Mutagenetix > Incidental Mutation

Incidental Mutation 'R4631:Bod1l'

349179

Institutional Source

Beutler Lab

Gene Symbol

Bod1l

Ensembl Gene

ENSMUSG00000061755

Gene Name

biorientation of chromosomes in cell division 1-like

Synonyms

A230054D04Rik

MMRRC Submission

041896-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.957) question?

Stock #

R4631 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

41944881-42001658 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 41975078 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 2079 (F2079L)

Ref Sequence

ENSEMBL: ENSMUSP00000144359 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000050556] [ENSMUST00000202908]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000050556
AA Change: F2079L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000058618
Gene: ENSMUSG00000061755
AA Change: F2079L

Domain	Start	End	E-Value	Type
low complexity region	5	47	N/A	INTRINSIC
Pfam:COMPASS-Shg1	54	150	1.8e-28	PFAM
low complexity region	328	343	N/A	INTRINSIC
low complexity region	415	435	N/A	INTRINSIC
low complexity region	475	484	N/A	INTRINSIC
coiled coil region	495	520	N/A	INTRINSIC
coiled coil region	553	580	N/A	INTRINSIC
low complexity region	820	840	N/A	INTRINSIC
low complexity region	895	916	N/A	INTRINSIC
low complexity region	996	1005	N/A	INTRINSIC
low complexity region	1023	1041	N/A	INTRINSIC
low complexity region	1272	1286	N/A	INTRINSIC
low complexity region	1791	1809	N/A	INTRINSIC
low complexity region	2695	2701	N/A	INTRINSIC
low complexity region	2711	2729	N/A	INTRINSIC
AT_hook	2807	2819	3.21e-1	SMART
coiled coil region	2908	2929	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000201291

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000202200

Predicted Effect

probably damaging
Transcript: ENSMUST00000202908
AA Change: F2079L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000144359
Gene: ENSMUSG00000061755
AA Change: F2079L

Domain	Start	End	E-Value	Type
low complexity region	5	47	N/A	INTRINSIC
Pfam:COMPASS-Shg1	54	150	2.9e-24	PFAM
low complexity region	328	343	N/A	INTRINSIC
low complexity region	415	435	N/A	INTRINSIC
low complexity region	475	484	N/A	INTRINSIC
coiled coil region	495	520	N/A	INTRINSIC
coiled coil region	553	580	N/A	INTRINSIC
low complexity region	820	840	N/A	INTRINSIC
low complexity region	895	916	N/A	INTRINSIC
low complexity region	996	1005	N/A	INTRINSIC
low complexity region	1023	1041	N/A	INTRINSIC
low complexity region	1272	1286	N/A	INTRINSIC
low complexity region	1791	1809	N/A	INTRINSIC
low complexity region	2695	2701	N/A	INTRINSIC
low complexity region	2711	2729	N/A	INTRINSIC
AT_hook	2807	2819	1.9e-3	SMART
coiled coil region	2908	2929	N/A	INTRINSIC

Meta Mutation Damage Score

0.0809

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.0%

Validation Efficiency

100% (84/84)

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017B05Rik	A	T	9: 57,165,270 (GRCm39)	L368Q	probably damaging	Het
Abcc2	C	T	19: 43,803,146 (GRCm39)	P661S	possibly damaging	Het
Adgre4	T	G	17: 56,121,305 (GRCm39)	M457R	probably null	Het
Ank	C	A	15: 27,467,176 (GRCm39)	F29L	probably benign	Het
Arhgap20	T	C	9: 51,751,653 (GRCm39)		probably benign	Het
Atf6	T	C	1: 170,574,766 (GRCm39)		probably null	Het
Bhmt1b	G	A	18: 87,774,525 (GRCm39)	R16H	probably damaging	Het
Cd163	T	C	6: 124,306,045 (GRCm39)	*1122Q	probably null	Het
Ces2g	T	C	8: 105,694,094 (GRCm39)		probably null	Het
Cntnap3	A	G	13: 64,926,697 (GRCm39)	Y558H	probably benign	Het
Ctsm	T	A	13: 61,685,510 (GRCm39)	S301C	probably null	Het
Dlc1	A	C	8: 37,404,712 (GRCm39)		probably null	Het
Dlg2	A	T	7: 91,737,822 (GRCm39)	I435F	probably damaging	Het
Dnah5	T	C	15: 28,402,099 (GRCm39)	V3420A	probably damaging	Het
Dnah5	T	A	15: 28,420,140 (GRCm39)	Y3813N	probably damaging	Het
Dnajc13	A	G	9: 104,067,616 (GRCm39)	M1181T	probably damaging	Het
Drc3	C	A	11: 60,255,734 (GRCm39)	T107N	probably benign	Het
Dydc2	T	C	14: 40,771,286 (GRCm39)	E131G	probably benign	Het
Eif5b	T	C	1: 38,080,828 (GRCm39)	V723A	probably damaging	Het
Fndc9	C	A	11: 46,128,675 (GRCm39)	H65N	possibly damaging	Het
Fzd1	A	T	5: 4,805,865 (GRCm39)	Y572*	probably null	Het
Gps1	T	A	11: 120,679,065 (GRCm39)		probably null	Het
Gvin3	A	G	7: 106,198,730 (GRCm39)		noncoding transcript	Het
Kazn	G	A	4: 141,845,471 (GRCm39)		probably benign	Het
Kcnd3	C	T	3: 105,566,082 (GRCm39)	A421V	probably damaging	Het
Kcnip1	T	A	11: 33,942,821 (GRCm39)		noncoding transcript	Het
Kif19a	A	G	11: 114,675,673 (GRCm39)	I382V	possibly damaging	Het
Krt1	C	T	15: 101,754,622 (GRCm39)	G543S	unknown	Het
Malsu1	A	T	6: 49,061,467 (GRCm39)	E177V	probably damaging	Het
Man2a2	A	G	7: 80,012,211 (GRCm39)	F649L	probably benign	Het
Map3k11	A	G	19: 5,740,941 (GRCm39)	I223V	probably benign	Het
Mroh2a	A	G	1: 88,186,386 (GRCm39)	S64G	probably benign	Het
Myh9	T	G	15: 77,681,228 (GRCm39)	D164A	probably damaging	Het
Myo16	T	C	8: 10,556,984 (GRCm39)	I1040T	probably damaging	Het
Myo18b	C	T	5: 112,994,266 (GRCm39)	A896T	probably damaging	Het
Myocd	G	T	11: 65,069,685 (GRCm39)	N798K	probably benign	Het
Or13c7b	T	C	4: 43,820,563 (GRCm39)	D266G	probably benign	Het
Or1n1b	T	G	2: 36,780,630 (GRCm39)	T77P	probably benign	Het
Or2l13b	G	A	16: 19,348,891 (GRCm39)	R260*	probably null	Het
Or4c11	C	T	2: 88,695,174 (GRCm39)	T75I	probably benign	Het
Or4g7	T	A	2: 111,309,908 (GRCm39)	W260R	probably damaging	Het
Or52a5	A	T	7: 103,426,682 (GRCm39)	L290Q	probably damaging	Het
Or5b105	T	A	19: 13,080,636 (GRCm39)	I11F	probably benign	Het
Pcdh18	T	A	3: 49,710,890 (GRCm39)	I142F	probably damaging	Het
Pcyox1	T	C	6: 86,366,212 (GRCm39)	E334G	possibly damaging	Het
Pcyox1	T	C	6: 86,366,125 (GRCm39)	D363G	probably benign	Het
Pgm2	A	G	5: 64,263,290 (GRCm39)		probably null	Het
Plagl1	T	G	10: 13,003,743 (GRCm39)		probably benign	Het
Ppp1r9a	A	G	6: 4,906,537 (GRCm39)	D364G	possibly damaging	Het
Rab2b	T	A	14: 52,503,699 (GRCm39)	H141L	possibly damaging	Het
Rev3l	A	G	10: 39,704,412 (GRCm39)	K279E	probably benign	Het
Rnf111	G	T	9: 70,357,678 (GRCm39)	T607N	probably benign	Het
Scn8a	C	A	15: 100,914,384 (GRCm39)	S1130*	probably null	Het
Selenbp1	A	G	3: 94,851,879 (GRCm39)	*473W	probably null	Het
Sh3bp4	A	C	1: 89,071,995 (GRCm39)	D281A	probably damaging	Het
Skint5	T	A	4: 113,486,314 (GRCm39)		probably null	Het
Slc1a4	A	G	11: 20,258,452 (GRCm39)	L249P	probably damaging	Het
Slc45a2	T	A	15: 11,012,662 (GRCm39)	S222T	probably benign	Het
Slc7a4	A	G	16: 17,392,255 (GRCm39)	F393S	probably damaging	Het
Slc9a2	A	T	1: 40,801,078 (GRCm39)	D536V	possibly damaging	Het
Stra6	T	A	9: 58,048,115 (GRCm39)		probably benign	Het
Tmem145	A	G	7: 25,007,250 (GRCm39)	D156G	probably benign	Het
Tns3	A	C	11: 8,401,119 (GRCm39)	F1060V	probably benign	Het
Trak1	G	A	9: 121,283,491 (GRCm39)	R419Q	probably benign	Het
Trappc8	A	G	18: 21,000,865 (GRCm39)	S273P	probably benign	Het
Trmt11	A	G	10: 30,435,200 (GRCm39)	S320P	probably benign	Het
Ugt1a6a	A	T	1: 88,066,980 (GRCm39)	Y262F	probably benign	Het
Vmn1r73	G	A	7: 11,490,758 (GRCm39)	C192Y	probably benign	Het
Vmn2r103	T	C	17: 20,013,958 (GRCm39)	I250T	probably benign	Het
Vmn2r25	T	A	6: 123,829,962 (GRCm39)	D63V	possibly damaging	Het
Vps13b	C	T	15: 35,646,278 (GRCm39)	H1461Y	possibly damaging	Het
Ythdc2	A	T	18: 45,020,698 (GRCm39)	E1427D	probably benign	Het
Zbed6	A	T	1: 133,586,482 (GRCm39)	V285E	probably damaging	Het
Zbtb26	A	G	2: 37,326,968 (GRCm39)	F23L	probably benign	Het
Zfp62	T	A	11: 49,108,632 (GRCm39)	*908R	probably null	Het
Zfp975	A	T	7: 42,312,369 (GRCm39)	N81K	probably benign	Het
Zkscan16	G	A	4: 58,951,918 (GRCm39)	V198M	probably damaging	Het

Other mutations in Bod1l

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00944:Bod1l	APN	5	41,974,166 (GRCm39)	missense	probably benign	0.00
IGL00990:Bod1l	APN	5	41,986,208 (GRCm39)	missense	probably benign	0.00
IGL01021:Bod1l	APN	5	41,995,516 (GRCm39)	splice site	probably benign
IGL01022:Bod1l	APN	5	41,951,652 (GRCm39)	missense	probably damaging	1.00
IGL01303:Bod1l	APN	5	41,974,942 (GRCm39)	missense	probably benign	0.00
IGL01654:Bod1l	APN	5	41,975,519 (GRCm39)	missense	probably damaging	0.99
IGL01748:Bod1l	APN	5	41,974,304 (GRCm39)	missense	probably benign	0.23
IGL01758:Bod1l	APN	5	41,983,953 (GRCm39)	splice site	probably benign
IGL01783:Bod1l	APN	5	41,966,055 (GRCm39)	missense	probably benign	0.02
IGL01790:Bod1l	APN	5	41,989,593 (GRCm39)	missense	probably benign	0.14
IGL01803:Bod1l	APN	5	41,974,732 (GRCm39)	missense	probably damaging	0.97
IGL01829:Bod1l	APN	5	41,977,811 (GRCm39)	missense	probably benign	0.25
IGL01952:Bod1l	APN	5	41,974,297 (GRCm39)	missense	possibly damaging	0.70
IGL02005:Bod1l	APN	5	41,973,682 (GRCm39)	missense	probably benign	0.01
IGL02110:Bod1l	APN	5	41,973,796 (GRCm39)	missense	probably damaging	0.97
IGL02129:Bod1l	APN	5	41,979,193 (GRCm39)	missense	probably benign	0.36
IGL02572:Bod1l	APN	5	41,978,573 (GRCm39)	nonsense	probably null
IGL02583:Bod1l	APN	5	41,973,550 (GRCm39)	critical splice donor site	probably null
IGL02643:Bod1l	APN	5	41,976,148 (GRCm39)	missense	possibly damaging	0.65
IGL02714:Bod1l	APN	5	41,973,682 (GRCm39)	missense	probably benign	0.01
IGL02728:Bod1l	APN	5	41,983,846 (GRCm39)	missense	probably damaging	1.00
IGL02752:Bod1l	APN	5	41,973,806 (GRCm39)	missense	possibly damaging	0.58
IGL02822:Bod1l	APN	5	41,951,688 (GRCm39)	missense	possibly damaging	0.94
IGL03032:Bod1l	APN	5	41,988,927 (GRCm39)	missense	probably benign	0.16
IGL03372:Bod1l	APN	5	41,962,578 (GRCm39)	splice site	probably benign
capacitance	UTSW	5	41,949,156 (GRCm39)	missense	possibly damaging	0.91
gauss	UTSW	5	41,974,210 (GRCm39)	missense	probably benign	0.01
Tesla	UTSW	5	41,952,411 (GRCm39)	critical splice donor site	probably null
R0102:Bod1l	UTSW	5	41,974,612 (GRCm39)	missense	probably benign	0.36
R0147:Bod1l	UTSW	5	41,976,040 (GRCm39)	missense	possibly damaging	0.48
R0148:Bod1l	UTSW	5	41,976,040 (GRCm39)	missense	possibly damaging	0.48
R0490:Bod1l	UTSW	5	41,979,235 (GRCm39)	missense	probably damaging	0.96
R0577:Bod1l	UTSW	5	41,952,230 (GRCm39)	missense	probably damaging	1.00
R0587:Bod1l	UTSW	5	41,978,980 (GRCm39)	missense	probably benign	0.16
R0620:Bod1l	UTSW	5	41,958,576 (GRCm39)	missense	probably benign	0.16
R0626:Bod1l	UTSW	5	41,988,880 (GRCm39)	missense	probably damaging	1.00
R0785:Bod1l	UTSW	5	41,977,359 (GRCm39)	missense	probably benign	0.00
R1139:Bod1l	UTSW	5	41,988,814 (GRCm39)	missense	possibly damaging	0.64
R1165:Bod1l	UTSW	5	41,978,396 (GRCm39)	missense	probably benign	0.02
R1418:Bod1l	UTSW	5	41,976,814 (GRCm39)	missense	probably damaging	1.00
R1509:Bod1l	UTSW	5	41,976,883 (GRCm39)	missense	probably damaging	0.99
R1533:Bod1l	UTSW	5	41,979,498 (GRCm39)	nonsense	probably null
R1538:Bod1l	UTSW	5	41,973,772 (GRCm39)	missense	probably benign	0.00
R1591:Bod1l	UTSW	5	41,976,563 (GRCm39)	missense	probably benign	0.06
R1616:Bod1l	UTSW	5	41,966,058 (GRCm39)	missense	probably benign
R1628:Bod1l	UTSW	5	41,974,325 (GRCm39)	missense	probably benign	0.01
R1667:Bod1l	UTSW	5	41,974,118 (GRCm39)	missense	probably benign	0.01
