SPANXN1 (SPANX family member N1)

Gene Gene information from NCBI Gene database.
Gene miRNA Other IDs Protein Associated diseases
Entrez ID 494118
Gene name SPANX family member N1
Gene symbol SPANXN1
Synonyms (NCBI Gene)
CT11.6
Chromosome X
Chromosome location Xq27.3
Summary This gene represents one of several duplicated family members that are located on chromosome X. This gene family encodes proteins that play a role in spermiogenesis. These proteins represent a specific subgroup of cancer/testis-associated antigens, and th
miRNA miRNA information provided by mirtarbase database.
91
Gene miRNA Other IDs Protein Associated diseases
Show/Hide all (91)
miRTarBase ID miRNA Experiments Reference
MIRT615613 hsa-miR-1245b-5p HITS-CLIP 23824327
MIRT615612 hsa-miR-3142 HITS-CLIP 23824327
MIRT615611 hsa-miR-5193 HITS-CLIP 23824327
MIRT615610 hsa-miR-660-3p HITS-CLIP 23824327
MIRT615609 hsa-miR-877-3p HITS-CLIP 23824327
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
300664 33174 ENSG00000203923
Protein Protein information from UniProt database.
Gene miRNA Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5VSR9
Protein name Sperm protein associated with the nucleus on the X chromosome N1 (Nuclear-associated protein SPAN-Xn1) (SPANX-N1) (SPANX family member N1)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07458 SPAN-X 1 → 72 Sperm protein associated with nucleus, mapped to X chromosome Family
Sequence
Sequence length 72
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Gene miRNA Other IDs Protein Associated diseases
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 (1)
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
CHROMOSOME XQ28 DUPLICATION SYNDROME — Disgenet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations