Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
T |
C |
6: 83,139,568 (GRCm39) |
S498P |
probably damaging |
Het |
3100002H09Rik |
A |
G |
4: 124,504,487 (GRCm39) |
W22R |
probably damaging |
Het |
AA986860 |
A |
G |
1: 130,670,831 (GRCm39) |
E351G |
probably damaging |
Het |
Acsl5 |
T |
C |
19: 55,268,924 (GRCm39) |
V195A |
probably benign |
Het |
Actmap |
A |
G |
7: 26,902,105 (GRCm39) |
H244R |
probably damaging |
Het |
Adamts10 |
A |
G |
17: 33,756,293 (GRCm39) |
D312G |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,452,466 (GRCm39) |
M211V |
probably damaging |
Het |
Ankfy1 |
C |
T |
11: 72,646,693 (GRCm39) |
R859* |
probably null |
Het |
Atp8b1 |
T |
A |
18: 64,683,503 (GRCm39) |
I742L |
probably benign |
Het |
B3galnt2 |
T |
A |
13: 14,145,354 (GRCm39) |
V89E |
probably damaging |
Het |
Brinp3 |
A |
C |
1: 146,777,628 (GRCm39) |
T692P |
probably damaging |
Het |
C9 |
T |
A |
15: 6,516,243 (GRCm39) |
F349I |
probably damaging |
Het |
Cacna1a |
T |
A |
8: 85,360,062 (GRCm39) |
M1976K |
probably benign |
Het |
Castor2 |
T |
G |
5: 134,154,726 (GRCm39) |
S43R |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,927,975 (GRCm39) |
V1170A |
possibly damaging |
Het |
Celsr1 |
A |
G |
15: 85,815,477 (GRCm39) |
V1846A |
probably benign |
Het |
Ces1f |
A |
T |
8: 93,998,517 (GRCm39) |
Y160N |
possibly damaging |
Het |
Cfap45 |
A |
G |
1: 172,368,139 (GRCm39) |
E377G |
probably damaging |
Het |
Clca3a1 |
T |
A |
3: 144,460,932 (GRCm39) |
M240L |
probably benign |
Het |
Clnk |
G |
A |
5: 38,952,309 (GRCm39) |
T10M |
probably damaging |
Het |
Cntrl |
T |
A |
2: 35,045,291 (GRCm39) |
I781K |
possibly damaging |
Het |
Col11a2 |
G |
A |
17: 34,274,228 (GRCm39) |
G375S |
probably damaging |
Het |
Col6a5 |
T |
A |
9: 105,817,193 (GRCm39) |
I373F |
unknown |
Het |
Dmxl1 |
C |
T |
18: 49,985,434 (GRCm39) |
A227V |
probably benign |
Het |
Dok5 |
A |
G |
2: 170,574,052 (GRCm39) |
N4D |
probably benign |
Het |
Dpysl3 |
A |
T |
18: 43,496,622 (GRCm39) |
V138D |
probably damaging |
Het |
Efs |
A |
T |
14: 55,157,172 (GRCm39) |
Y380N |
probably damaging |
Het |
Eme2 |
G |
A |
17: 25,111,892 (GRCm39) |
S263F |
probably damaging |
Het |
Farp2 |
A |
G |
1: 93,546,275 (GRCm39) |
Q855R |
possibly damaging |
Het |
Gadl1 |
C |
T |
9: 115,773,297 (GRCm39) |
A113V |
probably damaging |
Het |
Gda |
T |
A |
19: 21,389,903 (GRCm39) |
E219D |
probably benign |
Het |
Gli1 |
A |
T |
10: 127,168,446 (GRCm39) |
M469K |
probably damaging |
Het |
Gm4847 |
A |
T |
1: 166,469,219 (GRCm39) |
S148R |
probably damaging |
Het |
Golga2 |
T |
C |
2: 32,192,216 (GRCm39) |
V325A |
probably benign |
Het |
Hpf1 |
A |
G |
8: 61,349,783 (GRCm39) |
D137G |
probably damaging |
Het |
Htr2a |
C |
G |
14: 74,943,293 (GRCm39) |
S291* |
probably null |
Het |
Itga5 |
G |
A |
15: 103,265,209 (GRCm39) |
Q233* |
probably null |
Het |
Jazf1 |
C |
A |
6: 52,789,168 (GRCm39) |
R102L |
probably damaging |
Het |
Kif6 |
T |
G |
17: 50,021,141 (GRCm39) |
L322R |
probably damaging |
Het |
Ktn1 |
A |
C |
14: 47,904,873 (GRCm39) |
K217T |
probably damaging |
Het |
Lig4 |
A |
T |
8: 10,023,012 (GRCm39) |
V256E |
possibly damaging |
Het |
Lrp1 |
G |
T |
10: 127,403,233 (GRCm39) |
D2113E |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,411,155 (GRCm39) |
D1399E |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,979,443 (GRCm39) |
E717G |
probably damaging |
Het |
Mndal |
G |
T |
1: 173,699,032 (GRCm39) |
P155H |
possibly damaging |
Het |
Mycbpap |
A |
G |
11: 94,402,449 (GRCm39) |
|
probably null |
Het |
Nedd1 |
T |
C |
10: 92,555,476 (GRCm39) |
E3G |
probably damaging |
Het |
Nlgn1 |
A |
T |
3: 25,490,073 (GRCm39) |
N551K |
probably damaging |
Het |
Nup210 |
G |
A |
6: 91,046,148 (GRCm39) |
P595L |
possibly damaging |
Het |
Or2ag15 |
A |
G |
7: 106,340,212 (GRCm39) |
C310R |
probably benign |
Het |
Or2g25 |
A |
T |
17: 37,970,661 (GRCm39) |
C188S |
probably damaging |
Het |
Or4k52 |
A |
T |
2: 111,610,693 (GRCm39) |
|
probably null |
Het |
Or5ac17 |
T |
G |
16: 59,036,347 (GRCm39) |
T210P |
probably damaging |
Het |
Or5p56 |
A |
G |
7: 107,589,740 (GRCm39) |
H56R |
probably benign |
Het |
Pank3 |
G |
A |
11: 35,672,508 (GRCm39) |
V304M |
probably benign |
Het |
Phf3 |
G |
A |
1: 30,844,729 (GRCm39) |
T1410I |
probably benign |
Het |
Ppm1k |
A |
G |
6: 57,502,142 (GRCm39) |
I7T |
possibly damaging |
Het |
Ppp1r12c |
T |
C |
7: 4,500,424 (GRCm39) |
D73G |
probably damaging |
Het |
Prelid2 |
T |
G |
18: 42,014,332 (GRCm39) |
M165L |
probably benign |
Het |
Prkd3 |
A |
C |
17: 79,260,125 (GRCm39) |
L826R |
probably damaging |
Het |
Ptchd4 |
A |
T |
17: 42,814,433 (GRCm39) |
N778I |
probably damaging |
Het |
Ptprm |
T |
C |
17: 67,000,866 (GRCm39) |
D1063G |
possibly damaging |
Het |
Rab27a |
C |
A |
9: 72,982,764 (GRCm39) |
T23N |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 92,044,205 (GRCm39) |
F949L |
probably benign |
Het |
Rbm33 |
A |
G |
5: 28,542,002 (GRCm39) |
N68D |
probably damaging |
Het |
Rgl1 |
A |
T |
1: 152,462,284 (GRCm39) |
L109Q |
probably damaging |
Het |
Rnf20 |
A |
G |
4: 49,638,197 (GRCm39) |
N103S |
possibly damaging |
Het |
Sbno1 |
G |
A |
5: 124,530,675 (GRCm39) |
L875F |
probably damaging |
Het |
Scube1 |
T |
A |
15: 83,512,277 (GRCm39) |
|
probably null |
Het |
Selenbp1 |
G |
A |
3: 94,844,669 (GRCm39) |
V109M |
probably damaging |
Het |
Serpina3c |
T |
A |
12: 104,117,805 (GRCm39) |
I178F |
probably damaging |
Het |
Shisa8 |
C |
T |
15: 82,092,702 (GRCm39) |
G63D |
probably damaging |
Het |
Snx14 |
T |
C |
9: 88,284,277 (GRCm39) |
R464G |
possibly damaging |
Het |
Snx25 |
A |
T |
8: 46,577,119 (GRCm39) |
M1K |
probably null |
Het |
Sorcs3 |
C |
A |
19: 48,694,448 (GRCm39) |
T574K |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,150,557 (GRCm39) |
E6528G |
probably damaging |
Het |
Syt5 |
T |
C |
7: 4,543,245 (GRCm39) |
E338G |
probably damaging |
Het |
Tbk1 |
T |
C |
10: 121,387,223 (GRCm39) |
K691E |
probably benign |
Het |
Tenm3 |
G |
A |
8: 48,848,611 (GRCm39) |
T11I |
probably damaging |
Het |
Thrb |
A |
G |
14: 18,002,597 (GRCm38) |
H87R |
probably damaging |
Het |
Tlr4 |
T |
A |
4: 66,757,933 (GRCm39) |
M242K |
possibly damaging |
Het |
Tm4sf19 |
T |
C |
16: 32,224,820 (GRCm39) |
M56T |
possibly damaging |
Het |
Tmem212 |
T |
A |
3: 27,940,620 (GRCm39) |
R66* |
probably null |
Het |
Tmem39b |
G |
T |
4: 129,578,275 (GRCm39) |
D315E |
probably benign |
Het |
Tnxb |
T |
C |
17: 34,937,612 (GRCm39) |
F3834L |
probably damaging |
Het |
Trim36 |
A |
T |
18: 46,319,250 (GRCm39) |
L225* |
probably null |
Het |
Trim42 |
A |
T |
9: 97,247,732 (GRCm39) |
H321Q |
probably damaging |
Het |
Trio |
G |
T |
15: 27,732,726 (GRCm39) |
Q3052K |
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,955,698 (GRCm39) |
I1091T |
probably benign |
Het |
Tst |
T |
C |
15: 78,284,143 (GRCm39) |
E228G |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,702,060 (GRCm39) |
|
probably benign |
Het |
Uap1 |
A |
C |
1: 169,978,510 (GRCm39) |
|
probably null |
Het |
Ush2a |
T |
C |
1: 188,530,011 (GRCm39) |
S3267P |
possibly damaging |
Het |
Usp5 |
T |
C |
6: 124,802,129 (GRCm39) |
T38A |
probably benign |
Het |
Uvssa |
A |
T |
5: 33,545,152 (GRCm39) |
Q84L |
probably damaging |
Het |
Vmn1r159 |
T |
G |
7: 22,542,693 (GRCm39) |
H113P |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,824,742 (GRCm39) |
|
probably null |
Het |
Zfp182 |
T |
A |
X: 20,897,799 (GRCm39) |
I166L |
probably benign |
Het |
Zfp811 |
A |
T |
17: 33,016,622 (GRCm39) |
Y472N |
probably damaging |
Het |
|
Other mutations in Fcrl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01568:Fcrl2
|
APN |
3 |
87,163,986 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01959:Fcrl2
|
APN |
3 |
87,166,939 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02409:Fcrl2
|
APN |
3 |
87,160,030 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02677:Fcrl2
|
APN |
3 |
87,166,694 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02957:Fcrl2
|
APN |
3 |
87,169,501 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02974:Fcrl2
|
APN |
3 |
87,164,704 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02992:Fcrl2
|
APN |
3 |
87,166,773 (GRCm39) |
missense |
probably damaging |
0.99 |
BB001:Fcrl2
|
UTSW |
3 |
87,166,840 (GRCm39) |
missense |
probably damaging |
0.99 |
BB011:Fcrl2
|
UTSW |
3 |
87,166,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R0052:Fcrl2
|
UTSW |
3 |
87,164,085 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0052:Fcrl2
|
UTSW |
3 |
87,164,085 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0131:Fcrl2
|
UTSW |
3 |
87,166,266 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1171:Fcrl2
|
UTSW |
3 |
87,164,167 (GRCm39) |
missense |
probably benign |
0.24 |
R1319:Fcrl2
|
UTSW |
3 |
87,169,484 (GRCm39) |
critical splice donor site |
probably null |
|
R1696:Fcrl2
|
UTSW |
3 |
87,166,825 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1742:Fcrl2
|
UTSW |
3 |
87,166,350 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2156:Fcrl2
|
UTSW |
3 |
87,164,648 (GRCm39) |
missense |
probably benign |
0.43 |
R2255:Fcrl2
|
UTSW |
3 |
87,164,655 (GRCm39) |
nonsense |
probably null |
|
R2257:Fcrl2
|
UTSW |
3 |
87,166,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R2434:Fcrl2
|
UTSW |
3 |
87,164,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Fcrl2
|
UTSW |
3 |
87,164,656 (GRCm39) |
missense |
probably damaging |
0.99 |
R3552:Fcrl2
|
UTSW |
3 |
87,166,717 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4866:Fcrl2
|
UTSW |
3 |
87,170,773 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4883:Fcrl2
|
UTSW |
3 |
87,166,922 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5654:Fcrl2
|
UTSW |
3 |
87,164,851 (GRCm39) |
missense |
probably benign |
|
R5771:Fcrl2
|
UTSW |
3 |
87,170,775 (GRCm39) |
missense |
probably damaging |
0.98 |
R5917:Fcrl2
|
UTSW |
3 |
87,164,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R6349:Fcrl2
|
UTSW |
3 |
87,159,803 (GRCm39) |
missense |
probably damaging |
0.99 |
R6562:Fcrl2
|
UTSW |
3 |
87,164,635 (GRCm39) |
missense |
probably benign |
|
R6954:Fcrl2
|
UTSW |
3 |
87,170,983 (GRCm39) |
critical splice donor site |
probably benign |
|
R7059:Fcrl2
|
UTSW |
3 |
87,164,647 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7188:Fcrl2
|
UTSW |
3 |
87,166,830 (GRCm39) |
missense |
probably benign |
0.13 |
R7201:Fcrl2
|
UTSW |
3 |
87,159,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R7369:Fcrl2
|
UTSW |
3 |
87,164,008 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7431:Fcrl2
|
UTSW |
3 |
87,166,233 (GRCm39) |
missense |
probably damaging |
0.99 |
R7610:Fcrl2
|
UTSW |
3 |
87,160,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R7924:Fcrl2
|
UTSW |
3 |
87,166,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R8018:Fcrl2
|
UTSW |
3 |
87,166,933 (GRCm39) |
nonsense |
probably null |
|
R8280:Fcrl2
|
UTSW |
3 |
87,166,364 (GRCm39) |
nonsense |
probably null |
|
R8981:Fcrl2
|
UTSW |
3 |
87,164,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R9368:Fcrl2
|
UTSW |
3 |
87,164,906 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9477:Fcrl2
|
UTSW |
3 |
87,159,803 (GRCm39) |
missense |
probably damaging |
0.98 |
R9522:Fcrl2
|
UTSW |
3 |
87,164,101 (GRCm39) |
missense |
possibly damaging |
0.95 |
|