Genomics England
GMS Panels
Panels
Genes and Entities

SPATA5

spermatogenesis associated 5
OMIM: 613940
PanelMode of inheritanceDetails
6 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME 616577
Green
in Early onset or syndromic epilepsy
Component of the following Super Panels:
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R59
Signed-off version 6.9
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities, OMIM:616577
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities, OMIM:616577
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 7.51
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities, OMIM:616577
Green
in Mitochondrial disorders
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
Signed-off version 7.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities, OMIM:616577
Green
in Monogenic hearing loss
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.51
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities, OMIM:616577