Mutagenetix > Incidental Mutation

Incidental Mutation 'R4581:2410089E03Rik'

343699

Institutional Source

Beutler Lab

Gene Symbol

2410089E03Rik

Ensembl Gene

ENSMUSG00000039801

Gene Name

RIKEN cDNA 2410089E03 gene

Synonyms

b2b012Clo

MMRRC Submission

041802-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4581 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

8169106-8271158 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 8171798 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Proline to Threonine at position 20 (P20T)

Ref Sequence

ENSEMBL: ENSMUSP00000106247 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000110617]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000110617
AA Change: P20T

PolyPhen 2 Score 0.846 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000106247
Gene: ENSMUSG00000039801
AA Change: P20T

Domain	Start	End	E-Value	Type
low complexity region	144	157	N/A	INTRINSIC
low complexity region	338	352	N/A	INTRINSIC
low complexity region	466	476	N/A	INTRINSIC
low complexity region	868	883	N/A	INTRINSIC
low complexity region	949	962	N/A	INTRINSIC
low complexity region	1400	1415	N/A	INTRINSIC
low complexity region	1449	1464	N/A	INTRINSIC
low complexity region	1827	1838	N/A	INTRINSIC
low complexity region	1919	1930	N/A	INTRINSIC
low complexity region	2130	2145	N/A	INTRINSIC
coiled coil region	2750	2782	N/A	INTRINSIC
low complexity region	2838	2850	N/A	INTRINSIC
Pfam:Joubert	2894	3207	1.9e-136	PFAM

