Mutagenetix > Incidental Mutation

Incidental Mutation 'R0480:Prune2'

41991

Institutional Source

Beutler Lab

Gene Symbol

Prune2

Ensembl Gene

ENSMUSG00000039126

Gene Name

prune homolog 2

Synonyms

A230083H22Rik, 6330414G02Rik, A330102H22Rik

MMRRC Submission

038680-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0480 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

16956118-17223932 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 17006792 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000084977 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087689]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000087689

SMART Domains

Protein: ENSMUSP00000084977
Gene: ENSMUSG00000039126

Domain	Start	End	E-Value	Type
DHHA2	208	351	8.32e-17	SMART
low complexity region	433	445	N/A	INTRINSIC
low complexity region	476	488	N/A	INTRINSIC
low complexity region	547	553	N/A	INTRINSIC
low complexity region	962	975	N/A	INTRINSIC
low complexity region	1071	1082	N/A	INTRINSIC
low complexity region	1368	1378	N/A	INTRINSIC
low complexity region	1533	1545	N/A	INTRINSIC
low complexity region	1668	1685	N/A	INTRINSIC
low complexity region	1740	1751	N/A	INTRINSIC
low complexity region	2162	2175	N/A	INTRINSIC
low complexity region	2222	2233	N/A	INTRINSIC
low complexity region	2591	2606	N/A	INTRINSIC
low complexity region	2731	2744	N/A	INTRINSIC
SEC14	2882	3037	2.08e-12	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224145

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.3%
20x: 92.6%

Validation Efficiency

99% (117/118)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the B-cell CLL/lymphoma 2 and adenovirus E1B 19 kDa interacting family, whose members play roles in many cellular processes including apotosis, cell transformation, and synaptic function. Several functions for this protein have been demonstrated including suppression of Ras homolog family member A activity, which results in reduced stress fiber formation and suppression of oncogenic cellular transformation. A high molecular weight isoform of this protein has also been shown to colocalize with Adaptor protein complex 2, beta-Adaptin and endodermal markers, suggesting an involvement in post-endocytic trafficking. In prostate cancer cells, this gene acts as a tumor suppressor and its expression is regulated by prostate cancer antigen 3, a non-protein coding gene on the opposite DNA strand in an intron of this gene. Prostate cancer antigen 3 regulates levels of this gene through formation of a double-stranded RNA that undergoes adenosine deaminase actin on RNA-dependent adenosine-to-inosine RNA editing. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]

Allele List at MGI

All alleles(160) : Gene trapped(160)

Other mutations in this stock

Total: 113 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810021J22Rik	C	T	11: 58,880,186 (GRCm38)	L165F	probably damaging	Het
Adamts18	A	G	8: 113,738,818 (GRCm38)	V714A	possibly damaging	Het
Adamtsl1	G	T	4: 86,252,818 (GRCm38)	A518S	probably benign	Het
Adcy2	C	T	13: 68,732,112 (GRCm38)	V363M	probably damaging	Het
Ago4	G	T	4: 126,526,077 (GRCm38)	Q36K	probably benign	Het
Akr1a1	A	G	4: 116,639,847 (GRCm38)	V172A	possibly damaging	Het
Alkbh2	T	A	5: 114,125,535 (GRCm38)	N137I	probably damaging	Het
Ank3	T	A	10: 69,879,926 (GRCm38)	S470T	probably damaging	Het
Ankrd12	T	C	17: 66,049,828 (GRCm38)	T65A	possibly damaging	Het
Aox1	A	T	1: 58,043,651 (GRCm38)		probably benign	Het
Arhgap11a	A	T	2: 113,839,818 (GRCm38)	I320N	probably benign	Het
Arhgap17	G	A	7: 123,294,644 (GRCm38)	H518Y	probably damaging	Het
Ascc3	T	C	10: 50,735,252 (GRCm38)	V1563A	probably damaging	Het
Atf2	G	A	2: 73,819,156 (GRCm38)		probably benign	Het
Bmpr2	C	T	1: 59,845,659 (GRCm38)	T268I	probably damaging	Het
Bpifb9a	A	G	2: 154,264,688 (GRCm38)	I380V	probably benign	Het
C2cd2	G	A	16: 97,877,148 (GRCm38)	T363I	probably benign	Het
Catsperg2	T	G	7: 29,721,298 (GRCm38)	N190H	probably damaging	Het
Ccdc138	T	C	10: 58,561,967 (GRCm38)	L543S	probably damaging	Het
Ccdc170	A	T	10: 4,518,939 (GRCm38)	K162N	probably benign	Het
Cdca5	G	T	19: 6,090,298 (GRCm38)	R163L	probably damaging	Het
Cdh24	A	G	14: 54,632,597 (GRCm38)	F239S	probably benign	Het
Cdkl3	T	C	11: 52,005,055 (GRCm38)	V43A	probably damaging	Het
Cep152	G	T	2: 125,581,719 (GRCm38)	Q921K	possibly damaging	Het
Cftr	G	A	6: 18,274,518 (GRCm38)		probably benign	Het
Chmp5	T	C	4: 40,948,690 (GRCm38)		probably benign	Het
Cit	T	A	5: 115,933,393 (GRCm38)		probably benign	Het
Cngb3	T	A	4: 19,309,517 (GRCm38)		probably benign	Het
Cnr2	A	G	4: 135,917,601 (GRCm38)	E330G	probably benign	Het
Cyp21a1	A	T	17: 34,801,826 (GRCm38)	L473Q	probably damaging	Het
Dchs1	T	C	7: 105,771,489 (GRCm38)	T575A	probably benign	Het
Dedd2	A	G	7: 25,203,625 (GRCm38)	V303A	probably damaging	Het
Dmd	G	T	X: 84,425,738 (GRCm38)	A2370S	probably benign	Het
Dnah10	T	A	5: 124,808,851 (GRCm38)	N3009K	probably damaging	Het
Dnajc13	G	T	9: 104,200,509 (GRCm38)	N934K	probably damaging	Het
Dock1	C	T	7: 134,737,718 (GRCm38)	L106F	probably damaging	Het
Fat3	A	G	9: 15,997,729 (GRCm38)	Y2326H	probably benign	Het
Fhl5	A	T	4: 25,207,101 (GRCm38)	C222*	probably null	Het
Gm10639	C	T	9: 78,302,817 (GRCm38)	A135V	probably benign	Het
Gm1840	A	G	8: 5,639,888 (GRCm38)		noncoding transcript	Het
Gnmt	T	C	17: 46,725,928 (GRCm38)	T252A	probably benign	Het
Gtf2f1	A	G	17: 57,004,307 (GRCm38)		probably null	Het
Gtf3a	T	C	5: 146,953,229 (GRCm38)	Y187H	probably damaging	Het
Hdac2	A	G	10: 36,974,792 (GRCm38)	Y14C	probably damaging	Het
Hnrnph1	T	G	11: 50,385,762 (GRCm38)		probably benign	Het
Homer2	T	C	7: 81,618,603 (GRCm38)	D92G	possibly damaging	Het
Hspg2	T	C	4: 137,550,024 (GRCm38)	S2885P	probably damaging	Het
Insr	A	G	8: 3,161,770 (GRCm38)	S1084P	probably damaging	Het
Ints11	T	A	4: 155,887,624 (GRCm38)	V362E	probably damaging	Het
Kank2	T	C	9: 21,779,899 (GRCm38)	N513S	probably damaging	Het
Kdelc1	C	T	1: 44,110,757 (GRCm38)	W424*	probably null	Het
Kl	T	G	5: 150,953,288 (GRCm38)	V191G	probably damaging	Het
Krt23	A	G	11: 99,486,698 (GRCm38)		probably null	Het
Lama3	A	C	18: 12,450,424 (GRCm38)	T690P	possibly damaging	Het
Lamb1	G	A	12: 31,282,721 (GRCm38)	A281T	possibly damaging	Het
Lck	T	C	4: 129,555,640 (GRCm38)	E299G	probably damaging	Het
Lonrf1	A	G	8: 36,222,710 (GRCm38)	V703A	probably damaging	Het
Ly6f	T	C	15: 75,271,677 (GRCm38)	C78R	probably damaging	Het
Mapkap1	C	T	2: 34,533,781 (GRCm38)		probably benign	Het
Mast1	T	A	8: 84,913,089 (GRCm38)	I1204F	probably damaging	Het
Mbd6	C	T	10: 127,285,873 (GRCm38)		probably benign	Het
Mef2c	A	T	13: 83,592,901 (GRCm38)	T60S	probably damaging	Het
Mgat4c	C	T	10: 102,389,119 (GRCm38)	T398I	probably damaging	Het
Mmp12	C	A	9: 7,350,016 (GRCm38)	H102Q	probably damaging	Het
Mmp20	G	A	9: 7,645,373 (GRCm38)	G308E	probably damaging	Het
Mms19	A	T	19: 41,954,846 (GRCm38)	L395Q	probably damaging	Het
Mus81	A	G	19: 5,487,931 (GRCm38)		probably benign	Het
Mypn	C	T	10: 63,193,203 (GRCm38)	R27H	probably benign	Het
Nav3	T	C	10: 109,853,300 (GRCm38)	E372G	probably damaging	Het
Ncoa1	T	A	12: 4,339,105 (GRCm38)	I57F	probably damaging	Het
Ncstn	T	C	1: 172,082,592 (GRCm38)		probably benign	Het
Nefm	C	T	14: 68,124,159 (GRCm38)	D219N	probably damaging	Het
Notch2	C	T	3: 98,146,537 (GRCm38)	T2172I	possibly damaging	Het
Obscn	T	A	11: 59,133,946 (GRCm38)	K423*	probably null	Het
Olfr1164	A	C	2: 88,093,628 (GRCm38)	S103A	probably benign	Het
Olfr173	T	C	16: 58,797,321 (GRCm38)	N175S	probably benign	Het
Olfr459	A	T	6: 41,772,264 (GRCm38)	C12S	probably benign	Het
Olfr606	A	G	7: 103,451,628 (GRCm38)	N97S	probably benign	Het
Ostm1	T	A	10: 42,696,347 (GRCm38)	M242K	probably damaging	Het
Oxnad1	T	A	14: 32,099,480 (GRCm38)	I154N	probably damaging	Het
Pcdhb10	T	A	18: 37,413,099 (GRCm38)	D409E	probably damaging	Het
Pdcd11	T	C	19: 47,125,037 (GRCm38)		probably benign	Het
Peak1	C	A	9: 56,258,632 (GRCm38)	V671L	probably benign	Het
Pex1	G	A	5: 3,606,444 (GRCm38)		probably null	Het
Plk4	T	A	3: 40,805,640 (GRCm38)	F324I	probably benign	Het
Ppfibp1	C	A	6: 147,019,031 (GRCm38)		probably null	Het
Prcp	T	A	7: 92,919,082 (GRCm38)	W276R	probably damaging	Het
Prr14l	T	C	5: 32,829,880 (GRCm38)	E757G	probably benign	Het
Prss52	T	A	14: 64,113,644 (GRCm38)	Y293N	probably damaging	Het
Ptprk	G	C	10: 28,585,947 (GRCm38)	A84P	probably damaging	Het
Ptprk	C	T	10: 28,585,948 (GRCm38)	A84V	probably damaging	Het
Rock1	A	G	18: 10,079,120 (GRCm38)	L1116P	possibly damaging	Het
Sdha	A	T	13: 74,327,333 (GRCm38)	F526Y	probably benign	Het
Sema4b	T	C	7: 80,220,206 (GRCm38)	F414S	probably damaging	Het
Serpina12	T	C	12: 104,035,701 (GRCm38)	D252G	probably damaging	Het
Siglecg	C	T	7: 43,411,126 (GRCm38)	A310V	probably benign	Het
Slc30a8	A	G	15: 52,325,570 (GRCm38)	I194V	probably benign	Het
Spred3	A	G	7: 29,162,975 (GRCm38)	S148P	probably damaging	Het
Taf9b	A	G	X: 106,218,408 (GRCm38)	S58P	probably damaging	Het
Tgm4	A	T	9: 123,062,419 (GRCm38)	Y109F	probably benign	Het
Tmprss11c	T	G	5: 86,237,609 (GRCm38)		probably benign	Het
Tmtc3	A	T	10: 100,471,404 (GRCm38)	V246D	probably damaging	Het
Tnip1	C	T	11: 54,937,994 (GRCm38)	G116R	probably damaging	Het
Tpr	A	G	1: 150,428,241 (GRCm38)	E1455G	possibly damaging	Het
Ttc3	T	A	16: 94,432,004 (GRCm38)	L986*	probably null	Het
Txndc15	A	G	13: 55,724,623 (GRCm38)	I275V	possibly damaging	Het
Ugt2b1	T	A	5: 86,926,456 (GRCm38)	I15L	probably benign	Het
Upf2	T	C	2: 5,957,634 (GRCm38)	V49A	possibly damaging	Het
Vmn1r117	G	A	7: 20,883,446 (GRCm38)	P226S	probably benign	Het
Vmn2r28	A	T	7: 5,490,457 (GRCm38)	H163Q	probably benign	Het
Vstm2a	T	A	11: 16,263,240 (GRCm38)	S208R	probably damaging	Het
Zfp346	T	A	13: 55,113,097 (GRCm38)	C79*	probably null	Het
Zfp628	A	T	7: 4,921,616 (GRCm38)	T946S	probably benign	Het

Other mutations in Prune2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00234:Prune2	APN	19	17,168,344 (GRCm38)	critical splice donor site	probably null
IGL00848:Prune2	APN	19	17,119,118 (GRCm38)	missense	probably damaging	1.00
IGL00862:Prune2	APN	19	17,119,349 (GRCm38)	missense	probably benign	0.41
IGL00915:Prune2	APN	19	17,016,253 (GRCm38)	missense	probably damaging	1.00
IGL01084:Prune2	APN	19	17,118,209 (GRCm38)	missense	probably benign	0.19
IGL01109:Prune2	APN	19	17,123,879 (GRCm38)	missense	probably benign	0.03
IGL01372:Prune2	APN	19	17,125,069 (GRCm38)	missense	probably damaging	1.00
IGL01650:Prune2	APN	19	17,168,292 (GRCm38)	missense	possibly damaging	0.95
IGL01752:Prune2	APN	19	17,123,903 (GRCm38)	missense	possibly damaging	0.50
IGL01812:Prune2	APN	19	17,003,777 (GRCm38)	missense	possibly damaging	0.50
IGL01902:Prune2	APN	19	17,118,638 (GRCm38)	missense	probably benign	0.00
IGL02195:Prune2	APN	19	17,119,557 (GRCm38)	missense	probably benign	0.00
IGL02502:Prune2	APN	19	17,123,881 (GRCm38)	missense	probably benign	0.00
IGL02569:Prune2	APN	19	17,178,859 (GRCm38)	missense	probably damaging	0.99
IGL02693:Prune2	APN	19	17,124,491 (GRCm38)	missense	probably benign	0.03
IGL02737:Prune2	APN	19	17,193,411 (GRCm38)	nonsense	probably null
IGL02794:Prune2	APN	19	17,119,361 (GRCm38)	missense	probably benign	0.19
IGL02985:Prune2	APN	19	17,016,359 (GRCm38)	critical splice donor site	probably null
IGL03349:Prune2	APN	19	17,123,346 (GRCm38)	missense	probably damaging	1.00
3-1:Prune2	UTSW	19	17,125,282 (GRCm38)	missense	probably benign	0.00
R0060:Prune2	UTSW	19	17,003,733 (GRCm38)	missense	probably damaging	1.00
R0098:Prune2	UTSW	19	17,123,903 (GRCm38)	missense	possibly damaging	0.50
R0098:Prune2	UTSW	19	17,123,903 (GRCm38)	missense	possibly damaging	0.50
R0165:Prune2	UTSW	19	17,122,610 (GRCm38)	missense	probably benign	0.00
R0277:Prune2	UTSW	19	17,121,389 (GRCm38)	missense	probably damaging	0.99
R0321:Prune2	UTSW	19	17,122,454 (GRCm38)	missense	probably benign	0.39
R0321:Prune2	UTSW	19	17,120,927 (GRCm38)	missense	possibly damaging	0.78
R0374:Prune2	UTSW	19	17,120,910 (GRCm38)	missense	probably benign	0.00
R0380:Prune2	UTSW	19	17,124,007 (GRCm38)	missense	probably damaging	1.00
R0396:Prune2	UTSW	19	17,123,080 (GRCm38)	missense	probably benign	0.35
R0408:Prune2	UTSW	19	17,122,310 (GRCm38)	missense	probably benign	0.00
R0421:Prune2	UTSW	19	17,123,311 (GRCm38)	missense	probably benign	0.02
R0531:Prune2	UTSW	19	17,006,753 (GRCm38)	missense	probably damaging	1.00
R0546:Prune2	UTSW	19	17,020,666 (GRCm38)	splice site	probably benign
R0554:Prune2	UTSW	19	17,125,218 (GRCm38)	nonsense	probably null
R0659:Prune2	UTSW	19	17,122,835 (GRCm38)	missense	probably damaging	1.00
R0699:Prune2	UTSW	19	17,123,955 (GRCm38)	missense	probably damaging	1.00
R0781:Prune2	UTSW	19	17,125,222 (GRCm38)	missense	probably benign
R1110:Prune2	UTSW	19	17,125,222 (GRCm38)	missense	probably benign
R1178:Prune2	UTSW	19	17,123,105 (GRCm38)	missense	probably benign	0.22
R1181:Prune2	UTSW	19	17,123,105 (GRCm38)	missense	probably benign	0.22
