Entry Search - 156100 618774 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '156100 618774 (Search in: MIM number)'
Results: 2 entries.

1:
* 156100. MN1 PROTOONCOGENE, TRANSCRIPTIONAL REGULATOR; MN1
MN1/TEL FUSION GENE, INCLUDED
Cytogenetic location: 22q12.1, Genomic coordinates (GRCh38): 22:27,748,277-27,801,756
Matching terms: 156100
 Gene-Phenotype Relationships   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
22q12.1 CEBALID syndrome 618774 AD 3
Meningioma 607174 AD 3

2:
# 618774. CEBALID SYNDROME; CEBALID
Cytogenetic location: 22q12.1
Matching terms: 618774
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
22q12.1 CEBALID syndrome 618774 AD 3 MN1 156100
ICD+
ORPHA: 693549
Search: 156100 618774 (Search in: MIM number)
Results: 2 entries.

1:
* 156100. MN1 PROTOONCOGENE, TRANSCRIPTIONAL REGULATOR; MN1
MN1/TEL FUSION GENE, INCLUDED
Cytogenetic location: 22q12.1, Genomic coordinates (GRCh38): 22:27,748,277-27,801,756
Matching terms: 156100

2:
# 618774. CEBALID SYNDROME; CEBALID
Cytogenetic location: 22q12.1
Matching terms: 618774