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]
PHENOTYPE: Homozygotes exhibit double outlet right ventricle {SDD}, pulmonary atresia/hypolastic pulmonary artery, atrioventricular septal defect, and right aortic arch. Non-cardiovascular defects include cleft palate, polydactyly, transparent chest wall (sternal bone hypoplasia) and hypoplastic lungs. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	G	T	14: 32,661,871 (GRCm38)	S712R	possibly damaging	Het
4933427I04Rik	A	G	4: 123,860,353 (GRCm38)	D20G	possibly damaging	Het
Abca7	A	G	10: 80,006,568 (GRCm38)	D1112G	probably benign	Het
Actc1	G	T	2: 114,049,608 (GRCm38)	H175N	possibly damaging	Het
Adgrd1	C	T	5: 129,202,531 (GRCm38)	A863V	possibly damaging	Het
Ankrd17	T	C	5: 90,283,120 (GRCm38)	D935G	possibly damaging	Het
Ankrd7	T	A	6: 18,868,021 (GRCm38)	N95K	probably damaging	Het
Arhgef4	G	A	1: 34,732,124 (GRCm38)	E1171K	possibly damaging	Het
Ascc3	T	C	10: 50,711,025 (GRCm38)	I991T	probably damaging	Het
Cacna1s	T	A	1: 136,070,970 (GRCm38)		probably null	Het
Camk1d	A	T	2: 5,354,704 (GRCm38)	V177E	probably benign	Het
Cdh18	T	A	15: 23,226,783 (GRCm38)	I110N	probably damaging	Het
Cenpe	A	G	3: 135,247,000 (GRCm38)	K1484E	probably benign	Het
Cep68	A	G	11: 20,239,333 (GRCm38)	S560P	probably benign	Het
Cog3	G	T	14: 75,732,951 (GRCm38)	T352K	probably benign	Het
Cox6a2	A	G	7: 128,205,980 (GRCm38)	S44P	possibly damaging	Het
Csmd2	T	C	4: 128,369,088 (GRCm38)	V689A	probably benign	Het
Ddx60	A	T	8: 62,023,261 (GRCm38)	M1548L	possibly damaging	Het
Dennd5b	G	T	6: 149,016,984 (GRCm38)		silent	Het
Dlgap2	T	C	8: 14,846,679 (GRCm38)	Y1052H	probably damaging	Het
Dnaaf5	T	A	5: 139,184,685 (GRCm38)	D502E	probably damaging	Het
Efhb	C	A	17: 53,426,275 (GRCm38)	A523S	probably damaging	Het
Epha8	C	T	4: 136,933,464 (GRCm38)	V648M	probably damaging	Het
Fanca	C	T	8: 123,274,338 (GRCm38)		probably null	Het
Fbxw7	G	A	3: 84,967,545 (GRCm38)	E205K	probably benign	Het
Fer1l6	C	T	15: 58,640,226 (GRCm38)	T1514I	probably damaging	Het
Gm12886	T	C	4: 121,416,683 (GRCm38)	E112G	probably damaging	Het
Gm7535	T	C	17: 17,911,083 (GRCm38)		probably benign	Het
Irf2bp2	T	A	8: 126,591,255 (GRCm38)	Q524L	probably damaging	Het
Itih4	A	G	14: 30,900,968 (GRCm38)	D864G	probably benign	Het
Kdm4c	T	G	4: 74,357,339 (GRCm38)		probably null	Het
Ltn1	A	T	16: 87,402,024 (GRCm38)		probably null	Het
Mafa	G	T	15: 75,747,736 (GRCm38)	P63T	unknown	Het
Mars2	T	A	1: 55,237,862 (GRCm38)	L208H	probably damaging	Het
Myom2	A	G	8: 15,106,459 (GRCm38)	I769V	probably benign	Het
Nyap1	A	G	5: 137,736,022 (GRCm38)	S250P	probably damaging	Het
Olfr1082	A	T	2: 86,594,228 (GRCm38)	M200K	probably benign	Het
Osmr	C	T	15: 6,842,894 (GRCm38)	V240I	probably benign	Het
Pcdhga3	A	G	18: 37,676,881 (GRCm38)	T796A	probably benign	Het
Pclo	T	C	5: 14,675,505 (GRCm38)	V1459A	unknown	Het
Phactr3	A	C	2: 178,283,172 (GRCm38)	H300P	probably damaging	Het
Pla2g4e	T	G	2: 120,186,382 (GRCm38)	H226P	possibly damaging	Het
Plcd4	T	A	1: 74,548,224 (GRCm38)	W48R	probably damaging	Het
Prdm16	A	G	4: 154,323,353 (GRCm38)	S1140P	probably damaging	Het
Rarg	A	C	15: 102,252,551 (GRCm38)	S18A	possibly damaging	Het
Rfx4	T	A	10: 84,844,300 (GRCm38)	S114T	possibly damaging	Het
Sec14l4	G	A	11: 4,043,375 (GRCm38)		probably null	Het
Six1	T	G	12: 73,045,934 (GRCm38)	T165P	probably benign	Het
Skint4	T	C	4: 112,087,042 (GRCm38)	L17P	probably damaging	Het
Slc25a23	T	A	17: 57,052,740 (GRCm38)	Y337F	probably damaging	Het
Slc9a3	A	G	13: 74,164,165 (GRCm38)	Y627C	probably damaging	Het
Smu1	A	C	4: 40,737,401 (GRCm38)		probably null	Het
Spryd3	A	G	15: 102,130,364 (GRCm38)	S141P	probably damaging	Het
Src	A	T	2: 157,463,038 (GRCm38)	N175I	probably damaging	Het
Srcap	GCTCCTCCTCCTCCTCCT	GCTCCTCCTCCTCCT	7: 127,558,310 (GRCm38)		probably benign	Het
Stc2	A	G	11: 31,365,326 (GRCm38)		probably null	Het
Taf6l	T	C	19: 8,778,208 (GRCm38)	D261G	probably damaging	Het
Tal1	T	G	4: 115,064,722 (GRCm38)	V167G	probably damaging	Het
Tfec	G	A	6: 16,834,125 (GRCm38)	T261I	probably damaging	Het
Tgfb1	G	T	7: 25,697,230 (GRCm38)	S273I	possibly damaging	Het
Tmem8b	T	A	4: 43,685,760 (GRCm38)	V636E	probably damaging	Het
Top2b	T	G	14: 16,409,189 (GRCm38)	I777M	probably damaging	Het
Trappc11	A	T	8: 47,493,345 (GRCm38)	M1084K	probably damaging	Het
Trem3	A	C	17: 48,249,611 (GRCm38)	T37P	possibly damaging	Het
Ttc7b	G	A	12: 100,500,117 (GRCm38)	R79C	probably damaging	Het
Urb1	T	C	16: 90,788,146 (GRCm38)	D529G	probably benign	Het
Vmn2r8	T	A	5: 108,801,704 (GRCm38)	T426S	probably benign	Het
Yipf4	T	C	17: 74,499,094 (GRCm38)	Y243H	probably benign	Het
Zfp574	T	A	7: 25,081,313 (GRCm38)	C587S	probably damaging	Het
Zfp93	C	A	7: 24,275,668 (GRCm38)	H359Q	probably damaging	Het
Znfx1	T	C	2: 167,050,316 (GRCm38)	E660G	probably damaging	Het

Other mutations in 2410089E03Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00756:2410089E03Rik	APN	15	8,264,447 (GRCm38)	splice site	probably benign
IGL00766:2410089E03Rik	APN	15	8,252,164 (GRCm38)	missense	unknown
IGL01483:2410089E03Rik	APN	15	8,187,107 (GRCm38)	missense	probably damaging	0.98
IGL01520:2410089E03Rik	APN	15	8,221,911 (GRCm38)	missense	probably damaging	0.96
IGL01578:2410089E03Rik	APN	15	8,270,710 (GRCm38)	missense	unknown
IGL01701:2410089E03Rik	APN	15	8,203,257 (GRCm38)	splice site	probably benign
IGL01892:2410089E03Rik	APN	15	8,242,265 (GRCm38)	splice site	probably benign
IGL01895:2410089E03Rik	APN	15	8,229,107 (GRCm38)	missense	possibly damaging	0.63
IGL01922:2410089E03Rik	APN	15	8,270,821 (GRCm38)	missense	unknown
IGL01978:2410089E03Rik	APN	15	8,219,382 (GRCm38)	missense	probably damaging	0.98
IGL02031:2410089E03Rik	APN	15	8,179,769 (GRCm38)	missense	probably damaging	0.99
IGL02318:2410089E03Rik	APN	15	8,175,025 (GRCm38)	missense	probably damaging	0.98
IGL02321:2410089E03Rik	APN	15	8,216,572 (GRCm38)	missense	probably benign	0.04
IGL02363:2410089E03Rik	APN	15	8,218,437 (GRCm38)	missense	possibly damaging	0.68
IGL02404:2410089E03Rik	APN	15	8,187,284 (GRCm38)	missense	possibly damaging	0.48
IGL02535:2410089E03Rik	APN	15	8,174,838 (GRCm38)	missense	probably damaging	1.00
IGL02732:2410089E03Rik	APN	15	8,179,891 (GRCm38)	missense	probably benign	0.03
IGL02895:2410089E03Rik	APN	15	8,232,107 (GRCm38)	splice site	probably benign
IGL02903:2410089E03Rik	APN	15	8,269,778 (GRCm38)	missense	unknown
IGL02903:2410089E03Rik	APN	15	8,269,779 (GRCm38)	missense	unknown
IGL02979:2410089E03Rik	APN	15	8,218,554 (GRCm38)	missense	possibly damaging	0.82
IGL03077:2410089E03Rik	APN	15	8,212,795 (GRCm38)	splice site	probably benign
IGL03196:2410089E03Rik	APN	15	8,201,342 (GRCm38)	missense	probably damaging	0.98
IGL03344:2410089E03Rik	APN	15	8,187,458 (GRCm38)	missense	possibly damaging	0.63
IGL03368:2410089E03Rik	APN	15	8,222,373 (GRCm38)	missense	probably benign	0.06
IGL03403:2410089E03Rik	APN	15	8,201,342 (GRCm38)	missense	probably damaging	0.98
agnes	UTSW	15	8,246,938 (GRCm38)	nonsense	probably null
dei	UTSW	15	8,186,165 (GRCm38)	missense	probably damaging	1.00
R0015:2410089E03Rik	UTSW	15	8,186,184 (GRCm38)	missense	probably damaging	1.00
R0015:2410089E03Rik	UTSW	15	8,186,184 (GRCm38)	missense	probably damaging	1.00
R0101:2410089E03Rik	UTSW	15	8,220,960 (GRCm38)	missense	probably benign	0.00
R0105:2410089E03Rik	UTSW	15	8,187,392 (GRCm38)	missense	probably benign
R0105:2410089E03Rik	UTSW	15	8,187,392 (GRCm38)	missense	probably benign
R0165:2410089E03Rik	UTSW	15	8,216,382 (GRCm38)	missense	probably damaging	1.00
R0306:2410089E03Rik	UTSW	15	8,179,889 (GRCm38)	missense	probably damaging	1.00
R0433:2410089E03Rik	UTSW	15	8,216,562 (GRCm38)	missense	probably benign	0.00
R0491:2410089E03Rik	UTSW	15	8,182,243 (GRCm38)	missense	probably damaging	1.00
R0523:2410089E03Rik	UTSW	15	8,194,386 (GRCm38)	missense	probably damaging	1.00
R0571:2410089E03Rik	UTSW	15	8,259,793 (GRCm38)	missense	unknown
R0679:2410089E03Rik	UTSW	15	8,223,122 (GRCm38)	missense	probably benign	0.39
