OMIM Gene/Loci: 1 - 10 of 167 on Chromosome 21 (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) |
|---|---|---|---|---|---|---|---|---|---|
|
21:0-15,000,000
21p13-q11 |
AUTS12 | Autism, susceptibility to, 12 | 610838 | {Autism susceptibility 12} | 610838 | 2 | max lod at D21S1437 | ||
|
21:3,100,000-7,000,000
21p12 |
RNR4 | Ribosomal RNA-4 | 180453 | ||||||
|
21:10,521,513-10,606,269
21p11.2 |
TPTE | Transmembrane phosphatase with tensin homology | 604336 | ||||||
|
21:13,000,000-15,000,000
21q11.2 |
NRCLP3 | Narcolepsy 3 | 609039 | Narcolepsy 3 | 609039 | Autosomal dominant | 2 | max lod at D21S1245 | |
|
21:13,000,000-15,000,000
21q11.2 |
TAM, MST | Myeloproliferative syndrome, transient (transient abnormal myelopoiesis) | 159595 | Leukemia, transient, of Down syndrome | 159595 | 2 | |||
|
21:13,610,080-13,641,584
21q11.2 |
POTED, ANKRD21, POTE | POTE ankyrin domain family, member D | 607549 | ||||||
|
21:14,108,812-14,210,952
21q11.2 |
LIPI, LPDL, PRED5 | Lipase I | 609252 | {Hypertriglyceridemia, susceptibility to} | 145750 | Autosomal dominant | 3 | Lipi | |
|
21:14,273,798-14,301,385
21q11.2 |
ABCC13 | ATP-binding cassette, subfamily C, member 13 | 608835 | ||||||
|
21:14,371,114-14,383,187
21q11.2 |
STCH | Stress 70 protein chaperone, microsome-associated, p60 | 601100 | Hspa13 | |||||
|
21:14,485,227-14,583,401
21q11.2 |
SAMSN1, HACS1 | SAM domain, SH3 domain, and nuclear localization signals 1 | 607978 | Samsn1 |