Mutagenetix > Incidental Mutation

Incidental Mutation 'R1779:Gm11639'

197370

Institutional Source

Beutler Lab

Gene Symbol

Gm11639

Ensembl Gene

ENSMUSG00000040838

Gene Name

predicted gene 11639

Synonyms

MMRRC Submission

039810-MU

Accession Numbers

Essential gene?

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

Stock #

R1779 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

104685707-105117394 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 104720939 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 536 (S536T)

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: S463T

SMART Domains

Protein: ENSMUSP00000116040
Gene: ENSMUSG00000040838
AA Change: S463T

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: S536T

PolyPhen 2 Score 0.146 (Sensitivity: 0.92; Specificity: 0.87)

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.5%
20x: 93.0%

Validation Efficiency

97% (101/104)

Allele List at MGI

Other mutations in this stock

Total: 103 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700006A11Rik	T	G	3: 124,406,514 (GRCm38)	L476F	probably damaging	Het
1700061G19Rik	T	A	17: 56,885,169 (GRCm38)	Y577*	probably null	Het
4930432E11Rik	A	T	7: 29,579,166 (GRCm38)		noncoding transcript	Het
A930011G23Rik	A	T	5: 99,223,038 (GRCm38)		probably benign	Het
Abcd3	A	G	3: 121,781,963 (GRCm38)	Y217H	probably damaging	Het
Abraxas1	A	T	5: 100,817,956 (GRCm38)		probably benign	Het
Acsbg1	T	C	9: 54,616,062 (GRCm38)	Y427C	probably damaging	Het
Adam10	T	A	9: 70,776,369 (GRCm38)		probably benign	Het
Adam24	G	A	8: 40,680,965 (GRCm38)	V491I	possibly damaging	Het
Adamts2	T	G	11: 50,756,697 (GRCm38)	V299G	probably damaging	Het
Adh7	A	G	3: 138,223,991 (GRCm38)	T143A	probably damaging	Het
Ahcyl1	A	G	3: 107,674,103 (GRCm38)	S81P	probably benign	Het
Arhgap20	C	A	9: 51,849,915 (GRCm38)	T986K	probably benign	Het
Atp13a5	A	T	16: 29,314,660 (GRCm38)	I391N	possibly damaging	Het
Atp6v0a1	C	A	11: 101,026,685 (GRCm38)	A143E	probably benign	Het
Calcrl	A	G	2: 84,351,285 (GRCm38)	I173T	probably damaging	Het
Casz1	A	G	4: 148,932,937 (GRCm38)	T228A	probably benign	Het
Cckar	A	G	5: 53,699,979 (GRCm38)	I292T	probably damaging	Het
Cfhr2	T	A	1: 139,858,645 (GRCm38)		probably null	Het
Chkb	T	C	15: 89,429,057 (GRCm38)	I109V	possibly damaging	Het
Clec2i	T	C	6: 128,888,106 (GRCm38)		probably null	Het
Clec4a4	T	A	6: 123,023,975 (GRCm38)	W216R	probably damaging	Het
Cntnap1	A	C	11: 101,186,511 (GRCm38)	I1000L	probably damaging	Het
Cp	C	A	3: 19,957,385 (GRCm38)	D34E	possibly damaging	Het
Cse1l	T	C	2: 166,940,124 (GRCm38)		probably null	Het
Dennd3	T	C	15: 73,522,508 (GRCm38)		probably null	Het
Dnah7a	A	G	1: 53,577,223 (GRCm38)	V1193A	probably benign	Het
Eaf2	A	G	16: 36,810,470 (GRCm38)		probably null	Het
Ephb2	T	C	4: 136,693,825 (GRCm38)	T405A	possibly damaging	Het
Fam117a	G	A	11: 95,378,953 (GRCm38)	V348M	probably damaging	Het
Fh1	T	C	1: 175,601,424 (GRCm38)	*167W	probably null	Het
Fmo9	T	A	1: 166,663,299 (GRCm38)	I486F	probably benign	Het
Gabbr1	T	A	17: 37,054,879 (GRCm38)	I150N	probably damaging	Het
Gfpt1	T	C	6: 87,077,197 (GRCm38)	V478A	possibly damaging	Het
Gm2663	A	T	6: 40,997,960 (GRCm38)	V59E	probably damaging	Het
Gm4868	T	A	5: 125,848,112 (GRCm38)		noncoding transcript	Het
Heatr4	T	A	12: 83,980,160 (GRCm38)	T108S	probably benign	Het
Hells	G	T	19: 38,946,842 (GRCm38)	A319S	probably benign	Het
Helz2	T	A	2: 181,238,459 (GRCm38)	Q488L	possibly damaging	Het
Helz2	A	G	2: 181,234,987 (GRCm38)	V1238A	probably benign	Het
Hkdc1	A	G	10: 62,391,383 (GRCm38)	F765S	probably damaging	Het
Hspg2	T	A	4: 137,518,509 (GRCm38)	W938R	probably damaging	Het
Itpr2	G	A	6: 146,158,901 (GRCm38)	R2473*	probably null	Het
Kctd1	C	T	18: 15,061,782 (GRCm38)	V595I	probably benign	Het
Krt7	A	G	15: 101,423,409 (GRCm38)	Y369C	probably damaging	Het
