Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
T |
A |
2: 35,279,599 (GRCm39) |
Y34F |
possibly damaging |
Het |
Abcb6 |
A |
T |
1: 75,149,588 (GRCm39) |
S664T |
probably benign |
Het |
Abcc4 |
C |
T |
14: 118,853,804 (GRCm39) |
V443M |
probably damaging |
Het |
Abhd2 |
G |
A |
7: 78,998,095 (GRCm39) |
G209D |
probably damaging |
Het |
Acte1 |
A |
G |
7: 143,437,680 (GRCm39) |
N126S |
possibly damaging |
Het |
Ampd2 |
C |
A |
3: 107,987,432 (GRCm39) |
V134L |
probably benign |
Het |
Apbb2 |
T |
A |
5: 66,520,179 (GRCm39) |
M449L |
probably benign |
Het |
Ccdc81 |
T |
A |
7: 89,526,786 (GRCm39) |
|
probably null |
Het |
Cd209b |
A |
T |
8: 3,976,559 (GRCm39) |
C42* |
probably null |
Het |
Cdhr18 |
G |
A |
14: 13,814,954 (GRCm38) |
Q860* |
probably null |
Het |
Clec18a |
A |
T |
8: 111,808,689 (GRCm39) |
M11K |
probably benign |
Het |
Clock |
A |
T |
5: 76,402,269 (GRCm39) |
S130R |
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,512,465 (GRCm39) |
A2910V |
possibly damaging |
Het |
Col6a4 |
C |
T |
9: 105,952,414 (GRCm39) |
A495T |
probably benign |
Het |
Cyp4f37 |
A |
T |
17: 32,853,952 (GRCm39) |
N467I |
probably damaging |
Het |
Ddo |
G |
A |
10: 40,513,375 (GRCm39) |
V106M |
possibly damaging |
Het |
Dennd5a |
A |
G |
7: 109,500,332 (GRCm39) |
L931P |
probably damaging |
Het |
Dgcr6 |
A |
G |
16: 17,884,598 (GRCm39) |
D82G |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,179,032 (GRCm39) |
S902P |
probably damaging |
Het |
Dnal4 |
T |
G |
15: 79,646,711 (GRCm39) |
I57L |
probably benign |
Het |
Dst |
T |
A |
1: 34,156,592 (GRCm39) |
I174N |
probably damaging |
Het |
Dync2i1 |
T |
C |
12: 116,219,705 (GRCm39) |
E79G |
probably damaging |
Het |
Dync2i2 |
A |
G |
2: 29,922,201 (GRCm39) |
L420P |
probably damaging |
Het |
Eeig2 |
G |
A |
3: 108,934,658 (GRCm39) |
|
probably benign |
Het |
Efhb |
T |
C |
17: 53,756,563 (GRCm39) |
T363A |
probably damaging |
Het |
Ehbp1l1 |
A |
G |
19: 5,767,103 (GRCm39) |
F1245S |
probably damaging |
Het |
Eif4g1 |
A |
G |
16: 20,507,578 (GRCm39) |
D1453G |
probably benign |
Het |
Gm10782 |
T |
G |
13: 56,510,948 (GRCm39) |
F79V |
noncoding transcript |
Het |
Gpaa1 |
C |
G |
15: 76,216,160 (GRCm39) |
R47G |
possibly damaging |
Het |
Hs2st1 |
G |
A |
3: 144,143,365 (GRCm39) |
S226L |
possibly damaging |
Het |
Hydin |
A |
G |
8: 111,334,534 (GRCm39) |
Y4992C |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,191,065 (GRCm39) |
C549* |
probably null |
Het |
Insrr |
G |
A |
3: 87,717,749 (GRCm39) |
G817S |
probably benign |
Het |
Itgb5 |
G |
A |
16: 33,685,923 (GRCm39) |
V88I |
probably benign |
Het |
Krt78 |
A |
G |
15: 101,854,922 (GRCm39) |
V963A |
probably benign |
Het |
Lars1 |
T |
C |
18: 42,376,093 (GRCm39) |
Y239C |
possibly damaging |
Het |
Map2k5 |
A |
G |
9: 63,246,361 (GRCm39) |
|
probably null |
Het |
Mfn2 |
A |
T |
4: 147,974,693 (GRCm39) |
W118R |
probably benign |
Het |
Mga |
T |
A |
2: 119,791,411 (GRCm39) |
I2550N |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,722,111 (GRCm39) |
I401V |
possibly damaging |
Het |
Mrps18c |
A |
G |
5: 100,952,264 (GRCm39) |
Y141C |
probably damaging |
Het |
Myo1e |
A |
T |
9: 70,254,045 (GRCm39) |
I565L |
possibly damaging |
Het |
Nfatc4 |
G |
A |
14: 56,063,848 (GRCm39) |
E112K |
probably damaging |
Het |
Nubp1 |
A |
G |
16: 10,239,486 (GRCm39) |
M255V |
probably benign |
Het |
Or13n4 |
A |
C |
7: 106,423,620 (GRCm39) |
S38A |
probably benign |
Het |
Or52a33 |
A |
G |
7: 103,288,658 (GRCm39) |
S230P |
probably damaging |
Het |
Or8g33 |
C |
T |
9: 39,337,966 (GRCm39) |
V134I |
probably benign |
Het |
Pask |
A |
T |
1: 93,240,573 (GRCm39) |
C1264* |
probably null |
Het |
Pcgf2 |
T |
C |
11: 97,582,569 (GRCm39) |
T173A |
probably benign |
Het |
Plcg1 |
T |
C |
2: 160,595,853 (GRCm39) |
I574T |
probably benign |
Het |
Plin4 |
T |
C |
17: 56,411,437 (GRCm39) |
T865A |
probably damaging |
Het |
Pnpt1 |
T |
C |
11: 29,103,277 (GRCm39) |
V514A |
probably benign |
Het |
Ppp1r3a |
T |
A |
6: 14,719,700 (GRCm39) |
I405F |
probably benign |
Het |
Qpctl |
A |
G |
7: 18,882,398 (GRCm39) |
V86A |
probably benign |
Het |
Rab3gap1 |
G |
T |
1: 127,837,655 (GRCm39) |
W239L |
possibly damaging |
Het |
Ralgapa2 |
T |
A |
2: 146,246,786 (GRCm39) |
T939S |
possibly damaging |
Het |
Rapgef2 |
G |
T |
3: 78,990,509 (GRCm39) |
T923N |
possibly damaging |
Het |
Rit2 |
T |
A |
18: 31,286,898 (GRCm39) |
I96F |
probably damaging |
Het |
Rnase13 |
A |
T |
14: 52,159,893 (GRCm39) |
I82N |
probably damaging |
Het |
Rp1 |
C |
A |
1: 4,417,312 (GRCm39) |
V1267L |
probably benign |
Het |
Serpinb9b |
G |
A |
13: 33,223,554 (GRCm39) |
E249K |
probably damaging |
Het |
Serpinb9c |
G |
T |
13: 33,334,094 (GRCm39) |
T344K |
possibly damaging |
Het |
Serpinh1 |
T |
C |
7: 98,998,151 (GRCm39) |
I160V |
possibly damaging |
Het |
Sipa1 |
A |
G |
19: 5,704,964 (GRCm39) |
S544P |
probably damaging |
Het |
Slc17a5 |
A |
T |
9: 78,478,311 (GRCm39) |
Y231* |
probably null |
Het |
Srcap |
T |
C |
7: 127,148,529 (GRCm39) |
V1959A |
probably damaging |
Het |
Srrm4 |
G |
A |
5: 116,729,626 (GRCm39) |
|
probably benign |
Het |
Stat1 |
T |
C |
1: 52,190,404 (GRCm39) |
I553T |
possibly damaging |
Het |
Stpg1 |
A |
G |
4: 135,256,903 (GRCm39) |
I231M |
probably benign |
Het |
Szt2 |
G |
GC |
4: 118,232,679 (GRCm39) |
|
probably null |
Het |
Trpv3 |
C |
T |
11: 73,170,747 (GRCm39) |
T209M |
probably damaging |
Het |
Tsc22d2 |
G |
T |
3: 58,324,544 (GRCm39) |
G479C |
unknown |
Het |
Ttc3 |
A |
G |
16: 94,267,838 (GRCm39) |
H1950R |
probably damaging |
Het |
Tusc3 |
A |
G |
8: 39,617,882 (GRCm39) |
*348W |
probably null |
Het |
Utp4 |
A |
T |
8: 107,642,853 (GRCm39) |
T504S |
probably benign |
Het |
Vmn1r15 |
A |
G |
6: 57,235,635 (GRCm39) |
M168V |
probably benign |
Het |
Wdsub1 |
C |
T |
2: 59,704,578 (GRCm39) |
|
probably benign |
Het |
Xrcc5 |
T |
A |
1: 72,358,286 (GRCm39) |
M207K |
possibly damaging |
Het |
Zc3h7a |
A |
T |
16: 10,964,417 (GRCm39) |
|
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,345,750 (GRCm39) |
N1376K |
possibly damaging |
Het |
Zfp558 |
A |
C |
9: 18,368,213 (GRCm39) |
S192A |
probably benign |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
Zfp964 |
A |
G |
8: 70,115,924 (GRCm39) |
T175A |
possibly damaging |
Het |
Zfp988 |
A |
G |
4: 147,416,765 (GRCm39) |
R400G |
probably damaging |
Het |
|
Other mutations in Fbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02199:Fbp1
|
APN |
13 |
63,015,193 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02224:Fbp1
|
APN |
13 |
63,035,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02751:Fbp1
|
APN |
13 |
63,022,957 (GRCm39) |
splice site |
probably null |
|
IGL02887:Fbp1
|
APN |
13 |
63,016,894 (GRCm39) |
missense |
probably benign |
|
fruko
|
UTSW |
13 |
63,023,075 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4362001:Fbp1
|
UTSW |
13 |
63,015,194 (GRCm39) |
missense |
probably damaging |
0.99 |
R0400:Fbp1
|
UTSW |
13 |
63,012,882 (GRCm39) |
missense |
probably benign |
0.04 |
R0656:Fbp1
|
UTSW |
13 |
63,019,099 (GRCm39) |
missense |
probably benign |
0.23 |
R1672:Fbp1
|
UTSW |
13 |
63,015,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R2420:Fbp1
|
UTSW |
13 |
63,019,120 (GRCm39) |
missense |
probably benign |
0.00 |
R2422:Fbp1
|
UTSW |
13 |
63,019,120 (GRCm39) |
missense |
probably benign |
0.00 |
R3859:Fbp1
|
UTSW |
13 |
63,012,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R4474:Fbp1
|
UTSW |
13 |
63,023,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4990:Fbp1
|
UTSW |
13 |
63,012,888 (GRCm39) |
missense |
probably benign |
0.09 |
R4991:Fbp1
|
UTSW |
13 |
63,012,888 (GRCm39) |
missense |
probably benign |
0.09 |
R4992:Fbp1
|
UTSW |
13 |
63,012,888 (GRCm39) |
missense |
probably benign |
0.09 |
R5656:Fbp1
|
UTSW |
13 |
63,023,010 (GRCm39) |
missense |
probably damaging |
0.97 |
R6463:Fbp1
|
UTSW |
13 |
63,012,824 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7381:Fbp1
|
UTSW |
13 |
63,012,867 (GRCm39) |
missense |
probably benign |
0.01 |
R7448:Fbp1
|
UTSW |
13 |
63,020,564 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8318:Fbp1
|
UTSW |
13 |
63,012,825 (GRCm39) |
missense |
probably benign |
0.00 |
R8781:Fbp1
|
UTSW |
13 |
63,016,831 (GRCm39) |
missense |
probably benign |
|
R8962:Fbp1
|
UTSW |
13 |
63,023,067 (GRCm39) |
missense |
probably benign |
0.37 |
R9605:Fbp1
|
UTSW |
13 |
63,019,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|