Gene Gene information from NCBI Gene database.
Entrez ID 26127
Gene name FGFR1 oncogene partner 2
Gene symbol FGFR1OP2
Synonyms (NCBI Gene)
HSPC123-likeWIT3.0
Chromosome 12
Chromosome location 12p11.23
miRNA miRNA information provided by mirtarbase database.
259
miRTarBase ID miRNA Experiments Reference
MIRT020087 hsa-miR-361-5p Sequencing 20371350
MIRT712710 hsa-miR-3127-3p HITS-CLIP 19536157
MIRT712709 hsa-miR-6756-3p HITS-CLIP 19536157
MIRT712708 hsa-miR-6859-3p HITS-CLIP 19536157
MIRT712707 hsa-miR-711 HITS-CLIP 19536157
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:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol TAS
GO:0009611 Process Response to wounding IBA
GO:0042060 Process Wound healing IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608858 23098 ENSG00000111790
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NVK5
Protein name FGFR1 oncogene partner 2
Protein function May be involved in wound healing pathway.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05769 SIKE 2 142 SIKE family Family
PF05769 SIKE 146 221 SIKE family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in bone marrow, spleen and thymus.
Sequence
Sequence length 253
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Signaling by cytosolic FGFR1 fusion mutants
Signaling by FGFR1 in disease
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
Cervical cancer Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MYELOPROLIFERATIVE DISORDERS CTD
★★☆☆☆
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
Atrophy Atrophy Pubtator 22880093 Associate
★☆☆☆☆
Found in Text Mining only
Chronic myeloproliferative disorder Myeloproliferative disorder BEFREE 21745565
★☆☆☆☆
Found in Text Mining only
Myeloproliferative disease Myeloproliferative disorder BEFREE 21745565
★☆☆☆☆
Found in Text Mining only
Myeloproliferative disease Myeloproliferative disorder CTD_human_DG 22875613
★☆☆☆☆
Found in Text Mining only