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Gene

MINPP1

multiple inositol-polyphosphate phosphatase 1

Summary

Cytogenetic location
10q23.2
Coordinates
Chromosome 10: 87,504,893–87,553,461 (GRCh38)
Exons
5 exons across 48.6 kb
Protein
487 amino acids
Also known as
MIPP
MANE Select transcript
ENST00000371996.9NM_004897.5
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 MINPP1 yet. The test sequences your whole genome, so your data includes it all the same.

How MINPP1 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 10, with a bracket where MINPP1 sits. MINPP1 and 10 genes near it on chromosome 10, from 87,029,177 to 88,029,176.Chromosome 1010q23.2p15.3p15.2p15.1p14p13p12.33p12.32p12.31p12.2p12.1p11.23p11.22p11.21p11.1q11.1q11.21q11.22q11.23q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.31q23.32q23.33q24.1q24.2q24.31q24.32q24.33q25.1q25.2q25.3q26.11q26.12q26.13q26.2q26.387.2 Mb87.4 Mb87.6 Mb87.8 Mb88 MbFAM25A: 87,020,238–87,060,609, forward strandFAM25AGLUD1: 87,050,202–87,095,405, reverse strandGLUD1SHLD2: 87,094,006–87,191,478, forward strandSHLD2NUTM2A: 87,225,448–87,236,908, forward strandNUTM2ANUTM2D: 87,357,720–87,370,695, forward strandNUTM2DMINPP1: 87,504,893–87,553,461, forward strandMINPP1PAPSS2: 87,659,613–87,747,708, forward strandPAPSS2ATAD1: 87,744,644–87,842,355, reverse strandATAD1KLLN: 87,859,158–87,863,533, reverse strandKLLNPTEN: 87,862,638–87,971,930, forward strandPTENMLDHR: 87,863,559–87,863,654, forward strandMLDHRDiagram of MINPP1: 5 exons on the forward strand of chromosome 10Exon 1: 4 known disease-causing sitesExon 3: 2 known disease-causing sitesExon 4: 2 known disease-causing sitesExon 5: 3 known disease-causing sitesExon 1: 87,504,893–87,505,552, 660 basesExon 2: 87,508,336–87,508,533, 198 basesExon 3: 87,513,124–87,513,221, 98 basesExon 4: 87,521,036–87,521,169, 134 basesExon 5: 87,552,082–87,553,461, 1,380 bases123455′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 2.5 kb of the gene's 48.6 kb; 1,464 of those bases code for the protein.

How a genome test reads MINPP1

11

positions in MINPP1 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 48.6 kb of MINPP1, introns included, not only the 2.5 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.). MINPP1 gene: multiple inositol-polyphosphate phosphatase 1. Retrieved 16 October 2026, from https://dantelabs.com/genes/minpp1

Vancouver

Dante Labs. MINPP1 gene: multiple inositol-polyphosphate phosphatase 1 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/minpp1

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