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GENATLAS PHENOTYPE

last update : 22-03-2019

Symbol	NSMI
Location	11q13.1
Name	nonsyndromic male infertility
Other name(s)	Spermatogenic failure 7
Corresponding gene	CATSPER1
Other symbol(s)	MILM, SPGF7
Main clinical features	nonsyndromic male infertility with absence of spermatozoa motility semen showed sperm defects and reduced fertility, nonmotile sperm or sperm motility below the normal threshold, low sperm count, increased abnormally structured spermatozoa, and reduced semen volume
Genetic determination	autosomal recessive
Function/system disorder	sex-genitalia
Type	disease

Remark(s)