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Gene

ANKRD17

ankyrin repeat domain 17

Summary

Cytogenetic location
4q13.3
Coordinates
Chromosome 4: 73,073,376–73,258,798 (GRCh38)
Exons
34 exons across 185.4 kb
Protein
2,603 amino acids
Also known as
GTAR, KIAA0697, FLJ22206, NY-BR-16, MASK2
MANE Select transcript
ENST00000358602.9NM_032217.5
Locus type
Protein-coding
  • Very high
  • Confident
  • Low
  • Very low

Curated reports relevant to this gene

No Genome Test report reads ANKRD17 yet. The test sequences your whole genome, so your data includes it all the same.

How ANKRD17 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 ANKRD17 sits. ANKRD17 and 5 genes near it on chromosome 4, from 72,666,087 to 73,666,086.Chromosome 44q13.3p16.3p16.2p16.1p15.33p15.32p15.31p15.2p15.1p14p13p12p11q11q12q13.1q13.2q13.3q21.1q21.21q21.22q21.23q21.3q22.1q22.2q22.3q23q24q25q26q27q28.1q28.2q28.3q31.1q31.21q31.22q31.23q31.3q32.1q32.2q32.3q33q34.1q34.2q34.3q35.1q35.272.8 Mb73 Mb73.2 Mb73.4 Mb73.6 MbCOX18: 73,052,362–73,069,755, reverse strandCOX18ANKRD17: 73,073,376–73,258,798, reverse strandANKRD17ALB: 73,397,114–73,426,607, forward strandALBAFP: 73,431,138–73,456,174, forward strandAFPAFM: 73,481,659–73,504,173, forward strandAFMRASSF6: 73,571,550–73,620,631, reverse strandRASSF6Diagram of ANKRD17: 34 exons on the reverse strand of chromosome 4Exon 32: 3 known disease-causing sitesExon 31: 2 known disease-causing sitesExon 29: 7 known disease-causing sitesExon 26: 1 known disease-causing siteExon 25: 2 known disease-causing sitesExon 22: 2 known disease-causing sitesExon 21: 1 known disease-causing siteExon 20: 2 known disease-causing sitesExon 19: 2 known disease-causing sitesExon 18: 1 known disease-causing siteExon 17: 2 known disease-causing sitesExon 15: 2 known disease-causing sitesExon 13: 1 known disease-causing siteExon 11: 1 known disease-causing siteExon 8: 1 known disease-causing siteExon 4: 1 known disease-causing siteExon 1: 1 known disease-causing siteExon 34: 73,073,376–73,076,290, 2,915 basesExon 33: 73,076,940–73,077,104, 165 basesExon 32: 73,077,355–73,077,533, 179 basesExon 31: 73,078,642–73,078,890, 249 basesExon 30: 73,085,249–73,085,446, 198 basesExon 29: 73,090,667–73,092,300, 1,634 basesExon 28: 73,094,079–73,094,228, 150 basesExon 27: 73,097,117–73,097,272, 156 basesExon 26: 73,098,073–73,098,520, 448 basesExon 25: 73,102,376–73,102,547, 172 basesExon 24: 73,113,792–73,113,908, 117 basesExon 23: 73,115,821–73,115,916, 96 basesExon 22: 73,118,688–73,118,850, 163 basesExon 21: 73,120,162–73,120,337, 176 basesExon 20: 73,120,881–73,121,094, 214 basesExon 19: 73,121,617–73,121,759, 143 basesExon 18: 73,124,913–73,125,058, 146 basesExon 17: 73,125,201–73,125,312, 112 basesExon 16: 73,135,117–73,135,265, 149 basesExon 15: 73,139,531–73,140,283, 753 basesExon 14: 73,141,741–73,141,843, 103 basesExon 13: 73,142,242–73,142,385, 144 basesExon 12: 73,142,640–73,142,767, 128 basesExon 11: 73,144,745–73,144,832, 88 basesExon 10: 73,146,764–73,146,873, 110 basesExon 9: 73,147,241–73,147,432, 192 basesExon 8: 73,148,813–73,149,050, 238 basesExon 7: 73,151,430–73,151,524, 95 basesExon 6: 73,153,880–73,154,113, 234 basesExon 5: 73,155,631–73,155,778, 148 basesExon 4: 73,156,019–73,156,166, 148 basesExon 3: 73,161,192–73,161,348, 157 basesExon 2: 73,177,380–73,177,533, 154 basesExon 1: 73,258,276–73,258,798, 523 bases343025201510515′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 10.8 kb of the gene's 185.4 kb; 7,812 of those bases code for the protein.

Sequencing ANKRD17

2Low

How hard ANKRD17 is to sequence with short reads, out of 100

  • Mappability0%
  • Homology0%
  • Repeats6.1%
  • GC content14%
  • Reference coverage0%

32

positions in ANKRD17 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 185.4 kb of ANKRD17, introns included, not only the 10.8 kb of exons.

Traits linked to ANKRD17

The Human Phenotype Ontology lists these as features of the rare conditions ANKRD17 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 Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
  • Data release 2026.10.17-8666dff2.

Cite this page

APA

Dante Labs. (n.d.). ANKRD17 gene: ankyrin repeat domain 17. Retrieved 18 October 2026, from https://dantelabs.com/genes/ankrd17

Vancouver

Dante Labs. ANKRD17 gene: ankyrin repeat domain 17 [Internet]. [cited 18 October 2026]. Available from: https://dantelabs.com/genes/ankrd17

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