Gene table: search width pubmed_id = 37119330


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Spastic paraplegia 89, autosomal recessive - (AR)
15.78
37119330
AMFR (16q13)
Autocrine motility factor receptor
* Spastic paraplegia 89, autosomal recessive - SPG89