Mutagenetix > Incidental Mutation

Incidental Mutation 'R7219:Chd9'

561665

Institutional Source

Beutler Lab

Gene Symbol

Chd9

Ensembl Gene

ENSMUSG00000056608

Gene Name

chromodomain helicase DNA binding protein 9

Synonyms

AD013, 1810014J18Rik, 9030205D12Rik, A330063D19Rik

MMRRC Submission

045291-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7219 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

91554980-91781144 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 91728394 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 1270 (D1270G)

Ref Sequence

ENSEMBL: ENSMUSP00000046356 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048665] [ENSMUST00000109614] [ENSMUST00000209203] [ENSMUST00000209423] [ENSMUST00000210947]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000048665
AA Change: D1270G

SMART Domains

Protein: ENSMUSP00000046356
Gene: ENSMUSG00000056608
AA Change: D1270G

Domain	Start	End	E-Value	Type
low complexity region	323	334	N/A	INTRINSIC
low complexity region	586	605	N/A	INTRINSIC
CHROMO	687	753	2.41e-10	SMART
CHROMO	770	828	4.35e-8	SMART
DEXDc	855	1056	3.8e-36	SMART
Blast:DEXDc	1149	1174	7e-6	BLAST
HELICc	1211	1295	2.86e-22	SMART
low complexity region	1462	1475	N/A	INTRINSIC
Blast:DEXDc	1506	1551	3e-16	BLAST
low complexity region	2048	2067	N/A	INTRINSIC
low complexity region	2127	2199	N/A	INTRINSIC
BRK	2456	2505	6.77e-25	SMART
BRK	2530	2574	1.5e-17	SMART
low complexity region	2594	2608	N/A	INTRINSIC
low complexity region	2609	2639	N/A	INTRINSIC
low complexity region	2642	2659	N/A	INTRINSIC
low complexity region	2690	2704	N/A	INTRINSIC
low complexity region	2746	2771	N/A	INTRINSIC
low complexity region	2802	2813	N/A	INTRINSIC
low complexity region	2843	2869	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000109614
AA Change: D1270G

SMART Domains

Protein: ENSMUSP00000105243
Gene: ENSMUSG00000056608
AA Change: D1270G

Domain	Start	End	E-Value	Type
low complexity region	323	334	N/A	INTRINSIC
low complexity region	586	605	N/A	INTRINSIC
CHROMO	687	753	2.41e-10	SMART
CHROMO	770	828	4.35e-8	SMART
DEXDc	855	1056	3.8e-36	SMART
Blast:DEXDc	1149	1174	7e-6	BLAST
HELICc	1211	1295	2.86e-22	SMART
low complexity region	1462	1475	N/A	INTRINSIC
Blast:DEXDc	1506	1551	3e-16	BLAST
low complexity region	2048	2067	N/A	INTRINSIC
low complexity region	2127	2199	N/A	INTRINSIC
BRK	2472	2521	6.77e-25	SMART
BRK	2546	2590	1.5e-17	SMART
low complexity region	2610	2624	N/A	INTRINSIC
low complexity region	2625	2655	N/A	INTRINSIC
low complexity region	2658	2675	N/A	INTRINSIC
low complexity region	2706	2720	N/A	INTRINSIC
low complexity region	2762	2787	N/A	INTRINSIC
low complexity region	2818	2829	N/A	INTRINSIC
low complexity region	2859	2885	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000209203
AA Change: D1270G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Predicted Effect

unknown
Transcript: ENSMUST00000209423
AA Change: D1270G

Predicted Effect

probably damaging
Transcript: ENSMUST00000210947
AA Change: D797G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

97% (77/79)

