Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
G |
6: 142,547,500 (GRCm39) |
|
probably null |
Het |
Ahnak |
T |
A |
19: 8,989,420 (GRCm39) |
V3568E |
probably damaging |
Het |
Alpi |
T |
C |
1: 87,027,487 (GRCm39) |
E293G |
possibly damaging |
Het |
Apoa4 |
A |
G |
9: 46,153,822 (GRCm39) |
D141G |
probably benign |
Het |
Atg9a |
T |
C |
1: 75,161,143 (GRCm39) |
Y701C |
probably damaging |
Het |
Baz2b |
C |
T |
2: 59,762,510 (GRCm39) |
R922Q |
probably damaging |
Het |
Bmal2 |
T |
G |
6: 146,731,216 (GRCm39) |
V507G |
probably benign |
Het |
Bpnt1 |
G |
A |
1: 185,073,413 (GRCm39) |
|
probably benign |
Het |
Brms1 |
T |
A |
19: 5,096,727 (GRCm39) |
C136* |
probably null |
Het |
Ccdc180 |
T |
A |
4: 45,890,900 (GRCm39) |
V24E |
probably benign |
Het |
Cdh17 |
A |
G |
4: 11,785,186 (GRCm39) |
Y326C |
possibly damaging |
Het |
Cgn |
A |
T |
3: 94,669,899 (GRCm39) |
D1080E |
possibly damaging |
Het |
Clec4f |
C |
T |
6: 83,629,911 (GRCm39) |
V216M |
probably benign |
Het |
Cpd |
C |
G |
11: 76,681,664 (GRCm39) |
G1160R |
probably damaging |
Het |
Ddb2 |
G |
T |
2: 91,065,165 (GRCm39) |
Q87K |
probably benign |
Het |
Defb41 |
A |
G |
1: 18,321,471 (GRCm39) |
Y48H |
probably damaging |
Het |
Dido1 |
T |
C |
2: 180,303,267 (GRCm39) |
N1546D |
probably benign |
Het |
Dll1 |
A |
T |
17: 15,589,216 (GRCm39) |
H486Q |
probably damaging |
Het |
Dmac1 |
A |
G |
4: 75,196,337 (GRCm39) |
V51A |
possibly damaging |
Het |
Dnajb11 |
C |
T |
16: 22,681,369 (GRCm39) |
A49V |
probably damaging |
Het |
Dnajc14 |
G |
A |
10: 128,643,448 (GRCm39) |
D457N |
probably damaging |
Het |
Eif3a |
C |
A |
19: 60,755,264 (GRCm39) |
D973Y |
unknown |
Het |
Entpd3 |
T |
A |
9: 120,386,608 (GRCm39) |
N196K |
probably damaging |
Het |
Fam53a |
C |
A |
5: 33,765,076 (GRCm39) |
G210V |
probably damaging |
Het |
Farsb |
T |
A |
1: 78,439,011 (GRCm39) |
K395* |
probably null |
Het |
Fem1b |
A |
G |
9: 62,704,082 (GRCm39) |
S393P |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,806,952 (GRCm39) |
D1090E |
probably damaging |
Het |
Fsip2 |
A |
C |
2: 82,817,299 (GRCm39) |
N4344T |
possibly damaging |
Het |
Gata3 |
G |
A |
2: 9,863,258 (GRCm39) |
P419S |
probably damaging |
Het |
Gm7247 |
T |
A |
14: 51,807,057 (GRCm39) |
|
probably benign |
Het |
Gphn |
A |
G |
12: 78,684,277 (GRCm39) |
S558G |
probably damaging |
Het |
Gpr142 |
C |
A |
11: 114,689,755 (GRCm39) |
H2Q |
probably benign |
Het |
Grhpr |
T |
C |
4: 44,988,915 (GRCm39) |
|
probably benign |
Het |
Grik3 |
C |
A |
4: 125,517,368 (GRCm39) |
N70K |
probably damaging |
Het |
Gsap |
T |
A |
5: 21,455,933 (GRCm39) |
|
probably benign |
Het |
Iars1 |
T |
A |
13: 49,846,611 (GRCm39) |
C237S |
probably damaging |
Het |
Itprid1 |
T |
C |
6: 55,849,457 (GRCm39) |
|
probably benign |
Het |
Kank2 |
G |
A |
9: 21,685,970 (GRCm39) |
R635* |
probably null |
Het |
Kcnj16 |
G |
T |
11: 110,915,549 (GRCm39) |
W70C |
probably damaging |
Het |
Kpna6 |
T |
C |
4: 129,551,251 (GRCm39) |
M85V |
probably benign |
Het |
Kri1 |
G |
A |
9: 21,186,661 (GRCm39) |
S447L |
probably damaging |
Het |
L2hgdh |
G |
A |
12: 69,768,105 (GRCm39) |
P131L |
possibly damaging |
Het |
Lrp1b |
A |
G |
2: 40,632,829 (GRCm39) |
V3528A |
probably benign |
Het |
Lrrc46 |
A |
T |
11: 96,929,605 (GRCm39) |
L77Q |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 36,159,925 (GRCm39) |
T678A |
probably benign |
Het |
Mrpl44 |
T |
C |
1: 79,757,212 (GRCm39) |
L219S |
probably damaging |
Het |
Myo7a |
T |
C |
7: 97,714,905 (GRCm39) |
D112G |
probably damaging |
Het |
Ncoa3 |
A |
G |
2: 165,897,098 (GRCm39) |
T630A |
possibly damaging |
Het |
Nsl1 |
T |
C |
1: 190,814,381 (GRCm39) |
L194P |
probably damaging |
Het |
Or4k39 |
G |
A |
2: 111,239,140 (GRCm39) |
G127S |
probably benign |
Het |
Or5ac23 |
T |
C |
16: 59,149,428 (GRCm39) |
Y148C |
possibly damaging |
Het |
Or8u10 |
T |
C |
2: 85,915,705 (GRCm39) |
K139E |
probably benign |
Het |
Pde4d |
A |
G |
13: 109,876,955 (GRCm39) |
S159G |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,142,978 (GRCm39) |
R845G |
probably null |
Het |
Pld1 |
A |
G |
3: 28,150,033 (GRCm39) |
|
probably benign |
Het |
Pramel25 |
T |
A |
4: 143,521,572 (GRCm39) |
L396H |
probably damaging |
Het |
Psd |
T |
A |
19: 46,311,781 (GRCm39) |
I300F |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 22,986,195 (GRCm39) |
W332R |
probably damaging |
Het |
Rab3d |
A |
T |
9: 21,827,222 (GRCm39) |
S3T |
possibly damaging |
Het |
Rnf212 |
T |
A |
5: 108,893,530 (GRCm39) |
M70L |
possibly damaging |
Het |
Scd3 |
A |
G |
19: 44,204,076 (GRCm39) |
Y88C |
probably damaging |
Het |
Sema4f |
A |
G |
6: 82,896,674 (GRCm39) |
|
probably benign |
Het |
Sez6 |
C |
A |
11: 77,844,699 (GRCm39) |
T7K |
possibly damaging |
Het |
Skint2 |
T |
C |
4: 112,502,660 (GRCm39) |
I290T |
probably benign |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc35e1 |
T |
C |
8: 73,246,415 (GRCm39) |
|
probably benign |
Het |
Slc4a4 |
A |
C |
5: 89,304,195 (GRCm39) |
H502P |
possibly damaging |
Het |
Slc5a3 |
T |
A |
16: 91,874,522 (GRCm39) |
I193N |
probably damaging |
Het |
Slc5a4a |
A |
G |
10: 76,014,031 (GRCm39) |
I413V |
probably null |
Het |
Snip1 |
T |
A |
4: 124,966,633 (GRCm39) |
Y354* |
probably null |
Het |
Spata31d1c |
A |
G |
13: 65,180,876 (GRCm39) |
|
probably benign |
Het |
Speer2 |
G |
A |
16: 69,655,640 (GRCm39) |
T62M |
probably damaging |
Het |
Tmco5 |
A |
G |
2: 116,717,768 (GRCm39) |
Y200C |
probably damaging |
Het |
Tmem87b |
T |
A |
2: 128,673,361 (GRCm39) |
|
probably benign |
Het |
Trim43c |
A |
T |
9: 88,729,568 (GRCm39) |
K336N |
probably damaging |
Het |
Trim60 |
T |
C |
8: 65,453,973 (GRCm39) |
E92G |
probably benign |
Het |
Ttc21a |
C |
A |
9: 119,773,006 (GRCm39) |
Q228K |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,626,804 (GRCm39) |
D13067E |
possibly damaging |
Het |
Ufl1 |
A |
T |
4: 25,269,087 (GRCm39) |
I168N |
probably damaging |
Het |
Vmn1r167 |
T |
G |
7: 23,204,334 (GRCm39) |
R227S |
possibly damaging |
Het |
Vmn2r25 |
T |
A |
6: 123,829,984 (GRCm39) |
I56L |
probably benign |
Het |
Zfp385c |
G |
A |
11: 100,520,782 (GRCm39) |
P293S |
probably benign |
Het |
Zfp473 |
T |
A |
7: 44,383,899 (GRCm39) |
S144C |
probably damaging |
Het |
|
Other mutations in Csf2ra |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01304:Csf2ra
|
APN |
19 |
61,215,271 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01465:Csf2ra
|
APN |
19 |
61,214,436 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01693:Csf2ra
|
APN |
19 |
61,214,434 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02474:Csf2ra
|
APN |
19 |
61,214,975 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02950:Csf2ra
|
APN |
19 |
61,215,607 (GRCm39) |
missense |
probably benign |
0.01 |
R0201:Csf2ra
|
UTSW |
19 |
61,214,006 (GRCm39) |
missense |
probably benign |
0.14 |
R0452:Csf2ra
|
UTSW |
19 |
61,215,333 (GRCm39) |
missense |
probably benign |
0.02 |
R1735:Csf2ra
|
UTSW |
19 |
61,214,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R2016:Csf2ra
|
UTSW |
19 |
61,215,331 (GRCm39) |
missense |
probably benign |
0.01 |
R2157:Csf2ra
|
UTSW |
19 |
61,215,509 (GRCm39) |
missense |
probably benign |
0.05 |
R3149:Csf2ra
|
UTSW |
19 |
61,215,758 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3150:Csf2ra
|
UTSW |
19 |
61,215,758 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4747:Csf2ra
|
UTSW |
19 |
61,214,491 (GRCm39) |
nonsense |
probably null |
|
R4825:Csf2ra
|
UTSW |
19 |
61,214,990 (GRCm39) |
missense |
probably benign |
0.10 |
R5580:Csf2ra
|
UTSW |
19 |
61,214,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R5831:Csf2ra
|
UTSW |
19 |
61,213,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:Csf2ra
|
UTSW |
19 |
61,215,766 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7105:Csf2ra
|
UTSW |
19 |
61,213,458 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7123:Csf2ra
|
UTSW |
19 |
61,215,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R7419:Csf2ra
|
UTSW |
19 |
61,215,491 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7721:Csf2ra
|
UTSW |
19 |
61,215,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8918:Csf2ra
|
UTSW |
19 |
61,214,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R8972:Csf2ra
|
UTSW |
19 |
61,213,597 (GRCm39) |
missense |
probably null |
0.09 |
R9320:Csf2ra
|
UTSW |
19 |
61,215,280 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9686:Csf2ra
|
UTSW |
19 |
61,213,629 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Csf2ra
|
UTSW |
19 |
61,213,591 (GRCm39) |
missense |
probably benign |
0.03 |
|