Gene Gene information from NCBI Gene database.
Entrez ID 6650
Gene name Calpain 15
Gene symbol CAPN15
Synonyms (NCBI Gene)
OGINSOLH
Chromosome 16
Chromosome location 16p13.3
Summary This gene encodes a protein containing zinc-finger-like repeats and a calpain-like protease domain. The encoded protein may function as a transcription factor, RNA-binding protein, or in protein-protein interactions during visual system development. [prov
miRNA miRNA information provided by mirtarbase database.
112
miRTarBase ID miRNA Experiments Reference
MIRT115781 hsa-miR-93-5p PAR-CLIP 23592263
MIRT115779 hsa-miR-20a-5p PAR-CLIP 23592263
MIRT115778 hsa-miR-17-5p PAR-CLIP 23592263
MIRT115786 hsa-miR-20b-5p PAR-CLIP 23592263
MIRT115784 hsa-miR-106b-5p PAR-CLIP 23592263
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0004198 Function Calcium-dependent cysteine-type endopeptidase activity IBA
GO:0004198 Function Calcium-dependent cysteine-type endopeptidase activity IEA
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0005737 Component Cytoplasm IBA
GO:0006508 Process Proteolysis IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603267 11182 ENSG00000103326
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75808
Protein name Calpain-15 (EC 3.4.22.-) (Small optic lobes homolog)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00641 zf-RanBP 4 32 Zn-finger in Ran binding protein and others Domain
PF00641 zf-RanBP 143 172 Zn-finger in Ran binding protein and others Domain
PF00641 zf-RanBP 412 441 Zn-finger in Ran binding protein and others Domain
PF00648 Peptidase_C2 488 791 Calpain family cysteine protease Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed with higher expression in brain. {ECO:0000269|PubMed:9722942}.
Sequence
MATVGEWSCVRCTFLNPAGQRQCSICEAPRHKPDLNHILRLSVEEQKWPCARCTFRNFLG
KEACEVCGFTPEPAPGAAFLPVLNGVLPKPPAILGEPKGSCQEEAGPVRTAGLVATEPAR
GQCEDKDEEEKEEQEEEEGAAEPRGGWACPRCTLHNTPVASSCSVCGGPRRLSLPRIPPE
ALVVPEVVAPAGFHVVPAAPPPGLPGEGAEANPPATSQGPAAEPEPPRVPPFSPFSSTLQ
NNPVPRSRREVPPQLQPPVPEAAQPSPSAGCRGAPQGSGWAGASRLAELLSGKRLSVLEE
EATEGGTSRVEAGSSTSGSDIIDLAGDTVRYTPASPSSPDFTTWSCAKCTLRNPTVAPRC
SACGCSKLHGFQEHGEPPTHCPDCGADKPSPCGRSCGRVSSAQKAARVLPERPGQWACPA
CTLLNALRAKHCAACHTPQLL
VAQRRGAAPLRRRESMHVEQRRQTDEGEAKALWENIVAF
CRENNVSFVDDSFPPGPESVGFPAGDSVQQRVRQWLRPQEINCSVFRDHRATWSVFHTLR
PSDILQGLLGNCWFLSALAVLAERPDLVERVMVTRSLCAEGAYQVRLCKDGTWTTVLVDD
MLPCDEAGCLLFSQAQRKQLWVALIEKALAKLHGSYFALQAGRAIEGLATLTGAPCESLA
LQLSSTNPREEPVDTDLIWAKMLSSKEAGFLMGASCGGGNMKVDDSAYESLGLRPRHAYS
ILDVRDVQGTRLLRLRNPWGRFSWNGSWSDEWPHWPGHLRGELMPHGSSEGVFWMEYGDF
VRYFDSVDICK
VHSDWQEARVQGCFPSSASAPVGVTALTVLERASLEFALFQEGSRRSDA
VDSHLLDLCILVFRATFGSGGHLSLGRLLAHSKRAVKKFVSCDVMLEPGEYAVVCCAFNH
WGPPLPGTPAPQASSPSAGVPRASPEPPGHVLAVYSSRLVMVEPVEAQPTTLADAIILLT
ESRGERHEGREGMTCYYLTHGWAGLIVVVENRHPKAYLHVQCDCTDSFNVVSTRGSLRTQ
DSVPPLHRQVLVILSQLEGNAGFSITHRLAHRKAAQAFLSDWTASKGTHSPPLTPEVAGL
HGPRPL
Sequence length 1086
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Degradation of the extracellular matrix
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
75
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Oculogastrointestinal-neurodevelopmental syndrome Pathogenic rs2142085042, rs2142072159, rs762523863, rs2142086271, rs2142084042 RCV001387527
RCV001387528
RCV001387530
RCV001387531
RCV001387533
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Likely benign rs146637756 RCV005927303
Adrenocortical carcinoma, hereditary Conflicting classifications of pathogenicity rs1441582052 RCV005871162
CAPN15-related disorder Uncertain significance; Likely benign; Benign; Conflicting classifications of pathogenicity rs144209708, rs773799955, rs763566668, rs145595428, rs146637756, rs2505842019, rs141227716, rs572003179, rs141612773, rs149502771, rs145916590, rs142810996, rs147299088, rs371731942, rs373834069
View all (34 more)
RCV003933697
RCV003936647
RCV003928923
RCV003984354
RCV003973779
RCV003412437
RCV003938929
RCV003929062
RCV003938930
RCV003938931
RCV003938932
RCV003938933
RCV003966363
RCV003919123
RCV003929063
RCV003919124
RCV003929064
RCV003966364
RCV003949092
RCV003956644
RCV003909487
RCV003924155
RCV003929597
RCV003906860
RCV003984678
RCV003903883
RCV003899459
RCV003941945
RCV003944561
RCV003944599
RCV003954935
RCV003927139
RCV003939718
RCV003914357
RCV003924741
RCV003969267
RCV003922156
RCV003922243
RCV003922283
RCV003924681
RCV003934336
RCV003956808
RCV003971748
RCV003971499
RCV003971545
RCV003967164
RCV003969422
RCV004753749
RCV003935911
Cervical cancer Likely benign rs144075530 RCV005938834
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Dehydrated Hereditary Stomatocytosis Pseudohyperkalemia and Perinatal Edema Associate 29221444
Leiomyosarcoma Associate 22419440
Plaque Atherosclerotic Associate 29221444