Mutagenetix > Incidental Mutation

Incidental Mutation 'R1838:Wdr95'

205483

Institutional Source

Beutler Lab

Gene Symbol

Wdr95

Ensembl Gene

ENSMUSG00000029658

Gene Name

WD40 repeat domain 95

Synonyms

4930434E21Rik

MMRRC Submission

039865-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.078) question?

Stock #

R1838 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

149528679-149611894 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 149599366 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 663 (D663G)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000110502] [ENSMUST00000201525] [ENSMUST00000202902]

AlphaFold

D3Z7A8

Predicted Effect

probably benign
Transcript: ENSMUST00000110502
AA Change: D521G

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

SMART Domains

Protein: ENSMUSP00000106128
Gene: ENSMUSG00000029658
AA Change: D521G

Domain	Start	End	E-Value	Type
Pfam:WD40	4	28	3.3e-3	PFAM
WD40	32	71	4.38e-5	SMART
WD40	120	159	3.27e-4	SMART
WD40	162	203	1.71e-7	SMART
WD40	206	249	3.57e0	SMART
WD40	263	301	1.7e-2	SMART
Blast:WD40	315	363	3e-14	BLAST
Blast:WD40	367	408	4e-13	BLAST
WD40	421	460	2.01e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000121108
AA Change: D663G

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

SMART Domains

Protein: ENSMUSP00000113092
Gene: ENSMUSG00000029658
AA Change: D663G

Domain	Start	End	E-Value	Type
Blast:WD40	44	83	9e-11	BLAST
WD40	132	170	1.61e-3	SMART
WD40	174	213	4.38e-5	SMART
WD40	262	301	3.27e-4	SMART
WD40	304	345	1.71e-7	SMART
WD40	348	391	3.57e0	SMART
WD40	405	443	1.7e-2	SMART
Blast:WD40	457	505	3e-14	BLAST
Blast:WD40	509	550	4e-13	BLAST
WD40	563	602	2.01e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000201525

SMART Domains

Protein: ENSMUSP00000144234
Gene: ENSMUSG00000029658

Domain	Start	End	E-Value	Type
WD40	104	143	2e-6	SMART
WD40	146	187	1.1e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000202902
AA Change: D663G

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

SMART Domains

Protein: ENSMUSP00000144385
Gene: ENSMUSG00000029658
AA Change: D663G

Domain	Start	End	E-Value	Type
Blast:WD40	44	83	9e-11	BLAST
WD40	132	170	1.61e-3	SMART
WD40	174	213	4.38e-5	SMART
WD40	262	301	3.27e-4	SMART
WD40	304	345	1.71e-7	SMART
WD40	348	391	3.57e0	SMART
WD40	405	443	1.7e-2	SMART
Blast:WD40	457	505	3e-14	BLAST
Blast:WD40	509	550	4e-13	BLAST
WD40	563	602	2.01e-4	SMART

Coding Region Coverage

1x: 97.4%
3x: 96.9%
10x: 95.2%
20x: 92.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 88 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630073D07Rik	T	C	6: 132,626,727	D22G	unknown	Het
Abca4	G	A	3: 122,128,305	R1170K	probably benign	Het
Adam28	T	C	14: 68,639,210	N197S	possibly damaging	Het
Adamtsl3	G	T	7: 82,493,373	R267L	probably damaging	Het
Adgrb2	A	T	4: 130,010,231	T717S	probably benign	Het
Adgrb3	A	G	1: 25,084,270	S1417P	probably damaging	Het
Afg3l2	A	T	18: 67,414,172	V561D	probably damaging	Het
Atp13a2	T	A	4: 140,994,332	Y244*	probably null	Het
BB014433	C	G	8: 15,042,629	V75L	unknown	Het
Btnl6	T	A	17: 34,515,542	D82V	probably damaging	Het
Ccdc178	A	G	18: 22,067,638	Y421H	probably damaging	Het
Cdc123	A	T	2: 5,794,891		probably null	Het
Cdhr5	C	T	7: 141,272,603	V367I	possibly damaging	Het
Celsr3	A	G	9: 108,829,906	H1196R	probably benign	Het
Chd8	T	C	14: 52,204,883	S2077G	probably benign	Het
Col6a5	G	A	9: 105,864,833	H2296Y	probably benign	Het
Ctnna2	T	C	6: 77,845,542	D26G	probably damaging	Het
Ctr9	G	T	7: 111,052,303	R910L	possibly damaging	Het
Cyp2t4	G	T	7: 27,158,416	R455L	possibly damaging	Het
Cyp3a13	A	T	5: 137,911,632		probably null	Het
Dennd3	T	C	15: 73,565,100	S1059P	probably damaging	Het
Dennd4c	A	G	4: 86,825,178	T1135A	probably benign	Het
Dnah7b	T	C	1: 46,116,177	V295A	probably benign	Het
Dnah7b	C	A	1: 46,277,105	T3126K	probably damaging	Het
Ehbp1l1	C	T	19: 5,717,691	E1195K	probably benign	Het
Exoc6b	T	A	6: 84,853,678	I447L	probably benign	Het
Glt1d1	G	A	5: 127,678,129	V202I	probably benign	Het
Grk1	T	C	8: 13,416,155	V533A	possibly damaging	Het
Gsdma3	C	T	11: 98,629,858	A105V	probably benign	Het
Gzma	T	A	13: 113,095,984	I131F	probably damaging	Het
Helq	A	T	5: 100,771,879	L35*	probably null	Het
Hnrnpll	T	C	17: 80,038,623	N403S	probably damaging	Het
Hsf5	A	G	11: 87,636,055	K518E	probably benign	Het
Ighe	T	A	12: 113,271,850	H258L	unknown	Het
Il6ra	T	C	3: 89,890,272	D96G	probably benign	Het
Ints13	C	T	6: 146,566,611	A129T	possibly damaging	Het
Ipo7	T	A	7: 110,042,109	H345Q	probably damaging	Het
Kcna2	A	T	3: 107,104,512	E136D	probably benign	Het
Kif5a	G	A	10: 127,236,815	Q702*	probably null	Het
Klhdc7a	G	T	4: 139,967,070	P189T	probably benign	Het
Krtap4-9	A	G	11: 99,785,396		probably benign	Het
Lamc3	T	C	2: 31,925,582	S1097P	possibly damaging	Het
Ldlrad2	A	T	4: 137,572,170	N114K	probably benign	Het
Lrfn1	A	T	7: 28,459,768	I371L	probably damaging	Het
Lrwd1	A	G	5: 136,132,388	V240A	probably benign	Het
Lypd1	A	T	1: 125,873,371		probably benign	Het
Magi2	A	T	5: 20,465,827	T163S	probably damaging	Het
Man2c1	A	G	9: 57,137,337	N354S	probably benign	Het
Map3k13	T	C	16: 21,914,189	Y514H	possibly damaging	Het
Med15	T	C	16: 17,653,562	D577G	probably benign	Het
Mroh4	A	T	15: 74,616,113	M320K	probably benign	Het
Ms4a10	T	A	19: 10,964,047	D186V	possibly damaging	Het
Myh7	T	C	14: 54,973,180	N1725S	possibly damaging	Het
Myo5c	A	T	9: 75,273,553	R741S	probably damaging	Het
Naip6	T	C	13: 100,316,136	D139G	probably damaging	Het
Nat6	G	A	9: 107,583,017	R37H	possibly damaging	Het
Olfr1252	A	T	2: 89,721,709	M134K	probably damaging	Het
Olfr1370	A	T	13: 21,072,425	L292*	probably null	Het
Olfr229	A	T	9: 39,909,841	I13F	possibly damaging	Het
Olfr982	A	T	9: 40,074,309	M5L	probably benign	Het
Pcdhb3	A	G	18: 37,301,317	D112G	probably benign	Het
Pdpr	C	A	8: 111,134,734	P787T	probably damaging	Het
Pgm3	C	T	9: 86,569,233	V123I	probably benign	Het
Pms1	A	C	1: 53,192,098		probably null	Het
Prl2b1	A	G	13: 27,388,566	S14P	possibly damaging	Het
Prune2	T	A	19: 17,199,878	W212R	probably damaging	Het
Rabgef1	A	G	5: 130,213,021	E422G	probably benign	Het
Ralyl	A	G	3: 14,143,412	E204G	probably damaging	Het
Rbpms2	ACTGCTGCTGCTGCTGC	ACTGCTGCTGCTGCTGCTGC	9: 65,651,666		probably benign	Het
Rbpms2	TGCCGCCGCC	TGCCGCCGCCGCC	9: 65,651,680		probably benign	Het
Rit1	C	G	3: 88,729,170	T127S	probably damaging	Het
Slc16a7	C	T	10: 125,231,198	V191M	probably damaging	Het
Slc34a2	A	T	5: 53,058,436	H63L	probably benign	Het
Smpd4	G	A	16: 17,642,302		probably null	Het
Sp3	A	G	2: 72,938,176	S748P	possibly damaging	Het
Spata31d1b	G	A	13: 59,715,857	C273Y	probably benign	Het
Spata31d1b	G	A	13: 59,717,465	R809K	probably benign	Het
Tmco5	A	T	2: 116,880,879	E90V	probably damaging	Het
Tnxb	A	T	17: 34,678,910	D844V	probably damaging	Het
Tpi1	T	C	6: 124,814,152	T41A	probably benign	Het
Ttn	T	C	2: 76,727,192	I29853V	probably damaging	Het
Vmn2r26	C	T	6: 124,024,771	T5I	probably benign	Het
Zbtb39	T	C	10: 127,742,700	F381S	probably damaging	Het
Zfp523	T	A	17: 28,194,993	I34N	probably damaging	Het
Zfp646	T	A	7: 127,879,739	Y363N	probably damaging	Het
Zfp712	A	C	13: 67,042,047	C139G	probably damaging	Het
Zfp958	A	G	8: 4,628,590	H205R	probably damaging	Het
Zfp974	G	A	7: 27,910,356	P648L	possibly damaging	Het

