Mutagenetix > Incidental Mutation

Incidental Mutation 'R9779:Cplane1'

733934

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 #

R9779 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

8198590-8300642 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 8230786 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Lysine at position 1021 (T1021K)

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: T1021K

PolyPhen 2 Score 0.928 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000106247
Gene: ENSMUSG00000039801
AA Change: T1021K

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: 99.9%
3x: 99.8%
10x: 99.5%
20x: 98.6%

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: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aff4	T	G	11: 53,263,734 (GRCm39)	Y251*	probably null	Het
Amdhd1	G	T	10: 93,370,474 (GRCm39)	F121L	possibly damaging	Het
Apon	A	T	10: 128,091,065 (GRCm39)	T248S	probably benign	Het
Arhgap28	A	T	17: 68,152,764 (GRCm39)	I719K	probably benign	Het
Atf7ip2	A	T	16: 10,055,044 (GRCm39)	K270N	possibly damaging	Het
Atp2c1	A	G	9: 105,291,919 (GRCm39)	V881A	probably damaging	Het
Atp6v0a1	C	T	11: 100,924,938 (GRCm39)	T341M	probably damaging	Het
Cep192	T	C	18: 67,968,348 (GRCm39)	V944A	probably damaging	Het
Cyp26b1	T	C	6: 84,552,113 (GRCm39)	T342A	probably benign	Het
Cyp2c37	A	G	19: 39,998,323 (GRCm39)	E405G	probably benign	Het
Dab2	T	C	15: 6,460,525 (GRCm39)	S478P	probably benign	Het
Diablo	A	G	5: 123,662,132 (GRCm39)		probably null	Het
Dnajc8	A	G	4: 132,277,737 (GRCm39)	E174G	possibly damaging	Het
Eif4g1	T	C	16: 20,498,251 (GRCm39)	V336A	probably damaging	Het
Eif5a	C	T	11: 69,810,021 (GRCm39)	V41I	probably benign	Het
Epb41l5	C	T	1: 119,545,093 (GRCm39)		probably null	Het
F12	A	C	13: 55,566,012 (GRCm39)	V565G	probably damaging	Het
Fras1	C	A	5: 96,717,353 (GRCm39)	T389N	probably damaging	Het
Galnt13	T	A	2: 54,623,062 (GRCm39)	D69E	probably benign	Het
Golph3l	C	T	3: 95,499,041 (GRCm39)	T61I	probably damaging	Het
Grm3	A	T	5: 9,561,656 (GRCm39)	N731K	possibly damaging	Het
Hmgxb4	C	T	8: 75,750,629 (GRCm39)	S484F	possibly damaging	Het
Hsd17b11	C	A	5: 104,157,771 (GRCm39)	V114F	probably damaging	Het
Hspa1a	C	T	17: 35,190,778 (GRCm39)	V42M	probably damaging	Het
Igf1r	A	G	7: 67,654,065 (GRCm39)	Y201C	probably damaging	Het
Inf2	C	A	12: 112,574,786 (GRCm39)	P786T	unknown	Het
Ints12	T	G	3: 132,812,752 (GRCm39)	V236G	probably benign	Het
Itga2b	T	C	11: 102,348,147 (GRCm39)	N818S	probably damaging	Het
Itgb4	T	C	11: 115,882,485 (GRCm39)	L853P	probably damaging	Het
Kap	A	G	6: 133,829,006 (GRCm39)	V42A	probably benign	Het
Kcnk1	T	C	8: 126,751,807 (GRCm39)	S138P	probably damaging	Het
Klra2	G	A	6: 131,198,801 (GRCm39)	P247S	unknown	Het
Lrba	T	C	3: 86,233,078 (GRCm39)	I813T	probably damaging	Het
Lrrc27	A	T	7: 138,816,886 (GRCm39)	Q428L	possibly damaging	Het
Macf1	G	A	4: 123,348,789 (GRCm39)	T4046I	probably benign	Het
Mast3	T	C	8: 71,238,127 (GRCm39)	T521A	probably damaging	Het
Meox1	T	C	11: 101,769,470 (GRCm39)	E242G	probably benign	Het
Neo1	A	T	9: 58,886,009 (GRCm39)	L316*	probably null	Het
Notch3	A	G	17: 32,372,757 (GRCm39)	Y605H	probably damaging	Het
Nsf	T	C	11: 103,719,352 (GRCm39)	D650G	probably damaging	Het
Obscn	C	A	11: 59,026,441 (GRCm39)	R254L	probably benign	Het
Odam	G	A	5: 88,037,327 (GRCm39)		probably null	Het
Or5v1b	A	T	17: 37,841,048 (GRCm39)	Y60F	probably damaging	Het
Or7g12	A	T	9: 18,900,135 (GRCm39)	M284L	probably benign	Het
Pcdhb9	A	T	18: 37,535,253 (GRCm39)	M416L	probably benign	Het
Plcz1	A	T	6: 139,947,882 (GRCm39)	I500N	possibly damaging	Het
Prkn	T	C	17: 11,854,318 (GRCm39)	S285P	possibly damaging	Het
Rab14	G	A	2: 35,080,047 (GRCm39)	T50I		Het
Rag1	A	T	2: 101,474,153 (GRCm39)	Y330N	probably damaging	Het
Rapgef3	T	C	15: 97,643,479 (GRCm39)	I911V	probably damaging	Het
Rasgrf1	G	T	9: 89,873,551 (GRCm39)	C620F	probably damaging	Het
Rhbdl3	A	G	11: 80,214,317 (GRCm39)	T143A	probably damaging	Het
Robo2	A	C	16: 73,767,965 (GRCm39)	M609R	probably damaging	Het
Selplg	GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT	GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT	5: 113,957,756 (GRCm39)		probably benign	Het
Slc49a4	T	C	16: 35,543,186 (GRCm39)	D316G	probably benign	Het
Sod3	G	A	5: 52,525,435 (GRCm39)	V45I	probably benign	Het
Ticrr	A	G	7: 79,328,802 (GRCm39)	D647G	probably benign	Het
Tmem119	G	A	5: 113,933,204 (GRCm39)	S199L	possibly damaging	Het
Tmem63c	T	A	12: 87,104,419 (GRCm39)	I80N	probably damaging	Het
Trp53bp1	A	T	2: 121,066,469 (GRCm39)	D752E	probably damaging	Het
Ttn	A	G	2: 76,550,570 (GRCm39)	S31571P	probably damaging	Het
Ttn	A	T	2: 76,667,146 (GRCm39)	S11487T	unknown	Het
Vmn1r123	T	C	7: 20,896,111 (GRCm39)	M1T	probably null	Het
Vmn1r85	A	T	7: 12,818,308 (GRCm39)	S279T	probably benign	Het
Vps13d	A	G	4: 144,798,972 (GRCm39)	V3635A		Het
Wdr95	A	G	5: 149,505,293 (GRCm39)	D358G	probably benign	Het
Zfp1005	A	G	2: 150,108,064 (GRCm39)	D8G	possibly damaging	Het
Zfp764l1	A	T	7: 126,991,469 (GRCm39)	C173S	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
R7543:Cplane1	UTSW	15	8,254,876 (GRCm39)	missense	unknown
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
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'- TGATTCACAGAGCATTCCCTG -3'
(R):5'- TGGAATGTTTCTGGCCTTACC -3'

Sequencing Primer
(F):5'- TGCGACTTATTCCTCTACAACAC -3'
(R):5'- AGTCAGTGCTCTTAACCGCTGAG -3'

Posted On

2022-11-14