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Transcription factor SPT20 homolog-like 2 (SUPT20HL2)

Homo sapiens — UniProt P0C7V6

Gene: SUPT20HL2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Transcription factor SPT20 homolog-like 2 (SUPT20HL2) is a protein from Homo sapiens identified by UniProt accession P0C7V6, 817 residues long. MolForge cross-references it against 0 known binders and 2 disease associations.

  • UniProt accession: P0C7V6; gene symbol SUPT20HL2.
  • Organism: Homo sapiens.
  • Length: 817 amino acids.
  • Top disease associations (Open Targets): craniodiaphyseal dysplasia and Bardet-Biedl syndrome.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameTranscription factor SPT20 homolog-like 2
UniProt accessionP0C7V6
GeneSUPT20HL2
OrganismHomo sapiens
Length817 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 (2)

Diseases linked to this target (Open Targets).

  • craniodiaphyseal dysplasia · score 0.00
  • Bardet-Biedl syndrome · score 0.00

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P0C7V6-F1alphafoldPREDICTED50.05—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for P0C7V6.

Amino-acid sequence (817 residues)

MDRDLEQALD RTENITEIAQ QRRPRRRYSP RAGKTLQEKL YDIYVEECGK EPEDPQELRS NVNLLEKLVR RESLPCLLVN LYPGNQGYSV MLQREDGSFA ETIRLPYEER ALLDYLDAEE LPPALGDVLD KASVNIFHSG CVIVEVRDYR QSSNMQPPGY QSRHILLRPT MQTLAPEVKT MTRDGEKWSQ EDKFPLESQL ILATAEPLCL DPSVAVACTA NRLLYNKQKM NTDPMEQCLQ RYSWPSVKPQ QEQSDCPPPP ELRVSTSGQK EERKVGQPCE LNITKAGSCV DTWKGRPCDL AVPSEVDVEK LAKGYQSVTA ADPQLPVWPA QEVEDPFRHA WEAGCQAWDT KPNIMQSFND PLLCGKIRPR KKARQKSQKS PWQPFPDDHS ACLRPGSETD AGRAVSQAQE SVQSKVKGPG KMSHSSSGPA SVSQLSSWKT PEQPDPVWVQ SSVSGKGEKH PPPRTQLPSS SGKISSGNSF PPQQAGSPLK RPFPAAAPAV AAAAPAPAPA PAAAPALAAA AVAAAAGGAA PSHSQKPSVP LIKASRRRPA AGRPTRFVKI APAIQVRTGS TGLKATNVEG PVRGAQVLGC SFKPVQAPGS GAPAPAGISG SGLQSSGGPL PDARPGAVQA SSPAPLQFFL NTPEGLRPLT LQVPQGWAVL TGPQQQSHQL VSLQQLQQPT AAHPPQPGPQ GSTLGLSTQG QAFPAQQLLN VNLTGAGSGL QPQPQAAVLS LLGSAQVPQQ GVQLPFVLGQ QPQPLLLLQP QPQPQQIQLQ TQPLRVLQQP VFLATGAVQI VQPHPGVQAG SQLVGQRKGG KPTPPAP

Frequently asked questions

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

Which diseases are associated with SUPT20HL2?

The strongest Open Targets associations for SUPT20HL2 are craniodiaphyseal dysplasia and Bardet-Biedl syndrome.

How long is the SUPT20HL2 protein?

The Homo sapiens SUPT20HL2 protein (UniProt P0C7V6) is 817 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.

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Quick facts

UniProtP0C7V6
GeneSUPT20HL2
OrganismHomo sapiens
Length817
Binders0
Diseases2
View on UniProt