KIDINS220 Chromosome 2
Kinase D interacting substrate 220
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 |