Entry Search - 608732 616721 - OMIM
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Search: '608732 616721 (Search in: MIM number)'
Results: 2 entries.

1:
* 608732. SOLUTE CARRIER FAMILY 39 (ZINC TRANSPORTER), MEMBER 8; SLC39A8
Cytogenetic location: 4q24, Genomic coordinates (GRCh38): 4:102,251,041-102,345,482
Matching terms: 608732
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
4q24 Congenital disorder of glycosylation, type IIn 616721 AR 3
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ICD+
SNOMEDCT: 1187171005
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2:
# 616721. CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn; CDG2N
Cytogenetic location: 4q24
Matching terms: 616721
► 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
4q24 Congenital disorder of glycosylation, type IIn 616721 AR 3 SLC39A8 608732
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Congenital disorders of glycosylation, type II - PS212066 - 26 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
1q25.3 Congenital disorder of glycosylation, type IIv AR 3 619493 EDEM3 610214
1q42.13 Congenital disorder of glycosylation, type IIt AR 3 618885 GALNT2 602274
1q42.2 ?Congenital disorder of glycosylation, type IIq AR 3 617395 COG2 606974
2p13.1 Congenital disorder of glycosylation, type IIb AR 3 606056 MOGS 601336
2q21.1 Congenital disorder of glycosylation, type IIo AR 3 616828 CCDC115 613734
4q12 Congenital disorder of glycosylation, type IIk AR 3 614727 TMEM165 614726
4q24 Congenital disorder of glycosylation, type IIn AR 3 616721 SLC39A8 608732
5q31.1 ?Congenital disorder of glycosylation, type IIz AR 3 620201 CAMLG 601118
6q15 Congenital disorder of glycosylation, type IIf AR 3 603585 SLC35A1 605634
7p22.3 ?Congenital disorder of glycosylation, type IIy AR 3 620200 GET4 612056
7q22.3 Congenital disorder of glycosylation, type IIi AR 3 613612 COG5 606821
9p21.1 Congenital disorder of glycosylation, type IId AR 3 607091 B4GALT1 137060
11p11.2 Congenital disorder of glycosylation, type IIc AR 3 266265 SLC35C1 605881
11q12.3 ?Congenital disorder of glycosylation, type IIaa AR 3 620454 STX5 603189
11q23.3 Congenital disorder of glycosylation, type IIw AD 3 619525 SLC37A4 602671
13q14.11 Congenital disorder of glycosylation, type IIl AR 3 614576 COG6 606977
13q14.13 Congenital disorder of glycosylation, type IIbb AR 3 620546 COG3 606975
14q21.3 Congenital disorder of glycosylation, type IIa AR 3 212066 MGAT2 602616
16p12.2 Congenital disorder of glycosylation, type IIe AR 3 608779 COG7 606978
16q22.1 Congenital disorder of glycosylation, type IIh 3 611182 COG8 606979
16q22.1 Congenital disorder of glycosylation, type IIj AR 3 613489 COG4 606976
17q11.2 Congenital disorder of glycosylation, type IIp AR 3 616829 TMEM199 616815
17q25.1 Congenital disorder of glycosylation, type IIg AR 3 611209 COG1 606973
Xp11.4 Congenital disorder of glycosylation, type IIr XLR 3 301045 ATP6AP2 300556
Xp11.23 Congenital disorder of glycosylation, type IIm SMo, XLD 3 300896 SLC35A2 314375
Xq28 Immunodeficiency 47 XLR 3 300972 ATP6AP1 300197
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ICD+
SNOMEDCT: 1187171005
ORPHA: 468699
DO: 0070266
▲ Close
Search: 608732 616721 (Search in: MIM number)
Results: 2 entries.

1:
* 608732. SOLUTE CARRIER FAMILY 39 (ZINC TRANSPORTER), MEMBER 8; SLC39A8
Cytogenetic location: 4q24, Genomic coordinates (GRCh38): 4:102,251,041-102,345,482
Matching terms: 608732

2:
# 616721. CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn; CDG2N
Cytogenetic location: 4q24
Matching terms: 616721


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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