Mutagenetix > Incidental Mutation

Incidental Mutation 'R7411:Gm11639'

575099

Institutional Source

Beutler Lab

Gene Symbol

Gm11639

Ensembl Gene

ENSMUSG00000040838

Gene Name

predicted gene 11639

Synonyms

MMRRC Submission

045492-MU

Accession Numbers

Essential gene?

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

Stock #

R7411 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

104685707-105117394 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 104999723 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 4210 (N4210K)

Ref Sequence

ENSEMBL: ENSMUSP00000148433 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000212287
AA Change: N4210K

PolyPhen 2 Score 0.096 (Sensitivity: 0.93; Specificity: 0.85)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810055G02Rik	C	T	19: 3,717,241 (GRCm38)	T276I	possibly damaging	Het
9130011E15Rik	A	C	19: 45,965,435 (GRCm38)	V170G	probably benign	Het
Abca17	A	G	17: 24,328,569 (GRCm38)	I277T	possibly damaging	Het
Abcb11	C	T	2: 69,303,936 (GRCm38)		probably null	Het
Abcc12	C	A	8: 86,560,850 (GRCm38)	R122L	possibly damaging	Het
Abcc8	A	G	7: 46,165,917 (GRCm38)		probably null	Het
Adam28	C	T	14: 68,626,947 (GRCm38)	R469K	probably damaging	Het
Adamts18	T	C	8: 113,777,730 (GRCm38)	Y243C	probably damaging	Het
Agbl3	T	C	6: 34,814,819 (GRCm38)	S619P	probably damaging	Het
Alpk3	A	T	7: 81,092,852 (GRCm38)	T806S	probably benign	Het
Atoh1	T	A	6: 64,729,930 (GRCm38)	I203N	probably damaging	Het
Cables1	A	G	18: 11,840,515 (GRCm38)	E237G	probably benign	Het
Cacna1d	A	G	14: 30,352,990 (GRCm38)	M1T	probably null	Het
Ccdc91	C	T	6: 147,592,198 (GRCm38)	Q363*	probably null	Het
Ceacam5	T	A	7: 17,750,753 (GRCm38)	D473E	probably damaging	Het
Cfap54	T	A	10: 92,868,755 (GRCm38)	D2821V	unknown	Het
Clca3a2	A	G	3: 144,802,099 (GRCm38)	S737P	probably damaging	Het
Clec4n	T	A	6: 123,232,186 (GRCm38)	M70K	probably benign	Het
Dstyk	G	A	1: 132,417,666 (GRCm38)	G21S	probably benign	Het
Enpp5	A	G	17: 44,081,475 (GRCm38)	D265G	probably damaging	Het
Gabrb1	T	C	5: 72,122,195 (GRCm38)		probably null	Het
Gm28710	A	T	5: 16,824,765 (GRCm38)	T500S	possibly damaging	Het
Gm40460	CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	7: 142,240,817 (GRCm38)		probably benign	Het
Gm5861	T	A	5: 11,183,149 (GRCm38)		probably null	Het
Gm9513	T	C	9: 36,475,684 (GRCm38)	V16A	possibly damaging	Het
Guk1	A	G	11: 59,185,985 (GRCm38)	F91L		Het
Ints1	C	T	5: 139,764,260 (GRCm38)	E961K	possibly damaging	Het
Irx2	T	A	13: 72,629,063 (GRCm38)	M1K	probably null	Het
Jrk	C	T	15: 74,707,199 (GRCm38)	R79H	possibly damaging	Het
Kcnu1	G	T	8: 25,892,088 (GRCm38)	V489L	probably damaging	Het
Kctd7	C	T	5: 130,152,424 (GRCm38)	T209M	probably benign	Het
Kdm5a	T	A	6: 120,426,815 (GRCm38)	V1127E	probably damaging	Het
