Incidental Mutation 'R4782:Bod1l'
| ID |
366585 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Bod1l
|
| Ensembl Gene |
ENSMUSG00000061755 |
| Gene Name |
biorientation of chromosomes in cell division 1-like |
| Synonyms |
A230054D04Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.952)
|
| Stock # |
R4782 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
5 |
| Chromosomal Location |
41944881-42001658 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 41991006 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 183
(T183I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000144359
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050556]
[ENSMUST00000202908]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000050556
AA Change: T183I
PolyPhen 2
Score 0.062 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000058618
Gene: ENSMUSG00000061755
AA Change: T183I
| 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: ENSMUST00000202200
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000202908
AA Change: T183I
PolyPhen 2
Score 0.062 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000144359
Gene: ENSMUSG00000061755
AA Change: T183I
| 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 |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.4%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 121 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
A |
G |
11: 9,278,096 (GRCm39) |
E3092G |
probably damaging |
Het |
| Abhd12b |
C |
G |
12: 70,215,838 (GRCm39) |
S170C |
probably damaging |
Het |
| Abtb2 |
A |
T |
2: 103,547,644 (GRCm39) |
D1006V |
probably benign |
Het |
| Abtb3 |
A |
C |
10: 85,490,414 (GRCm39) |
I1027L |
probably damaging |
Het |
| Adgrl1 |
A |
G |
8: 84,662,202 (GRCm39) |
H1021R |
probably benign |
Het |
| Ago3 |
A |
T |
4: 126,241,665 (GRCm39) |
|
probably null |
Het |
| Ahnak |
A |
G |
19: 8,989,863 (GRCm39) |
|
probably benign |
Het |
| Akap6 |
CA |
C |
12: 52,934,406 (GRCm39) |
|
probably null |
Het |
| Amotl2 |
T |
G |
9: 102,597,322 (GRCm39) |
|
probably null |
Het |
| Ankrd34b |
T |
A |
13: 92,574,813 (GRCm39) |
I15N |
probably damaging |
Het |
| Ap3d1 |
C |
T |
10: 80,557,420 (GRCm39) |
|
probably null |
Het |
| Appl2 |
A |
T |
10: 83,436,855 (GRCm39) |
D635E |
probably damaging |
Het |
| Arid1b |
C |
T |
17: 5,389,496 (GRCm39) |
P1681S |
probably damaging |
Het |
| Atp10a |
T |
C |
7: 58,440,843 (GRCm39) |
M496T |
probably benign |
Het |
| Atp2c2 |
A |
G |
8: 120,475,891 (GRCm39) |
K595E |
probably damaging |
Het |
| Atpaf2 |
T |
C |
11: 60,295,238 (GRCm39) |
H204R |
probably damaging |
Het |
| Atr |
G |
A |
9: 95,744,850 (GRCm39) |
V56I |
probably benign |
Het |
| Ccdc168 |
T |
C |
1: 44,098,203 (GRCm39) |
D965G |
possibly damaging |
Het |
| Ccdc171 |
A |
T |
4: 83,599,253 (GRCm39) |
E689D |
probably damaging |
Het |
| Cdc73 |
T |
A |
1: 143,503,613 (GRCm39) |
Q346L |
probably benign |
Het |
| Cert1 |
T |
C |
13: 96,748,773 (GRCm39) |
V281A |
probably benign |
Het |
| Chd2 |
A |
T |
7: 73,134,184 (GRCm39) |
M721K |
possibly damaging |
Het |
| Col22a1 |
T |
A |
15: 71,673,774 (GRCm39) |
T981S |
unknown |
Het |
| Cpox |
G |
A |
16: 58,492,986 (GRCm39) |
A207T |
probably damaging |
Het |
| Cym |
G |
A |
3: 107,123,413 (GRCm39) |
T160I |
possibly damaging |
Het |
| D130043K22Rik |
T |
C |
13: 25,062,023 (GRCm39) |
I664T |
probably damaging |
Het |
| Ddx4 |
C |
T |
13: 112,750,230 (GRCm39) |
|
probably null |
Het |
| Ddx4 |
A |
T |
13: 112,787,894 (GRCm39) |
V15E |
probably benign |
Het |
| Depdc1a |
G |
A |
3: 159,232,273 (GRCm39) |
E675K |
probably damaging |
Het |
| Dglucy |
A |
T |
12: 100,816,602 (GRCm39) |
M415L |
probably benign |
Het |
| Dlg4 |
C |
T |
11: 69,917,780 (GRCm39) |
P21L |
probably damaging |
Het |
| Dmxl1 |
A |
T |
18: 49,996,059 (GRCm39) |
N395I |
probably damaging |
Het |
| Dzank1 |
A |
T |
2: 144,346,319 (GRCm39) |
C249S |
probably damaging |
Het |
| Efnb2 |
A |
T |
8: 8,673,104 (GRCm39) |
|
probably null |
Het |
| Ercc6l2 |
T |
G |
13: 63,982,552 (GRCm39) |
I244S |
probably damaging |
Het |
| Ewsr1 |
A |
T |
11: 5,020,423 (GRCm39) |
M584K |
unknown |
Het |
| Fam193b |
A |
G |
13: 55,691,284 (GRCm39) |
S197P |
probably damaging |
Het |
| Fanca |
A |
G |
8: 124,014,941 (GRCm39) |
V689A |
probably damaging |
Het |
| Fbxo31 |
A |
T |
8: 122,279,178 (GRCm39) |
Y436* |
probably null |
Het |
| Fbxo31 |
A |
G |
8: 122,279,180 (GRCm39) |
Y436H |
probably damaging |
Het |
| Fcna |
T |
A |
2: 25,515,338 (GRCm39) |
D215V |
probably damaging |
Het |
| Foxj3 |
A |
T |
4: 119,478,857 (GRCm39) |
S438C |
unknown |
Het |
| Gcm2 |
T |
C |
13: 41,256,970 (GRCm39) |
K260E |
possibly damaging |
Het |
| Gcnt4 |
A |
T |
13: 97,083,914 (GRCm39) |
L403F |
possibly damaging |
Het |
| Gdf10 |
A |
G |
14: 33,653,870 (GRCm39) |
T126A |
probably benign |
Het |
| Ggcx |
A |
G |
6: 72,405,875 (GRCm39) |
K569E |
probably benign |
Het |
| Gm10250 |
C |
T |
15: 5,150,578 (GRCm39) |
|
probably benign |
Het |
| Gpnmb |
G |
T |
6: 49,022,417 (GRCm39) |
|
probably null |
Het |
| Ifi44 |
G |
A |
3: 151,451,229 (GRCm39) |
P241S |
probably damaging |
Het |
| Irs1 |
T |
C |
1: 82,265,184 (GRCm39) |
T1011A |
probably benign |
Het |
| Jag2 |
A |
T |
12: 112,877,869 (GRCm39) |
S595T |
probably benign |
Het |
| Kif5a |
T |
A |
10: 127,066,823 (GRCm39) |
Q960L |
probably benign |
Het |
| Kifc2 |
A |
G |
15: 76,548,548 (GRCm39) |
E430G |
possibly damaging |
Het |
| Lama3 |
T |
A |
18: 12,544,627 (GRCm39) |
C323* |
probably null |
Het |
| Lgsn |
T |
C |
1: 31,242,823 (GRCm39) |
Y302H |
probably benign |
Het |
| Lmbrd1 |
G |
A |
1: 24,784,056 (GRCm39) |
|
probably null |
Het |
| Lrpap1 |
A |
G |
5: 35,256,622 (GRCm39) |
V120A |
probably damaging |
Het |
| Macrod2 |
T |
A |
2: 140,261,858 (GRCm39) |
D46E |
possibly damaging |
Het |
| Mbd4 |
C |
A |
6: 115,822,283 (GRCm39) |
R63L |
possibly damaging |
Het |
| Mfsd10 |
T |
C |
5: 34,792,293 (GRCm39) |
|
probably benign |
Het |
| Mib2 |
G |
T |
4: 155,744,229 (GRCm39) |
S144R |
probably benign |
Het |
| Muc5b |
T |
A |
7: 141,401,453 (GRCm39) |
C566* |
probably null |
Het |
| Ndufs1 |
C |
A |
1: 63,200,108 (GRCm39) |
G268V |
probably damaging |
Het |
| Nfs1 |
A |
G |
2: 155,976,369 (GRCm39) |
V175A |
possibly damaging |
Het |
| Ngb |
G |
A |
12: 87,146,999 (GRCm39) |
H73Y |
probably benign |
Het |
| Npepps |
G |
A |
11: 97,117,652 (GRCm39) |
T549I |
probably damaging |
Het |
| Nr1h2 |
A |
G |
7: 44,199,923 (GRCm39) |
V329A |
possibly damaging |
Het |
| Nsun6 |
T |
C |
2: 15,041,137 (GRCm39) |
I151M |
possibly damaging |
Het |
| Ofcc1 |
T |
C |
13: 40,155,368 (GRCm39) |
|
probably null |
Het |
| Or1e31 |
C |
T |
11: 73,689,665 (GRCm39) |
C306Y |
probably benign |
Het |
| Or2y16 |
T |
A |
11: 49,334,696 (GRCm39) |
F6Y |
probably benign |
Het |
| Or2z8 |
A |
G |
8: 72,811,938 (GRCm39) |
N138S |
probably benign |
Het |
| Or51h1 |
T |
A |
7: 102,308,041 (GRCm39) |
N4K |
possibly damaging |
Het |
| Or5an1c |
C |
T |
19: 12,218,936 (GRCm39) |
V30I |
probably benign |
Het |
| Or8b46 |
A |
G |
9: 38,450,371 (GRCm39) |
Y60C |
probably damaging |
Het |
| Parp6 |
A |
G |
9: 59,542,267 (GRCm39) |
|
probably null |
Het |
| Pcnt |
C |
A |
10: 76,245,411 (GRCm39) |
R1075S |
possibly damaging |
Het |
| Pla2g4f |
T |
C |
2: 120,133,757 (GRCm39) |
E548G |
probably damaging |
Het |
| Polrmt |
G |
T |
10: 79,575,357 (GRCm39) |
H725N |
probably benign |
Het |
| Pou2f3 |
T |
C |
9: 43,051,153 (GRCm39) |
T178A |
probably damaging |
Het |
| Prtn3 |
C |
A |
10: 79,717,899 (GRCm39) |
P169H |
probably damaging |
Het |
| Ptprd |
A |
G |
4: 76,009,769 (GRCm39) |
I764T |
probably benign |
Het |
| Ptprh |
A |
T |
7: 4,572,576 (GRCm39) |
H467Q |
probably benign |
Het |
| Raph1 |
A |
T |
1: 60,528,273 (GRCm39) |
I996N |
probably damaging |
Het |
| Rasa4 |
G |
A |
5: 136,120,083 (GRCm39) |
W53* |
probably null |
Het |
| Rasgrp1 |
C |
T |
2: 117,115,356 (GRCm39) |
R744Q |
probably benign |
Het |
| Rmnd5a |
T |
C |
6: 71,390,333 (GRCm39) |
E141G |
probably damaging |
Het |
| Rps12 |
T |
C |
10: 23,662,688 (GRCm39) |
I51M |
possibly damaging |
Het |
| Scn10a |
T |
G |
9: 119,451,976 (GRCm39) |
S1316R |
possibly damaging |
Het |
| Sdhb |
A |
G |
4: 140,704,777 (GRCm39) |
H246R |
possibly damaging |
Het |
| Setx |
G |
A |
2: 29,034,058 (GRCm39) |
R332Q |
probably damaging |
Het |
| Siglec1 |
A |