R0704:2410089E03Rik	UTSW	15	8,210,083 (GRCm38)	missense	possibly damaging	0.93
R0707:2410089E03Rik	UTSW	15	8,258,321 (GRCm38)	missense	unknown
R0715:2410089E03Rik	UTSW	15	8,223,092 (GRCm38)	missense	probably benign	0.14
R0762:2410089E03Rik	UTSW	15	8,218,416 (GRCm38)	unclassified	probably benign
R0830:2410089E03Rik	UTSW	15	8,247,185 (GRCm38)	missense	unknown
R0924:2410089E03Rik	UTSW	15	8,251,070 (GRCm38)	splice site	probably benign
R1071:2410089E03Rik	UTSW	15	8,218,426 (GRCm38)	missense	probably benign	0.20
R1184:2410089E03Rik	UTSW	15	8,216,487 (GRCm38)	missense	probably benign
R1224:2410089E03Rik	UTSW	15	8,178,385 (GRCm38)	missense	probably benign	0.06
R1416:2410089E03Rik	UTSW	15	8,246,938 (GRCm38)	nonsense	probably null
R1428:2410089E03Rik	UTSW	15	8,219,369 (GRCm38)	missense	possibly damaging	0.83
R1487:2410089E03Rik	UTSW	15	8,186,231 (GRCm38)	missense	probably damaging	1.00
R1641:2410089E03Rik	UTSW	15	8,228,959 (GRCm38)	missense	probably benign	0.41
R1652:2410089E03Rik	UTSW	15	8,201,146 (GRCm38)	missense	probably damaging	1.00
R1688:2410089E03Rik	UTSW	15	8,228,609 (GRCm38)	missense	probably benign	0.00
R1715:2410089E03Rik	UTSW	15	8,226,900 (GRCm38)	splice site	probably null
R1820:2410089E03Rik	UTSW	15	8,269,645 (GRCm38)	missense	unknown
R1863:2410089E03Rik	UTSW	15	8,228,593 (GRCm38)	missense	probably benign	0.00
R1940:2410089E03Rik	UTSW	15	8,233,852 (GRCm38)	missense	probably damaging	0.98
R1967:2410089E03Rik	UTSW	15	8,203,420 (GRCm38)	missense	probably benign	0.09
R2064:2410089E03Rik	UTSW	15	8,186,165 (GRCm38)	missense	probably damaging	1.00
R2076:2410089E03Rik	UTSW	15	8,219,257 (GRCm38)	missense	possibly damaging	0.93
R2163:2410089E03Rik	UTSW	15	8,203,251 (GRCm38)	splice site	probably null
R2208:2410089E03Rik	UTSW	15	8,194,403 (GRCm38)	missense	probably benign	0.33
R2504:2410089E03Rik	UTSW	15	8,219,216 (GRCm38)	missense	probably damaging	0.99
R2568:2410089E03Rik	UTSW	15	8,201,269 (GRCm38)	missense	possibly damaging	0.70
R2845:2410089E03Rik	UTSW	15	8,216,380 (GRCm38)	missense	probably damaging	1.00
R2913:2410089E03Rik	UTSW	15	8,270,685 (GRCm38)	missense	unknown
R3056:2410089E03Rik	UTSW	15	8,251,007 (GRCm38)	missense	unknown
R3706:2410089E03Rik	UTSW	15	8,259,816 (GRCm38)	missense	unknown
R3707:2410089E03Rik	UTSW	15	8,259,816 (GRCm38)	missense	unknown
R3870:2410089E03Rik	UTSW	15	8,218,464 (GRCm38)	missense	probably damaging	0.98
R3877:2410089E03Rik	UTSW	15	8,221,943 (GRCm38)	missense	probably benign
R3886:2410089E03Rik	UTSW	15	8,171,805 (GRCm38)	missense	probably damaging	0.98
R4057:2410089E03Rik	UTSW	15	8,219,025 (GRCm38)	missense	probably benign	0.08
R4090:2410089E03Rik	UTSW	15	8,212,358 (GRCm38)	splice site	probably null
R4362:2410089E03Rik	UTSW	15	8,270,745 (GRCm38)	missense	unknown
R4363:2410089E03Rik	UTSW	15	8,270,745 (GRCm38)	missense	unknown
R4445:2410089E03Rik	UTSW	15	8,252,188 (GRCm38)	missense	unknown
R4587:2410089E03Rik	UTSW	15	8,201,152 (GRCm38)	missense	possibly damaging	0.50
R4659:2410089E03Rik	UTSW	15	8,216,276 (GRCm38)	intron	probably benign
R4663:2410089E03Rik	UTSW	15	8,218,455 (GRCm38)	missense	probably benign	0.31
