Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55536
Gene name Gene Name - the full gene name approved by the HGNC.
Cell division cycle associated 7 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CDCA7L
Synonyms (NCBI Gene) Gene synonyms aliases
JPO2, R1, RAM2
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p15.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019850 hsa-miR-375 Microarray 20215506
MIRT002722 hsa-miR-124-3p Microarray 15685193
MIRT002722 hsa-miR-124-3p Proteomics 18668037
MIRT041933 hsa-miR-484 CLASH 23622248
MIRT879064 hsa-miR-129-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001650 Component Fibrillar center IDA
GO:0005515 Function Protein binding IPI 24705354, 25082813, 25416956, 25910212, 26871637, 27229929, 28169274, 29892012, 29997176, 32296183, 32814053
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IDA 15994933
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609685 30777 ENSG00000164649
Protein
UniProt ID Q96GN5
Protein name Cell division cycle-associated 7-like protein (Protein JPO2) (Transcription factor RAM2)
Protein function Plays a role in transcriptional regulation as a repressor that inhibits monoamine oxidase A (MAOA) activity and gene expression by binding to the promoter. Plays an important oncogenic role in mediating the full transforming effect of MYC in med
PDB 5YI9 , 6EMO
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10497 zf-4CXXC_R1 345 443 Zinc-finger domain of monoamine-oxidase A repressor R1 Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Overexpressed in medulloblastoma. {ECO:0000269|PubMed:15654081, ECO:0000269|PubMed:15994933}.
Sequence
MELATRYQIPKEVADIFNAPSDDEEFVGFRDDVPMETLSSEESCDSFDSLESGKQQDVRF
HSKYFTEELRRIFIEDTDSETEDFAGFTQSDLNGKTNPEVMVVESDLSDDGKASLVSEEE
EDEEEDKATPRRSRSRRSSIGLRVAFQFPTKKLANKPDKNSSSEQLFSSARLQNEKKTIL
ERKKDCRQVIQREDSTSESEDDSRDESQESSDALLKRTMNIKENKAMLAQLLAELNSMPD
FFPVRTPTSASRKKTVRRAFSEGQITRRMNPTRSARPPEKFALENFTVSAAKFAEEFYSF
RRRKTIGGKCREYRRRHRISSFRPVEDITEEDLENVAITVRDKIYDKVLGNTCHQCRQKT
IDTKTVCRNQGCCGVRGQFCGPCLRNRYGEDVRSALLDPDWVCPPCRGICNCSYCRKRDG
RCATGILIHLAKFYGYDNVKEYL
ESLQKELVEDN
Sequence length 454
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Breast Cancer Breast cancer N/A N/A GWAS
Dementia Dementia N/A N/A GWAS
Mental Depression Major depressive disorder N/A N/A GWAS
Neuroticism Neuroticism N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 39566392
Multiple Endocrine Neoplasia Type 1 Associate 30620390
Multiple Myeloma Associate 27882933, 35013207
Neuroendocrine Tumors Associate 30620390
Urinary Bladder Neoplasms Associate 37968767