LBR Chromosome 1

Lamin B receptor
62 variants 62 Health Risk

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What This Gene Does
The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Tudor domain containing
Locus Type
gene with protein product
Location
1q42.12
Ensembl
ENSG00000143815
Associated Conditions (19)
Pelger-Huët anomaly
6 conditions
RHIZOMELIC SKELETAL DYSPLASIA WITH PELGER-HUET ANOMALY
Greenberg dysplasia
Sarcoma
Malignant tumor of esophagus
Lung cancer
Cervical cancer
LBR-related disorder
Inborn genetic diseases
Connective tissue disorder
Reynolds syndrome
Regressive spondylometaphyseal dysplasia
RHIZOMELIC SKELETAL DYSPLASIA WITHOUT PELGER-HUET ANOMALY
Malignant tumor of urinary bladder
Jeune thoracic dystrophy
Anadysplasia-like
spontaneously remitting spondylometaphyseal dysplasia
Acute myeloid leukemia
Key Variants
All Variants (62)
RSID Category Clinical Significance Conditions
RS1057516045 Health Risk Conflicting classifications of pathogenicity Pelger-Huët anomaly, 6 conditions, Pelger-Huët anomaly
RS1131691304 Health Risk Conflicting classifications of pathogenicity RHIZOMELIC SKELETAL DYSPLASIA WITH PELGER-HUET ANOMALY, RHIZOMELIC SKELETAL DYSPLASIA WITH PELGER-HUET ANOMALY
RS1216210580 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Sarcoma, Malignant tumor of esophagus
RS137852605 Health Risk Conflicting classifications of pathogenicity Pelger-Huët anomaly, Pelger-Huët anomaly
RS138731836 Health Risk Conflicting classifications of pathogenicity
RS138769892 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, LBR-related disorder, Greenberg dysplasia
RS140355742 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS142747191 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS144672633 Health Risk Conflicting classifications of pathogenicity
RS146953852 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Connective tissue disorder, Greenberg dysplasia
RS148541545 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, LBR-related disorder, Greenberg dysplasia
RS150177807 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS151100686 Health Risk Conflicting classifications of pathogenicity Connective tissue disorder, Connective tissue disorder
RS184378202 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS199675363 Health Risk Conflicting classifications of pathogenicity
RS199748938 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS199796274 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Inborn genetic diseases, Greenberg dysplasia
RS200180113 Health Risk Conflicting classifications of pathogenicity Reynolds syndrome, Greenberg dysplasia, Regressive spondylometaphyseal dysplasia
RS200756121 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, LBR-related disorder, Greenberg dysplasia
RS200781118 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS200998506 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, LBR-related disorder, Greenberg dysplasia
RS201003932 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Inborn genetic diseases, Reynolds syndrome
RS201626710 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2230422 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Inborn genetic diseases, Connective tissue disorder
RS2275601 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS369094974 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Connective tissue disorder, Greenberg dysplasia
RS371750924 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS372673408 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, LBR-related disorder, Greenberg dysplasia
RS374289757 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS377110126 Health Risk Conflicting classifications of pathogenicity RHIZOMELIC SKELETAL DYSPLASIA WITHOUT PELGER-HUET ANOMALY, Connective tissue disorder, Reynolds syndrome
RS549177877 Health Risk Conflicting classifications of pathogenicity
RS553408012 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, LBR-related disorder, Greenberg dysplasia
RS565288775 Health Risk Conflicting classifications of pathogenicity Connective tissue disorder, Malignant tumor of urinary bladder, Connective tissue disorder
RS61749338 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Connective tissue disorder, Greenberg dysplasia
RS746272856 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS777146629 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Greenberg dysplasia
RS80299691 Health Risk Conflicting classifications of pathogenicity Greenberg dysplasia, Connective tissue disorder, Greenberg dysplasia
RS1236962991 Health Risk Likely pathogenic Jeune thoracic dystrophy, Jeune thoracic dystrophy
RS1363715209 Health Risk Likely pathogenic Pelger-Huët anomaly, Pelger-Huët anomaly
RS2527778968 Health Risk Likely pathogenic LBR-related disorder, LBR-related disorder
RS1193780362 Health Risk Pathogenic
RS137852606 Health Risk Pathogenic Pelger-Huët anomaly, Pelger-Huët anomaly
RS1558655670 Health Risk Pathogenic RHIZOMELIC SKELETAL DYSPLASIA WITH PELGER-HUET ANOMALY, RHIZOMELIC SKELETAL DYSPLASIA WITH PELGER-HUET ANOMALY
RS192681330 Health Risk Pathogenic
RS2150942257 Health Risk Pathogenic
RS2150945343 Health Risk Pathogenic Greenberg dysplasia, Greenberg dysplasia
RS2150958142 Health Risk Pathogenic Greenberg dysplasia, Greenberg dysplasia
RS2527822176 Health Risk Pathogenic
RS2527842814 Health Risk Pathogenic
RS374343844 Health Risk Pathogenic Anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia, Greenberg dysplasia
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