CERKL Chromosome 2

CERK like autophagy regulator
200 variants 200 Health Risk

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

What This Gene Does
This gene was initially identified as a locus (RP26) associated with an autosomal recessive form of retinitis pigmentosa (arRP) disease. This gene encodes a protein with ceramide kinase-like domains, however, the protein does not phosphorylate ceramide and its target substrate is currently unknown. This protein may be a negative regulator of apoptosis in photoreceptor cells. Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD). Alternative splicing of this gene results in multiple transcript variants encoding different isoforms and non-coding transcripts.[provided by RefSeq, May 2010]
Associated Conditions (21)
Isolated macular dystrophy
Retinal dystrophy
Retinitis pigmentosa 26
Cone-rod dystrophy
Inborn genetic diseases
Retinitis pigmentosa
Malignant tumor of esophagus
Ovarian serous cystadenocarcinoma
CERKL-related disorder
Acute myeloid leukemia
Chronic lymphocytic leukemia/small lymphocytic lymphoma
Stargardt disease
Autosomal recessive retinitis pigmentosa
Severe photosensitivity
Macular dystrophy
Adult-onset night blindness
Cone dystrophy
Retinal pigment epithelial atrophy
See cases
CERKL-related retinopathy
+1 more conditions
Key Variants
RS1064797278
Conflicting classifications of pathogenicity
Isolated macular dystrophy, Retinal dystrophy, Retinitis pigmentosa 26
Health Risk
RS1201433512
Conflicting classifications of pathogenicity
Cone-rod dystrophy, Retinal dystrophy, Cone-rod dystrophy
Health Risk
RS1343928865
Conflicting classifications of pathogenicity
Retinitis pigmentosa 26, Inborn genetic diseases, Retinitis pigmentosa 26
Health Risk
RS1344137236
Conflicting classifications of pathogenicity
Retinitis pigmentosa 26, Retinal dystrophy, Retinitis pigmentosa 26
Health Risk
RS139300604
Conflicting classifications of pathogenicity
Retinal dystrophy, Retinitis pigmentosa 26, Retinal dystrophy
Health Risk
RS140898616
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Retinitis pigmentosa 26, Malignant tumor of esophagus
Health Risk
RS141389059
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Retinitis pigmentosa 26, CERKL-related disorder
Health Risk
RS141656965
Conflicting classifications of pathogenicity
Retinitis pigmentosa, CERKL-related disorder, Retinitis pigmentosa
Health Risk
RS145489428
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Retinitis pigmentosa 26, Inborn genetic diseases
Health Risk
RS146279858
Conflicting classifications of pathogenicity
Retinitis pigmentosa 26, Inborn genetic diseases, Retinitis pigmentosa 26
Health Risk
RS146913105
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Retinal dystrophy, Inborn genetic diseases
Health Risk
RS1481841151
Conflicting classifications of pathogenicity
Retinal dystrophy, Retinal dystrophy
Health Risk
All Variants (200)
RSID Category Clinical Significance Conditions
RS1064797278 Health Risk Conflicting classifications of pathogenicity Isolated macular dystrophy, Retinal dystrophy, Retinitis pigmentosa 26
RS1201433512 Health Risk Conflicting classifications of pathogenicity Cone-rod dystrophy, Retinal dystrophy, Cone-rod dystrophy
RS1343928865 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Inborn genetic diseases, Retinitis pigmentosa 26
RS1344137236 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinal dystrophy, Retinitis pigmentosa 26
RS139300604 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinitis pigmentosa 26, Retinal dystrophy
RS140898616 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Malignant tumor of esophagus
RS141389059 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, CERKL-related disorder
RS141656965 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, CERKL-related disorder, Retinitis pigmentosa
RS145489428 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Inborn genetic diseases
RS146279858 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Inborn genetic diseases, Retinitis pigmentosa 26
RS146913105 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinal dystrophy, Inborn genetic diseases
RS1481841151 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS148507801 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS149078111 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa 26
RS149346187 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinitis pigmentosa, Retinitis pigmentosa 26
RS149505471 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS150587104 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS151110889 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS1574454654 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinitis pigmentosa 26, Retinal dystrophy
RS1688188231 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS183252158 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS186100602 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS187829374 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, CERKL-related disorder, Retinitis pigmentosa
RS189638090 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS199762900 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS2105846538 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinitis pigmentosa, Retinitis pigmentosa 26
RS368855330 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, CERKL-related disorder
RS371788033 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Acute myeloid leukemia, Retinitis pigmentosa
RS372089851 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Inborn genetic diseases, Retinitis pigmentosa 26
RS375177042 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS554167374 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS556744419 Health Risk Conflicting classifications of pathogenicity
RS568128856 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinitis pigmentosa 26
RS727503857 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS745341953 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinitis pigmentosa 26
RS746220721 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinal dystrophy, Retinitis pigmentosa 26
RS750109553 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS752334385 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS758960994 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Inborn genetic diseases, Retinitis pigmentosa
RS762405291 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS765901307 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS766131721 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS768292284 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Inborn genetic diseases, Retinal dystrophy
RS771126203 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinitis pigmentosa, Retinitis pigmentosa 26
RS773497189 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinitis pigmentosa 26
RS77741297 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 26, Retinitis pigmentosa
RS779653459 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 26, Retinitis pigmentosa 26
RS863224855 Health Risk Conflicting classifications of pathogenicity
RS1044562973 Health Risk Likely pathogenic Retinitis pigmentosa 26, Retinitis pigmentosa, Retinitis pigmentosa 26
RS113425928 Health Risk Likely pathogenic
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