GenTIGSA Gene Database on Rare Genetic Disorders

Lists of Rare Genetic Disorders  

Fibromylagia 
An Unknown mode(s) within the Pain syndrome category
Reported Pathogenic variants
Candidate Gene Information
S.No. Name/GeneID Description Cytogentic Band Gene Location on genomic DNA Gene Length Exons Details Gene Cross-References
1 TRPV2/51393 transient receptor potential cation channel subfamily V member 2 17p11.2 Chr17, NC_000017.11
(16415571..16437003)
21433 nt 16 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

2 MYT1L/23040 myelin transcription factor 1 like 2p25.3 Chr2, NC_000002.12
(1789113..2331275, complement)
542163 nt 34 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

3 NRXN3/9369 neurexin 3 14q24.3 Chr14, NC_000014.9
(78170373..79868291)
1697919 nt 27 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information    
Disorder Cross-References:                GTR          MalaCards          NORD     

Patient care services
Clinical Symptoms & Disabilities