1. Panels
  2. Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic
  3. HOXA13
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Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic

Gene: HOXA13

Green List (high evidence)
HOXA13 (homeobox A13)
EnsemblGeneIds (GRCh38): ENSG00000106031
EnsemblGeneIds (GRCh37): ENSG00000106031
OMIM: 142959, Gene2Phenotype
HOXA13 is in 8 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Well established gene-disease association.
Created: 4 May 2022, 6:04 a.m. | Last Modified: 4 May 2022, 6:04 a.m.
Panel Version: 0.13702

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Hand-foot-uterus syndrome, MIM# 140000

Publications

Created: 4 May 2022, 6:04 a.m.
Last Modified: 4 May 2022, 6:04 a.m.
Panel version: Imported from Mendeliome panel version 0.13702

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • Victorian Clinical Genetics Services
  • Expert Review Green
OMIM
142959
Clinvar variants
Variants in HOXA13
Penetrance
None
Panels with this gene

History Filter Activity

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: HOXA13 was added gene: HOXA13 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: HOXA13 was set to Unknown