R4779:2410089E03Rik	UTSW	15	8,218,838 (GRCm38)	missense	probably benign	0.04
R4812:2410089E03Rik	UTSW	15	8,201,123 (GRCm38)	splice site	probably null
R4850:2410089E03Rik	UTSW	15	8,262,938 (GRCm38)	missense	unknown
R4896:2410089E03Rik	UTSW	15	8,221,937 (GRCm38)	missense	probably benign	0.00
R5273:2410089E03Rik	UTSW	15	8,262,938 (GRCm38)	missense	unknown
R5273:2410089E03Rik	UTSW	15	8,244,341 (GRCm38)	missense	probably damaging	0.98
R5303:2410089E03Rik	UTSW	15	8,260,690 (GRCm38)	splice site	probably null
R5307:2410089E03Rik	UTSW	15	8,260,690 (GRCm38)	splice site	probably null
R5308:2410089E03Rik	UTSW	15	8,260,690 (GRCm38)	splice site	probably null
R5373:2410089E03Rik	UTSW	15	8,270,803 (GRCm38)	missense	unknown
R5374:2410089E03Rik	UTSW	15	8,270,803 (GRCm38)	missense	unknown
R5386:2410089E03Rik	UTSW	15	8,194,413 (GRCm38)	missense	probably damaging	1.00
R5534:2410089E03Rik	UTSW	15	8,228,835 (GRCm38)	missense	probably benign	0.06
R5720:2410089E03Rik	UTSW	15	8,203,687 (GRCm38)	missense	probably benign	0.35
R5891:2410089E03Rik	UTSW	15	8,188,589 (GRCm38)	missense	probably benign	0.00
R5932:2410089E03Rik	UTSW	15	8,244,595 (GRCm38)	splice site	probably null
R6053:2410089E03Rik	UTSW	15	8,188,461 (GRCm38)	missense	probably benign	0.35
R6166:2410089E03Rik	UTSW	15	8,186,560 (GRCm38)	missense	probably benign	0.00
R6245:2410089E03Rik	UTSW	15	8,178,418 (GRCm38)	missense	probably benign	0.01
R6246:2410089E03Rik	UTSW	15	8,210,014 (GRCm38)	missense	probably damaging	1.00
R6541:2410089E03Rik	UTSW	15	8,219,295 (GRCm38)	missense	possibly damaging	0.48
R6622:2410089E03Rik	UTSW	15	8,244,222 (GRCm38)	missense	probably damaging	0.98
R6707:2410089E03Rik	UTSW	15	8,223,122 (GRCm38)	missense	probably benign	0.39
R6729:2410089E03Rik	UTSW	15	8,188,601 (GRCm38)	splice site	probably null
R6805:2410089E03Rik	UTSW	15	8,244,306 (GRCm38)	missense	probably benign	0.07
R6806:2410089E03Rik	UTSW	15	8,186,858 (GRCm38)	missense	possibly damaging	0.55
R6813:2410089E03Rik	UTSW	15	8,229,282 (GRCm38)	missense	probably benign
R6830:2410089E03Rik	UTSW	15	8,176,184 (GRCm38)	missense	probably benign	0.04
R6845:2410089E03Rik	UTSW	15	8,221,904 (GRCm38)	missense	possibly damaging	0.84
R6894:2410089E03Rik	UTSW	15	8,187,368 (GRCm38)	missense	probably damaging	0.99
R6970:2410089E03Rik	UTSW	15	8,187,548 (GRCm38)	missense	probably benign	0.01
R6991:2410089E03Rik	UTSW	15	8,252,206 (GRCm38)	missense	unknown
R7003:2410089E03Rik	UTSW	15	8,228,762 (GRCm38)	missense	probably damaging	0.99
R7088:2410089E03Rik	UTSW	15	8,218,947 (GRCm38)	missense	probably benign	0.16
R7104:2410089E03Rik	UTSW	15	8,194,444 (GRCm38)	missense	possibly damaging	0.83
R7311:2410089E03Rik	UTSW	15	8,180,915 (GRCm38)	missense	probably damaging	1.00
R7374:2410089E03Rik	UTSW	15	8,247,247 (GRCm38)	missense	unknown
R7446:2410089E03Rik	UTSW	15	8,232,080 (GRCm38)	missense	probably damaging	0.98
R7539:2410089E03Rik	UTSW	15	8,201,244 (GRCm38)	missense	probably benign	0.19
R7543:2410089E03Rik	UTSW	15	8,225,392 (GRCm38)	missense	unknown
R7558:2410089E03Rik	UTSW	15	8,225,367 (GRCm38)	missense	unknown
R7629:2410089E03Rik	UTSW	15	8,227,067 (GRCm38)	nonsense	probably null
R7635:2410089E03Rik	UTSW	15	8,226,920 (GRCm38)	missense	probably benign	0.01
