Entry Search - 261540 610308 - OMIM
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Search: '261540 610308 (Search in: MIM number)'
Results: 2 entries.

1:
* 610308. BETA-3-GLUCOSYLTRANSFERASE; B3GLCT
Cytogenetic location: 13q12.3, Genomic coordinates (GRCh38): 13:31,199,975-31,332,276
Matching terms: 610308
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
13q12.3 Peters-plus syndrome 261540 AR 3
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ICD+
SNOMEDCT: 449817000
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2:
# 261540. PETERS-PLUS SYNDROME; PTRPLS
Cytogenetic location: 13q12.3
Matching terms: 261540
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
13q12.3 Peters-plus syndrome 261540 AR 3 B3GLCT 610308
▲ Close
ICD+
SNOMEDCT: 449817000
ORPHA: 709
DO: 0080201
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Search: 261540 610308 (Search in: MIM number)
Results: 2 entries.

1:
* 610308. BETA-3-GLUCOSYLTRANSFERASE; B3GLCT
Cytogenetic location: 13q12.3, Genomic coordinates (GRCh38): 13:31,199,975-31,332,276
Matching terms: 610308

2:
# 261540. PETERS-PLUS SYNDROME; PTRPLS
Cytogenetic location: 13q12.3
Matching terms: 261540


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.

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