Gene
GLIS2
GLIS family zinc finger 2
- HGNC 29450↗(opens in a new tab)
- Ensembl gene ENSG00000126603↗(opens in a new tab)
- NCBI Gene 84662↗(opens in a new tab)
Summary
- Cytogenetic location
- 16p13.3
- Coordinates
- Chromosome 16: 4,316,067–4,339,595 (GRCh38)
- Exons
- 7 exons across 23.5 kb
- Protein
- 524 amino acids
- Inheritance
- Autosomal recessive
- Also known as
- NPHP7
- MANE Select transcript
- ENST00000433375.2NM_032575.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read GLIS2, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated report relevant to this gene
Nephronophthisis and Senior-Løken Syndrome
- NephronophthisisAutosomal recessive
A recessively inherited kidney disease, caused by variants in NPHP1 and other cilia genes, in which progressive tubulointerstitial scarring leads to kidney failure, typically in the first three decades of life.
- ClinGen rates the link moderate
- 3 GenCC submitters rate it definitive or strong
What knowing changes
Knowing allows regular kidney function monitoring, timely planning for dialysis or transplantation, and carrier testing for relatives.
Inheritance
- Autosomal recessive
- It takes a changed copy from each parent. With one, you are a carrier and usually unaffected; when both parents are carriers, each child has a one-in-four chance of inheriting two.
How GLIS2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
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 3.9 kb of the gene's 23.5 kb; 1,575 of those bases code for the protein.
Genes linked to the same conditions
- ADAMTS9ADAM metallopeptidase with thrombospondin type 1 motif 9Shares 1 condition
- ANKS6ankyrin repeat and sterile alpha motif domain containing 6Shares 1 condition
- CEP164centrosomal protein 164Shares 1 condition
- CEP83centrosomal protein 83Shares 1 condition
- DCDC2doublecortin domain containing 2Shares 1 condition
- INVSinversinShares 1 condition
- MAPKBP1mitogen-activated protein kinase binding protein 1Shares 1 condition
- NEK8NIMA related kinase 8Shares 1 condition
- NPHP1nephrocystin 1Shares 1 condition
- NPHP3nephrocystin 3Shares 1 condition
- NPHP4nephrocystin 4Shares 1 condition
- TMEM67transmembrane protein 67Shares 1 condition
Traits linked to GLIS2
The Human Phenotype Ontology lists these as features of the rare conditions GLIS2 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
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.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- 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
Dante Labs. (n.d.). GLIS2 gene: GLIS family zinc finger 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/glis2
Dante Labs. GLIS2 gene: GLIS family zinc finger 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/glis2
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks