Gene: Flcn (folliculin) Rattus norvegicus | ![]() Analyze |
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Imported Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:12204536 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube syndrome | ClinVar | PMID:12204536 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:23891399 PMID:28492532 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18234728 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18234728 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:14627671 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:19802896 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:28202063 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:22703879 PMID:28492532 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:15852235 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18234728 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:15805188 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube syndrome | ClinVar | PMID:12204536 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:12843323 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:25741868 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18234728 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:15852235 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by OMIM:135150 | ClinVar | PMID:15657874 PMID:19562744 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube syndrome | ClinVar | PMID:12204536 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:24033266 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:14627671 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18794106 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:24033266 PMID:25741868 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18234728 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18794106 PMID:21506000 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18234728 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by OMIM:135150 | ClinVar | PMID:18234728 PMID:19562744 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by OMIM:135150 | ClinVar | PMID:23414156 PMID:24033266 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by OMIM:135150 | ClinVar | PMID:25637381 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:12204536 PMID:23784378 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:22703879 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:15852235 PMID:18234728 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by OMIM:135150 | ClinVar | PMID:12204536 PMID:19562744 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:22703879 PMID:24728327 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by OMIM:135150 | ClinVar | | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18505456 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:11100034 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:24728327 PMID:28492532 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by OMIM:135150 | ClinVar | PMID:12204536 PMID:24033266 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:23264078 more ... | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:28492532 | Birt-Hogg-Dube Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube Syndrome | ClinVar | PMID:18794106 more ... | Carcinoma, Renal Cell | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Renal cell carcinoma | ClinVar | PMID:18794106 more ... | Chromosome 17, Trisomy 17p11 2 | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Chromosome 17, trisomy 17p11 2 | ClinVar | PMID:28837307 | colon cancer | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Colon cancer | ClinVar | PMID:12843323 | colon cancer | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Colon cancer | ClinVar | PMID:12843323 more ... | colon carcinoma | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Colonic carcinoma | ClinVar | PMID:12843323 | colon carcinoma | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Colonic carcinoma | ClinVar | PMID:12843323 more ... | Colonic Neoplasms | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Colon cancer | ClinVar | PMID:12843323 | Colonic Neoplasms | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Colon cancer | ClinVar | PMID:12843323 more ... | colorectal cancer | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Colorectal cancer | ClinVar | PMID:12843323 | colorectal cancer | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Colorectal cancer | ClinVar | PMID:12843323 more ... | cutaneous malignant melanoma, susceptibility to, 1 | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Malignant melanoma | ClinVar | PMID:28492532 | Melanoma | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Malignant melanoma, somatic | ClinVar | PMID:28492532 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18794106 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:22679611 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:12204536 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:12204536 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18234728 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:15852235 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18234728 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:20403193 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:18234728 PMID:28151982 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:14627671 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:19802896 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:28202063 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:15852235 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:18505456 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18234728 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:17611575 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:15805188 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:12204536 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:12843323 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18234728 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:15852235 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:12204536 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:24728327 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:24033266 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18794106 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:15657874 PMID:19562744 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:15805188 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18234728 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18794106 PMID:21506000 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18234728 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:18505456 PMID:19802896 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:12204536 PMID:23784378 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:22703879 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by null | ClinVar | | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:18505456 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:11100034 more ... | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:24728327 PMID:28492532 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:18579543 PMID:22068306 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar | PMID:15852235 PMID:18234728 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:28492532 | Neoplastic Syndromes, Hereditary | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary | ClinVar | PMID:23264078 more ... | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:24728327 PMID:28492532 | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Pneumothorax, primary spontaneous | ClinVar | PMID:20413710 | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Pneumothorax, primary spontaneous | ClinVar | PMID:17496196 PMID:19562744 | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Pneumothorax, primary spontaneous | ClinVar | PMID:15657874 PMID:19562744 | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:14627671 more ... | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Pneumothorax, primary spontaneous | ClinVar | PMID:18505456 PMID:19562744 | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Pneumothorax, primary spontaneous | ClinVar | PMID:12204536 more ... | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:12843323 more ... | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:25741868 | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:24033266 more ... | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:14627671 more ... | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:24033266 PMID:25741868 | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:22703879 more ... | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Pneumothorax, primary spontaneous | ClinVar | PMID:18505456 more ... | pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Spontaneous pneumothorax | ClinVar | PMID:28492532 | primary spontaneous pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by null | ClinVar | PMID:15657874 PMID:19562744 | primary spontaneous pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Pneumothorax, primary spontaneous | ClinVar | PMID:12204536 more ... | primary spontaneous pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by OMIM:173600 | ClinVar | | primary spontaneous pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by null | ClinVar | PMID:20413710 | primary spontaneous pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Pneumothorax, primary spontaneous | ClinVar | PMID:18505456 more ... | primary spontaneous pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by null | ClinVar | PMID:17496196 PMID:19562744 | primary spontaneous pneumothorax | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by null | ClinVar | PMID:18505456 PMID:19562744 | Tumor Predisposition Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Tumor predisposition syndrome | ClinVar | PMID:11100034 more ... | Tumor Predisposition Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Tumor predisposition syndrome | ClinVar | PMID:28492532 | Tumor Predisposition Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Tumor predisposition syndrome | ClinVar | PMID:20403193 | Tumor Predisposition Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Tumor predisposition syndrome | ClinVar | PMID:15852235 | Tumor Predisposition Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Tumor predisposition syndrome | ClinVar | PMID:18234728 more ... | Tumor Predisposition Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Tumor predisposition syndrome | ClinVar | | Tumor Predisposition Syndrome | | ISO | RGD:1604509 | 8554872 | ClinVar Annotator: match by term: Tumor predisposition syndrome | ClinVar | PMID:15657874 PMID:19562744 | |
