Mutagenetix > Incidental Mutation

Incidental Mutation 'R7182:Chd9'

559050

Institutional Source

Beutler Lab

Gene Symbol

Chd9

Ensembl Gene

ENSMUSG00000056608

Gene Name

chromodomain helicase DNA binding protein 9

Synonyms

1810014J18Rik, AD013, 9030205D12Rik, A330063D19Rik

MMRRC Submission

045234-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7182 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

90828352-91054516 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 91006622 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 1373 (F1373S)

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: F1373S

SMART Domains

Protein: ENSMUSP00000046356
Gene: ENSMUSG00000056608
AA Change: F1373S

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: F1373S

SMART Domains

Protein: ENSMUSP00000105243
Gene: ENSMUSG00000056608
AA Change: F1373S

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: F1373S

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

Predicted Effect

unknown
Transcript: ENSMUST00000209423
AA Change: F1373S

Predicted Effect

probably benign
Transcript: ENSMUST00000210947

Meta Mutation Damage Score

0.5202

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

96% (70/73)

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930562C15Rik	T	C	16: 4,849,714 (GRCm38)	V323A	unknown	Het
AC117241.1	A	G	17: 7,352,688 (GRCm38)	V158A	unknown	Het
Acadm	A	G	3: 153,941,881 (GRCm38)		probably null	Het
Adcy10	T	G	1: 165,543,470 (GRCm38)		probably null	Het
Aldh6a1	C	T	12: 84,441,831 (GRCm38)	A94T	probably benign	Het
Ano2	T	A	6: 125,790,293 (GRCm38)	L229Q	probably damaging	Het
Cacna1h	C	T	17: 25,377,655 (GRCm38)	R1828H	probably damaging	Het
Ccdc33	A	T	9: 58,034,173 (GRCm38)		probably null	Het
Cep112	A	C	11: 108,682,844 (GRCm38)	D6A	probably benign	Het
Cog5	T	C	12: 31,685,708 (GRCm38)	L158P	probably damaging	Het
Col6a3	G	A	1: 90,803,678 (GRCm38)	Q1618*	probably null	Het
Dlg5	A	G	14: 24,244,856 (GRCm38)	V3A		Het
Dnah7a	T	A	1: 53,620,461 (GRCm38)		probably null	Het
Dpp10	A	T	1: 123,341,151 (GRCm38)	H716Q	probably benign	Het
Epor	A	G	9: 21,963,329 (GRCm38)	F35L	probably benign	Het
Ergic1	A	T	17: 26,654,882 (GRCm38)	Y92F		Het
Fam71a	C	T	1: 191,163,351 (GRCm38)	R365H	probably damaging	Het
Fam98a	G	A	17: 75,539,018 (GRCm38)	Q273*	probably null	Het
Fhdc1	G	A	3: 84,448,850 (GRCm38)	T429I	probably damaging	Het
Fmnl2	T	A	2: 53,107,441 (GRCm38)	L468Q	unknown	Het
Fmnl3	C	T	15: 99,321,782 (GRCm38)	R695Q	probably damaging	Het
Gabrg2	T	C	11: 41,920,506 (GRCm38)	M271V	probably damaging	Het
Gk5	G	T	9: 96,119,526 (GRCm38)	V26L	possibly damaging	Het
Gm14412	A	C	2: 177,315,615 (GRCm38)	N162K	probably benign	Het
Gm3604	T	C	13: 62,371,875 (GRCm38)	D22G	probably damaging	Het
