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Query results
Results for
HDAC9
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HDAC9
Description
histone deacetylase 9
Aliases
HD7, HD7b, HD9, HDAC, HDAC7, HDAC7BB, HDAC9FL, HDRP, MITR, HDAC9
Gene Identifiers
mRNA Identifiers
RefSeq (mRNA)
NM_001204144.3; NM_001204145.3; NM_001204146.2; NM_001204147.3; NM_001204148.3; NM_001321868.2; NM_001321869.2; NM_001321870.2; NM_001321871.2; NM_001321872.2; NM_001321873.2; NM_001321874.2; NM_001321875.2; NM_001321876.2; NM_001321877.2; NM_001321878.2; NM_001321879.2; NM_001321884.2; NM_001321885.2; NM_001321886.2; NM_001321887.2; NM_001321888.2; NM_001321889.2; NM_001321890.2; NM_001321891.2; NM_001321893.2; NM_001321894.2; NM_001321895.2; NM_001321896.1; NM_001321897.2; NM_001321898.2; NM_001321899.2; NM_001321900.2; NM_001321901.2; NM_001321902.2; NM_014707.4; NM_058176.2; NM_178423.3; NM_178425.3
Protein Identifiers
RefSeq (protein)
NP_001191073.1; NP_001191074.1; NP_001191075.1; NP_001191076.1; NP_001191077.1; NP_001308797.1; NP_001308798.1; NP_001308799.1; NP_001308800.1; NP_001308801.1; NP_001308802.1; NP_001308803.1; NP_001308804.1; NP_001308805.1; NP_001308806.1; NP_001308807.1; NP_001308808.1; NP_001308813.1; NP_001308814.1; NP_001308815.1; NP_001308816.1; NP_001308817.1; NP_001308818.1; NP_001308819.1; NP_001308820.1; NP_001308822.1; NP_001308823.1; NP_001308824.1; NP_001308825.1; NP_001308826.1; NP_001308827.1; NP_001308828.1; NP_001308829.1; NP_001308830.1; NP_001308831.1; NP_055522.1; NP_478056.1; NP_848510.1; NP_848512.1
Uniprot ID
Q9UKV0; Q9UKV0; Q9UKV0; B7Z3P7; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; B7Z3P7; B7Z3P7; Q9UKV0; Q9UKV0; Q9UKV0; B7Z3P7; Q9UKV0; B7Z3P7; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; B7Z3P7; Q9UKV0; B7Z3P7; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0; Q9UKV0
Ensembl protein ID
Protein Architecture
SMART
Disease Mapping
Druggability
- Candidate cancer driver
- Damaged in 269/7921 TCGA samples
- Damaged in 26/1291 cell lines
- Fewer loss of function mutations
- Equal damaging SNVs/indels
- Fewer structural variants