Incidental Mutation 'R7445:Brd7'
ID 577233
Institutional Source Beutler Lab
Gene Symbol Brd7
Ensembl Gene ENSMUSG00000031660
Gene Name bromodomain containing 7
Synonyms bromodomain protein 75 kDa, CELTIX1, BP75
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.785) question?
Stock # R7445 (G1)
Quality Score 225.009
Status Validated
Chromosome 8
Chromosomal Location 88331039-88362194 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 88361708 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 18 (Y18N)
Ref Sequence ENSEMBL: ENSMUSP00000034085 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034085]
AlphaFold O88665
Predicted Effect probably damaging
Transcript: ENSMUST00000034085
AA Change: Y18N

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000034085
Gene: ENSMUSG00000031660
AA Change: Y18N

DomainStartEndE-ValueType
low complexity region 51 68 N/A INTRINSIC
low complexity region 76 96 N/A INTRINSIC
BROMO 129 237 9.72e-38 SMART
Pfam:DUF3512 287 534 2.4e-93 PFAM
coiled coil region 535 564 N/A INTRINSIC
Meta Mutation Damage Score 0.1081 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 100% (67/67)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein which is a member of the bromodomain-containing protein family. The product of this gene has been identified as a component of one form of the SWI/SNF chromatin remodeling complex, and as a protein which interacts with p53 and is required for p53-dependent oncogene-induced senescence which prevents tumor growth. Pseudogenes have been described on chromosomes 2, 3, 6, 13 and 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired cognitive behavior and dendrite morphology in the medial prefrontal cortex. Mice homozygous for a different knock-out allele die in utero prior to E16.5, showing fetal growth retardation and altered limb, blood vessel and organ development. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610040J01Rik T A 5: 63,898,619 S233T probably damaging Het
1700034E13Rik T A 18: 52,660,481 C29S probably damaging Het
1700061G19Rik G A 17: 56,882,973 R333Q possibly damaging Het
9130409I23Rik A G 1: 181,055,012 N113S possibly damaging Het
Ank3 A G 10: 69,992,124 T2208A Het
Ap4s1 T C 12: 51,738,641 L132P probably damaging Het
Ascl4 C T 10: 85,928,500 R4C probably benign Het
Cacna2d3 A G 14: 29,058,618 S648P possibly damaging Het
Camta1 C T 4: 151,144,291 E695K possibly damaging Het
Ccdc28b A G 4: 129,622,607 F53L probably benign Het
Chaf1a A G 17: 56,062,170 D467G possibly damaging Het
Cnnm1 G A 19: 43,440,821 R126H possibly damaging Het
Cog5 T G 12: 31,919,672 S730R possibly damaging Het
Col11a1 A T 3: 114,193,929 E1374D unknown Het
Csmd1 A G 8: 16,158,254 I1229T possibly damaging Het
Dnajc30 T C 5: 135,064,378 L43P probably damaging Het
Eif3f C T 7: 108,934,658 T76M unknown Het
Ermap G A 4: 119,188,710 T42I unknown Het
Gpd1l C T 9: 114,920,674 G25S probably damaging Het
Heatr1 G T 13: 12,431,038 W1632L possibly damaging Het
Ice1 T C 13: 70,596,167 D29G Het
Ipo8 T C 6: 148,789,817 D685G probably benign Het
Klra10 T C 6: 130,275,856 T152A probably benign Het
Lmntd1 T A 6: 145,429,967 S82C probably damaging Het
Maip1 T C 1: 57,407,031 S87P possibly damaging Het
Mapkapk2 A G 1: 131,097,519 S3P unknown Het
Mei4 A G 9: 81,890,239 Y35C possibly damaging Het
Ms4a14 T G 19: 11,302,972 K741Q probably benign Het
Naip2 A C 13: 100,161,782 I582S probably benign Het
Ncapg2 A G 12: 116,419,268 I240V possibly damaging Het
Ncbp1 T A 4: 46,149,914 M145K probably damaging Het
Nmur2 A G 11: 56,032,940 F263L probably damaging Het
Ntrk2 A G 13: 58,846,762 E164G probably benign Het
Olfr48 T A 2: 89,844,272 T234S probably damaging Het
Olfr705 A G 7: 106,873,342 L301S possibly damaging Het
Olfr785 A T 10: 129,409,885 D173V probably benign Het
P3h2 T A 16: 25,985,065 Y317F probably damaging Het
Pcmtd1 C T 1: 7,120,420 R38C probably damaging Het
Pcyox1 T C 6: 86,391,679 T286A possibly damaging Het
Pdxk T C 10: 78,447,967 D131G probably benign Het
Ppl T C 16: 5,089,068 D1121G probably damaging Het
Prkra T C 2: 76,633,598 D240G probably benign Het
Ptgs1 C A 2: 36,245,210 N395K probably benign Het
Ptprq A T 10: 107,590,959 Y1572N probably damaging Het
Pyroxd1 A T 6: 142,358,501 H326L probably benign Het
Rapgef5 A G 12: 117,755,969 D778G probably benign Het
Rbm46 T A 3: 82,864,210 E366V probably damaging Het
Rnd1 G T 15: 98,670,669 H209Q probably benign Het
Rnf122 A T 8: 31,118,500 D32V possibly damaging Het
Samd4b G A 7: 28,406,456 P446S probably benign Het
Slco1a5 C A 6: 142,259,008 A187S possibly damaging Het
Smarca4 G A 9: 21,686,247 V1436M probably damaging Het
Smok2a G A 17: 13,226,639 G368R possibly damaging Het
Smok3c T A 5: 138,064,495 H81Q probably damaging Het
Soga3 T C 10: 29,197,003 S764P possibly damaging Het
Stk16 T C 1: 75,213,652 V245A probably damaging Het
Svep1 A T 4: 58,094,122 N1505K possibly damaging Het
Tigd4 G A 3: 84,595,164 A463T probably benign Het
Tmem117 T C 15: 94,714,918 F112L probably benign Het
Tmem72 A G 6: 116,698,330 I67T probably benign Het
Tnik A G 3: 28,663,909 probably null Het
Trav14-2 A G 14: 53,641,058 Q66R probably damaging Het
Trpv6 T A 6: 41,621,342 D677V probably damaging Het
Vgll4 C T 6: 114,862,196 S278N unknown Het
Wdfy4 C T 14: 33,070,618 W2157* probably null Het
Other mutations in Brd7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01947:Brd7 APN 8 88332875 unclassified probably benign
IGL02172:Brd7 APN 8 88351824 missense probably benign 0.41
IGL02441:Brd7 APN 8 88343590 missense probably damaging 1.00
R0241:Brd7 UTSW 8 88345850 missense probably benign 0.01
R0241:Brd7 UTSW 8 88345850 missense probably benign 0.01
R0845:Brd7 UTSW 8 88342767 nonsense probably null
R1613:Brd7 UTSW 8 88346950 missense probably benign 0.00
R1659:Brd7 UTSW 8 88333792 missense probably damaging 1.00
R1663:Brd7 UTSW 8 88358023 missense possibly damaging 0.87
R2237:Brd7 UTSW 8 88346913 missense probably benign 0.22
R2280:Brd7 UTSW 8 88342757 missense probably benign 0.00
R2916:Brd7 UTSW 8 88342780 missense probably damaging 0.98
R2917:Brd7 UTSW 8 88342780 missense probably damaging 0.98
R3770:Brd7 UTSW 8 88339407 critical splice donor site probably null
R4030:Brd7 UTSW 8 88332931 missense probably damaging 1.00
R5287:Brd7 UTSW 8 88357541 missense probably damaging 1.00
R5403:Brd7 UTSW 8 88357541 missense probably damaging 1.00
R6333:Brd7 UTSW 8 88345191 missense probably damaging 1.00
R7021:Brd7 UTSW 8 88347004 missense probably benign 0.00
R7072:Brd7 UTSW 8 88346987 missense probably benign
R7482:Brd7 UTSW 8 88361626 missense probably damaging 0.99
R7977:Brd7 UTSW 8 88334141 missense probably benign
R7987:Brd7 UTSW 8 88334141 missense probably benign
R8205:Brd7 UTSW 8 88343615 missense probably damaging 1.00
R8814:Brd7 UTSW 8 88345154 missense probably benign 0.00
R8984:Brd7 UTSW 8 88354712 missense probably benign 0.00
R9190:Brd7 UTSW 8 88354646 missense probably damaging 1.00
R9296:Brd7 UTSW 8 88332932 missense possibly damaging 0.46
X0067:Brd7 UTSW 8 88343697 splice site probably null
Predicted Primers PCR Primer
(F):5'- TGGGACAAGACTTGCTGAGC -3'
(R):5'- ACTTCTACGAGGGTGAGGAG -3'

Sequencing Primer
(F):5'- CAGACTTCCCAGACGTCTG -3'
(R):5'- GAGGAGCGGCTGGCCTG -3'
Posted On 2019-10-07