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930562C15Rik	T	C	16: 4,667,508 (GRCm39)	S300P	unknown	Het
Abhd17a	T	A	10: 80,420,008 (GRCm39)	K226*	probably null	Het
Alkbh7	T	A	17: 57,305,508 (GRCm39)	H108Q	probably damaging	Het
Ankrd44	A	C	1: 54,806,069 (GRCm39)	H112Q	probably damaging	Het
Capn3	A	G	2: 120,333,935 (GRCm39)	E790G	probably damaging	Het
Cd47	C	A	16: 49,728,440 (GRCm39)	N330K	possibly damaging	Het
Cd55	A	G	1: 130,390,343 (GRCm39)	S22P	possibly damaging	Het
Cdc25a	A	G	9: 109,718,154 (GRCm39)	I373V	probably damaging	Het
Cfap43	T	C	19: 47,779,912 (GRCm39)	I514V	probably benign	Het
Cfap73	A	T	5: 120,768,200 (GRCm39)	M186K	probably benign	Het
Ciita	A	G	16: 10,330,121 (GRCm39)	T802A	probably benign	Het
Dlgap2	A	G	8: 14,793,296 (GRCm39)	E430G	probably benign	Het
Dlx1	C	A	2: 71,360,513 (GRCm39)	S59*	probably null	Het
Dnaaf3	T	C	7: 4,531,076 (GRCm39)	N119S	probably damaging	Het
Dnah11	T	G	12: 118,004,830 (GRCm39)	I2164L	possibly damaging	Het
Dnah11	T	C	12: 118,090,624 (GRCm39)	K1079R	probably benign	Het
Dnah12	C	T	14: 26,576,837 (GRCm39)	T3029I	probably damaging	Het
Dppa3	A	T	6: 122,606,918 (GRCm39)	Y136F	probably damaging	Het
Enox1	T	A	14: 77,958,284 (GRCm39)	M611K	probably benign	Het
Fam149a	A	T	8: 45,803,600 (GRCm39)	I378N	possibly damaging	Het
Farp2	T	C	1: 93,488,040 (GRCm39)	F89S	probably damaging	Het
Fbn2	C	T	18: 58,186,099 (GRCm39)	V1750M	probably benign	Het
Frs3	A	G	17: 48,013,620 (GRCm39)	T181A	probably damaging	Het
Heatr4	T	A	12: 84,004,644 (GRCm39)	I726F	possibly damaging	Het
Ighg1	T	G	12: 113,290,216 (GRCm39)	E375A		Het
Ikzf4	G	T	10: 128,470,252 (GRCm39)	Q476K	possibly damaging	Het
Kcnh1	G	T	1: 192,187,945 (GRCm39)	C829F	probably benign	Het
Krtap19-4	T	C	16: 88,681,797 (GRCm39)	Y53C	unknown	Het
Loricrin	C	A	3: 91,988,705 (GRCm39)	G194C	unknown	Het
Lrp1	A	C	10: 127,393,097 (GRCm39)	D2720E	probably benign	Het
Lrp4	A	G	2: 91,322,368 (GRCm39)	Y1068C	probably damaging	Het
Mbnl1	A	G	3: 60,511,244 (GRCm39)	N67D	probably benign	Het
Mrpl21	A	G	19: 3,336,998 (GRCm39)	E123G	probably benign	Het
Mst1	A	T	9: 107,958,485 (GRCm39)	D65V	probably damaging	Het
Myo15b	T	A	11: 115,767,921 (GRCm39)		probably null	Het
Myo5a	A	G	9: 75,028,052 (GRCm39)	Y79C	probably damaging	Het
Oas1c	A	T	5: 120,940,957 (GRCm39)	W279R	probably damaging	Het
Or4f4-ps1	A	T	2: 111,330,532 (GRCm39)	M312L	probably benign	Het
Or4k77	A	T	2: 111,199,882 (GRCm39)	I302L	probably benign	Het
