Gene Gene information from NCBI Gene database.
Entrez ID 339345
Gene name Nanos C2HC-type zinc finger 2
Gene symbol NANOS2
Synonyms (NCBI Gene)
NOS2ZC2HC12B
Chromosome 19
Chromosome location 19q13.32
miRNA miRNA information provided by mirtarbase database.
36
miRTarBase ID miRNA Experiments Reference
MIRT1173405 hsa-miR-2110 CLIP-seq
MIRT1173406 hsa-miR-3150a-3p CLIP-seq
MIRT1173407 hsa-miR-4260 CLIP-seq
MIRT1173408 hsa-miR-4450 CLIP-seq
MIRT1173409 hsa-miR-4488 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
33
GO ID Ontology Definition Evidence Reference
GO:0000932 Component P-body IEA
GO:0000932 Component P-body ISS
GO:0003723 Function RNA binding IEA
GO:0003729 Function MRNA binding IBA
GO:0003729 Function MRNA binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608228 23292 ENSG00000188425
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P60321
Protein name Nanos homolog 2 (NOS-2)
Protein function Plays a key role in the sexual differentiation of germ cells by promoting the male fate but suppressing the female fate. Represses the female fate pathways by suppressing meiosis, which in turn results in the promotion of the male fate. Maintain
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05741 zf-nanos 63 116 Nanos RNA binding domain Family
Tissue specificity TISSUE SPECIFICITY: Testis and ovary. Expression found in several spermatogenic stages: in cells on the periphery of the tubules which could correspond to spermatogonia, in spermatocytes and in round spermatids (at protein level). {ECO:0000269|PubMed:1916
Sequence
MQLPPFDMWKDYFNLSQVVWALIASRGQRLETQEIEEPSPGPPLGQDQGLGAPGANGGLG
TLCNFCKHNGESRHVYSSHQLKTPDGVVVCPILRHYVCPVCGATGDQAHTLKYCPLNGGQ
QSLYRRSGRNSAGRRVKR
Sequence length 138
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INFERTILITY, MALE CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MALE INFERTILITY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEUROTIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Azoospermia Nonobstructive Associate 29790874
★☆☆☆☆
Found in Text Mining only
Neoplasm Metastasis Associate 36012673
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 36012673, 37454491
★☆☆☆☆
Found in Text Mining only
Sertoli Cell Only Syndrome Associate 37296437
★☆☆☆☆
Found in Text Mining only