Entrez Gene ID | 140862 |
---|---|
Official Gene Symbol | ISM1 (GeneCards) |
Full name | isthmin 1 |
Location | 20p12.1 |
Other ids | Vega : OTTHUMG00000031902 MIM : 615793 HGNC : HGNC:16213 Ensembl : ENSG00000101230 |
Other names | ISM, Isthmin, C20orf82, bA149I18.1, dJ1077I2.1 |
Summary | None |
Found 4 variants in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
21467 | 140862 | ISM1 | 20 | 13254478 | 13254478 | Cockayne syndrome | HiSeq X Ten |
21553 | 140862 | ISM1 | 20 | 13293088 | 13293088 | Xeroderma Pigmentosum | HiSeq X Ten |
28550 | 140862 | ISM1 | 20 | 13303198 | 13303198 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |
28630 | 140862 | ISM1 | 20 | 13263727 | 13263727 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |