Mutagenetix > Incidental Mutation

Incidental Mutation 'R7410:Wdfy4'

575034

Institutional Source

Beutler Lab

Gene Symbol

Wdfy4

Ensembl Gene

ENSMUSG00000051506

Gene Name

WD repeat and FYVE domain containing 4

Synonyms

MMRRC Submission

045491-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7410 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

32681504-32907465 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 32696191 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 2784 (D2784G)

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: D2625G

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000057556
Gene: ENSMUSG00000051506
AA Change: D2625G

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: D2784G

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: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210017I01Rik	A	G	3: 92,512,551 (GRCm39)	S3P	unknown	Het
Adgrv1	A	T	13: 81,711,738 (GRCm39)	D1079E	probably benign	Het
Agbl5	A	T	5: 31,048,032 (GRCm39)	Y102F	possibly damaging	Het
Ankfy1	T	C	11: 72,652,330 (GRCm39)	L1094S	probably damaging	Het
Ankrd42	A	T	7: 92,259,762 (GRCm39)	V337E	possibly damaging	Het
Axl	A	G	7: 25,458,208 (GRCm39)	L849P	probably benign	Het
Bmpr2	T	C	1: 59,907,652 (GRCm39)	I915T	probably benign	Het
Cables1	T	A	18: 12,074,282 (GRCm39)	F494L	probably benign	Het
Cacna1e	A	C	1: 154,347,980 (GRCm39)	V927G	probably benign	Het
Cavin1	A	T	11: 100,849,670 (GRCm39)	V320E	probably damaging	Het
Cemip	T	G	7: 83,602,042 (GRCm39)	S916R	probably damaging	Het
Cep57	G	A	9: 13,729,980 (GRCm39)		probably benign	Het
Ces1d	T	C	8: 93,919,433 (GRCm39)	N120D	probably damaging	Het
Cfap44	A	T	16: 44,288,776 (GRCm39)	S1509C	probably damaging	Het
Chga	A	G	12: 102,528,866 (GRCm39)	D281G	probably benign	Het
Clstn2	A	G	9: 97,423,920 (GRCm39)	F282L	probably benign	Het
Cnot1	A	T	8: 96,459,787 (GRCm39)	V1855E	possibly damaging	Het
Cnr1	T	A	4: 33,944,119 (GRCm39)	V169D	probably damaging	Het
Cpd	T	A	11: 76,673,134 (GRCm39)	H1337L	probably damaging	Het
Crabp2	T	A	3: 87,859,585 (GRCm39)	D78E	probably damaging	Het
Crat	C	T	2: 30,294,577 (GRCm39)	R497Q	probably benign	Het
Cyp2ab1	G	A	16: 20,135,475 (GRCm39)	A9V	probably benign	Het
Cyp3a41b	T	C	5: 145,514,967 (GRCm39)	D86G	probably damaging	Het
Dner	T	A	1: 84,563,332 (GRCm39)	D96V	probably damaging	Het
Duox1	C	A	2: 122,176,874 (GRCm39)	T1465N	probably damaging	Het
Ehd3	T	A	17: 74,112,428 (GRCm39)	V64E	probably benign	Het
Ehmt1	A	G	2: 24,738,080 (GRCm39)	V508A	probably benign	Het
Ephb3	G	A	16: 21,040,158 (GRCm39)	V761I	possibly damaging	Het
Fam161b	T	C	12: 84,404,575 (GRCm39)	Q35R	probably benign	Het
Fam186a	T	A	15: 99,844,826 (GRCm39)	K473*	probably null	Het
Fam227b	A	T	2: 125,960,983 (GRCm39)	D215E	probably damaging	Het