Gm5565	G	T	5: 146,158,055 (GRCm38)	H294N	probably benign	Het
Hsf2	T	A	10: 57,505,176 (GRCm38)	D287E	possibly damaging	Het
Impdh2	G	A	9: 108,563,208 (GRCm38)	R231H	possibly damaging	Het
Irak3	T	C	10: 120,166,511 (GRCm38)	H234R	probably damaging	Het
Lrba	GTTCCCTTC	GTTC	3: 86,741,458 (GRCm38)		probably null	Het
Lrch3	T	A	16: 32,993,779 (GRCm38)	D551E	probably benign	Het
Manba	A	T	3: 135,567,513 (GRCm38)	N736I	probably benign	Het
Map2	A	G	1: 66,412,653 (GRCm38)	D234G	possibly damaging	Het
Mdk	C	A	2: 91,930,852 (GRCm38)	K121N	unknown	Het
Mfn1	T	A	3: 32,564,220 (GRCm38)	L526Q	probably damaging	Het
Mfsd2b	A	G	12: 4,866,157 (GRCm38)		probably null	Het
Mnat1	G	T	12: 73,230,678 (GRCm38)	E233*	probably null	Het
Mtmr4	T	C	11: 87,604,605 (GRCm38)		probably null	Het
Mtrf1	A	G	14: 79,423,464 (GRCm38)	E432G	possibly damaging	Het
Muc5b	C	T	7: 141,842,645 (GRCm38)	R165C	unknown	Het
Naip6	T	A	13: 100,316,149 (GRCm38)	I135F	probably benign	Het
Nod2	A	G	8: 88,663,832 (GRCm38)	T256A	probably benign	Het
Notch4	T	A	17: 34,583,499 (GRCm38)	V1298E	probably damaging	Het
Nudc	G	T	4: 133,534,465 (GRCm38)	D169E	possibly damaging	Het
Obscn	A	T	11: 59,035,101 (GRCm38)	I5602N	probably damaging	Het
Olfr1468-ps1	G	A	19: 13,375,844 (GRCm38)	G294E	unknown	Het
Osbpl10	G	A	9: 115,067,251 (GRCm38)	D18N	probably damaging	Het
Pigk	G	A	3: 152,722,551 (GRCm38)	V72I	possibly damaging	Het
Prl8a6	C	T	13: 27,437,170 (GRCm38)	E26K	probably damaging	Het
Prpf8	A	G	11: 75,490,727 (GRCm38)	Y318C	possibly damaging	Het
Rab13	A	G	3: 90,224,763 (GRCm38)	D159G	possibly damaging	Het
Rgl2	T	C	17: 33,934,990 (GRCm38)	F457L	possibly damaging	Het
Ryr2	T	C	13: 11,759,757 (GRCm38)	H1171R	probably benign	Het
Scn4a	T	A	11: 106,330,308 (GRCm38)	I842F	probably benign	Het
Scnm1	A	T	3: 95,133,854 (GRCm38)	N14K	possibly damaging	Het
Serinc1	A	T	10: 57,524,361 (GRCm38)	I137N	probably benign	Het
Slc30a3	A	C	5: 31,089,670 (GRCm38)	M103R	probably damaging	Het
Slc30a3	T	C	5: 31,086,825 (GRCm38)	Q371R	probably benign	Het
Slco1a1	A	T	6: 141,911,839 (GRCm38)	C589S	probably damaging	Het
Slco1b2	A	G	6: 141,656,930 (GRCm38)	Y203C	probably damaging	Het
Spty2d1	A	T	7: 46,998,523 (GRCm38)	D219E	probably benign	Het
Svep1	A	T	4: 58,043,991 (GRCm38)	S3552T	probably benign	Het
Tmem62	A	G	2: 121,004,743 (GRCm38)	I516M	probably benign	Het
Trim61	A	T	8: 65,013,614 (GRCm38)	S332T	probably damaging	Het
Trmt10b	A	C	4: 45,308,520 (GRCm38)	T227P	probably benign	Het
Trpc3	T	C	3: 36,655,109 (GRCm38)	Q406R	probably benign	Het
Ttc30b	A	T	2: 75,937,949 (GRCm38)	Y153*	probably null	Het
Ush2a	A	T	1: 188,753,543 (GRCm38)	Y2950F	probably benign	Het
Usp32	C	T	11: 85,040,170 (GRCm38)	G478D	probably benign	Het
Wdfy3	A	G	5: 101,943,892 (GRCm38)	L527P	possibly damaging	Het
Wdr73	A	G	7: 80,893,678 (GRCm38)	V163A	possibly damaging	Het

Other mutations in Chd9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00420:Chd9	APN	8	91,025,392 (GRCm38)	missense	possibly damaging	0.79
IGL00547:Chd9	APN	8	91,005,798 (GRCm38)	missense	probably damaging	1.00
IGL00589:Chd9	APN	8	91,015,846 (GRCm38)	missense	probably damaging	1.00
IGL00640:Chd9	APN	8	90,986,132 (GRCm38)	missense	probably damaging	0.99
IGL00663:Chd9	APN	8	90,983,490 (GRCm38)	missense	probably damaging	1.00
IGL00852:Chd9	APN	8	90,973,207 (GRCm38)	missense	probably benign	0.29
IGL00908:Chd9	APN	8	90,996,880 (GRCm38)	missense	probably damaging	1.00
IGL00911:Chd9	APN	8	91,051,692 (GRCm38)	missense	probably damaging	1.00
IGL01068:Chd9	APN	8	91,042,116 (GRCm38)	missense	probably benign	0.13
IGL01668:Chd9	APN	8	91,026,776 (GRCm38)	missense	possibly damaging	0.53
IGL01873:Chd9	APN	8	90,933,767 (GRCm38)	missense	probably benign	0.00
IGL01969:Chd9	APN	8	91,033,510 (GRCm38)	missense	possibly damaging	0.72
IGL02105:Chd9	APN	8	90,932,488 (GRCm38)	missense	probably damaging	1.00
IGL02153:Chd9	APN	8	90,956,494 (GRCm38)	nonsense	probably null
IGL02164:Chd9	APN	8	90,933,221 (GRCm38)	missense	possibly damaging	0.94
IGL02725:Chd9	APN	8	91,051,684 (GRCm38)	missense	possibly damaging	0.78
IGL02755:Chd9	APN	8	91,033,582 (GRCm38)	missense	probably benign	0.33
IGL02892:Chd9	APN	8	90,976,915 (GRCm38)	splice site	probably benign
IGL02897:Chd9	APN	8	90,933,868 (GRCm38)	splice site	probably benign
IGL03005:Chd9	APN	8	91,011,447 (GRCm38)	missense	probably damaging	0.98
IGL03062:Chd9	APN	8	91,015,267 (GRCm38)	splice site	probably benign
IGL03140:Chd9	APN	8	91,042,228 (GRCm38)	missense	possibly damaging	0.91
hovel	UTSW	8	91,015,204 (GRCm38)	missense	probably benign	0.19
shack	UTSW	8	90,932,798 (GRCm38)	missense	probably damaging	1.00
R0056:Chd9	UTSW	8	90,933,537 (GRCm38)	missense	possibly damaging	0.62
R0157:Chd9	UTSW	8	91,008,836 (GRCm38)	splice site	probably null
R0238:Chd9	UTSW	8	90,932,828 (GRCm38)	missense	probably damaging	1.00
R0238:Chd9	UTSW	8	90,932,828 (GRCm38)	missense	probably damaging	1.00
R0432:Chd9	UTSW	8	90,994,450 (GRCm38)	splice site	probably benign
R0454:Chd9	UTSW	8	90,973,231 (GRCm38)	missense	possibly damaging	0.83
R0573:Chd9	UTSW	8	90,998,595 (GRCm38)	missense	probably damaging	1.00
R0580:Chd9	UTSW	8	90,994,563 (GRCm38)	missense	possibly damaging	0.91
R0604:Chd9	UTSW	8	91,036,542 (GRCm38)	missense	possibly damaging	0.82
R0662:Chd9	UTSW	8	90,977,676 (GRCm38)	missense	probably damaging	0.99
R0825:Chd9	UTSW	8	91,051,197 (GRCm38)	missense	probably benign	0.06
R0945:Chd9	UTSW	8	90,933,002 (GRCm38)	missense	possibly damaging	0.60
R0964:Chd9	UTSW	8	91,015,204 (GRCm38)	missense	probably benign	0.19
R0967:Chd9	UTSW	8	90,989,479 (GRCm38)	missense	probably damaging	1.00
R1015:Chd9	UTSW	8	90,932,578 (GRCm38)	missense	probably damaging	0.99
R1066:Chd9	UTSW	8	90,986,136 (GRCm38)	nonsense	probably null
R1244:Chd9	UTSW	8	91,022,929 (GRCm38)	missense	probably damaging	0.99
R1505:Chd9	UTSW	8	91,006,495 (GRCm38)	splice site	probably null
R1570:Chd9	UTSW	8	91,036,542 (GRCm38)	missense	probably benign	0.03
R1591:Chd9	UTSW	8	90,983,538 (GRCm38)	missense	probably damaging	0.97
R1624:Chd9	UTSW	8	90,998,535 (GRCm38)	missense	probably benign	0.17
R1626:Chd9	UTSW	8	90,994,596 (GRCm38)	missense	probably benign	0.00
R1632:Chd9	UTSW	8	90,956,707 (GRCm38)	nonsense	probably null
R1649:Chd9	UTSW	8	90,932,601 (GRCm38)	missense	possibly damaging	0.88
R1664:Chd9	UTSW	8	91,022,790 (GRCm38)	splice site	probably null
R1668:Chd9	UTSW	8	91,041,186 (GRCm38)	missense	probably damaging	0.99
R1681:Chd9	UTSW	8	90,973,135 (GRCm38)	missense	probably damaging	0.98
R1695:Chd9	UTSW	8	91,001,782 (GRCm38)	missense	probably damaging	1.00
R1714:Chd9	UTSW	8	91,034,225 (GRCm38)	utr 3 prime	probably benign
R1746:Chd9	UTSW	8	91,010,698 (GRCm38)	missense	probably benign	0.01
R1843:Chd9	UTSW	8	91,010,794 (GRCm38)	missense	probably benign	0.19
R1844:Chd9	UTSW	8	90,956,695 (GRCm38)	nonsense	probably null
R1941:Chd9	UTSW	8	90,977,069 (GRCm38)	critical splice donor site	probably null
R2022:Chd9	UTSW	8	91,035,054 (GRCm38)	missense	probably benign	0.17
R2027:Chd9	UTSW	8	90,907,991 (GRCm38)	unclassified	probably benign
R2098:Chd9	UTSW	8	91,033,987 (GRCm38)	missense	probably benign	0.01
R2099:Chd9	UTSW	8	91,033,987 (GRCm38)	missense	probably benign	0.01
R2100:Chd9	UTSW	8	91,033,987 (GRCm38)	missense	probably benign	0.01
R2101:Chd9	UTSW	8	91,033,987 (GRCm38)	missense	probably benign	0.01
R2224:Chd9	UTSW	8	91,011,285 (GRCm38)	missense	probably benign	0.04
R2276:Chd9	UTSW	8	91,033,987 (GRCm38)	missense	probably benign	0.01
R2278:Chd9	UTSW	8	91,033,987 (GRCm38)	missense	probably benign	0.01
R2316:Chd9	UTSW	8	91,051,128 (GRCm38)	missense	probably damaging	0.99
R2507:Chd9	UTSW	8	91,033,987 (GRCm38)	missense	probably benign	0.01
R2508:Chd9	UTSW	8	91,033,987 (GRCm38)	missense	probably benign	0.01
R2988:Chd9	UTSW	8	91,030,460 (GRCm38)	splice site	probably null
R3418:Chd9	UTSW	8	91,036,591 (GRCm38)	missense	probably damaging	1.00
R3817:Chd9	UTSW	8	90,984,265 (GRCm38)	splice site	probably benign
R3923:Chd9	UTSW	8	90,933,519 (GRCm38)	missense	probably benign	0.16
R4001:Chd9	UTSW	8	90,956,557 (GRCm38)	missense	probably damaging	1.00
R4003:Chd9	UTSW	8	90,956,557 (GRCm38)	missense	probably damaging	1.00
R4006:Chd9	UTSW	8	90,933,560 (GRCm38)	missense	probably benign	0.12
R4013:Chd9	UTSW	8	90,973,169 (GRCm38)	missense	possibly damaging	0.82
R4067:Chd9	UTSW	8	91,023,574 (GRCm38)	missense	possibly damaging	0.53
R4108:Chd9	UTSW	8	91,010,676 (GRCm38)	missense	probably benign	0.04
R4125:Chd9	UTSW	8	91,051,284 (GRCm38)	missense	probably damaging	0.99
R4126:Chd9	UTSW	8	91,051,284 (GRCm38)	missense	probably damaging	0.99
R4452:Chd9	UTSW	8	90,977,680 (GRCm38)	missense	probably damaging	0.99
R4463:Chd9	UTSW	8	90,978,999 (GRCm38)	missense	probably benign	0.01
R4478:Chd9	UTSW	8	91,034,031 (GRCm38)	utr 3 prime	probably benign
R4587:Chd9	UTSW	8	91,036,506 (GRCm38)	missense	possibly damaging	0.95
R4628:Chd9	UTSW	8	90,983,463 (GRCm38)	missense	probably benign	0.05
