Mutagenetix > Incidental Mutation

Incidental Mutation 'R1698:Cep350'

192371

Institutional Source

Beutler Lab

Gene Symbol

Cep350

Ensembl Gene

ENSMUSG00000033671

Gene Name

centrosomal protein 350

Synonyms

6430546F08Rik, 4933409L06Rik

MMRRC Submission

039731-MU

Accession Numbers

Genbank: NM_001039184.1; Ensembl: ENSMUST00000138762, ENSMUST00000124495, ENSMUST00000078888

Essential gene?

Probably essential (E-score: 0.960) question?

Stock #

R1698 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

155844964-155973255 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 155953358 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 267 (I267V)

Ref Sequence

ENSEMBL: ENSMUSP00000120085 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000124495] [ENSMUST00000138762]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000104231

Predicted Effect

possibly damaging
Transcript: ENSMUST00000124495
AA Change: I207V

PolyPhen 2 Score 0.621 (Sensitivity: 0.87; Specificity: 0.91)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000138762
AA Change: I267V

PolyPhen 2 Score 0.621 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000120085
Gene: ENSMUSG00000033671
AA Change: I267V

Domain	Start	End	E-Value	Type
low complexity region	251	265	N/A	INTRINSIC
low complexity region	376	394	N/A	INTRINSIC
low complexity region	481	491	N/A	INTRINSIC
coiled coil region	596	641	N/A	INTRINSIC
low complexity region	659	669	N/A	INTRINSIC
low complexity region	701	719	N/A	INTRINSIC
low complexity region	754	763	N/A	INTRINSIC
low complexity region	979	994	N/A	INTRINSIC
low complexity region	1153	1175	N/A	INTRINSIC
low complexity region	1250	1267	N/A	INTRINSIC
coiled coil region	1363	1402	N/A	INTRINSIC
low complexity region	1517	1531	N/A	INTRINSIC
low complexity region	1536	1546	N/A	INTRINSIC
low complexity region	1694	1714	N/A	INTRINSIC
coiled coil region	1732	1794	N/A	INTRINSIC
low complexity region	1800	1811	N/A	INTRINSIC
low complexity region	1819	1835	N/A	INTRINSIC
coiled coil region	1853	1893	N/A	INTRINSIC
low complexity region	1980	1994	N/A	INTRINSIC
coiled coil region	2042	2092	N/A	INTRINSIC
low complexity region	2383	2394	N/A	INTRINSIC
low complexity region	2409	2421	N/A	INTRINSIC
low complexity region	2470	2482	N/A	INTRINSIC
CAP_GLY	2486	2551	5.91e-31	SMART
coiled coil region	2700	2731	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.6%
20x: 93.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene is a large protein with a CAP-Gly domain typically found in cytoskeleton-associated proteins. The encoded protein primarily localizes to the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. The encoded protein directly interacts with another large centrosomal protein and is required to anchor microtubules at the centrosome. It is also implicated in the regulation of a class of nuclear hormone receptors in the nucleus. Several alternatively spliced transcript variants have been found, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]

Allele List at MGI

All alleles(5) : Gene trapped(5)

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	A	C	6: 121,645,158 (GRCm38)	E340A	possibly damaging	Het
Abca13	A	G	11: 9,314,507 (GRCm38)	D2963G	probably benign	Het
Actn3	T	C	19: 4,862,207 (GRCm38)	D783G	possibly damaging	Het
Adamtsl2	A	G	2: 27,103,127 (GRCm38)	E723G	possibly damaging	Het
Agrn	G	T	4: 156,166,558 (GRCm38)	Q1931K	probably benign	Het
Ankrd27	G	A	7: 35,614,521 (GRCm38)	A426T	probably benign	Het
Atg9b	C	A	5: 24,388,188 (GRCm38)	G406C	probably damaging	Het
BC005561	C	T	5: 104,520,510 (GRCm38)	A966V	probably benign	Het
C1ra	A	T	6: 124,522,766 (GRCm38)	Q637L	probably benign	Het
Cdhr2	A	T	13: 54,719,581 (GRCm38)	M438L	probably benign	Het
Chrna5	A	G	9: 55,004,642 (GRCm38)	Y138C	probably damaging	Het
Chst3	T	A	10: 60,185,703 (GRCm38)	M441L	probably benign	Het
Cmya5	G	A	13: 93,063,519 (GRCm38)	P3434S	probably benign	Het
Cog2	T	A	8: 124,525,683 (GRCm38)	L42Q	probably damaging	Het
Cpq	A	T	15: 33,250,126 (GRCm38)	I210F	probably benign	Het
Crnn	C	A	3: 93,148,458 (GRCm38)	Q184K	probably damaging	Het
Csnka2ip	A	T	16: 64,478,059 (GRCm38)	Y647*	probably null	Het
D5Ertd579e	C	T	5: 36,604,530 (GRCm38)	R1331H	probably benign	Het
Dennd5a	C	T	7: 109,917,380 (GRCm38)		probably null	Het
Dync1h1	A	G	12: 110,626,992 (GRCm38)	Q1231R	possibly damaging	Het
Erbin	T	A	13: 103,833,731 (GRCm38)	I1126F	possibly damaging	Het
Fastkd1	T	C	2: 69,702,469 (GRCm38)	D518G	probably benign	Het
Gcc1	A	G	6: 28,421,111 (GRCm38)	L69P	possibly damaging	Het
Gkn1	T	C	6: 87,347,169 (GRCm38)	Y119C	probably damaging	Het
Gmpr	T	G	13: 45,517,044 (GRCm38)	W81G	probably benign	Het
Gyg	T	A	3: 20,138,051 (GRCm38)	I236F	probably benign	Het
Hcrtr2	T	C	9: 76,246,453 (GRCm38)	Y219C	probably damaging	Het
Hmcn1	G	A	1: 150,565,369 (GRCm38)	Q5379*	probably null	Het
Kank1	T	C	19: 25,411,317 (GRCm38)	C785R	probably benign	Het
Lrp1b	A	T	2: 40,851,806 (GRCm38)	C3036*	probably null	Het
Mdga2	T	C	12: 66,689,335 (GRCm38)	D373G	probably damaging	Het
Mgat2	A	T	12: 69,185,719 (GRCm38)	I356F	probably benign	Het
Miga2	A	G	2: 30,377,997 (GRCm38)	D346G	probably damaging	Het
Mprip	T	A	11: 59,760,258 (GRCm38)	L1596Q	possibly damaging	Het
Mroh2b	G	A	15: 4,914,140 (GRCm38)	R386Q	probably benign	Het
Mst1r	T	A	9: 107,919,980 (GRCm38)	S1349R	probably benign	Het
Mtmr3	C	T	11: 4,492,825 (GRCm38)	R403H	possibly damaging	Het
Mycbpap	G	A	11: 94,508,143 (GRCm38)	Q460*	probably null	Het
Myo9a	T	C	9: 59,868,181 (GRCm38)	V1025A	probably benign	Het
Ncapd2	C	T	6: 125,168,590 (GRCm38)	E1365K	probably null	Het
