Skip to content

Sodium channel and clathrin linker 1 (SCLT1)

Homo sapiens — UniProt Q96NL6

Gene: SCLT1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Sodium channel and clathrin linker 1 (SCLT1) is a protein from Homo sapiens identified by UniProt accession Q96NL6, 688 residues long. MolForge cross-references it against 0 known binders and 154 disease associations.

  • UniProt accession: Q96NL6; gene symbol SCLT1.
  • Organism: Homo sapiens.
  • Length: 688 amino acids.
  • Top disease associations (Open Targets): Astigmatism, Nystagmus and congenital hypothalamic hamartoma syndrome.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameSodium channel and clathrin linker 1
UniProt accessionQ96NL6
GeneSCLT1
OrganismHomo sapiens
Length688 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 (154)

Diseases linked to this target (Open Targets).

  • Astigmatism · score 0.41
  • Nystagmus · score 0.41
  • congenital hypothalamic hamartoma syndrome · score 0.41
  • Hypermetropia · score 0.41
  • Global developmental delay · score 0.41
  • Bardet-Biedl syndrome · score 0.38
  • hip bone mineral density · score 0.27
  • hip bone size · score 0.26
  • neurodegenerative disease · score 0.25
  • fat body mass · score 0.21

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q96NL6-F1alphafoldPREDICTED82.09—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q96NL6.

Amino-acid sequence (688 residues)

MAAEIDFLRE QNRRLNEDFR RYQMESFSKY SSVQKAVCQG EGDDTFENLV FDQSFLAPLV TEYDKHLGEL NGQLKYYQKQ VGEMKLQLEN VIKENERLHS ELKDAVEKKL EAFPLGTEVG TDIYADDETV RNLQEQLQLA NQEKTQAVEL WQTVSQELDR LHKLYQEHMT EAQIHVFESQ KQKDQLFDFQ QLTKQLHVTN ENMEVTNQQF LKTVTEQSVI IEQLRKKLRQ AKLELRVAVA KVEELTNVTE DLQGQMKKKE KDVVSAHGRE EASDRRLQQL QSSIKQLEIR LCVTIQEANQ LRTENTHLEK QTRELQAKCN ELENERYEAI VRARNSMQLL EEANLQKSQA LLEEKQKEED IEKMKETVSR FVQDATIRTK KEVANTKKQC NIQISRLTEE LSALQMECAE KQGQIERVIK EKKAVEEELE KIYREGRGNE SDYRKLEEMH QRFLVSERSK DDLQLRLTRA ENRIKQLETD SSEEISRYQE MIQKLQNVLE SERENCGLVS EQRLKLQQEN KQLRKETESL RKIALEAQKK AKVKISTMEH EFSIKERGFE VQLREMEDSN RNSIVELRHL LATQQKAANR WKEETKKLTE SAEIRINNLK SELSRQKLHT QELLSQLEMA NEKVAENEKL ILEHQEKANR LQRRLSQAEE RAASASQQLS VITVQRRKAA SLMNLENI

Frequently asked questions

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

Which diseases are associated with SCLT1?

The strongest Open Targets associations for SCLT1 are Astigmatism, Nystagmus, congenital hypothalamic hamartoma syndrome, Hypermetropia and Global developmental delay.

How long is the SCLT1 protein?

The Homo sapiens SCLT1 protein (UniProt Q96NL6) is 688 amino acids long.

Browse: Targets: S · 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.

Explore Sodium channel and clathrin linker 1 with MolForge

Find binders, run structure-based screening, and map this target across diseases and approved drugs with our AI-powered platform.

Browse all targets

Quick facts

UniProtQ96NL6
GeneSCLT1
OrganismHomo sapiens
Length688
Binders0
Diseases154
View on UniProt