Mutagenetix > Incidental Mutation

Incidental Mutation 'R7543:Cplane1'

584037

Institutional Source

Beutler Lab

Gene Symbol

Cplane1

Ensembl Gene

ENSMUSG00000039801

Gene Name

ciliogenesis and planar polarity effector 1

Synonyms

Hug, 2410089E03Rik, b2b012Clo, Jbts17

MMRRC Submission

045615-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7543 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

8198590-8300642 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 8254876 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 21 (I21T)

Ref Sequence

ENSEMBL: ENSMUSP00000154760 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000110617] [ENSMUST00000228039]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000110617

SMART Domains

Protein: ENSMUSP00000106247
Gene: ENSMUSG00000039801

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

Predicted Effect

unknown
Transcript: ENSMUST00000228039
AA Change: I21T

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

100% (71/71)

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
Aacs	T	A	5: 125,559,920 (GRCm39)	S54T	probably damaging	Het
Acsl5	G	A	19: 55,266,615 (GRCm39)	V59I		Het
Acss2	A	T	2: 155,391,755 (GRCm39)	I203F	probably damaging	Het
Add2	A	G	6: 86,083,207 (GRCm39)	N435S	probably damaging	Het
Afap1l1	T	C	18: 61,889,972 (GRCm39)	D88G	probably benign	Het
Ajm1	C	A	2: 25,467,410 (GRCm39)	A834S	possibly damaging	Het
Ank3	C	T	10: 69,786,846 (GRCm39)	T970M	possibly damaging	Het
Ap3b2	A	T	7: 81,115,894 (GRCm39)		probably null	Het
Apc2	A	G	10: 80,150,720 (GRCm39)	K1925E	possibly damaging	Het
Aspscr1	A	G	11: 120,600,249 (GRCm39)	N130D	unknown	Het
B3glct	A	G	5: 149,677,604 (GRCm39)	D411G	probably damaging	Het
Bard1	T	C	1: 71,114,589 (GRCm39)	K131E	probably damaging	Het
Bche	T	C	3: 73,609,066 (GRCm39)	D120G	probably damaging	Het
Brms1l	A	T	12: 55,914,997 (GRCm39)	D302V	probably damaging	Het
Ccdc191	T	A	16: 43,718,572 (GRCm39)	Y56*	probably null	Het
Cela3a	T	A	4: 137,129,883 (GRCm39)	H246L	probably damaging	Het
Col11a2	A	T	17: 34,269,430 (GRCm39)	D440V	unknown	Het
Dag1	C	T	9: 108,095,280 (GRCm39)	V71I	probably benign	Het
Ddx23	A	G	15: 98,556,139 (GRCm39)	S60P	unknown	Het
Dync1h1	G	T	12: 110,580,541 (GRCm39)	R134L	probably benign	Het
Dync1i1	T	C	6: 5,784,464 (GRCm39)	S103P	possibly damaging	Het
Erap1	T	A	13: 74,822,753 (GRCm39)	D755E	probably damaging	Het
Exosc8	T	C	3: 54,636,669 (GRCm39)	T221A	probably benign	Het
Fbxo4	T	C	15: 4,007,385 (GRCm39)	D93G	probably damaging	Het
Fzd5	A	G	1: 64,774,999 (GRCm39)	V254A	probably damaging	Het
Gbp3	T	C	3: 142,272,341 (GRCm39)	V281A	probably damaging	Het
Gcc2	T	A	10: 58,107,086 (GRCm39)	I774K	probably benign	Het
Gpr132	A	C	12: 112,815,822 (GRCm39)	C335G	probably benign	Het
Gpr162	G	T	6: 124,838,355 (GRCm39)	Y98*	probably null	Het
H2-T24	T	C	17: 36,325,743 (GRCm39)	T283A	possibly damaging	Het
Hoxc6	A	G	15: 102,918,186 (GRCm39)	Y50C	probably damaging	Het
Il4i1	A	G	7: 44,486,199 (GRCm39)	N53S	possibly damaging	Het
Iqcf3	T	C	9: 106,431,425 (GRCm39)	K60R	possibly damaging	Het
Kif24	A	T	4: 41,413,993 (GRCm39)	Y316*	probably null	Het
Krt18	A	G	15: 101,939,896 (GRCm39)	K365E	probably damaging	Het
Lrguk	T	A	6: 34,025,870 (GRCm39)	L222*	probably null	Het
Mbd1	T	G	18: 74,407,520 (GRCm39)	V210G	probably damaging	Het
Ms4a6b	A	G	19: 11,499,155 (GRCm39)	I90V	not run	Het
Muc16	A	G	9: 18,556,028 (GRCm39)	S3422P	unknown	Het
Mynn	G	A	3: 30,661,188 (GRCm39)	W90*	probably null	Het
Or5p5	T	A	7: 107,414,308 (GRCm39)	N172K	probably damaging	Het
Pdpr	T	A	8: 111,859,520 (GRCm39)	H687Q	probably damaging	Het
Pkd1	A	G	17: 24,814,227 (GRCm39)	E4199G	probably damaging	Het
Plekhg5	A	G	4: 152,192,491 (GRCm39)	E517G	probably damaging	Het
Plxna1	T	C	6: 89,299,837 (GRCm39)	D1644G	probably damaging	Het
Pon1	C	T	6: 5,168,400 (GRCm39)	V336M	possibly damaging	Het
Pop1	T	A	15: 34,530,593 (GRCm39)	L1027Q	probably damaging	Het
Pramel1	T	C	4: 143,124,993 (GRCm39)	S306P	probably damaging	Het
Prpsap2	A	T	11: 61,635,797 (GRCm39)	F168I	possibly damaging	Het
Rabgap1	T	A	2: 37,359,444 (GRCm39)	D2E	probably damaging	Het
Rgmb	A	T	17: 16,027,777 (GRCm39)	L314Q	probably damaging	Het
Ryr2	C	T	13: 11,653,317 (GRCm39)		probably null	Het
Samd4b	A	T	7: 28,113,711 (GRCm39)	S85T	probably benign	Het
Sfrp5	T	C	19: 42,187,302 (GRCm39)	D256G	possibly damaging	Het
Slc25a23	A	G	17: 57,365,106 (GRCm39)		probably null	Het
Sox5	A	G	6: 143,786,905 (GRCm39)	I589T	probably damaging	Het
Sybu	T	A	15: 44,546,848 (GRCm39)		probably null	Het
Syne2	A	G	12: 75,953,616 (GRCm39)	E515G	possibly damaging	Het
Tbc1d17	G	A	7: 44,495,503 (GRCm39)	A107V	probably benign	Het
Tcstv2c	A	C	13: 120,616,290 (GRCm39)	E43A	probably damaging	Het
Tex50	G	T	1: 160,984,817 (GRCm39)	T141K	possibly damaging	Het
Tmc7	A	G	7: 118,144,979 (GRCm39)	L527P	probably benign	Het
Tns4	T	A	11: 98,963,079 (GRCm39)	D547V	probably benign	Het
Topors	A	G	4: 40,268,312 (GRCm39)	S65P	probably damaging	Het
Trdc	T	A	14: 54,381,692 (GRCm39)	S126T		Het
Ttc27	A	T	17: 75,024,745 (GRCm39)		probably benign	Het
Wdfy3	A	C	5: 102,083,925 (GRCm39)	I787S	probably benign	Het
Zc3h11a	T	C	1: 133,554,768 (GRCm39)	D404G	possibly damaging	Het
Zfp799	A	G	17: 33,039,534 (GRCm39)	I244T	probably benign	Het
Zfp93	A	G	7: 23,974,533 (GRCm39)	T173A	probably benign	Het
Zfp953	T	A	13: 67,495,953 (GRCm39)	L29F	probably damaging	Het

Other mutations in Cplane1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00756:Cplane1	APN	15	8,293,931 (GRCm39)	splice site	probably benign
IGL00766:Cplane1	APN	15	8,281,648 (GRCm39)	missense	unknown
IGL01483:Cplane1	APN	15	8,216,591 (GRCm39)	missense	probably damaging	0.98
IGL01520:Cplane1	APN	15	8,251,395 (GRCm39)	missense	probably damaging	0.96
IGL01578:Cplane1	APN	15	8,300,194 (GRCm39)	missense	unknown
IGL01701:Cplane1	APN	15	8,232,741 (GRCm39)	splice site	probably benign
IGL01892:Cplane1	APN	15	8,271,749 (GRCm39)	splice site	probably benign
IGL01895:Cplane1	APN	15	8,258,591 (GRCm39)	missense	possibly damaging	0.63
IGL01922:Cplane1	APN	15	8,300,305 (GRCm39)	missense	unknown
IGL01978:Cplane1	APN	15	8,248,866 (GRCm39)	missense	probably damaging	0.98
IGL02031:Cplane1	APN	15	8,209,253 (GRCm39)	missense	probably damaging	0.99
IGL02318:Cplane1	APN	15	8,204,509 (GRCm39)	missense	probably damaging	0.98
IGL02321:Cplane1	APN	15	8,246,056 (GRCm39)	missense	probably benign	0.04
IGL02363:Cplane1	APN	15	8,247,921 (GRCm39)	missense	possibly damaging	0.68
IGL02404:Cplane1	APN	15	8,216,768 (GRCm39)	missense	possibly damaging	0.48
IGL02535:Cplane1	APN	15	8,204,322 (GRCm39)	missense	probably damaging	1.00
IGL02732:Cplane1	APN	15	8,209,375 (GRCm39)	missense	probably benign	0.03
IGL02895:Cplane1	APN	15	8,261,591 (GRCm39)	splice site	probably benign
IGL02903:Cplane1	APN	15	8,299,262 (GRCm39)	missense	unknown
IGL02903:Cplane1	APN	15	8,299,263 (GRCm39)	missense	unknown
IGL02979:Cplane1	APN	15	8,248,038 (GRCm39)	missense	possibly damaging	0.82
IGL03077:Cplane1	APN	15	8,242,279 (GRCm39)	splice site	probably benign
IGL03196:Cplane1	APN	15	8,230,826 (GRCm39)	missense	probably damaging	0.98
IGL03344:Cplane1	APN	15	8,216,942 (GRCm39)	missense	possibly damaging	0.63
IGL03368:Cplane1	APN	15	8,251,857 (GRCm39)	missense	probably benign	0.06
IGL03403:Cplane1	APN	15	8,230,826 (GRCm39)	missense	probably damaging	0.98
agnes	UTSW	15	8,276,422 (GRCm39)	nonsense	probably null
dei	UTSW	15	8,215,649 (GRCm39)	missense	probably damaging	1.00
R0015:Cplane1	UTSW	15	8,215,668 (GRCm39)	missense	probably damaging	1.00
R0015:Cplane1	UTSW	15	8,215,668 (GRCm39)	missense	probably damaging	1.00
R0101:Cplane1	UTSW	15	8,250,444 (GRCm39)	missense	probably benign	0.00
R0105:Cplane1	UTSW	15	8,216,876 (GRCm39)	missense	probably benign
R0105:Cplane1	UTSW	15	8,216,876 (GRCm39)	missense	probably benign
R0165:Cplane1	UTSW	15	8,245,866 (GRCm39)	missense	probably damaging	1.00
R0306:Cplane1	UTSW	15	8,209,373 (GRCm39)	missense	probably damaging	1.00
R0433:Cplane1	UTSW	15	8,246,046 (GRCm39)	missense	probably benign	0.00
R0491:Cplane1	UTSW	15	8,211,727 (GRCm39)	missense	probably damaging	1.00
R0523:Cplane1	UTSW	15	8,223,870 (GRCm39)	missense	probably damaging	1.00
R0571:Cplane1	UTSW	15	8,289,277 (GRCm39)	missense	unknown
R0679:Cplane1	UTSW	15	8,252,606 (GRCm39)	missense	probably benign	0.39
R0704:Cplane1	UTSW	15	8,239,567 (GRCm39)	missense	possibly damaging	0.93
R0707:Cplane1	UTSW	15	8,287,805 (GRCm39)	missense	unknown
R0715:Cplane1	UTSW	15	8,252,576 (GRCm39)	missense	probably benign	0.14
R0762:Cplane1	UTSW	15	8,247,900 (GRCm39)	unclassified	probably benign
R0830:Cplane1	UTSW	15	8,276,669 (GRCm39)	missense	unknown
R0924:Cplane1	UTSW	15	8,280,554 (GRCm39)	splice site	probably benign
R1071:Cplane1	UTSW	15	8,247,910 (GRCm39)	missense	probably benign	0.20
R1184:Cplane1	UTSW	15	8,245,971 (GRCm39)	missense	probably benign
R1224:Cplane1	UTSW	15	8,207,869 (GRCm39)	missense	probably benign	0.06
R1416:Cplane1	UTSW	15	8,276,422 (GRCm39)	nonsense	probably null
R1428:Cplane1	UTSW	15	8,248,853 (GRCm39)	missense	possibly damaging	0.83
R1487:Cplane1	UTSW	15	8,215,715 (GRCm39)	missense	probably damaging	1.00
R1641:Cplane1	UTSW	15	8,258,443 (GRCm39)	missense	probably benign	0.41
R1652:Cplane1	UTSW	15	8,230,630 (GRCm39)	missense	probably damaging	1.00
R1688:Cplane1	UTSW	15	8,258,093 (GRCm39)	missense	probably benign	0.00
R1715:Cplane1	UTSW	15	8,256,384 (GRCm39)	splice site	probably null
R1820:Cplane1	UTSW	15	8,299,129 (GRCm39)	missense	unknown
R1863:Cplane1	UTSW	15	8,258,077 (GRCm39)	missense	probably benign	0.00
R1940:Cplane1	UTSW	15	8,263,336 (GRCm39)	missense	probably damaging	0.98
R1967:Cplane1	UTSW	15	8,232,904 (GRCm39)	missense	probably benign	0.09
R2064:Cplane1	UTSW	15	8,215,649 (GRCm39)	missense	probably damaging	1.00
R2076:Cplane1	UTSW	15	8,248,741 (GRCm39)	missense	possibly damaging	0.93
R2163:Cplane1	UTSW	15	8,232,735 (GRCm39)	splice site	probably null
R2208:Cplane1	UTSW	15	8,223,887 (GRCm39)	missense	probably benign	0.33
R2504:Cplane1	UTSW	15	8,248,700 (GRCm39)	missense	probably damaging	0.99
R2568:Cplane1	UTSW	15	8,230,753 (GRCm39)	missense	possibly damaging	0.70
R2845:Cplane1	UTSW	15	8,245,864 (GRCm39)	missense	probably damaging	1.00
R2913:Cplane1	UTSW	15	8,300,169 (GRCm39)	missense	unknown
R3056:Cplane1	UTSW	15	8,280,491 (GRCm39)	missense	unknown
R3706:Cplane1	UTSW	15	8,289,300 (GRCm39)	missense	unknown
R3707:Cplane1	UTSW	15	8,289,300 (GRCm39)	missense	unknown
R3870:Cplane1	UTSW	15	8,247,948 (GRCm39)	missense	probably damaging	0.98
R3877:Cplane1	UTSW	15	8,251,427 (GRCm39)	missense	probably benign
R3886:Cplane1	UTSW	15	8,201,289 (GRCm39)	missense	probably damaging	0.98
R4057:Cplane1	UTSW	15	8,248,509 (GRCm39)	missense	probably benign	0.08
R4090:Cplane1	UTSW	15	8,241,842 (GRCm39)	splice site	probably null
R4362:Cplane1	UTSW	15	8,300,229 (GRCm39)	missense	unknown
R4363:Cplane1	UTSW	15	8,300,229 (GRCm39)	missense	unknown
R4445:Cplane1	UTSW	15	8,281,672 (GRCm39)	missense	unknown
R4581:Cplane1	UTSW	15	8,201,282 (GRCm39)	missense	possibly damaging	0.85
R4587:Cplane1	UTSW	15	8,230,636 (GRCm39)	missense	possibly damaging	0.50
R4659:Cplane1	UTSW	15	8,245,760 (GRCm39)	intron	probably benign
R4663:Cplane1	UTSW	15	8,247,939 (GRCm39)	missense	probably benign	0.31
