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Gene

RB1CC1

RB1 inducible coiled-coil 1

Summary

Cytogenetic location
8q11.23
Coordinates
Chromosome 8: 52,622,458–52,714,435 (GRCh38)
Exons
24 exons across 92 kb
Protein
1,594 amino acids
Also known as
KIAA0203, Cc1, DRAGOU14, FIP200, ATG17, PPP1R131
MANE Select transcript
ENST00000025008.10NM_014781.5
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Curated reports relevant to this gene

No Genome Test report reads RB1CC1 yet. The test sequences your whole genome, so your data includes it all the same.

How RB1CC1 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 8, with a bracket where RB1CC1 sits. RB1CC1 and 3 genes near it on chromosome 8, from 52,168,447 to 53,168,446.Chromosome 88q11.23p23.3p23.2p23.1p22p21.3p21.2p21.1p12p11.23p11.22p11.21p11.1q11.1q11.21q11.22q11.23q12.1q12.2q12.3q13.1q13.2q13.3q21.11q21.12q21.13q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.3q24.11q24.12q24.13q24.21q24.22q24.23q24.352.2 Mb52.4 Mb52.6 Mb52.8 Mb53 MbST18: 52,110,415–52,460,983, reverse strandST18ALKAL1: 52,534,025–52,565,437, reverse strandALKAL1RB1CC1: 52,622,458–52,714,435, reverse strandRB1CC1NPBWR1: 52,915,635–52,943,734, forward strandNPBWR1Diagram of RB1CC1: 24 exons on the reverse strand of chromosome 8Exon 13: 1 known disease-causing siteExon 24: 52,622,458–52,623,859, 1,402 basesExon 23: 52,624,717–52,624,787, 71 basesExon 22: 52,628,032–52,628,168, 137 basesExon 21: 52,630,470–52,630,528, 59 basesExon 20: 52,634,921–52,634,968, 48 basesExon 19: 52,636,015–52,636,069, 55 basesExon 18: 52,642,351–52,642,591, 241 basesExon 17: 52,642,704–52,642,812, 109 basesExon 16: 52,645,702–52,645,867, 166 basesExon 15: 52,656,008–52,657,908, 1,901 basesExon 14: 52,657,998–52,658,124, 127 basesExon 13: 52,658,873–52,658,976, 104 basesExon 12: 52,660,596–52,660,657, 62 basesExon 11: 52,660,926–52,661,007, 82 basesExon 10: 52,661,095–52,661,281, 187 basesExon 9: 52,661,535–52,661,719, 185 basesExon 8: 52,668,021–52,668,191, 171 basesExon 7: 52,673,845–52,674,274, 430 basesExon 6: 52,676,369–52,676,571, 203 basesExon 5: 52,683,549–52,683,719, 171 basesExon 4: 52,683,887–52,684,013, 127 basesExon 3: 52,685,399–52,685,520, 122 basesExon 2: 52,686,853–52,686,967, 115 basesExon 1: 52,714,075–52,714,435, 361 bases24201510515′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 6.6 kb of the gene's 92 kb; 4,785 of those bases code for the protein.

How a genome test reads RB1CC1

1

position in RB1CC1 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 92 kb of RB1CC1, introns included, not only the 6.6 kb of exons.

Traits linked to RB1CC1

The Human Phenotype Ontology lists these as features of the rare conditions RB1CC1 can cause. Each trait's page lists the other genes linked to it.

External links

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.). RB1CC1 gene: RB1 inducible coiled-coil 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/rb1cc1

Vancouver

Dante Labs. RB1CC1 gene: RB1 inducible coiled-coil 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/rb1cc1

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