Or51f5	A	G	7: 102,430,913 (GRCm39)	I77V	probably benign	Het
Pcdh9	C	T	14: 93,253,216 (GRCm39)	G1149D	possibly damaging	Het
Pcid2	G	A	8: 13,129,907 (GRCm39)	T283I	probably benign	Het
Pdhx	A	G	2: 102,858,760 (GRCm39)	V348A	probably benign	Het
Pi16	C	A	17: 29,538,208 (GRCm39)	P7Q	possibly damaging	Het
Psmb3	T	A	11: 97,602,023 (GRCm39)	M131K	probably null	Het
Raph1	A	G	1: 60,542,032 (GRCm39)	Y309H	unknown	Het
Rasgrf1	A	G	9: 89,866,341 (GRCm39)	N593S	probably damaging	Het
Rbm38	A	C	2: 172,863,990 (GRCm39)	E53A	possibly damaging	Het
Rufy3	A	G	5: 88,797,715 (GRCm39)	T631A	probably benign	Het
Sbno1	A	T	5: 124,543,722 (GRCm39)	D272E	probably benign	Het
Scamp1	T	A	13: 94,361,415 (GRCm39)	Y207F	probably damaging	Het
Scn8a	T	A	15: 100,866,984 (GRCm39)	S263R	probably damaging	Het
Setbp1	T	G	18: 78,798,960 (GRCm39)	T1407P	probably damaging	Het
Skor2	T	C	18: 76,948,096 (GRCm39)	L606P	possibly damaging	Het
Slc35f6	A	G	5: 30,814,796 (GRCm39)	N241S	probably benign	Het
Slc36a2	T	G	11: 55,059,744 (GRCm39)	D247A	probably benign	Het
Smim10l1	T	A	6: 133,084,895 (GRCm39)	F87L	unknown	Het
Son	T	C	16: 91,461,889 (GRCm39)	S2265P	unknown	Het
Spta1	A	G	1: 174,050,203 (GRCm39)	N1748D	probably damaging	Het
Sptbn2	A	G	19: 4,774,201 (GRCm39)	D84G	probably damaging	Het
Tasor2	T	A	13: 3,640,521 (GRCm39)	L205F	probably damaging	Het
Tbc1d24	G	A	17: 24,404,266 (GRCm39)	R293C	probably damaging	Het
Tex15	A	G	8: 34,036,268 (GRCm39)	T65A	probably benign	Het
Thyn1	A	G	9: 26,916,506 (GRCm39)	Y97C	probably damaging	Het
Tmem64	T	C	4: 15,266,700 (GRCm39)	L250P	probably damaging	Het
Tnfrsf9	A	T	4: 151,019,991 (GRCm39)	K217N	probably damaging	Het
Tnxb	A	G	17: 34,898,039 (GRCm39)	T896A	probably benign	Het
Trpm1	T	A	7: 63,854,333 (GRCm39)	I285N	possibly damaging	Het
Try5	T	A	6: 41,288,637 (GRCm39)	D194V	probably damaging	Het
U2surp	G	A	9: 95,372,215 (GRCm39)	R316*	probably null	Het
Ubr2	G	T	17: 47,246,360 (GRCm39)	S1618*	probably null	Het
Ugp2	T	C	11: 21,273,271 (GRCm39)	I449M	probably damaging	Het
Umodl1	A	G	17: 31,201,236 (GRCm39)		probably null	Het
Vmn2r31	C	T	7: 7,390,105 (GRCm39)	V538I	probably benign	Het
Vmn2r31	A	T	7: 7,397,397 (GRCm39)	M287K	probably damaging	Het
Wwc2	A	G	8: 48,311,919 (GRCm39)	V748A	unknown	Het
Zfp800	A	C	6: 28,243,662 (GRCm39)	H434Q	probably benign	Het
Zfp869	A	G	8: 70,159,356 (GRCm39)	C406R	probably damaging	Het
Zhx1	A	G	15: 57,917,733 (GRCm39)	V171A	probably benign	Het

Other mutations in Chd9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00420:Chd9	APN	8	91,752,020 (GRCm39)	missense	possibly damaging	0.79
IGL00547:Chd9	APN	8	91,732,426 (GRCm39)	missense	probably damaging	1.00
IGL00589:Chd9	APN	8	91,742,474 (GRCm39)	missense	probably damaging	1.00
IGL00640:Chd9	APN	8	91,712,760 (GRCm39)	missense	probably damaging	0.99
IGL00663:Chd9	APN	8	91,710,118 (GRCm39)	missense	probably damaging	1.00
IGL00852:Chd9	APN	8	91,699,835 (GRCm39)	missense	probably benign	0.29
IGL00908:Chd9	APN	8	91,723,508 (GRCm39)	missense	probably damaging	1.00
IGL00911:Chd9	APN	8	91,778,320 (GRCm39)	missense	probably damaging	1.00
IGL01068:Chd9	APN	8	91,768,744 (GRCm39)	missense	probably benign	0.13
IGL01668:Chd9	APN	8	91,753,404 (GRCm39)	missense	possibly damaging	0.53
IGL01873:Chd9	APN	8	91,660,395 (GRCm39)	missense	probably benign	0.00
IGL01969:Chd9	APN	8	91,760,138 (GRCm39)	missense	possibly damaging	0.72
IGL02105:Chd9	APN	8	91,659,116 (GRCm39)	missense	probably damaging	1.00
IGL02153:Chd9	APN	8	91,683,122 (GRCm39)	nonsense	probably null
IGL02164:Chd9	APN	8	91,659,849 (GRCm39)	missense	possibly damaging	0.94
IGL02725:Chd9	APN	8	91,778,312 (GRCm39)	missense	possibly damaging	0.78
IGL02755:Chd9	APN	8	91,760,210 (GRCm39)	missense	probably benign	0.33
IGL02892:Chd9	APN	8	91,703,543 (GRCm39)	splice site	probably benign
IGL02897:Chd9	APN	8	91,660,496 (GRCm39)	splice site	probably benign
IGL03005:Chd9	APN	8	91,738,075 (GRCm39)	missense	probably damaging	0.98
IGL03062:Chd9	APN	8	91,741,895 (GRCm39)	splice site	probably benign
IGL03140:Chd9	APN	8	91,768,856 (GRCm39)	missense	possibly damaging	0.91
hovel	UTSW	8	91,741,832 (GRCm39)	missense	probably benign	0.19
shack	UTSW	8	91,659,426 (GRCm39)	missense	probably damaging	1.00
R0056:Chd9	UTSW	8	91,660,165 (GRCm39)	missense	possibly damaging	0.62
R0157:Chd9	UTSW	8	91,735,464 (GRCm39)	splice site	probably null
R0238:Chd9	UTSW	8	91,659,456 (GRCm39)	missense	probably damaging	1.00
R0238:Chd9	UTSW	8	91,659,456 (GRCm39)	missense	probably damaging	1.00
R0432:Chd9	UTSW	8	91,721,078 (GRCm39)	splice site	probably benign
R0454:Chd9	UTSW	8	91,699,859 (GRCm39)	missense	possibly damaging	0.83
R0573:Chd9	UTSW	8	91,725,223 (GRCm39)	missense	probably damaging	1.00
R0580:Chd9	UTSW	8	91,721,191 (GRCm39)	missense	possibly damaging	0.91
R0604:Chd9	UTSW	8	91,763,170 (GRCm39)	missense	possibly damaging	0.82
R0662:Chd9	UTSW	8	91,704,304 (GRCm39)	missense	probably damaging	0.99
R0825:Chd9	UTSW	8	91,777,825 (GRCm39)	missense	probably benign	0.06
R0945:Chd9	UTSW	8	91,659,630 (GRCm39)	missense	possibly damaging	0.60
R0964:Chd9	UTSW	8	91,741,832 (GRCm39)	missense	probably benign	0.19
R0967:Chd9	UTSW	8	91,716,107 (GRCm39)	missense	probably damaging	1.00
R1015:Chd9	UTSW	8	91,659,206 (GRCm39)	missense	probably damaging	0.99
R1066:Chd9	UTSW	8	91,712,764 (GRCm39)	nonsense	probably null
R1244:Chd9	UTSW	8	91,749,557 (GRCm39)	missense	probably damaging	0.99
R1505:Chd9	UTSW	8	91,733,123 (GRCm39)	splice site	probably null
R1570:Chd9	UTSW	8	91,763,170 (GRCm39)	missense	probably benign	0.03
R1591:Chd9	UTSW	8	91,710,166 (GRCm39)	missense	probably damaging	0.97
R1624:Chd9	UTSW	8	91,725,163 (GRCm39)	missense	probably benign	0.17
R1626:Chd9	UTSW	8	91,721,224 (GRCm39)	missense	probably benign	0.00
R1632:Chd9	UTSW	8	91,683,335 (GRCm39)	nonsense	probably null
R1649:Chd9	UTSW	8	91,659,229 (GRCm39)	missense	possibly damaging	0.88
R1664:Chd9	UTSW	8	91,749,418 (GRCm39)	splice site	probably null
R1668:Chd9	UTSW	8	91,767,814 (GRCm39)	missense	probably damaging	0.99
R1681:Chd9	UTSW	8	91,699,763 (GRCm39)	missense	probably damaging	0.98
R1695:Chd9	UTSW	8	91,728,410 (GRCm39)	missense	probably damaging	1.00
R1714:Chd9	UTSW	8	91,760,853 (GRCm39)	utr 3 prime	probably benign
R1746:Chd9	UTSW	8	91,737,326 (GRCm39)	missense	probably benign	0.01
R1843:Chd9	UTSW	8	91,737,422 (GRCm39)	missense	probably benign	0.19
R1844:Chd9	UTSW	8	91,683,323 (GRCm39)	nonsense	probably null
R1941:Chd9	UTSW	8	91,703,697 (GRCm39)	critical splice donor site	probably null
R2022:Chd9	UTSW	8	91,761,682 (GRCm39)	missense	probably benign	0.17
R2027:Chd9	UTSW	8	91,634,619 (GRCm39)	unclassified	probably benign
R2098:Chd9	UTSW	8	91,760,615 (GRCm39)	missense	probably benign	0.01
R2099:Chd9	UTSW	8	91,760,615 (GRCm39)	missense	probably benign	0.01
R2100:Chd9	UTSW	8	91,760,615 (GRCm39)	missense	probably benign	0.01
R2101:Chd9	UTSW	8	91,760,615 (GRCm39)	missense	probably benign	0.01
R2224:Chd9	UTSW	8	91,737,913 (GRCm39)	missense	probably benign	0.04
R2276:Chd9	UTSW	8	91,760,615 (GRCm39)	missense	probably benign	0.01
R2278:Chd9	UTSW	8	91,760,615 (GRCm39)	missense	probably benign	0.01
R2316:Chd9	UTSW	8	91,777,756 (GRCm39)	missense	probably damaging	0.99
R2507:Chd9	UTSW	8	91,760,615 (GRCm39)	missense	probably benign	0.01
R2508:Chd9	UTSW	8	91,760,615 (GRCm39)	missense	probably benign	0.01
R2988:Chd9	UTSW	8	91,757,088 (GRCm39)	splice site	probably null
R3418:Chd9	UTSW	8	91,763,219 (GRCm39)	missense	probably damaging	1.00
R3817:Chd9	UTSW	8	91,710,893 (GRCm39)	splice site	probably benign
R3923:Chd9	UTSW	8	91,660,147 (GRCm39)	missense	probably benign	0.16
R4001:Chd9	UTSW	8	91,683,185 (GRCm39)	missense	probably damaging	1.00
R4003:Chd9	UTSW	8	91,683,185 (GRCm39)	missense	probably damaging	1.00
R4006:Chd9	UTSW	8	91,660,188 (GRCm39)	missense	probably benign	0.12
R4013:Chd9	UTSW	8	91,699,797 (GRCm39)	missense	possibly damaging	0.82
R4067:Chd9	UTSW	8	91,750,202 (GRCm39)	missense	possibly damaging	0.53
R4108:Chd9	UTSW	8	91,737,304 (GRCm39)	missense	probably benign	0.04
R4125:Chd9	UTSW	8	91,777,912 (GRCm39)	missense	probably damaging	0.99
R4126:Chd9	UTSW	8	91,777,912 (GRCm39)	missense	probably damaging	0.99
R4452:Chd9	UTSW	8	91,704,308 (GRCm39)	missense	probably damaging	0.99
R4463:Chd9	UTSW	8	91,705,627 (GRCm39)	missense	probably benign	0.01
R4478:Chd9	UTSW	8	91,760,659 (GRCm39)	utr 3 prime	probably benign
R4587:Chd9	UTSW	8	91,763,134 (GRCm39)	missense	possibly damaging	0.95
R4628:Chd9	UTSW	8	91,710,091 (GRCm39)	missense	probably benign	0.05
