Trait

Ureterocele

A ureterocele is a congenital saccular dilatation of the distal segment of the ureter.

Body system: Abnormality of the genitourinary system

This page as data

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library(jsonlite)

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page <- fromJSON(url)
page$trait$name

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32 genes linked to Ureterocele

Changes in these genes cause rare conditions in which Ureterocele is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.

Gene	How often it is seen	Conditions
ITGA6integrin subunit alpha 6	Often (30–79%)	In 1 condition
ITGB4integrin subunit beta 4	Often (30–79%)	In 2 conditions
HNF1BHNF1 homeobox B	Sometimes (5–29%)	In 1 condition
LAMA3laminin subunit alpha 3	Sometimes (5–29%)	In 1 condition
LAMB3laminin subunit beta 3	Sometimes (5–29%)	In 1 condition
LAMC2laminin subunit gamma 2	Sometimes (5–29%)	In 1 condition
LHX1LIM homeobox 1	Sometimes (5–29%)	In 1 condition
MAPRE2microtubule associated protein RP/EB family member 2	Sometimes (5–29%)	In 1 condition
PLECplectin	Sometimes (5–29%)	In 1 condition
ARXaristaless related homeobox	Rarely (1–4%)	In 1 condition
CACNA1Ecalcium voltage-gated channel subunit alpha1 E	Rarely (1–4%)	In 1 condition
CASKcalcium/calmodulin dependent serine protein kinase	Rarely (1–4%)	In 1 condition
CDKL5cyclin dependent kinase like 5	Rarely (1–4%)	In 1 condition
DMXL2Dmx like 2	Rarely (1–4%)	In 1 condition
GNAO1G protein subunit alpha o1	Rarely (1–4%)	In 1 condition
GRIN1glutamate ionotropic receptor NMDA type subunit 1	Rarely (1–4%)	In 1 condition
GRM7glutamate metabotropic receptor 7	Rarely (1–4%)	In 1 condition
KCNA1potassium voltage-gated channel subfamily A member 1	Rarely (1–4%)	In 1 condition
LGI1leucine rich glioma inactivated 1	Rarely (1–4%)	In 1 condition
NEUROD2neuronal differentiation 2	Rarely (1–4%)	In 1 condition
PIGPphosphatidylinositol glycan anchor biosynthesis class P	Rarely (1–4%)	In 1 condition
PIGQphosphatidylinositol glycan anchor biosynthesis class Q	Rarely (1–4%)	In 1 condition
PNKPpolynucleotide kinase 3'-phosphatase	Rarely (1–4%)	In 1 condition
RHOBTB2Rho related BTB domain containing 2	Rarely (1–4%)	In 1 condition
SCN1Bsodium voltage-gated channel beta subunit 1	Rarely (1–4%)	In 1 condition
SCN2Asodium voltage-gated channel alpha subunit 2	Rarely (1–4%)	In 1 condition
SIK1salt inducible kinase 1	Rarely (1–4%)	In 1 condition
SLC25A22solute carrier family 25 member 22	Rarely (1–4%)	In 1 condition
SLC32A1solute carrier family 32 member 1	Rarely (1–4%)	In 1 condition
TRIM8tripartite motif containing 8	Rarely (1–4%)	In 1 condition
PEX6peroxisomal biogenesis factor 6	Not recorded	In 1 condition
TP63tumor protein p63	Not recorded	In 1 condition

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Broader traits

Abnormal ureter morphology

Where this comes from

The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
Data release 2026.10.16-c6eea6bf.

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