Incidental Mutation 'R6247:Hdac4'
ID 505657
Institutional Source Beutler Lab
Gene Symbol Hdac4
Ensembl Gene ENSMUSG00000026313
Gene Name histone deacetylase 4
Synonyms 4932408F19Rik
MMRRC Submission 044366-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6247 (G1)
Quality Score 224.009
Status Not validated
Chromosome 1
Chromosomal Location 91856501-92123421 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 91940560 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000095249 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000008995] [ENSMUST00000097644]
AlphaFold Q6NZM9
Predicted Effect probably null
Transcript: ENSMUST00000008995
SMART Domains Protein: ENSMUSP00000008995
Gene: ENSMUSG00000026313

DomainStartEndE-ValueType
Pfam:HDAC4_Gln 61 151 5e-38 PFAM
low complexity region 289 310 N/A INTRINSIC
low complexity region 354 368 N/A INTRINSIC
low complexity region 472 502 N/A INTRINSIC
low complexity region 517 529 N/A INTRINSIC
low complexity region 558 575 N/A INTRINSIC
Pfam:Hist_deacetyl 661 985 1.4e-85 PFAM
low complexity region 1066 1075 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000097644
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.4%
  • 20x: 95.4%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class II of the histone deacetylase/acuc/apha family. It possesses histone deacetylase activity and represses transcription when tethered to a promoter. This protein does not bind DNA directly, but through transcription factors MEF2C and MEF2D. It seems to interact in a multiprotein complex with RbAp48 and HDAC3. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a gene trap allele exhibit increased thermal nociception threshold and seizures. Mice homozygous for a knock-out allele exhibit postnatal lethality, exencephaly, and abnormal skeleton morphology and physiology. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 86 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427D14Rik T C 11: 72,049,768 (GRCm39) D871G probably benign Het
A4galt G T 15: 83,112,020 (GRCm39) H254Q probably damaging Het
AA986860 C A 1: 130,670,780 (GRCm39) T334K possibly damaging Het
Abca13 T C 11: 9,353,874 (GRCm39) I3732T probably benign Het
Abcf1 C T 17: 36,271,956 (GRCm39) D353N probably damaging Het
Adss1 A G 12: 112,594,790 (GRCm39) H83R probably damaging Het
Amer2 C A 14: 60,616,321 (GRCm39) A172E probably damaging Het
Ankhd1 A G 18: 36,787,199 (GRCm39) T2300A probably benign Het
Ano5 G A 7: 51,215,879 (GRCm39) probably null Het
Apob G A 12: 8,051,801 (GRCm39) G1109D probably damaging Het
Arhgef26 A T 3: 62,288,381 (GRCm39) N484Y probably damaging Het
C6 A G 15: 4,793,023 (GRCm39) D376G probably damaging Het
Caml T C 13: 55,772,986 (GRCm39) probably null Het
Capn12 T C 7: 28,588,077 (GRCm39) L473S probably benign Het
Cdk6 G A 5: 3,394,553 (GRCm39) probably null Het
Cers5 A T 15: 99,643,805 (GRCm39) C153S probably benign Het
Cfap206 T C 4: 34,692,530 (GRCm39) M499V probably benign Het
Chd6 A G 2: 160,791,968 (GRCm39) M2463T probably damaging Het
Chn1 T C 2: 73,537,350 (GRCm39) E58G possibly damaging Het
Clec4a1 T C 6: 122,905,001 (GRCm39) V100A probably benign Het
Col7a1 G C 9: 108,810,130 (GRCm39) probably benign Het
Csmd1 A G 8: 16,246,249 (GRCm39) V1050A possibly damaging Het
Dab1 C T 4: 104,588,948 (GRCm39) A524V probably benign Het
Dennd5a A T 7: 109,497,889 (GRCm39) C1044S probably damaging Het
Dnah7b A G 1: 46,265,048 (GRCm39) T2181A probably benign Het
Dnai1 T C 4: 41,605,775 (GRCm39) V255A probably benign Het
Dync2h1 A G 9: 7,135,078 (GRCm39) C1518R probably damaging Het
Dysf T C 6: 84,043,981 (GRCm39) V273A probably damaging Het
Eif1 C T 11: 100,211,223 (GRCm39) probably benign Het