Other mutations in Wdr95

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00429:Wdr95	APN	5	149595244	critical splice acceptor site	probably benign	0.00
IGL02352:Wdr95	APN	5	149580619	missense	probably damaging	0.99
IGL02359:Wdr95	APN	5	149580619	missense	probably damaging	0.99
IGL02478:Wdr95	APN	5	149596321	missense	probably benign	0.02
IGL03078:Wdr95	APN	5	149611597	missense	possibly damaging	0.63
IGL03201:Wdr95	APN	5	149581887	splice site	probably null
P0037:Wdr95	UTSW	5	149588071	missense	probably benign	0.27
R0115:Wdr95	UTSW	5	149564390	missense	probably damaging	1.00
R0538:Wdr95	UTSW	5	149580806	missense	probably damaging	1.00
R0606:Wdr95	UTSW	5	149588130	missense	probably damaging	1.00
R0723:Wdr95	UTSW	5	149574048	missense	probably damaging	1.00
R1104:Wdr95	UTSW	5	149606337	missense	probably benign	0.00
R1233:Wdr95	UTSW	5	149581858	missense	possibly damaging	0.61
R1233:Wdr95	UTSW	5	149595364	missense	probably benign	0.00
R1344:Wdr95	UTSW	5	149588098	missense	probably damaging	1.00
R1513:Wdr95	UTSW	5	149599294	missense	probably benign	0.00
R1623:Wdr95	UTSW	5	149574116	missense	probably damaging	1.00
R1633:Wdr95	UTSW	5	149593172	missense	probably damaging	0.98
R1664:Wdr95	UTSW	5	149595287	missense	probably damaging	0.98
R1686:Wdr95	UTSW	5	149593101	missense	probably damaging	1.00
R1741:Wdr95	UTSW	5	149595396	splice site	probably null
R1750:Wdr95	UTSW	5	149581886	splice site	probably null
R1774:Wdr95	UTSW	5	149564392	nonsense	probably null
R1831:Wdr95	UTSW	5	149552426	missense	probably damaging	1.00
R1907:Wdr95	UTSW	5	149552426	missense	probably damaging	1.00
R2019:Wdr95	UTSW	5	149574148	splice site	probably benign
R2063:Wdr95	UTSW	5	149579162	splice site	probably null
R2392:Wdr95	UTSW	5	149580670	missense	probably benign	0.03
R2863:Wdr95	UTSW	5	149581856	nonsense	probably null
R4116:Wdr95	UTSW	5	149597575	missense	probably benign	0.02
R4237:Wdr95	UTSW	5	149563337	nonsense	probably null
R4420:Wdr95	UTSW	5	149532666	missense	probably damaging	0.99
R4639:Wdr95	UTSW	5	149581814	splice site	probably benign
R4824:Wdr95	UTSW	5	149595332	missense	probably damaging	1.00
R4911:Wdr95	UTSW	5	149611692	nonsense	probably null
R5016:Wdr95	UTSW	5	149544801	missense	probably benign	0.00
R5458:Wdr95	UTSW	5	149564414	missense	probably damaging	1.00
R5486:Wdr95	UTSW	5	149596330	nonsense	probably null
R5613:Wdr95	UTSW	5	149584470	missense	probably damaging	1.00
R5906:Wdr95	UTSW	5	149564227	missense	possibly damaging	0.50
R5956:Wdr95	UTSW	5	149594482	missense	probably benign	0.00
R6309:Wdr95	UTSW	5	149580803	critical splice acceptor site	probably null
R6867:Wdr95	UTSW	5	149580923	splice site	probably null
R6964:Wdr95	UTSW	5	149581850	missense	probably damaging	1.00
R7008:Wdr95	UTSW	5	149611540	missense	probably benign	0.00
R7208:Wdr95	UTSW	5	149595371	missense	probably benign	0.02
R7309:Wdr95	UTSW	5	149606293	missense	probably benign	0.01
R7504:Wdr95	UTSW	5	149581846	missense	probably damaging	0.99
R7660:Wdr95	UTSW	5	149594480	missense	possibly damaging	0.86
R7997:Wdr95	UTSW	5	149579157	critical splice donor site	probably null
R8084:Wdr95	UTSW	5	149588133	missense	probably damaging	1.00
R8356:Wdr95	UTSW	5	149579107	missense	probably damaging	1.00
R8456:Wdr95	UTSW	5	149579107	missense	probably damaging	1.00
R8523:Wdr95	UTSW	5	149573996	missense	probably damaging	1.00
R8682:Wdr95	UTSW	5	149595287	missense	possibly damaging	0.94
R9451:Wdr95	UTSW	5	149580700	missense	probably benign	0.01
R9453:Wdr95	UTSW	5	149552452	missense	probably damaging	0.99
R9779:Wdr95	UTSW	5	149581828	missense	probably benign	0.01
X0024:Wdr95	UTSW	5	149588167	missense	possibly damaging	0.81
Z1176:Wdr95	UTSW	5	149566436	missense	probably benign	0.34
Z1177:Wdr95	UTSW	5	149544776	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- ATTCCTCCAGGGACCTTTGG -3'
(R):5'- GTCCTTTACCTCACAGATGGATCG -3'

Sequencing Primer
(F):5'- TTTGGGCAGAATCACCCCTG -3'
(R):5'- TGGTCCAGATCAGTGCCAATG -3'

Posted On

2014-06-23