Mutagenetix > Incidental Mutation

Incidental Mutation 'R1993:Fryl'

223858

Institutional Source

Beutler Lab

Gene Symbol

Fryl

Ensembl Gene

ENSMUSG00000070733

Gene Name

FRY like transcription coactivator

Synonyms

9030227G01Rik, 2310004H21Rik, 2510002A14Rik

MMRRC Submission

040004-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.740) question?

Stock #

R1993 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

73177534-73414042 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 73265836 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Lysine at position 495 (T495K)

Ref Sequence

ENSEMBL: ENSMUSP00000098687 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000094700] [ENSMUST00000101127] [ENSMUST00000153903]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000094700
AA Change: T495K

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000092289
Gene: ENSMUSG00000070733
AA Change: T495K

Domain	Start	End	E-Value	Type
Pfam:MOR2-PAG1_N	117	649	5.7e-176	PFAM
low complexity region	873	884	N/A	INTRINSIC
Pfam:MOR2-PAG1_mid	896	1141	1.3e-5	PFAM
Pfam:MOR2-PAG1_mid	1145	1331	2e-19	PFAM
Pfam:MOR2-PAG1_mid	1351	1450	1.2e-5	PFAM
low complexity region	1476	1487	N/A	INTRINSIC
low complexity region	1530	1548	N/A	INTRINSIC
Pfam:MOR2-PAG1_mid	1590	1660	1.1e-5	PFAM
Pfam:MOR2-PAG1_mid	1725	1866	3.2e-15	PFAM
low complexity region	1973	1984	N/A	INTRINSIC
Pfam:MOR2-PAG1_C	2002	2255	9.9e-78	PFAM
low complexity region	2329	2341	N/A	INTRINSIC
low complexity region	2473	2482	N/A	INTRINSIC
low complexity region	2485	2500	N/A	INTRINSIC
low complexity region	2523	2534	N/A	INTRINSIC
coiled coil region	2625	2649	N/A	INTRINSIC
low complexity region	2827	2841	N/A	INTRINSIC
coiled coil region	2854	2893	N/A	INTRINSIC
coiled coil region	2963	2989	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000101127
AA Change: T495K

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000098687
Gene: ENSMUSG00000070733
AA Change: T495K

Domain	Start	End	E-Value	Type
Pfam:MOR2-PAG1_N	116	649	3e-172	PFAM
low complexity region	873	884	N/A	INTRINSIC
Pfam:MOR2-PAG1_mid	898	1115	7.8e-6	PFAM
Pfam:MOR2-PAG1_mid	1147	1331	9.5e-19	PFAM
Pfam:MOR2-PAG1_mid	1351	1503	1.1e-5	PFAM
low complexity region	1530	1548	N/A	INTRINSIC
Pfam:MOR2-PAG1_mid	1589	1664	6e-6	PFAM
Pfam:MOR2-PAG1_mid	1725	1866	1.6e-14	PFAM
low complexity region	1973	1984	N/A	INTRINSIC
Pfam:MOR2-PAG1_C	1998	2260	4.4e-76	PFAM
low complexity region	2329	2341	N/A	INTRINSIC
low complexity region	2473	2482	N/A	INTRINSIC
low complexity region	2485	2500	N/A	INTRINSIC
low complexity region	2523	2534	N/A	INTRINSIC
coiled coil region	2625	2649	N/A	INTRINSIC
low complexity region	2827	2841	N/A	INTRINSIC
coiled coil region	2854	2893	N/A	INTRINSIC
coiled coil region	2963	2989	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000153903

SMART Domains

Protein: ENSMUSP00000119385
Gene: ENSMUSG00000070733

Domain	Start	End	E-Value	Type
Pfam:MOR2-PAG1_N	1	199	4.4e-58	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153923

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.0%
20x: 94.3%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Most mice homozygous for a knock-out allele exhibit postnatal lethality and defects in kidney development; rare survivors display growth retardation, decreased body weight, and premature death associated with chronic hydronephrosis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 104 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb1b	T	G	5: 8,871,322 (GRCm39)	I292S	possibly damaging	Het
Abcc4	T	C	14: 118,763,694 (GRCm39)	N1047S	probably benign	Het
Abcc8	G	T	7: 45,766,847 (GRCm39)		probably null	Het
Akap9	T	A	5: 4,088,520 (GRCm39)		probably null	Het
Alox5	T	A	6: 116,392,424 (GRCm39)	I366F	probably damaging	Het
Amn	A	G	12: 111,242,526 (GRCm39)	N447S	probably damaging	Het
Ankrd22	A	T	19: 34,143,174 (GRCm39)	M1K	probably null	Het
Asic1	G	T	15: 99,569,765 (GRCm39)	G29C	probably damaging	Het
Atxn7l1	A	G	12: 33,395,976 (GRCm39)	N235S	probably benign	Het
AY358078	T	A	14: 52,063,519 (GRCm39)	D388E	probably damaging	Het
Bod1l	A	G	5: 41,974,679 (GRCm39)	S2212P	probably damaging	Het
Cacna1e	T	A	1: 154,353,563 (GRCm39)	Q423L	probably damaging	Het
Calu	T	C	6: 29,366,974 (GRCm39)	I62T	possibly damaging	Het
Cars2	A	G	8: 11,564,515 (GRCm39)	V75A	probably benign	Het
Catsperb	T	A	12: 101,569,026 (GRCm39)	N899K	possibly damaging	Het
Ccdc50	T	A	16: 27,228,089 (GRCm39)	C86*	probably null	Het
Cdh5	G	T	8: 104,864,447 (GRCm39)	L469F	probably damaging	Het
Clrn3	A	T	7: 135,115,848 (GRCm39)	D167E	probably benign	Het
Csmd1	A	T	8: 16,396,698 (GRCm39)	C411S	probably damaging	Het
Dchs1	A	T	7: 105,411,755 (GRCm39)	S1454T	probably benign	Het
Ddx20	G	A	3: 105,586,660 (GRCm39)	Q562*	probably null	Het
Dgkg	T	G	16: 22,419,344 (GRCm39)	Y52S	probably damaging	Het
Dhx58	T	C	11: 100,594,316 (GRCm39)		probably null	Het
Dpp6	A	T	5: 27,604,004 (GRCm39)	I145L	probably benign	Het
Efna2	A	T	10: 80,022,711 (GRCm39)	Y85F	possibly damaging	Het
Eif3a	C	T	19: 60,769,954 (GRCm39)	V127I	probably benign	Het
Exph5	A	T	9: 53,284,935 (GRCm39)	H672L	possibly damaging	Het
Fam131b	T	C	6: 42,297,818 (GRCm39)	T112A	possibly damaging	Het
Fcgr1	A	T	3: 96,193,184 (GRCm39)	V271E	probably damaging	Het
Fgfr4	A	G	13: 55,313,715 (GRCm39)	D508G	probably damaging	Het
Fndc3b	A	G	3: 27,473,549 (GRCm39)	M1172T	probably benign	Het
Garin5b	A	T	7: 4,761,017 (GRCm39)	V565E	probably damaging	Het
Gm5134	A	T	10: 75,802,227 (GRCm39)	I93F	probably damaging	Het
Gpbar1	G	A	1: 74,318,603 (GRCm39)	G282D	possibly damaging	Het
Gria2	G	A	3: 80,709,664 (GRCm39)	L10F	probably benign	Het
Grm7	T	C	6: 111,184,769 (GRCm39)	Y367H	probably benign	Het
H1f9	T	A	11: 94,858,858 (GRCm39)	V51E	probably damaging	Het
Hivep1	G	A	13: 42,310,969 (GRCm39)	A1070T	probably benign	Het
Il33	A	G	19: 29,934,304 (GRCm39)	D155G	possibly damaging	Het
Kdm6b	T	C	11: 69,297,129 (GRCm39)	S408G	probably null	Het
Kntc1	A	G	5: 123,948,874 (GRCm39)		probably null	Het
Kntc1	G	A	5: 123,897,162 (GRCm39)		probably null	Het
Ltbp2	T	G	12: 84,855,220 (GRCm39)		probably null	Het
Mapk8ip3	G	T	17: 25,133,562 (GRCm39)	L83I	probably damaging	Het
Meltf	C	A	16: 31,711,440 (GRCm39)	Y554*	probably null	Het
Mov10	A	C	3: 104,706,735 (GRCm39)	F725C	probably damaging	Het
Ms4a6d	A	C	19: 11,567,523 (GRCm39)	L18R	probably damaging	Het
Naip2	T	C	13: 100,298,515 (GRCm39)	N507S	probably benign	Het
Nodal	A	G	10: 61,254,113 (GRCm39)	Q12R	probably benign	Het
Npy6r	T	C	18: 44,409,575 (GRCm39)	L332P	probably damaging	Het
Nrxn3	A	G	12: 89,227,181 (GRCm39)	K272R	possibly damaging	Het
Obox2	G	T	7: 15,131,174 (GRCm39)	K93N	probably benign	Het
Or10j27	C	T	1: 172,958,418 (GRCm39)	R122H	possibly damaging	Het
Or51a6	G	T	7: 102,603,953 (GRCm39)	P285Q	probably damaging	Het
Or5b112	A	G	19: 13,319,178 (GRCm39)	T19A	possibly damaging	Het
Or5w13	C	T	2: 87,523,777 (GRCm39)	V150M	probably benign	Het
Pcdh12	T	A	18: 38,415,196 (GRCm39)	D643V	possibly damaging	Het
Pcsk2	A	G	2: 143,529,539 (GRCm39)	D112G	probably benign	Het
Pms1	A	G	1: 53,234,174 (GRCm39)	S781P	probably benign	Het
Prtg	A	G	9: 72,752,178 (GRCm39)	D188G	probably benign	Het
Psg21	A	T	7: 18,388,695 (GRCm39)	N132K	probably benign	Het
Psip1	A	G	4: 83,400,769 (GRCm39)	V25A	probably damaging	Het
Psmd13	T	A	7: 140,478,107 (GRCm39)	I319N	probably damaging	Het
Ptges2	A	G	2: 32,290,104 (GRCm39)	T173A	probably benign	Het
Ptprm	G	A	17: 67,054,155 (GRCm39)	R975W	probably damaging	Het
Rdh1	A	G	10: 127,601,214 (GRCm39)	D254G	probably benign	Het
Rnf138	T	G	18: 21,157,540 (GRCm39)	N212K	probably damaging	Het
Serpine2	A	G	1: 79,799,159 (GRCm39)	S32P	probably damaging	Het
Serpini1	G	T	3: 75,521,971 (GRCm39)	W154L	probably damaging	Het
Sf3a1	C	A	11: 4,129,177 (GRCm39)	Q713K	possibly damaging	Het
Sgo2b	A	T	8: 64,379,867 (GRCm39)	H988Q	probably benign	Het
Sin3a	T	C	9: 57,008,483 (GRCm39)	F468L	probably damaging	Het
Slamf6	A	T	1: 171,761,776 (GRCm39)	I66F	possibly damaging	Het
Slc22a28	A	T	19: 8,094,488 (GRCm39)	C178S	possibly damaging	Het
Slc35a1	A	C	4: 34,675,181 (GRCm39)	V119G	probably damaging	Het
Slc39a12	A	T	2: 14,439,030 (GRCm39)	H428L	probably damaging	Het
Speer2	A	G	16: 69,654,965 (GRCm39)	S167P	probably benign	Het
Sphkap	G	A	1: 83,255,236 (GRCm39)	R838*	probably null	Het
Spsb2	T	C	6: 124,786,329 (GRCm39)		probably null	Het
Stam2	A	T	2: 52,593,168 (GRCm39)	Y341*	probably null	Het
Sv2b	G	A	7: 74,856,089 (GRCm39)	A67V	probably benign	Het
Svep1	A	G	4: 58,064,170 (GRCm39)		probably null	Het
Syt15	A	T	14: 33,944,969 (GRCm39)	Q172L	probably benign	Het
T	G	A	17: 8,660,634 (GRCm39)	S415N	probably benign	Het
Tep1	A	G	14: 51,061,641 (GRCm39)	F2625S	possibly damaging	Het
Tex14	T	C	11: 87,427,581 (GRCm39)	V11A	possibly damaging	Het
Tiam2	A	T	17: 3,465,401 (GRCm39)	R377*	probably null	Het
Tirap	A	G	9: 35,102,312 (GRCm39)		probably null	Het
Tm4sf20	T	C	1: 82,737,938 (GRCm39)	T118A	probably benign	Het
Trank1	A	T	9: 111,207,900 (GRCm39)	Q1715L	probably benign	Het
Trpm2	C	T	10: 77,783,823 (GRCm39)	V217M	probably damaging	Het
Ubap1l	G	A	9: 65,279,078 (GRCm39)	E126K	possibly damaging	Het
Urgcp	G	T	11: 5,666,526 (GRCm39)	P604Q	probably damaging	Het
Vmn1r63	A	G	7: 5,806,254 (GRCm39)	V126A	probably benign	Het
Vmn2r90	T	C	17: 17,933,525 (GRCm39)	C362R	probably damaging	Het
Vmn2r96	A	G	17: 18,804,138 (GRCm39)	I271V	probably damaging	Het
Vps13a	A	T	19: 16,699,822 (GRCm39)	I740K	probably benign	Het
Vps13c	A	G	9: 67,883,138 (GRCm39)	T3562A	probably damaging	Het
Wdr91	T	A	6: 34,869,297 (GRCm39)	H409L	probably damaging	Het
Wnt7a	T	A	6: 91,342,938 (GRCm39)	T315S	possibly damaging	Het
Zfp616	A	G	11: 73,975,795 (GRCm39)	H688R	probably benign	Het
Zfp763	A	T	17: 33,237,413 (GRCm39)	H577Q	probably damaging	Het
Zfp808	G	A	13: 62,320,721 (GRCm39)	S650N	probably benign	Het
Zfp977	A	T	7: 42,229,409 (GRCm39)	M372K	probably benign	Het

Other mutations in Fryl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00819:Fryl	APN	5	73,305,451 (GRCm39)	missense	possibly damaging	0.92
IGL01518:Fryl	APN	5	73,244,305 (GRCm39)	missense	possibly damaging	0.76
IGL01545:Fryl	APN	5	73,211,940 (GRCm39)	missense	probably damaging	1.00
IGL01646:Fryl	APN	5	73,179,844 (GRCm39)	critical splice donor site	probably null
IGL01938:Fryl	APN	5	73,279,707 (GRCm39)	missense	probably damaging	0.98
IGL01962:Fryl	APN	5	73,190,134 (GRCm39)	missense	possibly damaging	0.62
IGL02064:Fryl	APN	5	73,282,112 (GRCm39)	unclassified	probably benign
IGL02148:Fryl	APN	5	73,233,302 (GRCm39)	missense	probably benign	0.35
IGL02418:Fryl	APN	5	73,267,519 (GRCm39)	splice site	probably benign
IGL02431:Fryl	APN	5	73,255,651 (GRCm39)	missense	probably benign	0.02
IGL02513:Fryl	APN	5	73,222,636 (GRCm39)	missense	probably damaging	1.00
IGL02557:Fryl	APN	5	73,255,736 (GRCm39)	missense	probably damaging	1.00
IGL02625:Fryl	APN	5	73,227,220 (GRCm39)	intron	probably benign
IGL02642:Fryl	APN	5	73,252,809 (GRCm39)	missense	probably benign
IGL02657:Fryl	APN	5	73,212,203 (GRCm39)	missense	probably benign	0.01
IGL02706:Fryl	APN	5	73,250,506 (GRCm39)	missense	probably benign	0.45
IGL03022:Fryl	APN	5	73,216,726 (GRCm39)	missense	possibly damaging	0.82
IGL03144:Fryl	APN	5	73,258,798 (GRCm39)	missense	probably null	0.22
IGL03155:Fryl	APN	5	73,234,038 (GRCm39)	missense	probably benign
IGL03183:Fryl	APN	5	73,234,038 (GRCm39)	missense	probably benign
IGL03275:Fryl	APN	5	73,305,376 (GRCm39)	missense	possibly damaging	0.47
IGL03310:Fryl	APN	5	73,293,659 (GRCm39)	splice site	probably benign
IGL03341:Fryl	APN	5	73,234,038 (GRCm39)	missense	probably benign
IGL03343:Fryl	APN	5	73,234,038 (GRCm39)	missense	probably benign
IGL03350:Fryl	APN	5	73,290,649 (GRCm39)	missense	probably damaging	0.99
IGL03357:Fryl	APN	5	73,211,402 (GRCm39)	missense	probably damaging	1.00
IGL03374:Fryl	APN	5	73,267,624 (GRCm39)	splice site	probably benign
IGL03375:Fryl	APN	5	73,245,792 (GRCm39)	missense	possibly damaging	0.91
bedeviled	UTSW	5	73,216,843 (GRCm39)	missense	probably damaging	1.00
Besotted	UTSW	5	73,230,255 (GRCm39)	missense	probably damaging	1.00
R0062:Fryl	UTSW	5	73,179,621 (GRCm39)	missense	probably benign	0.02
R0062:Fryl	UTSW	5	73,179,621 (GRCm39)	missense	probably benign	0.02
R0308:Fryl	UTSW	5	73,198,947 (GRCm39)	splice site	probably benign
R0312:Fryl	UTSW	5	73,230,231 (GRCm39)	missense	probably damaging	1.00
R0415:Fryl	UTSW	5	73,255,757 (GRCm39)	missense	probably damaging	0.99
R0440:Fryl	UTSW	5	73,244,315 (GRCm39)	missense	possibly damaging	0.91
R0446:Fryl	UTSW	5	73,254,760 (GRCm39)	missense	possibly damaging	0.91
R0566:Fryl	UTSW	5	73,221,840 (GRCm39)	splice site	probably benign
R0567:Fryl	UTSW	5	73,222,734 (GRCm39)	missense	possibly damaging	0.50
R0606:Fryl	UTSW	5	73,282,077 (GRCm39)	missense	probably benign	0.15
R0619:Fryl	UTSW	5	73,226,074 (GRCm39)	missense	probably benign	0.22
R0654:Fryl	UTSW	5	73,240,715 (GRCm39)	missense	probably benign	0.17
R0658:Fryl	UTSW	5	73,222,702 (GRCm39)	missense	probably damaging	1.00
R0707:Fryl	UTSW	5	73,240,715 (GRCm39)	missense	probably benign	0.17
R0744:Fryl	UTSW	5	73,246,424 (GRCm39)	unclassified	probably benign
R0745:Fryl	UTSW	5	73,228,469 (GRCm39)	missense	probably damaging	0.96
R0833:Fryl	UTSW	5	73,246,424 (GRCm39)	unclassified	probably benign
R0885:Fryl	UTSW	5	73,246,539 (GRCm39)	missense	probably damaging	0.97
R0894:Fryl	UTSW	5	73,198,675 (GRCm39)	splice site	probably benign
R1076:Fryl	UTSW	5	73,282,016 (GRCm39)	unclassified	probably benign
R1241:Fryl	UTSW	5	73,267,614 (GRCm39)	missense	probably damaging	1.00
R1241:Fryl	UTSW	5	73,222,268 (GRCm39)	splice site	probably benign
R1394:Fryl	UTSW	5	73,230,255 (GRCm39)	missense	probably damaging	1.00
R1395:Fryl	UTSW	5	73,230,255 (GRCm39)	missense	probably damaging	1.00
R1608:Fryl	UTSW	5	73,232,094 (GRCm39)	nonsense	probably null
R1664:Fryl	UTSW	5	73,216,778 (GRCm39)	missense	probably damaging	1.00
R1745:Fryl	UTSW	5	73,190,204 (GRCm39)	splice site	probably benign
R1937:Fryl	UTSW	5	73,290,710 (GRCm39)	missense	probably damaging	1.00
R1969:Fryl	UTSW	5	73,255,609 (GRCm39)	missense	probably benign	0.18
R1994:Fryl	UTSW	5	73,265,836 (GRCm39)	missense	probably damaging	1.00
R2029:Fryl	UTSW	5	73,179,465 (GRCm39)	nonsense	probably null
R2036:Fryl	UTSW	5	73,265,305 (GRCm39)	critical splice donor site	probably null
R2036:Fryl	UTSW	5	73,179,887 (GRCm39)	missense	probably benign
R2088:Fryl	UTSW	5	73,222,804 (GRCm39)	missense	probably benign	0.02
R2105:Fryl	UTSW	5	73,279,642 (GRCm39)	missense	probably benign
R2106:Fryl	UTSW	5	73,255,674 (GRCm39)	missense	probably damaging	1.00
R2186:Fryl	UTSW	5	73,222,318 (GRCm39)	missense	probably damaging	1.00
R2239:Fryl	UTSW	5	73,265,890 (GRCm39)	missense	probably damaging	0.99
R2256:Fryl	UTSW	5	73,230,187 (GRCm39)	missense	possibly damaging	0.47
R2257:Fryl	UTSW	5	73,230,187 (GRCm39)	missense	possibly damaging	0.47
R2280:Fryl	UTSW	5	73,198,707 (GRCm39)	missense	possibly damaging	0.47
R2281:Fryl	UTSW	5	73,198,707 (GRCm39)	missense	possibly damaging	0.47
R2911:Fryl	UTSW	5	73,207,799 (GRCm39)	missense	probably damaging	0.99
R3019:Fryl	UTSW	5	73,240,193 (GRCm39)	missense	probably benign	0.01
R3416:Fryl	UTSW	5	73,265,417 (GRCm39)	missense	possibly damaging	0.84
R3783:Fryl	UTSW	5	73,258,819 (GRCm39)	missense	probably benign
R3787:Fryl	UTSW	5	73,258,819 (GRCm39)	missense	probably benign
R3837:Fryl	UTSW	5	73,228,608 (GRCm39)	missense	probably benign	0.03
R3969:Fryl	UTSW	5	73,269,766 (GRCm39)	missense	probably damaging	0.97
R4387:Fryl	UTSW	5	73,243,903 (GRCm39)	missense	possibly damaging	0.91
R4502:Fryl	UTSW	5	73,245,740 (GRCm39)	missense	probably damaging	1.00
R4658:Fryl	UTSW	5	73,238,396 (GRCm39)	missense	probably damaging	1.00
R4664:Fryl	UTSW	5	73,248,022 (GRCm39)	missense	possibly damaging	0.80
R4690:Fryl	UTSW	5	73,257,636 (GRCm39)	missense	probably benign
R4700:Fryl	UTSW	5	73,222,881 (GRCm39)	missense	possibly damaging	0.88
R4709:Fryl	UTSW	5	73,238,315 (GRCm39)	missense	probably benign	0.03
R4807:Fryl	UTSW	5	73,198,705 (GRCm39)	missense	probably benign	0.00
R4912:Fryl	UTSW	5	73,226,125 (GRCm39)	frame shift	probably null
R4948:Fryl	UTSW	5	73,246,473 (GRCm39)	missense	probably benign	0.08
R4959:Fryl	UTSW	5	73,192,401 (GRCm39)	missense	probably benign	0.00
R5062:Fryl	UTSW	5	73,233,236 (GRCm39)	missense	possibly damaging	0.89
R5067:Fryl	UTSW	5	73,215,098 (GRCm39)	missense	probably benign	0.13
R5071:Fryl	UTSW	5	73,232,110 (GRCm39)	missense	probably damaging	0.99
R5072:Fryl	UTSW	5	73,232,110 (GRCm39)	missense	probably damaging	0.99
R5073:Fryl	UTSW	5	73,232,110 (GRCm39)	missense	probably damaging	0.99
R5074:Fryl	UTSW	5	73,232,110 (GRCm39)	missense	probably damaging	0.99
R5139:Fryl	UTSW	5	73,248,061 (GRCm39)	missense	probably damaging	1.00
R5172:Fryl	UTSW	5	73,259,016 (GRCm39)	missense	possibly damaging	0.95
R5187:Fryl	UTSW	5	73,243,943 (GRCm39)	missense	possibly damaging	0.95
R5272:Fryl	UTSW	5	73,222,479 (GRCm39)	nonsense	probably null
R5275:Fryl	UTSW	5	73,270,134 (GRCm39)	missense	probably damaging	1.00
R5295:Fryl	UTSW	5	73,270,134 (GRCm39)	missense	probably damaging	1.00
R5344:Fryl	UTSW	5	73,262,117 (GRCm39)	missense	probably damaging	1.00
R5355:Fryl	UTSW	5	73,231,247 (GRCm39)	missense	probably damaging	1.00
R5716:Fryl	UTSW	5	73,257,808 (GRCm39)	missense	probably benign
R5778:Fryl	UTSW	5	73,230,121 (GRCm39)	missense	probably damaging	1.00
R5810:Fryl	UTSW	5	73,248,098 (GRCm39)	missense	probably benign	0.06
R5934:Fryl	UTSW	5	73,248,060 (GRCm39)	missense	probably damaging	1.00
R5948:Fryl	UTSW	5	73,254,715 (GRCm39)	critical splice donor site	probably null
R6005:Fryl	UTSW	5	73,240,638 (GRCm39)	missense	probably damaging	1.00
R6026:Fryl	UTSW	5	73,257,340 (GRCm39)	missense	probably benign	0.04
R6045:Fryl	UTSW	5	73,275,894 (GRCm39)	missense	probably damaging	0.99
R6185:Fryl	UTSW	5	73,270,131 (GRCm39)	missense	probably benign	0.43
R6247:Fryl	UTSW	5	73,222,824 (GRCm39)	missense	probably damaging	0.98
R6294:Fryl	UTSW	5	73,349,102 (GRCm39)	intron	probably benign
R6310:Fryl	UTSW	5	73,349,104 (GRCm39)	intron	probably benign
R6429:Fryl	UTSW	5	73,248,094 (GRCm39)	missense	possibly damaging	0.84
R6568:Fryl	UTSW	5	73,216,859 (GRCm39)	missense	probably damaging	1.00
R6636:Fryl	UTSW	5	73,290,655 (GRCm39)	missense	probably benign	0.01
R6664:Fryl	UTSW	5	73,289,824 (GRCm39)	missense	probably damaging	1.00
R6732:Fryl	UTSW	5	73,212,124 (GRCm39)	missense	probably damaging	1.00
R6750:Fryl	UTSW	5	73,179,575 (GRCm39)	missense	probably damaging	1.00
R6805:Fryl	UTSW	5	73,222,437 (GRCm39)	missense	probably benign	0.03
R6823:Fryl	UTSW	5	73,222,560 (GRCm39)	missense	probably damaging	0.99
R6855:Fryl	UTSW	5	73,216,843 (GRCm39)	missense	probably damaging	1.00
R6858:Fryl	UTSW	5	73,222,375 (GRCm39)	missense	probably damaging	1.00
R6868:Fryl	UTSW	5	73,226,146 (GRCm39)	missense	probably damaging	1.00
R6898:Fryl	UTSW	5	73,179,485 (GRCm39)	missense	probably damaging	0.96
R6908:Fryl	UTSW	5	73,179,554 (GRCm39)	missense	probably damaging	1.00
R6958:Fryl	UTSW	5	73,231,272 (GRCm39)	missense	possibly damaging	0.89
R6980:Fryl	UTSW	5	73,207,773 (GRCm39)	missense	probably benign	0.06
R7036:Fryl	UTSW	5	73,212,951 (GRCm39)	missense	probably benign	0.03
R7065:Fryl	UTSW	5	73,248,099 (GRCm39)	missense	probably damaging	0.96
R7097:Fryl	UTSW	5	73,231,251 (GRCm39)	missense	probably benign	0.31
R7171:Fryl	UTSW	5	73,279,653 (GRCm39)	missense	probably damaging	0.97
R7191:Fryl	UTSW	5	73,230,255 (GRCm39)	missense	probably damaging	1.00
R7207:Fryl	UTSW	5	73,222,438 (GRCm39)	missense	probably benign
R7236:Fryl	UTSW	5	73,265,821 (GRCm39)	missense	possibly damaging	0.66
R7334:Fryl	UTSW	5	73,204,839 (GRCm39)	splice site	probably null
R7425:Fryl	UTSW	5	73,262,091 (GRCm39)	missense	probably damaging	1.00
R7452:Fryl	UTSW	5	73,181,331 (GRCm39)	missense	probably damaging	1.00
R7479:Fryl	UTSW	5	73,254,904 (GRCm39)	missense	possibly damaging	0.71
R7535:Fryl	UTSW	5	73,255,539 (GRCm39)	missense	probably benign	0.15
R7538:Fryl	UTSW	5	73,180,019 (GRCm39)	missense	probably benign	0.09
R7544:Fryl	UTSW	5	73,238,382 (GRCm39)	missense	probably benign
R7548:Fryl	UTSW	5	73,349,105 (GRCm39)	missense	unknown
R7565:Fryl	UTSW	5	73,191,063 (GRCm39)	missense	probably benign	0.18
R7572:Fryl	UTSW	5	73,245,739 (GRCm39)	missense	possibly damaging	0.91
R7582:Fryl	UTSW	5	73,179,843 (GRCm39)	critical splice donor site	probably null
R7630:Fryl	UTSW	5	73,267,588 (GRCm39)	missense	possibly damaging	0.62
R7774:Fryl	UTSW	5	73,240,727 (GRCm39)	missense	probably benign	0.12
R7777:Fryl	UTSW	5	73,228,641 (GRCm39)	missense	probably damaging	0.98
