Entry Search - 608148 612313

Search: '608148 612313 (Search in: MIM number)'

Results: 2 entries.

* 608148. SPECIAL AT-RICH SEQUENCE-BINDING PROTEIN 2; SATB2
Cytogenetic location: 2q33.1, Genomic coordinates (GRCh38): 2:199,269,500-199,471,266
Matching terms: 608148
► Gene-Phenotype Relationships ► Links

Gene-Phenotype Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key
2q33.1	Glass syndrome	612313	AD	3

▲ Close

Links
Testing GTR	Genome Ensembl NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl (MANE Select) NCBI RefSeq NCBI RefSeq (MANE Select) UCSC Genome Browser	Protein HPRD Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene UCSC	Clinical Resources ClinGen Dosage ClinGen Validity MedlinePlus Genetics GTR	Variation ClinVar DECIPHER gnomAD GWAS Catalog GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB Wormbase Gene Wormbase Gene ZFin	Cellular Pathways Reactome

▲ Close

# 612313. GLASS SYNDROME; GLASS
Cytogenetic location: 2q33.1
Matching terms: 612313
► Phenotype-Gene Relationships ► ICD+ ► Links

Phenotype-Gene Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key	Gene/Locus	Gene/Locus MIM number
2q33.1	Glass syndrome	612313	AD	3	SATB2	608148

▲ Close

Links
Testing GTR EuroGentest 2q32q33 deletion syndrome SATB2-associated syndrome … SATB2-associated syndrome SATB2-associated syndrome …	Clinical Resources Clinical Trials DECIPHER EuroGentest 2q32q33 deletion syndrome SATB2-associated syndrome … SATB2-associated syndrome SATB2-associated syndrome … Gene Reviews MedlinePlus Genetics GTR OrphaNet 2q32q33 deletion syndrome SATB2-associated syndrome … SATB2-associated syndrome SATB2-associated syndrome … POSSUM	Animal Models Alliance Genome MGI Mouse Phenotype Wormbase Disease Ontology

▲ Close

ICD+
ORPHA: 251019, 251028, 576278, 576283 DO: 0060428

▲ Close

Search: 608148 612313 (Search in: MIM number)

Results: 2 entries.

* 608148. SPECIAL AT-RICH SEQUENCE-BINDING PROTEIN 2; SATB2
Cytogenetic location: 2q33.1, Genomic coordinates (GRCh38): 2:199,269,500-199,471,266
Matching terms: 608148

# 612313. GLASS SYNDROME; GLASS
Cytogenetic location: 2q33.1
Matching terms: 612313

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM^® and Online Mendelian Inheritance in Man^® are registered trademarks of the Johns Hopkins University.
Copyright^® 1966-2025 Johns Hopkins University.
Printed: March 5, 2025