Mutagenetix > Incidental Mutation

Incidental Mutation 'R7412:Wdfy4'

575174

Institutional Source

Beutler Lab

Gene Symbol

Wdfy4

Ensembl Gene

ENSMUSG00000051506

Gene Name

WD repeat and FYVE domain containing 4

Synonyms

MMRRC Submission

045493-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7412 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

32959547-33185508 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 33149584 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 290 (L290P)

Ref Sequence

ENSEMBL: ENSMUSP00000117068 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000061753] [ENSMUST00000130509]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000061753
AA Change: L290P

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000057556
Gene: ENSMUSG00000051506
AA Change: L290P

Domain	Start	End	E-Value	Type
low complexity region	69	77	N/A	INTRINSIC
low complexity region	204	222	N/A	INTRINSIC
low complexity region	508	522	N/A	INTRINSIC
low complexity region	618	632	N/A	INTRINSIC
low complexity region	644	661	N/A	INTRINSIC
low complexity region	1585	1604	N/A	INTRINSIC
low complexity region	1899	1909	N/A	INTRINSIC
Pfam:PH_BEACH	2237	2348	1.2e-9	PFAM
Beach	2378	2660	3.69e-196	SMART
WD40	2761	2801	1.98e1	SMART
WD40	2811	2850	5.18e-7	SMART
WD40	2853	2891	9.94e-1	SMART
WD40	2893	2940	3.17e-2	SMART
WD40	2986	3021	3.31e0	SMART

Predicted Effect

SMART Domains

Protein: ENSMUSP00000117068
Gene: ENSMUSG00000051506
AA Change: L290P

Domain	Start	End	E-Value	Type
low complexity region	69	77	N/A	INTRINSIC
low complexity region	204	222	N/A	INTRINSIC
low complexity region	508	522	N/A	INTRINSIC
low complexity region	618	632	N/A	INTRINSIC
low complexity region	644	661	N/A	INTRINSIC
low complexity region	1596	1615	N/A	INTRINSIC
low complexity region	1795	1819	N/A	INTRINSIC
low complexity region	2019	2029	N/A	INTRINSIC
Pfam:PH_BEACH	2362	2473	1.2e-9	PFAM
Beach	2503	2785	3.69e-196	SMART
WD40	2886	2926	1.98e1	SMART
WD40	2936	2975	5.18e-7	SMART
WD40	2978	3016	9.94e-1	SMART
WD40	3018	3065	3.17e-2	SMART
WD40	3111	3146	3.31e0	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

97% (71/73)

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017N19Rik	T	A	10: 100,612,829 (GRCm38)	Y335*	probably null	Het
Alpk1	A	T	3: 127,672,494 (GRCm38)	L1121Q	probably damaging	Het
Alpk1	A	G	3: 127,695,733 (GRCm38)	I99T	probably damaging	Het
Ap2a2	T	A	7: 141,626,136 (GRCm38)	F717I	probably damaging	Het
Arhgap33	C	T	7: 30,523,052 (GRCm38)	D1152N	probably benign	Het
Arvcf	A	G	16: 18,401,600 (GRCm38)	D642G	probably benign	Het
Astn1	T	G	1: 158,502,349 (GRCm38)	M258R	probably damaging	Het
Brinp3	C	G	1: 146,902,010 (GRCm38)	L732V	possibly damaging	Het
Carmil1	T	C	13: 24,098,810 (GRCm38)	D547G	possibly damaging	Het
Ccdc177	A	G	12: 80,759,018 (GRCm38)	F161L	possibly damaging	Het
Cfap57	C	T	4: 118,614,931 (GRCm38)	V84I	probably benign	Het
Cnot10	A	G	9: 114,625,903 (GRCm38)	Y221H	probably damaging	Het
Col6a3	T	A	1: 90,828,133 (GRCm38)	I145F	probably damaging	Het
Crybg2	A	G	4: 134,074,123 (GRCm38)	T865A	probably benign	Het
Cyp4f37	A	G	17: 32,629,844 (GRCm38)	S229G	possibly damaging	Het
Ddx56	G	A	11: 6,261,720 (GRCm38)	T462I	probably damaging	Het
Dhx30	T	C	9: 110,092,898 (GRCm38)	M239V	probably benign	Het
Dusp9	TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG	TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG	X: 73,640,611 (GRCm38)		probably benign	Het
Enpp5	G	A	17: 44,085,264 (GRCm38)	G356S	probably damaging	Het
Ephb6	A	G	6: 41,620,239 (GRCm38)	K994E	probably damaging	Het
Fam83a	A	C	15: 57,986,425 (GRCm38)	T122P	probably benign	Het
Fbxo24	C	A	5: 137,619,623 (GRCm38)	C293F	possibly damaging	Het
Fech	A	T	18: 64,458,184 (GRCm38)	S390T	probably benign	Het
Fras1	A	G	5: 96,614,889 (GRCm38)	H750R	probably benign	Het
Frmpd2	A	G	14: 33,571,969 (GRCm38)	D1364G	probably benign	Het
Ganab	T	C	19: 8,912,528 (GRCm38)	I652T	probably benign	Het
Gm21103	T	A	14: 6,301,955 (GRCm38)	T153S	probably benign	Het
Gm21886	GGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGTTAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAG	GGGCCTGCAGACAGTAGGTACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAG	18: 80,089,752 (GRCm38)		probably benign	Het
Gm5799	A	G	14: 43,544,538 (GRCm38)	I56V	possibly damaging	Het
Gm7276	T	C	18: 77,185,487 (GRCm38)	R184G	unknown	Het
Gmip	T	G	8: 69,820,499 (GRCm38)	D845E	probably benign	Het
Hspa9	T	C	18: 34,949,029 (GRCm38)	K175E	probably damaging	Het
Ipo13	A	G	4: 117,894,871 (GRCm38)	F890L	probably benign	Het
Klrb1f	C	T	6: 129,056,345 (GRCm38)	R179*	probably null	Het
