OMIM Gene/Loci: 1 - 10 of 422 on Chromosome 20 (All Entries)
| Location (from NCBI, GRCh38) |
Gene/Locus | Gene/Locus name | Gene/Locus MIM number |
Phenotype | Phenotype MIM number |
Inheritance | Pheno map key |
Comments | Mouse symbol (from MGI) |
|---|---|---|---|---|---|---|---|---|---|
|
20:0-28,100,000
20p |
AD8 | Alzheimer disease 8 | 607116 | Alzheimer disease 8 | 607116 | 2 | ?related to CST3 | ||
|
20:0-5,100,000
20p13 |
ALS7 | Amyotrophic lateral sclerosis 7 | 608031 | Amyotrophic lateral sclerosis 7 | 608031 | 2 | max lod at D20S103 | ||
|
20:0-28,100,000
20p |
ATOD3 | Dermatitis, atopic, 3 | 605804 | {Dermatitis, atopic, susceptibility to, 3} | 605804 | 2 | max lod at D20S115 | ||
|
20:0-25,700,000
20pter-p11.2 |
BMIQ6 | Body mass index quantitative trait locus 6 | 608559 | [Body mass index QTL6] | 608559 | 2 | near D20S482 and D20S851 | ||
|
20:0-5,100,000
20p13 |
RLS5 | Restless legs syndrome, susceptibility to, 5 | 611242 | {Restless legs syndrome 5} | 611242 | 2 | max lod at D20S849 | ||
|
20:325,570-330,227
20p13 |
SOX12, SOX22 | SRY (sex-determining region Y)-box 12 | 601947 | Sox12 | |||||
|
20:346,725-359,704
20p13 |
NRSN2 | Neurensin 2 | 610666 | Nrsn2 | |||||
|
20:380,628-397,558
20p13 |
TRIB3, NIPK, SINK, C20orf97, SKIP3 | Tribbles, Drosophila, homolog of, 3 | 607898 | Trib3 | |||||
|
20:408,049-432,138
20p13 |
RBCK1, HOIL1, PGBM1, PBMEI | RANBP-type and C3HC4-type zinc finger-containing 1 | 610924 | Polyglucosan body myopathy 1 with or without immunodeficiency | 615895 | Autosomal recessive | 3 | Rbck1 | |
|
20:435,476-462,552
20p13 |
TBC1D20, C20orf140, WARBM4 | TBC1 domain family, member 20 | 611663 | Warburg micro syndrome 4 | 615663 | Autosomal recessive | 3 | Tbc1d20 |