IGLL1 Chromosome 22

Immunoglobulin lambda like polypeptide 1
7 variants 7 Health Risk

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What This Gene Does
The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"CD molecules|C1-set domain containing"
Locus Type
gene with protein product
Location
22q11.23
Ensembl
ENSG00000128322
Associated Conditions (3)
Agammaglobulinemia 2
autosomal recessive
IGLL1-related condition
Key Variants
All Variants (7)
RSID Category Clinical Significance Conditions
RS1064422 Health Risk Conflicting classifications of pathogenicity Agammaglobulinemia 2, autosomal recessive, IGLL1-related condition
RS112775194 Health Risk Conflicting classifications of pathogenicity Agammaglobulinemia 2, autosomal recessive, Agammaglobulinemia 2
RS114766892 Health Risk Conflicting classifications of pathogenicity Agammaglobulinemia 2, autosomal recessive, Agammaglobulinemia 2
RS139491925 Health Risk Conflicting classifications of pathogenicity Agammaglobulinemia 2, autosomal recessive, Agammaglobulinemia 2
RS143780139 Health Risk Conflicting classifications of pathogenicity Agammaglobulinemia 2, autosomal recessive, Agammaglobulinemia 2
RS149986237 Health Risk Conflicting classifications of pathogenicity Agammaglobulinemia 2, autosomal recessive, Agammaglobulinemia 2
RS532338576 Health Risk Conflicting classifications of pathogenicity Agammaglobulinemia 2, autosomal recessive, Agammaglobulinemia 2
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