Gene
ZFYVE19
zinc finger FYVE-type containing 19
- HGNC 20758↗(opens in a new tab)
- Ensembl gene ENSG00000166140↗(opens in a new tab)
- NCBI Gene 84936↗(opens in a new tab)
Summary
- Cytogenetic location
- 15q15.1
- Coordinates
- Chromosome 15: 40,807,089–40,815,084 (GRCh38)
- Exons
- 11 exons across 8 kb
- Protein
- 471 amino acids
- Inheritance
- Autosomal recessive
- Also known as
- FLJ14840, ANCHR, MPFYVE
- MANE Select transcript
- ENST00000355341.8NM_001077268.2
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
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Familial Intrahepatic Cholestasis
- Autosomal recessive
An instance of intrahepatic cholestasis that is caused by an inherited modification of the individual's genome.
- 3 GenCC submitters rate it definitive or strong
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 ZFYVE19 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
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 2.8 kb of the gene's 8 kb; 1,416 of those bases code for the protein.
How a genome test reads ZFYVE19
3
positions in ZFYVE19 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 8 kb of ZFYVE19, introns included, not only the 2.8 kb of exons.
Genes linked to the same conditions
- ABCB11ATP binding cassette subfamily B member 11Shares 1 condition
- ABCB4ATP binding cassette subfamily B member 4Shares 1 condition
- ATP8B1ATPase phospholipid transporting 8B1Shares 1 condition
- KIF12kinesin family member 12Shares 1 condition
- MYO5Bmyosin VBShares 1 condition
- NR1H4nuclear receptor subfamily 1 group H member 4Shares 1 condition
- PSKH1protein serine kinase H1Shares 1 condition
- TJP2tight junction protein 2Shares 1 condition
- USP53ubiquitin specific peptidase 53Shares 1 condition
Traits linked to ZFYVE19
The Human Phenotype Ontology lists these as features of the rare conditions ZFYVE19 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.
- 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
Dante Labs. (n.d.). ZFYVE19 gene: zinc finger FYVE-type containing 19. Retrieved 17 October 2026, from https://dantelabs.com/genes/zfyve19
Dante Labs. ZFYVE19 gene: zinc finger FYVE-type containing 19 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/zfyve19
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