Neonatal Diabetes Mellitus(NDM)
An Autosomal dominant, Autosomal recessive mode(s) within the Metabolic disorders category
Candidate Gene Information
An Autosomal dominant, Autosomal recessive mode(s) within the Metabolic disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | GLIS3/169792 | GLIS family zinc finger 3 | 9p24.2 | Chr9, NC_000009.12 (3824127..4490465, complement) |
666339 nt | 20 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | ABCC8/6833 | ATP binding cassette subfamily C member 8 | 11p15.1 | Chr11, NC_000011.10 (17392498..17476845, complement) |
84348 nt | 38 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 3 | GCK/2645 | glucokinase | 7p13 | Chr7, NC_000007.14 (44143213..44189439, complement) |
46227 nt | 15 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 4 | INS/3630 | insulin | 11p15.5 | Chr11, NC_000011.10 (2159779..2161209, complement) |
1431 nt | 3 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 5 | PDX1/3651 | pancreatic and duodenal homeobox 1 | 13q12.2 | Chr13, NC_000013.11 (27920000..27926313) |
6314 nt | 2 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 6 | KCNJ11/3767 | potassium inwardly rectifying channel subfamily J member 11 | 11p15.1 | Chr11, NC_000011.10 (17385248..17389346, complement) |
4099 nt | 4 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information Highlighted rows indicate variants are reported from India | ||||||||
| Disorder Cross-References: GTR MalaCards NORD | ||||||||