Gene Gene information from NCBI Gene database.
Entrez ID 171483
Gene name Family with sequence similarity 9 member B
Gene symbol FAM9B
Synonyms (NCBI Gene)
TEX39B
Chromosome X
Chromosome location Xp22.31
Summary This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be localized to the nucleus as the protein contains several nuclear localization signals, and has similarity to a synaptonemal complex prot
miRNA miRNA information provided by mirtarbase database.
78
miRTarBase ID miRNA Experiments Reference
MIRT021936 hsa-miR-128-3p Microarray 17612493
MIRT637332 hsa-miR-1245a HITS-CLIP 23824327
MIRT637331 hsa-miR-8079 HITS-CLIP 23824327
MIRT637330 hsa-miR-6513-3p HITS-CLIP 23824327
MIRT637329 hsa-miR-6777-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0000795 Component Synaptonemal complex IBA
GO:0005515 Function Protein binding IPI 24722188, 25416956, 25910212, 26871637, 31515488, 32296183, 33961781
GO:0005634 Component Nucleus IDA 34507348
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300478 18404 ENSG00000177138
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IZU0
Protein name Protein FAM9B
Protein function May play a role in meiosis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04803 Cor1 61 186 Cor1/Xlr/Xmr conserved region Coiled-coil
Tissue specificity TISSUE SPECIFICITY: Expressed in testis and ovary (at protein level). {ECO:0000269|PubMed:34507348}.
Sequence
Sequence length 186
Interactions View interactions
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
DERMATOPHYTOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
UTERINE FIBROID GWAS catalog
★★☆☆☆
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
Azoospermia Nonobstructive Nonobstructive azoospermia Pubtator 36017582 Associate
★☆☆☆☆
Found in Text Mining only