R7917:Fryl	UTSW	5	73,211,875 (GRCm39)	missense	probably damaging	1.00
R7920:Fryl	UTSW	5	73,259,150 (GRCm39)	splice site	probably null
R8110:Fryl	UTSW	5	73,290,620 (GRCm39)	missense	probably benign	0.10
R8120:Fryl	UTSW	5	73,228,527 (GRCm39)	missense	probably benign	0.01
R8143:Fryl	UTSW	5	73,207,682 (GRCm39)	missense	probably benign	0.00
R8207:Fryl	UTSW	5	73,257,843 (GRCm39)	splice site	probably null
R8263:Fryl	UTSW	5	73,238,348 (GRCm39)	missense	probably damaging	1.00
R8350:Fryl	UTSW	5	73,226,073 (GRCm39)	missense	probably benign
R8359:Fryl	UTSW	5	73,233,276 (GRCm39)	missense	probably benign	0.39
R8387:Fryl	UTSW	5	73,293,663 (GRCm39)	critical splice donor site	probably null
R8403:Fryl	UTSW	5	73,275,790 (GRCm39)	makesense	probably null
R8450:Fryl	UTSW	5	73,226,073 (GRCm39)	missense	probably benign
R8514:Fryl	UTSW	5	73,242,699 (GRCm39)	missense	probably benign
R8536:Fryl	UTSW	5	73,257,696 (GRCm39)	missense	probably damaging	0.99
R8703:Fryl	UTSW	5	73,247,997 (GRCm39)	missense	probably damaging	0.99
R8708:Fryl	UTSW	5	73,289,905 (GRCm39)	missense	probably benign	0.01
R8783:Fryl	UTSW	5	73,226,185 (GRCm39)	missense	probably benign	0.45
R9028:Fryl	UTSW	5	73,255,609 (GRCm39)	missense	probably benign	0.18
R9045:Fryl	UTSW	5	73,182,118 (GRCm39)	missense
R9063:Fryl	UTSW	5	73,238,346 (GRCm39)	missense	possibly damaging	0.70
R9096:Fryl	UTSW	5	73,265,920 (GRCm39)	missense	probably benign	0.01
R9244:Fryl	UTSW	5	73,348,862 (GRCm39)	intron	probably benign
R9345:Fryl	UTSW	5	73,207,754 (GRCm39)	missense	probably benign
R9381:Fryl	UTSW	5	73,240,637 (GRCm39)	missense	probably benign	0.24
R9386:Fryl	UTSW	5	73,349,152 (GRCm39)	missense	unknown
R9401:Fryl	UTSW	5	73,222,563 (GRCm39)	nonsense	probably null
R9497:Fryl	UTSW	5	73,215,134 (GRCm39)	missense
R9514:Fryl	UTSW	5	73,262,115 (GRCm39)	missense	probably damaging	1.00
R9570:Fryl	UTSW	5	73,179,498 (GRCm39)	missense	probably benign	0.02
R9654:Fryl	UTSW	5	73,275,801 (GRCm39)	missense	probably benign
R9665:Fryl	UTSW	5	73,222,299 (GRCm39)	missense	probably damaging	1.00
R9685:Fryl	UTSW	5	73,216,879 (GRCm39)	missense	probably damaging	0.99
R9798:Fryl	UTSW	5	73,192,402 (GRCm39)	missense	probably benign
Z1088:Fryl	UTSW	5	73,248,081 (GRCm39)	missense	probably damaging	1.00
Z1088:Fryl	UTSW	5	73,248,052 (GRCm39)	missense	probably damaging	0.99
Z1176:Fryl	UTSW	5	73,230,180 (GRCm39)	missense	probably benign
Z1177:Fryl	UTSW	5	73,198,938 (GRCm39)	critical splice acceptor site	probably null

Predicted Primers

PCR Primer
(F):5'- ACTGCGTACAAATTGCACAG -3'
(R):5'- CTTAGCCTAGGCAGTGCTTG -3'

Sequencing Primer
(F):5'- CATTTAACAGGAAGACTCTTGACAGG -3'
(R):5'- CAGTGCTTGGCCCTGATC -3'

Posted On

2014-08-25