Skip to content
Use your HSA or FSA funds

Gene

QRICH1

glutamine rich 1

Summary

Cytogenetic location
3p21.31
Coordinates
Chromosome 3: 49,029,707–49,094,071 (GRCh38)
Exons
10 exons across 64.4 kb
Protein
776 amino acids
Also known as
FLJ20259, VERBRAS, AB-DIP
MANE Select transcript
ENST00000395443.7NM_198880.3
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 report relevant to this gene

    How QRICH1 is laid out

    • Coding sequence
    • Untranslated region
    • Intron
    • Direction of transcription
    • Known disease-causing sites
    • Stretches short reads find hard
    Chromosome 3, with a bracket where QRICH1 sits. QRICH1 and 36 genes near it on chromosome 3, from 48,561,889 to 49,561,888.Chromosome 33p21.31p26.3p26.2p26.1p25.3p25.2p25.1p24.3p24.2p24.1p23p22.3p22.2p22.1p21.33p21.32p21.31p21.2p21.1p14.3p14.2p14.1p13p12.3p12.2p12.1p11.2p11.1q11.1q11.2q12.1q12.2q12.3q13.11q13.12q13.13q13.2q13.31q13.32q13.33q21.1q21.2q21.3q22.1q22.2q22.3q23q24q25.1q25.2q25.31q25.32q25.33q26.1q26.2q26.31q26.32q26.33q27.1q27.2q27.3q28q2948.6 Mb48.8 Mb49 Mb49.2 Mb49.4 MbPFKFB4: 48,517,668–48,562,015, reverse strandUCN2: 48,561,718–48,563,781, reverse strandUCN2COL7A1: 48,564,073–48,595,596, reverse strandCOL7A1UQCRC1: 48,598,990–48,610,976, reverse strandUQCRC1TMEM89: 48,620,759–48,621,769, reverse strandTMEM89SLC26A6: 48,625,718–48,635,510, reverse strandSLC26A6CELSR3: 48,636,463–48,662,886, reverse strandCELSR3NCKIPSD: 48,662,986–48,686,364, reverse strandNCKIPSDIP6K2: 48,688,003–48,740,353, reverse strandIP6K2PRKAR2A: 48,744,591–48,847,894, reverse strandPRKAR2ASLC25A20: 48,856,926–48,898,993, reverse strandSLC25A20ARIH2: 48,918,217–48,986,382, forward strandARIH2P4HTM: 48,989,858–49,007,153, forward strandWDR6: 49,007,062–49,015,953, forward strandDALRD3: 49,015,474–49,022,293, reverse strandNDUFAF3: 49,020,459–49,027,593, forward strandNDUFAF3IMPDH2: 49,024,315–49,029,452, reverse strandIMPDH2: 49,024,345–49,094,071, reverse strandQRICH1: 49,029,707–49,094,071, reverse strandQRICH1QARS1: 49,095,932–49,105,130, reverse strandQARS1USP19: 49,105,758–49,120,940, reverse strandUSP19LAMB2: 49,121,113–49,133,118, reverse strandLAMB2CCDC71: 49,161,063–49,166,357, reverse strandCCDC71KLHDC8B: 49,171,239–49,176,487, forward strandKLHDC8BCIMIP7: 49,177,634–49,191,858, reverse strandCIMIP7IHO1: 49,198,428–49,277,629, forward strandIHO1C3orf62: 49,268,596–49,277,236, reverse strandC3orf62USP4: 49,277,144–49,340,712, reverse strandUSP4GPX1: 49,357,174–49,358,605, reverse strandGPX1: 49,357,176–49,412,051, reverse strandRHOA: 49,359,136–49,412,998, reverse strandRHOATCTA: 49,412,212–49,455,826, forward strandAMT: 49,416,771–49,422,685, reverse strandAMT: 49,416,777–49,429,314, reverse strandNICN1: 49,422,333–49,429,331, reverse strandDAG1: 49,468,649–49,535,624, forward strandDAG1BSN: 49,554,477–49,671,549, forward strandBSNDiagram of QRICH1: 10 exons on the reverse strand of chromosome 3Exon 10: 4 known disease-causing sitesExon 8: 2 known disease-causing sitesExon 7: 3 known disease-causing sitesExon 6: 1 known disease-causing siteExon 5: 6 known disease-causing sitesExon 4: 2 known disease-causing sitesExon 3: 25 known disease-causing sitesExon 2: 6 known disease-causing sitesExon 10: 49,029,707–49,030,644, 938 basesExon 9: 49,032,183–49,032,273, 91 basesExon 8: 49,032,622–49,032,773, 152 basesExon 7: 49,033,120–49,033,228, 109 basesExon 6: 49,044,390–49,044,504, 115 basesExon 5: 49,046,425–49,046,579, 155 basesExon 4: 49,047,069–49,047,246, 178 basesExon 3: 49,056,862–49,057,890, 1,029 basesExon 2: 49,076,709–49,077,038, 330 basesExon 1: 49,093,912–49,094,071, 160 bases10864215′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 3.3 kb of the gene's 64.4 kb; 2,331 of those bases code for the protein.

    How a genome test reads QRICH1

    55

    positions in QRICH1 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 64.4 kb of QRICH1, introns included, not only the 3.3 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.
    • GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
    • The ACMG secondary findings list, SF v3.2.
    • 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.). QRICH1 gene: glutamine rich 1. Retrieved 16 October 2026, from https://dantelabs.com/genes/qrich1

    Vancouver

    Dante Labs. QRICH1 gene: glutamine rich 1 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/qrich1

    One test. A lifetime of answers.

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

    Get my Genome Test