Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
339855
Gene name Gene Name - the full gene name approved by the HGNC.
Kyphoscoliosis peptidase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KY
Synonyms (NCBI Gene) Gene synonyms aliases
MFM7
Disease Acronyms (UniProt) Disease acronyms from UniProt database
MFM7
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q22.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the transglutaminase-like superfamily. The protein is involved in the function, maturation and stabilization of the neuromuscular junction and may be required for normal muscle growth. Mutations in this gene are
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT526294 hsa-miR-4724-5p PAR-CLIP 22012620
MIRT526293 hsa-miR-4499 PAR-CLIP 22012620
MIRT526292 hsa-miR-4463 PAR-CLIP 22012620
MIRT526290 hsa-miR-4539 PAR-CLIP 22012620
MIRT526291 hsa-miR-18a-3p PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005856 Component Cytoskeleton IEA
GO:0006508 Process Proteolysis IEA
GO:0008233 Function Peptidase activity IEA
GO:0030018 Component Z disc ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605739 26576 ENSG00000174611
Protein
UniProt ID Q8NBH2
Protein name Kyphoscoliosis peptidase (EC 3.4.-.-)
Protein function Probable cytoskeleton-associated protease required for normal muscle growth. Involved in function, maturation and stabilization of the neuromuscular junction. May act by cleaving muscle-specific proteins such as FLNC (By similarity). {ECO:000025
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01841 Transglut_core 169 283 Transglutaminase-like superfamily Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in skeletal muscle. {ECO:0000269|PubMed:27485408}.
Sequence
MELKKDINAVSIDMLLIVHSEKRRAAQGTLSDQQANPSSLLQRGGGFQGVGNGVRRWQKL
EGNDFHENLVEKQHPQQPQVITSYNSQGTQLTVEVHPRDAMPQLLKKFSLAKRLQGDKNG
NTRPRQPGGKDAHAYPWDRSSLKSMSLDLQQFEKLDIYASQVTAKSGLDELVSDLLQEAH
TDLERVRAIWIWICHHIEYDIAAAQEKDRQAFKPTDILRTQKTNCDGYAGLFERMCRLAG
VQCMTVPGYSKGFGYQTGQSFSGEFDHAWNAVYLEGRWHLVDS
TWGSGLVDTITSKFTFL
YNEFYFLTHPALFIEDHFPDNKNWQLLKPPQSLRQFENNMYHKSEFYNKGMLSAHPETSM
IRTVNGKATVTIESCAPTLFMFMLNGKQEHGLLSLRKNGMKLEVYPPTMGTHKLQIFAKG
NSDIYSSVLEYTLKCNYVDMGVQLPAELHQPVGPSWFSEQMGIMKPSHPDPIIHTSDGRC
SISFSVEEGINVLASLHGDDGPITEETQRRYIFQLHREKQTELKVQLPHAGKFALKIFVK
KRQEPGNYIFVFNYLVCCANTKVNWPMFPESFGNWGQDNELLEPLSGVLPANRNVPFKLK
LHGIAKVLVKGQDTWPLTLNHEGYWEGSCSTAGCQEVYVMVLENANHNFYSYILKYKVNA
Q
Sequence length 661
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Congenital myopathy Congenital myopathy (disorder) rs80358247, rs199474720, rs80358248, rs121964852, rs199474719, rs121964853, rs121964854, rs104894129, rs137853306, rs199476153, rs199476147, rs137853307, rs28930068, rs121909519, rs121909521
View all (43 more)
27484770
Developmental delay Gross motor development delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
Mental retardation Intellectual Disability rs5742905, rs267607136, rs267607137, rs2131714307, rs267607038, rs267607042, rs80338685, rs137853127, rs80338815, rs28940893, rs387906309, rs121908096, rs121908099, rs587784365, rs121918315
View all (1024 more)
Myofibrillar myopathy Myofibrillar Myopathy, MYOPATHY, MYOFIBRILLAR, 7 rs121908333, rs121908334, rs28937597, rs121908457, rs121908458, rs121908460, rs121908461, rs121913000, rs60538473, rs57639980, rs121913003, rs57955682, rs121913004, rs121913005, rs57965306
View all (75 more)
27484770, 27485408
Unknown
Disease term Disease name Evidence References Source
Kyphosis-Lateral Tongue Atrophy-Myofibrillar Myopathy Syndrome kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome GenCC
Kyphoscoliosis-Lateral Tongue Atrophy-Hereditary Spastic Paraplegia Syndrome kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome GenCC
Associations from Text Mining
Disease Name Relationship Type References
Myofibrillar Myopathy Associate 32818658
Neurologic Manifestations Associate 32818658
Neuromuscular Diseases Associate 27485408
Spastic Paraplegia Hereditary Associate 32818658