R4667:Chd9	UTSW	8	91,760,428 (GRCm39)	missense	possibly damaging	0.73
R4908:Chd9	UTSW	8	91,741,877 (GRCm39)	missense	possibly damaging	0.50
R4912:Chd9	UTSW	8	91,760,858 (GRCm39)	missense	possibly damaging	0.84
R4977:Chd9	UTSW	8	91,760,336 (GRCm39)	missense	possibly damaging	0.96
R5016:Chd9	UTSW	8	91,733,254 (GRCm39)	nonsense	probably null
R5083:Chd9	UTSW	8	91,711,002 (GRCm39)	missense	probably damaging	1.00
R5088:Chd9	UTSW	8	91,704,147 (GRCm39)	missense	possibly damaging	0.94
R5090:Chd9	UTSW	8	91,753,462 (GRCm39)	nonsense	probably null
R5307:Chd9	UTSW	8	91,723,777 (GRCm39)	missense	probably damaging	1.00
R5541:Chd9	UTSW	8	91,778,132 (GRCm39)	missense	probably benign	0.09
R5559:Chd9	UTSW	8	91,742,553 (GRCm39)	critical splice donor site	probably null
R5638:Chd9	UTSW	8	91,738,078 (GRCm39)	missense	possibly damaging	0.67
R5640:Chd9	UTSW	8	91,763,190 (GRCm39)	missense	probably damaging	1.00
R5793:Chd9	UTSW	8	91,728,384 (GRCm39)	missense	probably damaging	1.00
R5827:Chd9	UTSW	8	91,716,078 (GRCm39)	missense	probably damaging	1.00
R5834:Chd9	UTSW	8	91,723,792 (GRCm39)	missense	probably damaging	1.00
R5875:Chd9	UTSW	8	91,778,464 (GRCm39)	missense	probably damaging	0.99
R6002:Chd9	UTSW	8	91,705,515 (GRCm39)	missense	probably damaging	1.00
R6091:Chd9	UTSW	8	91,761,691 (GRCm39)	missense	probably damaging	1.00
R6185:Chd9	UTSW	8	91,775,765 (GRCm39)	missense	probably damaging	1.00
R6246:Chd9	UTSW	8	91,659,045 (GRCm39)	missense	probably damaging	1.00
R6292:Chd9	UTSW	8	91,659,550 (GRCm39)	missense	probably benign	0.05
R6305:Chd9	UTSW	8	91,757,174 (GRCm39)	missense	possibly damaging	0.93
R6348:Chd9	UTSW	8	91,737,903 (GRCm39)	missense	possibly damaging	0.95
R6438:Chd9	UTSW	8	91,725,149 (GRCm39)	missense	probably benign	0.02
R6470:Chd9	UTSW	8	91,659,426 (GRCm39)	missense	probably damaging	1.00
R6798:Chd9	UTSW	8	91,778,182 (GRCm39)	missense	possibly damaging	0.56
R6902:Chd9	UTSW	8	91,769,579 (GRCm39)	missense	probably damaging	1.00
R6908:Chd9	UTSW	8	91,683,044 (GRCm39)	missense	probably benign	0.02
R6929:Chd9	UTSW	8	91,769,573 (GRCm39)	missense	probably damaging	1.00
R6969:Chd9	UTSW	8	91,705,542 (GRCm39)	missense	probably benign	0.34
R7043:Chd9	UTSW	8	91,760,843 (GRCm39)	utr 3 prime	probably benign
R7094:Chd9	UTSW	8	91,716,189 (GRCm39)	missense	unknown
R7126:Chd9	UTSW	8	91,741,853 (GRCm39)	missense	unknown
R7182:Chd9	UTSW	8	91,733,250 (GRCm39)	missense	unknown
R7260:Chd9	UTSW	8	91,721,171 (GRCm39)	missense	unknown
R7293:Chd9	UTSW	8	91,760,707 (GRCm39)	missense	unknown
R7303:Chd9	UTSW	8	91,778,532 (GRCm39)	missense	unknown
R7358:Chd9	UTSW	8	91,760,846 (GRCm39)	missense	unknown
R7358:Chd9	UTSW	8	91,710,115 (GRCm39)	missense	unknown
R7451:Chd9	UTSW	8	91,760,446 (GRCm39)	missense	probably benign	0.27
R7451:Chd9	UTSW	8	91,760,418 (GRCm39)	frame shift	probably null
R7456:Chd9	UTSW	8	91,659,153 (GRCm39)	nonsense	probably null
R7481:Chd9	UTSW	8	91,683,066 (GRCm39)	missense	unknown
R7532:Chd9	UTSW	8	91,721,193 (GRCm39)	missense	unknown
