|
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) |
|---|---|---|---|---|---|---|---|---|---|
|
X:61,000,001-156,040,895
Xq |
CGF1 | Cognitive function-1, social | 300082 | [Social cognition] | 300082 | X-linked | 2 | imprinted locus | |
|
X:61,000,001-156,040,895
Xq |
DXS435E, A11 | A-11 gene | 300010 | ||||||
|
X:61,000,001-156,040,895
Xq |
MGR2 | Migraine, familial typical, susceptibility to, 2 | 300125 | {Migraine, familial typical, susceptibility to, 2} | 300125 | X-linked | 2 | ||
|
X:61,000,001-156,040,895
Xq |
MTBSX | Mycobacterium tuberculosis, susceptibility to, X-linked | 300259 | {Mycobacterium tuberculosis, susceptibility, X-linked} | 300259 | 2 | |||
|
X:76,800,001-129,500,000
Xq21-q25 |
PARK12 | Parkinson disease-12 | 300557 | {Parkinson disease 12} | 300557 | 2 | max lod with DXS1106, DXS8055, DXS1001 | ||
|
X:99,100,001-156,040,895
Xq22-q28 |
AI1E2, AIH3 | Amelogenesis imperfecta, hypomaturation or hypoplastic type, X-linked 2 | 301201 | ?Amelogenesis imperfecta, type IE, X-linked 2 | 301201 | X-linked | 2 | ||
|
X:103,300,001-138,900,000
Xq22.2-q26 |
XLID53, MRX53 | Intellectual developmental disorder, X-linked 53 | 300324 | Intellectual developmental disorder, X-linked 53 | 300324 | X-linked recessive | 2 | ||
|
X:109,400,001-138,900,000
Xq23-q26 |
CHDS3 | Coronary heart disease, susceptibility to, 3 | 300464 | {Coronary heart disease, susceptibility to, 3} | 300464 | 2 | |||
|
X:109,400,001-143,000,000
Xq23-q27.2 |
MYP13 | Myopia 13 | 300613 | Myopia 13 | 300613 | 2 | between DXS1210 and DXS1227 | ||
|
X:117,400,001-138,900,000
Xq24-q26 |
ADFN, ALDS | Albinism-deafness syndrome | 300700 | Albinism-deafness syndrome | 300700 | X-linked | 2 | ~8cM proximal to F9 |