Gene
ZMYM2
zinc finger MYM-type containing 2
- HGNC 12989↗(opens in a new tab)
- Ensembl gene ENSG00000121741↗(opens in a new tab)
- NCBI Gene 7750↗(opens in a new tab)
Summary
- Cytogenetic location
- 13q12.11
- Coordinates
- Chromosome 13: 19,958,727–20,089,115 (GRCh38)
- Exons
- 25 exons across 130.4 kb
- Protein
- 1,377 amino acids
- Also known as
- RAMP, FIM, MYM
- Previous symbols
- ZNF198
- MANE Select transcript
- ENST00000610343.5NM_197968.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read ZMYM2, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads ZMYM2 yet. The test sequences your whole genome, so your data includes it all the same.
How ZMYM2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
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 7.4 kb of the gene's 130.4 kb; 4,134 of those bases code for the protein.
How a genome test reads ZMYM2
43
positions in ZMYM2 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 130.4 kb of ZMYM2, introns included, not only the 7.4 kb of exons.
Traits linked to ZMYM2
The Human Phenotype Ontology lists these as features of the rare conditions ZMYM2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Global developmental delay
- Attention deficit
- Autism spectrum disorder
- Delayed speech and language development
- Epilepsy
- Exaggerated startle response
- Intellectual disability
- Intellectual disability, mild
Show 4 more traits
Abnormality of limbs
- Abnormality of the palm lines
- Broad toe
- Curvature of little finger
- Short 5th finger
- Short finger
- Short foot
- Short thumb
- Single transverse palmar crease
Show 1 more trait
External links
Gene records
Transcript
Protein
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
Dante Labs. (n.d.). ZMYM2 gene: zinc finger MYM-type containing 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/zmym2
Dante Labs. ZMYM2 gene: zinc finger MYM-type containing 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/zmym2
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks