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Epidermal growth factor receptor kinase substrate 8-like protein 2 (EPS8L2)

Homo sapiens — UniProt Q9H6S3

Gene: EPS8L2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Epidermal growth factor receptor kinase substrate 8-like protein 2 (EPS8L2) is a protein from Homo sapiens identified by UniProt accession Q9H6S3, 715 residues long. MolForge cross-references it against 0 known binders and 46 disease associations.

  • UniProt accession: Q9H6S3; gene symbol EPS8L2.
  • Organism: Homo sapiens.
  • Length: 715 amino acids.
  • Top disease associations (Open Targets): deafness, hearing loss, autosomal recessive and intellectual disability, autosomal dominant 24.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameEpidermal growth factor receptor kinase substrate 8-like protein 2
UniProt accessionQ9H6S3
GeneEPS8L2
OrganismHomo sapiens
Length715 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 (46)

Diseases linked to this target (Open Targets).

  • deafness · score 0.60
  • hearing loss, autosomal recessive · score 0.59
  • intellectual disability, autosomal dominant 24 · score 0.41
  • genetic disorder · score 0.19
  • nonsyndromic genetic hearing loss · score 0.18
  • intellectual disability-epilepsy-extrapyramidal syndrome · score 0.18
  • intellectual developmental disorder with paroxysmal dyskinesia or seizures · score 0.18
  • Meniere disease · score 0.16
  • body height · score 0.14
  • blood protein measurement · score 0.07

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H6S3-F1alphafoldPREDICTED73.04—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H6S3.

Amino-acid sequence (715 residues)

MSQSGAVSCC PGATNGSLGR SDGVAKMSPK DLFEQRKKYS NSNVIMHETS QYHVQHLATF IMDKSEAITS VDDAIRKLVQ LSSKEKIWTQ EMLLQVNDQS LRLLDIESQE ELEDFPLPTV QRSQTVLNQL RYPSVLLLVC QDSEQSKPDV HFFHCDEVEA ELVHEDIESA LADCRLGKKM RPQTLKGHQE KIRQRQSILP PPQGPAPIPF QHRGGDSPEA KNRVGPQVPL SEPGFRRRES QEEPRAVLAQ KIEKETQILN CALDDIEWFV ARLQKAAEAF KQLNQRKKGK KKGKKAPAEG VLTLRARPPS EGEFIDCFQK IKLAINLLAK LQKHIQNPSA AELVHFLFGP LDLIVNTCSG PDIARSVSCP LLSRDAVDFL RGHLVPKEMS LWESLGESWM RPRSEWPREP QVPLYVPKFH SGWEPPVDVL QEAPWEVEGL ASAPIEEVSP VSRQSIRNSQ KHSPTSEPTP PGDALPPVSS PHTHRGYQPT PAMAKYVKIL YDFTARNANE LSVLKDEVLE VLEDGRQWWK LRSRSGQAGY VPCNILGEAR PEDAGAPFEQ AGQKYWGPAS PTHKLPPSFP GNKDELMQHM DEVNDELIRK ISNIRAQPQR HFRVERSQPV SQPLTYESGP DEVRAWLEAK AFSPRIVENL GILTGPQLFS LNKEELKKVC GEEGVRVYSQ LTMQKAFLEK QQSGSELEEL MNKFHSMNQR RGEDS

Frequently asked questions

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

Which diseases are associated with EPS8L2?

The strongest Open Targets associations for EPS8L2 are deafness, hearing loss, autosomal recessive, intellectual disability, autosomal dominant 24, genetic disorder and nonsyndromic genetic hearing loss.

How long is the EPS8L2 protein?

The Homo sapiens EPS8L2 protein (UniProt Q9H6S3) is 715 amino acids long.

Browse: Targets: E · 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

UniProtQ9H6S3
GeneEPS8L2
OrganismHomo sapiens
Length715
Binders0
Diseases46
View on UniProt