Mutagenetix > Incidental Mutation

Incidental Mutation 'R1711:Gm11639'

190600

Institutional Source

Beutler Lab

Gene Symbol

Gm11639

Ensembl Gene

ENSMUSG00000040838

Gene Name

predicted gene 11639

Synonyms

MMRRC Submission

039744-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.082) question?

Stock #

R1711 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

104685707-105117394 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 104720688 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Arginine at position 452 (K452R)

Ref Sequence

ENSEMBL: ENSMUSP00000148433 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000148007] [ENSMUST00000212287]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000148007
AA Change: K379R

SMART Domains

Protein: ENSMUSP00000116040
Gene: ENSMUSG00000040838
AA Change: K379R

Domain	Start	End	E-Value	Type
low complexity region	40	55	N/A	INTRINSIC
low complexity region	116	129	N/A	INTRINSIC
internal_repeat_4	146	233	3.42e-6	PROSPERO
internal_repeat_3	165	247	2.21e-6	PROSPERO
low complexity region	331	348	N/A	INTRINSIC
internal_repeat_2	349	361	4.38e-8	PROSPERO
internal_repeat_2	371	383	4.38e-8	PROSPERO
low complexity region	385	640	N/A	INTRINSIC
Pfam:EF-hand_8	677	729	8.7e-6	PFAM
low complexity region	835	842	N/A	INTRINSIC
internal_repeat_1	879	1106	2.47e-14	PROSPERO
internal_repeat_4	1015	1108	3.42e-6	PROSPERO

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000175713

Predicted Effect

probably benign
Transcript: ENSMUST00000212287
AA Change: K452R

PolyPhen 2 Score 0.074 (Sensitivity: 0.93; Specificity: 0.85)

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.6%
20x: 93.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 111 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210408I21Rik	C	T	13: 77,269,920 (GRCm38)	T741I	possibly damaging	Het
Acot3	A	T	12: 84,053,573 (GRCm38)	Q41L	probably damaging	Het
Actl7b	G	A	4: 56,740,165 (GRCm38)	Q398*	probably null	Het
Adgrb2	C	A	4: 129,992,624 (GRCm38)	Q186K	probably damaging	Het
Akr1a1	A	G	4: 116,637,974 (GRCm38)		probably null	Het
Ap3s2	A	T	7: 79,880,490 (GRCm38)	F192L	probably damaging	Het
Apobr	T	G	7: 126,584,979 (GRCm38)		probably null	Het
Arhgap5	A	G	12: 52,519,345 (GRCm38)	N1033S	probably damaging	Het
Arid3c	G	T	4: 41,725,947 (GRCm38)	R219S	probably damaging	Het
Bves	C	T	10: 45,347,865 (GRCm38)	T207M	probably damaging	Het
C330027C09Rik	A	C	16: 49,017,486 (GRCm38)	I850L	probably benign	Het
Cacna1d	T	C	14: 30,066,056 (GRCm38)	K1619R	probably damaging	Het
Caps2	A	T	10: 112,190,978 (GRCm38)	D223V	possibly damaging	Het
Cd163l1	G	T	7: 140,220,609 (GRCm38)	C101F	probably damaging	Het
Cd3g	A	C	9: 44,974,342 (GRCm38)	L35R	probably damaging	Het
Cdh23	A	T	10: 60,523,536 (GRCm38)	V261E	probably benign	Het
Cfap54	T	G	10: 93,011,020 (GRCm38)	T1028P	probably damaging	Het
Ch25h	C	A	19: 34,474,286 (GRCm38)	V281L	probably benign	Het
Clu	G	T	14: 65,980,905 (GRCm38)	V405L	possibly damaging	Het
Col6a3	A	T	1: 90,830,213 (GRCm38)	H6Q	probably damaging	Het
Cps1	G	A	1: 67,168,374 (GRCm38)		probably null	Het
Ctr9	T	C	7: 111,055,663 (GRCm38)	S1134P	unknown	Het
Cts7	C	T	13: 61,352,810 (GRCm38)	G308S	probably damaging	Het
Cyp2c39	C	A	19: 39,566,891 (GRCm38)	T385K	probably damaging	Het
Dennd5a	A	T	7: 109,918,712 (GRCm38)	D596E	probably benign	Het
Disc1	T	A	8: 125,124,610 (GRCm38)	I413K	probably benign	Het
Dll3	C	T	7: 28,294,497 (GRCm38)	G505D	probably damaging	Het
Dnah3	A	G	7: 120,078,571 (GRCm38)	W377R	probably damaging	Het
Dopey2	A	G	16: 93,799,926 (GRCm38)	D1792G	probably damaging	Het
Dpep3	T	A	8: 105,973,693 (GRCm38)	R460S	probably benign	Het
Ebf4	A	G	2: 130,358,831 (GRCm38)	N302S	probably damaging	Het
Egflam	T	C	15: 7,289,915 (GRCm38)	E194G	possibly damaging	Het
Ep400	A	T	5: 110,693,308 (GRCm38)		probably benign	Het
Ercc6	T	C	14: 32,526,176 (GRCm38)	M228T	probably damaging	Het
Fbxo9	T	C	9: 78,087,247 (GRCm38)	T264A	probably damaging	Het
Fcrl5	C	A	3: 87,457,414 (GRCm38)	P486T	possibly damaging	Het
Fyb	T	C	15: 6,580,479 (GRCm38)	F178L	probably damaging	Het
Gaa	T	A	11: 119,280,460 (GRCm38)	I646N	probably damaging	Het
Gm13124	A	T	4: 144,555,406 (GRCm38)	I272K	probably damaging	Het
Gm5431	A	T	11: 48,895,026 (GRCm38)	V174E	possibly damaging	Het
Gnpat	T	G	8: 124,886,952 (GRCm38)		probably null	Het
Gucy1a2	G	T	9: 3,759,622 (GRCm38)	R476I	probably benign	Het
Hars	A	G	18: 36,771,103 (GRCm38)	L241P	probably damaging	Het
Haus5	G	A	7: 30,657,903 (GRCm38)	Q399*	probably null	Het
Hephl1	T	C	9: 15,059,246 (GRCm38)	E984G	probably damaging	Het
Hmces	C	T	6: 87,921,592 (GRCm38)	Q132*	probably null	Het
Hsp90b1	G	T	10: 86,694,525 (GRCm38)	T490K	probably damaging	Het
Idh2	T	G	7: 80,099,158 (GRCm38)	E125A	probably damaging	Het
Ipo13	G	T	4: 117,904,522 (GRCm38)	H465Q	probably benign	Het
Isca2	C	A	12: 84,773,619 (GRCm38)	T31K	probably damaging	Het
Itga9	T	C	9: 118,698,461 (GRCm38)	V560A	probably benign	Het
Jhy	G	A	9: 40,911,157 (GRCm38)	Q562*	probably null	Het
Kcnj5	A	G	9: 32,322,569 (GRCm38)	I150T	probably damaging	Het
Kmt2a	A	G	9: 44,841,621 (GRCm38)	I1419T	unknown	Het
