Skip to content
Use your HSA or FSA funds

Gene

MSTO1

misato mitochondrial distribution and morphology regulator 1

Summary

Cytogenetic location
1q22
Coordinates
Chromosome 1: 155,610,218–155,614,951 (GRCh38)
Exons
14 exons across 4.7 kb
Protein
570 amino acids
Also known as
FLJ10504, LST005, MST, misato
MANE Select transcript
ENST00000245564.8NM_018116.4
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads MSTO1 yet. The test sequences your whole genome, so your data includes it all the same.

How MSTO1 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 1, with a bracket where MSTO1 sits. MSTO1 and 33 genes near it on chromosome 1, from 155,112,585 to 156,112,584.Chromosome 11q22p36.33p36.32p36.31p36.23p36.22p36.21p36.13p36.12p36.11p35.3p35.2p35.1p34.3p34.2p34.1p33p32.3p32.2p32.1p31.3p31.2p31.1p22.3p22.2p22.1p21.3p21.2p21.1p13.3p13.2p13.1p12p11.2p11.1q11q12q21.1q21.2q21.3q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.3q31.1q31.2q31.3q32.1q32.2q32.3q41q42.11q42.12q42.13q42.2q42.3q43q44155.2 Mb155.4 Mb155.6 Mb155.8 Mb156 MbEFNA1: 155,127,452–155,134,899, forward strandEFNA1SLC50A1: 155,135,344–155,138,857, forward strandDPM3: 155,138,457–155,140,595, reverse strandDPM3KRTCAP2: 155,169,182–155,173,475, reverse strand: 155,169,409–155,187,272, reverse strandTRIM46: 155,173,787–155,184,971, forward strandTRIM46MUC1: 155,185,824–155,192,916, reverse strandMUC1THBS3: 155,195,584–155,209,203, reverse strandTHBS3MTX1: 155,208,695–155,213,824, forward strandMTX1GBA1: 155,231,270–155,245,178, reverse strandGBA1ENTREP3: 155,247,205–155,255,824, reverse strandSCAMP3: 155,255,979–155,262,433, reverse strandSCAMP3CLK2: 155,262,747–155,278,491, reverse strandCLK2HCN3: 155,277,328–155,289,848, forward strandHCN3PKLR: 155,289,265–155,301,443, reverse strandPKLRFDPS: 155,304,786–155,320,666, forward strandFDPSRUSC1: 155,320,739–155,331,422, forward strandRUSC1ASH1L: 155,335,268–155,563,162, reverse strandASH1LMSTO1: 155,610,218–155,614,951, forward strandMSTO1: 155,626,755–155,648,640, reverse strandYY1AP1: 155,659,446–155,689,334, reverse strandYY1AP1DAP3: 155,687,833–155,740,132, forward strandDAP3GON4L: 155,749,659–155,859,439, reverse strandGON4LSYT11: 155,859,449–155,885,199, forward strandSYT11RIT1: 155,897,808–155,911,408, reverse strandRIT1KHDC4: 155,913,043–155,934,416, reverse strandKHDC4RXFP4: 155,941,638–155,943,087, forward strandRXFP4ARHGEF2: 155,944,685–156,007,070, reverse strandARHGEF2SSR2: 156,009,041–156,020,972, reverse strandSSR2UBQLN4: 156,026,961–156,053,814, reverse strandUBQLN4LAMTOR2: 156,053,916–156,058,817, forward strandLAMTOR2RAB25: 156,061,147–156,070,514, forward strandRAB25MEX3A: 156,072,013–156,082,465, reverse strandMEX3ALMNA: 156,082,572–156,140,085, forward strandLMNADiagram of MSTO1: 14 exons on the forward strand of chromosome 1Exon 2: 1 known disease-causing siteExon 3: 1 known disease-causing siteExon 7: 3 known disease-causing sitesExon 8: 2 known disease-causing sitesExon 9: 2 known disease-causing sitesExon 10: 2 known disease-causing sitesExon 11: 2 known disease-causing sitesExon 12: 1 known disease-causing siteExon 1: 155,610,218–155,610,332, 115 basesExon 2: 155,610,425–155,610,560, 136 basesExon 3: 155,611,039–155,611,108, 70 basesExon 4: 155,611,216–155,611,291, 76 basesExon 5: 155,611,549–155,611,603, 55 basesExon 6: 155,611,689–155,611,827, 139 basesExon 7: 155,611,983–155,612,100, 118 basesExon 8: 155,612,182–155,612,316, 135 basesExon 9: 155,612,418–155,612,570, 153 basesExon 10: 155,612,844–155,612,975, 132 basesExon 11: 155,613,049–155,613,233, 185 basesExon 12: 155,613,462–155,613,566, 105 basesExon 13: 155,613,657–155,613,766, 110 basesExon 14: 155,614,059–155,614,951, 893 bases12345678910111213145′3′

Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.

Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).

Nearby genes from Ensembl release 116, on GRCh38.

Exons make up 2.4 kb of the gene's 4.7 kb; 1,713 of those bases code for the protein.

How a genome test reads MSTO1

16

positions in MSTO1 where ClinVar classes a change as pathogenic or likely pathogenic

16 of them (100%) fall in regions short reads find hard.

  • Low mappability (13 sites)Regions where 100 bp or 250 bp reads cannot be placed uniquely.
  • Segmental duplications (16 sites)Copies of at least 1 kb sharing at least 90% identity with another part of the genome (paralogues, pseudogenes); reads may align to the wrong copy.

A whole genome covers all 4.7 kb of MSTO1, introns included, not only the 2.4 kb of exons.

Where this comes from

  • HGNC: the gene's symbol, name, other symbols and location.
  • MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). MSTO1 gene: misato mitochondrial distribution and morphology regulator 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/msto1

Vancouver

Dante Labs. MSTO1 gene: misato mitochondrial distribution and morphology regulator 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/msto1

One test. A lifetime of answers.

From $449Free shipping · Results in 6–8 weeks

Get my Genome Test