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Gene Gene information from NCBI Gene database.
Entrez ID 10917
Gene name Butyrophilin like 3
Gene symbol BTNL3
Synonyms (NCBI Gene)
BTN9.1BTNLR
Chromosome 5
Chromosome location 5q35.3
miRNA miRNA information provided by mirtarbase database.
117 Show/Hide all (117)
miRTarBase ID miRNA Experiments Reference
MIRT019277 hsa-miR-148b-3p Microarray 17612493
MIRT710451 hsa-miR-3192-5p HITS-CLIP 19536157
MIRT710450 hsa-miR-377-5p HITS-CLIP 19536157
MIRT710449 hsa-miR-6086 HITS-CLIP 19536157
MIRT710448 hsa-miR-661 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9 Show/Hide all (9)
GO ID Ontology Definition Evidence Reference
GO:0001817 Process Regulation of cytokine production IBA
GO:0003674 Function Molecular_function ND
GO:0005102 Function Signaling receptor binding IBA
GO:0005515 Function Protein binding IPI 29339503
GO:0005575 Component Cellular_component ND
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606192 1143 ENSG00000168903
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UXE8
Protein name Butyrophilin-like protein 3 (Butyrophilin-like receptor)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00622 SPRY 340 → 458 SPRY domain Family
PF07686 V-set 22 → 132 Immunoglobulin V-set domain Domain
PF13765 PRY 290 → 336 SPRY-associated domain Family
Tissue specificity TISSUE SPECIFICITY: Expressed in small intestine, colon, testis, spleen, and leukocyte. {ECO:0000269|PubMed:10429365}.
Sequence
MAFVLILVLSFYELVSGQWQVTGPGKFVQALVGEDAVFSCSLFPETSAEAMEVRFFRNQF
HAVVHLYRDGEDWESKQMPQYRGRTEFVKDSIAGGRVSLRLKNITPSDIGLYGCWFSSQI
YDEEATWELRVA
ALGSLPLISIVGYVDGGIQLLCLSSGWFPQPTAKWKGPQGQDLSSDSR
ANADGYSLYDVEISIIVQENAGSILCSIHLAEQSHEVESKVLIGETFFQPSPWRLASILL
GLLCGALCGVVMGMIIVFFKSKGKIQAELDWRRKHGQAELRDARKHAVEVTLDPETAHPK
LCVSDLKTVTHRKAPQEVPHSEKRFTRKSVVASQGF
QAGKHYWEVDVGQNVGWYVGVCRD
DVDRGKNNVTLSPNNGYWVLRLTTEHLYFTFNPHFISLPPSTPPTRVGVFLDYEGGTISF
FNTNDQSLIYTLLTCQFEGLLRPYIQHAMYDEEKGTPI
FICPVSWG
Sequence length 466
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 Reference Evidence Score
Adrenocortical carcinoma, hereditary Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Celiac Disease Celiac disease BEFREE 30739797
★★★★★
★☆☆☆☆
Found in Text Mining only
Celiac Disease Celiac disease Pubtator 30739797 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Inflammatory Bowel Diseases Inflammatory bowel disease Pubtator 30137272 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only