Gene Gene information from NCBI Gene database.
Entrez ID 116159
Gene name Cysteine and tyrosine rich 1
Gene symbol CYYR1
Synonyms (NCBI Gene)
C21orf95
Chromosome 21
Chromosome location 21q21.3
miRNA miRNA information provided by mirtarbase database.
128
miRTarBase ID miRNA Experiments Reference
MIRT019006 hsa-miR-335-5p Microarray 18185580
MIRT711132 hsa-miR-5692a HITS-CLIP 19536157
MIRT711131 hsa-miR-3156-5p HITS-CLIP 19536157
MIRT711130 hsa-miR-130b-5p HITS-CLIP 19536157
MIRT711129 hsa-miR-1267 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0008150 Process Biological_process ND
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616020 16274 ENSG00000166265
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96J86
Protein name Cysteine and tyrosine-rich protein 1 (Proline-rich domain-containing protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10873 CYYR1 7 154 Cysteine and tyrosine-rich protein 1 Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed. {ECO:0000269|PubMed:12036297, ECO:0000269|PubMed:17442112}.
Sequence
Sequence length 154
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEMENTIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LATE-ONSET ALZHEIMER'S DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Bronchopulmonary Dysplasia Associate 38277517
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Associate 26646589
★☆☆☆☆
Found in Text Mining only