Mutagenetix > Incidental Mutations

Incidental Mutation 'R0420:Brd9'

37014

Institutional Source

Beutler Lab

Gene Symbol

Brd9

Ensembl Gene

ENSMUSG00000057649

Gene Name

bromodomain containing 9

Synonyms

MMRRC Submission

038622-MU

Accession Numbers

Is this an essential gene?

Essential (E-score: 1.000) question?

Stock #

R0420 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

73937811-73960895 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 73955473 bp

Zygosity

Heterozygous

Amino Acid Change

Methionine to Valine at position 491 (M491V)

Ref Sequence

ENSEMBL: ENSMUSP00000152390 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099384] [ENSMUST00000222399]

Predicted Effect

probably benign
Transcript: ENSMUST00000099384
AA Change: M492V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000096982
Gene: ENSMUSG00000057649
AA Change: M492V

Domain	Start	End	E-Value	Type
low complexity region	23	34	N/A	INTRINSIC
coiled coil region	53	104	N/A	INTRINSIC
low complexity region	116	127	N/A	INTRINSIC
BROMO	134	242	1.52e-30	SMART
low complexity region	249	264	N/A	INTRINSIC
Pfam:DUF3512	274	505	1.6e-82	PFAM
low complexity region	544	557	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220488

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221324

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222191

Predicted Effect

probably benign
Transcript: ENSMUST00000222399
AA Change: M491V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222479

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223446

Predicted Effect

probably benign
Transcript: ENSMUST00000223525

Meta Mutation Damage Score

0.0728

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.1%
20x: 95.2%

Validation Efficiency

100% (76/76)

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930415O20Rik	A	G	15: 98,571,094	S17G	probably benign	Het
Abcb4	T	C	5: 8,941,050	V870A	probably benign	Het
Adam6b	A	T	12: 113,489,994	M144L	probably benign	Het
Adrb2	T	A	18: 62,179,539	I72L	possibly damaging	Het
Ankrd53	A	T	6: 83,763,692	H99L	probably damaging	Het
Ap4e1	C	T	2: 127,049,360	T17M	probably damaging	Het
Arnt	T	A	3: 95,470,394		probably benign	Het
Atp1a3	C	T	7: 24,980,627	G884E	probably benign	Het
Atp6v1b1	T	C	6: 83,752,844		probably benign	Het
Atp8a2	G	T	14: 59,773,744	T971K	probably damaging	Het
BC048562	A	T	9: 108,445,966	T167S	probably benign	Het
Btnl10	A	T	11: 58,923,451	D319V	probably damaging	Het
Cadps	T	A	14: 12,491,800	R783S	probably damaging	Het
Ccdc149	A	G	5: 52,400,239		probably benign	Het
Ccm2l	A	T	2: 153,070,862	D107V	probably null	Het
Cep192	A	G	18: 67,813,893	E213G	possibly damaging	Het
Cyp2c37	A	C	19: 39,995,794	N242T	probably benign	Het
Dnah17	A	G	11: 118,039,939	V3750A	probably damaging	Het
Ehbp1	T	A	11: 22,151,836	I231L	probably benign	Het
Emilin3	A	G	2: 160,910,879		probably benign	Het
Eya4	T	C	10: 23,155,963	N254S	possibly damaging	Het
Fam184b	A	G	5: 45,584,512	S126P	probably damaging	Het
Fancd2	T	C	6: 113,536,979	L108P	probably damaging	Het
Fgf12	A	T	16: 28,162,529	M145K	possibly damaging	Het
Gabbr1	A	G	17: 37,046,762	N23S	possibly damaging	Het
Ggt1	T	A	10: 75,576,213		probably benign	Het
Gm1966	T	A	7: 106,603,883	L51F	probably damaging	Het
Gm6434	T	A	7: 25,882,361		noncoding transcript	Het
Gm6614	T	G	6: 141,985,477		probably benign	Het
Grik4	A	T	9: 42,622,096	L376*	probably null	Het
Gzf1	A	G	2: 148,683,833	T75A	probably benign	Het
Hcn1	T	C	13: 117,975,375	I625T	unknown	Het
Hhat	C	T	1: 192,552,934		probably null	Het
Ifit1bl1	T	C	19: 34,594,514	E181G	probably damaging	Het
Kif21a	T	C	15: 90,968,054		probably benign	Het
Lrrc45	A	C	11: 120,715,219	S118R	probably damaging	Het
Mcm9	T	C	10: 53,548,527	I656V	probably benign	Het
Ms4a5	A	G	19: 11,283,654	L47S	probably damaging	Het
Mynn	A	T	3: 30,607,459	N230I	probably benign	Het
Nck2	T	C	1: 43,554,118	S162P	probably damaging	Het
Nfat5	T	C	8: 107,367,461	F259S	probably damaging	Het
Obox1	T	G	7: 15,556,253	S174A	possibly damaging	Het
Ociad1	T	A	5: 73,313,429		probably null	Het
Pgbd1	A	T	13: 21,423,166	V286E	possibly damaging	Het
Phlpp2	T	C	8: 109,939,935	V1032A	probably damaging	Het
Ppm1e	C	T	11: 87,240,614	A318T	probably damaging	Het
Prex1	T	A	2: 166,589,571	D757V	probably benign	Het
Ptpdc1	C	A	13: 48,589,119		probably null	Het
Rbbp5	T	G	1: 132,493,844	I94R	possibly damaging	Het
Rnpc3	A	G	3: 113,621,869	V173A	probably benign	Het
Sgsm1	A	T	5: 113,263,759	N700K	probably benign	Het
Sox14	T	A	9: 99,875,122	H188L	probably damaging	Het
Supt5	T	A	7: 28,317,329		probably benign	Het
Synpo	A	G	18: 60,602,418	S819P	probably damaging	Het
Tenm2	A	G	11: 36,207,124		probably benign	Het
Tenm4	T	C	7: 96,873,766	V1468A	possibly damaging	Het
Tiam2	A	G	17: 3,502,918	N83S	probably benign	Het
Tle6	T	C	10: 81,595,311		probably benign	Het
Tm2d2	T	G	8: 25,018,114	N91K	probably damaging	Het
Tmem132d	T	G	5: 127,864,646	Q463H	probably benign	Het
Tmf1	A	G	6: 97,176,141	S324P	probably damaging	Het
Tnc	T	C	4: 64,000,159	T1172A	probably benign	Het
Usp17lb	A	T	7: 104,840,539	C393S	probably benign	Het
Usp42	G	A	5: 143,714,861	L1136F	probably damaging	Het
Vmn2r92	T	G	17: 18,168,921	M499R	probably benign	Het
Vps54	T	A	11: 21,311,071		probably benign	Het
Wdr6	C	T	9: 108,573,101	R1076H	probably benign	Het
Wdr72	T	A	9: 74,210,757	M917K	possibly damaging	Het
Wee2	T	C	6: 40,456,995	V281A	probably benign	Het
Zc3h6	A	G	2: 129,014,827	D609G	probably benign	Het
Zfp345	G	A	2: 150,473,243	H125Y	possibly damaging	Het
Zhx2	A	G	15: 57,821,840	K202E	probably damaging	Het
Zic2	CCCACCACCACCATCACCACCACCACC	CCCACCATCACCACCACCACC	14: 122,476,364		probably benign	Het

Other mutations in Brd9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00340:Brd9	APN	13	73938547	missense	probably damaging	0.98
IGL01461:Brd9	APN	13	73951598	nonsense	probably null
IGL01928:Brd9	APN	13	73955511	missense	probably benign	0.02
R0379:Brd9	UTSW	13	73942683	splice site	probably benign
R0788:Brd9	UTSW	13	73944867	splice site	probably benign
R1539:Brd9	UTSW	13	73944743	missense	probably damaging	0.99
R4095:Brd9	UTSW	13	73944799	missense	probably benign	0.19
R4582:Brd9	UTSW	13	73947733	missense	probably benign	0.00
R4648:Brd9	UTSW	13	73940776	missense	probably benign	0.37
R4915:Brd9	UTSW	13	73938455	missense	probably damaging	0.99
R6054:Brd9	UTSW	13	73940741	missense	probably damaging	1.00
R6175:Brd9	UTSW	13	73960314	missense	probably damaging	0.98
R6462:Brd9	UTSW	13	73940669	missense	probably damaging	1.00
R6520:Brd9	UTSW	13	73942794	missense	probably benign	0.00
R7217:Brd9	UTSW	13	73938944	missense	probably damaging	1.00
R7360:Brd9	UTSW	13	73944823	missense	probably benign	0.07
R7422:Brd9	UTSW	13	73954578	missense	probably benign
R7556:Brd9	UTSW	13	73944767	missense	possibly damaging	0.83
R7844:Brd9	UTSW	13	73938533	missense	probably damaging	1.00
Z1176:Brd9	UTSW	13	73944751	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGATGGCCTCAACTTTAGCACATCC -3'
(R):5'- AGTGACATGCAACAAGACCTGTCTG -3'

Sequencing Primer
(F):5'- CACATCCTATTGACTTACATAGCTGG -3'
(R):5'- cacagggcaaccagcag -3'

Posted On

2013-05-09