Mutagenetix > Incidental Mutation

Incidental Mutation 'R9294:Cplane1'

704495

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

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R9294 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

8169106-8271158 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 8203327 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 1110 (V1110A)

Ref Sequence

ENSEMBL: ENSMUSP00000106247 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000110617
AA Change: V1110A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000106247
Gene: ENSMUSG00000039801
AA Change: V1110A

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: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.8%

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: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700067K01Rik	A	G	8: 84,003,379 (GRCm38)	Y165C	probably damaging	Het
Abcb11	T	A	2: 69,265,496 (GRCm38)	K833N	possibly damaging	Het
Abcb1a	T	A	5: 8,686,171 (GRCm38)	M188K	probably benign	Het
Akap1	A	T	11: 88,837,140 (GRCm38)	V672D	probably damaging	Het
Anapc4	A	G	5: 52,864,525 (GRCm38)	T650A	possibly damaging	Het
Ash1l	C	A	3: 88,982,990 (GRCm38)	S725R	possibly damaging	Het
Axdnd1	T	A	1: 156,420,347 (GRCm38)	K28*	probably null	Het
C8b	C	A	4: 104,786,995 (GRCm38)	H286Q	probably benign	Het
Cacna2d1	A	G	5: 16,012,398 (GRCm38)	K34E	probably damaging	Het
Ccdc14	T	A	16: 34,697,358 (GRCm38)	H154Q	probably damaging	Het
Ccdc184	A	G	15: 98,168,512 (GRCm38)	D66G	probably damaging	Het
Ccdc62	A	G	5: 123,954,709 (GRCm38)	I586V	possibly damaging	Het
Cfap20dc	A	G	14: 8,578,361 (GRCm38)	I127T	possibly damaging	Het
Chadl	A	T	15: 81,694,490 (GRCm38)	C313S	probably damaging	Het
Clec14a	C	A	12: 58,268,750 (GRCm38)	A29S	probably damaging	Het
Col26a1	C	T	5: 136,757,754 (GRCm38)	G161D	probably benign	Het
Ctbp2	A	G	7: 133,014,232 (GRCm38)	S325P	probably damaging	Het
Dcaf13	A	G	15: 39,130,292 (GRCm38)	D260G	possibly damaging	Het
Dele1	T	G	18: 38,261,076 (GRCm38)	L442R	probably damaging	Het
Dhx37	G	A	5: 125,422,672 (GRCm38)	P575L	probably benign	Het
Dnajc6	T	C	4: 101,550,857 (GRCm38)		probably null	Het
Eapp	T	C	12: 54,690,276 (GRCm38)	T145A	unknown	Het
Efcab5	A	G	11: 77,121,238 (GRCm38)	M730T	probably benign	Het
Eif4g3	T	A	4: 138,190,657 (GRCm38)	D1305E	probably damaging	Het
Endou	A	T	15: 97,712,065 (GRCm38)	V450E	probably benign	Het
F10	A	T	8: 13,048,177 (GRCm38)	K127*	probably null	Het
Fbxw21	A	G	9: 109,143,762 (GRCm38)	F368S	probably damaging	Het
Fezf1	A	T	6: 23,245,798 (GRCm38)	L456Q	possibly damaging	Het
Foxo3	C	T	10: 42,197,025 (GRCm38)	V499M	probably damaging	Het
Fyco1	A	C	9: 123,794,813 (GRCm38)	C1384G	probably damaging	Het
Galnt6	G	T	15: 100,704,151 (GRCm38)	S258R	possibly damaging	Het
Gemin5	A	G	11: 58,137,748 (GRCm38)	V882A	probably benign	Het
Gm10750	A	G	2: 149,016,187 (GRCm38)	L48P	unknown	Het
Gm11639	A	G	11: 104,831,300 (GRCm38)	I1913V	probably benign	Het
Gm16503	T	A	4: 147,541,114 (GRCm38)	F22I	unknown	Het
Hdac10	A	G	15: 89,126,277 (GRCm38)	C281R	probably damaging	Het
