Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene information from NCBI Gene database. Gene miRNA Other IDs Protein Associated diseases
Entrez ID	27146
Gene name	Family with sequence similarity 184 member B
Gene symbol	FAM184B
Synonyms (NCBI Gene)	-
Chromosome	4
Chromosome location	4p15.32-p15.31

Show/Hide all (92)

miRTarBase ID	miRNA	Experiments
MIRT982430	hsa-miR-1245	CLIP-seq
MIRT982431	hsa-miR-1254	CLIP-seq
MIRT982432	hsa-miR-1297	CLIP-seq
MIRT982433	hsa-miR-1298	CLIP-seq
MIRT982434	hsa-miR-205	CLIP-seq
MIRT982435	hsa-miR-26a	CLIP-seq
MIRT982436	hsa-miR-26b	CLIP-seq
MIRT982437	hsa-miR-3116	CLIP-seq
MIRT982438	hsa-miR-3149	CLIP-seq
MIRT982439	hsa-miR-3152-3p	CLIP-seq
MIRT982440	hsa-miR-3160-3p	CLIP-seq
MIRT982441	hsa-miR-3610	CLIP-seq
MIRT982442	hsa-miR-3674	CLIP-seq
MIRT982443	hsa-miR-4438	CLIP-seq
MIRT982444	hsa-miR-4465	CLIP-seq
MIRT982445	hsa-miR-4487	CLIP-seq
MIRT982446	hsa-miR-4735-5p	CLIP-seq
MIRT982447	hsa-miR-4775	CLIP-seq
MIRT982448	hsa-miR-4794	CLIP-seq
MIRT982449	hsa-miR-5095	CLIP-seq
MIRT982450	hsa-miR-558	CLIP-seq
MIRT982451	hsa-miR-568	CLIP-seq
MIRT982452	hsa-miR-590-3p	CLIP-seq
MIRT982453	hsa-miR-661	CLIP-seq
MIRT982431	hsa-miR-1254	CLIP-seq
MIRT1991276	hsa-miR-140-3p	CLIP-seq
MIRT982437	hsa-miR-3116	CLIP-seq
MIRT1991277	hsa-miR-4269	CLIP-seq
MIRT982446	hsa-miR-4735-5p	CLIP-seq
MIRT982447	hsa-miR-4775	CLIP-seq
MIRT982448	hsa-miR-4794	CLIP-seq
MIRT982452	hsa-miR-590-3p	CLIP-seq
MIRT982453	hsa-miR-661	CLIP-seq
MIRT982431	hsa-miR-1254	CLIP-seq
MIRT982432	hsa-miR-1297	CLIP-seq
MIRT2225334	hsa-miR-1305	CLIP-seq
MIRT1991276	hsa-miR-140-3p	CLIP-seq
MIRT982435	hsa-miR-26a	CLIP-seq
MIRT982436	hsa-miR-26b	CLIP-seq
MIRT982437	hsa-miR-3116	CLIP-seq
MIRT2225335	hsa-miR-3649	CLIP-seq
MIRT1991277	hsa-miR-4269	CLIP-seq
MIRT2225336	hsa-miR-4307	CLIP-seq
MIRT982444	hsa-miR-4465	CLIP-seq
MIRT2225337	hsa-miR-4677-3p	CLIP-seq
MIRT2225338	hsa-miR-4679	CLIP-seq
MIRT982446	hsa-miR-4735-5p	CLIP-seq
MIRT982447	hsa-miR-4775	CLIP-seq
MIRT982448	hsa-miR-4794	CLIP-seq
MIRT2225339	hsa-miR-498	CLIP-seq
MIRT982452	hsa-miR-590-3p	CLIP-seq
MIRT982453	hsa-miR-661	CLIP-seq
MIRT2387786	hsa-miR-1343	CLIP-seq
MIRT2387787	hsa-miR-3663-5p	CLIP-seq
MIRT2387788	hsa-miR-3690	CLIP-seq
MIRT2387789	hsa-miR-371-5p	CLIP-seq
MIRT2387790	hsa-miR-371b-5p	CLIP-seq
MIRT2387791	hsa-miR-378	CLIP-seq
MIRT2387792	hsa-miR-378b	CLIP-seq
MIRT2387793	hsa-miR-378c	CLIP-seq
MIRT2387794	hsa-miR-378d	CLIP-seq
MIRT2387795	hsa-miR-378e	CLIP-seq
MIRT2387796	hsa-miR-378f	CLIP-seq
MIRT2387797	hsa-miR-378h	CLIP-seq
MIRT2387798	hsa-miR-378i	CLIP-seq
MIRT2387799	hsa-miR-422a	CLIP-seq
MIRT2387800	hsa-miR-4254	CLIP-seq
MIRT2387801	hsa-miR-455-3p	CLIP-seq
MIRT2449263	hsa-miR-1	CLIP-seq
MIRT2449264	hsa-miR-1286	CLIP-seq
MIRT2449265	hsa-miR-206	CLIP-seq
MIRT2449266	hsa-miR-3673	CLIP-seq
MIRT2449267	hsa-miR-4433	CLIP-seq
MIRT2449268	hsa-miR-4722-5p	CLIP-seq
MIRT2449269	hsa-miR-613	CLIP-seq
MIRT982431	hsa-miR-1254	CLIP-seq
MIRT982437	hsa-miR-3116	CLIP-seq
MIRT982446	hsa-miR-4735-5p	CLIP-seq
MIRT982447	hsa-miR-4775	CLIP-seq
MIRT982448	hsa-miR-4794	CLIP-seq
MIRT982452	hsa-miR-590-3p	CLIP-seq
MIRT982453	hsa-miR-661	CLIP-seq
MIRT982431	hsa-miR-1254	CLIP-seq
MIRT982432	hsa-miR-1297	CLIP-seq
MIRT1991276	hsa-miR-140-3p	CLIP-seq
MIRT982435	hsa-miR-26a	CLIP-seq
MIRT982436	hsa-miR-26b	CLIP-seq
MIRT982437	hsa-miR-3116	CLIP-seq
MIRT2225335	hsa-miR-3649	CLIP-seq
MIRT1991277	hsa-miR-4269	CLIP-seq
MIRT982444	hsa-miR-4465	CLIP-seq
MIRT982453	hsa-miR-661	CLIP-seq

