Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100049707
Gene name Gene Name - the full gene name approved by the HGNC.
-
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SPG38
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16-p15
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612335 N/A N/A
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Spastic paraplegia SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT (disorder), Autosomal dominant spastic paraplegia type 38 rs118204049, rs121918262, rs104894490, rs119476046, rs281865117, rs281865118, rs137853017, rs72554620, rs121908610, rs121908611, rs121908613, rs116171274, rs121434442, rs121434443, rs137852520
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