Entry Search - 120470 157600 179617 601614 614508 618264 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '120470 157600 179617 601614 614508 618264 (Search in: MIM number)'
Results: 6 entries.

1:
# 157600. MIRROR MOVEMENTS 1; MRMV1
Cytogenetic location: 18q21.2
Matching terms: 157600
 Phenotype-Gene Relationships   Phenotypic Series   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
18q21.2 Mirror movements 1 and/or agenesis of the corpus callosum 157600 AD 3 DCC 120470
ICD+
ORPHA: 238722

2:
* 120470. DCC NETRIN 1 RECEPTOR; DCC
Cytogenetic location: 18q21.2, Genomic coordinates (GRCh38): 18:52,340,197-53,535,899
Matching terms: 120470
 Gene-Phenotype Relationships   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
18q21.2 Colorectal cancer, somatic 114500 3
Esophageal carcinoma, somatic 133239 3
Gaze palsy, familial horizontal, with progressive scoliosis, 2 617542 AR 3
Mirror movements 1 and/or agenesis of the corpus callosum 157600 AD 3

3:
# 614508. MIRROR MOVEMENTS 2; MRMV2
Cytogenetic location: 15q15.1
Matching terms: 614508
 Phenotype-Gene Relationships   Phenotypic Series   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
15q15.1 Mirror movements 2 614508 AD 3 RAD51 179617
ICD+
ORPHA: 238722

4:
# 618264. MIRROR MOVEMENTS 4; MRMV4
Cytogenetic location: 17p13.1
Matching terms: 618264
 Phenotype-Gene Relationships   Phenotypic Series   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
17p13.1 Mirror movements 4 618264 AD 3 NTN1 601614
ICD+
ORPHA: 238722

5:
* 179617. RAD51 RECOMBINASE; RAD51
Cytogenetic location: 15q15.1, Genomic coordinates (GRCh38): 15:40,694,733-40,732,340
Matching terms: 179617
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
15q15.1 {Breast cancer, susceptibility to} 114480 AD, SMu 3
Fanconi anemia, complementation group R 617244 AD 3
Mirror movements 2 614508 AD 3
ICD+
SNOMEDCT: 254843006

6:
* 601614. NETRIN 1; NTN1
Cytogenetic location: 17p13.1, Genomic coordinates (GRCh38): 17:9,003,087-9,244,000
Matching terms: 601614
 Gene-Phenotype Relationships   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
17p13.1 Mirror movements 4 618264 AD 3
Search: 120470 157600 179617 601614 614508 618264 (Search in: MIM number)
Results: 6 entries.

1:
# 157600. MIRROR MOVEMENTS 1; MRMV1
Cytogenetic location: 18q21.2
Matching terms: 157600

2:
* 120470. DCC NETRIN 1 RECEPTOR; DCC
Cytogenetic location: 18q21.2, Genomic coordinates (GRCh38): 18:52,340,197-53,535,899
Matching terms: 120470

3:
# 614508. MIRROR MOVEMENTS 2; MRMV2
Cytogenetic location: 15q15.1
Matching terms: 614508

4:
# 618264. MIRROR MOVEMENTS 4; MRMV4
Cytogenetic location: 17p13.1
Matching terms: 618264

5:
* 179617. RAD51 RECOMBINASE; RAD51
Cytogenetic location: 15q15.1, Genomic coordinates (GRCh38): 15:40,694,733-40,732,340
Matching terms: 179617

6:
* 601614. NETRIN 1; NTN1
Cytogenetic location: 17p13.1, Genomic coordinates (GRCh38): 17:9,003,087-9,244,000
Matching terms: 601614