Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
90362
Gene name Gene Name - the full gene name approved by the HGNC.
Family with sequence similarity 110 member B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM110B
Synonyms (NCBI Gene) Gene synonyms aliases
C8orf72
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q12.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT047048 hsa-miR-183-5p CLASH 23622248
MIRT038074 hsa-miR-423-5p CLASH 23622248
MIRT717705 hsa-miR-7109-3p HITS-CLIP 19536157
MIRT717705 hsa-miR-7109-3p HITS-CLIP 19536157
MIRT717705 hsa-miR-7109-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005739 Component Mitochondrion IDA
GO:0005815 Component Microtubule organizing center IEA
GO:0005829 Component Cytosol IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611394 28587 ENSG00000169122
Protein
UniProt ID Q8TC76
Protein name Protein FAM110B
Protein function May be involved in tumor progression.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14161 FAM110_N 13 118 Centrosome-associated N terminus Family
PF14160 FAM110_C 253 361 Centrosome-associated C terminus Family
Tissue specificity TISSUE SPECIFICITY: Detected in thyroid, spleen and testis, and at lower levels in stomach, spinal cord, lymph node, trachea, adrenal gland, prostate, ovary and intestine. {ECO:0000269|PubMed:17499476}.
Sequence
MPTETLQTGSMVKPVSPAGTFTSAVPLRILNKGPDYFRRQAEPNPKRLSAVERLEADKAK
YVKSQEVINAKQEPVKPAVLAKPPVCPAAKRALGSPTLKVFGNHAKTESGVQRENLKL
EI
LKNIINSSEGSSSGSGHKHSSRNWPPHRSEATDLHRHSFAESLKVYPTQGRRSPQEGGSH
VGRRLLEQSAESFLHVSHSSSDIRKVTSVKPLKAIPCSSSAPPLPPKPKIAAIASMKSPE
ADPVEPACGVSRRPSLQRSKSDLSDRYFRVDADVERFFNYCGLDPEELENLGMENFARAN
SDIISLNFRSASMISSDCEQSQDSNSDLRNDDSANDRVPYGISAIERNARIIKWLYSIKQ
A
RESQKVSHV
Sequence length 370
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Unknown
Disease term Disease name Evidence References Source
Schizophrenia Schizophrenia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Colorectal Neoplasms Associate 32859214
Neoplasms Associate 29596435
Pancreatic Neoplasms Associate 29596435