• Gene id: 83856

Gene Summary

• Gene Symbol: FSD1L   Gene   UCSC   Ensembl
• Aliases: CCDC10, CSDUFD1, FSD1CL, FSD1NL, MIR1
• Gene name: fibronectin type III and SPRY domain containing 1 like
• Alternate names: FSD1-like protein, FSD1 C-terminal like, FSD1 N-terminal like, coiled-coil domain containing 10, cystatin and DUF19 domain containing 1,
• Gene location: 9q31.2 (105442182: 105552432)     Exons: 18     NC_000009.12

Protein Summary

• Protein general information: Q9BXM9  
  • Name: FSD1 like protein (Coiled coil domain containing protein 10) (FSD1 N terminal like protein)
  • Length: 530  
  • Mass: 59578
• Sequence:

  MDSQKYCFKENENVTVDKACFLISNITIGPESINLQQEALQRIISTLANKNDEIQNFIDTLHHTLKGVQENSSNI
  LSELDEEFDSLYSILDEVKESMINCIKQEQARKSQELQSQISQCNNALENSEELLEFATRSLDIKEPEEFSKAAR
  QIKDRVTMASAFRLSLKPKVSDNMTHLMVDFSQERQMLQTLKFLPVPKAPEIDPVECLVADNSVTVAWRMPEEDN
  KIDHFILEHRKTNFDGLPRVKDERCWEIIDNIKGTEYTLSGLKFDSKYMNFRVRACNKAVAGEYSDPVTLETKAL
  NFNLDNSSSHLNLKVEDTCVEWDPTGGKGQESKIKGKENKGRSGTPSPKRTSVGSRPPAVRGSRDRFTGESYTVL
  GDTAIESGQHYWEVKAQKDCKSYSVGVAYKTLGKFDQLGKTNTSWCIHVNNWLQNTFAAKHNNKVKALDVTVPEK
  IGVFCDFDGGQLSFYDANSKQLLYSFKTKFTQPVLPGFMVWCGGLSLSTGMQVPSAVRTLQKSENGMTGSASSLN
  NVVTQ

• Structural information:
  • Protein Domains: (137..19-)
    (/note="COS-)
    (/evidence="ECO:0000255|PROSITE-ProRule:PRU00586-)
    (196..30-)
    (/note="Fibronectin-type-III)
    (/evidence="ECO:0000255|PROSITE-ProRule:PRU00316-)
    (300..50-)
    (/note="B30.2/SPRY-)
    (/evidence="ECO:0000255|PROSITE-ProR-)
  • Interpro: IPR001870  IPR003649  IPR003879  IPR013320  IPR017903   IPR003961  IPR036116  IPR013783  IPR035742  IPR003877  
  • Prosite: PS50188 PS51262 PS50853
  • CDD: cd00063 cd12901
  • STRING: ENSP00000417492
• Other Databases: GeneCards:  FSD1L  Malacards:  FSD1L

Gene ontology

GO accession	Term name	Evidence code	Go category
GO:0005575	cellular_component	ND	cellular component
GO:0003674	molecular_function	ND	molecular function
GO:0008150	biological_process	ND	biological process

Diseases

Associated diseases	References
Spermatogenic defects	MIK: 31037746

PubMed references

PMID	Condition	Mutation	Ethnicity	Population details	Infertility_type	Associated_genes
31037746	Spermatogenic defects			16 (1 control, 15 cases)	Male infertility	GSE6023 analyzed using GEO2R