R4779:Cplane1	UTSW	15	8,248,322 (GRCm39)	missense	probably benign	0.04
R4812:Cplane1	UTSW	15	8,230,607 (GRCm39)	splice site	probably null
R4850:Cplane1	UTSW	15	8,292,422 (GRCm39)	missense	unknown
R4896:Cplane1	UTSW	15	8,251,421 (GRCm39)	missense	probably benign	0.00
R5273:Cplane1	UTSW	15	8,292,422 (GRCm39)	missense	unknown
R5273:Cplane1	UTSW	15	8,273,825 (GRCm39)	missense	probably damaging	0.98
R5303:Cplane1	UTSW	15	8,290,174 (GRCm39)	splice site	probably null
R5307:Cplane1	UTSW	15	8,290,174 (GRCm39)	splice site	probably null
R5308:Cplane1	UTSW	15	8,290,174 (GRCm39)	splice site	probably null
R5373:Cplane1	UTSW	15	8,300,287 (GRCm39)	missense	unknown
R5374:Cplane1	UTSW	15	8,300,287 (GRCm39)	missense	unknown
R5386:Cplane1	UTSW	15	8,223,897 (GRCm39)	missense	probably damaging	1.00
R5534:Cplane1	UTSW	15	8,258,319 (GRCm39)	missense	probably benign	0.06
R5720:Cplane1	UTSW	15	8,233,171 (GRCm39)	missense	probably benign	0.35
R5891:Cplane1	UTSW	15	8,218,073 (GRCm39)	missense	probably benign	0.00
R5932:Cplane1	UTSW	15	8,274,079 (GRCm39)	splice site	probably null
R6053:Cplane1	UTSW	15	8,217,945 (GRCm39)	missense	probably benign	0.35
R6166:Cplane1	UTSW	15	8,216,044 (GRCm39)	missense	probably benign	0.00
R6245:Cplane1	UTSW	15	8,207,902 (GRCm39)	missense	probably benign	0.01
R6246:Cplane1	UTSW	15	8,239,498 (GRCm39)	missense	probably damaging	1.00
R6541:Cplane1	UTSW	15	8,248,779 (GRCm39)	missense	possibly damaging	0.48
R6622:Cplane1	UTSW	15	8,273,706 (GRCm39)	missense	probably damaging	0.98
R6707:Cplane1	UTSW	15	8,252,606 (GRCm39)	missense	probably benign	0.39
R6729:Cplane1	UTSW	15	8,218,085 (GRCm39)	splice site	probably null
R6805:Cplane1	UTSW	15	8,273,790 (GRCm39)	missense	probably benign	0.07
R6806:Cplane1	UTSW	15	8,216,342 (GRCm39)	missense	possibly damaging	0.55
R6813:Cplane1	UTSW	15	8,258,766 (GRCm39)	missense	probably benign
R6830:Cplane1	UTSW	15	8,205,668 (GRCm39)	missense	probably benign	0.04
R6845:Cplane1	UTSW	15	8,251,388 (GRCm39)	missense	possibly damaging	0.84
R6894:Cplane1	UTSW	15	8,216,852 (GRCm39)	missense	probably damaging	0.99
R6970:Cplane1	UTSW	15	8,217,032 (GRCm39)	missense	probably benign	0.01
R6991:Cplane1	UTSW	15	8,281,690 (GRCm39)	missense	unknown
R7003:Cplane1	UTSW	15	8,258,246 (GRCm39)	missense	probably damaging	0.99
R7088:Cplane1	UTSW	15	8,248,431 (GRCm39)	missense	probably benign	0.16
R7104:Cplane1	UTSW	15	8,223,928 (GRCm39)	missense	possibly damaging	0.83
R7311:Cplane1	UTSW	15	8,210,399 (GRCm39)	missense	probably damaging	1.00
R7374:Cplane1	UTSW	15	8,276,731 (GRCm39)	missense	unknown
R7446:Cplane1	UTSW	15	8,261,564 (GRCm39)	missense	probably damaging	0.98
R7539:Cplane1	UTSW	15	8,230,728 (GRCm39)	missense	probably benign	0.19
R7558:Cplane1	UTSW	15	8,254,851 (GRCm39)	missense	unknown
R7629:Cplane1	UTSW	15	8,256,551 (GRCm39)	nonsense	probably null
R7635:Cplane1	UTSW	15	8,256,404 (GRCm39)	missense	probably benign	0.01
