KIDINS220 Chromosome 2

Kinase D interacting substrate 220
81 variants 81 Health Risk

Upload your DNA to see your personal genotypes for variants in KIDINS220.

What This Gene Does
This gene encodes a transmembrane protein that is preferentially expressed in the nervous system where it controls neuronal cell survival, differentiation into exons and dendrites, and synaptic plasticity. The encoded protein interacts with membrane receptors, cytosolic signaling components, and cytoskeletal proteins, serving as a scaffold that mediates crosstalk between the neurotrophin pathway and several other intracellular signaling pathways. Aberrant expression of this gene is associated with the onset of various neuropsychiatric disorders and neurodegenerative diseases, including Alzheimer's disease. Naturally occurring mutations in this gene are associated with a syndrome characterized by spastic paraplegia, intellectual disability, nystagmus and obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]
Gene Info
Gene Group
Ankyrin repeat domain containing
Locus Type
gene with protein product
Location
2p25.1
Ensembl
ENSG00000134313
Associated Conditions (14)
Inborn genetic diseases
KIDINS220-related disorder
Nonpapillary renal cell carcinoma
Spastic paraplegia
intellectual disability
nystagmus
and obesity
Ventriculomegaly and arthrogryposis
Early onset severe obesity
Kabuki syndrome 1
Ovarian serous cystadenocarcinoma
Clear cell carcinoma of kidney
Cerebral palsy
KCNA1-related disorder
Key Variants
RS139252608
Conflicting classifications of pathogenicity
Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
Health Risk
RS146753792
Conflicting classifications of pathogenicity
Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
Health Risk
RS181372484
Conflicting classifications of pathogenicity
Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
Health Risk
RS182521570
Conflicting classifications of pathogenicity
KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
Health Risk
RS185330217
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS199536870
Conflicting classifications of pathogenicity
KIDINS220-related disorder, Inborn genetic diseases, Nonpapillary renal cell carcinoma
Health Risk
RS199682748
Conflicting classifications of pathogenicity
KIDINS220-related disorder, KIDINS220-related disorder
Health Risk
RS199962701
Conflicting classifications of pathogenicity
Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
Health Risk
RS199990643
Conflicting classifications of pathogenicity
KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
Health Risk
RS200081016
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS200104720
Conflicting classifications of pathogenicity
Inborn genetic diseases, Spastic paraplegia, intellectual disability
Health Risk
RS200846235
Conflicting classifications of pathogenicity
Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
Health Risk
All Variants (81)
RSID Category Clinical Significance Conditions
RS139252608 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS146753792 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS181372484 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS182521570 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS185330217 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS199536870 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, Nonpapillary renal cell carcinoma
RS199682748 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, KIDINS220-related disorder
RS199962701 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS199990643 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS200081016 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200104720 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Spastic paraplegia, intellectual disability
RS200846235 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS200899102 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS201077051 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Ventriculomegaly and arthrogryposis, Early onset severe obesity
RS201363981 Health Risk Conflicting classifications of pathogenicity Ventriculomegaly and arthrogryposis, Ventriculomegaly and arthrogryposis
RS201478192 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS201557833 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, KIDINS220-related disorder
RS201737651 Health Risk Conflicting classifications of pathogenicity Spastic paraplegia, intellectual disability, nystagmus
RS201780168 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS202036173 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS202094672 Health Risk Conflicting classifications of pathogenicity Spastic paraplegia, intellectual disability, nystagmus
RS202154759 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS2527406250 Health Risk Conflicting classifications of pathogenicity Kabuki syndrome 1, Spastic paraplegia, intellectual disability
RS367886108 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, KIDINS220-related disorder
RS368903999 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS370574933 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Spastic paraplegia, intellectual disability
RS374716369 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Spastic paraplegia, intellectual disability
RS529873727 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS538261513 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS749584082 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS749707556 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS752601543 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS753935388 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS764865735 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS767119807 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Ovarian serous cystadenocarcinoma, Early onset severe obesity
RS769837969 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS772773265 Health Risk Conflicting classifications of pathogenicity Clear cell carcinoma of kidney, Clear cell carcinoma of kidney
RS775189420 Health Risk Conflicting classifications of pathogenicity Early onset severe obesity, Early onset severe obesity
RS775892620 Health Risk Conflicting classifications of pathogenicity Ventriculomegaly and arthrogryposis, KIDINS220-related disorder, Ventriculomegaly and arthrogryposis
RS776227065 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, KIDINS220-related disorder, Inborn genetic diseases
RS776518265 Health Risk Conflicting classifications of pathogenicity KIDINS220-related disorder, Inborn genetic diseases, KIDINS220-related disorder
RS777873298 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778173916 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778339888 Health Risk Conflicting classifications of pathogenicity Spastic paraplegia, intellectual disability, nystagmus
RS77973158 Health Risk Conflicting classifications of pathogenicity Spastic paraplegia, intellectual disability, nystagmus
RS1219040737 Health Risk Likely pathogenic
RS1311041431 Health Risk Likely pathogenic
RS1553305080 Health Risk Likely pathogenic Spastic paraplegia, intellectual disability, nystagmus
RS1572428834 Health Risk Likely pathogenic
RS1664160163 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
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