R1869:Bod1l	UTSW	5	41,991,018 (GRCm39)	missense	possibly damaging	0.93
R1870:Bod1l	UTSW	5	41,991,018 (GRCm39)	missense	possibly damaging	0.93
R1993:Bod1l	UTSW	5	41,974,679 (GRCm39)	missense	probably damaging	1.00
R2060:Bod1l	UTSW	5	41,966,085 (GRCm39)	missense	possibly damaging	0.58
R2066:Bod1l	UTSW	5	41,962,499 (GRCm39)	missense	probably damaging	0.99
R2067:Bod1l	UTSW	5	41,974,429 (GRCm39)	missense	probably benign	0.11
R2073:Bod1l	UTSW	5	41,976,532 (GRCm39)	missense	probably benign	0.19
R2092:Bod1l	UTSW	5	41,988,860 (GRCm39)	missense	probably damaging	1.00
R2105:Bod1l	UTSW	5	41,989,622 (GRCm39)	missense	probably benign	0.00
R2243:Bod1l	UTSW	5	41,978,888 (GRCm39)	missense	possibly damaging	0.58
R2322:Bod1l	UTSW	5	41,984,463 (GRCm39)	missense	probably benign	0.09
R2849:Bod1l	UTSW	5	41,995,419 (GRCm39)	missense	probably damaging	1.00
R2883:Bod1l	UTSW	5	41,989,602 (GRCm39)	missense	probably benign	0.03
R3037:Bod1l	UTSW	5	41,979,380 (GRCm39)	missense	probably damaging	0.99
R3910:Bod1l	UTSW	5	41,974,441 (GRCm39)	missense	probably damaging	0.99
R3911:Bod1l	UTSW	5	41,974,441 (GRCm39)	missense	probably damaging	0.99
R3962:Bod1l	UTSW	5	41,966,064 (GRCm39)	missense	probably benign	0.07
R4235:Bod1l	UTSW	5	41,978,798 (GRCm39)	missense	probably damaging	1.00
R4308:Bod1l	UTSW	5	41,949,156 (GRCm39)	missense	possibly damaging	0.91
R4414:Bod1l	UTSW	5	41,977,870 (GRCm39)	missense	probably benign	0.04
R4535:Bod1l	UTSW	5	41,989,574 (GRCm39)	missense	probably benign	0.06
R4657:Bod1l	UTSW	5	41,975,955 (GRCm39)	missense	probably benign	0.00
R4782:Bod1l	UTSW	5	41,991,006 (GRCm39)	missense	probably benign	0.06
R4786:Bod1l	UTSW	5	41,976,781 (GRCm39)	missense	probably benign	0.43
R4840:Bod1l	UTSW	5	41,975,815 (GRCm39)	missense	probably damaging	1.00
R4877:Bod1l	UTSW	5	41,977,337 (GRCm39)	missense	probably benign	0.00
R4982:Bod1l	UTSW	5	41,977,816 (GRCm39)	missense	probably benign	0.00
R5152:Bod1l	UTSW	5	41,973,886 (GRCm39)	missense	probably benign	0.04
R5284:Bod1l	UTSW	5	41,977,810 (GRCm39)	missense	probably benign	0.05
R5354:Bod1l	UTSW	5	41,988,880 (GRCm39)	missense	probably damaging	1.00
R5369:Bod1l	UTSW	5	41,984,526 (GRCm39)	missense	probably damaging	1.00
R5486:Bod1l	UTSW	5	41,964,524 (GRCm39)	missense	possibly damaging	0.56
R5541:Bod1l	UTSW	5	41,949,276 (GRCm39)	missense	probably benign	0.06
R5610:Bod1l	UTSW	5	41,979,217 (GRCm39)	missense	probably damaging	1.00
R5655:Bod1l	UTSW	5	41,974,387 (GRCm39)	missense	probably benign	0.06
R5705:Bod1l	UTSW	5	41,974,345 (GRCm39)	missense	probably benign	0.01
R5819:Bod1l	UTSW	5	41,989,948 (GRCm39)	missense	probably benign	0.27
R5890:Bod1l	UTSW	5	41,977,921 (GRCm39)	missense	probably benign	0.43
R5923:Bod1l	UTSW	5	41,974,762 (GRCm39)	missense	probably damaging	1.00
R5991:Bod1l	UTSW	5	41,974,206 (GRCm39)	nonsense	probably null
R6017:Bod1l	UTSW	5	41,976,103 (GRCm39)	missense	probably benign	0.01
R6253:Bod1l	UTSW	5	41,983,881 (GRCm39)	missense	probably damaging	0.96
R6284:Bod1l	UTSW	5	41,976,130 (GRCm39)	missense	probably benign	0.35
R6483:Bod1l	UTSW	5	41,978,425 (GRCm39)	missense	probably benign	0.03
R6485:Bod1l	UTSW	5	41,974,459 (GRCm39)	missense	possibly damaging	0.93
R6575:Bod1l	UTSW	5	41,995,411 (GRCm39)	missense	probably damaging	1.00
R6679:Bod1l	UTSW	5	41,974,009 (GRCm39)	missense	probably damaging	0.97
R6788:Bod1l	UTSW	5	41,979,216 (GRCm39)	nonsense	probably null