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1. | Goberdhan DC, etal., Cell Metab. 2016 Apr 12;23(4):580-9. doi: 10.1016/j.cmet.2016.03.013. |
2. | Nickerson ML, etal., Cancer Cell. 2002 Aug;2(2):157-64. |
3. | Okimoto K, etal., Proc Natl Acad Sci U S A 2004 Feb 17;101(7):2023-7. Epub 2004 Feb 09. |
4. | OMIM Disease Annotation Pipeline |
5. | Pipeline to import KEGG annotations from KEGG into RGD |
6. | RGD automated data pipeline |
7. | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
8. | RGD automated import pipeline for gene-chemical interactions |
9. | RGD comprehensive gene curation |
10. | Wang L, etal., FEBS Lett. 2010 Jan 4;584(1):39-43. doi: 10.1016/j.febslet.2009.11.033. Epub . |
PubMed | 12477932 15489334 16447066 17028174 18182616 18663353 18974783 19234517 19695222 19843504 19850877 20573232 21209915 21258407 22709692 22965878 23150719 25126726 |
Flcn has been annotated in the following RGD Disease Portals. |
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Flcn (Rattus norvegicus - Norway rat) |
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FLCN (Homo sapiens - human) |
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Flcn (Mus musculus - house mouse) |
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Flcn (Chinchilla lanigera - long-tailed chinchilla) |
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FLCN (Pan paniscus - bonobo/pygmy chimpanzee) |
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FLCN (Canis lupus familiaris - dog) |
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Flcn (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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PMC357045P1 |
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PMC357045P6 |
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RH130087 |
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PMC357045P10 |
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PMC357045P11 |
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PMC357045P12 |
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PMC357045P2 |
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PMC357045P3 |
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PMC357045P4 |
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PMC357045P5 |
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PMC357045P7 |
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PMC357045P8 |
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PMC357045P9 |
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The following QTLs overlap with this region. | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer | ![]() | Gviewer |
The detailed report is available here: | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer |
miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/). For more information about miRGate, see PMID:25858286 or access the full paper here. |
RefSeq Transcripts | NM_199390 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
XM_006246489 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006246490 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017597267 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017597269 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017597270 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AAHX01064213 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AAHX01064214 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AAHX01064215 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AB096213 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AC097038 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC085848 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH473948 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
FQ212214 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_199390 | ||||||||||||||||||||||||
RefSeq Status: | PROVISIONAL | ||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||
Position: |
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Sequence: |
GGACTCTTGGCTTGGAAGAGCGTAACGCAGCACAGCGTGGCTCGGCGCATCCTAGTCTCCTGTChide sequence |
RefSeq Acc Id: | XM_006246490 | ||||||||||||||
RefSeq Status: | |||||||||||||||
Type: | CODING | ||||||||||||||
Position: |
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Sequence: |
CGATTGTTGCCGAGGGCGCTTGGACTCTTGGCTTGGAAGAGCGTAACGCAGCACAGCGTGGCTChide sequence |
RefSeq Acc Id: | XM_006246489 | ||||||||||||||
RefSeq Status: | |||||||||||||||
Type: | CODING | ||||||||||||||
Position: |
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Sequence: |
TCACGCGCTAGACTCGGTGCAAGGGCCTGCGGAACGGGCGAGGGGCAGAACGGTGGCGACAGCChide sequence |
RefSeq Acc Id: | XM_006246491 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
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Sequence: |
ACCAGGGAGAGGGAGGTGACAGGTTCCATCCCTCGGTCGGGGTAATTGCTGTAGTTTGAACACThide sequence |
RefSeq Acc Id: | XM_006246492 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