R7644:Cplane1	UTSW	15	8,252,611 (GRCm39)	missense	probably benign	0.00
R7705:Cplane1	UTSW	15	8,211,736 (GRCm39)	missense	probably damaging	1.00
R7752:Cplane1	UTSW	15	8,299,190 (GRCm39)	missense	unknown
R7754:Cplane1	UTSW	15	8,273,310 (GRCm39)	missense	possibly damaging	0.53
R7757:Cplane1	UTSW	15	8,281,711 (GRCm39)	missense	unknown
R7836:Cplane1	UTSW	15	8,233,241 (GRCm39)	missense	probably damaging	0.97
R7875:Cplane1	UTSW	15	8,239,446 (GRCm39)	missense	probably benign	0.18
R7901:Cplane1	UTSW	15	8,299,190 (GRCm39)	missense	unknown
R7983:Cplane1	UTSW	15	8,251,299 (GRCm39)	missense	probably benign	0.01
R8030:Cplane1	UTSW	15	8,259,787 (GRCm39)	missense	probably damaging	1.00
R8088:Cplane1	UTSW	15	8,215,802 (GRCm39)	missense	probably benign	0.00
R8231:Cplane1	UTSW	15	8,248,511 (GRCm39)	missense	probably benign	0.16
R8443:Cplane1	UTSW	15	8,230,635 (GRCm39)	missense	probably benign	0.03
R8480:Cplane1	UTSW	15	8,216,942 (GRCm39)	missense	possibly damaging	0.63
R8693:Cplane1	UTSW	15	8,258,492 (GRCm39)	missense	probably benign	0.15
R8785:Cplane1	UTSW	15	8,204,244 (GRCm39)	missense	probably benign	0.39
R8791:Cplane1	UTSW	15	8,216,744 (GRCm39)	missense	probably damaging	1.00
R8822:Cplane1	UTSW	15	8,201,262 (GRCm39)	missense	probably damaging	1.00
R8831:Cplane1	UTSW	15	8,211,620 (GRCm39)	missense	probably benign	0.09
R8932:Cplane1	UTSW	15	8,223,859 (GRCm39)	missense	probably damaging	1.00
R8968:Cplane1	UTSW	15	8,230,765 (GRCm39)	missense	possibly damaging	0.84
R8973:Cplane1	UTSW	15	8,233,277 (GRCm39)	missense	probably damaging	1.00
R9036:Cplane1	UTSW	15	8,252,622 (GRCm39)	missense	possibly damaging	0.63
R9134:Cplane1	UTSW	15	8,228,716 (GRCm39)	missense	probably damaging	0.99
R9197:Cplane1	UTSW	15	8,280,536 (GRCm39)	missense	unknown
R9259:Cplane1	UTSW	15	8,232,787 (GRCm39)	missense	possibly damaging	0.82
R9269:Cplane1	UTSW	15	8,248,500 (GRCm39)	missense	probably damaging	0.97
R9294:Cplane1	UTSW	15	8,232,811 (GRCm39)	missense	probably benign	0.00
R9328:Cplane1	UTSW	15	8,215,692 (GRCm39)	missense	probably damaging	1.00
R9563:Cplane1	UTSW	15	8,216,563 (GRCm39)	missense	probably benign	0.20
R9680:Cplane1	UTSW	15	8,231,785 (GRCm39)	missense	possibly damaging	0.68
R9721:Cplane1	UTSW	15	8,254,893 (GRCm39)	missense	unknown
R9779:Cplane1	UTSW	15	8,230,786 (GRCm39)	missense	possibly damaging	0.93
R9780:Cplane1	UTSW	15	8,258,123 (GRCm39)	missense	probably benign	0.00
U24488:Cplane1	UTSW	15	8,211,694 (GRCm39)	missense	probably damaging	1.00
X0023:Cplane1	UTSW	15	8,276,515 (GRCm39)	missense	unknown
Z1177:Cplane1	UTSW	15	8,239,473 (GRCm39)	missense	probably damaging	0.98
Z1177:Cplane1	UTSW	15	8,204,456 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATTAAGCCATGGAGTCTTTGCTG -3'
(R):5'- AACGGTGTGCCTACATTGC -3'

Sequencing Primer
(F):5'- CAGACTGTGATTATGAGCTAAGTGC -3'
(R):5'- AACGGTGTGCCTACATTGCTTTTTC -3'

Posted On

2019-10-17