Lix1	T	C	17: 17,446,058 (GRCm38)	F160L	possibly damaging	Het
Lonrf2	G	A	1: 38,813,276 (GRCm38)	P165S	probably benign	Het
Map4k1	A	T	7: 28,989,352 (GRCm38)	Q276L	possibly damaging	Het
Mmp9	G	A	2: 164,949,422 (GRCm38)	G171S	probably damaging	Het
Mvp	C	A	7: 126,995,735 (GRCm38)		probably null	Het
Mylk3	T	A	8: 85,364,831 (GRCm38)	E115V	probably damaging	Het
Nebl	T	A	2: 17,388,754 (GRCm38)	T603S	probably damaging	Het
Nudt15	T	C	14: 73,523,336 (GRCm38)	D105G	probably benign	Het
Olfr1369-ps1	G	A	13: 21,116,306 (GRCm38)	V205I	probably benign	Het
Olfr527	A	C	7: 140,335,999 (GRCm38)	T46P	possibly damaging	Het
Olfr556	G	T	7: 102,670,162 (GRCm38)	V81L	probably damaging	Het
Olfr65	T	A	7: 103,906,699 (GRCm38)	W87R	probably damaging	Het
Olfr685	A	T	7: 105,180,760 (GRCm38)	H199Q	probably damaging	Het
Olfr971	A	G	9: 39,840,285 (GRCm38)	M284V	probably benign	Het
Osbpl9	A	T	4: 109,066,218 (GRCm38)	C495S	probably damaging	Het
Pamr1	A	G	2: 102,640,852 (GRCm38)	T507A	probably benign	Het
Pcdhb9	T	A	18: 37,403,327 (GRCm38)	C791*	probably null	Het
Pcgf6	T	C	19: 47,050,518 (GRCm38)	E101G	probably damaging	Het
Pdgfrl	A	T	8: 40,985,794 (GRCm38)	I256F	probably benign	Het
Pdzd7	T	C	19: 45,045,511 (GRCm38)	R45G	possibly damaging	Het
Pecr	C	T	1: 72,277,409 (GRCm38)	V46I	possibly damaging	Het
Pgr	A	G	9: 8,922,714 (GRCm38)		probably null	Het
Pik3c2a	A	T	7: 116,417,927 (GRCm38)	Y198*	probably null	Het
Pp2d1	T	A	17: 53,515,310 (GRCm38)	M243L	possibly damaging	Het
Ppp1r1a	T	A	15: 103,533,492 (GRCm38)	I50L	possibly damaging	Het
Proc	T	C	18: 32,127,406 (GRCm38)	D222G	probably benign	Het
Ptprq	T	A	10: 107,534,699 (GRCm38)	R2044*	probably null	Het
Ranbp2	T	C	10: 58,460,519 (GRCm38)	V326A	probably benign	Het
Reep6	T	A	10: 80,333,981 (GRCm38)	F122I	possibly damaging	Het
Rubcn	C	A	16: 32,843,101 (GRCm38)	R388S	probably damaging	Het
Rusc1	A	G	3: 89,089,293 (GRCm38)	L62P	probably damaging	Het
Satb2	T	C	1: 56,850,289 (GRCm38)	N423S	probably damaging	Het
Serpinb9d	A	G	13: 33,200,748 (GRCm38)	K236R	probably benign	Het
Slc4a7	A	G	14: 14,765,709 (GRCm38)	R680G	probably benign	Het
Slitrk1	T	A	14: 108,913,096 (GRCm38)	Y61F	probably benign	Het
Son	A	G	16: 91,660,226 (GRCm38)		probably benign	Het
Sparc	T	A	11: 55,395,776 (GRCm38)		probably null	Het
Spon2	A	G	5: 33,216,385 (GRCm38)	F194S	probably damaging	Het
Spta1	A	G	1: 174,241,042 (GRCm38)	E2136G	probably damaging	Het
Stat4	T	C	1: 52,106,925 (GRCm38)	S746P	probably damaging	Het
Stk31	T	A	6: 49,469,304 (GRCm38)	S958R	probably benign	Het
Stom	T	A	2: 35,315,917 (GRCm38)	I267F	probably damaging	Het
Stx12	A	T	4: 132,858,477 (GRCm38)	D197E	probably damaging	Het
Taok3	A	T	5: 117,255,926 (GRCm38)	N588I	possibly damaging	Het
Tgs1	A	G	4: 3,598,658 (GRCm38)	D657G	probably damaging	Het
Trim6	A	G	7: 104,232,837 (GRCm38)	T432A	probably damaging	Het
Trim72	C	G	7: 128,004,585 (GRCm38)	C34W	probably damaging	Het
Trpc4ap	A	T	2: 155,657,744 (GRCm38)	I286N	probably benign	Het
Ttn	A	G	2: 76,863,561 (GRCm38)	V321A	possibly damaging	Het
Utp4	T	A	8: 106,918,720 (GRCm38)	I583N	probably damaging	Het
Wdfy2	G	T	14: 62,944,097 (GRCm38)	M225I	probably benign	Het
Wfdc1	A	G	8: 119,681,037 (GRCm38)	T134A	probably benign	Het
Wnt9b	A	G	11: 103,732,128 (GRCm38)	S150P	probably damaging	Het
Zbtb46	A	T	2: 181,411,684 (GRCm38)	F412I	probably damaging	Het
Zc3h15	G	A	2: 83,661,148 (GRCm38)	R240H	probably benign	Het
Zfp11	A	T	5: 129,656,673 (GRCm38)	Y575N	probably benign	Het
Zfp687	T	C	3: 95,011,889 (GRCm38)	M191V	probably benign	Het

Other mutations in Gm11639

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00897:Gm11639	APN	11	105,100,021 (GRCm38)	missense	probably damaging	1.00
IGL01308:Gm11639	APN	11	104,720,697 (GRCm38)	missense	probably benign	0.03
IGL01483:Gm11639	APN	11	104,739,347 (GRCm38)	missense	probably benign	0.03
IGL01695:Gm11639	APN	11	104,736,063 (GRCm38)	missense	probably damaging	1.00
IGL01860:Gm11639	APN	11	104,690,921 (GRCm38)	missense	probably benign	0.16
IGL01981:Gm11639	APN	11	104,721,432 (GRCm38)	intron	probably benign
IGL01984:Gm11639	APN	11	104,738,308 (GRCm38)	missense	probably benign	0.20
IGL02023:Gm11639	APN	11	104,721,432 (GRCm38)	intron	probably benign
IGL02252:Gm11639	APN	11	104,753,927 (GRCm38)	missense	possibly damaging	0.68
IGL02886:Gm11639	APN	11	105,095,874 (GRCm38)	missense	possibly damaging	0.95
IGL03116:Gm11639	APN	11	104,721,533 (GRCm38)	missense	probably benign	0.02
IGL03141:Gm11639	APN	11	105,095,870 (GRCm38)	missense	probably damaging	0.99
IGL03242:Gm11639	APN	11	105,106,404 (GRCm38)	missense	probably damaging	1.00
IGL03274:Gm11639	APN	11	104,721,093 (GRCm38)	missense	probably benign	0.03
IGL03408:Gm11639	APN	11	104,710,621 (GRCm38)	missense	probably benign	0.03
R0018:Gm11639	UTSW	11	104,721,552 (GRCm38)	critical splice donor site	probably null
R0068:Gm11639	UTSW	11	104,720,822 (GRCm38)	missense	probably benign	0.29
R0350:Gm11639	UTSW	11	104,690,880 (GRCm38)	missense	probably benign	0.03
R0646:Gm11639	UTSW	11	104,720,501 (GRCm38)	missense	probably benign	0.03
R0668:Gm11639	UTSW	11	104,720,492 (GRCm38)	missense	probably benign	0.16
R0715:Gm11639	UTSW	11	104,720,880 (GRCm38)	missense	possibly damaging	0.90
R0944:Gm11639	UTSW	11	104,710,730 (GRCm38)	splice site	probably null
R1330:Gm11639	UTSW	11	104,746,290 (GRCm38)	missense	possibly damaging	0.84
R1508:Gm11639	UTSW	11	104,710,677 (GRCm38)	missense	probably benign	0.03
R1643:Gm11639	UTSW	11	104,698,978 (GRCm38)	missense	probably benign	0.16
R1651:Gm11639	UTSW	11	104,720,666 (GRCm38)	missense	probably benign	0.03
R1665:Gm11639	UTSW	11	104,721,114 (GRCm38)	missense	probably benign	0.07
R1702:Gm11639	UTSW	11	104,691,006 (GRCm38)	missense	probably benign	0.03
R1779:Gm11639	UTSW	11	104,720,939 (GRCm38)	missense	probably benign	0.15
R1813:Gm11639	UTSW	11	104,720,688 (GRCm38)	missense	probably benign	0.07
R1818:Gm11639	UTSW	11	104,721,507 (GRCm38)	missense	probably benign	0.10
R1896:Gm11639	UTSW	11	104,720,688 (GRCm38)	missense	probably benign	0.07
R1969:Gm11639	UTSW	11	104,746,264 (GRCm38)	missense	probably damaging	1.00
R2139:Gm11639	UTSW	11	104,751,911 (GRCm38)	missense	possibly damaging	0.53
R2165:Gm11639	UTSW	11	104,751,862 (GRCm38)	missense	possibly damaging	0.93
R2359:Gm11639	UTSW	11	104,739,280 (GRCm38)	missense	possibly damaging	0.80
R2394:Gm11639	UTSW	11	104,738,295 (GRCm38)	missense	probably benign	0.17
R2406:Gm11639	UTSW	11	104,720,631 (GRCm38)	missense	probably benign	0.03
R2570:Gm11639	UTSW	11	104,733,664 (GRCm38)	missense	probably damaging	1.00
R3795:Gm11639	UTSW	11	104,733,675 (GRCm38)	missense	possibly damaging	0.94
R4352:Gm11639	UTSW	11	104,739,314 (GRCm38)	missense	probably null	0.25
R4359:Gm11639	UTSW	11	104,733,721 (GRCm38)	splice site	probably null
R4424:Gm11639	UTSW	11	104,736,114 (GRCm38)	critical splice donor site	probably null
R4895:Gm11639	UTSW	11	104,720,286 (GRCm38)	missense	probably benign	0.16
R4895:Gm11639	UTSW	11	104,749,670 (GRCm38)	missense	probably damaging	1.00
R5006:Gm11639	UTSW	11	104,729,677 (GRCm38)	splice site	probably null
R5066:Gm11639	UTSW	11	104,720,664 (GRCm38)	missense	probably benign	0.03
R5329:Gm11639	UTSW	11	104,753,806 (GRCm38)	splice site	probably null
R5405:Gm11639	UTSW	11	104,721,192 (GRCm38)	missense	probably benign	0.07
R5814:Gm11639	UTSW	11	104,736,114 (GRCm38)	critical splice donor site	probably benign
R5888:Gm11639	UTSW	11	104,721,401 (GRCm38)	splice site	probably benign
R5910:Gm11639	UTSW	11	104,690,934 (GRCm38)	missense	probably benign	0.01
R5975:Gm11639	UTSW	11	104,687,549 (GRCm38)	start gained	probably benign
R6019:Gm11639	UTSW	11	105,042,902 (GRCm38)	critical splice donor site	probably null
R6028:Gm11639	UTSW	11	104,769,655 (GRCm38)	critical splice donor site	probably null
R6048:Gm11639	UTSW	11	104,944,433 (GRCm38)	missense	unknown
R6059:Gm11639	UTSW	11	105,036,769 (GRCm38)	missense	probably benign	0.03
R6147:Gm11639	UTSW	11	104,967,740 (GRCm38)	missense	unknown
R6176:Gm11639	UTSW	11	104,792,557 (GRCm38)	missense	probably benign	0.16
R6181:Gm11639	UTSW	11	104,831,333 (GRCm38)	missense	probably benign	0.25
R6196:Gm11639	UTSW	11	104,855,560 (GRCm38)	missense	probably benign	0.07
R6245:Gm11639	UTSW	11	104,785,008 (GRCm38)	missense	probably benign	0.03
R6262:Gm11639	UTSW	11	104,893,753 (GRCm38)	missense	probably benign	0.24
R6263:Gm11639	UTSW	11	104,919,486 (GRCm38)	missense	unknown
R6277:Gm11639	UTSW	11	105,010,322 (GRCm38)	missense	possibly damaging	0.49
R6338:Gm11639	UTSW	11	104,843,208 (GRCm38)	nonsense	probably null
R6355:Gm11639	UTSW	11	105,005,685 (GRCm38)	missense	probably benign	0.29
R6356:Gm11639	UTSW	11	104,893,707 (GRCm38)	missense	probably benign	0.19
R6365:Gm11639	UTSW	11	104,924,586 (GRCm38)	missense	unknown
R6391:Gm11639	UTSW	11	104,994,317 (GRCm38)	missense	possibly damaging	0.92