R1337:Prune2	UTSW	19	17,119,607 (GRCm38)	missense	possibly damaging	0.70
R1356:Prune2	UTSW	19	17,212,317 (GRCm38)	missense	probably benign	0.40
R1385:Prune2	UTSW	19	17,124,948 (GRCm38)	missense	possibly damaging	0.50
R1659:Prune2	UTSW	19	17,120,651 (GRCm38)	missense	possibly damaging	0.59
R1738:Prune2	UTSW	19	17,125,010 (GRCm38)	missense	probably benign	0.01
R1756:Prune2	UTSW	19	17,123,704 (GRCm38)	missense	probably benign	0.01
R1765:Prune2	UTSW	19	17,125,598 (GRCm38)	missense	probably damaging	1.00
R1782:Prune2	UTSW	19	17,122,173 (GRCm38)	missense	probably benign	0.00
R1817:Prune2	UTSW	19	17,122,081 (GRCm38)	missense	probably benign	0.00
R1838:Prune2	UTSW	19	17,199,878 (GRCm38)	missense	probably damaging	1.00
R1851:Prune2	UTSW	19	17,199,139 (GRCm38)	missense	probably damaging	1.00
R1852:Prune2	UTSW	19	17,199,139 (GRCm38)	missense	probably damaging	1.00
R1866:Prune2	UTSW	19	17,123,492 (GRCm38)	missense	probably damaging	1.00
R1911:Prune2	UTSW	19	17,113,674 (GRCm38)	missense	probably benign	0.02
R1983:Prune2	UTSW	19	17,020,642 (GRCm38)	missense	probably damaging	0.97
R2014:Prune2	UTSW	19	17,120,523 (GRCm38)	missense	probably damaging	1.00
R2066:Prune2	UTSW	19	17,120,678 (GRCm38)	missense	possibly damaging	0.57
R2088:Prune2	UTSW	19	17,119,745 (GRCm38)	missense	possibly damaging	0.95
R2111:Prune2	UTSW	19	17,208,238 (GRCm38)	missense	probably damaging	1.00
R2128:Prune2	UTSW	19	17,122,422 (GRCm38)	missense	probably benign	0.00
R2165:Prune2	UTSW	19	17,120,182 (GRCm38)	missense	probably benign	0.19
R2241:Prune2	UTSW	19	17,123,092 (GRCm38)	missense	probably damaging	0.96
R2278:Prune2	UTSW	19	17,118,555 (GRCm38)	missense	possibly damaging	0.93
R2504:Prune2	UTSW	19	17,000,036 (GRCm38)	missense	probably damaging	1.00
R2508:Prune2	UTSW	19	17,122,622 (GRCm38)	missense	probably benign	0.43
R3055:Prune2	UTSW	19	17,125,043 (GRCm38)	missense	probably damaging	0.98
R3086:Prune2	UTSW	19	17,121,413 (GRCm38)	missense	possibly damaging	0.75
R3104:Prune2	UTSW	19	17,119,156 (GRCm38)	missense	probably damaging	1.00
R3105:Prune2	UTSW	19	17,119,156 (GRCm38)	missense	probably damaging	1.00
R3547:Prune2	UTSW	19	17,124,348 (GRCm38)	missense	probably damaging	0.96
R3702:Prune2	UTSW	19	17,178,871 (GRCm38)	missense	probably damaging	1.00
R3753:Prune2	UTSW	19	17,125,454 (GRCm38)	missense	probably benign	0.38
R3933:Prune2	UTSW	19	17,123,954 (GRCm38)	missense	probably damaging	1.00
R3935:Prune2	UTSW	19	17,199,786 (GRCm38)	missense	probably damaging	1.00
R4022:Prune2	UTSW	19	17,000,020 (GRCm38)	missense	probably damaging	1.00
R4042:Prune2	UTSW	19	17,003,826 (GRCm38)	critical splice donor site	probably null
R4164:Prune2	UTSW	19	17,003,734 (GRCm38)	missense	possibly damaging	0.87
R4453:Prune2	UTSW	19	17,121,910 (GRCm38)	missense	probably benign	0.00
R4642:Prune2	UTSW	19	17,020,655 (GRCm38)	critical splice donor site	probably null
R4661:Prune2	UTSW	19	17,000,023 (GRCm38)	missense	probably damaging	1.00
R4666:Prune2	UTSW	19	17,120,188 (GRCm38)	nonsense	probably null
R4823:Prune2	UTSW	19	17,120,504 (GRCm38)	missense	probably damaging	1.00
R4897:Prune2	UTSW	19	17,121,855 (GRCm38)	missense	probably benign	0.03
R4922:Prune2	UTSW	19	17,122,752 (GRCm38)	missense	probably benign	0.00
R4962:Prune2	UTSW	19	17,122,273 (GRCm38)	missense	probably benign	0.11
R5026:Prune2	UTSW	19	17,199,142 (GRCm38)	missense	probably damaging	1.00
R5042:Prune2	UTSW	19	17,119,797 (GRCm38)	missense	possibly damaging	0.94
R5124:Prune2	UTSW	19	17,199,910 (GRCm38)	missense	probably damaging	1.00
R5133:Prune2	UTSW	19	17,003,631 (GRCm38)	missense	probably damaging	1.00
R5184:Prune2	UTSW	19	17,216,357 (GRCm38)	missense	possibly damaging	0.95
R5234:Prune2	UTSW	19	17,118,668 (GRCm38)	missense	probably damaging	1.00
R5339:Prune2	UTSW	19	17,120,872 (GRCm38)	missense	probably damaging	1.00
R5363:Prune2	UTSW	19	17,118,266 (GRCm38)	missense	probably damaging	1.00
R5382:Prune2	UTSW	19	17,003,659 (GRCm38)	missense	probably damaging	1.00
R5436:Prune2	UTSW	19	17,020,643 (GRCm38)	missense	probably damaging	1.00
R5480:Prune2	UTSW	19	17,120,947 (GRCm38)	missense	possibly damaging	0.66
R5635:Prune2	UTSW	19	17,118,209 (GRCm38)	missense	probably benign	0.19
R5678:Prune2	UTSW	19	17,118,668 (GRCm38)	missense	probably damaging	1.00
R5814:Prune2	UTSW	19	17,016,361 (GRCm38)	splice site	probably null
R5894:Prune2	UTSW	19	17,121,391 (GRCm38)	missense	possibly damaging	0.88
R6011:Prune2	UTSW	19	17,118,716 (GRCm38)	missense	probably benign	0.35
R6207:Prune2	UTSW	19	17,118,116 (GRCm38)	missense	probably damaging	1.00
R6218:Prune2	UTSW	19	17,121,562 (GRCm38)	missense	probably benign	0.00
R6573:Prune2	UTSW	19	17,121,158 (GRCm38)	missense	possibly damaging	0.61
R6573:Prune2	UTSW	19	17,121,157 (GRCm38)	missense	probably damaging	1.00
R6734:Prune2	UTSW	19	17,003,733 (GRCm38)	missense	probably damaging	1.00
R6805:Prune2	UTSW	19	17,120,590 (GRCm38)	missense	probably benign
R6837:Prune2	UTSW	19	17,178,928 (GRCm38)	missense	probably damaging	1.00
R6850:Prune2	UTSW	19	17,122,188 (GRCm38)	missense	probably benign	0.00
R6858:Prune2	UTSW	19	17,118,106 (GRCm38)	missense	possibly damaging	0.70
R6874:Prune2	UTSW	19	17,123,228 (GRCm38)	missense	probably damaging	1.00
R6954:Prune2	UTSW	19	17,000,021 (GRCm38)	missense	probably damaging	1.00
R7098:Prune2	UTSW	19	17,120,602 (GRCm38)	missense	probably benign	0.39
R7102:Prune2	UTSW	19	17,121,213 (GRCm38)	missense	probably benign	0.24
R7246:Prune2	UTSW	19	17,121,368 (GRCm38)	missense	probably damaging	0.99
R7284:Prune2	UTSW	19	17,119,886 (GRCm38)	missense	probably damaging	1.00
R7295:Prune2	UTSW	19	17,119,897 (GRCm38)	missense	probably benign	0.01
R7371:Prune2	UTSW	19	17,119,370 (GRCm38)	missense	probably benign	0.02
R7651:Prune2	UTSW	19	17,120,408 (GRCm38)	missense	probably damaging	1.00
R7830:Prune2	UTSW	19	17,122,674 (GRCm38)	missense	probably benign	0.21
R7872:Prune2	UTSW	19	17,119,434 (GRCm38)	missense	probably benign	0.05
R7881:Prune2	UTSW	19	17,123,029 (GRCm38)	missense	possibly damaging	0.50
R7966:Prune2	UTSW	19	17,178,859 (GRCm38)	missense	probably damaging	0.99
