Gene Gene information from NCBI Gene database.
Entrez ID 83690
Gene name Cysteine rich secretory protein LCCL domain containing 1
Gene symbol CRISPLD1
Synonyms (NCBI Gene)
CRISP-10CRISP10LCRISP1
Chromosome 8
Chromosome location 8q21.13
miRNA miRNA information provided by mirtarbase database.
46
miRTarBase ID miRNA Experiments Reference
MIRT909813 hsa-miR-1 CLIP-seq
MIRT909814 hsa-miR-181a CLIP-seq
MIRT909815 hsa-miR-181b CLIP-seq
MIRT909816 hsa-miR-181c CLIP-seq
MIRT909817 hsa-miR-181d CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
GO:0060325 Process Face morphogenesis IEA
GO:0060325 Process Face morphogenesis IMP 21254358
GO:0061484 Process Hematopoietic stem cell homeostasis IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H336
Protein name Cysteine-rich secretory protein LCCL domain-containing 1 (CocoaCrisp) (Cysteine-rich secretory protein 10) (CRISP-10) (LCCL domain-containing cysteine-rich secretory protein 1) (Trypsin inhibitor Hl)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00188 CAP 66 206 Cysteine-rich secretory protein family Domain
PF03815 LCCL 293 384 LCCL domain Domain
PF03815 LCCL 394 491 LCCL domain Domain
Sequence
Sequence length 500
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
COLON CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLONIC NEOPLASM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OLIGODENDROGLIOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PARKINSON 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
Carcinoma Squamous Cell Associate 30896821
★☆☆☆☆
Found in Text Mining only
Cleft Palate Associate 31262291
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 30896821
★☆☆☆☆
Found in Text Mining only