Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
*611592 - PHENYLALANYL-tRNA SYNTHETASE 2, MITOCHONDRIAL; FARS2
Cytogenetic locations: 26553276
Gene summaries Genetic tests Medical literature
#617046 - SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE; SPG77
#615595 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19
Cytogenetic locations: 23814038
#614946 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14
Cytogenetic locations: 27095821
*613311 - LYR MOTIF-CONTAINING PROTEIN 4; LYRM4
Cytogenetic locations: 19454487
#609060 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1
Cytogenetic locations: 17160893
*602918 - PHENYLALANINE-tRNA SYNTHETASE, ALPHA SUBUNIT; FARSA
Cytogenetic locations: 614611
*590070 - TRANSFER RNA, MITOCHONDRIAL, PHENYLALANINE; MTTF
#270800 - SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A
Cytogenetic locations: 12874406
#203700 - MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE); MTDPS4A
Cytogenetic locations: 15q24.2
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on