NALCN Chromosome 13

Sodium leak channel, non-selective
159 variants 159 Health Risk

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

What This Gene Does
This gene encodes a voltage-independent, nonselective cation channel which belongs to a family of voltage-gated sodium and calcium channels that regulates the resting membrane potential and excitability of neurons. This family is expressed throughout the nervous system and conducts a persistent sodium leak current that contributes to tonic neuronal excitability. The encoded protein forms a channelosome complex that includes G-protein-coupled receptors, UNC-79, UNC-80, NCA localization factor-1, and src family tyrosine kinases. Naturally occurring mutations in this gene are associated with infantile neuroaxonal dystrophy, infantile hypotonia with psychomotor retardation and characteristic facies (IHPRF) syndrome, and congenital contractures of the limbs and face with hypotonia and developmental delay (CLIFAHDD) syndrome. A knockout of the orthologous gene in mice results in paralysis with a severely disrupted respiratory rhythm, and lethality within 24 hours after birth. [provided by RefSeq, Apr 2017]
Gene Info
Gene Group
"Sodium leak channels, non selective|NALCN channel complex subunits"
Locus Type
gene with protein product
Location
13q32.3-q33.1
Ensembl
ENSG00000102452
Associated Conditions (23)
Autism spectrum disorder
NALCN-related disorder
Hypotonia
infantile
with psychomotor retardation and characteristic facies 1
Congenital contractures of the limbs and face
hypotonia
and developmental delay
Inborn genetic diseases
Developmental disorder
See cases
Arthrogryposis multiplex congenita
Fetal akinesia deformation sequence 1
Abnormality of the nervous system
Neurodevelopmental disorder
Intellectual disability
Seizure
Cachexia
Severe intellectual disability
Abnormal pattern of respiration
+3 more conditions
Key Variants
All Variants (159)
RSID Category Clinical Significance Conditions
RS1594211051 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS1594211244 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS1594211334 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS1594212468 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS1594218864 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS1594761911 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS2033731019 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS2034773072 Health Risk Pathogenic
RS2042316930 Health Risk Pathogenic
RS2139408863 Health Risk Pathogenic Neurodevelopmental disorder, Neurodevelopmental disorder
RS2139426437 Health Risk Pathogenic
RS2139465605 Health Risk Pathogenic Intellectual disability, Intellectual disability
RS2139597781 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS2139938691 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS2140156819 Health Risk Pathogenic Abnormality of the nervous system, Abnormality of the nervous system
RS2501833379 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS2501976400 Health Risk Pathogenic
RS2502043671 Health Risk Pathogenic
RS2502452053 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS2503581243 Health Risk Pathogenic
RS2548588606 Health Risk Pathogenic
RS376152742 Health Risk Pathogenic Inborn genetic diseases, Hypotonia, infantile
RS527789070 Health Risk Pathogenic
RS587777038 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS587777068 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS751434431 Health Risk Pathogenic
RS757674263 Health Risk Pathogenic Inborn genetic diseases, Congenital contractures of the limbs and face, hypotonia
RS766421214 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS767029163 Health Risk Pathogenic
RS772394714 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS774096141 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS779930597 Health Risk Pathogenic
RS786203984 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS786203985 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS786203986 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS786203987 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS869025188 Health Risk Pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
RS869312873 Health Risk Pathogenic Seizure, Cachexia, Severe intellectual disability
RS869312952 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS878853127 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS878853130 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS878853131 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS878853132 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS878853133 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS878853134 Health Risk Pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS972964381 Health Risk Pathogenic
RS1057516040 Health Risk Pathogenic/Likely pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS1057519433 Health Risk Pathogenic/Likely pathogenic Congenital contractures of the limbs and face, hypotonia, and developmental delay
RS1158141270 Health Risk Pathogenic/Likely pathogenic Inborn genetic diseases, Hypotonia, infantile
RS1333710212 Health Risk Pathogenic/Likely pathogenic Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
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