R7969:Prune2	UTSW	19	17,201,670 (GRCm38)	missense	probably damaging	0.98
R8092:Prune2	UTSW	19	17,119,993 (GRCm38)	missense	probably damaging	1.00
R8110:Prune2	UTSW	19	17,120,719 (GRCm38)	missense	probably benign	0.22
R8115:Prune2	UTSW	19	17,123,924 (GRCm38)	missense	probably benign	0.02
R8129:Prune2	UTSW	19	17,118,836 (GRCm38)	missense	probably benign	0.01
R8169:Prune2	UTSW	19	17,125,091 (GRCm38)	missense	probably benign	0.10
R8171:Prune2	UTSW	19	17,120,518 (GRCm38)	missense	probably damaging	1.00
R8176:Prune2	UTSW	19	17,118,292 (GRCm38)	missense	probably damaging	1.00
R8200:Prune2	UTSW	19	17,124,973 (GRCm38)	missense	probably benign	0.01
R8217:Prune2	UTSW	19	17,120,116 (GRCm38)	missense	probably benign	0.01
R8258:Prune2	UTSW	19	17,212,308 (GRCm38)	missense	unknown
R8259:Prune2	UTSW	19	17,212,308 (GRCm38)	missense	unknown
R8289:Prune2	UTSW	19	17,123,009 (GRCm38)	missense	probably benign	0.43
R8329:Prune2	UTSW	19	17,121,265 (GRCm38)	missense	probably benign	0.02
R8342:Prune2	UTSW	19	17,125,663 (GRCm38)	missense	probably benign	0.01
R8558:Prune2	UTSW	19	17,122,238 (GRCm38)	missense	probably damaging	0.98
R8732:Prune2	UTSW	19	17,120,405 (GRCm38)	missense	probably damaging	1.00
R8743:Prune2	UTSW	19	17,119,556 (GRCm38)	missense	probably benign	0.22
R8769:Prune2	UTSW	19	17,123,078 (GRCm38)	missense	probably damaging	0.96
R8862:Prune2	UTSW	19	17,120,146 (GRCm38)	missense	probably benign	0.04
R8936:Prune2	UTSW	19	17,121,835 (GRCm38)	missense	probably benign	0.24
R9040:Prune2	UTSW	19	17,120,627 (GRCm38)	missense	probably damaging	1.00
R9084:Prune2	UTSW	19	17,120,377 (GRCm38)	missense	probably damaging	1.00
R9224:Prune2	UTSW	19	17,120,029 (GRCm38)	missense	probably damaging	1.00
R9273:Prune2	UTSW	19	17,118,326 (GRCm38)	missense	possibly damaging	0.74
R9275:Prune2	UTSW	19	17,123,780 (GRCm38)	missense	probably benign	0.06
R9278:Prune2	UTSW	19	17,123,780 (GRCm38)	missense	probably benign	0.06
R9290:Prune2	UTSW	19	17,168,327 (GRCm38)	missense	probably benign	0.41
R9305:Prune2	UTSW	19	17,120,261 (GRCm38)	missense	probably benign	0.14
R9317:Prune2	UTSW	19	17,121,670 (GRCm38)	missense	probably benign	0.00
R9354:Prune2	UTSW	19	17,122,622 (GRCm38)	missense	probably benign	0.43
R9373:Prune2	UTSW	19	17,122,138 (GRCm38)	missense	probably benign
R9394:Prune2	UTSW	19	17,003,689 (GRCm38)	missense	probably damaging	1.00
R9405:Prune2	UTSW	19	17,216,344 (GRCm38)	missense	probably damaging	0.99
R9476:Prune2	UTSW	19	17,119,342 (GRCm38)	missense	possibly damaging	0.64
R9532:Prune2	UTSW	19	17,122,430 (GRCm38)	missense	probably benign	0.00
X0019:Prune2	UTSW	19	17,121,517 (GRCm38)	missense	probably benign	0.16
X0028:Prune2	UTSW	19	17,122,885 (GRCm38)	missense	probably damaging	1.00
X0064:Prune2	UTSW	19	17,122,375 (GRCm38)	missense	probably damaging	1.00
X0066:Prune2	UTSW	19	17,118,790 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGAGGACAGAACTTTGGAATCGGC -3'
(R):5'- AGGAACTGGCTCTCGCTCTCTAAC -3'

Sequencing Primer
(F):5'- GCAGTTGTCAGAGTCATTAACCC -3'
(R):5'- CTTGTCTAGTGAAACAGTGCAG -3'

Posted On

2013-05-23