Krt72	T	C	15: 101,780,929 (GRCm38)	T323A	probably benign	Het
Krt76	A	G	15: 101,892,687 (GRCm38)	L58P	unknown	Het
Liph	C	A	16: 21,968,050 (GRCm38)	R272L	probably benign	Het
Lrrc9	A	T	12: 72,455,998 (GRCm38)	K248*	probably null	Het
Mei4	T	A	9: 81,927,142 (GRCm38)	S93T	probably damaging	Het
Mgll	T	A	6: 88,813,948 (GRCm38)	Y183*	probably null	Het
Myo5b	A	G	18: 74,742,147 (GRCm38)	M1541V	probably benign	Het
Napg	A	G	18: 62,982,691 (GRCm38)	E66G	probably benign	Het
Npr3	T	C	15: 11,851,486 (GRCm38)	D406G	probably damaging	Het
Nr2c2	A	G	6: 92,159,243 (GRCm38)	T355A	possibly damaging	Het
Olfr1243	A	T	2: 89,527,645 (GRCm38)	I255K	probably benign	Het
Olfr1461	T	C	19: 13,165,040 (GRCm38)	Y9H	probably benign	Het
Olfr26	A	G	9: 38,855,550 (GRCm38)	M163V	possibly damaging	Het
Olfr618	A	T	7: 103,597,900 (GRCm38)	I195F	probably damaging	Het
Olfr624	A	G	7: 103,670,638 (GRCm38)	I131T	probably benign	Het
Olfr631	G	T	7: 103,929,461 (GRCm38)	V213L	probably benign	Het
Olfr71	G	A	4: 43,706,041 (GRCm38)	H176Y	probably damaging	Het
Orai2	T	C	5: 136,150,939 (GRCm38)	E80G	probably damaging	Het
Pcdhb14	T	A	18: 37,449,482 (GRCm38)	V547E	probably damaging	Het
Pcdhb15	T	C	18: 37,476,031 (GRCm38)	I772T	possibly damaging	Het
Pcnt	T	C	10: 76,408,796 (GRCm38)	Q1150R	probably damaging	Het
Pdcd6	A	G	13: 74,305,581 (GRCm38)	I146T	probably damaging	Het
Phldb2	T	A	16: 45,801,625 (GRCm38)	D664V	probably damaging	Het
Pik3ap1	A	T	19: 41,332,234 (GRCm38)	V182E	probably damaging	Het
Pip4k2a	A	G	2: 18,847,622 (GRCm38)	V283A	probably benign	Het
Pkdrej	A	G	15: 85,821,171 (GRCm38)	V188A	possibly damaging	Het
Pnpla6	T	C	8: 3,541,404 (GRCm38)	W1151R	probably damaging	Het
Ppp1r14c	A	G	10: 3,366,890 (GRCm38)	Y75C	probably damaging	Het
Prl2b1	C	T	13: 27,383,469 (GRCm38)	D224N	probably benign	Het
Ptgis	A	G	2: 167,214,858 (GRCm38)	S270P	probably benign	Het
Rgs11	C	A	17: 26,210,666 (GRCm38)	A446D	probably damaging	Het
Rims2	A	G	15: 39,681,702 (GRCm38)	T1531A	probably damaging	Het
Sbno1	A	T	5: 124,388,517 (GRCm38)		probably benign	Het
Scarb2	C	G	5: 92,448,557 (GRCm38)	M409I	probably benign	Het
Scube3	C	T	17: 28,168,379 (GRCm38)		probably benign	Het
Slc44a4	T	C	17: 34,921,925 (GRCm38)	I180T	probably damaging	Het
Slc9a2	T	C	1: 40,742,643 (GRCm38)	M344T	probably damaging	Het
Smc3	A	T	19: 53,639,369 (GRCm38)	T860S	probably benign	Het
Snrpa	A	G	7: 27,191,749 (GRCm38)	I99T	probably benign	Het
Sorcs1	A	G	19: 50,175,043 (GRCm38)		probably benign	Het
Sorl1	C	T	9: 41,991,482 (GRCm38)		probably null	Het
Suds3	T	C	5: 117,105,244 (GRCm38)	K143R	probably benign	Het
Supt20	A	T	3: 54,714,743 (GRCm38)	M424L	probably benign	Het
Tgtp2	T	C	11: 49,058,924 (GRCm38)	M274V	probably benign	Het
Tmem158	T	A	9: 123,259,909 (GRCm38)	M213L	probably benign	Het
Tnks	C	A	8: 34,857,518 (GRCm38)	R639L	probably benign	Het
Tns2	C	T	15: 102,108,934 (GRCm38)	R281C	probably damaging	Het
Trmt10c	A	C	16: 56,034,575 (GRCm38)	N232K	possibly damaging	Het
Trpm6	C	T	19: 18,856,217 (GRCm38)	R1587W	probably damaging	Het
Trrap	G	A	5: 144,828,590 (GRCm38)	V2539I	probably benign	Het
Tsg101	A	G	7: 46,907,087 (GRCm38)	S115P	probably benign	Het
Ttll13	G	T	7: 80,260,508 (GRCm38)	V800L	probably benign	Het
Vmn1r57	A	G	7: 5,220,577 (GRCm38)	T34A	possibly damaging	Het
Vmn2r118	T	A	17: 55,611,530 (GRCm38)	T121S	probably benign	Het
Wdr35	A	G	12: 8,985,772 (GRCm38)	I238M	possibly damaging	Het
Wisp2	G	A	2: 163,828,986 (GRCm38)	V138M	probably damaging	Het
Zfp81	T	A	17: 33,335,106 (GRCm38)	T245S	probably benign	Het
Zfyve26	G	T	12: 79,278,463 (GRCm38)	P824Q	probably damaging	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
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'- TACCGGATAGACGTGATTCAAGCCTC -3'
(R):5'- AGCCTCCTCATAGCCAACTTCTGAT -3'

Sequencing Primer
(F):5'- TCAAGCCTCAAGAAGTCACC -3'
(R):5'- GAGACTTGAATCACGTCTATCCG -3'

Posted On

2014-05-23