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Gene

LARP7

La ribonucleoprotein 7, transcriptional regulator

Summary

Cytogenetic location
4q25
Coordinates
Chromosome 4: 112,637,143–112,657,586 (GRCh38)
Exons
13 exons across 20.4 kb
Protein
582 amino acids
Also known as
HDCMA18P, PIP7S, DKFZP564K112
MANE Select transcript
ENST00000344442.10NM_016648.4
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 LARP7 yet. The test sequences your whole genome, so your data includes it all the same.

How LARP7 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 4, with a bracket where LARP7 sits. LARP7 and 7 genes near it on chromosome 4, from 112,147,365 to 113,147,364.Chromosome 44q25p16.3p16.2p16.1p15.33p15.32p15.31p15.2p15.1p14p13p12p11q11q12q13.1q13.2q13.3q21.1q21.21q21.22q21.23q21.3q22.1q22.2q22.3q23q24q25q26q27q28.1q28.2q28.3q31.1q31.21q31.22q31.23q31.3q32.1q32.2q32.3q33q34.1q34.2q34.3q35.1q35.2112.2 Mb112.4 Mb112.6 Mb112.8 Mb113 MbFAM241A: 112,145,408–112,195,256, forward strandFAM241AAP1AR: 112,231,363–112,273,110, forward strandAP1ARTIFA: 112,272,966–112,302,436, reverse strandTIFAALPK1: 112,285,509–112,442,621, forward strandALPK1NEUROG2: 112,513,516–112,516,180, reverse strandNEUROG2ZGRF1: 112,534,428–112,637,402, reverse strandZGRF1LARP7: 112,637,143–112,657,586, forward strandLARP7ANK2: 112,818,032–113,384,237, forward strandANK2Diagram of LARP7: 13 exons on the forward strand of chromosome 4Exon 2: 3 known disease-causing sitesExon 3: 4 known disease-causing sitesExon 5: 6 known disease-causing sitesExon 6: 1 known disease-causing siteExon 7: 13 known disease-causing sitesExon 8: 5 known disease-causing sitesExon 9: 1 known disease-causing siteExon 11: 1 known disease-causing siteExon 12: 1 known disease-causing siteExon 1: 112,637,143–112,637,239, 97 basesExon 2: 112,644,668–112,644,871, 204 basesExon 3: 112,646,351–112,646,451, 101 basesExon 4: 112,646,588–112,646,671, 84 basesExon 5: 112,646,791–112,646,955, 165 basesExon 6: 112,647,034–112,647,127, 94 basesExon 7: 112,647,199–112,647,549, 351 basesExon 8: 112,647,690–112,647,834, 145 basesExon 9: 112,649,535–112,649,686, 152 basesExon 10: 112,650,461–112,650,582, 122 basesExon 11: 112,653,077–112,653,236, 160 basesExon 12: 112,654,068–112,654,159, 92 basesExon 13: 112,657,247–112,657,586, 340 bases124681012135′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 2.1 kb of the gene's 20.4 kb; 1,749 of those bases code for the protein.

How a genome test reads LARP7

39

positions in LARP7 where ClinVar classes a change as pathogenic or likely pathogenic

1 of them (2.6%) falls in a region short reads find hard.

  • Low mappability (1 site)Regions where 100 bp or 250 bp reads cannot be placed uniquely.

A whole genome covers all 20.4 kb of LARP7, introns included, not only the 2.1 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.). LARP7 gene: La ribonucleoprotein 7, transcriptional regulator. Retrieved 17 October 2026, from https://dantelabs.com/genes/larp7

Vancouver

Dante Labs. LARP7 gene: La ribonucleoprotein 7, transcriptional regulator [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/larp7

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