% 608031

AMYOTROPHIC LATERAL SCLEROSIS 7; ALS7


HGNC Approved Gene Symbol: ALS7

Cytogenetic location: 20p13     Genomic coordinates (GRCh38): 20:0-5,100,000


Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
20p13 Amyotrophic lateral sclerosis 7 608031 2
Phenotypic Series
 

Amyotrophic lateral sclerosis - PS105400 - 35 Entries
Location Phenotype Inheritance Phenotype
mapping key
Phenotype
MIM number
Gene/Locus Gene/Locus
MIM number
1p36.22 Frontotemporal lobar degeneration, TARDBP-related AD 3 612069 TARDBP 605078
1p36.22 Amyotrophic lateral sclerosis 10, with or without FTD AD 3 612069 TARDBP 605078
2p13.1 {Amyotrophic lateral sclerosis, susceptibility to} AR, AD 3 105400 DCTN1 601143
2q33.1 Amyotrophic lateral sclerosis 2, juvenile AR 3 205100 ALS2 606352
2q34 Amyotrophic lateral sclerosis 19 AD 3 615515 ERBB4 600543
2q35 Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia AD 3 616208 TUBA4A 191110
3p11.2 Amyotrophic lateral sclerosis 17 AD 3 614696 CHMP2B 609512
4q33 {Amyotrophic lateral sclerosis, susceptibility to, 24} AD 3 617892 NEK1 604588
5q31.2 Amyotrophic lateral sclerosis 21 AD 3 606070 MATR3 164015
5q35.3 Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 AD 3 616437 SQSTM1 601530
6q21 Amyotrophic lateral sclerosis 11 AD 3 612577 FIG4 609390
9p21.2 Frontotemporal dementia and/or amyotrophic lateral sclerosis 1 AD 3 105550 C9orf72 614260
9p13.3 ?Amyotrophic lateral sclerosis 16, juvenile AR 3 614373 SIGMAR1 601978
9p13.3 Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia 3 613954 VCP 601023
9q34.13 Amyotrophic lateral sclerosis 4, juvenile AD 3 602433 SETX 608465
10p13 Amyotrophic lateral sclerosis 12 3 613435 OPTN 602432
10q22.3 Amytrophic lateral sclerosis 23 AD 3 617839 ANXA11 602572
12q13.12 {Amyotrophic lateral sclerosis, susceptibility to} AR, AD 3 105400 PRPH 170710
12q13.13 Amyotrophic lateral sclerosis 20 AD 3 615426 HNRNPA1 164017
12q13.3 {Amyotrophic lateral sclerosis, susceptibility to, 25} AD 3 617921 KIF5A 602821
12q14.2 Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 AD 3 616439 TBK1 604834
12q24.12 {Amyotrophic lateral sclerosis, susceptibility to, 13} AD 3 183090 ATXN2 601517
12q24.12 Spinocerebellar ataxia 2 AD 3 183090 ATXN2 601517
14q11.2 Amyotrophic lateral sclerosis 9 3 611895 ANG 105850
15q21.1 Amyotrophic lateral sclerosis 5, juvenile AR 3 602099 SPG11 610844
16p11.2 Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia 3 608030 FUS 137070
17p13.2 Amyotrophic lateral sclerosis 18 3 614808 PFN1 176610
18q21 Amyotrophic lateral sclerosis 3 AD 2 606640 ALS3 606640
20p13 Amyotrophic lateral sclerosis 7 2 608031 ALS7 608031
20q13.32 Amyotrophic lateral sclerosis 8 AD 3 608627 VAPB 605704
21q22.11 Amyotrophic lateral sclerosis 1 AR, AD 3 105400 SOD1 147450
22q11.23 Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 AD 3 615911 CHCHD10 615903
22q12.2 ?{Amyotrophic lateral sclerosis, susceptibility to} AR, AD 3 105400 NEFH 162230
Xp11.21 Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia XLD 3 300857 UBQLN2 300264
Not Mapped Amyotrophic lateral sclerosis, juvenile, with dementia 205200 ALSDC 205200

TEXT

For a phenotypic description and a discussion of genetic heterogeneity of amyotrophic lateral sclerosis (ALS), see ALS1 (105400).


Mapping

Sapp et al. (2003) performed a genetic linkage screen in 16 U.S. pedigrees with familial ALS and no evidence for mutations in the SOD1 gene (147450). In 1 of the 16 families, they identified a novel ALS locus, designated ALS7, spanning a 6.25-cM (1-Mb) region on chromosome 20p. A multipoint lod score calculated for this family had a peak value of 3.46 at D20S103. In another family, Sapp et al. (2003) identified a novel ALS locus on chromosome 16 (ALS6; 608030).


REFERENCES

  1. Sapp, P. C., Hosler, B. A., McKenna-Yasek, D., Chin, W., Gann, A., Genise, H., Gorenstein, J., Huang, M., Sailer, W., Scheffler, M., Valesky, M., Haines, J. L., Pericak-Vance, M., Siddique, T., Horvitz, H. R., Brown, R. H., Jr. Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis. Am. J. Hum. Genet. 73: 397-403, 2003. [PubMed: 12858291, images, related citations] [Full Text]


Creation Date:
Victor A. McKusick : 8/12/2003
carol : 08/12/2011
terry : 1/20/2010
wwang : 9/1/2009
carol : 6/20/2006
tkritzer : 4/30/2004
terry : 4/29/2004
carol : 3/18/2004
mgross : 8/12/2003

% 608031

AMYOTROPHIC LATERAL SCLEROSIS 7; ALS7


HGNC Approved Gene Symbol: ALS7

ORPHA: 803;   DO: 0060199;  


Cytogenetic location: 20p13     Genomic coordinates (GRCh38): 20:0-5,100,000


Gene-Phenotype Relationships

Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
20p13 Amyotrophic lateral sclerosis 7 608031 2

TEXT

For a phenotypic description and a discussion of genetic heterogeneity of amyotrophic lateral sclerosis (ALS), see ALS1 (105400).


Mapping

Sapp et al. (2003) performed a genetic linkage screen in 16 U.S. pedigrees with familial ALS and no evidence for mutations in the SOD1 gene (147450). In 1 of the 16 families, they identified a novel ALS locus, designated ALS7, spanning a 6.25-cM (1-Mb) region on chromosome 20p. A multipoint lod score calculated for this family had a peak value of 3.46 at D20S103. In another family, Sapp et al. (2003) identified a novel ALS locus on chromosome 16 (ALS6; 608030).


REFERENCES

  1. Sapp, P. C., Hosler, B. A., McKenna-Yasek, D., Chin, W., Gann, A., Genise, H., Gorenstein, J., Huang, M., Sailer, W., Scheffler, M., Valesky, M., Haines, J. L., Pericak-Vance, M., Siddique, T., Horvitz, H. R., Brown, R. H., Jr. Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis. Am. J. Hum. Genet. 73: 397-403, 2003. [PubMed: 12858291] [Full Text: https://linkinghub.elsevier.com/retrieve/pii/S0002-9297(07)61928-4]


Creation Date:
Victor A. McKusick : 8/12/2003
Edit History:
carol : 08/12/2011
terry : 1/20/2010
wwang : 9/1/2009
carol : 6/20/2006
tkritzer : 4/30/2004
terry : 4/29/2004
carol : 3/18/2004
mgross : 8/12/2003