Nkiras2	C	A	11: 100,625,163 (GRCm38)	D105E	probably damaging	Het
Nolc1	T	G	19: 46,081,431 (GRCm38)		probably null	Het
Nos1	T	C	5: 117,867,232 (GRCm38)	F6L	probably benign	Het
Olfr1112	G	T	2: 87,191,737 (GRCm38)	V17L	probably benign	Het
Olfr1278	T	A	2: 111,292,560 (GRCm38)	C97*	probably null	Het
Olfr1369-ps1	C	T	13: 21,116,565 (GRCm38)	T291I	probably benign	Het
Olfr218	A	T	1: 173,203,371 (GRCm38)	N5I	probably damaging	Het
Olfr325	T	C	11: 58,581,251 (GRCm38)	Y136H	probably damaging	Het
Olfr910	T	A	9: 38,539,256 (GRCm38)	Y120*	probably null	Het
Pfkm	A	G	15: 98,128,318 (GRCm38)	E598G	possibly damaging	Het
Phf2	A	T	13: 48,807,630 (GRCm38)	D861E	unknown	Het
Polr2a	A	G	11: 69,739,877 (GRCm38)		probably null	Het
Popdc2	G	A	16: 38,369,491 (GRCm38)	V167M	probably damaging	Het
Ptpn22	T	C	3: 103,885,798 (GRCm38)	S422P	probably benign	Het
Rasa2	T	C	9: 96,568,375 (GRCm38)	K490R	possibly damaging	Het
Rbfox3	T	A	11: 118,495,221 (GRCm38)	D286V	probably damaging	Het
Rdh13	A	G	7: 4,427,791 (GRCm38)	W223R	probably damaging	Het
Riok3	T	C	18: 12,128,929 (GRCm38)	S7P	probably benign	Het
Rnaseh2b	A	G	14: 62,353,632 (GRCm38)	E144G	probably benign	Het
Rnf20	C	T	4: 49,651,498 (GRCm38)	Q655*	probably null	Het
Rpap2	T	C	5: 107,603,550 (GRCm38)	Y8H	probably damaging	Het
Slc5a10	T	C	11: 61,709,602 (GRCm38)	Y181C	probably benign	Het
Snd1	G	T	6: 28,888,253 (GRCm38)	G896*	probably null	Het
Spast	C	T	17: 74,356,160 (GRCm38)	Q158*	probably null	Het
Tas2r104	G	A	6: 131,685,584 (GRCm38)	S54F	probably damaging	Het
Tcaf2	C	T	6: 42,628,017 (GRCm38)	W611*	probably null	Het
Timp4	G	A	6: 115,250,403 (GRCm38)		probably null	Het
Tmem45a	G	A	16: 56,823,570 (GRCm38)	S72L	probably benign	Het
Tnrc18	T	C	5: 142,788,703 (GRCm38)	T124A	possibly damaging	Het
Tns2	C	T	15: 102,108,934 (GRCm38)	R281C	probably damaging	Het
Ttn	T	C	2: 76,942,915 (GRCm38)	D2381G	probably damaging	Het
Uevld	T	C	7: 46,955,624 (GRCm38)	T41A	possibly damaging	Het
Ugcg	C	T	4: 59,207,798 (GRCm38)	P46S	probably benign	Het
Unc5d	T	C	8: 28,696,478 (GRCm38)	E527G	probably damaging	Het
Vmn2r125	C	T	4: 156,351,038 (GRCm38)	T237I	probably benign	Het
Vmn2r63	A	C	7: 42,933,614 (GRCm38)	I59S	probably benign	Het
Vps72	G	A	3: 95,118,695 (GRCm38)	S106N	probably benign	Het
Zan	A	C	5: 137,409,669 (GRCm38)		probably benign	Het
Zbtb38	T	C	9: 96,685,462 (GRCm38)	K1190E	probably benign	Het
Zc3h6	T	C	2: 129,017,358 (GRCm38)	V1103A	probably benign	Het
Zfp407	G	A	18: 84,562,157 (GRCm38)	T277I	probably damaging	Het
Zfp804b	A	G	5: 6,769,509 (GRCm38)	S1149P	probably damaging	Het

Other mutations in Cep350

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00764:Cep350	APN	1	155,940,746 (GRCm38)	missense	possibly damaging	0.68
IGL00821:Cep350	APN	1	155,862,204 (GRCm38)	missense	probably benign
IGL00837:Cep350	APN	1	155,953,391 (GRCm38)	missense	probably damaging	1.00
IGL00977:Cep350	APN	1	155,932,865 (GRCm38)	missense	probably null	0.99
IGL01544:Cep350	APN	1	155,953,187 (GRCm38)	missense	probably damaging	1.00
IGL01616:Cep350	APN	1	155,953,247 (GRCm38)	missense	probably benign	0.00
IGL01695:Cep350	APN	1	155,944,158 (GRCm38)	missense	probably damaging	1.00
IGL01902:Cep350	APN	1	155,861,985 (GRCm38)	missense	probably damaging	1.00
IGL01977:Cep350	APN	1	155,911,968 (GRCm38)	missense	probably benign	0.01
IGL02388:Cep350	APN	1	155,953,753 (GRCm38)	missense	probably benign	0.28
IGL02475:Cep350	APN	1	155,862,595 (GRCm38)	missense	probably damaging	1.00
IGL02528:Cep350	APN	1	155,894,615 (GRCm38)	missense	probably damaging	1.00
IGL02598:Cep350	APN	1	155,862,967 (GRCm38)	missense	probably benign	0.00
IGL02676:Cep350	APN	1	155,862,231 (GRCm38)	missense	possibly damaging	0.82
IGL02728:Cep350	APN	1	155,953,222 (GRCm38)	missense	probably benign	0.02
IGL02744:Cep350	APN	1	155,931,533 (GRCm38)	missense	probably damaging	0.98
IGL02817:Cep350	APN	1	155,928,842 (GRCm38)	missense	probably damaging	1.00
IGL02892:Cep350	APN	1	155,868,806 (GRCm38)	missense	possibly damaging	0.51
IGL03156:Cep350	APN	1	155,858,042 (GRCm38)	missense	probably damaging	1.00
IGL03166:Cep350	APN	1	155,863,600 (GRCm38)	missense	possibly damaging	0.78
IGL03216:Cep350	APN	1	155,860,627 (GRCm38)	missense	probably benign	0.06
IGL03268:Cep350	APN	1	155,953,549 (GRCm38)	missense	probably benign	0.16
IGL03358:Cep350	APN	1	155,928,539 (GRCm38)	missense	probably benign
primed	UTSW	1	155,953,588 (GRCm38)	missense	probably damaging	0.98
stoked	UTSW	1	155,915,575 (GRCm38)	missense	probably benign	0.03
NA:Cep350	UTSW	1	155,958,648 (GRCm38)	missense	probably damaging	1.00
R0060:Cep350	UTSW	1	155,928,626 (GRCm38)	missense	probably damaging	1.00
R0060:Cep350	UTSW	1	155,928,626 (GRCm38)	missense	probably damaging	1.00
R0066:Cep350	UTSW	1	155,911,218 (GRCm38)	missense	probably damaging	0.99
R0066:Cep350	UTSW	1	155,911,218 (GRCm38)	missense	probably damaging	0.99
R0172:Cep350	UTSW	1	155,953,447 (GRCm38)	missense	probably benign	0.00
R0365:Cep350	UTSW	1	155,906,571 (GRCm38)	missense	probably benign	0.00
R0472:Cep350	UTSW	1	155,914,723 (GRCm38)	missense	probably damaging	0.99
R0502:Cep350	UTSW	1	155,900,883 (GRCm38)	splice site	probably null
R0538:Cep350	UTSW	1	155,848,620 (GRCm38)	missense	possibly damaging	0.80
R0547:Cep350	UTSW	1	155,901,435 (GRCm38)	splice site	probably null
R0565:Cep350	UTSW	1	155,961,195 (GRCm38)	splice site	probably benign
R0607:Cep350	UTSW	1	155,872,048 (GRCm38)	missense	probably damaging	1.00
R0645:Cep350	UTSW	1	155,940,712 (GRCm38)	splice site	probably null
R0675:Cep350	UTSW	1	155,959,753 (GRCm38)	missense	possibly damaging	0.63
R0828:Cep350	UTSW	1	155,953,246 (GRCm38)	missense	probably benign	0.00
R0863:Cep350	UTSW	1	155,862,235 (GRCm38)	missense	probably benign	0.00
R0969:Cep350	UTSW	1	155,940,826 (GRCm38)	missense	possibly damaging	0.81
R1102:Cep350	UTSW	1	155,931,518 (GRCm38)	missense	probably damaging	1.00