Eml3 T C 19: 8,908,313 (GRCm39) I58T probably benign Het
Fam171b T A 2: 83,709,552 (GRCm39) I408N probably damaging Het
Fchsd2 A G 7: 100,902,747 (GRCm39) E351G probably benign Het
Focad G A 4: 88,325,377 (GRCm39) A81T possibly damaging Het
Fpr-rs4 G A 17: 18,242,748 (GRCm39) V252I probably benign Het
Fryl A G 5: 73,222,824 (GRCm39) L1919P probably damaging Het
Gm12185 C T 11: 48,806,735 (GRCm39) R152H probably damaging Het
Gm14410 C T 2: 176,885,517 (GRCm39) G249E probably damaging Het
Gm6685 A T 11: 28,289,706 (GRCm39) S37T possibly damaging Het
Greb1 G A 12: 16,766,676 (GRCm39) P374L probably damaging Het
Hecw1 A T 13: 14,409,010 (GRCm39) L1099* probably null Het
Hivep1 T C 13: 42,310,966 (GRCm39) S1069P probably benign Het
Itgad T C 7: 127,784,959 (GRCm39) I288T possibly damaging Het
Kif9 A G 9: 110,317,612 (GRCm39) M96V possibly damaging Het
Kncn T A 4: 115,741,987 (GRCm39) V18E probably damaging Het
Lrrc74a G A 12: 86,805,330 (GRCm39) G384D probably damaging Het
Ltb4r2 T C 14: 56,000,108 (GRCm39) V243A probably damaging Het
Mtnr1b T A 9: 15,774,082 (GRCm39) I326L probably benign Het
Mylip C T 13: 45,561,957 (GRCm39) T253I probably damaging Het
Necap1 T A 6: 122,857,611 (GRCm39) probably null Het
Nedd4 C T 9: 72,633,720 (GRCm39) P409S probably damaging Het
Npat A T 9: 53,456,538 (GRCm39) E36D probably damaging Het
Ovch2 C T 7: 107,384,648 (GRCm39) V490M probably damaging Het
Pax9 T C 12: 56,756,480 (GRCm39) S273P probably benign Het
Plce1 A G 19: 38,734,289 (GRCm39) E1563G probably damaging Het
Podxl2 C A 6: 88,826,299 (GRCm39) G336* probably null Het
Prdm1 A G 10: 44,322,782 (GRCm39) probably null Het
Psme4 T C 11: 30,803,245 (GRCm39) I29T possibly damaging Het
Ptprd A T 4: 75,984,528 (GRCm39) D780E probably benign Het
Retsat T C 6: 72,581,918 (GRCm39) M294T probably benign Het
Robo2 A T 16: 73,764,672 (GRCm39) V652D probably damaging Het
Rptn C G 3: 93,305,437 (GRCm39) H923Q possibly damaging Het
Serpinb3d G T 1: 107,010,490 (GRCm39) T66K probably benign Het
Setd1b A T 5: 123,296,461 (GRCm39) probably benign Het
Slc7a10 G T 7: 34,886,012 (GRCm39) A36S possibly damaging Het
Sstr3 T A 15: 78,423,788 (GRCm39) I320F probably damaging Het
Syne1 G T 10: 5,299,071 (GRCm39) A1005E probably damaging Het
Syngap1 C A 17: 27,181,931 (GRCm39) S975* probably null Het
Tinagl1 C T 4: 130,066,725 (GRCm39) C124Y probably null Het
Tm9sf1 C T 14: 55,873,827 (GRCm39) R557H probably damaging Het
Tmed2 T A 5: 124,685,055 (GRCm39) I68K possibly damaging Het
Tmem104 A G 11: 115,134,819 (GRCm39) T451A probably benign Het
Tmem141 T C 2: 25,511,693 (GRCm39) probably null Het
Tmem184a C A 5: 139,798,827 (GRCm39) V41L probably benign Het
Tmem39b C T 4: 129,580,584 (GRCm39) V303I possibly damaging Het
Tsn T C 1: 118,232,939 (GRCm39) I122V probably benign Het
Ttc41 G T 10: 86,612,527 (GRCm39) V1267L probably benign Het
Uggt1 A T 1: 36,202,309 (GRCm39) L1096Q probably damaging Het
Usp50 A T 2: 126,617,713 (GRCm39) I244N probably benign Het
Vil1 A G 1: 74,471,498 (GRCm39) S760G probably benign Het
Wasf1 T A 10: 40,813,741 (GRCm39) V541E unknown Het
Zc3h13 G T 14: 75,581,176 (GRCm39) S1721I probably benign Het
Zfp180 G T 7: 23,804,530 (GRCm39) K316N probably damaging Het
Zfp582 T C 7: 6,356,945 (GRCm39) C253R probably damaging Het
Zfp709 TCGACG TCG 8: 72,644,552 (GRCm39) probably benign Het
Zfp759 A G 13: 67,288,524 (GRCm39) T692A probably benign Het
Zfyve26 A G 12: 79,329,758 (GRCm39) V476A probably benign Het
Other mutations in Hdac4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01324:Hdac4 APN 1 91,887,137 (GRCm39) missense probably damaging 0.99
IGL01396:Hdac4 APN 1 91,887,196 (GRCm39) splice site probably benign
IGL01536:Hdac4 APN 1 91,857,868 (GRCm39) utr 3 prime probably benign
