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Gene

MAU2

MAU2 sister chromatid cohesion factor

Summary

Cytogenetic location
19p13.11
Coordinates
Chromosome 19: 19,320,829–19,358,754 (GRCh38)
Exons
19 exons across 37.9 kb
Protein
613 amino acids
Also known as
MGC75361, mau-2, MAU2L, SCC4
Previous symbols
KIAA0892
MANE Select transcript
ENST00000262815.13NM_015329.4
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 MAU2 yet. The test sequences your whole genome, so your data includes it all the same.

How MAU2 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 MAU2 sits. MAU2 and 33 genes near it on chromosome 19, from 18,839,792 to 19,839,791.Chromosome 1919p13.11p13.3p13.2p13.13p13.12p13.11p12p11q11q12q13.11q13.12q13.13q13.2q13.31q13.32q13.33q13.41q13.42q13.4319 Mb19.2 Mb19.4 Mb19.6 Mb19.8 MbUPF1: 18,831,905–18,868,232, forward strandUPF1CERS1: 18,868,545–18,896,727, reverse strandGDF1: 18,868,545–18,896,158, reverse strandCOPE: 18,899,511–18,919,407, reverse strandCOPE: 18,907,013–18,934,397, reverse strandDDX49: 18,919,667–18,929,189, forward strandDDX49HOMER3: 18,929,201–18,941,728, reverse strandHOMER3SUGP2: 18,990,887–19,061,647, reverse strandSUGP2ARMC6: 19,033,575–19,060,311, forward strandARMC6SLC25A42: 19,061,697–19,113,030, forward strandSLC25A42TMEM161A: 19,119,148–19,138,513, reverse strandMEF2B: 19,145,563–19,192,589, reverse strandMEF2BBORCS8-MEF2B: 19,145,569–19,192,158, reverse strandBORCS8: 19,163,148–19,192,591, reverse strandBORCS8RFXANK: 19,191,957–19,202,844, forward strandRFXANKNR2C2AP: 19,201,409–19,203,729, reverse strandNR2C2APNCAN: 19,211,948–19,252,247, forward strandNCANHAPLN4: 19,254,731–19,262,827, reverse strandHAPLN4TM6SF2: 19,263,385–19,273,406, reverse strandTM6SF2SUGP1: 19,276,018–19,320,511, reverse strandSUGP1MAU2: 19,320,829–19,358,754, forward strandMAU2GATAD2A: 19,385,638–19,508,932, forward strandGATAD2ATSSK6: 19,512,396–19,515,553, reverse strandTSSK6NDUFA13: 19,515,728–19,529,054, forward strandNDUFA13: 19,516,227–19,536,076, forward strandYJEFN3: 19,528,851–19,537,584, forward strandCILP2: 19,538,248–19,546,659, forward strandPBX4: 19,561,707–19,618,746, reverse strandPBX4LPAR2: 19,623,639–19,628,930, reverse strandLPAR2GMIP: 19,629,473–19,643,669, reverse strandGMIPATP13A1: 19,645,196–19,663,700, reverse strandATP13A1ZNF101: 19,668,781–19,683,509, forward strandZNF101ZNF14: 19,708,130–19,733,119, reverse strandZNF14ZNF506: 19,761,038–19,821,784, reverse strandZNF506Diagram of MAU2: 19 exons on the forward strand of chromosome 19Exon 1: 1 known disease-causing siteExon 4: 1 known disease-causing siteExon 7: 1 known disease-causing siteExon 9: 2 known disease-causing sitesExon 11: 2 known disease-causing sitesExon 17: 1 known disease-causing siteExon 1: 19,320,829–19,321,135, 307 basesExon 2: 19,335,718–19,335,735, 18 basesExon 3: 19,336,122–19,336,187, 66 basesExon 4: 19,337,170–19,337,265, 96 basesExon 5: 19,338,845–19,338,939, 95 basesExon 6: 19,340,846–19,340,873, 28 basesExon 7: 19,341,252–19,341,407, 156 basesExon 8: 19,342,535–19,342,681, 147 basesExon 9: 19,342,776–19,342,866, 91 basesExon 10: 19,343,837–19,343,940, 104 basesExon 11: 19,344,849–19,344,926, 78 basesExon 12: 19,345,304–19,345,369, 66 basesExon 13: 19,347,280–19,347,366, 87 basesExon 14: 19,348,889–19,348,938, 50 basesExon 15: 19,349,155–19,349,232, 78 basesExon 16: 19,349,325–19,349,436, 112 basesExon 17: 19,354,355–19,354,445, 91 basesExon 18: 19,355,264–19,355,391, 128 basesExon 19: 19,355,708–19,358,754, 3,047 bases151015195′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 4.8 kb of the gene's 37.9 kb; 1,842 of those bases code for the protein.

How a genome test reads MAU2

8

positions in MAU2 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 37.9 kb of MAU2, introns included, not only the 4.8 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.). MAU2 gene: MAU2 sister chromatid cohesion factor. Retrieved 17 October 2026, from https://dantelabs.com/genes/mau2

Vancouver

Dante Labs. MAU2 gene: MAU2 sister chromatid cohesion factor [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/mau2

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