Incidental Mutation 'R1869:Bod1l'
| ID |
210517 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Bod1l
|
| Ensembl Gene |
ENSMUSG00000061755 |
| Gene Name |
biorientation of chromosomes in cell division 1-like |
| Synonyms |
A230054D04Rik |
| MMRRC Submission |
039891-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.957)
|
| Stock # |
R1869 (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 41991018 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Phenylalanine
at position 179
(S179F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000144359
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050556]
[ENSMUST00000202908]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000050556
AA Change: S179F
PolyPhen 2
Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000058618
Gene: ENSMUSG00000061755
AA Change: S179F
| 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 |
possibly damaging
Transcript: ENSMUST00000202908
AA Change: S179F
PolyPhen 2
Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000144359
Gene: ENSMUSG00000061755
AA Change: S179F
| 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 |
0.1795 |
| Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.4%
- 20x: 92.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 127 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4921536K21Rik |
A |
G |
11: 3,840,067 (GRCm39) |
L110P |
probably damaging |
Het |
| 6030458C11Rik |
T |
C |
15: 12,817,993 (GRCm39) |
D168G |
probably damaging |
Het |
| Abca13 |
A |
T |
11: 9,242,134 (GRCm39) |
E1332D |
probably benign |
Het |
| Abhd11 |
A |
G |
5: 135,040,471 (GRCm39) |
Y168C |
probably damaging |
Het |
| Actr5 |
A |
C |
2: 158,480,643 (GRCm39) |
T554P |
probably damaging |
Het |
| Adam34l |
A |
T |
8: 44,078,132 (GRCm39) |
Y697* |
probably null |
Het |
| Adamts16 |
A |
G |
13: 70,883,866 (GRCm39) |
L1103P |
probably damaging |
Het |
| Adgrb3 |
A |
T |
1: 25,865,519 (GRCm39) |
I108K |
possibly damaging |
Het |
| Agbl4 |
T |
A |
4: 111,423,826 (GRCm39) |
M284K |
possibly damaging |
Het |
| Aoc3 |
T |
A |
11: 101,222,293 (GRCm39) |
Y176* |
probably null |
Het |
| Aox1 |
A |
G |
1: 58,115,262 (GRCm39) |
E749G |
probably damaging |
Het |
| Ap4b1 |
T |
A |
3: 103,728,184 (GRCm39) |
Y399* |
probably null |
Het |
| Arhgef5 |
A |
T |
6: 43,265,616 (GRCm39) |
I1553F |
probably damaging |
Het |
| Bag6 |
T |
C |
17: 35,361,802 (GRCm39) |
V541A |
probably benign |
Het |
| Bdp1 |
A |
C |
13: 100,178,709 (GRCm39) |
V1879G |
probably damaging |
Het |
| Bsnd |
C |
T |
4: 106,343,833 (GRCm39) |
V158I |
probably benign |
Het |
| Cachd1 |
C |
A |
4: 100,840,587 (GRCm39) |
H880N |
probably damaging |
Het |
| Ccdc27 |
T |
C |
4: 154,111,220 (GRCm39) |
|
probably null |
Het |
| Cd74 |
C |
T |
18: 60,943,484 (GRCm39) |
P190S |
probably benign |
Het |
| Cep68 |
A |
T |
11: 20,190,217 (GRCm39) |
L265Q |
probably damaging |
Het |
| Cfap70 |
G |
A |
14: 20,458,678 (GRCm39) |
Q772* |
probably null |
Het |
| CK137956 |
T |
A |
4: 127,864,327 (GRCm39) |
S101C |
possibly damaging |
Het |
| Clca3a2 |
G |
A |
3: 144,512,164 (GRCm39) |
T524M |
probably benign |
Het |
| Cxcr6 |
T |
C |
9: 123,639,022 (GRCm39) |
S15P |
probably benign |
Het |
| Cyfip2 |
T |
A |
11: 46,114,995 (GRCm39) |
Y904F |
probably benign |
Het |
| D130040H23Rik |
T |
A |
8: 69,755,354 (GRCm39) |
I253N |
probably benign |
Het |
| Ddx56 |
C |
T |
11: 6,213,993 (GRCm39) |
V389M |
possibly damaging |
Het |
| Dmp1 |
A |
T |
5: 104,359,942 (GRCm39) |
D206V |
probably damaging |
Het |
| Dnah17 |
A |
T |
11: 117,938,015 (GRCm39) |
C3350* |
probably null |
Het |
| Dst |
A |
T |
1: 34,291,913 (GRCm39) |
S877C |
probably damaging |
Het |
| Ermp1 |
A |
G |
19: 29,623,415 (GRCm39) |
S192P |
possibly damaging |
Het |
| F13b |
G |
A |
1: 139,438,672 (GRCm39) |
D359N |
probably benign |
Het |
| Fam171a1 |
A |
T |
2: 3,227,189 (GRCm39) |
Q769L |
possibly damaging |
Het |
| Fap |
T |
C |
2: 62,359,071 (GRCm39) |
R411G |
probably damaging |
Het |
| Fbn1 |
A |
G |
2: 125,193,947 (GRCm39) |
V1340A |
probably benign |
Het |
| Fbxw19 |
T |
C |
9: 109,311,100 (GRCm39) |
I370V |
probably benign |
Het |
| Foxi1 |
A |
T |
11: 34,157,937 (GRCm39) |
N29K |
possibly damaging |
Het |
| Frem2 |
T |
G |
3: 53,442,617 (GRCm39) |
D2640A |
probably benign |
Het |
| Fzd4 |
T |
C |
7: 89,056,454 (GRCm39) |
V167A |
probably benign |
Het |
| Galnt3 |
T |
C |
2: 65,928,123 (GRCm39) |
I258V |
possibly damaging |
Het |
| Galr2 |
T |
C |
11: 116,174,069 (GRCm39) |
V233A |
possibly damaging |
Het |
| Gldc |
G |
T |
19: 30,116,732 (GRCm39) |
Q407K |
probably benign |
Het |
| Gmcl1 |
T |
C |
6: 86,674,498 (GRCm39) |
D460G |
probably benign |
Het |
| Gpr89 |
A |
G |
3: 96,782,975 (GRCm39) |
I325T |
probably benign |
Het |
| Grap |
T |
A |
11: 61,555,015 (GRCm39) |
Y61N |
possibly damaging |
Het |
| Hbs1l |
G |
T |
10: 21,234,305 (GRCm39) |
|
probably null |
Het |
| Hexb |
T |
A |
13: 97,327,767 (GRCm39) |
E134D |
probably benign |
Het |
| Hydin |
T |
A |
8: 111,227,337 (GRCm39) |
V1507D |
possibly damaging |
Het |
| Igkv8-16 |
C |
A |
6: 70,363,971 (GRCm39) |
G17V |
probably benign |
Het |
| Kdm4a |
T |
A |
4: 117,996,068 (GRCm39) |
Q987L |
probably null |
Het |
| Krt76 |
A |
G |
15: 101,797,922 (GRCm39) |
|
probably null |
Het |
| Lap3 |
T |
C |
5: 45,660,729 (GRCm39) |
S238P |
probably benign |
Het |
| Letm2 |
T |
C |
8: 26,071,729 (GRCm39) |
D391G |
probably damaging |
Het |
| Lipn |
A |
G |
19: 34,058,139 (GRCm39) |
T287A |
possibly damaging |
Het |
| Macf1 |
T |
C |
4: 123,244,921 (GRCm39) |
S466G |
probably damaging |
Het |
| Map3k5 |
C |
A |
10: 20,007,855 (GRCm39) |
S1220* |
probably null |
Het |
| Map4 |
T |
A |
9: 109,897,996 (GRCm39) |
S754R |
possibly damaging |
Het |
| Map4 |
T |
C |
9: 109,864,032 (GRCm39) |
V419A |
probably benign |
Het |
| Mroh9 |
A |
G |
1: 162,854,082 (GRCm39) |
S773P |
probably damaging |
Het |
| Mtus1 |
A |
C |
8: 41,529,267 (GRCm39) |
|
probably null |
Het |
| Muc1 |
C |
T |
3: 89,139,117 (GRCm39) |
P533S |
probably damaging |
Het |
| Muc13 |
A |
T |
16: 33,624,970 (GRCm39) |
I282F |
probably damaging |
Het |
| Mucl3 |
A |
G |
17: 35,949,305 (GRCm39) |
L98P |
possibly damaging |
Het |
| Myh14 |
T |
A |
7: 44,261,067 (GRCm39) |
Q1816L |
possibly damaging |
Het |
| Nalcn |
A |
C |
14: 123,831,965 (GRCm39) |
V103G |
possibly damaging |
Het |
| Nlrp9c |
G |
A |
7: 26,084,245 (GRCm39) |
Q445* |
probably null |
Het |
| Olfml2b |
A |
G |
1: 170,496,812 (GRCm39) |
D481G |
probably damaging |
Het |
| Or13g1 |
T |
A |
7: 85,955,875 (GRCm39) |
I149F |
possibly damaging |
Het |
| Or2ag19 |
T |
G |
7: 106,444,301 (GRCm39) |
I161S |
probably benign |
Het |
| Or5g23 |
A |
G |
2: 85,438,844 (GRCm39) |
S137P |
probably benign |
Het |
| Or8b37 |
T |
A |
9: 37,959,498 (GRCm39) |
|
probably null |
Het |
| Or8k3b |
T |
A |
2: 86,520,735 (GRCm39) |
I195F |
probably damaging |
Het |
| Pcdhb2 |
A |
T |
18: 37,430,408 (GRCm39) |
|
probably null |
Het |
| Pcdhb22 |
A |
C |
18: 37,652,200 (GRCm39) |
T223P |
probably damaging |
Het |
| Pcdhga1 |
T |
A |
18: 37,973,143 (GRCm39) |
N907K |
probably damaging |
Het |
| Pcnt |
T |
C |
10: 76,215,740 (GRCm39) |
E2347G |
probably null |
Het |
| Phax |
T |
A |
18: 56,706,176 (GRCm39) |
V22D |
probably benign |
Het |
| Pik3ca |
T |
C |
3: 32,504,499 (GRCm39) |
F667S |
probably damaging |
Het |
| Pkd1 |
T |
C |
17: 24,813,905 (GRCm39) |
F4123S |
probably damaging |
Het |
| Pkhd1 |
A |
G |
1: 20,685,491 (GRCm39) |
|
probably null |
Het |
| Plcb1 |
G |
A |
2: 135,152,934 (GRCm39) |
R368K |
probably benign |
Het |
| Prrc2a |
G |
T |
17: 35,372,284 (GRCm39) |
R1739S |
possibly damaging |
Het |
| Psg23 |
A |
T |
7: 18,348,543 (GRCm39) |
M88K |
probably benign |
Het |
| Pstk |
T |
A |
7: 130,989,526 (GRCm39) |
Y354N |
probably damaging |
Het |
| Rab39 |
A |
G |
9: 53,617,231 (GRCm39) |
I62T |
possibly damaging |
Het |
| Ranbp2 |
A |
G |
10: 58,328,383 (GRCm39) |
I2800V |
probably damaging |
Het |
| Rasgrp1 |
T |
C |
2: 117,120,828 (GRCm39) |
Y431C |
probably damaging |
Het |
| Rest |
T |
A |
5: 77,416,209 (GRCm39) |
V141E |
possibly damaging |
Het |
| Rnf167 |
T |
A |
11: 70,540,965 (GRCm39) |
I197N |
possibly damaging |
Het |
| Rtn1 |
A |
G |
12: 72,354,942 (GRCm39) |
S335P |
probably damaging |
Het |
| Ryr2 |
G |
T |
13: 11,676,961 (GRCm39) |
R3297S |
probably damaging |
Het |
| S1pr3 |
A |
C |
13: 51,573,952 (GRCm39) |
K378Q |
probably benign |
Het |
| Scgb1b24 |
T |
C |
7: 33,443,469 (GRCm39) |
Y43H |
probably damaging |
Het |
| Sh3rf3 |
T |
A |
10: 58,919,335 (GRCm39) |
M484K |
probably damaging |
Het |
| Shank1 |
A |
T |
7: 43,991,539 (GRCm39) |
R69* |
probably null |
Het |
| Siglecf |
A |
G |
7: 43,004,967 (GRCm39) |
N399S |
probably benign |
Het |
| Slc1a7 |
A |
G |
4: 107,865,561 (GRCm39) |
T350A |
probably damaging |
Het |
| Slc25a54 |
T |
A |
3: 108,987,932 (GRCm39) |
Y24* |
probably null |
Het |
| Slk |
T |
C |
19: 47,613,891 (GRCm39) |
F916L |
probably damaging |
Het |
| Snap91 |
T |
A |
9: 86,672,194 (GRCm39) |
|
probably null |
Het |
| Snrpb2 |
A |
T |
2: 142,907,106 (GRCm39) |
R25S |
possibly damaging |
Het |
| Specc1l |
T |
C |
10: 75,097,659 (GRCm39) |
Y811H |
probably damaging |
Het |
| Sprr2h |
A |
G |
3: 92,293,925 (GRCm39) |
|
probably benign |
Het |
| Sult2a5 |
A |
T |
7: 13,358,045 (GRCm39) |
I26F |
probably benign |
Het |
| Syt13 |
C |
T |
2: 92,776,448 (GRCm39) |
T245I |
possibly damaging |
Het |
| Tecrl |
T |
A |
5: 83,502,706 (GRCm39) |
T33S |
probably benign |
Het |
| Telo2 |
T |
A |
17: 25,333,968 (GRCm39) |
D93V |
probably benign |
Het |
| Tet2 |
A |
T |
3: 133,187,202 (GRCm39) |
|
probably null |
Het |
| Tgm7 |
A |
T |
2: 120,931,570 (GRCm39) |
C198S |
probably damaging |
Het |
| Ticrr |
T |
C |
7: 79,328,883 (GRCm39) |
F674S |
probably damaging |
Het |
| Tmem129 |
C |
A |
5: 33,811,843 (GRCm39) |
C31F |
probably damaging |
Het |
| Tmem132a |
T |
A |
19: 10,836,052 (GRCm39) |
D826V |
possibly damaging |
Het |
| Tpd52 |
T |
C |
3: 9,018,862 (GRCm39) |
|
probably null |
Het |
| Trub2 |
A |
G |
2: 29,667,678 (GRCm39) |
S321P |
probably benign |
Het |
| Ttc29 |
A |
G |
8: 79,009,014 (GRCm39) |
T295A |
probably benign |
Het |
| Tubb1 |
G |
A |
2: 174,298,482 (GRCm39) |
S89N |
probably benign |
Het |
| Tut4 |
T |
A |
4: 108,386,497 (GRCm39) |
F1122L |
probably damaging |
Het |
| Ubap2 |
C |
A |
4: 41,233,617 (GRCm39) |
G91V |
probably damaging |
Het |
| Ugt2b35 |
A |
G |
5: 87,149,147 (GRCm39) |
N133D |
probably damaging |
Het |
| Usp34 |
A |
G |
11: 23,314,479 (GRCm39) |
H807R |
probably benign |
Het |
| Vmn1r220 |
A |
C |
13: 23,368,457 (GRCm39) |
C80G |
probably damaging |
Het |
| Vmn1r79 |
A |
G |
7: 11,910,574 (GRCm39) |
E152G |
probably benign |
Het |
| Vmn2r28 |
T |
C |
7: 5,489,345 (GRCm39) |
Y498C |
probably benign |
Het |
| Wif1 |
A |
G |
10: 120,920,824 (GRCm39) |
I215M |
probably benign |
Het |
| Wnk1 |
T |
C |
6: 119,928,050 (GRCm39) |
T1134A |
probably damaging |
Het |
| Zfp90 |
A |
G |
8: 107,145,755 (GRCm39) |
H29R |
probably benign |
Het |
| Zfp972 |
A |
G |
2: 177,563,480 (GRCm39) |
|
probably null |
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 |
|
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 |
|
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'- TCTTATAGCGAGTGTGCACAC -3'
(R):5'- TCAGATCAGGAATGCTGGAGTC -3'
Sequencing Primer
(F):5'- GTGCACACACACACACAC -3'
(R):5'- AATGCTGGAGTCTGGTATTGAC -3'
|
| Posted On |
2014-06-30 |
Incidental Mutation