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Gene

WDR62

WD repeat domain 62

Summary

Cytogenetic location
19q13.12
Coordinates
Chromosome 19: 36,054,897–36,105,108 (GRCh38)
Exons
32 exons across 50.2 kb
Protein
1,523 amino acids
Also known as
DKFZP434J046, FLJ33298
Previous symbols
C19orf14, MCPH2
MANE Select transcript
ENST00000401500.7NM_001083961.2
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 WDR62 yet. The test sequences your whole genome, so your data includes it all the same.

How WDR62 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 19, with a bracket where WDR62 sits. WDR62 and 42 genes near it on chromosome 19, from 35,580,003 to 36,580,002.Chromosome 1919q13.12p13.3p13.2p13.13p13.12p13.11p12p11q11q12q13.11q13.12q13.13q13.2q13.31q13.32q13.33q13.41q13.42q13.4335.6 Mb35.8 Mb36 Mb36.2 Mb36.4 MbPMIS2: 35,586,161–35,587,296, forward strandPMIS2HAUS5: 35,612,735–35,625,355, forward strandHAUS5RBM42: 35,628,989–35,638,927, forward strandRBM42ETV2: 35,641,730–35,644,871, forward strandETV2COX6B1: 35,648,230–35,662,890, forward strandCOX6B1UPK1A: 35,666,516–35,678,481, forward strandUPK1AZBTB32: 35,704,558–35,717,048, forward strandKMT2B: 35,717,973–35,738,880, forward strandIGFLR1: 35,738,798–35,742,459, reverse strand: 35,739,252–35,745,432, reverse strandU2AF1L4: 35,742,464–35,745,460, reverse strandPSENEN: 35,745,070–35,747,519, forward strand: 35,745,678–35,754,519, forward strandLIN37: 35,748,361–35,754,519, forward strandHSPB6: 35,754,566–35,758,079, reverse strandHSPB6PROSER3: 35,758,143–35,771,398, forward strandPROSER3ARHGAP33: 35,774,532–35,788,822, forward strandARHGAP33PRODH2: 35,799,975–35,813,299, reverse strandPRODH2NPHS1: 35,825,372–35,869,287, reverse strandNPHS1KIRREL2: 35,851,369–35,867,145, forward strandAPLP1: 35,867,899–35,879,803, forward strandAPLP1NFKBID: 35,887,129–35,902,303, reverse strandNFKBIDHCST: 35,899,017–35,904,377, forward strandHCSTTYROBP: 35,904,398–35,908,318, reverse strandTYROBPLRFN3: 35,935,358–35,946,624, forward strandLRFN3SDHAF1: 35,995,188–35,996,312, forward strandSYNE4: 36,000,545–36,008,831, reverse strandSYNE4ALKBH6: 36,009,113–36,014,297, reverse strandALKBH6CLIP3: 36,014,660–36,033,343, reverse strandCLIP3THAP8: 36,033,393–36,054,739, reverse strandTHAP8WDR62: 36,054,897–36,105,108, forward strandWDR62OVOL3: 36,111,116–36,113,711, forward strandOVOL3POLR2I: 36,111,817–36,115,213, reverse strandPOLR2ITBCB: 36,114,289–36,125,948, forward strandTBCBCAPNS1: 36,139,953–36,150,356, forward strandCAPNS1COX7A1: 36,150,287–36,152,699, reverse strandZNF565: 36,181,542–36,246,257, reverse strandZNF565ZNF146: 36,214,602–36,239,969, forward strandZNF146ZFP14: 36,334,453–36,379,208, reverse strandZFP14ZFP82: 36,383,120–36,418,924, reverse strandZFP82ZNF566: 36,445,119–36,489,902, reverse strandZNF566ZNF260: 36,510,687–36,528,696, reverse strandZNF260ZNF529: 36,534,774–36,605,554, reverse strandZNF529Diagram of WDR62: 32 exons on the forward strand of chromosome 19Exon 1: 1 known disease-causing siteExon 2: 2 known disease-causing sitesExon 3: 1 known disease-causing siteExon 4: 2 known disease-causing sitesExon 5: 1 known disease-causing siteExon 6: 2 known disease-causing sitesExon 7: 1 known disease-causing siteExon 8: 1 known disease-causing siteExon 9: 5 known disease-causing sitesExon 10: 2 known disease-causing sitesExon 11: 6 known disease-causing sitesExon 12: 3 known disease-causing sitesExon 13: 1 known disease-causing siteExon 15: 1 known disease-causing siteExon 17: 3 known disease-causing sitesExon 18: 1 known disease-causing siteExon 19: 1 known disease-causing siteExon 20: 1 known disease-causing siteExon 22: 7 known disease-causing sitesExon 23: 2 known disease-causing sitesExon 25: 2 known disease-causing sitesExon 27: 1 known disease-causing siteExon 28: 2 known disease-causing sitesExon 29: 1 known disease-causing siteExon 30: 5 known disease-causing sitesExon 31: 2 known disease-causing sitesExon 32: 2 known disease-causing sitesExon 1: 36,054,897–36,055,148, 252 basesExon 2: 36,058,780–36,058,871, 92 basesExon 3: 36,059,968–36,060,030, 63 basesExon 4: 36,065,958–36,066,015, 58 basesExon 5: 36,066,257–36,066,427, 171 basesExon 6: 36,067,306–36,067,443, 138 basesExon 7: 36,067,828–36,068,010, 183 basesExon 8: 36,071,556–36,071,716, 161 basesExon 9: 36,073,342–36,073,531, 190 basesExon 10: 36,081,433–36,081,570, 138 basesExon 11: 36,083,063–36,083,241, 179 basesExon 12: 36,084,653–36,084,744, 92 basesExon 13: 36,086,687–36,086,812, 126 basesExon 14: 36,089,038–36,089,105, 68 basesExon 15: 36,089,185–36,089,306, 122 basesExon 16: 36,090,445–36,090,520, 76 basesExon 17: 36,091,200–36,091,311, 112 basesExon 18: 36,091,402–36,091,465, 64 basesExon 19: 36,092,689–36,092,811, 123 basesExon 20: 36,094,031–36,094,164, 134 basesExon 21: 36,097,027–36,097,079, 53 basesExon 22: 36,099,399–36,099,617, 219 basesExon 23: 36,100,748–36,100,875, 128 basesExon 24: 36,101,214–36,101,317, 104 basesExon 25: 36,101,664–36,101,774, 111 basesExon 26: 36,102,014–36,102,151, 138 basesExon 27: 36,102,737–36,102,851, 115 basesExon 28: 36,102,948–36,103,074, 127 basesExon 29: 36,103,156–36,103,207, 52 basesExon 30: 36,103,343–36,103,981, 639 basesExon 31: 36,104,518–36,104,675, 158 basesExon 32: 36,104,768–36,105,108, 341 bases151015202530325′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 4.7 kb of the gene's 50.2 kb; 4,572 of those bases code for the protein.

How a genome test reads WDR62

72

positions in WDR62 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 50.2 kb of WDR62, introns included, not only the 4.7 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.). WDR62 gene: WD repeat domain 62. Retrieved 16 October 2026, from https://dantelabs.com/genes/wdr62

Vancouver

Dante Labs. WDR62 gene: WD repeat domain 62 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/wdr62

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