R6556:Gm11639	UTSW	11	105,008,251 (GRCm38)	missense	probably null	0.03
R6604:Gm11639	UTSW	11	104,698,946 (GRCm38)	nonsense	probably null
R6605:Gm11639	UTSW	11	104,999,281 (GRCm38)	splice site	probably null
R6634:Gm11639	UTSW	11	104,893,783 (GRCm38)	missense	probably benign	0.17
R6851:Gm11639	UTSW	11	105,005,695 (GRCm38)	missense	probably benign	0.03
R6862:Gm11639	UTSW	11	104,721,458 (GRCm38)	nonsense	probably null
R6949:Gm11639	UTSW	11	104,909,070 (GRCm38)	missense	probably damaging	1.00
R6970:Gm11639	UTSW	11	104,776,356 (GRCm38)	missense	probably benign	0.03
R7014:Gm11639	UTSW	11	104,693,422 (GRCm38)	missense	probably benign	0.03
R7097:Gm11639	UTSW	11	105,008,961 (GRCm38)	missense	possibly damaging	0.68
R7122:Gm11639	UTSW	11	105,008,961 (GRCm38)	missense	possibly damaging	0.68
R7124:Gm11639	UTSW	11	104,738,274 (GRCm38)	missense	probably benign	0.17
R7146:Gm11639	UTSW	11	105,022,938 (GRCm38)	missense	probably benign	0.03
R7146:Gm11639	UTSW	11	104,967,752 (GRCm38)	missense	unknown
R7154:Gm11639	UTSW	11	104,699,140 (GRCm38)	splice site	probably null
R7175:Gm11639	UTSW	11	104,947,411 (GRCm38)	missense	unknown
R7198:Gm11639	UTSW	11	104,751,885 (GRCm38)	missense	probably benign	0.15
R7211:Gm11639	UTSW	11	104,724,609 (GRCm38)	critical splice donor site	probably null
R7211:Gm11639	UTSW	11	104,710,713 (GRCm38)	missense	probably benign	0.01
R7216:Gm11639	UTSW	11	104,880,549 (GRCm38)	missense	possibly damaging	0.49
R7221:Gm11639	UTSW	11	104,900,606 (GRCm38)	missense	probably benign	0.36
R7233:Gm11639	UTSW	11	104,839,843 (GRCm38)	missense	possibly damaging	0.69
R7236:Gm11639	UTSW	11	104,899,267 (GRCm38)	missense	probably benign	0.10
R7262:Gm11639	UTSW	11	104,854,606 (GRCm38)	critical splice donor site	probably null
R7289:Gm11639	UTSW	11	105,038,358 (GRCm38)	missense	probably benign	0.24
R7323:Gm11639	UTSW	11	105,030,011 (GRCm38)	missense	probably benign	0.07
R7378:Gm11639	UTSW	11	104,714,702 (GRCm38)	missense	probably benign	0.03
R7388:Gm11639	UTSW	11	104,721,045 (GRCm38)	missense	probably damaging	0.97
R7390:Gm11639	UTSW	11	104,724,585 (GRCm38)	missense	possibly damaging	0.46
R7411:Gm11639	UTSW	11	104,999,723 (GRCm38)	missense	probably benign	0.10
R7468:Gm11639	UTSW	11	104,749,700 (GRCm38)	missense	probably benign	0.17
R7497:Gm11639	UTSW	11	104,762,690 (GRCm38)	critical splice donor site	probably null
R7620:Gm11639	UTSW	11	104,832,143 (GRCm38)	missense	possibly damaging	0.95
R7638:Gm11639	UTSW	11	105,036,799 (GRCm38)	missense	probably benign	0.03
R7661:Gm11639	UTSW	11	104,726,677 (GRCm38)	missense	probably benign	0.03
R7667:Gm11639	UTSW	11	104,751,911 (GRCm38)	missense	possibly damaging	0.53
R7682:Gm11639	UTSW	11	104,964,348 (GRCm38)	splice site	probably null
R7708:Gm11639	UTSW	11	104,964,571 (GRCm38)	missense	unknown
R7721:Gm11639	UTSW	11	104,724,540 (GRCm38)	nonsense	probably null
R7747:Gm11639	UTSW	11	104,842,603 (GRCm38)	missense	probably damaging	0.96
R7840:Gm11639	UTSW	11	104,733,713 (GRCm38)	missense	probably benign	0.07
R7846:Gm11639	UTSW	11	104,714,745 (GRCm38)	critical splice donor site	probably null
R7893:Gm11639	UTSW	11	104,979,360 (GRCm38)	missense	unknown
R7897:Gm11639	UTSW	11	104,998,235 (GRCm38)	missense	probably benign	0.24
R7936:Gm11639	UTSW	11	105,046,559 (GRCm38)	critical splice donor site	probably null
R7936:Gm11639	UTSW	11	104,999,698 (GRCm38)	missense	possibly damaging	0.89
R7959:Gm11639	UTSW	11	105,042,801 (GRCm38)	missense	probably damaging	0.96
R8031:Gm11639	UTSW	11	104,881,469 (GRCm38)	missense	possibly damaging	0.49
R8041:Gm11639	UTSW	11	104,919,479 (GRCm38)	missense	unknown
R8054:Gm11639	UTSW	11	104,730,400 (GRCm38)	missense	probably benign	0.07
R8056:Gm11639	UTSW	11	104,909,070 (GRCm38)	missense	probably damaging	0.98
R8088:Gm11639	UTSW	11	104,998,246 (GRCm38)	missense	probably benign	0.10
R8112:Gm11639	UTSW	11	104,950,200 (GRCm38)	missense	unknown
R8340:Gm11639	UTSW	11	104,986,030 (GRCm38)	missense	unknown
R8405:Gm11639	UTSW	11	104,721,198 (GRCm38)	missense	probably benign	0.02
R8413:Gm11639	UTSW	11	104,920,309 (GRCm38)	missense	unknown
R8472:Gm11639	UTSW	11	104,818,637 (GRCm38)	missense	probably benign	0.07
R8549:Gm11639	UTSW	11	104,999,695 (GRCm38)	missense	probably damaging	0.99
R8699:Gm11639	UTSW	11	104,781,246 (GRCm38)	missense	probably benign	0.03
R8711:Gm11639	UTSW	11	104,852,545 (GRCm38)	missense	probably benign	0.03
R8732:Gm11639	UTSW	11	104,804,274 (GRCm38)	missense	probably benign	0.03
R8745:Gm11639	UTSW	11	104,858,478 (GRCm38)	missense	possibly damaging	0.57
R8806:Gm11639	UTSW	11	105,037,869 (GRCm38)	missense	probably benign	0.07
R8810:Gm11639	UTSW	11	104,914,895 (GRCm38)	missense	unknown
R8845:Gm11639	UTSW	11	105,008,961 (GRCm38)	missense	possibly damaging	0.68
R8870:Gm11639	UTSW	11	104,900,674 (GRCm38)	missense	probably benign	0.07
R8872:Gm11639	UTSW	11	104,870,054 (GRCm38)	missense	probably benign	0.19
R8879:Gm11639	UTSW	11	104,690,955 (GRCm38)	missense	probably benign	0.03
R8924:Gm11639	UTSW	11	104,915,427 (GRCm38)	frame shift	probably null
R8954:Gm11639	UTSW	11	105,018,699 (GRCm38)	critical splice donor site	probably null
R8960:Gm11639	UTSW	11	104,929,946 (GRCm38)	splice site	probably benign
R8975:Gm11639	UTSW	11	105,063,589 (GRCm38)	missense	probably benign	0.17
