Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
165215
Gene name Gene Name - the full gene name approved by the HGNC.
Family with sequence similarity 171 member B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM171B
Synonyms (NCBI Gene) Gene synonyms aliases
KIAA1946
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q32.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022182 hsa-miR-124-3p Microarray 18668037
MIRT024632 hsa-miR-215-5p Microarray 19074876
MIRT026167 hsa-miR-192-5p Microarray 19074876
MIRT048646 hsa-miR-99a-5p CLASH 23622248
MIRT981958 hsa-miR-1183 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620309 29412 ENSG00000144369
Protein
UniProt ID Q6P995
Protein name Protein FAM171B
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10577 UPF0560 82 612 Uncharacterised protein family UPF0560 Family
PF10577 UPF0560 592 826 Uncharacterised protein family UPF0560 Family
Sequence
MARLCRRVPCTLLLGLAVVLLKARLVPAAARAELSRSDLSLIQQQQQQQQQQQQQQKQLE
EAEEERTEVPGATSTLTVPVSVFMLKVQVNDIISRQYLSQAVVEVFVNYTKTNSTVTKSN
GAVLIKVPYKLGLSLTIIAYKDGYVLTPLPWKTRRMPIYSSVTLSLFPQSQANIWLFEDT
VLITGKLADAKSQPSVQFSKALIKLPDNHHISNVTGYLTVLQQFLKVDNFLHTTGITLNK
PGFENIELTPLAAICVKIYSGGKELKVNGSIQVSLPLLRLNDISAGDRIPAWTFDMNTGA
WVNHGRGMVKEHNNHLIWTYDAPHLGYWIAAPLPGTRGSGINEDSKDITAYHTVFLTAIL
GGTIVIVIGFFAVLLCYCRDKCGTPQKRERNITKLEVLKRDQTTSTTHINHISTVKVALK
AEDKSQLFNAKNSSYSPQKKEPSKAETEERVSMVKTRDDFKIYNEDVSFLSVNQNNYSRN
PTQSLEPNVGSKQPKHINNNLSSSLGDAQDEKRYLTGNEEAYGRSHIPEQLMHIYSQPIA
ILQTSDLFSTPEQLHTAKSATLPRKGQLVYGQLMEPVNRENFTQTLPKMPI
HSHAQPPDA
REEDIILEGQQS
LPSQASDWSRYSSSLLESVSVPGTLNEAVVMTPFSSELQGISEQTLLE
LSKGKPSPHPRAWFVSLDGKPVAQVRHSFIDLKKGKRTQSNDTSLDSGVDMNELHSSRKL
EREKTFIKSMHQPKILYLEDLDLSSSESGTTVCSPEDPALRHILDGGSGVIMEHPGEESP
GRKSTVEDFEANTSPTKRRGRPPLAKRDSKTNIWKKREERPLIPIN
Sequence length 826
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Inflammatory bowel disease Inflammatory Bowel Diseases rs137853579, rs137853580, rs121909601, rs149491038, rs368287711, rs387907326, rs587777338, rs758439420, rs1329427406, rs1264862631, rs1192830343, rs1373354533, rs1419560997, rs1591263883, rs1989014468 28067908
Unknown
Disease term Disease name Evidence References Source
Crohn disease Crohn Disease 28067908 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Colorectal Neoplasms Associate 30861353
Pulmonary Arterial Hypertension Associate 36248192