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Gene

CEP112

centrosomal protein 112

Summary

Cytogenetic location
17q24.1
Coordinates
Chromosome 17: 65,635,537–66,192,133 (GRCh38)
Exons
27 exons across 556.6 kb
Protein
955 amino acids
Also known as
MGC33887
Previous symbols
CCDC46
MANE Select transcript
ENST00000535342.7NM_001199165.4
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 CEP112 yet. The test sequences your whole genome, so your data includes it all the same.

How CEP112 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 17, with a bracket where CEP112 sits. CEP112 and 5 genes near it on chromosome 17, from 65,078,940 to 66,748,730.Chromosome 1717q24.1p13.3p13.2p13.1p12p11.2p11.1q11.1q11.2q12q21.1q21.2q21.31q21.32q21.33q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.365.2 Mb65.4 Mb65.6 Mb65.8 Mb66 Mb66.2 Mb66.4 Mb66.6 MbRGS9: 65,100,812–65,227,703, forward strandRGS9AXIN2: 65,528,561–65,562,067, reverse strandAXIN2: 65,538,102–65,641,033, reverse strandCEP112: 65,635,537–66,192,133, reverse strandCEP112APOH: 66,211,543–66,256,525, reverse strandAPOHPRKCA: 66,302,567–66,810,743, forward strandPRKCADiagram of CEP112: 27 exons on the reverse strand of chromosome 17Exon 13: 1 known disease-causing siteExon 27: 65,635,537–65,635,974, 438 basesExon 26: 65,637,124–65,637,188, 65 basesExon 25: 65,640,964–65,641,065, 102 basesExon 24: 65,689,129–65,689,218, 90 basesExon 23: 65,743,068–65,743,217, 150 basesExon 22: 65,750,662–65,750,724, 63 basesExon 21: 65,851,804–65,852,034, 231 basesExon 20: 65,902,152–65,902,334, 183 basesExon 19: 65,927,582–65,927,689, 108 basesExon 18: 65,961,463–65,961,598, 136 basesExon 17: 66,005,690–66,005,769, 80 basesExon 16: 66,027,501–66,027,560, 60 basesExon 15: 66,028,313–66,028,405, 93 basesExon 14: 66,029,123–66,029,252, 130 basesExon 13: 66,029,869–66,030,023, 155 basesExon 12: 66,053,736–66,053,879, 144 basesExon 11: 66,062,963–66,063,081, 119 basesExon 10: 66,066,778–66,066,877, 100 basesExon 9: 66,069,915–66,070,001, 87 basesExon 8: 66,096,251–66,096,328, 78 basesExon 7: 66,096,585–66,096,632, 48 basesExon 6: 66,129,746–66,129,823, 78 basesExon 5: 66,132,670–66,132,763, 94 basesExon 4: 66,175,044–66,175,216, 173 basesExon 3: 66,176,830–66,177,020, 191 basesExon 2: 66,183,194–66,183,307, 114 basesExon 1: 66,191,997–66,192,133, 137 bases27201015′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 3.4 kb of the gene's 556.6 kb; 2,868 of those bases code for the protein.

How a genome test reads CEP112

2

positions in CEP112 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 556.6 kb of CEP112, introns included, not only the 3.4 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.). CEP112 gene: centrosomal protein 112. Retrieved 17 October 2026, from https://dantelabs.com/genes/cep112

Vancouver

Dante Labs. CEP112 gene: centrosomal protein 112 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/cep112

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