Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019A02Rik |
C |
T |
1: 53,221,665 (GRCm39) |
D55N |
possibly damaging |
Het |
Abcc2 |
G |
A |
19: 43,806,471 (GRCm39) |
G762S |
probably damaging |
Het |
Acta2 |
C |
A |
19: 34,225,865 (GRCm39) |
A110S |
probably damaging |
Het |
Adam26a |
T |
C |
8: 44,022,456 (GRCm39) |
T345A |
possibly damaging |
Het |
Anapc11 |
T |
C |
11: 120,496,250 (GRCm39) |
*85R |
probably null |
Het |
Ang2 |
A |
C |
14: 51,433,071 (GRCm39) |
C104G |
probably damaging |
Het |
Ankzf1 |
G |
A |
1: 75,174,596 (GRCm39) |
V529I |
probably benign |
Het |
Aox4 |
G |
T |
1: 58,288,097 (GRCm39) |
V737F |
probably benign |
Het |
Aqr |
T |
C |
2: 113,934,528 (GRCm39) |
N1371S |
probably benign |
Het |
Bach1 |
T |
A |
16: 87,526,733 (GRCm39) |
S732T |
probably benign |
Het |
Bcr |
T |
A |
10: 74,967,431 (GRCm39) |
I555N |
probably damaging |
Het |
Bicra |
T |
C |
7: 15,705,717 (GRCm39) |
T1575A |
probably damaging |
Het |
Bop1 |
A |
G |
15: 76,338,076 (GRCm39) |
L598P |
probably damaging |
Het |
Cacna1d |
A |
T |
14: 29,845,419 (GRCm39) |
F605L |
possibly damaging |
Het |
Capn15 |
C |
T |
17: 26,184,353 (GRCm39) |
V109I |
possibly damaging |
Het |
Cdkn1b |
T |
C |
6: 134,897,815 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,406,617 (GRCm39) |
T542A |
possibly damaging |
Het |
Dsc2 |
A |
T |
18: 20,180,276 (GRCm39) |
I159N |
probably damaging |
Het |
Ecel1 |
A |
T |
1: 87,075,716 (GRCm39) |
V774E |
probably damaging |
Het |
Eif5b |
T |
G |
1: 38,084,560 (GRCm39) |
C849W |
probably damaging |
Het |
Eif5b |
T |
A |
1: 38,058,451 (GRCm39) |
L251* |
probably null |
Het |
Ext2 |
T |
C |
2: 93,592,956 (GRCm39) |
D416G |
probably damaging |
Het |
Fancm |
G |
A |
12: 65,153,388 (GRCm39) |
W1281* |
probably null |
Het |
Foxk1 |
T |
C |
5: 142,437,389 (GRCm39) |
|
probably null |
Het |
Frem2 |
T |
A |
3: 53,560,905 (GRCm39) |
I1201F |
possibly damaging |
Het |
Gabra5 |
A |
G |
7: 57,157,873 (GRCm39) |
|
probably benign |
Het |
Gmpr2 |
G |
A |
14: 55,915,778 (GRCm39) |
V319I |
probably damaging |
Het |
Gna12 |
A |
T |
5: 140,746,338 (GRCm39) |
L369Q |
probably damaging |
Het |
Gpr160 |
A |
G |
3: 30,950,914 (GRCm39) |
R329G |
probably benign |
Het |
H2-M10.3 |
T |
C |
17: 36,677,423 (GRCm39) |
H285R |
probably benign |
Het |
H2-M2 |
A |
T |
17: 37,793,424 (GRCm39) |
V194E |
probably benign |
Het |
Hephl1 |
G |
A |
9: 14,995,830 (GRCm39) |
R431W |
possibly damaging |
Het |
Hr |
A |
G |
14: 70,793,877 (GRCm39) |
T46A |
probably benign |
Het |
Hr |
A |
G |
14: 70,794,205 (GRCm39) |
H126R |
possibly damaging |
Het |
Hsf1 |
T |
G |
15: 76,382,398 (GRCm39) |
D256E |
probably benign |
Het |
Ifi208 |
C |
T |
1: 173,510,961 (GRCm39) |
T372I |
probably damaging |
Het |
Ifi47 |
T |
G |
11: 48,986,620 (GRCm39) |
F129C |
probably damaging |
Het |
Il1rl2 |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
1: 40,366,470 (GRCm39) |
|
probably benign |
Het |
Irag2 |
A |
G |
6: 145,120,257 (GRCm39) |
I491V |
probably benign |
Het |
Itga11 |
A |
T |
9: 62,670,171 (GRCm39) |
N765I |
probably benign |
Het |
Klhl22 |
T |
A |
16: 17,589,663 (GRCm39) |
I108K |
probably benign |
Het |
Lancl1 |
T |
G |
1: 67,073,381 (GRCm39) |
H34P |
probably benign |
Het |
Lcor |
C |
A |
19: 41,573,685 (GRCm39) |