C |
2: 130,917,843 (GRCm39) |
S1011R |
probably damaging |
Het |
| Sin3b |
A |
C |
8: 73,452,271 (GRCm39) |
I126L |
probably benign |
Het |
| Slc11a1 |
T |
G |
1: 74,423,247 (GRCm39) |
L366R |
probably damaging |
Het |
| Slc12a1 |
C |
T |
2: 125,002,999 (GRCm39) |
R177* |
probably null |
Het |
| Slc30a1 |
A |
C |
1: 191,641,160 (GRCm39) |
K269Q |
probably benign |
Het |
| Slco1a5 |
T |
C |
6: 142,194,533 (GRCm39) |
Y370C |
possibly damaging |
Het |
| Slf2 |
T |
A |
19: 44,923,364 (GRCm39) |
|
probably null |
Het |
| Sltm |
A |
G |
9: 70,496,339 (GRCm39) |
H958R |
probably damaging |
Het |
| Snrnp40 |
A |
G |
4: 130,256,549 (GRCm39) |
I91M |
probably damaging |
Het |
| Spta1 |
A |
T |
1: 174,058,232 (GRCm39) |
Q1900L |
probably benign |
Het |
| Srgn |
C |
T |
10: 62,333,631 (GRCm39) |
E49K |
possibly damaging |
Het |
| Ssu2 |
A |
C |
6: 112,353,411 (GRCm39) |
C238G |
probably damaging |
Het |
| Terf2 |
G |
T |
8: 107,803,307 (GRCm39) |
H425Q |
probably benign |
Het |
| Thra |
G |
A |
11: 98,646,990 (GRCm39) |
S37N |
probably benign |
Het |
| Toporsl |
A |
G |
4: 52,610,845 (GRCm39) |
D246G |
probably damaging |
Het |
| Ubap2l |
G |
A |
3: 89,928,210 (GRCm39) |
T553M |
probably damaging |
Het |
| Usp10 |
A |
G |
8: 120,667,930 (GRCm39) |
Y77C |
probably benign |
Het |
| Utrn |
T |
C |
10: 12,625,813 (GRCm39) |
T123A |
probably damaging |
Het |
| Vmn1r204 |
T |
G |
13: 22,740,867 (GRCm39) |
F166C |
probably benign |
Het |
| Vmn2r14 |
T |
C |
5: 109,369,370 (GRCm39) |
I68V |
probably benign |
Het |
| Wls |
C |
T |
3: 159,603,082 (GRCm39) |
T165I |
probably benign |
Het |
| Wsb1 |
A |
G |
11: 79,131,199 (GRCm39) |
M399T |
probably benign |
Het |
| Xbp1 |
C |
T |
11: 5,471,167 (GRCm39) |
T58M |
probably damaging |
Het |
| Zbtb46 |
A |
T |
2: 181,032,929 (GRCm39) |
D577E |
probably benign |
Het |
| Zfp366 |
A |
G |
13: 99,382,991 (GRCm39) |
D718G |
probably damaging |
Het |
| Zfp408 |
A |
T |
2: 91,475,369 (GRCm39) |
V595E |
possibly damaging |
Het |
| Zfp493 |
T |
A |
13: 67,934,322 (GRCm39) |
W60R |
probably null |
Het |
| Zfp606 |
A |
T |
7: 12,227,932 (GRCm39) |
K626N |
probably damaging |
Het |
| Zfp820 |
A |
T |
17: 22,037,966 (GRCm39) |
L454Q |
probably benign |
Het |
| Zswim5 |
A |
G |
4: 116,830,169 (GRCm39) |
I515V |
probably benign |
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 |
|
R4631:Bod1l
|
UTSW |
5 |
41,975,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4657:Bod1l
|
UTSW |
5 |
41,975,955 (GRCm39) |
missense |
probably benign |
0.00 |
|
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'- GACATTCTCTCTTATAGCGAGTGTG -3'
(R):5'- AGATCAGGAATGCTGGAGTCTG -3'
Sequencing Primer
(F):5'- TCTTATAGCGAGTGTGCACAC -3'
(R):5'- GGTATTGACCGAATTATTTCTCAGG -3'
|
| Posted On |
2015-12-29 |
Incidental Mutation