Fkbp15	C	A	4: 62,258,536 (GRCm39)	D144Y	probably damaging	Het
Galt	T	C	4: 41,757,707 (GRCm39)	I259T	possibly damaging	Het
Gbp11	G	A	5: 105,491,774 (GRCm39)	P8S	probably damaging	Het
Gfap	A	T	11: 102,783,963 (GRCm39)	M339K	probably damaging	Het
Gm14443	C	T	2: 175,011,069 (GRCm39)	R459Q	possibly damaging	Het
Grip1	A	G	10: 119,855,925 (GRCm39)	N632S	probably benign	Het
H4c18	G	A	13: 22,016,211 (GRCm39)	R40W	probably damaging	Het
Hcar1	T	G	5: 124,017,161 (GRCm39)	I177L	possibly damaging	Het
Ighv1-37	A	G	12: 114,860,099 (GRCm39)	V37A	probably damaging	Het
Ilf3	T	A	9: 21,311,100 (GRCm39)	F657L	unknown	Het
Ints2	T	G	11: 86,124,052 (GRCm39)	T579P	probably benign	Het
Iqgap1	G	T	7: 80,372,778 (GRCm39)	Y1520*	probably null	Het
Kdm4a	T	C	4: 118,001,115 (GRCm39)	H884R	possibly damaging	Het
Krtap19-1	A	T	16: 88,666,132 (GRCm39)	Y52N	unknown	Het
Lama5	A	T	2: 179,844,183 (GRCm39)		probably null	Het
Lrrc72	T	C	12: 36,272,803 (GRCm39)	N89D	probably damaging	Het
Med13l	A	G	5: 118,698,897 (GRCm39)	D16G	possibly damaging	Het
Mefv	A	G	16: 3,533,545 (GRCm39)	L242P	probably damaging	Het
Mob3c	T	C	4: 115,688,784 (GRCm39)	Y106H	probably damaging	Het
Nlrp1a	A	G	11: 71,014,683 (GRCm39)	I189T	probably damaging	Het
Nudt7	T	C	8: 114,860,559 (GRCm39)		probably benign	Het
Or13p10	T	C	4: 118,523,629 (GRCm39)	L305P	probably benign	Het
Or4f7	T	A	2: 111,644,271 (GRCm39)	I267L	probably benign	Het
Pappa	A	G	4: 65,253,956 (GRCm39)	T1537A	probably damaging	Het
Pik3r4	T	A	9: 105,527,790 (GRCm39)	V381E	probably damaging	Het
Pkd1	T	A	17: 24,794,855 (GRCm39)	Y2181N	probably damaging	Het
Pmel	G	T	10: 128,552,353 (GRCm39)	V396F	probably benign	Het
Prdm9	A	G	17: 15,765,259 (GRCm39)	I507T	possibly damaging	Het
Psme4	C	T	11: 30,765,279 (GRCm39)	Q549*	probably null	Het
Ptprg	T	A	14: 11,962,657 (GRCm38)	W152R	probably damaging	Het
Ptprm	A	C	17: 67,000,561 (GRCm39)	V1141G	probably damaging	Het
Rapgef5	G	A	12: 117,685,063 (GRCm39)	V505M	probably damaging	Het
Rnf213	T	A	11: 119,325,877 (GRCm39)	M1558K		Het
Slc35a1	A	G	4: 34,675,034 (GRCm39)	V168A	probably benign	Het
Srebf1	T	C	11: 60,096,693 (GRCm39)	T347A	probably benign	Het
Stard9	T	A	2: 120,531,978 (GRCm39)	V2745D	probably benign	Het
Taar7e	A	T	10: 23,914,424 (GRCm39)	T305S	probably benign	Het
Tie1	T	C	4: 118,337,074 (GRCm39)	S551G	probably benign	Het
Tmc5	T	A	7: 118,222,820 (GRCm39)	Y173*	probably null	Het
Tns2	T	A	15: 102,018,961 (GRCm39)	V384D	probably damaging	Het
Tubgcp4	T	A	2: 121,014,890 (GRCm39)	Y267N	probably damaging	Het
Vmn1r53	A	G	6: 90,200,700 (GRCm39)	V208A	probably damaging	Het
Vwa8	A	C	14: 79,219,674 (GRCm39)		probably null	Het
Zfp712	A	C	13: 67,189,400 (GRCm39)	S376A	probably benign	Het
Znrf3	C	T	11: 5,238,955 (GRCm39)	C232Y	unknown	Het

Other mutations in Wdfy4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00231:Wdfy4	APN	14	32,824,496 (GRCm39)	missense	possibly damaging	0.93
IGL01116:Wdfy4	APN	14	32,681,934 (GRCm39)	missense	probably damaging	1.00
IGL01449:Wdfy4	APN	14	32,825,994 (GRCm39)	missense	probably damaging	0.99
IGL01567:Wdfy4	APN	14	32,873,618 (GRCm39)	missense	probably benign	0.01
IGL01700:Wdfy4	APN	14	32,742,195 (GRCm39)	splice site	probably benign
IGL01931:Wdfy4	APN	14	32,877,710 (GRCm39)	missense	probably damaging	1.00
IGL01981:Wdfy4	APN	14	32,855,673 (GRCm39)	missense	probably damaging	1.00
IGL01988:Wdfy4	APN	14	32,798,437 (GRCm39)	missense	possibly damaging	0.75
IGL02026:Wdfy4	APN	14	32,815,257 (GRCm39)	missense	probably damaging	1.00
IGL02066:Wdfy4	APN	14	32,871,523 (GRCm39)	missense	probably benign
IGL02468:Wdfy4	APN	14	32,688,389 (GRCm39)	missense	probably benign	0.01
IGL02512:Wdfy4	APN	14	32,764,448 (GRCm39)	missense	probably benign	0.01
IGL02597:Wdfy4	APN	14	32,812,818 (GRCm39)	nonsense	probably null
IGL02752:Wdfy4	APN	14	32,798,283 (GRCm39)	missense	probably damaging	1.00
IGL02792:Wdfy4	APN	14	32,817,262 (GRCm39)	missense	probably benign	0.01
IGL02826:Wdfy4	APN	14	32,693,707 (GRCm39)	missense	possibly damaging	0.47
IGL02903:Wdfy4	APN	14	32,831,607 (GRCm39)	missense	probably damaging	1.00
IGL02955:Wdfy4	APN	14	32,798,241 (GRCm39)	missense	probably damaging	1.00
IGL03031:Wdfy4	APN	14	32,862,608 (GRCm39)	missense	probably damaging	1.00
IGL03102:Wdfy4	APN	14	32,688,392 (GRCm39)	missense	probably damaging	1.00
IGL03123:Wdfy4	APN	14	32,884,827 (GRCm39)	missense	probably benign	0.01
IGL03198:Wdfy4	APN	14	32,847,844 (GRCm39)	missense	probably damaging	1.00
IGL03250:Wdfy4	APN	14	32,699,124 (GRCm39)	missense	probably damaging	0.99
IGL03277:Wdfy4	APN	14	32,790,861 (GRCm39)	missense	probably benign	0.01
IGL03398:Wdfy4	APN	14	32,769,247 (GRCm39)	missense	probably benign	0.14
dodgers	UTSW	14	32,699,063 (GRCm39)	nonsense	probably null
Dollar	UTSW	14	32,742,268 (GRCm39)	missense	probably damaging	1.00
Giants	UTSW	14	32,792,575 (GRCm39)	nonsense	probably null
gigantea	UTSW	14	32,696,111 (GRCm39)	critical splice donor site	probably null
kings_canyon	UTSW	14	32,831,476 (GRCm39)	nonsense	probably null
moro	UTSW	14	32,686,583 (GRCm39)	splice site	probably null
popped	UTSW	14	32,688,356 (GRCm39)	missense	probably damaging	0.99
sequoia	UTSW	14	32,822,860 (GRCm39)	critical splice donor site	probably null
Sherman	UTSW	14	32,817,908 (GRCm39)	missense	possibly damaging	0.89
stretched	UTSW	14	32,795,492 (GRCm39)	nonsense	probably null
watchtower	UTSW	14	32,805,596 (GRCm39)	critical splice donor site	probably null
R0014:Wdfy4	UTSW	14	32,829,130 (GRCm39)	missense	possibly damaging	0.72
R0067:Wdfy4	UTSW	14	32,884,708 (GRCm39)	missense	probably null	1.00
R0085:Wdfy4	UTSW	14	32,800,200 (GRCm39)	missense	possibly damaging	0.81
R0277:Wdfy4	UTSW	14	32,805,742 (GRCm39)	missense	possibly damaging	0.83
R0436:Wdfy4	UTSW	14	32,805,769 (GRCm39)	splice site	probably benign
R0496:Wdfy4	UTSW	14	32,862,695 (GRCm39)	splice site	probably benign
R0514:Wdfy4	UTSW	14	32,802,732 (GRCm39)	missense	probably benign	0.22
R0548:Wdfy4	UTSW	14	32,764,578 (GRCm39)	missense	probably benign
R0590:Wdfy4	UTSW	14	32,763,131 (GRCm39)	missense	probably benign	0.09
R0647:Wdfy4	UTSW	14	32,831,656 (GRCm39)	missense	possibly damaging	0.96
R0766:Wdfy4	UTSW	14	32,862,569 (GRCm39)	missense	probably damaging	1.00
R0981:Wdfy4	UTSW	14	32,869,049 (GRCm39)	missense	probably benign	0.03
R1024:Wdfy4	UTSW	14	32,801,923 (GRCm39)	missense	possibly damaging	0.81
R1113:Wdfy4	UTSW	14	32,693,695 (GRCm39)	missense	possibly damaging	0.47
R1252:Wdfy4	UTSW	14	32,693,729 (GRCm39)	splice site	probably null
R1415:Wdfy4	UTSW	14	32,763,137 (GRCm39)	missense	possibly damaging	0.60
R1475:Wdfy4	UTSW	14	32,830,645 (GRCm39)	missense	probably benign	0.14
R1483:Wdfy4	UTSW	14	32,822,923 (GRCm39)	missense	probably benign	0.41
R1490:Wdfy4	UTSW	14	32,874,495 (GRCm39)	critical splice donor site	probably null
R1512:Wdfy4	UTSW	14	32,682,765 (GRCm39)	missense	probably damaging	0.98
R1615:Wdfy4	UTSW	14	32,764,469 (GRCm39)	missense	probably damaging	1.00
R1628:Wdfy4	UTSW	14	32,681,918 (GRCm39)	missense	probably damaging	1.00
R1643:Wdfy4	UTSW	14	32,795,542 (GRCm39)	critical splice acceptor site	probably null
R1729:Wdfy4	UTSW	14	32,817,962 (GRCm39)	missense	possibly damaging	0.85
R1859:Wdfy4	UTSW	14	32,825,940 (GRCm39)	missense	probably damaging	0.99
R1933:Wdfy4	UTSW	14	32,855,301 (GRCm39)	missense	probably benign	0.08
R1957:Wdfy4	UTSW	14	32,693,641 (GRCm39)	missense	probably damaging	1.00
R1968:Wdfy4	UTSW	14	32,828,001 (GRCm39)	missense	possibly damaging	0.95
R2032:Wdfy4	UTSW	14	32,868,946 (GRCm39)	missense	probably benign	0.11
R2241:Wdfy4	UTSW	14	32,795,468 (GRCm39)	missense	possibly damaging	0.81
R2391:Wdfy4	UTSW	14	32,884,764 (GRCm39)	missense	possibly damaging	0.92
R2888:Wdfy4	UTSW	14	32,831,476 (GRCm39)	nonsense	probably null
R2889:Wdfy4	UTSW	14	32,831,476 (GRCm39)	nonsense	probably null
R3114:Wdfy4	UTSW	14	32,811,860 (GRCm39)	missense	probably damaging	0.97
R3757:Wdfy4	UTSW	14	32,745,331 (GRCm39)	missense	probably benign	0.17
R3758:Wdfy4	UTSW	14	32,745,331 (GRCm39)	missense	probably benign	0.17
R3797:Wdfy4	UTSW	14	32,862,602 (GRCm39)	missense	probably damaging	1.00
R3890:Wdfy4	UTSW	14	32,769,237 (GRCm39)	missense	probably damaging	1.00
R3892:Wdfy4	UTSW	14	32,769,237 (GRCm39)	missense	probably damaging	1.00
R3945:Wdfy4	UTSW	14	32,688,352 (GRCm39)	missense	probably damaging	0.99
R4011:Wdfy4	UTSW	14	32,824,637 (GRCm39)	splice site	probably benign
R4091:Wdfy4	UTSW	14	32,847,837 (GRCm39)	missense	possibly damaging	0.93
R4449:Wdfy4	UTSW	14	32,818,040 (GRCm39)	missense	probably damaging	1.00
R4585:Wdfy4	UTSW	14	32,809,912 (GRCm39)	missense	possibly damaging	0.89
R4628:Wdfy4	UTSW	14	32,824,515 (GRCm39)	missense	probably damaging	0.97
R4629:Wdfy4	UTSW	14	32,824,515 (GRCm39)	missense	probably damaging	0.97
R4655:Wdfy4	UTSW	14	32,711,893 (GRCm39)	missense	probably damaging	0.98
R4689:Wdfy4	UTSW	14	32,831,505 (GRCm39)	missense	possibly damaging	0.88
R4718:Wdfy4	UTSW	14	32,867,273 (GRCm39)	missense	probably benign	0.03
R4862:Wdfy4	UTSW	14	32,822,860 (GRCm39)	critical splice donor site	probably null
R4884:Wdfy4	UTSW	14	32,710,852 (GRCm39)	nonsense	probably null
R4894:Wdfy4	UTSW	14	32,877,717 (GRCm39)	missense	probably benign	0.03
R4929:Wdfy4	UTSW	14	32,769,213 (GRCm39)	missense	possibly damaging	0.90
R4932:Wdfy4	UTSW	14	32,750,970 (GRCm39)	missense	probably damaging	1.00
R5014:Wdfy4	UTSW	14	32,822,897 (GRCm39)	missense	probably benign	0.02
R5020:Wdfy4	UTSW	14	32,801,892 (GRCm39)	missense	probably damaging	1.00
R5049:Wdfy4	UTSW	14	32,874,627 (GRCm39)	missense	possibly damaging	0.78
R5276:Wdfy4	UTSW	14	32,769,232 (GRCm39)	missense	probably damaging	1.00
R5318:Wdfy4	UTSW	14	32,800,300 (GRCm39)	missense	possibly damaging	0.95
R5338:Wdfy4	UTSW	14	32,812,823 (GRCm39)	missense	probably damaging	1.00
R5349:Wdfy4	UTSW	14	32,710,856 (GRCm39)	missense	probably damaging	1.00
R5411:Wdfy4	UTSW	14	32,681,959 (GRCm39)	missense	probably damaging	1.00
R5435:Wdfy4	UTSW	14	32,742,268 (GRCm39)	missense	probably damaging	1.00
R5463:Wdfy4	UTSW	14	32,873,689 (GRCm39)	missense	probably benign	0.17
R5591:Wdfy4	UTSW	14	32,829,087 (GRCm39)	missense	probably benign	0.09
R5598:Wdfy4	UTSW	14	32,855,454 (GRCm39)	missense	probably damaging	1.00
R5654:Wdfy4	UTSW	14	32,829,575 (GRCm39)	splice site	probably null
R5890:Wdfy4	UTSW	14	32,824,534 (GRCm39)	missense	possibly damaging	0.91
R5894:Wdfy4	UTSW	14	32,855,317 (GRCm39)	missense	possibly damaging	0.86
R5964:Wdfy4	UTSW	14	32,827,968 (GRCm39)	missense	probably damaging	1.00
R6036:Wdfy4	UTSW	14	32,868,947 (GRCm39)	missense	probably damaging	0.97
R6036:Wdfy4	UTSW	14	32,868,947 (GRCm39)	missense	probably damaging	0.97
R6074:Wdfy4	UTSW	14	32,805,596 (GRCm39)	critical splice donor site	probably null
R6135:Wdfy4	UTSW	14	32,693,668 (GRCm39)	missense	probably damaging	0.99
R6276:Wdfy4	UTSW	14	32,831,482 (GRCm39)	missense	possibly damaging	0.54
R6357:Wdfy4	UTSW	14	32,823,006 (GRCm39)	nonsense	probably null
R6370:Wdfy4	UTSW	14	32,790,807 (GRCm39)	missense	probably benign	0.16
R6390:Wdfy4	UTSW	14	32,826,051 (GRCm39)	missense	probably damaging	0.99
R6413:Wdfy4	UTSW	14	32,689,604 (GRCm39)	missense	probably damaging	1.00
R6450:Wdfy4	UTSW	14	32,830,649 (GRCm39)	missense	probably damaging	1.00
R6522:Wdfy4	UTSW	14	32,868,901 (GRCm39)	missense	probably damaging	0.98
R6657:Wdfy4	UTSW	14	32,769,208 (GRCm39)	missense	possibly damaging	0.70
R6761:Wdfy4	UTSW	14	32,817,908 (GRCm39)	missense	possibly damaging	0.89
R6763:Wdfy4	UTSW	14	32,764,469 (GRCm39)	missense	probably damaging	1.00
R6952:Wdfy4	UTSW	14	32,681,923 (GRCm39)	missense	probably damaging	1.00
R6985:Wdfy4	UTSW	14	32,821,074 (GRCm39)	missense	possibly damaging	0.68
R7024:Wdfy4	UTSW	14	32,686,583 (GRCm39)	splice site	probably null
R7101:Wdfy4	UTSW	14	32,682,777 (GRCm39)	missense
R7114:Wdfy4	UTSW	14	32,693,531 (GRCm39)	splice site	probably null
R7139:Wdfy4	UTSW	14	32,873,535 (GRCm39)	missense
R7255:Wdfy4	UTSW	14	32,696,239 (GRCm39)	missense
R7324:Wdfy4	UTSW	14	32,769,271 (GRCm39)	missense
R7379:Wdfy4	UTSW	14	32,873,566 (GRCm39)	missense
R7399:Wdfy4	UTSW	14	32,790,863 (GRCm39)	missense
R7408:Wdfy4	UTSW	14	32,800,264 (GRCm39)	missense
R7411:Wdfy4	UTSW	14	32,828,088 (GRCm39)	missense
R7412:Wdfy4	UTSW	14	32,871,541 (GRCm39)	missense
R7445:Wdfy4	UTSW	14	32,792,575 (GRCm39)	nonsense	probably null
R7595:Wdfy4	UTSW	14	32,696,111 (GRCm39)	critical splice donor site	probably null
R7618:Wdfy4	UTSW	14	32,707,696 (GRCm39)	missense
R7622:Wdfy4	UTSW	14	32,800,231 (GRCm39)	missense
R7828:Wdfy4	UTSW	14	32,710,878 (GRCm39)	missense	possibly damaging	0.90
R7888:Wdfy4	UTSW	14	32,812,920 (GRCm39)	missense
R7946:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R7946:Wdfy4	UTSW	14	32,792,705 (GRCm39)	missense
R7986:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R7990:Wdfy4	UTSW	14	32,819,752 (GRCm39)	missense
R8001:Wdfy4	UTSW	14	32,695,492 (GRCm39)	critical splice donor site	probably null
R8010:Wdfy4	UTSW	14	32,693,584 (GRCm39)	missense
R8015:Wdfy4	UTSW	14	32,829,704 (GRCm39)	missense
R8032:Wdfy4	UTSW	14	32,751,043 (GRCm39)	nonsense	probably null
R8041:Wdfy4	UTSW	14	32,875,965 (GRCm39)	critical splice donor site	probably null
R8090:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R8092:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R8112:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R8114:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R8115:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R8117:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R8117:Wdfy4	UTSW	14	32,699,063 (GRCm39)	nonsense	probably null
R8118:Wdfy4	UTSW	14	32,826,072 (GRCm39)	missense
R8140:Wdfy4	UTSW	14	32,864,317 (GRCm39)	missense
R8155:Wdfy4	UTSW	14	32,884,776 (GRCm39)	missense
R8163:Wdfy4	UTSW	14	32,873,545 (GRCm39)	missense
R8293:Wdfy4	UTSW	14	32,696,218 (GRCm39)	missense
R8325:Wdfy4	UTSW	14	32,689,444 (GRCm39)	missense
R8353:Wdfy4	UTSW	14	32,695,581 (GRCm39)	missense	probably benign
R8370:Wdfy4	UTSW	14	32,815,208 (GRCm39)	missense
R8437:Wdfy4	UTSW	14	32,798,332 (GRCm39)	missense
R8497:Wdfy4	UTSW	14	32,688,356 (GRCm39)	missense	probably damaging	0.99
R8545:Wdfy4	UTSW	14	32,800,258 (GRCm39)	missense	probably benign	0.01
R8671:Wdfy4	UTSW	14	32,693,722 (GRCm39)	splice site	probably benign
R8708:Wdfy4	UTSW	14	32,689,489 (GRCm39)	missense
R8747:Wdfy4	UTSW	14	32,874,611 (GRCm39)	missense
R8794:Wdfy4	UTSW	14	32,869,049 (GRCm39)	missense	probably benign	0.03
R8846:Wdfy4	UTSW	14	32,867,105 (GRCm39)	missense
R8880:Wdfy4	UTSW	14	32,795,492 (GRCm39)	nonsense	probably null
R9109:Wdfy4	UTSW	14	32,760,704 (GRCm39)	splice site	probably null
R9131:Wdfy4	UTSW	14	32,819,807 (GRCm39)	missense
R9309:Wdfy4	UTSW	14	32,817,313 (GRCm39)	missense
R9349:Wdfy4	UTSW	14	32,875,996 (GRCm39)	missense
R9451:Wdfy4	UTSW	14	32,855,518 (GRCm39)	missense
R9563:Wdfy4	UTSW	14	32,692,833 (GRCm39)	missense
R9587:Wdfy4	UTSW	14	32,769,230 (GRCm39)	nonsense	probably null
R9599:Wdfy4	UTSW	14	32,855,428 (GRCm39)	missense
R9670:Wdfy4	UTSW	14	32,769,219 (GRCm39)	missense
R9718:Wdfy4	UTSW	14	32,847,893 (GRCm39)	missense
R9742:Wdfy4	UTSW	14	32,809,987 (GRCm39)	missense
X0028:Wdfy4	UTSW	14	32,802,593 (GRCm39)	missense	probably benign
X0053:Wdfy4	UTSW	14	32,884,899 (GRCm39)	start codon destroyed	probably null	0.99
X0062:Wdfy4	UTSW	14	32,829,575 (GRCm39)	splice site	probably null
Z1177:Wdfy4	UTSW	14	32,809,942 (GRCm39)	missense

Predicted Primers

PCR Primer
(F):5'- AGGGATGACTCTCCCTTCACTG -3'
(R):5'- GCTTAAATGTAGAGAACTGGGC -3'

Sequencing Primer
(F):5'- GGATGACTCTCCCTTCACTGCTAAC -3'
(R):5'- AAATGTAGAGAACTGGGCTTTTG -3'

Posted On

2019-10-07