R8988:Gm11639	UTSW	11	105,020,526 (GRCm38)	missense	probably benign	0.07
R8998:Gm11639	UTSW	11	104,749,651 (GRCm38)	missense	probably benign	0.09
R8999:Gm11639	UTSW	11	104,749,651 (GRCm38)	missense	probably benign	0.09
R9002:Gm11639	UTSW	11	105,029,996 (GRCm38)	missense	probably damaging	0.99
R9012:Gm11639	UTSW	11	104,820,521 (GRCm38)	critical splice donor site	probably null
R9036:Gm11639	UTSW	11	105,036,775 (GRCm38)	missense	probably benign	0.03
R9037:Gm11639	UTSW	11	104,912,965 (GRCm38)	missense	unknown
R9059:Gm11639	UTSW	11	104,751,863 (GRCm38)	missense	possibly damaging	0.73
R9066:Gm11639	UTSW	11	104,740,862 (GRCm38)	intron	probably benign
R9122:Gm11639	UTSW	11	104,965,779 (GRCm38)	missense	unknown
R9125:Gm11639	UTSW	11	104,845,534 (GRCm38)	missense	probably damaging	1.00
R9127:Gm11639	UTSW	11	104,850,581 (GRCm38)	missense	probably benign	0.07
R9171:Gm11639	UTSW	11	104,909,882 (GRCm38)	missense	probably benign	0.36
R9219:Gm11639	UTSW	11	104,945,865 (GRCm38)	missense	unknown
R9224:Gm11639	UTSW	11	104,770,975 (GRCm38)	missense	probably benign	0.07
R9235:Gm11639	UTSW	11	105,017,161 (GRCm38)	missense	probably benign	0.19
R9294:Gm11639	UTSW	11	104,831,300 (GRCm38)	missense	probably benign	0.24
R9318:Gm11639	UTSW	11	104,965,822 (GRCm38)	critical splice donor site	probably null
R9322:Gm11639	UTSW	11	104,874,373 (GRCm38)	missense	probably benign	0.36
R9361:Gm11639	UTSW	11	105,005,698 (GRCm38)	missense	probably benign	0.03
R9408:Gm11639	UTSW	11	104,730,429 (GRCm38)	critical splice donor site	probably null
R9434:Gm11639	UTSW	11	105,009,037 (GRCm38)	missense	probably benign	0.24
R9477:Gm11639	UTSW	11	104,945,872 (GRCm38)	missense	unknown
R9658:Gm11639	UTSW	11	104,720,294 (GRCm38)	missense	probably benign	0.03
R9719:Gm11639	UTSW	11	104,977,086 (GRCm38)	missense	unknown
R9751:Gm11639	UTSW	11	104,893,085 (GRCm38)	missense	probably benign	0.19
R9763:Gm11639	UTSW	11	104,999,659 (GRCm38)	missense	possibly damaging	0.89
X0026:Gm11639	UTSW	11	104,720,975 (GRCm38)	missense	probably benign	0.07
Z1088:Gm11639	UTSW	11	104,751,902 (GRCm38)	missense	probably damaging	0.96
Z1176:Gm11639	UTSW	11	105,001,967 (GRCm38)	missense	probably benign	0.29
Z1177:Gm11639	UTSW	11	104,820,518 (GRCm38)	missense	probably benign	0.03
Z1177:Gm11639	UTSW	11	104,739,338 (GRCm38)	nonsense	probably null
Z1177:Gm11639	UTSW	11	104,924,019 (GRCm38)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- CAGGATGAGGCTGAACTTAAACTCTCC -3'
(R):5'- CACTTCTATCCAGTGACTTCTTGAGGC -3'

Sequencing Primer
(F):5'- TCTCAAGTGGGATCATCAGC -3'
(R):5'- GCTTGAATCACGTCTATCCGATAAC -3'

Posted On

2014-05-14