Hikeshi	T	C	7: 89,935,760 (GRCm38)	S79G	probably damaging	Het
Ifitm2	AG	A	7: 140,955,901 (GRCm38)		probably null	Het
Itpr3	A	G	17: 27,111,217 (GRCm38)	E1603G	probably damaging	Het
Lrrc37a	A	T	11: 103,504,533 (GRCm38)	V22E	probably benign	Het
Man1a	C	T	10: 53,933,491 (GRCm38)		probably null	Het
Mdga1	A	G	17: 29,839,897 (GRCm38)	L5P	probably damaging	Het
Mup6	A	G	4: 60,004,838 (GRCm38)	I76M	probably benign	Het
Nbea	A	T	3: 56,091,092 (GRCm38)	M98K	probably benign	Het
Nckap1l	A	G	15: 103,473,539 (GRCm38)	E454G	probably damaging	Het
Notch3	A	T	17: 32,143,691 (GRCm38)	L1320Q	probably benign	Het
Nrn1	A	T	13: 36,726,674 (GRCm38)	L128H	probably damaging	Het
Numa1	T	C	7: 101,995,416 (GRCm38)	S200P	possibly damaging	Het
Numa1	A	G	7: 102,012,796 (GRCm38)	D1898G	probably damaging	Het
Or10ag58	G	A	2: 87,434,666 (GRCm38)	A60T	probably benign	Het
Or1af1	T	C	2: 37,220,110 (GRCm38)	I207T	possibly damaging	Het
Or2ag18	A	T	7: 106,806,398 (GRCm38)	S21R	possibly damaging	Het
Or5i1	A	C	2: 87,782,523 (GRCm38)		probably null	Het
P2ry6	A	T	7: 100,938,926 (GRCm38)	Y75*	probably null	Het
Pbrm1	T	A	14: 31,084,803 (GRCm38)	C1062*	probably null	Het
Pcdh15	A	G	10: 74,643,728 (GRCm38)	E557G	unknown	Het
Pcdh7	T	C	5: 57,721,335 (GRCm38)	L744P	probably benign	Het
Plekhg3	A	T	12: 76,562,278 (GRCm38)	I142L	possibly damaging	Het
Plk4	C	T	3: 40,811,891 (GRCm38)	H695Y	probably damaging	Het
Pms1	T	C	1: 53,208,057 (GRCm38)	H243R	probably benign	Het
Prdm14	T	C	1: 13,122,483 (GRCm38)	D344G	possibly damaging	Het
R3hdml	A	G	2: 163,502,332 (GRCm38)	I214V	probably benign	Het
Rab11fip5	T	C	6: 85,348,710 (GRCm38)	N238S	probably benign	Het
Resf1	T	A	6: 149,326,432 (GRCm38)	N325K	probably benign	Het
Sacs	T	A	14: 61,240,319 (GRCm38)	Y732N	possibly damaging	Het
Scfd1	T	A	12: 51,393,866 (GRCm38)	M187K	possibly damaging	Het
Serpina1d	A	G	12: 103,767,998 (GRCm38)	C16R	probably damaging	Het
Slc2a12	T	C	10: 22,665,095 (GRCm38)	I283T	possibly damaging	Het
Smarca5	A	G	8: 80,719,803 (GRCm38)	Y423H	probably damaging	Het
Srrm3	C	A	5: 135,868,261 (GRCm38)	A366E	unknown	Het
St7	A	T	6: 17,844,914 (GRCm38)	K134*	probably null	Het
St8sia5	T	G	18: 77,254,829 (GRCm38)	C412G	probably damaging	Het
Tanc2	A	T	11: 105,886,458 (GRCm38)	I821F	probably damaging	Het
Tbrg4	A	G	11: 6,624,204 (GRCm38)	M6T	probably benign	Het
Tcf20	A	T	15: 82,852,696 (GRCm38)	I1518N	probably benign	Het
Tctn3	A	G	19: 40,607,276 (GRCm38)	V355A	probably benign	Het
Tenm2	A	T	11: 36,024,500 (GRCm38)	F2070Y	probably damaging	Het
Tex2	A	G	11: 106,568,535 (GRCm38)	V23A	probably damaging	Het
Thrsp	C	G	7: 97,417,074 (GRCm38)	E144Q	probably damaging	Het
Tmt1a	A	G	15: 100,313,133 (GRCm38)	E213G	probably damaging	Het
Top2a	A	C	11: 99,001,078 (GRCm38)	S1114A	probably benign	Het
Tpm1	A	G	9: 67,029,716 (GRCm38)	Y267H	probably benign	Het
Txndc2	G	T	17: 65,639,024 (GRCm38)	P53T	unknown	Het
Ugt2b36	A	T	5: 87,081,017 (GRCm38)	I389N	probably damaging	Het
Virma	C	T	4: 11,513,507 (GRCm38)	R454*	probably null	Het
Vwa3b	T	A	1: 37,035,801 (GRCm38)	H16Q	probably damaging	Het
Zbp1	A	G	2: 173,210,643 (GRCm38)	M240T	possibly damaging	Het

