LIM homeobox transcription factor 1-alpha (LMX1A)

Homo sapiens — UniProt Q8TE12

Gene: LMX1AHomo sapiensSwissProt reviewed

About LIM homeobox transcription factor 1-alpha

LIM homeobox transcription factor 1-alpha (LMX1A) is a protein from Homo sapiens identified by UniProt accession Q8TE12, 382 residues long. MolForge cross-references it against 0 known binders and 292 disease associations.

Target properties

Protein nameLIM homeobox transcription factor 1-alpha
UniProt accessionQ8TE12
GeneLMX1A
OrganismHomo sapiens
Length382 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
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 (292)

Diseases linked to this target (Open Targets).

  • autosomal dominant nonsyndromic hearing loss 7 · score 0.67
  • autosomal dominant nonsyndromic hearing loss · score 0.51
  • BMI-adjusted waist-hip ratio · score 0.39
  • alcohol consumption measurement · score 0.35
  • mathematical ability · score 0.34
  • neurodegenerative disease · score 0.34
  • Sensorineural hearing impairment · score 0.33
  • sensorineural hearing loss · score 0.33
  • brain measurement · score 0.31
  • cortical thickness · score 0.31

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8TE12-F1alphafoldPREDICTED68.59—

Amino-acid sequence (382 residues)

MLDGLKMEEN FQSAIDTSAS FSSLLGRAVS PKSVCEGCQR VILDRFLLRL NDSFWHEQCV QCASCKEPLE TTCFYRDKKL YCKYDYEKLF AVKCGGCFEA IAPNEFVMRA QKSVYHLSCF CCCVCERQLQ KGDEFVLKEG QLLCKGDYEK ERELLSLVSP AASDSGKSDD EESLCKSAHG AGKGTAEEGK DHKRPKRPRT ILTTQQRRAF KASFEVSSKP CRKVRETLAA ETGLSVRVVQ VWFQNQRAKM KKLARRQQQQ QQDQQNTQRL SSAQTNGGGS AGMEGIMNPY TALPTPQQLL AIEQSVYSSD PFRQGLTPPQ MPGDHMHPYG AEPLFHDLDS DDTSLSNLGD CFLATSEAGP LQSRVGNPID HLYSMQNSYF TS

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Quick facts

UniProtQ8TE12
GeneLMX1A
OrganismHomo sapiens
Length382
Binders0
Diseases292
View on UniProt