R7570:Chd9	UTSW	8	91,721,208 (GRCm39)	missense	unknown
R7611:Chd9	UTSW	8	91,763,017 (GRCm39)	missense	probably damaging	1.00
R7673:Chd9	UTSW	8	91,778,325 (GRCm39)	missense	probably damaging	0.96
R7723:Chd9	UTSW	8	91,741,837 (GRCm39)	missense	unknown
R7739:Chd9	UTSW	8	91,761,653 (GRCm39)	missense	probably damaging	1.00
R7759:Chd9	UTSW	8	91,704,178 (GRCm39)	critical splice donor site	probably null
R7916:Chd9	UTSW	8	91,761,684 (GRCm39)	nonsense	probably null
R7921:Chd9	UTSW	8	91,768,909 (GRCm39)	critical splice donor site	probably null
R7957:Chd9	UTSW	8	91,778,326 (GRCm39)	missense	probably damaging	0.99
R7972:Chd9	UTSW	8	91,732,395 (GRCm39)	missense	unknown
R8108:Chd9	UTSW	8	91,659,852 (GRCm39)	missense	unknown
R8115:Chd9	UTSW	8	91,762,960 (GRCm39)	missense	probably damaging	0.99
R8165:Chd9	UTSW	8	91,767,769 (GRCm39)	missense	probably damaging	1.00
R8171:Chd9	UTSW	8	91,752,015 (GRCm39)	missense	possibly damaging	0.92
R8186:Chd9	UTSW	8	91,725,233 (GRCm39)	missense	unknown
R8208:Chd9	UTSW	8	91,763,891 (GRCm39)	splice site	probably null
R8256:Chd9	UTSW	8	91,660,129 (GRCm39)	missense	unknown
R8281:Chd9	UTSW	8	91,763,225 (GRCm39)	missense	probably damaging	1.00
R8504:Chd9	UTSW	8	91,723,472 (GRCm39)	missense	unknown
R8836:Chd9	UTSW	8	91,767,812 (GRCm39)	missense	probably damaging	0.99
R8892:Chd9	UTSW	8	91,660,468 (GRCm39)	missense	unknown
R8985:Chd9	UTSW	8	91,721,101 (GRCm39)	missense	unknown
R9029:Chd9	UTSW	8	91,683,198 (GRCm39)	missense	unknown
R9030:Chd9	UTSW	8	91,683,198 (GRCm39)	missense	unknown
R9038:Chd9	UTSW	8	91,716,233 (GRCm39)	missense	unknown
R9081:Chd9	UTSW	8	91,704,144 (GRCm39)	nonsense	probably null
R9134:Chd9	UTSW	8	91,659,754 (GRCm39)	missense	unknown
R9205:Chd9	UTSW	8	91,757,270 (GRCm39)	missense	probably benign	0.01
R9309:Chd9	UTSW	8	91,733,319 (GRCm39)	missense	unknown
R9375:Chd9	UTSW	8	91,725,335 (GRCm39)	critical splice donor site	probably null
R9449:Chd9	UTSW	8	91,659,174 (GRCm39)	missense	unknown
R9547:Chd9	UTSW	8	91,683,186 (GRCm39)	missense	unknown
R9573:Chd9	UTSW	8	91,704,302 (GRCm39)	missense	unknown
R9576:Chd9	UTSW	8	91,659,294 (GRCm39)	missense	unknown
R9601:Chd9	UTSW	8	91,732,360 (GRCm39)	nonsense	probably null
R9613:Chd9	UTSW	8	91,683,150 (GRCm39)	nonsense	probably null
R9639:Chd9	UTSW	8	91,760,840 (GRCm39)	missense	probably null
R9718:Chd9	UTSW	8	91,712,801 (GRCm39)	missense	unknown
R9746:Chd9	UTSW	8	91,738,063 (GRCm39)	missense	unknown
R9762:Chd9	UTSW	8	91,712,741 (GRCm39)	missense	unknown
R9764:Chd9	UTSW	8	91,721,220 (GRCm39)	missense	unknown
R9790:Chd9	UTSW	8	91,760,417 (GRCm39)	missense	possibly damaging	0.82
R9791:Chd9	UTSW	8	91,760,417 (GRCm39)	missense	possibly damaging	0.82
RF007:Chd9	UTSW	8	91,760,578 (GRCm39)	missense	possibly damaging	0.66
X0065:Chd9	UTSW	8	91,763,200 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CAGGGATGCTGACTTTGCCATATC -3'
(R):5'- ACTGAGCTAGGGGATCATGC -3'

Sequencing Primer
(F):5'- CTCAACATTTAAACTTCCTGCTTTTC -3'
(R):5'- TTGAGGCAAAGTCTCACTCCATGG -3'

Posted On

2019-06-26