N813K |
probably damaging |
Het |
Mbd3l1 |
G |
A |
9: 18,396,274 (GRCm39) |
G133D |
probably benign |
Het |
Med12l |
T |
C |
3: 59,155,353 (GRCm39) |
F1178L |
probably benign |
Het |
Mrm1 |
A |
T |
11: 84,705,531 (GRCm39) |
N289K |
probably damaging |
Het |
Myf6 |
A |
G |
10: 107,330,073 (GRCm39) |
Y165H |
probably benign |
Het |
Myo1g |
C |
A |
11: 6,456,913 (GRCm39) |
C971F |
probably benign |
Het |
Myo3a |
T |
C |
2: 22,245,862 (GRCm39) |
M3T |
probably benign |
Het |
Nsrp1 |
G |
A |
11: 76,937,114 (GRCm39) |
R361* |
probably null |
Het |
Or10d4 |
A |
C |
9: 39,580,611 (GRCm39) |
Q86P |
possibly damaging |
Het |
Or10h1b |
C |
A |
17: 33,395,548 (GRCm39) |
H57Q |
possibly damaging |
Het |
Or4a69 |
T |
C |
2: 89,312,756 (GRCm39) |
H241R |
probably damaging |
Het |
Or4a77 |
T |
C |
2: 89,487,731 (GRCm39) |
D18G |
probably damaging |
Het |
Or5p6 |
A |
T |
7: 107,631,163 (GRCm39) |
I129N |
possibly damaging |
Het |
Or8b41 |
G |
A |
9: 38,054,866 (GRCm39) |
C140Y |
probably benign |
Het |
Or8k53 |
T |
A |
2: 86,177,846 (GRCm39) |
D88V |
probably benign |
Het |
Oscar |
T |
G |
7: 3,614,663 (GRCm39) |
Y103S |
probably damaging |
Het |
Pdpr |
A |
G |
8: 111,852,925 (GRCm39) |
N610S |
probably benign |
Het |
Ppp4r3b |
T |
C |
11: 29,124,697 (GRCm39) |
I56T |
probably damaging |
Het |
Pxdn |
T |
A |
12: 30,044,552 (GRCm39) |
V510D |
possibly damaging |
Het |
Rab11fip5 |
T |
C |
6: 85,324,913 (GRCm39) |
S465G |
possibly damaging |
Het |
Rasgrf2 |
T |
C |
13: 92,267,759 (GRCm39) |
T82A |
probably benign |
Het |
Scmh1 |
G |
A |
4: 120,320,284 (GRCm39) |
W30* |
probably null |
Het |
Sema4g |
T |
C |
19: 44,981,071 (GRCm39) |
Y40H |
probably benign |
Het |
Serpinf2 |
A |
T |
11: 75,323,494 (GRCm39) |
M404K |
probably damaging |
Het |
Sgk3 |
T |
C |
1: 9,950,616 (GRCm39) |
|
probably null |
Het |
Slc16a5 |
A |
T |
11: 115,360,738 (GRCm39) |
Y307F |
possibly damaging |
Het |
Slc39a5 |
G |
A |
10: 128,233,628 (GRCm39) |
L290F |
probably damaging |
Het |
Snx32 |
A |
C |
19: 5,547,736 (GRCm39) |
D191E |
probably damaging |
Het |
Sp4 |
T |
C |
12: 118,262,859 (GRCm39) |
I396V |
probably benign |
Het |
Srrd |
A |
G |
5: 112,490,765 (GRCm39) |
V42A |
unknown |
Het |
Stim1 |
A |
G |
7: 102,080,257 (GRCm39) |
H547R |
unknown |
Het |
Svep1 |
G |
A |
4: 58,070,517 (GRCm39) |
A2423V |
probably benign |
Het |
Tep1 |
A |
G |
14: 51,066,687 (GRCm39) |
S2304P |
possibly damaging |
Het |
Tkt |
C |
G |
14: 30,281,795 (GRCm39) |
S104R |
probably benign |
Het |
Tkt |
T |
C |
14: 30,281,796 (GRCm39) |
S105P |
probably damaging |
Het |
Tln1 |
A |
T |
4: 43,542,893 (GRCm39) |
N1365K |
probably damaging |
Het |
Topaz1 |
G |
T |
9: 122,604,707 (GRCm39) |
A1104S |
probably benign |
Het |
Trmt2a |
A |
G |
16: 18,068,814 (GRCm39) |
H270R |
probably damaging |
Het |
Ttll10 |
G |
T |
4: 156,127,616 (GRCm39) |
T389K |
probably benign |
Het |
Tubal3 |
A |
G |
13: 3,980,674 (GRCm39) |
I129V |
probably benign |
Het |
Ucp3 |
A |
G |
7: 100,131,123 (GRCm39) |
E192G |
probably damaging |
Het |
Usp47 |
A |
G |
7: 111,677,063 (GRCm39) |
D448G |
probably damaging |
Het |
Vmn2r98 |
T |
A |
17: 19,301,496 (GRCm39) |
L833M |
possibly damaging |
Het |
Vps13d |
A |
G |
4: 144,807,869 (GRCm39) |
|
probably null |
Het |
Wdr7 |
A |
G |