R7644:2410089E03Rik	UTSW	15	8,223,127 (GRCm38)	missense	probably benign	0.00
R7705:2410089E03Rik	UTSW	15	8,182,252 (GRCm38)	missense	probably damaging	1.00
R7752:2410089E03Rik	UTSW	15	8,269,706 (GRCm38)	missense	unknown
R7754:2410089E03Rik	UTSW	15	8,243,826 (GRCm38)	missense	possibly damaging	0.53
R7757:2410089E03Rik	UTSW	15	8,252,227 (GRCm38)	missense	unknown
R7836:2410089E03Rik	UTSW	15	8,203,757 (GRCm38)	missense	probably damaging	0.97
R7875:2410089E03Rik	UTSW	15	8,209,962 (GRCm38)	missense	probably benign	0.18
R7901:2410089E03Rik	UTSW	15	8,269,706 (GRCm38)	missense	unknown
R7983:2410089E03Rik	UTSW	15	8,221,815 (GRCm38)	missense	probably benign	0.01
R8030:2410089E03Rik	UTSW	15	8,230,303 (GRCm38)	missense	probably damaging	1.00
R8088:2410089E03Rik	UTSW	15	8,186,318 (GRCm38)	missense	probably benign	0.00
R8231:2410089E03Rik	UTSW	15	8,219,027 (GRCm38)	missense	probably benign	0.16
R8443:2410089E03Rik	UTSW	15	8,201,151 (GRCm38)	missense	probably benign	0.03
R8480:2410089E03Rik	UTSW	15	8,187,458 (GRCm38)	missense	possibly damaging	0.63
R8693:2410089E03Rik	UTSW	15	8,229,008 (GRCm38)	missense	probably benign	0.15
R8785:2410089E03Rik	UTSW	15	8,174,760 (GRCm38)	missense	probably benign	0.39
R8791:2410089E03Rik	UTSW	15	8,187,260 (GRCm38)	missense	probably damaging	1.00
R8822:2410089E03Rik	UTSW	15	8,171,778 (GRCm38)	missense	probably damaging	1.00
R8831:2410089E03Rik	UTSW	15	8,182,136 (GRCm38)	missense	probably benign	0.09
R8932:2410089E03Rik	UTSW	15	8,194,375 (GRCm38)	missense	probably damaging	1.00
R8968:2410089E03Rik	UTSW	15	8,201,281 (GRCm38)	missense	possibly damaging	0.84
R8973:2410089E03Rik	UTSW	15	8,203,793 (GRCm38)	missense	probably damaging	1.00
R9036:2410089E03Rik	UTSW	15	8,223,138 (GRCm38)	missense	possibly damaging	0.63
R9134:2410089E03Rik	UTSW	15	8,199,232 (GRCm38)	missense	probably damaging	0.99
R9197:2410089E03Rik	UTSW	15	8,251,052 (GRCm38)	missense	unknown
R9259:2410089E03Rik	UTSW	15	8,203,303 (GRCm38)	missense	possibly damaging	0.82
R9269:2410089E03Rik	UTSW	15	8,219,016 (GRCm38)	missense	probably damaging	0.97
R9294:2410089E03Rik	UTSW	15	8,203,327 (GRCm38)	missense	probably benign	0.00
R9328:2410089E03Rik	UTSW	15	8,186,208 (GRCm38)	missense	probably damaging	1.00
R9563:2410089E03Rik	UTSW	15	8,187,079 (GRCm38)	missense	probably benign	0.20
R9680:2410089E03Rik	UTSW	15	8,202,301 (GRCm38)	missense	possibly damaging	0.68
R9721:2410089E03Rik	UTSW	15	8,225,409 (GRCm38)	missense	unknown
R9779:2410089E03Rik	UTSW	15	8,201,302 (GRCm38)	missense	possibly damaging	0.93
R9780:2410089E03Rik	UTSW	15	8,228,639 (GRCm38)	missense	probably benign	0.00
U24488:2410089E03Rik	UTSW	15	8,182,210 (GRCm38)	missense	probably damaging	1.00
X0023:2410089E03Rik	UTSW	15	8,247,031 (GRCm38)	missense	unknown
Z1177:2410089E03Rik	UTSW	15	8,209,989 (GRCm38)	missense	probably damaging	0.98
Z1177:2410089E03Rik	UTSW	15	8,174,972 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GTGTTGAGAAAACCTATCCTTTGT -3'
(R):5'- TAGATGCCTCAATTCTCTGTAAATGCT -3'

Sequencing Primer
(F):5'- ACCTATCCTTTGTAAATATTTCAGGC -3'
(R):5'- ATCCTCATTTTCTGAAGATGCTAAC -3'

Posted On

2015-09-24