Klk6	A	G	7: 43,826,943 (GRCm38)	H69R	probably damaging	Het
Lck	T	C	4: 129,551,970 (GRCm38)	K340R	probably benign	Het
Lrrc75a	A	G	11: 62,605,908 (GRCm38)	L276P	probably damaging	Het
Med25	A	G	7: 44,878,243 (GRCm38)	W730R	probably damaging	Het
Muc4	T	C	16: 32,751,322 (GRCm38)	V400A	probably benign	Het
Myl10	G	C	5: 136,697,971 (GRCm38)	V70L	probably benign	Het
Myt1	C	A	2: 181,815,106 (GRCm38)	H906Q	probably damaging	Het
Ncl	A	T	1: 86,350,842 (GRCm38)	F673I	probably damaging	Het
Nfe2l1	G	T	11: 96,822,183 (GRCm38)	T216N	probably benign	Het
Nos2	G	A	11: 78,944,855 (GRCm38)		probably null	Het
Nphp4	T	A	4: 152,554,717 (GRCm38)	I935N	probably benign	Het
Ntn1	G	A	11: 68,386,089 (GRCm38)	A11V	probably benign	Het
Olfr1257	T	C	2: 89,881,261 (GRCm38)	V145A	probably damaging	Het
Olfr1395	A	T	11: 49,148,994 (GRCm38)	M246L	probably benign	Het
Pcdha12	A	G	18: 37,021,608 (GRCm38)	Y460C	probably damaging	Het
Pcdha4	G	T	18: 36,953,058 (GRCm38)	R98L	probably benign	Het
Pitpnc1	A	G	11: 107,212,572 (GRCm38)	S234P	probably damaging	Het
Pmfbp1	A	T	8: 109,513,871 (GRCm38)	Y195F	probably damaging	Het
Prl6a1	T	C	13: 27,318,142 (GRCm38)	I164T	probably damaging	Het
Ptpn18	G	A	1: 34,472,192 (GRCm38)		probably null	Het
Rhbdl2	G	A	4: 123,829,642 (GRCm38)	A280T	possibly damaging	Het
Rsf1	CGGC	CGGCGGCGGGGGC	7: 97,579,932 (GRCm38)		probably benign	Het
Sema3a	T	G	5: 13,516,263 (GRCm38)	Y171*	probably null	Het
Set	A	G	2: 30,066,885 (GRCm38)	E22G	probably benign	Het
Sirpb1b	A	T	3: 15,542,997 (GRCm38)	D229E	probably benign	Het
Slc12a2	A	T	18: 57,941,013 (GRCm38)	I1096F	probably benign	Het
Slc30a5	T	C	13: 100,818,180 (GRCm38)	I159V	probably benign	Het
Slc35f3	CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	8: 126,389,038 (GRCm38)		probably benign	Het
Slc6a20b	A	G	9: 123,604,948 (GRCm38)	I275T	probably benign	Het
Stradb	A	C	1: 58,988,518 (GRCm38)	D69A	possibly damaging	Het
Supt16	A	T	14: 52,178,051 (GRCm38)	V409E	probably damaging	Het
Tcea2	A	G	2: 181,686,664 (GRCm38)	N195S	probably damaging	Het
Thumpd3	T	C	6: 113,056,111 (GRCm38)	V270A	possibly damaging	Het
Urgcp	T	A	11: 5,718,116 (GRCm38)	H117L	probably benign	Het
Vps13c	T	A	9: 67,972,001 (GRCm38)	M3408K	probably damaging	Het
Wdfy4	A	C	14: 33,106,131 (GRCm38)	M1078R		Het
Wdr63	A	G	3: 146,097,145 (GRCm38)	V97A	probably damaging	Het
Ypel5	G	A	17: 72,846,444 (GRCm38)		probably null	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
R1711:Gm11639	UTSW	11	104,720,688 (GRCm38)	missense	probably benign	0.07
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
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'- TGAGATACGACACCTGGTTTC -3'
(R):5'- GGCACCTGCTAGACTTGAAC -3'

Sequencing Primer
(F):5'- ATACGACACCTGGTTTCAATGTTTTC -3'
(R):5'- CACCTGCTAGACTTGAACTAATAAAG -3'

Posted On

2019-10-07