CRIP3 (cysteine rich protein 3)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
401262
Gene name Gene Name - the full gene name approved by the HGNC.
Cysteine rich protein 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CRIP3
Synonyms (NCBI Gene) Gene synonyms aliases
CRP-3, TLP, TLP-A, h6LIMo
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.1
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(9)
miRTarBase ID miRNA Experiments Reference
MIRT909753 hsa-miR-1224-3p CLIP-seq
MIRT909754 hsa-miR-1260 CLIP-seq
MIRT909755 hsa-miR-1260b CLIP-seq
MIRT909756 hsa-miR-1280 CLIP-seq
MIRT909757 hsa-miR-2355-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(3)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005737 Component Cytoplasm IEA
GO:0046872 Function Metal ion binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q6Q6R5
Protein name Cysteine-rich protein 3 (CRP-3) (Chromosome 6 LIM domain only protein) (h6LIMo)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00412 LIM 5 → 62 LIM domain Domain
PF00412 LIM 124 → 181 LIM domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in most tissues, but not in skeletal muscle. {ECO:0000269|PubMed:15380775}.
Sequence 
MSWTCPRCQQPVFFAEKVSSLGKNWHRFCLKCERCHSILSPGGHAEHNGRPYCHKPCYGA
LFGPRGVNIGGVGSYLYNPPTPSPGCTTPLSPSSFSPPRPRTGLPQGKKSPPHMKTFTGE
TSLCPGCGEPVYFAEKVMSLGRNWHRPCLRCQRCHKTLTAGSHAEHDGVPYCHVPCYGYL
FGPKGGQPHPRHWDGMYMPEVWHVHGLWVCVDNFPCG
Sequence length 217
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)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (2)
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
Diabetes Serum magnesium levels in type 2 diabetes, Type 2 diabetes N/A N/A GWAS
Hypertension Hypertension N/A N/A GWAS
Show/Hide Text Mining Associations (1)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Prostatic Neoplasms Associate 31605802