Skip to content
Use your HSA or FSA funds
Sequence your genome (opens in a new tab)

Gene

MYO1H

myosin IH

Summary

Cytogenetic location
12q24.11
Coordinates
Chromosome 12: 109,347,900–109,448,379 (GRCh38)
Exons
32 exons across 100.5 kb
Protein
1,038 amino acids
Also known as
FLJ37587
MANE Select transcript
ENST00000310903.10NM_001101421.4
Locus type
Protein-coding
  • Very high
  • Confident
  • Low
  • Very low

Curated reports relevant to this gene

No Genome Test report reads MYO1H yet. The test sequences your whole genome, so your data includes it all the same.

How MYO1H is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 12, with a bracket where MYO1H sits. MYO1H and 14 genes near it on chromosome 12, from 108,898,140 to 109,898,139.Chromosome 1212q24.11p13.33p13.32p13.31p13.2p13.1p12.3p12.2p12.1p11.23p11.22p11.21p11.1q11q12q13.11q13.12q13.13q13.2q13.3q14.1q14.2q14.3q15q21.1q21.2q21.31q21.32q21.33q22q23.1q23.2q23.3q24.11q24.12q24.13q24.21q24.22q24.23q24.31q24.32q24.33109 Mb109.2 Mb109.4 Mb109.6 Mb109.8 MbDAO: 108,858,932–108,901,052, forward strandDAOSVOP: 108,907,741–109,021,068, reverse strandSVOPUSP30: 109,023,089–109,088,023, forward strandUSP30ALKBH2: 109,085,154–109,098,462, reverse strandALKBH2UNG: 109,097,569–109,126,725, forward strandUNGACACB: 109,116,320–109,268,226, forward strandACACBFOXN4: 109,277,978–109,309,289, reverse strandFOXN4MYO1H: 109,347,900–109,448,379, forward strandMYO1HKCTD10: 109,448,655–109,477,359, reverse strandKCTD10UBE3B: 109,477,375–109,536,705, forward strandUBE3BMMAB: 109,553,715–109,573,580, reverse strandMMABMVK: 109,573,255–109,600,609, forward strandMVKFAM222A: 109,713,819–109,770,495, forward strandFAM222ATRPV4: 109,783,087–109,833,542, reverse strandTRPV4GLTP: 109,850,943–109,880,549, reverse strandGLTPDiagram of MYO1H: 32 exons on the forward strand of chromosome 12Exon 2: 1 known disease-causing siteExon 3: 1 known disease-causing siteExon 4: 1 known disease-causing siteExon 24: 1 known disease-causing siteExon 1: 109,347,900–109,347,972, 73 basesExon 2: 109,388,683–109,388,844, 162 basesExon 3: 109,393,331–109,393,446, 116 basesExon 4: 109,396,384–109,396,582, 199 basesExon 5: 109,397,732–109,397,812, 81 basesExon 6: 109,401,093–109,401,272, 180 basesExon 7: 109,403,982–109,404,080, 99 basesExon 8: 109,405,922–109,406,035, 114 basesExon 9: 109,406,789–109,406,860, 72 basesExon 10: 109,407,794–109,407,913, 120 basesExon 11: 109,409,557–109,409,624, 68 basesExon 12: 109,409,963–109,410,068, 106 basesExon 13: 109,410,688–109,410,768, 81 basesExon 14: 109,411,894–109,411,985, 92 basesExon 15: 109,415,526–109,415,620, 95 basesExon 16: 109,420,981–109,421,027, 47 basesExon 17: 109,424,748–109,424,828, 81 basesExon 18: 109,425,946–109,426,051, 106 basesExon 19: 109,427,469–109,427,586, 118 basesExon 20: 109,432,897–109,433,010, 114 basesExon 21: 109,435,037–109,435,113, 77 basesExon 22: 109,436,488–109,436,556, 69 basesExon 23: 109,438,536–109,438,620, 85 basesExon 24: 109,439,631–109,439,790, 160 basesExon 25: 109,440,744–109,440,827, 84 basesExon 26: 109,441,615–109,441,708, 94 basesExon 27: 109,442,217–109,442,272, 56 basesExon 28: 109,443,514–109,443,649, 136 basesExon 29: 109,444,213–109,444,283, 71 basesExon 30: 109,444,432–109,444,529, 98 basesExon 31: 109,445,513–109,445,612, 100 basesExon 32: 109,447,159–109,448,379, 1,221 bases151015202530325′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 4.4 kb of the gene's 100.5 kb; 3,117 of those bases code for the protein.

Sequencing MYO1H

6

positions in MYO1H where ClinVar classes a change as pathogenic or likely pathogenic

None of them falls in a region short reads find hard.

A whole genome covers all 100.5 kb of MYO1H, introns included, not only the 4.4 kb of exons.

Traits linked to MYO1H

The Human Phenotype Ontology lists these as features of the rare conditions MYO1H can cause. Each trait's page lists the other genes linked to it.

External links

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.). MYO1H gene: myosin IH. Retrieved 17 October 2026, from https://dantelabs.com/genes/myo1h

Vancouver

Dante Labs. MYO1H gene: myosin IH [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/myo1h

One test. A lifetime of answers.

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

Get my Genome Test