PITX2 Chromosome 4

Paired like homeodomain 2
75 variants 75 Health Risk

Upload your DNA to see your personal genotypes for variants in PITX2.

What This Gene Does
This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. The encoded protein acts as a transcription factor and regulates procollagen lysyl hydroxylase gene expression. This protein plays a role in the terminal differentiation of somatotroph and lactotroph cell phenotypes, is involved in the development of the eye, tooth and abdominal organs, and acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin. Mutations in this gene are associated with Axenfeld-Rieger syndrome, iridogoniodysgenesis syndrome, and sporadic cases of Peters anomaly. A similar protein in other vertebrates is involved in the determination of left-right asymmetry during development. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
PRD class homeoboxes and pseudogenes
Locus Type
gene with protein product
Location
4q25
Ensembl
ENSG00000164093
Associated Conditions (22)
Axenfeld-Rieger syndrome type 1
Inborn genetic diseases
Anterior segment dysgenesis 4
Irido-corneo-trabecular dysgenesis
Hypoplasia of the iris
PITX2-Related Eye Abnormalities
Ring dermoid of cornea
Cataract
Atrial fibrillation
familial
1
PITX2-related disorder
Uterine carcinosarcoma
Intellectual disability
Anterior segment dysgenesis
Rieger anomaly
ANTERIOR SEGMENT DYSGENESIS 4
PETERS ANOMALY SUBTYPE
Axenfeld-Rieger anomaly with partially absent eye muscles
distinctive face
+2 more conditions
Key Variants
RS104893859
Conflicting classifications of pathogenicity
Axenfeld-Rieger syndrome type 1, Inborn genetic diseases, Axenfeld-Rieger syndrome type 1
Health Risk
RS111733107
Conflicting classifications of pathogenicity
Axenfeld-Rieger syndrome type 1, Irido-corneo-trabecular dysgenesis, Hypoplasia of the iris
Health Risk
RS117231596
Conflicting classifications of pathogenicity
PITX2-Related Eye Abnormalities, Hypoplasia of the iris, Cataract
Health Risk
RS138163892
Conflicting classifications of pathogenicity
Atrial fibrillation, familial, 1
Health Risk
RS139401187
Conflicting classifications of pathogenicity
Ring dermoid of cornea, Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4
Health Risk
RS140614517
Conflicting classifications of pathogenicity
Hypoplasia of the iris, PITX2-Related Eye Abnormalities, Anterior segment dysgenesis 4
Health Risk
RS141176394
Conflicting classifications of pathogenicity
Irido-corneo-trabecular dysgenesis, PITX2-Related Eye Abnormalities, Hypoplasia of the iris
Health Risk
RS145044365
Conflicting classifications of pathogenicity
Cataract, Axenfeld-Rieger syndrome type 1, PITX2-Related Eye Abnormalities
Health Risk
RS149288560
Conflicting classifications of pathogenicity
Anterior segment dysgenesis 4, Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4
Health Risk
RS201628949
Conflicting classifications of pathogenicity
Axenfeld-Rieger syndrome type 1, Hypoplasia of the iris, Irido-corneo-trabecular dysgenesis
Health Risk
RS368647502
Conflicting classifications of pathogenicity
Irido-corneo-trabecular dysgenesis, Axenfeld-Rieger syndrome type 1, PITX2-Related Eye Abnormalities
Health Risk
RS535056127
Conflicting classifications of pathogenicity
PITX2-Related Eye Abnormalities, Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4
Health Risk
All Variants (75)
RSID Category Clinical Significance Conditions
RS2476649405 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476650692 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476650732 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476651963 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476656626 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476657038 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476657179 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4, Axenfeld-Rieger syndrome type 1
RS2476657335 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476657637 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4, Axenfeld-Rieger syndrome type 1
RS2476658099 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476658161 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2476658214 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2529772680 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2529773041 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2529773071 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2529773117 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS2529773540 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS387906810 Health Risk Pathogenic Axenfeld-Rieger syndrome type 1, Axenfeld-Rieger syndrome type 1
RS765382079 Health Risk Pathogenic Anterior segment dysgenesis 4, Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4
RS104893862 Health Risk Pathogenic/Likely pathogenic Ring dermoid of cornea, Anterior segment dysgenesis, Axenfeld-Rieger syndrome type 1
RS1553922583 Health Risk Pathogenic/Likely pathogenic ANTERIOR SEGMENT DYSGENESIS 4, PETERS ANOMALY SUBTYPE, Axenfeld-Rieger syndrome type 1
RS2110435742 Health Risk Pathogenic/Likely pathogenic Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4, Axenfeld-Rieger syndrome type 1
RS2476650016 Health Risk Pathogenic/Likely pathogenic Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly
RS772800095 Health Risk Pathogenic/Likely pathogenic Anterior segment dysgenesis 4, Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4
RS951710742 Health Risk Pathogenic/Likely pathogenic Axenfeld-Rieger syndrome type 1, Anterior segment dysgenesis 4, Axenfeld-Rieger syndrome type 1
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