Mutagenetix > Incidental Mutation

Incidental Mutation 'R2165:Gm11639'

235449

Institutional Source

Beutler Lab

Gene Symbol

Gm11639

Ensembl Gene

ENSMUSG00000040838

Gene Name

predicted gene 11639

Synonyms

MMRRC Submission

040168-MU

Accession Numbers

Essential gene?

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

Stock #

R2165 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

104685707-105117394 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 104751862 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 1104 (V1104I)

Ref Sequence

ENSEMBL: ENSMUSP00000148433 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000148007
AA Change: V1052I

PolyPhen 2 Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000116040
Gene: ENSMUSG00000040838
AA Change: V1052I

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

possibly damaging
Transcript: ENSMUST00000212287
AA Change: V1104I

PolyPhen 2 Score 0.933 (Sensitivity: 0.80; Specificity: 0.94)

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.6%
20x: 96.0%

Validation Efficiency

99% (71/72)

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	A	G	3: 122,112,399 (GRCm38)	T806A	possibly damaging	Het
Adgre1	T	G	17: 57,419,338 (GRCm38)	L403R	probably damaging	Het
Alox12	A	T	11: 70,242,572 (GRCm38)		probably null	Het
Ankib1	A	T	5: 3,713,210 (GRCm38)	D506E	possibly damaging	Het
Ascc3	T	G	10: 50,721,839 (GRCm38)	Y1268D	probably damaging	Het
Bik	A	G	15: 83,541,423 (GRCm38)	M42V	probably benign	Het
Bola1	A	T	3: 96,197,201 (GRCm38)	S26T	probably benign	Het
Bub1	T	C	2: 127,801,281 (GRCm38)	I1048V	probably benign	Het
Cad	A	G	5: 31,062,220 (GRCm38)	N621S	probably damaging	Het
Camkv	C	A	9: 107,945,600 (GRCm38)	N69K	possibly damaging	Het
Ccdc110	T	C	8: 45,942,839 (GRCm38)	M589T	probably benign	Het
Ccdc154	T	A	17: 25,170,890 (GRCm38)	V498E	probably damaging	Het
Ccr1l1	A	G	9: 123,977,654 (GRCm38)	L252P	probably damaging	Het
Cdh1	T	C	8: 106,664,321 (GRCm38)	C690R	probably damaging	Het
Cfap157	T	G	2: 32,778,163 (GRCm38)		probably null	Het
Cux2	A	G	5: 121,887,477 (GRCm38)	S43P	possibly damaging	Het
Cyb5rl	C	T	4: 107,068,683 (GRCm38)	P21S	probably damaging	Het
Cyp51	T	G	5: 4,086,594 (GRCm38)	Q400P	probably damaging	Het
Dnah7b	T	C	1: 46,097,992 (GRCm38)		probably benign	Het
Ephb4	A	G	5: 137,354,426 (GRCm38)	I90M	probably benign	Het
Fam13c	A	G	10: 70,542,693 (GRCm38)	N269S	probably damaging	Het
Fam83c	T	A	2: 155,831,524 (GRCm38)	Y248F	possibly damaging	Het
Fat2	A	G	11: 55,303,716 (GRCm38)	F1166L	probably benign	Het
Fem1a	A	G	17: 56,257,686 (GRCm38)	N260D	probably benign	Het
Fnbp4	T	A	2: 90,767,399 (GRCm38)		probably null	Het
Fut9	T	A	4: 25,619,733 (GRCm38)	*360Y	probably null	Het
Fut9	T	A	4: 25,619,734 (GRCm38)	*360L	probably null	Het
Gm3727	T	A	14: 7,264,625 (GRCm38)	Q10L	probably damaging	Het
Gpat2	G	A	2: 127,428,291 (GRCm38)	V75M	probably damaging	Het
Haspin	A	C	11: 73,136,630 (GRCm38)	N544K	probably damaging	Het
