Gene Gene information from NCBI Gene database.
Entrez ID 284759
Gene name Signal regulatory protein beta 2
Gene symbol SIRPB2
Synonyms (NCBI Gene)
PTPN1LPTPNS1L3dJ776F14.2
Chromosome 20
Chromosome location 20p13
miRNA miRNA information provided by mirtarbase database.
233
miRTarBase ID miRNA Experiments Reference
MIRT437535 hsa-miR-19b-3p Immunoprecipitaion 22382630
MIRT722765 hsa-miR-510-5p HITS-CLIP 19536157
MIRT722764 hsa-miR-3140-5p HITS-CLIP 19536157
MIRT722763 hsa-miR-371b-5p HITS-CLIP 19536157
MIRT722762 hsa-miR-373-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
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
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.
Q5JXA9
Protein name Signal-regulatory protein beta-2 (SIRP-beta-2) (Protein tyrosine phosphatase non-receptor type substrate 1-like 3) (Protein tyrosine phosphatase non-receptor type substrate protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07686 V-set 43 150 Immunoglobulin V-set domain Domain
PF07686 V-set 162 264 Immunoglobulin V-set domain Domain
Sequence
Sequence length 342
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations