Mutagenetix > Incidental Mutation

Incidental Mutation 'R1473:Wdr38'

165893

Institutional Source

Beutler Lab

Gene Symbol

Wdr38

Ensembl Gene

ENSMUSG00000035295

Gene Name

WD repeat domain 38

Synonyms

1700123D08Rik

MMRRC Submission

039526-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.065) question?

Stock #

R1473 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

38888287-38891600 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 38890991 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 261 (T261A)

Ref Sequence

ENSEMBL: ENSMUSP00000108493 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039535] [ENSMUST00000080861] [ENSMUST00000112872]

AlphaFold

Q9D994

Predicted Effect

probably benign
Transcript: ENSMUST00000039535
AA Change: T261A

PolyPhen 2 Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000043834
Gene: ENSMUSG00000035295
AA Change: T261A

Domain	Start	End	E-Value	Type
WD40	15	54	9.67e-7	SMART
WD40	57	96	9.22e-13	SMART
WD40	99	138	4.4e-10	SMART
WD40	141	180	1.21e-7	SMART
WD40	186	224	9.97e-9	SMART
WD40	227	266	4.34e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000080861

SMART Domains

Protein: ENSMUSP00000079672
Gene: ENSMUSG00000062997

Domain	Start	End	E-Value	Type
Pfam:Ribosomal_L29	7	63	2.7e-22	PFAM
low complexity region	95	108	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000112872
AA Change: T261A

PolyPhen 2 Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000108493
Gene: ENSMUSG00000035295
AA Change: T261A

Domain	Start	End	E-Value	Type
WD40	15	54	9.67e-7	SMART
WD40	57	96	9.22e-13	SMART
WD40	99	138	4.4e-10	SMART
WD40	141	180	1.21e-7	SMART
WD40	186	224	9.97e-9	SMART
WD40	227	266	4.34e-9	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000124062

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126246

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141133

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141467

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152441

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.5%
20x: 93.2%

Validation Efficiency

98% (88/90)

Allele List at MGI

Other mutations in this stock

Total: 89 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ablim1	T	C	19: 57,056,668 (GRCm39)	D342G	probably damaging	Het
Acad8	T	C	9: 26,890,337 (GRCm39)	T293A	probably benign	Het
Adamts13	C	A	2: 26,871,765 (GRCm39)	Y310*	probably null	Het
Adcy6	T	A	15: 98,490,624 (GRCm39)	Y1102F	probably damaging	Het
Ahctf1	G	A	1: 179,603,673 (GRCm39)	T791M	probably benign	Het
Ahctf1	A	G	1: 179,626,844 (GRCm39)	V18A	probably damaging	Het
Ahcyl	T	A	16: 45,975,182 (GRCm39)	E65V	probably damaging	Het
Ampd3	T	G	7: 110,404,142 (GRCm39)	S564R	probably damaging	Het
Anapc1	A	T	2: 128,459,617 (GRCm39)	I1814K	possibly damaging	Het
Arl4c	A	T	1: 88,629,331 (GRCm39)	L19Q	probably damaging	Het
Atp6v0e2	T	C	6: 48,516,198 (GRCm39)	Y49H	probably damaging	Het
Ccdc121rt3	T	C	5: 112,502,415 (GRCm39)	T430A	probably benign	Het
Ccdc24	G	T	4: 117,727,101 (GRCm39)		probably benign	Het
Ceacam23	A	G	7: 17,639,016 (GRCm39)		noncoding transcript	Het
Clcn6	A	C	4: 148,108,613 (GRCm39)	F139V	possibly damaging	Het
Col2a1	A	G	15: 97,880,789 (GRCm39)		probably benign	Het
Crip2	T	A	12: 113,107,120 (GRCm39)	C29S	probably damaging	Het
Cyp2a4	A	C	7: 26,014,188 (GRCm39)	N455T	probably benign	Het
Dhcr7	T	C	7: 143,400,805 (GRCm39)	Y323H	probably damaging	Het
Dhcr7	A	G	7: 143,395,105 (GRCm39)	D113G	probably damaging	Het
Dnah7a	A	C	1: 53,535,173 (GRCm39)	S2696A	probably benign	Het
Dnajc12	A	G	10: 63,233,023 (GRCm39)	T55A	probably benign	Het
Drosha	G	A	15: 12,912,606 (GRCm39)	E1075K	probably benign	Het
Duox2	A	G	2: 122,117,602 (GRCm39)	S911P	possibly damaging	Het
Ephb2	G	A	4: 136,421,369 (GRCm39)	A327V	possibly damaging	Het
Espl1	C	T	15: 102,228,878 (GRCm39)	T1711I	possibly damaging	Het
Fmnl2	A	G	2: 52,748,219 (GRCm39)	K22R	possibly damaging	Het
Fzd6	T	C	15: 38,894,358 (GRCm39)	F175L	probably damaging	Het
Gm6526	A	G	14: 43,986,303 (GRCm39)	I76M	probably damaging	Het
Gm9881	A	T	16: 90,967,623 (GRCm39)	F34I	unknown	Het
Gm9892	T	C	8: 52,649,649 (GRCm39)	D148G	possibly damaging	Het
Grb10	C	T	11: 11,884,249 (GRCm39)	V486I	probably damaging	Het
Gtf3c3	C	T	1: 54,456,937 (GRCm39)	A488T	probably damaging	Het
H2bc18	G	T	3: 96,177,388 (GRCm39)	L107F	probably damaging	Het
Hdac4	T	C	1: 91,957,690 (GRCm39)	H108R	possibly damaging	Het
Hmcn1	G	A	1: 150,648,303 (GRCm39)	T661I	probably benign	Het
Icam1	T	A	9: 20,939,172 (GRCm39)	I515N	probably damaging	Het
Ifi208	A	G	1: 173,523,220 (GRCm39)	R497G	possibly damaging	Het
Igsf10	A	T	3: 59,226,188 (GRCm39)	V2495E	probably damaging	Het
Iqgap1	T	C	7: 80,383,759 (GRCm39)	M1102V	probably benign	Het
Itgb4	A	T	11: 115,874,873 (GRCm39)	N410I	probably benign	Het
Jup	T	C	11: 100,270,427 (GRCm39)	H360R	possibly damaging	Het
Kif20b	T	A	19: 34,951,896 (GRCm39)	S1685T	possibly damaging	Het
Lins1	T	C	7: 66,361,794 (GRCm39)		probably null	Het
Lrig1	T	A	6: 94,584,294 (GRCm39)	T917S	probably benign	Het
Mast2	A	G	4: 116,169,152 (GRCm39)	S814P	probably damaging	Het
Mast4	T	C	13: 102,909,027 (GRCm39)	T483A	probably damaging	Het
Mcpt1	T	C	14: 56,256,990 (GRCm39)	M176T	probably benign	Het
Mettl22	A	G	16: 8,291,825 (GRCm39)	Q38R	probably damaging	Het
Mrm2	T	C	5: 140,314,443 (GRCm39)	T131A	probably benign	Het
Mtcl2	A	T	2: 156,862,368 (GRCm39)	Y1520*	probably null	Het
Nde1	T	G	16: 14,003,728 (GRCm39)	F71V	probably benign	Het
Nxn	C	T	11: 76,154,013 (GRCm39)	G274D	possibly damaging	Het
Or4c123	A	T	2: 89,127,250 (GRCm39)	Y121*	probably null	Het
Or5h17	A	T	16: 58,820,275 (GRCm39)	T76S	probably benign	Het
Or6k14	G	T	1: 173,927,315 (GRCm39)	C97F	probably damaging	Het
Or6p1	T	A	1: 174,258,209 (GRCm39)	W72R	probably damaging	Het
Osbp2	T	C	11: 3,667,175 (GRCm39)		probably null	Het
Otud7a	C	A	7: 63,404,377 (GRCm39)		probably benign	Het
Phf3	G	A	1: 30,845,021 (GRCm39)	L1313F	probably damaging	Het
Pkhd1	A	T	1: 20,593,207 (GRCm39)	D1635E	probably benign	Het
Plpp1	A	G	13: 112,996,198 (GRCm39)	H171R	probably damaging	Het
Pofut1	A	G	2: 153,103,166 (GRCm39)	M172V	probably damaging	Het
Prmt5	A	G	14: 54,746,372 (GRCm39)	F580L	probably damaging	Het
Rab11fip3	A	T	17: 26,210,296 (GRCm39)	L987Q	probably damaging	Het
Retnlb	T	A	16: 48,639,028 (GRCm39)	C76*	probably null	Het
Rnf38	T	C	4: 44,131,584 (GRCm39)	N399S	probably benign	Het
Sbk1	A	G	7: 125,891,424 (GRCm39)	E286G	possibly damaging	Het
Scin	T	A	12: 40,127,501 (GRCm39)	T430S	probably benign	Het
Sgsm1	T	A	5: 113,411,123 (GRCm39)	T868S	probably benign	Het
Sipa1l1	G	A	12: 82,387,885 (GRCm39)	R37H	probably damaging	Het
Smchd1	A	T	17: 71,668,832 (GRCm39)		probably benign	Het
Sned1	G	A	1: 93,209,376 (GRCm39)	V830M	possibly damaging	Het
Stk32c	C	T	7: 138,705,095 (GRCm39)	R23Q	probably damaging	Het
Sult1d1	A	G	5: 87,712,598 (GRCm39)	M82T	probably benign	Het
Tat	T	C	8: 110,723,550 (GRCm39)	L346P	probably damaging	Het
Tenm3	C	A	8: 48,763,660 (GRCm39)	G789V	probably damaging	Het
Thsd7a	C	T	6: 12,338,621 (GRCm39)	S1203N	probably benign	Het
Tmem191	G	A	16: 17,095,826 (GRCm39)		probably null	Het
Tmem268	A	G	4: 63,498,575 (GRCm39)	T239A	probably damaging	Het
Tmem82	A	C	4: 141,343,589 (GRCm39)	L227R	possibly damaging	Het
Ttn	A	T	2: 76,557,376 (GRCm39)	I29906N	probably damaging	Het
Txndc15	T	C	13: 55,869,387 (GRCm39)		probably benign	Het
Ubqln4	A	G	3: 88,473,152 (GRCm39)	I536V	probably benign	Het
Unc80	C	T	1: 66,560,740 (GRCm39)	H823Y	possibly damaging	Het
Vmn2r102	A	T	17: 19,914,843 (GRCm39)	I803F	probably benign	Het
Vmn2r6	G	T	3: 64,445,579 (GRCm39)	Y715*	probably null	Het
Vmn2r74	A	T	7: 85,610,618 (GRCm39)	C25S	probably damaging	Het
Zfp653	T	C	9: 21,969,516 (GRCm39)	E250G	possibly damaging	Het

Other mutations in Wdr38

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01549:Wdr38	APN	2	38,890,730 (GRCm39)	missense	probably damaging	1.00
IGL02019:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02020:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02137:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02138:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02172:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02178:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02422:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02423:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02525:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02526:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02621:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02623:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02624:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
IGL02625:Wdr38	APN	2	38,888,424 (GRCm39)	missense	probably damaging	0.97
PIT4696001:Wdr38	UTSW	2	38,889,984 (GRCm39)	critical splice acceptor site	probably null
R1794:Wdr38	UTSW	2	38,890,741 (GRCm39)	missense	probably damaging	1.00
R3964:Wdr38	UTSW	2	38,889,362 (GRCm39)	missense	probably damaging	1.00
R6005:Wdr38	UTSW	2	38,891,333 (GRCm39)	missense	possibly damaging	0.57
R6432:Wdr38	UTSW	2	38,890,723 (GRCm39)	missense	probably damaging	1.00
R6513:Wdr38	UTSW	2	38,889,970 (GRCm39)	splice site	probably null
R7266:Wdr38	UTSW	2	38,890,276 (GRCm39)	missense	probably damaging	1.00
R7454:Wdr38	UTSW	2	38,888,352 (GRCm39)	start gained	probably benign
R7834:Wdr38	UTSW	2	38,890,196 (GRCm39)	missense	possibly damaging	0.84
R8333:Wdr38	UTSW	2	38,889,361 (GRCm39)	missense	probably damaging	1.00
R9542:Wdr38	UTSW	2	38,890,210 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- ACCCCAGTTGTGTCCTACCACAATC -3'
(R):5'- AAGGCATTTCCCTGTGAGGCAGTC -3'

Sequencing Primer
(F):5'- GTGTCCTACCACAATCTGGAG -3'
(R):5'- GTCCCAGACTTTGACCTAGAAG -3'

Posted On

2014-03-28