Gene Gene information from NCBI Gene database.
Entrez ID 25903
Gene name Olfactomedin like 2B
Gene symbol OLFML2B
Synonyms (NCBI Gene)
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Chromosome 1
Chromosome location 1q23.3
Summary This gene encodes an olfactomedin domain-containing protein. Most olfactomedin domain-containing proteins are secreted glycoproteins. [provided by RefSeq, Dec 2016]
miRNA miRNA information provided by mirtarbase database.
49
miRTarBase ID miRNA Experiments Reference
MIRT046128 hsa-miR-30b-5p CLASH 23622248
MIRT1203265 hsa-miR-3135b CLIP-seq
MIRT1203266 hsa-miR-3184 CLIP-seq
MIRT1203267 hsa-miR-423-5p CLIP-seq
MIRT1203268 hsa-miR-432 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
GO:0007165 Process Signal transduction IBA
GO:0030198 Process Extracellular matrix organization IEA
GO:0031012 Component Extracellular matrix 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.
Q68BL8
Protein name Olfactomedin-like protein 2B (Photomedin-2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02191 OLF 498 748 Olfactomedin-like domain Family
Sequence
MAKPRLLVLYFALIVVPAWVSSIVLTGTSEPPDAQTVAPAEDETLQNEADNQENVLSQLL
GDYDKVKAMSEGSDCQCKCVVRPLGRDACQRINAGASRKEDFYTVETITSGSSCKCACVA
PPSALNPCEGDFRLQKLREADSQDLKLSTIIDMLEGAFYGLDLLKLHSVTTKLVGRVDKL
EEEVSKNLTKENEQIKEDMEEIRTEMNKRGKENCSENILDSMPDIRSALQRDAAAAYAHP
EYEERFLQEETVSQQINSIELLQTRPLALPEVVKSQRPLQRQVHLRGRPASQPTVIRGIT
YYKAKVSEEENDIEEQQDEFFSGDNGVDLLIEDQLLRHNGLMTSVTRRPAATRQGHSTAV
TSDLNARTAPWSSALPQPSTSDPSIANHASVGPTLQTTSVSPDPTRESVLQPSPQVPATT
VAHTATQQPAAPAPPAVSPREALMEAMHTVPVPPTTVRTDSLGKDAPAGWGTTPASPTLS
PEEEDDIRNVIGRCKDTLSTITGPTTQNTYGRNEGAWMKDPLAKDERIYVTNYYYGNTLV
EFRNLENFKQGRWSNSYKLPYSWIGTGHVVYNGAFYYNRAFTRNIIKYDLKQRYVAAWAM
LHDVAYEEATPWRWQGHSDVDFAVDENGLWLIYPALDDEGFSQEVIVLSKLNAADLSTQK
ETTWRTGLRRNFYGNCFVICGVLYAVDSYNQRNANISYAFDTHTNTQIVPRLLFENEYSY
TTQIDYNPKDRLLYAWDNGHQVTYHVIF
AY
Sequence length 750
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hepatocellular carcinoma Uncertain significance rs532457018 RCV005931050
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 37340445
Neoplasms Associate 37340445
Stomach Neoplasms Associate 30866865, 32908579, 33015704
Triple Negative Breast Neoplasms Associate 36999020
Urinary Bladder Neoplasms Associate 33204728