R7006:Bod1l	UTSW	5	41,989,895 (GRCm39)	missense	probably damaging	1.00
R7095:Bod1l	UTSW	5	41,952,411 (GRCm39)	critical splice donor site	probably null
R7111:Bod1l	UTSW	5	41,970,463 (GRCm39)	critical splice donor site	probably null
R7190:Bod1l	UTSW	5	41,977,281 (GRCm39)	missense	probably benign	0.14
R7311:Bod1l	UTSW	5	41,951,676 (GRCm39)	missense	possibly damaging	0.57
R7336:Bod1l	UTSW	5	41,978,867 (GRCm39)	missense	probably damaging	1.00
R7341:Bod1l	UTSW	5	41,946,200 (GRCm39)	missense	probably benign	0.00
R7396:Bod1l	UTSW	5	41,988,889 (GRCm39)	missense	probably damaging	1.00
R7431:Bod1l	UTSW	5	41,970,463 (GRCm39)	critical splice donor site	probably null
R7442:Bod1l	UTSW	5	41,964,522 (GRCm39)	missense	probably damaging	0.96
R7539:Bod1l	UTSW	5	41,975,203 (GRCm39)	missense	possibly damaging	0.65
R7583:Bod1l	UTSW	5	41,991,133 (GRCm39)	missense	probably damaging	1.00
R7679:Bod1l	UTSW	5	41,977,986 (GRCm39)	frame shift	probably null
R7748:Bod1l	UTSW	5	41,989,683 (GRCm39)	missense	probably damaging	0.97
R7767:Bod1l	UTSW	5	41,974,099 (GRCm39)	missense	probably benign	0.01
R7773:Bod1l	UTSW	5	41,990,055 (GRCm39)	missense	probably benign	0.14
R7782:Bod1l	UTSW	5	41,975,286 (GRCm39)	missense	probably benign	0.01
R7860:Bod1l	UTSW	5	41,976,608 (GRCm39)	missense	probably damaging	1.00
R7975:Bod1l	UTSW	5	41,973,620 (GRCm39)	missense	possibly damaging	0.90
R7977:Bod1l	UTSW	5	41,952,413 (GRCm39)	missense	probably damaging	1.00
R7987:Bod1l	UTSW	5	41,952,413 (GRCm39)	missense	probably damaging	1.00
R8104:Bod1l	UTSW	5	41,991,075 (GRCm39)	nonsense	probably null
R8217:Bod1l	UTSW	5	41,988,850 (GRCm39)	missense	probably damaging	1.00
R8307:Bod1l	UTSW	5	41,978,498 (GRCm39)	missense	probably damaging	1.00
R8469:Bod1l	UTSW	5	41,978,834 (GRCm39)	missense	possibly damaging	0.86
R8506:Bod1l	UTSW	5	41,976,398 (GRCm39)	nonsense	probably null
R8934:Bod1l	UTSW	5	41,976,944 (GRCm39)	missense	probably benign	0.11
R8984:Bod1l	UTSW	5	41,946,215 (GRCm39)	missense	probably damaging	1.00
R8989:Bod1l	UTSW	5	41,979,025 (GRCm39)	missense	probably benign	0.00
R8993:Bod1l	UTSW	5	41,974,210 (GRCm39)	missense	probably benign	0.01
R9128:Bod1l	UTSW	5	41,946,266 (GRCm39)	missense	probably benign	0.22
R9129:Bod1l	UTSW	5	41,976,220 (GRCm39)	missense	probably damaging	0.99
R9198:Bod1l	UTSW	5	41,957,129 (GRCm39)	missense	probably benign	0.08
R9254:Bod1l	UTSW	5	41,979,223 (GRCm39)	missense	probably damaging	1.00
R9445:Bod1l	UTSW	5	41,974,619 (GRCm39)	missense	probably benign	0.04
R9457:Bod1l	UTSW	5	41,979,310 (GRCm39)	missense	probably damaging	0.99
R9470:Bod1l	UTSW	5	41,974,439 (GRCm39)	missense	probably damaging	0.99
R9536:Bod1l	UTSW	5	41,974,305 (GRCm39)	missense	probably benign	0.01
R9654:Bod1l	UTSW	5	41,975,707 (GRCm39)	missense	probably benign	0.02
R9734:Bod1l	UTSW	5	41,962,573 (GRCm39)	missense	possibly damaging	0.91
R9771:Bod1l	UTSW	5	41,949,206 (GRCm39)	missense	probably damaging	0.96
X0027:Bod1l	UTSW	5	41,990,012 (GRCm39)	missense	probably benign	0.20
X0058:Bod1l	UTSW	5	41,981,361 (GRCm39)	missense	probably damaging	1.00
Z1088:Bod1l	UTSW	5	41,966,107 (GRCm39)	missense	possibly damaging	0.95
Z1088:Bod1l	UTSW	5	41,978,489 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAAAGTCCTCGGTGCTTACC -3'
(R):5'- CCAACAAGGACAGCTTAGCAGG -3'

Sequencing Primer
(F):5'- TCAACTGCTGCAACTGGTTG -3'
(R):5'- ACAGCTTAGCAGGTAGTAAAAGTC -3'

Posted On

2015-10-08