OMIM Gene/Loci: 1 - 10 of 372 on Chromosome 22 (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) |
|---|---|---|---|---|---|---|---|---|---|
|
22:0-15,000,000
22p |
ZNF72 | Zinc finger protein-72 (Cos8) | 194546 | ||||||
|
22:4,300,000-9,400,000
22p12 |
RNR5 | Ribosomal RNA-5 | 180454 | ||||||
|
22:11,303,799-11,486,223
22p11.2 |
ZNF73 | Zinc finger protein-73 (Cos12) | 194547 | ||||||
|
22:15,000,000-25,500,000
22q11 |
ACF | Asymmetric crying facies (Cayler cardiofacial syndrome) | 125520 | Cayler cardiofacial syndrome | 125520 | Autosomal dominant | 2 | ||
|
22:15,000,000-25,500,000
22q11 |
CECR, CES | Cat eye syndrome | 115470 | Cat eye syndrome | 115470 | Autosomal dominant | 4 | partial tetrasomy of 22q11 | |
|
22:15,000,000-25,500,000
22q11.1-q11.2 |
GGT1, GTG | Gamma-glutamyltransferase-1 | 231950 | Glutathioninuria | 1 | minor peak, q13.1 | |||
|
22:15,000,000-37,200,000
22q11-q12 |
LRE1, L1.2 | Line-1.2 retrotransposable element | 151626 | ||||||
|
22:15,690,025-15,721,630
22q11.1 |
POTEH, POTE22, ACTBL1 | POTE ankyrin domain family, member H | 608913 | ||||||
|
22:16,783,411-16,825,411
22q11.1 |
XKR3, XTES, XRG3 | X Kell blood group precursor-related family, member 3 | 611674 | ||||||
|
22:17,084,958-17,115,693
22q11.1 |
IL17RA, IL17R, IMD51 | Interleukin 17 receptor A | 605461 | Immunodeficiency 51 | 613953 | Autosomal recessive | 3 | Il17ra |