R4667:Chd9	UTSW	8	91,033,800 (GRCm38)	missense	possibly damaging	0.73
R4908:Chd9	UTSW	8	91,015,249 (GRCm38)	missense	possibly damaging	0.50
R4912:Chd9	UTSW	8	91,034,230 (GRCm38)	missense	possibly damaging	0.84
R4977:Chd9	UTSW	8	91,033,708 (GRCm38)	missense	possibly damaging	0.96
R5016:Chd9	UTSW	8	91,006,626 (GRCm38)	nonsense	probably null
R5083:Chd9	UTSW	8	90,984,374 (GRCm38)	missense	probably damaging	1.00
R5088:Chd9	UTSW	8	90,977,519 (GRCm38)	missense	possibly damaging	0.94
R5090:Chd9	UTSW	8	91,026,834 (GRCm38)	nonsense	probably null
R5307:Chd9	UTSW	8	90,997,149 (GRCm38)	missense	probably damaging	1.00
R5541:Chd9	UTSW	8	91,051,504 (GRCm38)	missense	probably benign	0.09
R5559:Chd9	UTSW	8	91,015,925 (GRCm38)	critical splice donor site	probably null
R5638:Chd9	UTSW	8	91,011,450 (GRCm38)	missense	possibly damaging	0.67
R5640:Chd9	UTSW	8	91,036,562 (GRCm38)	missense	probably damaging	1.00
R5793:Chd9	UTSW	8	91,001,756 (GRCm38)	missense	probably damaging	1.00
R5827:Chd9	UTSW	8	90,989,450 (GRCm38)	missense	probably damaging	1.00
R5834:Chd9	UTSW	8	90,997,164 (GRCm38)	missense	probably damaging	1.00
R5875:Chd9	UTSW	8	91,051,836 (GRCm38)	missense	probably damaging	0.99
R6002:Chd9	UTSW	8	90,978,887 (GRCm38)	missense	probably damaging	1.00
R6091:Chd9	UTSW	8	91,035,063 (GRCm38)	missense	probably damaging	1.00
R6185:Chd9	UTSW	8	91,049,137 (GRCm38)	missense	probably damaging	1.00
R6246:Chd9	UTSW	8	90,932,417 (GRCm38)	missense	probably damaging	1.00
R6292:Chd9	UTSW	8	90,932,922 (GRCm38)	missense	probably benign	0.05
R6305:Chd9	UTSW	8	91,030,546 (GRCm38)	missense	possibly damaging	0.93
R6348:Chd9	UTSW	8	91,011,275 (GRCm38)	missense	possibly damaging	0.95
R6438:Chd9	UTSW	8	90,998,521 (GRCm38)	missense	probably benign	0.02
R6470:Chd9	UTSW	8	90,932,798 (GRCm38)	missense	probably damaging	1.00
R6798:Chd9	UTSW	8	91,051,554 (GRCm38)	missense	possibly damaging	0.56
R6902:Chd9	UTSW	8	91,042,951 (GRCm38)	missense	probably damaging	1.00
R6908:Chd9	UTSW	8	90,956,416 (GRCm38)	missense	probably benign	0.02
R6929:Chd9	UTSW	8	91,042,945 (GRCm38)	missense	probably damaging	1.00
R6969:Chd9	UTSW	8	90,978,914 (GRCm38)	missense	probably benign	0.34
R7043:Chd9	UTSW	8	91,034,215 (GRCm38)	utr 3 prime	probably benign
R7094:Chd9	UTSW	8	90,989,561 (GRCm38)	missense	unknown
R7126:Chd9	UTSW	8	91,015,225 (GRCm38)	missense	unknown
R7219:Chd9	UTSW	8	91,001,766 (GRCm38)	missense	unknown
R7260:Chd9	UTSW	8	90,994,543 (GRCm38)	missense	unknown
R7293:Chd9	UTSW	8	91,034,079 (GRCm38)	missense	unknown
R7303:Chd9	UTSW	8	91,051,904 (GRCm38)	missense	unknown
R7358:Chd9	UTSW	8	91,034,218 (GRCm38)	missense	unknown
R7358:Chd9	UTSW	8	90,983,487 (GRCm38)	missense	unknown
R7451:Chd9	UTSW	8	91,033,818 (GRCm38)	missense	probably benign	0.27
R7451:Chd9	UTSW	8	91,033,790 (GRCm38)	frame shift	probably null
R7456:Chd9	UTSW	8	90,932,525 (GRCm38)	nonsense	probably null
R7481:Chd9	UTSW	8	90,956,438 (GRCm38)	missense	unknown
R7532:Chd9	UTSW	8	90,994,565 (GRCm38)	missense	unknown