Mrvi1	A	T	7: 110,923,756 (GRCm38)	V160D	probably benign	Het
Nasp	A	G	4: 116,610,588 (GRCm38)	V400A	possibly damaging	Het
Ncoa7	T	A	10: 30,722,851 (GRCm38)	K25N	possibly damaging	Het
Ndrg1	A	C	15: 66,960,533 (GRCm38)	M1R	probably null	Het
Nf1	G	A	11: 79,473,414 (GRCm38)	A1557T	probably damaging	Het
Nrde2	G	A	12: 100,142,250 (GRCm38)	Q361*	probably null	Het
Olfr1330	A	T	4: 118,893,130 (GRCm38)	I16F	possibly damaging	Het
Olfr150	T	C	9: 39,737,126 (GRCm38)	F104L	probably benign	Het
Olfr221	A	T	14: 52,035,853 (GRCm38)	L86*	probably null	Het
Olfr350	T	C	2: 36,850,466 (GRCm38)	L140P	probably benign	Het
Olfr366	C	T	2: 37,219,762 (GRCm38)	T91I	possibly damaging	Het
Olfr829	A	T	9: 18,856,789 (GRCm38)	I46F	possibly damaging	Het
Opn1sw	A	T	6: 29,379,857 (GRCm38)	L126Q	probably damaging	Het
Osmr	A	G	15: 6,823,567 (GRCm38)	Y616H	probably damaging	Het
Pagr1a	T	C	7: 127,016,564 (GRCm38)	T120A	probably benign	Het
Patj	A	G	4: 98,411,139 (GRCm38)	E166G	probably damaging	Het
Plk4	G	A	3: 40,812,178 (GRCm38)	V764I	probably benign	Het
Polr3h	G	A	15: 81,916,401 (GRCm38)		probably null	Het
Ptprb	T	A	10: 116,341,138 (GRCm38)	D989E	probably benign	Het
Sdk2	A	T	11: 113,868,083 (GRCm38)		probably null	Het
Setd1b	C	A	5: 123,152,576 (GRCm38)	R869S	unknown	Het
Sgcz	T	C	8: 37,523,411 (GRCm38)	I263V	probably benign	Het
Skint8	G	A	4: 111,928,561 (GRCm38)	G68D	probably benign	Het
Slc22a7	A	T	17: 46,434,627 (GRCm38)	V326E	probably benign	Het
Slc39a1	T	G	3: 90,249,089 (GRCm38)	L38R	probably damaging	Het
Slc4a4	A	G	5: 89,214,647 (GRCm38)		probably null	Het
Sptlc3	A	G	2: 139,589,617 (GRCm38)	E353G	possibly damaging	Het
Ssh2	G	T	11: 77,450,108 (GRCm38)	L695F	probably damaging	Het
Tacr2	C	A	10: 62,261,648 (GRCm38)	Y302*	probably null	Het
Tas2r117	T	C	6: 132,803,229 (GRCm38)	L110P	probably damaging	Het
Tex9	A	T	9: 72,486,778 (GRCm38)		probably null	Het
Tmem17	A	T	11: 22,518,645 (GRCm38)	T195S	probably benign	Het
Trcg1	T	A	9: 57,241,483 (GRCm38)	S113T	probably benign	Het
Trpa1	A	T	1: 14,884,198 (GRCm38)	F826I	probably benign	Het
Usp17lc	A	G	7: 103,418,368 (GRCm38)	Y290C	probably damaging	Het
Vmn2r32	T	A	7: 7,474,213 (GRCm38)	D393V	possibly damaging	Het
Xpnpep1	G	C	19: 53,006,291 (GRCm38)	A302G	probably benign	Het
Xrn2	T	C	2: 147,049,346 (GRCm38)	L692P	probably damaging	Het
Zgrf1	A	G	3: 127,563,071 (GRCm38)	S649G	probably benign	Het
Zscan4b	T	C	7: 10,901,893 (GRCm38)	D169G	probably benign	Het
Zscan4b	C	T	7: 10,900,864 (GRCm38)	C484Y	probably damaging	Het

Other mutations in Wdfy4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00231:Wdfy4	APN	14	33,102,539 (GRCm38)	missense	possibly damaging	0.93
IGL01116:Wdfy4	APN	14	32,959,977 (GRCm38)	missense	probably damaging	1.00
IGL01449:Wdfy4	APN	14	33,104,037 (GRCm38)	missense	probably damaging	0.99
IGL01567:Wdfy4	APN	14	33,151,661 (GRCm38)	missense	probably benign	0.01
IGL01700:Wdfy4	APN	14	33,020,238 (GRCm38)	splice site	probably benign
IGL01931:Wdfy4	APN	14	33,155,753 (GRCm38)	missense	probably damaging	1.00
IGL01981:Wdfy4	APN	14	33,133,716 (GRCm38)	missense	probably damaging	1.00
IGL01988:Wdfy4	APN	14	33,076,480 (GRCm38)	missense	possibly damaging	0.75
IGL02026:Wdfy4	APN	14	33,093,300 (GRCm38)	missense	probably damaging	1.00
IGL02066:Wdfy4	APN	14	33,149,566 (GRCm38)	missense	probably benign
IGL02468:Wdfy4	APN	14	32,966,432 (GRCm38)	missense	probably benign	0.01
IGL02512:Wdfy4	APN	14	33,042,491 (GRCm38)	missense	probably benign	0.01
IGL02597:Wdfy4	APN	14	33,090,861 (GRCm38)	nonsense	probably null
IGL02752:Wdfy4	APN	14	33,076,326 (GRCm38)	missense	probably damaging	1.00
IGL02792:Wdfy4	APN	14	33,095,305 (GRCm38)	missense	probably benign	0.01
IGL02826:Wdfy4	APN	14	32,971,750 (GRCm38)	missense	possibly damaging	0.47
IGL02903:Wdfy4	APN	14	33,109,650 (GRCm38)	missense	probably damaging	1.00
IGL02955:Wdfy4	APN	14	33,076,284 (GRCm38)	missense	probably damaging	1.00
IGL03031:Wdfy4	APN	14	33,140,651 (GRCm38)	missense	probably damaging	1.00
IGL03102:Wdfy4	APN	14	32,966,435 (GRCm38)	missense	probably damaging	1.00
IGL03123:Wdfy4	APN	14	33,162,870 (GRCm38)	missense	probably benign	0.01
IGL03198:Wdfy4	APN	14	33,125,887 (GRCm38)	missense	probably damaging	1.00
IGL03250:Wdfy4	APN	14	32,977,167 (GRCm38)	missense	probably damaging	0.99
IGL03277:Wdfy4	APN	14	33,068,904 (GRCm38)	missense	probably benign	0.01
IGL03398:Wdfy4	APN	14	33,047,290 (GRCm38)	missense	probably benign	0.14
dodgers	UTSW	14	32,977,106 (GRCm38)	nonsense	probably null
Dollar	UTSW	14	33,020,311 (GRCm38)	missense	probably damaging	1.00
Giants	UTSW	14	33,070,618 (GRCm38)	nonsense	probably null
gigantea	UTSW	14	32,974,154 (GRCm38)	critical splice donor site	probably null
kings_canyon	UTSW	14	33,109,519 (GRCm38)	nonsense	probably null
moro	UTSW	14	32,964,626 (GRCm38)	splice site	probably null
popped	UTSW	14	32,966,399 (GRCm38)	missense	probably damaging	0.99
sequoia	UTSW	14	33,100,903 (GRCm38)	critical splice donor site	probably null
Sherman	UTSW	14	33,095,951 (GRCm38)	missense	possibly damaging	0.89
stretched	UTSW	14	33,073,535 (GRCm38)	nonsense	probably null
watchtower	UTSW	14	33,083,639 (GRCm38)	critical splice donor site	probably null
R0014:Wdfy4	UTSW	14	33,107,173 (GRCm38)	missense	possibly damaging	0.72
R0067:Wdfy4	UTSW	14	33,162,751 (GRCm38)	missense	probably null	1.00
R0085:Wdfy4	UTSW	14	33,078,243 (GRCm38)	missense	possibly damaging	0.81
R0277:Wdfy4	UTSW	14	33,083,785 (GRCm38)	missense	possibly damaging	0.83
R0436:Wdfy4	UTSW	14	33,083,812 (GRCm38)	splice site	probably benign
R0496:Wdfy4	UTSW	14	33,140,738 (GRCm38)	splice site	probably benign
R0514:Wdfy4	UTSW	14	33,080,775 (GRCm38)	missense	probably benign	0.22
R0548:Wdfy4	UTSW	14	33,042,621 (GRCm38)	missense	probably benign
R0590:Wdfy4	UTSW	14	33,041,174 (GRCm38)	missense	probably benign	0.09
R0647:Wdfy4	UTSW	14	33,109,699 (GRCm38)	missense	possibly damaging	0.96
R0766:Wdfy4	UTSW	14	33,140,612 (GRCm38)	missense	probably damaging	1.00
R0981:Wdfy4	UTSW	14	33,147,092 (GRCm38)	missense	probably benign	0.03
R1024:Wdfy4	UTSW	14	33,079,966 (GRCm38)	missense	possibly damaging	0.81
R1113:Wdfy4	UTSW	14	32,971,738 (GRCm38)	missense	possibly damaging	0.47
R1252:Wdfy4	UTSW	14	32,971,772 (GRCm38)	splice site	probably null
R1415:Wdfy4	UTSW	14	33,041,180 (GRCm38)	missense	possibly damaging	0.60
R1475:Wdfy4	UTSW	14	33,108,688 (GRCm38)	missense	probably benign	0.14
R1483:Wdfy4	UTSW	14	33,100,966 (GRCm38)	missense	probably benign	0.41
R1490:Wdfy4	UTSW	14	33,152,538 (GRCm38)	critical splice donor site	probably null
R1512:Wdfy4	UTSW	14	32,960,808 (GRCm38)	missense	probably damaging	0.98
R1615:Wdfy4	UTSW	14	33,042,512 (GRCm38)	missense	probably damaging	1.00
R1628:Wdfy4	UTSW	14	32,959,961 (GRCm38)	missense	probably damaging	1.00
R1643:Wdfy4	UTSW	14	33,073,585 (GRCm38)	critical splice acceptor site	probably null
R1729:Wdfy4	UTSW	14	33,096,005 (GRCm38)	missense	possibly damaging	0.85
R1859:Wdfy4	UTSW	14	33,103,983 (GRCm38)	missense	probably damaging	0.99
R1933:Wdfy4	UTSW	14	33,133,344 (GRCm38)	missense	probably benign	0.08
R1957:Wdfy4	UTSW	14	32,971,684 (GRCm38)	missense	probably damaging	1.00
R1968:Wdfy4	UTSW	14	33,106,044 (GRCm38)	missense	possibly damaging	0.95
R2032:Wdfy4	UTSW	14	33,146,989 (GRCm38)	missense	probably benign	0.11
R2241:Wdfy4	UTSW	14	33,073,511 (GRCm38)	missense	possibly damaging	0.81
R2391:Wdfy4	UTSW	14	33,162,807 (GRCm38)	missense	possibly damaging	0.92
R2888:Wdfy4	UTSW	14	33,109,519 (GRCm38)	nonsense	probably null
R2889:Wdfy4	UTSW	14	33,109,519 (GRCm38)	nonsense	probably null
R3114:Wdfy4	UTSW	14	33,089,903 (GRCm38)	missense	probably damaging	0.97
R3757:Wdfy4	UTSW	14	33,023,374 (GRCm38)	missense	probably benign	0.17
R3758:Wdfy4	UTSW	14	33,023,374 (GRCm38)	missense	probably benign	0.17
R3797:Wdfy4	UTSW	14	33,140,645 (GRCm38)	missense	probably damaging	1.00
R3890:Wdfy4	UTSW	14	33,047,280 (GRCm38)	missense	probably damaging	1.00
R3892:Wdfy4	UTSW	14	33,047,280 (GRCm38)	missense	probably damaging	1.00
R3945:Wdfy4	UTSW	14	32,966,395 (GRCm38)	missense	probably damaging	0.99
R4011:Wdfy4	UTSW	14	33,102,680 (GRCm38)	splice site	probably benign
R4091:Wdfy4	UTSW	14	33,125,880 (GRCm38)	missense	possibly damaging	0.93
R4449:Wdfy4	UTSW	14	33,096,083 (GRCm38)	missense	probably damaging	1.00
R4585:Wdfy4	UTSW	14	33,087,955 (GRCm38)	missense	possibly damaging	0.89
R4628:Wdfy4	UTSW	14	33,102,558 (GRCm38)	missense	probably damaging	0.97
R4629:Wdfy4	UTSW	14	33,102,558 (GRCm38)	missense	probably damaging	0.97
R4655:Wdfy4	UTSW	14	32,989,936 (GRCm38)	missense	probably damaging	0.98
R4689:Wdfy4	UTSW	14	33,109,548 (GRCm38)	missense	possibly damaging	0.88
R4718:Wdfy4	UTSW	14	33,145,316 (GRCm38)	missense	probably benign	0.03
R4862:Wdfy4	UTSW	14	33,100,903 (GRCm38)	critical splice donor site	probably null
R4884:Wdfy4	UTSW	14	32,988,895 (GRCm38)	nonsense	probably null
R4894:Wdfy4	UTSW	14	33,155,760 (GRCm38)	missense	probably benign	0.03
R4929:Wdfy4	UTSW	14	33,047,256 (GRCm38)	missense	possibly damaging	0.90
R4932:Wdfy4	UTSW	14	33,029,013 (GRCm38)	missense	probably damaging	1.00
R5014:Wdfy4	UTSW	14	33,100,940 (GRCm38)	missense	probably benign	0.02
R5020:Wdfy4	UTSW	14	33,079,935 (GRCm38)	missense	probably damaging	1.00
R5049:Wdfy4	UTSW	14	33,152,670 (GRCm38)	missense	possibly damaging	0.78
R5276:Wdfy4	UTSW	14	33,047,275 (GRCm38)	missense	probably damaging	1.00
R5318:Wdfy4	UTSW	14	33,078,343 (GRCm38)	missense	possibly damaging	0.95
R5338:Wdfy4	UTSW	14	33,090,866 (GRCm38)	missense	probably damaging	1.00
R5349:Wdfy4	UTSW	14	32,988,899 (GRCm38)	missense	probably damaging	1.00
R5411:Wdfy4	UTSW	14	32,960,002 (GRCm38)	missense	probably damaging	1.00
R5435:Wdfy4	UTSW	14	33,020,311 (GRCm38)	missense	probably damaging	1.00
R5463:Wdfy4	UTSW	14	33,151,732 (GRCm38)	missense	probably benign	0.17
R5591:Wdfy4	UTSW	14	33,107,130 (GRCm38)	missense	probably benign	0.09
R5598:Wdfy4	UTSW	14	33,133,497 (GRCm38)	missense	probably damaging	1.00
R5654:Wdfy4	UTSW	14	33,107,618 (GRCm38)	splice site	probably null
R5890:Wdfy4	UTSW	14	33,102,577 (GRCm38)	missense	possibly damaging	0.91
R5894:Wdfy4	UTSW	14	33,133,360 (GRCm38)	missense	possibly damaging	0.86
R5964:Wdfy4	UTSW	14	33,106,011 (GRCm38)	missense	probably damaging	1.00
R6036:Wdfy4	UTSW	14	33,146,990 (GRCm38)	missense	probably damaging	0.97
R6036:Wdfy4	UTSW	14	33,146,990 (GRCm38)	missense	probably damaging	0.97
R6074:Wdfy4	UTSW	14	33,083,639 (GRCm38)	critical splice donor site	probably null
R6135:Wdfy4	UTSW	14	32,971,711 (GRCm38)	missense	probably damaging	0.99
R6276:Wdfy4	UTSW	14	33,109,525 (GRCm38)	missense	possibly damaging	0.54
R6357:Wdfy4	UTSW	14	33,101,049 (GRCm38)	nonsense	probably null
R6370:Wdfy4	UTSW	14	33,068,850 (GRCm38)	missense	probably benign	0.16
R6390:Wdfy4	UTSW	14	33,104,094 (GRCm38)	missense	probably damaging	0.99
R6413:Wdfy4	UTSW	14	32,967,647 (GRCm38)	missense	probably damaging	1.00
R6450:Wdfy4	UTSW	14	33,108,692 (GRCm38)	missense	probably damaging	1.00
R6522:Wdfy4	UTSW	14	33,146,944 (GRCm38)	missense	probably damaging	0.98
R6657:Wdfy4	UTSW	14	33,047,251 (GRCm38)	missense	possibly damaging	0.70
R6761:Wdfy4	UTSW	14	33,095,951 (GRCm38)	missense	possibly damaging	0.89
R6763:Wdfy4	UTSW	14	33,042,512 (GRCm38)	missense	probably damaging	1.00
R6952:Wdfy4	UTSW	14	32,959,966 (GRCm38)	missense	probably damaging	1.00
R6985:Wdfy4	UTSW	14	33,099,117 (GRCm38)	missense	possibly damaging	0.68
R7024:Wdfy4	UTSW	14	32,964,626 (GRCm38)	splice site	probably null
R7101:Wdfy4	UTSW	14	32,960,820 (GRCm38)	missense
R7114:Wdfy4	UTSW	14	32,971,574 (GRCm38)	splice site	probably null
R7139:Wdfy4	UTSW	14	33,151,578 (GRCm38)	missense
R7255:Wdfy4	UTSW	14	32,974,282 (GRCm38)	missense
R7324:Wdfy4	UTSW	14	33,047,314 (GRCm38)	missense
R7379:Wdfy4	UTSW	14	33,151,609 (GRCm38)	missense
R7399:Wdfy4	UTSW	14	33,068,906 (GRCm38)	missense
R7408:Wdfy4	UTSW	14	33,078,307 (GRCm38)	missense
R7410:Wdfy4	UTSW	14	32,974,234 (GRCm38)	missense
R7411:Wdfy4	UTSW	14	33,106,131 (GRCm38)	missense
R7445:Wdfy4	UTSW	14	33,070,618 (GRCm38)	nonsense	probably null
R7595:Wdfy4	UTSW	14	32,974,154 (GRCm38)	critical splice donor site	probably null
R7618:Wdfy4	UTSW	14	32,985,739 (GRCm38)	missense
R7622:Wdfy4	UTSW	14	33,078,274 (GRCm38)	missense
R7828:Wdfy4	UTSW	14	32,988,921 (GRCm38)	missense	possibly damaging	0.90
R7888:Wdfy4	UTSW	14	33,090,963 (GRCm38)	missense
R7946:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R7946:Wdfy4	UTSW	14	33,070,748 (GRCm38)	missense
R7986:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R7990:Wdfy4	UTSW	14	33,097,795 (GRCm38)	missense
R8001:Wdfy4	UTSW	14	32,973,535 (GRCm38)	critical splice donor site	probably null
R8010:Wdfy4	UTSW	14	32,971,627 (GRCm38)	missense
R8015:Wdfy4	UTSW	14	33,107,747 (GRCm38)	missense
R8032:Wdfy4	UTSW	14	33,029,086 (GRCm38)	nonsense	probably null
R8041:Wdfy4	UTSW	14	33,154,008 (GRCm38)	critical splice donor site	probably null
R8090:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R8092:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R8112:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R8114:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R8115:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R8117:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R8117:Wdfy4	UTSW	14	32,977,106 (GRCm38)	nonsense	probably null
R8118:Wdfy4	UTSW	14	33,104,115 (GRCm38)	missense
R8140:Wdfy4	UTSW	14	33,142,360 (GRCm38)	missense
R8155:Wdfy4	UTSW	14	33,162,819 (GRCm38)	missense
R8163:Wdfy4	UTSW	14	33,151,588 (GRCm38)	missense
R8293:Wdfy4	UTSW	14	32,974,261 (GRCm38)	missense
R8325:Wdfy4	UTSW	14	32,967,487 (GRCm38)	missense
R8353:Wdfy4	UTSW	14	32,973,624 (GRCm38)	missense	probably benign
R8370:Wdfy4	UTSW	14	33,093,251 (GRCm38)	missense
R8437:Wdfy4	UTSW	14	33,076,375 (GRCm38)	missense
R8497:Wdfy4	UTSW	14	32,966,399 (GRCm38)	missense	probably damaging	0.99
R8545:Wdfy4	UTSW	14	33,078,301 (GRCm38)	missense	probably benign	0.01
R8671:Wdfy4	UTSW	14	32,971,765 (GRCm38)	splice site	probably benign
R8708:Wdfy4	UTSW	14	32,967,532 (GRCm38)	missense
R8747:Wdfy4	UTSW	14	33,152,654 (GRCm38)	missense
R8794:Wdfy4	UTSW	14	33,147,092 (GRCm38)	missense	probably benign	0.03
R8846:Wdfy4	UTSW	14	33,145,148 (GRCm38)	missense
R8880:Wdfy4	UTSW	14	33,073,535 (GRCm38)	nonsense	probably null
R9109:Wdfy4	UTSW	14	33,038,747 (GRCm38)	splice site	probably null
R9131:Wdfy4	UTSW	14	33,097,850 (GRCm38)	missense
R9309:Wdfy4	UTSW	14	33,095,356 (GRCm38)	missense
R9349:Wdfy4	UTSW	14	33,154,039 (GRCm38)	missense
R9451:Wdfy4	UTSW	14	33,133,561 (GRCm38)	missense
R9563:Wdfy4	UTSW	14	32,970,876 (GRCm38)	missense
R9587:Wdfy4	UTSW	14	33,047,273 (GRCm38)	nonsense	probably null
R9599:Wdfy4	UTSW	14	33,133,471 (GRCm38)	missense
R9670:Wdfy4	UTSW	14	33,047,262 (GRCm38)	missense
R9718:Wdfy4	UTSW	14	33,125,936 (GRCm38)	missense
R9742:Wdfy4	UTSW	14	33,088,030 (GRCm38)	missense
X0028:Wdfy4	UTSW	14	33,080,636 (GRCm38)	missense	probably benign
X0053:Wdfy4	UTSW	14	33,162,942 (GRCm38)	start codon destroyed	probably null	0.99
X0062:Wdfy4	UTSW	14	33,107,618 (GRCm38)	splice site	probably null
Z1177:Wdfy4	UTSW	14	33,087,985 (GRCm38)	missense

Predicted Primers

PCR Primer
(F):5'- AGCAAGATGATTCTGGGCCC -3'
(R):5'- CAGAAAGTAGCCTCAAATTATTCTCCC -3'

Sequencing Primer
(F):5'- AAGATGATTCTGGGCCCCACAG -3'
(R):5'- GTAGCCTCAAATTATTCTCCCGCAAG -3'

Posted On

2019-10-07