Search: 'Xq25 '
Results: 37 entries.
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Genomic
context
table
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)
1: X:61,000,001
Xq
CGF1 Cognitive function-1, social 300082 [Social cognition] 300082 XL 2 imprinted locus
2: X:61,000,001
Xq
DXS435E, A11 A-11 gene 300010
3: X:61,000,001
Xq
MGR2 Migraine, familial typical, susceptibility to, 2 300125 {Migraine, familial typical, susceptibility to, 2} 300125 XL 2
4: X:61,000,001
Xq
MTBSX Mycobacterium tuberculosis, susceptibility to, X-linked 300259 {Mycobacterium tuberculosis, susceptibility, X-linked} 300259 2
5: X:76,800,001
Xq21-q25
PARK12 Parkinson disease-12 300557 {Parkinson disease 12} 300557 2 max lod with DXS1106, DXS8055, DXS1001
6: X:99,100,001
Xq22-q28
AI1E2, AIH3 Amelogenesis imperfecta, hypomaturation or hypoplastic type, X-linked 2 301201 ?Amelogenesis imperfecta, type IE, X-linked 2 301201 XL 2
7: X:103,300,001
Xq22.2-q26
XLID53, MRX53 Intellectual developmental disorder, X-linked 53 300324 Intellectual developmental disorder, X-linked 53 300324 XLR 2
8: X:109,400,001
Xq23-q26
CHDS3 Coronary heart disease, susceptibility to, 3 300464 {Coronary heart disease, susceptibility to, 3} 300464 2
9: X:109,400,001
Xq23-q27.2
MYP13 Myopia 13 300613 Myopia 13 300613 2 between DXS1210 and DXS1227
10: X:117,400,001
Xq24-q26
ADFN, ALDS Albinism-deafness syndrome 300700 Albinism-deafness syndrome 300700 XL 2 ~8cM proximal to F9

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Search: '{{ search.search.searchDescription }'}
Results: 37 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)
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