MIM	HGNC	e!Ensembl
619945	29235	ENSG00000047662

Q9ULE4

Protein name

Protein FAM184B

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF15665	FAM184	48 → 243	Family with sequence similarity 184, A and B	Coiled-coil

Sequence

MASALNSKINPPGTCQGSKADGGAGWRMDCDPQMHVKMCKKIAQLTKVIYALNTRQDEAE
ASMEALREAHQEELQNAVAETKARLLQEQGCAEEEALLQRIQALESALELQKRLTEEALA
ESASCRLETKERELRVEAEHAERVLTLSREMLELKADYERRLQHLTSHEATPQGRLPQES
PETKSEPGQGPEMQEVLLEVQRLRVENQQLSKDYARKAEELQATYERENEAIRQAMQQSV
SQALWQWQEKESDLRKNFQVQESALQAQVRKLEGDLEHRGRKISDLKKYAQKLKERIQDL
DVQLKEARQENSELKGTAKKLGEKLAVAKDRMMLQECRGTQQTDAMKTELVSENKVLREE
NDLEAGNLHPQQDQSCLKECPCMKGGTDMQTKKEASAETEYMKQQYEEDLRKIKHQTEEE
KKHLKDQLVKRLEDLVKKHTVEIKSVRSSVEAERKKLQREVEAQLEEVRKKSEKEIKQLE
EEKAALNVKLQNSLLEVLRLEEFIQQNKTRPTGAEESPQELGRQHCSILETQDPCLKLDE
TSPRGEEYQDKLAAEEGTSSDEEERTKVLLKEGSDPQPPLGSLLKEKTSKIQRLEEDWQS
QKAKLQAQVSQMQQALEQCTSNYREDLQALKQLSDLEREKLQRELQETTQQNHAMKAQLE
ASHQRALRMLEKARHQELKATEERLKKESSHSLQIQHQTHRLELQALEEKARQELQEERE
RMQAQQALLLESLRQELSEQQAACSGHQKDLEALQAELRALGRQQASSQCPGDSKDHIIA
TEERGGPGQAGSPPGAAGQGSGEGCGLWEENAQLQDAVRRLRAEVEQHQQEAQKLRDQRR
FLEETQQAQRAREVETLRQEHRKEMQAMVADFSSAQAQLQARLAALEAELKDSGEKPGKG
ASRPEDLQLIGRLQTRLKEREDIIKQLTEERRFHYAAFPSAMSHRNRSFSFNPHPGYLTP
SMKKKKVEDVPSRVVSVPNLASYAKNFLSGDLSSRINAPPITTSPSLDPSPSCGRTYKPN
QSTDAKTATRTPDGETAQAKEVQQKQGSPHQEWFTKYFSF

Sequence length

1060

Interactions

View interactions

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)

Show/Hide Unknown Diseases (3)

Phenotype Name	Clinical Significance	Source	Evidence Score
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.
INSOMNIA	—	GWAS catalog	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
SKIN DISEASE	—	GWAS catalog	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS	—	GWAS catalog	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Show/Hide Text Mining Associations (1)

Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Associations from Text Mining Disease associations identified through text mining
Pulmonary Disease Chronic Obstructive	Chronic obstructive pulmonary disease	Pubtator	30111857	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only

FAM184B (family with sequence similarity 184 member B)