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Gene

NIN

ninein

Summary

Cytogenetic location
14q22.1
Coordinates
Chromosome 14: 50,719,763–50,831,162 (GRCh38)
Exons
31 exons across 111.4 kb
Protein
2,133 amino acids
MANE Select transcript
ENST00000530997.7NM_020921.4
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 NIN yet. The test sequences your whole genome, so your data includes it all the same.

How NIN is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 14, with a bracket where NIN sits. NIN and 10 genes near it on chromosome 14, from 50,275,463 to 51,275,462.Chromosome 1414q22.1p13p12p11.2p11.1q11.1q11.2q12q13.1q13.2q13.3q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.3q24.1q24.2q24.3q31.1q31.2q31.3q32.11q32.12q32.13q32.2q32.31q32.32q32.3350.4 Mb50.6 Mb50.8 Mb51 Mb51.2 MbL2HGDH: 50,237,563–50,312,243, reverse strandL2HGDHDMAC2L: 50,311,516–50,356,756, forward strandDMAC2LCDKL1: 50,326,265–50,416,461, reverse strandCDKL1MAP4K5: 50,417,845–50,561,126, reverse strandMAP4K5ATL1: 50,532,509–50,634,017, forward strandATL1SAV1: 50,626,616–50,668,600, reverse strandSAV1NIN: 50,719,763–50,831,162, reverse strandNINPYGL: 50,857,891–50,944,734, reverse strandPYGLABHD12B: 50,872,046–50,904,970, forward strandABHD12BTRIM9: 50,975,254–51,096,084, reverse strandTRIM9TMX1: 51,240,152–51,259,059, forward strandTMX1Diagram of NIN: 31 exons on the reverse strand of chromosome 14Exon 30: 1 known disease-causing siteExon 23: 1 known disease-causing siteExon 18: 3 known disease-causing sitesExon 17: 2 known disease-causing sitesExon 31: 50,719,763–50,723,672, 3,910 basesExon 30: 50,725,953–50,726,066, 114 basesExon 29: 50,729,523–50,729,723, 201 basesExon 28: 50,735,516–50,735,617, 102 basesExon 27: 50,738,140–50,738,286, 147 basesExon 26: 50,739,308–50,739,487, 180 basesExon 25: 50,741,582–50,741,728, 147 basesExon 24: 50,743,416–50,743,529, 114 basesExon 23: 50,744,243–50,744,365, 123 basesExon 22: 50,747,992–50,748,105, 114 basesExon 21: 50,752,518–50,752,733, 216 basesExon 20: 50,754,563–50,754,632, 70 basesExon 19: 50,754,742–50,754,867, 126 basesExon 18: 50,756,492–50,758,630, 2,139 basesExon 17: 50,759,857–50,760,359, 503 basesExon 16: 50,761,790–50,761,911, 122 basesExon 15: 50,763,826–50,763,964, 139 basesExon 14: 50,766,307–50,766,396, 90 basesExon 13: 50,766,780–50,766,890, 111 basesExon 12: 50,770,388–50,770,562, 175 basesExon 11: 50,770,852–50,770,992, 141 basesExon 10: 50,771,332–50,771,468, 137 basesExon 9: 50,772,301–50,772,468, 168 basesExon 8: 50,772,949–50,773,095, 147 basesExon 7: 50,776,949–50,777,139, 191 basesExon 6: 50,778,765–50,778,804, 40 basesExon 5: 50,792,712–50,792,881, 170 basesExon 4: 50,806,737–50,806,818, 82 basesExon 3: 50,821,874–50,822,077, 204 basesExon 2: 50,830,464–50,830,517, 54 basesExon 1: 50,831,006–50,831,162, 157 bases313025201510515′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 10.3 kb of the gene's 111.4 kb; 6,402 of those bases code for the protein.

How a genome test reads NIN

8

positions in NIN 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 111.4 kb of NIN, introns included, not only the 10.3 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.
  • 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.). NIN gene: ninein. Retrieved 17 October 2026, from https://dantelabs.com/genes/nin

Vancouver

Dante Labs. NIN gene: ninein [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/nin

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