Havcr1	A	G	11: 46,778,552 (GRCm38)	N286S	probably benign	Het
Lrp6	A	C	6: 134,459,283 (GRCm38)	C1307G	probably damaging	Het
Lrrc2	A	C	9: 110,979,577 (GRCm38)	H294P	possibly damaging	Het
Mettl25b	A	T	3: 87,927,053 (GRCm38)		probably null	Het
Mon2	A	C	10: 123,042,364 (GRCm38)		probably null	Het
Mrc2	G	A	11: 105,348,431 (GRCm38)		probably null	Het
Mrgprb1	T	C	7: 48,447,322 (GRCm38)	I281V	probably benign	Het
Muc4	A	G	16: 32,750,476 (GRCm38)	E118G	probably damaging	Het
Nefh	T	C	11: 4,943,872 (GRCm38)	D394G	probably damaging	Het
Neurl4	A	G	11: 69,903,221 (GRCm38)	T168A	probably benign	Het
Or10s1	A	G	9: 40,074,915 (GRCm38)	N207D	possibly damaging	Het
Or1j18	T	A	2: 36,734,701 (GRCm38)	C127S	probably damaging	Het
Or51a10	T	C	7: 104,049,638 (GRCm38)	T239A	probably benign	Het
Or5ak4	A	T	2: 85,331,102 (GRCm38)	N265K	probably benign	Het
Oxsr1	A	C	9: 119,294,432 (GRCm38)	M92R	probably damaging	Het
Pde8a	T	C	7: 81,295,768 (GRCm38)		probably null	Het
Pex5l	T	A	3: 32,953,132 (GRCm38)		probably null	Het
Pik3r4	T	A	9: 105,672,785 (GRCm38)	M1025K	probably benign	Het
Plch1	C	T	3: 63,698,482 (GRCm38)	E1325K	probably benign	Het
Plin2	A	T	4: 86,668,432 (GRCm38)	V54E	probably damaging	Het
Prss47	A	T	13: 65,045,073 (GRCm38)	I298N	probably damaging	Het
Prune2	A	G	19: 17,120,182 (GRCm38)	R1017G	probably benign	Het
Psg19	T	A	7: 18,796,986 (GRCm38)	Y81F	possibly damaging	Het
Ptch1	T	G	13: 63,524,959 (GRCm38)	E944A	probably benign	Het
Serpinb1a	T	C	13: 32,850,414 (GRCm38)		probably benign	Het
Sh3pxd2a	A	T	19: 47,278,355 (GRCm38)	V265E	probably damaging	Het
Slc22a17	A	T	14: 54,908,825 (GRCm38)	Y337*	probably null	Het
Slc25a27	A	G	17: 43,657,772 (GRCm38)	V138A	probably benign	Het
Slc4a2	A	G	5: 24,431,316 (GRCm38)	Y220C	probably damaging	Het
Slc66a3	G	A	12: 16,989,839 (GRCm38)	L192F	probably damaging	Het
Stab1	A	T	14: 31,168,435 (GRCm38)	S20T	probably benign	Het
Tcstv2a	A	T	13: 120,264,097 (GRCm38)	Q99L	probably damaging	Het
Thsd1	G	T	8: 22,238,522 (GRCm38)		probably benign	Het
Tmem204	G	A	17: 25,080,592 (GRCm38)		probably benign	Het
Tom1l1	A	G	11: 90,649,895 (GRCm38)		probably benign	Het
Toporsl	T	A	4: 52,612,072 (GRCm38)	F655Y	possibly damaging	Het
Vmn2r98	A	G	17: 19,081,291 (GRCm38)	K852E	unknown	Het
Wdpcp	T	G	11: 21,691,884 (GRCm38)	L174R	probably damaging	Het
Zbbx	G	A	3: 75,112,107 (GRCm38)	P99S	probably damaging	Het
Zfhx4	C	T	3: 5,403,358 (GRCm38)	P2859S	probably benign	Het
Zfp600	A	T	4: 146,196,918 (GRCm38)	R719*	probably null	Het
Zfp697	C	A	3: 98,428,014 (GRCm38)	A365E	unknown	Het
Zfp957	A	C	14: 79,213,613 (GRCm38)	S249A	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
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
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'- TTGACTATCCAATGTGTTTGCCTG -3'
(R):5'- TGCTCCTCCACCTGTAGACAAC -3'

Sequencing Primer
(F):5'- GGACCTGTATTGCCCGAACTTAAATC -3'
(R):5'- CCTGTAGACAACAATCCATTTAAGG -3'

Posted On

2014-10-01