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Sequence: |
AAAAAAAAAAAAAAAAAGAATTCAAGTATGGTGGTGAGGAGACTGTCTTCAGCTTGGAAAAGTThide sequence |
RefSeq Acc Id: | XM_008767817 |
RefSeq Status: | |
Type: | CODING |
Position: | No map positions available. |
Sequence: |
GTCACGCGCTAGACTCGGTGCAAGGGCCTGCGGAACGGGCGAGGGGCAGAACGGTGGCGACAGChide sequence |
RefSeq Acc Id: | XM_008767816 |
RefSeq Status: | |
Type: | CODING |
Position: | No map positions available. |
Sequence: |
GGGTCACGCGCTAGACTCGGTGCAAGGGCCTGCGGAACGGGCGAGGGGCAGAACGGTGGCGACAhide sequence |
RefSeq Acc Id: | XM_017597270 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
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RefSeq Acc Id: | XM_017597267 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
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RefSeq Acc Id: | XM_017597269 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
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Protein RefSeqs | NP_955422 | (Get FASTA) | NCBI Sequence Viewer |
XP_006246551 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006246552 | (Get FASTA) | NCBI Sequence Viewer | |
XP_017452756 | (Get FASTA) | NCBI Sequence Viewer | |
XP_017452758 | (Get FASTA) | NCBI Sequence Viewer | |
XP_017452759 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAH85848 | (Get FASTA) | NCBI Sequence Viewer |
BAD01656 | (Get FASTA) | NCBI Sequence Viewer | |
EDM04621 | (Get FASTA) | NCBI Sequence Viewer | |
Q76JQ2 | (Get FASTA) | NCBI Sequence Viewer |
Protein Acc Id: | NP_955422 |
Sequence: |
MNAIVALCHFCELHGPRTLFCTEVLHAPLPQGAGSGDSPGQVEQAEEEEGGIQMSSRVRAHSPAhide sequence |
Protein Acc Id: | XP_006246552 |
Peptide Label: | isoform X1 |
Sequence: |
MNAIVALCHFCELHGPRTLFCTEVLHAPLPQGAGSGDSPGQVEQAEEEEGGIQMSSRVRAHSPAhide sequence |
Protein Acc Id: | XP_006246551 |
Peptide Label: | isoform X1 |
Sequence: |
MNAIVALCHFCELHGPRTLFCTEVLHAPLPQGAGSGDSPGQVEQAEEEEGGIQMSSRVRAHSPAhide sequence |
Protein Acc Id: | XP_006246553 |
Peptide Label: | isoform X1 |
Sequence: |
MNAIVALCHFCELHGPRTLFCTEVLHAPLPQGAGSGDSPGQVEQAEEEEGGIQMSSRVRAHSPAhide sequence |
Protein Acc Id: | XP_006246554 |
Sequence: |
MNAIVALCHFCELHGPRTLFCTEVLHAPLPQGAGSGDSPGQVEQAEEEEGGIQMSSRVRAHSPAhide sequence |
Protein Acc Id: | XP_008766039 |
Peptide Label: | isoform X3 |
Sequence: |
MNAIVALCHFCELHGPRTLFCTEVLHAPLPQGAGSGDSPGQVEQAEEEEGGIQMSSRVRAHSPAhide sequence |
Protein Acc Id: | XP_008766038 |
Peptide Label: | isoform X2 |
Sequence: |
MNAIVALCHFCELHGPRTLFCTEVLHAPLPQGAGSGDSPGQVEQAEEEEGGIQMSSRVRAHSPAhide sequence |
Protein Acc Id: | XP_017452759 |
Peptide Label: | isoform X3 |
Protein Acc Id: | XP_017452756 |
Peptide Label: | isoform X1 |
Protein Acc Id: | XP_017452758 |
Peptide Label: | isoform X2 |
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Database | Acc Id | Source(s) |
Ensembl Genes | ENSRNOG00000003302 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Protein | ENSRNOP00000004412 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENSRNOP00000075720 | ENTREZGENE, UniProtKB/TrEMBL | |
Ensembl Transcript | ENSRNOT00000004412 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENSRNOT00000091052 | ENTREZGENE, UniProtKB/TrEMBL | |
IMAGE_CLONE | IMAGE:7189414 | IMAGE-MGC_LOAD |
InterPro | FLCN/SMCR8_DENN | UniProtKB/Swiss-Prot |
Folliculin | UniProtKB/Swiss-Prot | |
Folliculin_C | UniProtKB/Swiss-Prot | |
Folliculin_N | UniProtKB/Swiss-Prot | |
KEGG Report | rno:303185 | UniProtKB/Swiss-Prot |
MGC_CLONE | MGC:94558 | IMAGE-MGC_LOAD |
NCBI Gene | 303185 | ENTREZGENE |
PANTHER | PTHR31441 | UniProtKB/Swiss-Prot |
Pfam | Folliculin | UniProtKB/Swiss-Prot |
Folliculin_C | UniProtKB/Swiss-Prot | |
PhenoGen | Flcn | PhenoGen |
PROSITE | DENN_FLCN_SMCR8 | UniProtKB/Swiss-Prot |
UniGene | Rn.12799 | ENTREZGENE |
UniProt | A0A0G2KBA8 | ENTREZGENE, UniProtKB/TrEMBL |
FLCN_RAT | UniProtKB/Swiss-Prot, ENTREZGENE |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
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2005-07-08 | Flcn | folliculin | Bhd | Symbol updated | 1299863 | APPROVED |
Note Type | Note | Reference |
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gene_disease | in heterozygotes, a germline insertion of one nucleotide resulting in a nonsense mutation gives rise to renal adenocarcinomas by the age of 6 months; homozygosity is lethal at an early stage of embryogenesis | 1302869 |
gene_homology | amino acid sequence is 93% and 97% homologous to human and mouse folliculin, respectively | 1302869 |
gene_mutations_overexpression | 10 of 11 renal carcinomas showed a loss of heterozygosity at the Bhd locus and the one LOH-negative case displayed a spontaneous nonsense point mutation at the second Bhd locus | 1302869 |
More on Flcn | |
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Alliance Gene |
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NCBI Gene |
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Ensembl Gene |
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JBrowse: rn5 rn6 |
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NCBI Genome Data Viewer |
RGD Object Information | |
RGD ID: | 735088 |
Created: | 2004-02-05 |
Species: | Rattus norvegicus |
Last Modified: | 2018-04-10 |
Status: | ACTIVE |
© Medical College of Wisconsin
RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.