R1186:Cep350	UTSW	1	155,875,376 (GRCm38)	missense	probably damaging	1.00
R1552:Cep350	UTSW	1	155,910,738 (GRCm38)	missense	possibly damaging	0.92
R1560:Cep350	UTSW	1	155,929,079 (GRCm38)	missense	possibly damaging	0.48
R1729:Cep350	UTSW	1	155,911,981 (GRCm38)	missense	probably benign	0.17
R1735:Cep350	UTSW	1	155,953,214 (GRCm38)	missense	probably damaging	0.99
R1740:Cep350	UTSW	1	155,928,833 (GRCm38)	missense	probably damaging	1.00
R1783:Cep350	UTSW	1	155,928,865 (GRCm38)	missense	probably damaging	1.00
R1844:Cep350	UTSW	1	155,848,628 (GRCm38)	missense	probably damaging	0.99
R1848:Cep350	UTSW	1	155,953,651 (GRCm38)	missense	probably benign	0.28
R1988:Cep350	UTSW	1	155,933,104 (GRCm38)	missense	possibly damaging	0.82
R2008:Cep350	UTSW	1	155,914,721 (GRCm38)	missense	probably benign	0.16
R2241:Cep350	UTSW	1	155,958,556 (GRCm38)	splice site	probably null
R2245:Cep350	UTSW	1	155,879,020 (GRCm38)	missense	probably benign	0.10
R2402:Cep350	UTSW	1	155,863,136 (GRCm38)	missense	probably benign
R2566:Cep350	UTSW	1	155,959,718 (GRCm38)	critical splice donor site	probably null
R3160:Cep350	UTSW	1	155,863,164 (GRCm38)	missense	probably benign	0.00
R3162:Cep350	UTSW	1	155,863,164 (GRCm38)	missense	probably benign	0.00
R3769:Cep350	UTSW	1	155,953,204 (GRCm38)	missense	probably damaging	1.00
R4035:Cep350	UTSW	1	155,959,795 (GRCm38)	missense	probably benign	0.06
R4158:Cep350	UTSW	1	155,932,875 (GRCm38)	missense	probably damaging	1.00
R4160:Cep350	UTSW	1	155,932,875 (GRCm38)	missense	probably damaging	1.00
R4213:Cep350	UTSW	1	155,935,961 (GRCm38)	missense	probably damaging	1.00
R4483:Cep350	UTSW	1	155,926,468 (GRCm38)	missense	probably benign	0.01
R4648:Cep350	UTSW	1	155,902,598 (GRCm38)	missense	possibly damaging	0.85
R4694:Cep350	UTSW	1	155,928,586 (GRCm38)	missense	probably damaging	1.00
R4836:Cep350	UTSW	1	155,928,833 (GRCm38)	missense	probably damaging	1.00
R4839:Cep350	UTSW	1	155,928,494 (GRCm38)	missense	probably benign	0.00
R4969:Cep350	UTSW	1	155,860,279 (GRCm38)	missense	probably damaging	0.99
R5014:Cep350	UTSW	1	155,928,206 (GRCm38)	missense	probably benign	0.00
R5027:Cep350	UTSW	1	155,933,354 (GRCm38)	missense	probably benign	0.01
R5144:Cep350	UTSW	1	155,911,150 (GRCm38)	missense	probably damaging	0.99
R5153:Cep350	UTSW	1	155,935,946 (GRCm38)	missense	probably damaging	1.00
R5165:Cep350	UTSW	1	155,928,368 (GRCm38)	missense	probably damaging	1.00
R5182:Cep350	UTSW	1	155,858,108 (GRCm38)	missense	probably damaging	1.00
R5445:Cep350	UTSW	1	155,894,723 (GRCm38)	missense	probably benign	0.01
R5738:Cep350	UTSW	1	155,866,078 (GRCm38)	missense	probably damaging	1.00
R5809:Cep350	UTSW	1	155,933,341 (GRCm38)	missense	probably damaging	0.98
R5855:Cep350	UTSW	1	155,953,762 (GRCm38)	missense	probably benign	0.00
R6103:Cep350	UTSW	1	155,924,576 (GRCm38)	missense	probably benign	0.05
R6139:Cep350	UTSW	1	155,953,279 (GRCm38)	missense	probably benign	0.03
R6285:Cep350	UTSW	1	155,953,374 (GRCm38)	missense	possibly damaging	0.48
R6430:Cep350	UTSW	1	155,894,673 (GRCm38)	missense	probably damaging	1.00
R6446:Cep350	UTSW	1	155,862,154 (GRCm38)	missense	probably benign
R6520:Cep350	UTSW	1	155,933,336 (GRCm38)	missense	probably benign	0.02
R6712:Cep350	UTSW	1	155,858,106 (GRCm38)	missense	possibly damaging	0.93
R6940:Cep350	UTSW	1	155,928,551 (GRCm38)	missense	probably benign	0.01
R7020:Cep350	UTSW	1	155,928,331 (GRCm38)	missense	probably damaging	1.00
R7056:Cep350	UTSW	1	155,848,627 (GRCm38)	missense	probably damaging	1.00
R7141:Cep350	UTSW	1	155,914,748 (GRCm38)	missense	probably damaging	1.00
R7215:Cep350	UTSW	1	155,894,707 (GRCm38)	missense	possibly damaging	0.89
R7247:Cep350	UTSW	1	155,910,753 (GRCm38)	missense	probably damaging	1.00
R7272:Cep350	UTSW	1	155,953,588 (GRCm38)	missense	probably damaging	0.98
R7336:Cep350	UTSW	1	155,862,276 (GRCm38)	missense	probably benign	0.17
R7361:Cep350	UTSW	1	155,901,491 (GRCm38)	missense	probably damaging	1.00
R7390:Cep350	UTSW	1	155,866,087 (GRCm38)	missense	possibly damaging	0.94
R7402:Cep350	UTSW	1	155,928,215 (GRCm38)	missense	probably benign	0.00
R7428:Cep350	UTSW	1	155,894,619 (GRCm38)	missense	probably benign	0.00
R7440:Cep350	UTSW	1	155,940,772 (GRCm38)	missense	probably damaging	0.98
R7520:Cep350	UTSW	1	155,915,629 (GRCm38)	missense	probably benign	0.05
R7529:Cep350	UTSW	1	155,861,923 (GRCm38)	missense	probably benign	0.08
R7635:Cep350	UTSW	1	155,879,021 (GRCm38)	nonsense	probably null
R7806:Cep350	UTSW	1	155,862,063 (GRCm38)	missense	probably benign	0.00
R8100:Cep350	UTSW	1	155,953,402 (GRCm38)	missense	probably damaging	0.97
R8192:Cep350	UTSW	1	155,940,783 (GRCm38)	missense	possibly damaging	0.94
R8193:Cep350	UTSW	1	155,862,079 (GRCm38)	missense	probably benign	0.01
R8351:Cep350	UTSW	1	155,872,034 (GRCm38)	missense	probably damaging	0.99
R8406:Cep350	UTSW	1	155,922,418 (GRCm38)	missense	probably benign	0.00
R8451:Cep350	UTSW	1	155,872,034 (GRCm38)	missense	probably damaging	0.99
R8467:Cep350	UTSW	1	155,915,575 (GRCm38)	missense	probably benign	0.03
R8543:Cep350	UTSW	1	155,862,376 (GRCm38)	missense	probably damaging	0.98
R8714:Cep350	UTSW	1	155,860,731 (GRCm38)	missense	probably damaging	0.98
R8810:Cep350	UTSW	1	155,928,116 (GRCm38)	missense	probably damaging	1.00
R8837:Cep350	UTSW	1	155,861,772 (GRCm38)	missense	probably benign	0.09
R8933:Cep350	UTSW	1	155,863,415 (GRCm38)	missense	probably benign	0.01
R9043:Cep350	UTSW	1	155,897,482 (GRCm38)	missense	probably damaging	1.00
R9050:Cep350	UTSW	1	155,862,941 (GRCm38)	missense	possibly damaging	0.81
R9067:Cep350	UTSW	1	155,861,739 (GRCm38)	missense	probably benign	0.00
R9105:Cep350	UTSW	1	155,959,815 (GRCm38)	missense	probably damaging	1.00
R9295:Cep350	UTSW	1	155,862,305 (GRCm38)	nonsense	probably null
R9304:Cep350	UTSW	1	155,953,718 (GRCm38)	missense	probably damaging	0.98
R9456:Cep350	UTSW	1	155,868,711 (GRCm38)	missense	probably benign	0.00
R9575:Cep350	UTSW	1	155,875,367 (GRCm38)	missense	probably benign	0.03
R9715:Cep350	UTSW	1	155,875,361 (GRCm38)	missense	probably benign	0.00
R9749:Cep350	UTSW	1	155,953,239 (GRCm38)	missense	probably benign	0.02
R9758:Cep350	UTSW	1	155,894,687 (GRCm38)	missense	probably damaging	0.96
R9767:Cep350	UTSW	1	155,863,272 (GRCm38)	missense	probably benign	0.01
RF020:Cep350	UTSW	1	155,915,478 (GRCm38)	missense	probably benign	0.34
X0018:Cep350	UTSW	1	155,953,286 (GRCm38)	missense	probably benign	0.13

Predicted Primers

PCR Primer
(F):5'- CCAACCTTTGTATGCTGGAGCAGG -3'
(R):5'- TGTATTCACGAGGAGAAGCCCGAG -3'

Sequencing Primer
(F):5'- GGTGCTGTTGCCACTTTC -3'
(R):5'- CCTCGGTCATCAGTGATACAG -3'

Posted On

2014-05-14