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Gene

SLC30A7

solute carrier family 30 member 7

Summary

Cytogenetic location
1p21.2
Coordinates
Chromosome 1: 100,896,090–100,981,757 (GRCh38)
Exons
11 exons across 85.7 kb
Protein
376 amino acids
Also known as
ZnTL2, ZNT7
MANE Select transcript
ENST00000357650.9NM_133496.5
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 SLC30A7 yet. The test sequences your whole genome, so your data includes it all the same.

How SLC30A7 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 SLC30A7 sits. SLC30A7 and 6 genes near it on chromosome 1, from 100,438,924 to 101,438,923.Chromosome 11p21.2p36.33p36.32p36.31p36.23p36.22p36.21p36.13p36.12p36.11p35.3p35.2p35.1p34.3p34.2p34.1p33p32.3p32.2p32.1p31.3p31.2p31.1p22.3p22.2p22.1p21.3p21.2p21.1p13.3p13.2p13.1p12p11.2p11.1q11q12q21.1q21.2q21.3q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.3q31.1q31.2q31.3q32.1q32.2q32.3q41q42.11q42.12q42.13q42.2q42.3q43q44100.6 Mb100.8 Mb101 Mb101.2 Mb101.4 MbCDC14A: 100,325,629–100,520,564, forward strandCDC14AGPR88: 100,538,105–100,542,021, forward strandGPR88VCAM1: 100,719,684–100,739,045, forward strandVCAM1EXTL2: 100,871,371–100,896,000, reverse strandEXTL2SLC30A7: 100,896,090–100,981,757, forward strandSLC30A7DPH5: 100,926,286–101,026,117, reverse strandDPH5S1PR1: 101,235,366–101,243,749, forward strandS1PR1Diagram of SLC30A7: 11 exons on the forward strand of chromosome 1Exon 4: 1 known disease-causing siteExon 1: 100,896,090–100,896,342, 253 basesExon 2: 100,896,570–100,896,671, 102 basesExon 3: 100,906,852–100,906,965, 114 basesExon 4: 100,911,063–100,911,150, 88 basesExon 5: 100,912,112–100,912,238, 127 basesExon 6: 100,913,663–100,913,806, 144 basesExon 7: 100,918,077–100,918,127, 51 basesExon 8: 100,921,706–100,921,841, 136 basesExon 9: 100,961,828–100,961,918, 91 basesExon 10: 100,965,769–100,965,918, 150 basesExon 11: 100,974,810–100,981,757, 6,948 bases1510115′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 8.2 kb of the gene's 85.7 kb; 1,131 of those bases code for the protein.

How a genome test reads SLC30A7

1

position in SLC30A7 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 85.7 kb of SLC30A7, introns included, not only the 8.2 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.). SLC30A7 gene: solute carrier family 30 member 7. Retrieved 16 October 2026, from https://dantelabs.com/genes/slc30a7

Vancouver

Dante Labs. SLC30A7 gene: solute carrier family 30 member 7 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/slc30a7

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