IGL01860:Hdac4 APN 1 91,861,417 (GRCm39) missense probably benign 0.31
IGL02110:Hdac4 APN 1 91,912,127 (GRCm39) missense probably benign 0.00
IGL02201:Hdac4 APN 1 91,915,382 (GRCm39) splice site probably null
IGL02294:Hdac4 APN 1 91,909,929 (GRCm39) missense probably benign
IGL02367:Hdac4 APN 1 91,886,171 (GRCm39) splice site probably benign
IGL02429:Hdac4 APN 1 91,940,417 (GRCm39) missense probably benign 0.00
IGL02966:Hdac4 APN 1 91,982,667 (GRCm39) missense possibly damaging 0.94
IGL03250:Hdac4 APN 1 91,862,322 (GRCm39) critical splice donor site probably null
R0067:Hdac4 UTSW 1 91,957,706 (GRCm39) missense probably damaging 1.00
R0103:Hdac4 UTSW 1 91,903,366 (GRCm39) missense possibly damaging 0.73
R0288:Hdac4 UTSW 1 91,898,728 (GRCm39) missense probably damaging 1.00
R0334:Hdac4 UTSW 1 91,883,760 (GRCm39) splice site probably benign
R1473:Hdac4 UTSW 1 91,957,690 (GRCm39) missense possibly damaging 0.88
R1732:Hdac4 UTSW 1 91,875,257 (GRCm39) missense probably benign 0.01
R1826:Hdac4 UTSW 1 91,912,421 (GRCm39) missense probably damaging 1.00
R1987:Hdac4 UTSW 1 91,862,367 (GRCm39) missense probably damaging 1.00
R2189:Hdac4 UTSW 1 91,903,244 (GRCm39) missense probably null 0.00
R2384:Hdac4 UTSW 1 91,912,207 (GRCm39) missense probably benign 0.02
R3705:Hdac4 UTSW 1 91,862,416 (GRCm39) splice site probably benign
R3894:Hdac4 UTSW 1 91,898,690 (GRCm39) missense possibly damaging 0.95
R4440:Hdac4 UTSW 1 91,873,717 (GRCm39) missense probably damaging 1.00
R5075:Hdac4 UTSW 1 91,923,842 (GRCm39) missense probably benign 0.00
R5431:Hdac4 UTSW 1 91,900,512 (GRCm39) nonsense probably null
R5505:Hdac4 UTSW 1 91,903,187 (GRCm39) missense probably benign
R5854:Hdac4 UTSW 1 91,887,143 (GRCm39) missense probably damaging 1.00
R6018:Hdac4 UTSW 1 91,886,120 (GRCm39) missense probably damaging 1.00
R6164:Hdac4 UTSW 1 91,957,876 (GRCm39) missense probably benign 0.04
R6239:Hdac4 UTSW 1 91,982,694 (GRCm39) missense probably benign 0.17
R6306:Hdac4 UTSW 1 91,923,896 (GRCm39) missense probably benign 0.00
R6381:Hdac4 UTSW 1 91,912,247 (GRCm39) missense possibly damaging 0.67
R6450:Hdac4 UTSW 1 91,912,433 (GRCm39) missense possibly damaging 0.81
R6504:Hdac4 UTSW 1 91,896,177 (GRCm39) missense possibly damaging 0.88
R6639:Hdac4 UTSW 1 91,898,670 (GRCm39) missense probably damaging 1.00
R6799:Hdac4 UTSW 1 91,929,935 (GRCm39) missense probably damaging 0.98
R6910:Hdac4 UTSW 1 91,909,875 (GRCm39) missense probably damaging 1.00
R7002:Hdac4 UTSW 1 91,896,083 (GRCm39) missense possibly damaging 0.85
R7781:Hdac4 UTSW 1 91,903,387 (GRCm39) missense probably benign 0.41
R7966:Hdac4 UTSW 1 91,861,402 (GRCm39) missense possibly damaging 0.71
R8156:Hdac4 UTSW 1 91,886,138 (GRCm39) missense probably damaging 0.99
R8732:Hdac4 UTSW 1 91,875,239 (GRCm39) missense probably damaging 1.00
R8957:Hdac4 UTSW 1 91,873,757 (GRCm39) critical splice acceptor site probably null
R9129:Hdac4 UTSW 1 91,909,929 (GRCm39) missense probably benign
R9167:Hdac4 UTSW 1 91,875,256 (GRCm39) missense probably benign 0.35
R9243:Hdac4 UTSW 1 91,900,512 (GRCm39) missense probably benign 0.14
R9243:Hdac4 UTSW 1 91,900,511 (GRCm39) missense probably damaging 0.98
R9255:Hdac4 UTSW 1 91,889,173 (GRCm39) critical splice donor site probably null
R9503:Hdac4 UTSW 1 91,929,956 (GRCm39) missense probably damaging 0.96
R9600:Hdac4 UTSW 1 91,889,277 (GRCm39) missense probably damaging 0.99
Z1177:Hdac4 UTSW 1 91,915,333 (GRCm39) missense probably damaging 0.96
Z1177:Hdac4 UTSW 1 91,883,769 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACTGATGACTCCTGTGTGGG -3'
(R):5'- AGTGCTCTGCAGAGATCCAAG -3'

Sequencing Primer
(F):5'- CTGAGTGCTCACTGTGCCTG -3'
(R):5'- CTGCAGAGATCCAAGACTATTTTATG -3'
Posted On 2018-02-28