Entry Search - 601501 614203 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '601501 614203 (Search in: MIM number)'
Results: 2 entries.

1:
* 601501. VPS35 RETROMER COMPLEX COMPONENT; VPS35
Cytogenetic location: 16q11.2, Genomic coordinates (GRCh38): 16:46,656,132-46,689,178
Matching terms: 601501
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
16q11.2 {Parkinson disease 17} 614203 AD 3
▲ Close

2:
# 614203. PARKINSON DISEASE 17; PARK17
Cytogenetic location: 16q11.2
Matching terms: 614203
► 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
16q11.2 {Parkinson disease 17} 614203 AD 3 VPS35 601501
▲ Close
Parkinson disease - PS168600 - 33 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
1p36.23 Parkinson disease 7, autosomal recessive early-onset AR 3 606324 DJ1 602533
1p36.13 Kufor-Rakeb syndrome AR 3 606693 ATP13A2 610513
1p36.12 Parkinson disease 6, early onset AR 3 605909 PINK1 608309
1p32 {Parkinson disease 10} 2 606852 PARK10 606852
1p31.3 Parkinson disease 19b, early-onset AR 3 615528 DNAJC6 608375
1p31.3 Parkinson disease 19a, juvenile-onset AR 3 615528 DNAJC6 608375
1q22 {Parkinson disease, late-onset, susceptibility to} AD, Mu 3 168600 GBA 606463
1q32 {Parkinson disease 16} 2 613164 PARK16 613164
2p13 {Parkinson disease 3} 2 602404 PARK3 602404
2p13.1 {Parkinson disease 13} 3 610297 HTRA2 606441
2q37.1 {Parkinson disease 11} 3 607688 GIGYF2 612003
3q22 Parkinson disease 21 AD 2 616361 PARK21 616361
3q27.1 {Parkinson disease 18} AD 3 614251 EIF4G1 600495
4p13 {?Parkinson disease 5, susceptibility to} AD 3 613643 UCHL1 191342
4q22.1 Parkinson disease 4 AD 3 605543 SNCA 163890
4q22.1 Parkinson disease 1 AD 3 168601 SNCA 163890
4q23 {Parkinson disease, susceptibility to} AD, Mu 3 168600 ADH1C 103730
6q26 Parkinson disease, juvenile, type 2 AR 3 600116 PRKN 602544
6q27 {Parkinson disease, susceptibility to} AD, Mu 3 168600 TBP 600075
7p11.2 Parkinson disease 22, autosomal dominant AD 3 616710 CHCHD2 616244
9q34.11 Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development AR 3 620482 PTPA 600756
10q22.1 {Parkinson disease 24, autosomal dominant, susceptibility to} AD 3 619491 PSAP 176801
12q12 {Parkinson disease 8} AD 3 607060 LRRK2 609007
12q24.12 {Parkinson disease, late-onset, susceptibility to} AD, Mu 3 168600 ATXN2 601517
13q21.33 {Parkinson disease, susceptibility to} AD, Mu 3 168600 ATXN8OS 603680
14q32.12 {Parkinson disease, late-onset, susceptibility to} AD, Mu 3 168600 ATXN3 607047
15q22.2 Parkinson disease 23, autosomal recessive, early onset AR 3 616840 VPS13C 608879
16q11.2 {Parkinson disease 17} AD 3 614203 VPS35 601501
17q21.31 {Parkinson disease, susceptibility to} AD, Mu 3 168600 MAPT 157140
21q22.11 Parkinson disease 20, early-onset AR 3 615530 SYNJ1 604297
22q12.3 Parkinson disease 15, autosomal recessive AR 3 260300 FBXO7 605648
22q13.1 Parkinson disease 14, autosomal recessive AR 3 612953 PLA2G6 603604
Xq21-q25 {Parkinson disease 12} 2 300557 PARK12 300557
▲ Close
ICD+
ORPHA: 411602
DO: 0060897
▲ Close
Search: 601501 614203 (Search in: MIM number)
Results: 2 entries.

1:
* 601501. VPS35 RETROMER COMPLEX COMPONENT; VPS35
Cytogenetic location: 16q11.2, Genomic coordinates (GRCh38): 16:46,656,132-46,689,178
Matching terms: 601501

2:
# 614203. PARKINSON DISEASE 17; PARK17
Cytogenetic location: 16q11.2
Matching terms: 614203


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® 1966-2024 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® 1966-2024 Johns Hopkins University.
Printed: May 7, 2024