Mutagenetix > Incidental Mutation

Incidental Mutation 'R8973:2410089E03Rik'

683274

Institutional Source

Beutler Lab

Gene Symbol

2410089E03Rik

Ensembl Gene

ENSMUSG00000039801

Gene Name

RIKEN cDNA 2410089E03 gene

Synonyms

b2b012Clo

MMRRC Submission

068807-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8973 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

8169106-8271158 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 8203793 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Arginine at position 1201 (W1201R)

Ref Sequence

ENSEMBL: ENSMUSP00000106247 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000110617
AA Change: W1201R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000106247
Gene: ENSMUSG00000039801
AA Change: W1201R

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

Meta Mutation Damage Score

0.4774

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.5%

Validation Efficiency

100% (77/77)

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: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700011I03Rik	T	G	18: 57,592,067 (GRCm38)	L123V	possibly damaging	Het
1810022K09Rik	C	T	3: 14,607,245 (GRCm38)	V97I	probably benign	Het
4930404N11Rik	T	C	10: 81,364,015 (GRCm38)	D129G	unknown	Het
Adamts16	A	T	13: 70,738,840 (GRCm38)	I975N	probably benign	Het
Adcy8	A	G	15: 64,699,135 (GRCm38)	*1250Q	probably null	Het
Anapc1	A	T	2: 128,664,032 (GRCm38)	I628N	probably damaging	Het
Ankrd39	C	T	1: 36,539,358 (GRCm38)		probably benign	Het
Ankub1	A	T	3: 57,665,511 (GRCm38)	S263R	possibly damaging	Het
Aoah	A	G	13: 20,840,155 (GRCm38)	I94V	probably benign	Het
Aox2	A	G	1: 58,289,954 (GRCm38)	D186G	probably benign	Het
Arap2	A	T	5: 62,698,325 (GRCm38)	C589*	probably null	Het
Armt1	T	C	10: 4,439,550 (GRCm38)	L69P	probably damaging	Het
Atxn7l3	T	A	11: 102,292,772 (GRCm38)	Y185F	probably benign	Het
BC067074	A	G	13: 113,319,759 (GRCm38)	T780A		Het
Cacna2d4	A	G	6: 119,241,181 (GRCm38)	D159G	probably damaging	Het
Camta2	C	A	11: 70,670,358 (GRCm38)	R1184L	probably benign	Het
Ccr7	G	A	11: 99,145,823 (GRCm38)	T91I	probably damaging	Het
Cdh9	A	G	15: 16,831,045 (GRCm38)	T323A	possibly damaging	Het
Cep250	C	T	2: 155,970,122 (GRCm38)	A446V	unknown	Het
Clec2e	C	A	6: 129,093,411 (GRCm38)	G216*	probably null	Het
Col25a1	T	C	3: 130,475,626 (GRCm38)	S176P	unknown	Het
Col4a3	A	C	1: 82,715,331 (GRCm38)	I1446L	probably benign	Het
Cse1l	A	G	2: 166,943,080 (GRCm38)	E823G	probably damaging	Het
Dchs2	A	G	3: 83,354,456 (GRCm38)	E2677G	possibly damaging	Het
Dis3l	T	C	9: 64,339,542 (GRCm38)	E77G	probably damaging	Het
Dnah6	T	C	6: 73,144,751 (GRCm38)	D1416G	probably benign	Het
Dpyd	T	C	3: 119,314,933 (GRCm38)		probably null	Het
Dst	A	G	1: 34,228,855 (GRCm38)	D3112G	probably damaging	Het
Dusp13	A	C	14: 21,734,906 (GRCm38)	N128K	probably benign	Het
Emilin2	T	G	17: 71,275,084 (GRCm38)	K216Q	probably benign	Het
Enam	T	C	5: 88,494,088 (GRCm38)	W254R	possibly damaging	Het
Esrrg	A	C	1: 188,198,750 (GRCm38)	N346T	possibly damaging	Het
Fbn2	C	T	18: 58,153,856 (GRCm38)	G244R	probably damaging	Het
Fbxw25	A	G	9: 109,650,064 (GRCm38)	L373P		Het
Gm21060	C	A	19: 61,296,928 (GRCm38)	V48L	possibly damaging	Het
Gm30302	A	T	13: 49,788,239 (GRCm38)	D80E	probably benign	Het
Gtpbp3	T	C	8: 71,491,162 (GRCm38)	V254A	possibly damaging	Het
H2-DMb2	A	G	17: 34,148,725 (GRCm38)	D171G	probably damaging	Het
Hrg	A	T	16: 22,959,218 (GRCm38)	T242S	probably benign	Het
Inf2	G	T	12: 112,607,515 (GRCm38)	C751F	unknown	Het
Krt13	A	T	11: 100,119,438 (GRCm38)	M239K	possibly damaging	Het
Lrrc72	A	G	12: 36,253,294 (GRCm38)	S7P	probably benign	Het
Matn2	A	G	15: 34,433,050 (GRCm38)	I867V	probably benign	Het
Mdh2	C	T	5: 135,790,165 (GRCm38)	A325V	possibly damaging	Het
Mki67	C	A	7: 135,695,635 (GRCm38)	A2557S	possibly damaging	Het
Mrpl16	A	T	19: 11,772,943 (GRCm38)	R64*	probably null	Het
Nav1	T	C	1: 135,584,725 (GRCm38)	D199G	probably benign	Het
Nbn	T	C	4: 15,986,585 (GRCm38)	V662A	probably damaging	Het
Nek10	G	A	14: 14,931,321 (GRCm38)		probably null	Het
Olfr141	C	A	2: 86,806,856 (GRCm38)	V48F	probably benign	Het
Olfr298	A	G	7: 86,489,279 (GRCm38)	S91P	probably damaging	Het
Olfr834	C	A	9: 18,988,678 (GRCm38)	S230*	probably null	Het
Olfr884	T	A	9: 38,047,543 (GRCm38)	V107D	possibly damaging	Het
Pcsk7	T	G	9: 45,927,642 (GRCm38)	S617R	probably benign	Het
Pde10a	C	A	17: 8,924,239 (GRCm38)	Q6K	probably benign	Het
Pigq	A	C	17: 25,932,167 (GRCm38)	M396R	probably damaging	Het
Pkhd1l1	T	A	15: 44,586,437 (GRCm38)	D3865E	probably damaging	Het
Prag1	C	T	8: 36,099,590 (GRCm38)		probably benign	Het
Rint1	A	G	5: 23,811,730 (GRCm38)	T498A	probably benign	Het
Rnf213	T	A	11: 119,461,930 (GRCm38)	F3921I		Het
Rpp14	A	G	14: 8,088,768 (GRCm38)	S95G	probably benign	Het
Ryk	T	G	9: 102,861,921 (GRCm38)	Y78D	possibly damaging	Het
Sez6	A	T	11: 77,974,571 (GRCm38)	Q678L	probably damaging	Het
Slc22a21	T	C	11: 53,969,576 (GRCm38)	K141E	probably damaging	Het
Slc30a5	A	T	13: 100,806,694 (GRCm38)	I609K	probably damaging	Het
Slc44a4	T	C	17: 34,921,562 (GRCm38)	F244L	probably damaging	Het
Susd5	T	C	9: 114,082,504 (GRCm38)	Y161H	possibly damaging	Het
Syne3	A	G	12: 104,959,395 (GRCm38)		probably null	Het
Tbcd	G	C	11: 121,496,853 (GRCm38)		probably benign	Het
Tmc1	A	T	19: 20,900,851 (GRCm38)	N93K	probably benign	Het
Tmem100	T	A	11: 90,035,476 (GRCm38)	M43K	probably benign	Het
Tmem131l	A	T	3: 83,928,732 (GRCm38)	V690D	probably damaging	Het
Trim8	A	G	19: 46,515,464 (GRCm38)	Q485R	possibly damaging	Het
Vmn2r63	A	T	7: 42,928,495 (GRCm38)	H206Q	probably benign	Het
Vmn2r77	T	A	7: 86,802,942 (GRCm38)	N443K	possibly damaging	Het
Zan	T	A	5: 137,389,316 (GRCm38)	I4878F	unknown	Het
Zfand4	A	G	6: 116,314,080 (GRCm38)	D344G	probably benign	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
R4581:2410089E03Rik	UTSW	15	8,171,798 (GRCm38)	missense	possibly damaging	0.85
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
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'- CTCTCAGTGAAAGTTGATTTTGTCTGC -3'
(R):5'- GCATCTCAGCCACAAACTGG -3'

Sequencing Primer
(F):5'- TCTGCTTTTTAAAAATGGCCTGG -3'
(R):5'- CACAAACTGGCCAGAGTTGTTTATTG -3'

Posted On

2021-10-11