R7570:Chd9	UTSW	8	90,994,580 (GRCm38)	missense	unknown
R7611:Chd9	UTSW	8	91,036,389 (GRCm38)	missense	probably damaging	1.00
R7673:Chd9	UTSW	8	91,051,697 (GRCm38)	missense	probably damaging	0.96
R7723:Chd9	UTSW	8	91,015,209 (GRCm38)	missense	unknown
R7739:Chd9	UTSW	8	91,035,025 (GRCm38)	missense	probably damaging	1.00
R7759:Chd9	UTSW	8	90,977,550 (GRCm38)	critical splice donor site	probably null
R7916:Chd9	UTSW	8	91,035,056 (GRCm38)	nonsense	probably null
R7921:Chd9	UTSW	8	91,042,281 (GRCm38)	critical splice donor site	probably null
R7957:Chd9	UTSW	8	91,051,698 (GRCm38)	missense	probably damaging	0.99
R7972:Chd9	UTSW	8	91,005,767 (GRCm38)	missense	unknown
R8108:Chd9	UTSW	8	90,933,224 (GRCm38)	missense	unknown
R8115:Chd9	UTSW	8	91,036,332 (GRCm38)	missense	probably damaging	0.99
R8165:Chd9	UTSW	8	91,041,141 (GRCm38)	missense	probably damaging	1.00
R8171:Chd9	UTSW	8	91,025,387 (GRCm38)	missense	possibly damaging	0.92
R8186:Chd9	UTSW	8	90,998,605 (GRCm38)	missense	unknown
R8208:Chd9	UTSW	8	91,037,263 (GRCm38)	splice site	probably null
R8256:Chd9	UTSW	8	90,933,501 (GRCm38)	missense	unknown
R8281:Chd9	UTSW	8	91,036,597 (GRCm38)	missense	probably damaging	1.00
R8504:Chd9	UTSW	8	90,996,844 (GRCm38)	missense	unknown
R8836:Chd9	UTSW	8	91,041,184 (GRCm38)	missense	probably damaging	0.99
R8892:Chd9	UTSW	8	90,933,840 (GRCm38)	missense	unknown
R8985:Chd9	UTSW	8	90,994,473 (GRCm38)	missense	unknown
R9029:Chd9	UTSW	8	90,956,570 (GRCm38)	missense	unknown
R9030:Chd9	UTSW	8	90,956,570 (GRCm38)	missense	unknown
R9038:Chd9	UTSW	8	90,989,605 (GRCm38)	missense	unknown
R9081:Chd9	UTSW	8	90,977,516 (GRCm38)	nonsense	probably null
R9134:Chd9	UTSW	8	90,933,126 (GRCm38)	missense	unknown
R9205:Chd9	UTSW	8	91,030,642 (GRCm38)	missense	probably benign	0.01
R9309:Chd9	UTSW	8	91,006,691 (GRCm38)	missense	unknown
R9375:Chd9	UTSW	8	90,998,707 (GRCm38)	critical splice donor site	probably null
R9449:Chd9	UTSW	8	90,932,546 (GRCm38)	missense	unknown
R9547:Chd9	UTSW	8	90,956,558 (GRCm38)	missense	unknown
R9573:Chd9	UTSW	8	90,977,674 (GRCm38)	missense	unknown
R9576:Chd9	UTSW	8	90,932,666 (GRCm38)	missense	unknown
R9601:Chd9	UTSW	8	91,005,732 (GRCm38)	nonsense	probably null
R9613:Chd9	UTSW	8	90,956,522 (GRCm38)	nonsense	probably null
R9639:Chd9	UTSW	8	91,034,212 (GRCm38)	missense	probably null
R9718:Chd9	UTSW	8	90,986,173 (GRCm38)	missense	unknown
R9746:Chd9	UTSW	8	91,011,435 (GRCm38)	missense	unknown
R9762:Chd9	UTSW	8	90,986,113 (GRCm38)	missense	unknown
R9764:Chd9	UTSW	8	90,994,592 (GRCm38)	missense	unknown
R9790:Chd9	UTSW	8	91,033,789 (GRCm38)	missense	possibly damaging	0.82
R9791:Chd9	UTSW	8	91,033,789 (GRCm38)	missense	possibly damaging	0.82
RF007:Chd9	UTSW	8	91,033,950 (GRCm38)	missense	possibly damaging	0.66
X0065:Chd9	UTSW	8	91,036,572 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTTCTCACATGTGGCCCAAGC -3'
(R):5'- ACAGGATATATGTGACCTCTGTGGG -3'

Sequencing Primer
(F):5'- AGCCCAAAATATGACACTGAATG -3'
(R):5'- CAAATGTTGACCCACGTC -3'

Posted On

2019-06-26