Other mutations in Cplane1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00756:Cplane1	APN	15	8,264,447 (GRCm38)	splice site	probably benign
IGL00766:Cplane1	APN	15	8,252,164 (GRCm38)	missense	unknown
IGL01483:Cplane1	APN	15	8,187,107 (GRCm38)	missense	probably damaging	0.98
IGL01520:Cplane1	APN	15	8,221,911 (GRCm38)	missense	probably damaging	0.96
IGL01578:Cplane1	APN	15	8,270,710 (GRCm38)	missense	unknown
IGL01701:Cplane1	APN	15	8,203,257 (GRCm38)	splice site	probably benign
IGL01892:Cplane1	APN	15	8,242,265 (GRCm38)	splice site	probably benign
IGL01895:Cplane1	APN	15	8,229,107 (GRCm38)	missense	possibly damaging	0.63
IGL01922:Cplane1	APN	15	8,270,821 (GRCm38)	missense	unknown
IGL01978:Cplane1	APN	15	8,219,382 (GRCm38)	missense	probably damaging	0.98
IGL02031:Cplane1	APN	15	8,179,769 (GRCm38)	missense	probably damaging	0.99
IGL02318:Cplane1	APN	15	8,175,025 (GRCm38)	missense	probably damaging	0.98
IGL02321:Cplane1	APN	15	8,216,572 (GRCm38)	missense	probably benign	0.04
IGL02363:Cplane1	APN	15	8,218,437 (GRCm38)	missense	possibly damaging	0.68
IGL02404:Cplane1	APN	15	8,187,284 (GRCm38)	missense	possibly damaging	0.48
IGL02535:Cplane1	APN	15	8,174,838 (GRCm38)	missense	probably damaging	1.00
IGL02732:Cplane1	APN	15	8,179,891 (GRCm38)	missense	probably benign	0.03
IGL02895:Cplane1	APN	15	8,232,107 (GRCm38)	splice site	probably benign
IGL02903:Cplane1	APN	15	8,269,778 (GRCm38)	missense	unknown
IGL02903:Cplane1	APN	15	8,269,779 (GRCm38)	missense	unknown
IGL02979:Cplane1	APN	15	8,218,554 (GRCm38)	missense	possibly damaging	0.82
IGL03077:Cplane1	APN	15	8,212,795 (GRCm38)	splice site	probably benign
IGL03196:Cplane1	APN	15	8,201,342 (GRCm38)	missense	probably damaging	0.98
IGL03344:Cplane1	APN	15	8,187,458 (GRCm38)	missense	possibly damaging	0.63
IGL03368:Cplane1	APN	15	8,222,373 (GRCm38)	missense	probably benign	0.06
IGL03403:Cplane1	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:Cplane1	UTSW	15	8,186,184 (GRCm38)	missense	probably damaging	1.00
R0015:Cplane1	UTSW	15	8,186,184 (GRCm38)	missense	probably damaging	1.00
R0101:Cplane1	UTSW	15	8,220,960 (GRCm38)	missense	probably benign	0.00
R0105:Cplane1	UTSW	15	8,187,392 (GRCm38)	missense	probably benign
R0105:Cplane1	UTSW	15	8,187,392 (GRCm38)	missense	probably benign
R0165:Cplane1	UTSW	15	8,216,382 (GRCm38)	missense	probably damaging	1.00
R0306:Cplane1	UTSW	15	8,179,889 (GRCm38)	missense	probably damaging	1.00
R0433:Cplane1	UTSW	15	8,216,562 (GRCm38)	missense	probably benign	0.00
R0491:Cplane1	UTSW	15	8,182,243 (GRCm38)	missense	probably damaging	1.00
R0523:Cplane1	UTSW	15	8,194,386 (GRCm38)	missense	probably damaging	1.00
R0571:Cplane1	UTSW	15	8,259,793 (GRCm38)	missense	unknown
R0679:Cplane1	UTSW	15	8,223,122 (GRCm38)	missense	probably benign	0.39
R0704:Cplane1	UTSW	15	8,210,083 (GRCm38)	missense	possibly damaging	0.93
R0707:Cplane1	UTSW	15	8,258,321 (GRCm38)	missense	unknown
R0715:Cplane1	UTSW	15	8,223,092 (GRCm38)	missense	probably benign	0.14
R0762:Cplane1	UTSW	15	8,218,416 (GRCm38)	unclassified	probably benign
R0830:Cplane1	UTSW	15	8,247,185 (GRCm38)	missense	unknown
R0924:Cplane1	UTSW	15	8,251,070 (GRCm38)	splice site	probably benign
R1071:Cplane1	UTSW	15	8,218,426 (GRCm38)	missense	probably benign	0.20
R1184:Cplane1	UTSW	15	8,216,487 (GRCm38)	missense	probably benign
R1224:Cplane1	UTSW	15	8,178,385 (GRCm38)	missense	probably benign	0.06
R1416:Cplane1	UTSW	15	8,246,938 (GRCm38)	nonsense	probably null
R1428:Cplane1	UTSW	15	8,219,369 (GRCm38)	missense	possibly damaging	0.83
R1487:Cplane1	UTSW	15	8,186,231 (GRCm38)	missense	probably damaging	1.00
R1641:Cplane1	UTSW	15	8,228,959 (GRCm38)	missense	probably benign	0.41
R1652:Cplane1	UTSW	15	8,201,146 (GRCm38)	missense	probably damaging	1.00
R1688:Cplane1	UTSW	15	8,228,609 (GRCm38)	missense	probably benign	0.00
R1715:Cplane1	UTSW	15	8,226,900 (GRCm38)	splice site	probably null
R1820:Cplane1	UTSW	15	8,269,645 (GRCm38)	missense	unknown
R1863:Cplane1	UTSW	15	8,228,593 (GRCm38)	missense	probably benign	0.00
R1940:Cplane1	UTSW	15	8,233,852 (GRCm38)	missense	probably damaging	0.98
R1967:Cplane1	UTSW	15	8,203,420 (GRCm38)	missense	probably benign	0.09
R2064:Cplane1	UTSW	15	8,186,165 (GRCm38)	missense	probably damaging	1.00
R2076:Cplane1	UTSW	15	8,219,257 (GRCm38)	missense	possibly damaging	0.93
R2163:Cplane1	UTSW	15	8,203,251 (GRCm38)	splice site	probably null
R2208:Cplane1	UTSW	15	8,194,403 (GRCm38)	missense	probably benign	0.33
R2504:Cplane1	UTSW	15	8,219,216 (GRCm38)	missense	probably damaging	0.99
R2568:Cplane1	UTSW	15	8,201,269 (GRCm38)	missense	possibly damaging	0.70
R2845:Cplane1	UTSW	15	8,216,380 (GRCm38)	missense	probably damaging	1.00
R2913:Cplane1	UTSW	15	8,270,685 (GRCm38)	missense	unknown
R3056:Cplane1	UTSW	15	8,251,007 (GRCm38)	missense	unknown
R3706:Cplane1	UTSW	15	8,259,816 (GRCm38)	missense	unknown
R3707:Cplane1	UTSW	15	8,259,816 (GRCm38)	missense	unknown
R3870:Cplane1	UTSW	15	8,218,464 (GRCm38)	missense	probably damaging	0.98
R3877:Cplane1	UTSW	15	8,221,943 (GRCm38)	missense	probably benign
R3886:Cplane1	UTSW	15	8,171,805 (GRCm38)	missense	probably damaging	0.98
R4057:Cplane1	UTSW	15	8,219,025 (GRCm38)	missense	probably benign	0.08
R4090:Cplane1	UTSW	15	8,212,358 (GRCm38)	splice site	probably null
R4362:Cplane1	UTSW	15	8,270,745 (GRCm38)	missense	unknown
R4363:Cplane1	UTSW	15	8,270,745 (GRCm38)	missense	unknown
R4445:Cplane1	UTSW	15	8,252,188 (GRCm38)	missense	unknown
R4581:Cplane1	UTSW	15	8,171,798 (GRCm38)	missense	possibly damaging	0.85
R4587:Cplane1	UTSW	15	8,201,152 (GRCm38)	missense	possibly damaging	0.50
R4659:Cplane1	UTSW	15	8,216,276 (GRCm38)	intron	probably benign
R4663:Cplane1	UTSW	15	8,218,455 (GRCm38)	missense	probably benign	0.31
R4779:Cplane1	UTSW	15	8,218,838 (GRCm38)	missense	probably benign	0.04
R4812:Cplane1	UTSW	15	8,201,123 (GRCm38)	splice site	probably null
R4850:Cplane1	UTSW	15	8,262,938 (GRCm38)	missense	unknown
R4896:Cplane1	UTSW	15	8,221,937 (GRCm38)	missense	probably benign	0.00
R5273:Cplane1	UTSW	15	8,262,938 (GRCm38)	missense	unknown
R5273:Cplane1	UTSW	15	8,244,341 (GRCm38)	missense	probably damaging	0.98
R5303:Cplane1	UTSW	15	8,260,690 (GRCm38)	splice site	probably null
R5307:Cplane1	UTSW	15	8,260,690 (GRCm38)	splice site	probably null
R5308:Cplane1	UTSW	15	8,260,690 (GRCm38)	splice site	probably null
R5373:Cplane1	UTSW	15	8,270,803 (GRCm38)	missense	unknown
R5374:Cplane1	UTSW	15	8,270,803 (GRCm38)	missense	unknown
R5386:Cplane1	UTSW	15	8,194,413 (GRCm38)	missense	probably damaging	1.00
R5534:Cplane1	UTSW	15	8,228,835 (GRCm38)	missense	probably benign	0.06
R5720:Cplane1	UTSW	15	8,203,687 (GRCm38)	missense	probably benign	0.35
R5891:Cplane1	UTSW	15	8,188,589 (GRCm38)	missense	probably benign	0.00
R5932:Cplane1	UTSW	15	8,244,595 (GRCm38)	splice site	probably null
R6053:Cplane1	UTSW	15	8,188,461 (GRCm38)	missense	probably benign	0.35
R6166:Cplane1	UTSW	15	8,186,560 (GRCm38)	missense	probably benign	0.00
R6245:Cplane1	UTSW	15	8,178,418 (GRCm38)	missense	probably benign	0.01
R6246:Cplane1	UTSW	15	8,210,014 (GRCm38)	missense	probably damaging	1.00
R6541:Cplane1	UTSW	15	8,219,295 (GRCm38)	missense	possibly damaging	0.48
R6622:Cplane1	UTSW	15	8,244,222 (GRCm38)	missense	probably damaging	0.98
R6707:Cplane1	UTSW	15	8,223,122 (GRCm38)	missense	probably benign	0.39
R6729:Cplane1	UTSW	15	8,188,601 (GRCm38)	splice site	probably null
R6805:Cplane1	UTSW	15	8,244,306 (GRCm38)	missense	probably benign	0.07
R6806:Cplane1	UTSW	15	8,186,858 (GRCm38)	missense	possibly damaging	0.55
R6813:Cplane1	UTSW	15	8,229,282 (GRCm38)	missense	probably benign
R6830:Cplane1	UTSW	15	8,176,184 (GRCm38)	missense	probably benign	0.04
R6845:Cplane1	UTSW	15	8,221,904 (GRCm38)	missense	possibly damaging	0.84
R6894:Cplane1	UTSW	15	8,187,368 (GRCm38)	missense	probably damaging	0.99
R6970:Cplane1	UTSW	15	8,187,548 (GRCm38)	missense	probably benign	0.01
R6991:Cplane1	UTSW	15	8,252,206 (GRCm38)	missense	unknown
R7003:Cplane1	UTSW	15	8,228,762 (GRCm38)	missense	probably damaging	0.99
R7088:Cplane1	UTSW	15	8,218,947 (GRCm38)	missense	probably benign	0.16
R7104:Cplane1	UTSW	15	8,194,444 (GRCm38)	missense	possibly damaging	0.83
R7311:Cplane1	UTSW	15	8,180,915 (GRCm38)	missense	probably damaging	1.00
R7374:Cplane1	UTSW	15	8,247,247 (GRCm38)	missense	unknown
R7446:Cplane1	UTSW	15	8,232,080 (GRCm38)	missense	probably damaging	0.98
R7539:Cplane1	UTSW	15	8,201,244 (GRCm38)	missense	probably benign	0.19
R7543:Cplane1	UTSW	15	8,225,392 (GRCm38)	missense	unknown
R7558:Cplane1	UTSW	15	8,225,367 (GRCm38)	missense	unknown
R7629:Cplane1	UTSW	15	8,227,067 (GRCm38)	nonsense	probably null
