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Protein FAM199X (FAM199X)

Homo sapiens — UniProt Q6PEV8

Gene: FAM199XHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Protein FAM199X (FAM199X) is a protein from Homo sapiens identified by UniProt accession Q6PEV8, 388 residues long. MolForge cross-references it against 0 known binders and 8 disease associations.

  • UniProt accession: Q6PEV8; gene symbol FAM199X.
  • Organism: Homo sapiens.
  • Length: 388 amino acids.
  • Top disease associations (Open Targets): neurodegenerative disease, 15q11q13 microduplication syndrome and isolated asymptomatic elevation of creatine phosphokinase.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameProtein FAM199X
UniProt accessionQ6PEV8
GeneFAM199X
OrganismHomo sapiens
Length388 residues
Molecular weight—
EC numbers—
Target class—
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (8)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.52
  • 15q11q13 microduplication syndrome · score 0.12
  • isolated asymptomatic elevation of creatine phosphokinase · score 0.05
  • pentosuria · score 0.04
  • 46,XX ovotesticular disorder of sex development · score 0.03
  • 46,XY complete gonadal dysgenesis · score 0.03
  • meningococcal infection · score 0.00
  • type 1 diabetes mellitus · score 0.00

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q6PEV8-F1alphafoldPREDICTED56.29—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q6PEV8.

Amino-acid sequence (388 residues)

MSDEASAITS YEKFLTPEEP FPLLGPPRGV GTCPSEEPGC LDISDFGCQL SSCHRTDPLH RFHTNRWNLT SCGTSVASSE GSEELFSSVS VGDQDDCYSL LDDQDFTSFD LFPEGSVCSD VSSSISTYWD WSDSEFEWQL PGSDIASGSD VLSDVIPSIP SSPCLLPKKK NKHRNLDELP WSAMTNDEQV EYIEYLSRKV STEMGLREQL DIIKIIDPSA QISPTDSEFI IELNCLTDEK LKQVRNYIKE HSPRQRPARE AWKRSNFSCA STSGVSGASA SASSSSASMV SSASSSGSSV GNSASNSSAN MSRAHSDSNL SASAAERIRD SKKRSKQRKL QQKAFRKRQL KEQRQARKER LSGLFLNEEV LSLKVTEEDH EADVDVLM

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with FAM199X?

The strongest Open Targets associations for FAM199X are neurodegenerative disease, 15q11q13 microduplication syndrome, isolated asymptomatic elevation of creatine phosphokinase, pentosuria and 46,XX ovotesticular disorder of sex development.

How long is the FAM199X protein?

The Homo sapiens FAM199X protein (UniProt Q6PEV8) is 388 amino acids long.

Browse: Targets: F · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ6PEV8
GeneFAM199X
OrganismHomo sapiens
Length388
Binders0
Diseases8
View on UniProt