18: 63,910,939 (GRCm39) |
D777G |
possibly damaging |
Het |
Zcchc8 |
A |
G |
5: 123,847,300 (GRCm39) |
I213T |
probably damaging |
Het |
Zfp281 |
T |
C |
1: 136,555,143 (GRCm39) |
I707T |
probably damaging |
Het |
Zfp335 |
T |
C |
2: 164,735,395 (GRCm39) |
H1158R |
probably damaging |
Het |
Zfp692 |
C |
T |
11: 58,199,765 (GRCm39) |
T118M |
probably damaging |
Het |
Zfr2 |
T |
A |
10: 81,075,969 (GRCm39) |
L192Q |
probably benign |
Het |
|
Other mutations in Flvcr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Flvcr1
|
APN |
1 |
190,747,686 (GRCm39) |
nonsense |
probably null |
|
IGL01089:Flvcr1
|
APN |
1 |
190,745,587 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02572:Flvcr1
|
APN |
1 |
190,757,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03248:Flvcr1
|
APN |
1 |
190,757,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Flvcr1
|
UTSW |
1 |
190,740,388 (GRCm39) |
missense |
probably benign |
|
R0122:Flvcr1
|
UTSW |
1 |
190,753,423 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0363:Flvcr1
|
UTSW |
1 |
190,744,451 (GRCm39) |
splice site |
probably benign |
|
R0417:Flvcr1
|
UTSW |
1 |
190,743,416 (GRCm39) |
missense |
probably benign |
0.05 |
R0718:Flvcr1
|
UTSW |
1 |
190,757,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R1061:Flvcr1
|
UTSW |
1 |
190,740,370 (GRCm39) |
missense |
probably benign |
0.01 |
R1815:Flvcr1
|
UTSW |
1 |
190,757,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Flvcr1
|
UTSW |
1 |
190,753,353 (GRCm39) |
missense |
probably benign |
0.01 |
R4590:Flvcr1
|
UTSW |
1 |
190,744,343 (GRCm39) |
missense |
probably benign |
0.05 |
R4766:Flvcr1
|
UTSW |
1 |
190,753,303 (GRCm39) |
missense |
probably benign |
0.00 |
R4889:Flvcr1
|
UTSW |
1 |
190,757,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R4956:Flvcr1
|
UTSW |
1 |
190,758,383 (GRCm39) |
unclassified |
probably benign |
|
R4976:Flvcr1
|
UTSW |
1 |
190,757,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R5434:Flvcr1
|
UTSW |
1 |
190,758,206 (GRCm39) |
missense |
probably benign |
0.07 |
R5508:Flvcr1
|
UTSW |
1 |
190,757,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Flvcr1
|
UTSW |
1 |
190,741,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6698:Flvcr1
|
UTSW |
1 |
190,757,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6927:Flvcr1
|
UTSW |
1 |
190,757,861 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7544:Flvcr1
|
UTSW |
1 |
190,758,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R7654:Flvcr1
|
UTSW |
1 |
190,743,802 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7853:Flvcr1
|
UTSW |
1 |
190,757,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R8185:Flvcr1
|
UTSW |
1 |
190,747,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R8387:Flvcr1
|
UTSW |
1 |
190,743,731 (GRCm39) |
critical splice donor site |
probably null |
|
R8995:Flvcr1
|
UTSW |
1 |
190,743,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R9092:Flvcr1
|
UTSW |
1 |
190,740,364 (GRCm39) |
missense |
|
|
R9202:Flvcr1
|
UTSW |
1 |
190,744,351 (GRCm39) |
missense |
probably benign |
0.04 |
R9448:Flvcr1
|
UTSW |
1 |
190,744,406 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0064:Flvcr1
|
UTSW |
1 |
190,757,644 (GRCm39) |
missense |
probably benign |
0.08 |
|