R7635:Cplane1	UTSW	15	8,226,920 (GRCm38)	missense	probably benign	0.01
R7644:Cplane1	UTSW	15	8,223,127 (GRCm38)	missense	probably benign	0.00
R7705:Cplane1	UTSW	15	8,182,252 (GRCm38)	missense	probably damaging	1.00
R7752:Cplane1	UTSW	15	8,269,706 (GRCm38)	missense	unknown
R7754:Cplane1	UTSW	15	8,243,826 (GRCm38)	missense	possibly damaging	0.53
R7757:Cplane1	UTSW	15	8,252,227 (GRCm38)	missense	unknown
R7836:Cplane1	UTSW	15	8,203,757 (GRCm38)	missense	probably damaging	0.97
R7875:Cplane1	UTSW	15	8,209,962 (GRCm38)	missense	probably benign	0.18
R7901:Cplane1	UTSW	15	8,269,706 (GRCm38)	missense	unknown
R7983:Cplane1	UTSW	15	8,221,815 (GRCm38)	missense	probably benign	0.01
R8030:Cplane1	UTSW	15	8,230,303 (GRCm38)	missense	probably damaging	1.00
R8088:Cplane1	UTSW	15	8,186,318 (GRCm38)	missense	probably benign	0.00
R8231:Cplane1	UTSW	15	8,219,027 (GRCm38)	missense	probably benign	0.16
R8443:Cplane1	UTSW	15	8,201,151 (GRCm38)	missense	probably benign	0.03
R8480:Cplane1	UTSW	15	8,187,458 (GRCm38)	missense	possibly damaging	0.63
R8693:Cplane1	UTSW	15	8,229,008 (GRCm38)	missense	probably benign	0.15
R8785:Cplane1	UTSW	15	8,174,760 (GRCm38)	missense	probably benign	0.39
R8791:Cplane1	UTSW	15	8,187,260 (GRCm38)	missense	probably damaging	1.00
R8822:Cplane1	UTSW	15	8,171,778 (GRCm38)	missense	probably damaging	1.00
R8831:Cplane1	UTSW	15	8,182,136 (GRCm38)	missense	probably benign	0.09
R8932:Cplane1	UTSW	15	8,194,375 (GRCm38)	missense	probably damaging	1.00
R8968:Cplane1	UTSW	15	8,201,281 (GRCm38)	missense	possibly damaging	0.84
R8973:Cplane1	UTSW	15	8,203,793 (GRCm38)	missense	probably damaging	1.00
R9036:Cplane1	UTSW	15	8,223,138 (GRCm38)	missense	possibly damaging	0.63
R9134:Cplane1	UTSW	15	8,199,232 (GRCm38)	missense	probably damaging	0.99
R9197:Cplane1	UTSW	15	8,251,052 (GRCm38)	missense	unknown
R9259:Cplane1	UTSW	15	8,203,303 (GRCm38)	missense	possibly damaging	0.82
R9269:Cplane1	UTSW	15	8,219,016 (GRCm38)	missense	probably damaging	0.97
R9328:Cplane1	UTSW	15	8,186,208 (GRCm38)	missense	probably damaging	1.00
R9563:Cplane1	UTSW	15	8,187,079 (GRCm38)	missense	probably benign	0.20
R9680:Cplane1	UTSW	15	8,202,301 (GRCm38)	missense	possibly damaging	0.68
R9721:Cplane1	UTSW	15	8,225,409 (GRCm38)	missense	unknown
R9779:Cplane1	UTSW	15	8,201,302 (GRCm38)	missense	possibly damaging	0.93
R9780:Cplane1	UTSW	15	8,228,639 (GRCm38)	missense	probably benign	0.00
U24488:Cplane1	UTSW	15	8,182,210 (GRCm38)	missense	probably damaging	1.00
X0023:Cplane1	UTSW	15	8,247,031 (GRCm38)	missense	unknown
Z1177:Cplane1	UTSW	15	8,209,989 (GRCm38)	missense	probably damaging	0.98
Z1177:Cplane1	UTSW	15	8,174,972 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCTTACAGCTCAGCAGTAG -3'
(R):5'- GACTCCAGTGACCTTACTTCAC -3'

Sequencing Primer
(F):5'- ACTTGCTTGACATGCACCAGG -3'
(R):5'- TACTTCACTAAGAACAGCTGGCTGG -3'

Posted On

2022-03-25