Genomics England
GMS Panels
Panels
Genes and Entities

ANOS1

anosmin 1
OMIM: 300836
PanelMode of inheritanceDetails
4 panels
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1) 308700
Green
in Hypogonadotropic hypogonadism (GMS)
R-numbers: R148
Signed-off version 3.0
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Hypogonadotropic hypogonadism type 1 (OMIM 308700)
Green
in Paediatric disorders - additional genes
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.10
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
CAKUT, Kallman syndrome, Hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), 308700
Green
in Unexplained young onset end-stage renal disease - additional genes
Component of the following Super Panels:
  • - Unexplained young onset end-stage renal disease
Signed-off version 1.0
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), OMIM:308700