Gene Gene information from NCBI Gene database.
Entrez ID 339855
Gene name Kyphoscoliosis peptidase
Gene symbol KY
Synonyms (NCBI Gene)
MFM7
Chromosome 3
Chromosome location 3q22.2
Summary 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.
309
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
GO:0005856 Component Cytoskeleton IEA
GO:0006508 Process Proteolysis IEA
GO:0007517 Process Muscle organ development IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605739 26576 ENSG00000174611
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
35
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hereditary spastic paraplegia Pathogenic rs1085307110 RCV000488883
Myofibrillar myopathy 7 Likely pathogenic; Pathogenic rs2107735424, rs2547432519, rs377332009, rs886037917, rs762212832, rs373240849 RCV001824281
RCV003146861
RCV000240829
RCV000240807
RCV003331854
RCV001293458
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
KY-related disorder Conflicting classifications of pathogenicity; Likely benign; Benign rs188233679, rs202115421, rs752132028, rs145706524, rs1275322585, rs777981227, rs141346785, rs548777705, rs376145121, rs201201519, rs34502271, rs200174527, rs372354601, rs371587266, rs35026874 RCV003918849
RCV003961634
RCV003931601
RCV003927068
RCV003939787
RCV003949290
RCV003932266
RCV003954448
RCV003920513
RCV003912947
RCV003933035
RCV003933031
RCV003923171
RCV003958326
RCV004758097
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Myofibrillar Myopathy Associate 32818658
Neurologic Manifestations Associate 32818658
Neuromuscular Diseases Associate 27485408
Spastic Paraplegia Hereditary Associate 32818658