TYROBP Chromosome 19

Transmembrane immune signaling adaptor TYROBP
13 variants 13 Health Risk

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What This Gene Does
This gene encodes a transmembrane signaling polypeptide which contains an immunoreceptor tyrosine-based activation motif (ITAM) in its cytoplasmic domain. The encoded protein may associate with the killer-cell inhibitory receptor (KIR) family of membrane glycoproteins and may act as an activating signal transduction element. This protein may bind zeta-chain (TCR) associated protein kinase 70kDa (ZAP-70) and spleen tyrosine kinase (SYK) and play a role in signal transduction, bone modeling, brain myelination, and inflammation. Mutations within this gene have been associated with polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), also known as Nasu-Hakola disease. Its putative receptor, triggering receptor expressed on myeloid cells 2 (TREM2), also causes PLOSL. Multiple alternative transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Mar 2010]
Associated Conditions (3)
Inborn genetic diseases
TYROBP-related disorder
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
Key Variants
RS138901102
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS140188939
Conflicting classifications of pathogenicity
TYROBP-related disorder, TYROBP-related disorder
Health Risk
RS147393700
Conflicting classifications of pathogenicity
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, TYROBP-related disorder, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
Health Risk
RS199583341
Conflicting classifications of pathogenicity
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
Health Risk
RS200649978
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS200694727
Conflicting classifications of pathogenicity
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
Health Risk
RS762708303
Conflicting classifications of pathogenicity
Health Risk
RS767032012
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS386833839
Likely pathogenic
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
Health Risk
RS386833842
Likely pathogenic
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
Health Risk
RS104894732
Pathogenic
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
Health Risk
RS2513975356
Pathogenic
Health Risk
All Variants (13)
RSID Category Clinical Significance Conditions
RS138901102 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS140188939 Health Risk Conflicting classifications of pathogenicity TYROBP-related disorder, TYROBP-related disorder
RS147393700 Health Risk Conflicting classifications of pathogenicity Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, TYROBP-related disorder, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
RS199583341 Health Risk Conflicting classifications of pathogenicity Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
RS200649978 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200694727 Health Risk Conflicting classifications of pathogenicity Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
RS762708303 Health Risk Conflicting classifications of pathogenicity
RS767032012 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS386833839 Health Risk Likely pathogenic Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
RS386833842 Health Risk Likely pathogenic Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
RS104894732 Health Risk Pathogenic Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
RS2513975356 Health Risk Pathogenic
RS386833840 Health Risk Pathogenic/Likely pathogenic Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
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