1 Q9HB07 DESI2 Homo sapiens Q9BSY9 32296183
Intra
MYG1 Q9HB07 DESI2 Homo sapiens Q9BSY9 32296183
Intra
MYG1 Q9HB07 REEP6 Homo sapiens Q96HR9-2 32296183
Intra
MYG1 Q9HB07 REEP6 Homo sapiens Q96HR9-2 32296183
Intra
MYG1 Q9HB07 RHBDD2 Homo sapiens Q6NTF9-3 32296183
Intra
MYG1 Q9HB07 RHBDD2 Homo sapiens Q6NTF9-3 32296183
Intra
MYG1 Q9HB07 TIMM17B Homo sapiens O60830 32296183
Intra
MYG1 Q9HB07 TIMM17B Homo sapiens O60830 32296183
Intra
MYG1 Q9HB07 CMTM5 Homo sapiens Q96DZ9 25416956
Intra
MYG1 Q9HB07 CMTM5 Homo sapiens Q96DZ9 25416956
Intra
MYG1 Q9HB07 CPLX2 Homo sapiens Q6PUV4 32296183
Intra
MYG1 Q9HB07 CPLX2 Homo sapiens Q6PUV4 32296183
Intra
MYG1 Q9HB07 YIF1A Homo sapiens O95070 32296183
Intra
MYG1 Q9HB07 YIF1A Homo sapiens O95070 32296183
Intra
MYG1 Q9HB07 METTL9 Homo sapiens Q9H1A3 32296183
Intra
MYG1 Q9HB07 METTL9 Homo sapiens Q9H1A3 32296183
Intra
MYG1 Q9HB07 SFT2D1 Homo sapiens Q8WV19 32296183
Intra
MYG1 Q9HB07 SFT2D1 Homo sapiens Q8WV19 32296183
Intra
MYG1 Q9HB07 MTNAP1 Homo sapiens Q9BSJ5 32814053
Intra
MYG1 Q9HB07 MTNAP1 Homo sapiens Q9BSJ5 32814053
Intra
MYG1 Q9HB07 MTNAP1 Homo sapiens Q9BSJ5 32814053
Intra
MYG1 Q9HB07 EEF1G Homo sapiens P26641 32814053
Intra
MYG1 Q9HB07 EEF1G Homo sapiens P26641 32814053
Intra
MYG1 Q9HB07 EEF1G Homo sapiens P26641 32814053
Intra
MYG1 Q9HB07 APOA5 Homo sapiens Q6Q788 32296183
Intra
MYG1 Q9HB07 APOA5 Homo sapiens Q6Q788 32296183
Intra
MYG1 Q9HB07 SLC17A9 Homo sapiens Q9BYT1 32296183
Intra
MYG1 Q9HB07 SLC17A9 Homo sapiens Q9BYT1 32296183
Intra
MYG1 Q9HB07 ARL6IP1 Homo sapiens Q15041 25416956
Intra
MYG1 Q9HB07 ARL6IP1 Homo sapiens Q15041 32296183
Intra
MYG1 Q9HB07 ARL6IP1 Homo sapiens Q15041 32296183
Intra
MYG1 Q9HB07 DCAF10 Homo sapiens Q5QP82 33961781
Intra
MYG1 Q9HB07 PLIN3 Homo sapiens O60664 32296183
Intra
MYG1 Q9HB07 PLIN3 Homo sapiens O60664 32296183
Intra
MYG1 Q9HB07 MAN1C1 Homo sapiens Q9NR34 32296183
Intra
MYG1 Q9HB07 MAN1C1 Homo sapiens Q9NR34 32296183
Intra
MYG1 Q9HB07 MAN1C1 Homo sapiens Q9NR34 32296183
Intra
MYG1 Q9HB07 AGTRAP Homo sapiens Q6RW13 25416956
Intra
MYG1 Q9HB07 AGTRAP Homo sapiens Q6RW13 25416956
Intra
MYG1 Q9HB07 AGTRAP Homo sapiens Q6RW13 25416956
Intra
MYG1 Q9HB07 RBM11 Homo sapiens P57052 32814053
Intra
MYG1 Q9HB07 RBM11 Homo sapiens P57052 32814053
Intra
MYG1 Q9HB07 RBM11 Homo sapiens P57052 32814053
Intra
MYG1 Q9HB07 DDIT4L Homo sapiens Q96D03 32296183
Intra
MYG1 Q9HB07 DDIT4L Homo sapiens Q96D03 32296183
Intra
MYG1 Q9HB07 SPG21 Homo sapiens Q9NZD8 32296183
Intra
MYG1 Q9HB07 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
MYG1 Q9HB07 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
MYG1 Q9HB07 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
MYG1 Q9HB07 BSND Homo sapiens Q8WZ55 32296183
Intra
MYG1 Q9HB07 BSND Homo sapiens Q8WZ55 32296183
Intra
MYG1 Q9HB07 SYP Homo sapiens P08247 32296183
Intra
MYG1 Q9HB07 SYP Homo sapiens P08247 32296183
Intra
MYG1 Q9HB07 ROM1 Homo sapiens Q03395 32296183
Intra
MYG1 Q9HB07 ROM1 Homo sapiens Q03395 32296183
Intra
MYG1 Q9HB07 MAL2 Homo sapiens Q969L2 32296183
Intra
MYG1 Q9HB07 MAL2 Homo sapiens Q969L2 32296183
Intra
MYG1 Q9HB07 TMEM239 Homo sapiens Q8WW34 25416956
Intra
MYG1 Q9HB07 TMEM239 Homo sapiens Q8WW34 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Nemaline Myopathy 4
  • Cap Myopathy 2

  • NEM4

  • Nemaline Myopathy 4, Autosomal Dominant

  • Nemaline Myopathy, Type 4

  • CAPM2

  • Cap Disease

  • Cap Myopathy Tpm2-Related

  • Tpm2-Related Nemaline Myopathy

  • Tpm2-Related Cap Myopathy

  • Myopathy, Nemaline, Type 4

  • Cap Myopathy

Dracunculiasis
  • Guinea Worm Disease

  • Dracontiasis

  • Dracunculosis

  • Infection By Dracunculus Medinensis

  • Gwd

  • Guinea Worm Infection

  • Parasitic Infection Caused By Dracunculus Medinensis

  • Medina Worm Disease

  • Medinensis

  • Medina Worm Infestation

  • Dracunculus Medinensis Infestation

  • Guinea Worm Infestation

Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1
  • Vitiligo

  • VAMAS1

  • Slev1

  • Vtlg

  • Systemic Lupus Erythematosus, Vitiligo-Related

  • Vitiligo-Associated Multiple Autoimmune Disease 1

  • Systemic Lupus Erythematosus Vitiligo-Related

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris MYG1 VGNC VGNC:49228
Mus musculus MYG1 MGD MGI:1929864
Macaca mulatta MYG1 VGNC VGNC:70338
Bos taurus MYG1 VGNC VGNC:49159
Rattus norvegicus MYG1 RGD RGD:1359237
Others MYG1 NCBI