Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
C |
T |
16: 4,678,912 (GRCm39) |
R245* |
probably null |
Het |
4930563I02Rik |
T |
A |
14: 60,333,477 (GRCm39) |
|
probably benign |
Het |
Acss1 |
T |
C |
2: 150,469,212 (GRCm39) |
T435A |
probably damaging |
Het |
Aoc2 |
T |
A |
11: 101,216,897 (GRCm39) |
S327T |
probably damaging |
Het |
Arid5a |
T |
A |
1: 36,357,645 (GRCm39) |
Y252N |
probably damaging |
Het |
AU040320 |
T |
C |
4: 126,733,465 (GRCm39) |
Y662H |
probably damaging |
Het |
B4gat1 |
T |
A |
19: 5,089,735 (GRCm39) |
L244* |
probably null |
Het |
Btbd16 |
A |
T |
7: 130,424,896 (GRCm39) |
T426S |
probably benign |
Het |
Btn1a1 |
C |
T |
13: 23,649,267 (GRCm39) |
|
probably null |
Het |
Cap2 |
T |
C |
13: 46,791,508 (GRCm39) |
|
probably benign |
Het |
Capn8 |
T |
A |
1: 182,429,677 (GRCm39) |
D299E |
probably damaging |
Het |
Cdipt |
G |
A |
7: 126,578,772 (GRCm39) |
V160I |
probably benign |
Het |
Cep164 |
A |
G |
9: 45,679,916 (GRCm39) |
S1267P |
possibly damaging |
Het |
Cic |
T |
A |
7: 24,986,565 (GRCm39) |
S1299T |
probably damaging |
Het |
Cic |
C |
A |
7: 24,986,566 (GRCm39) |
S1299Y |
probably damaging |
Het |
Col3a1 |
T |
C |
1: 45,369,701 (GRCm39) |
|
probably benign |
Het |
Cyb5r3 |
T |
C |
15: 83,046,137 (GRCm39) |
T60A |
probably benign |
Het |
Dgkb |
T |
G |
12: 38,654,112 (GRCm39) |
S744A |
probably benign |
Het |
Dock2 |
T |
A |
11: 34,647,111 (GRCm39) |
|
probably null |
Het |
Ece1 |
C |
T |
4: 137,675,892 (GRCm39) |
T422M |
probably benign |
Het |
Ece2 |
A |
G |
16: 20,461,067 (GRCm39) |
T442A |
probably benign |
Het |
Elapor2 |
T |
C |
5: 9,490,709 (GRCm39) |
|
probably benign |
Het |
Eml3 |
C |
A |
19: 8,915,842 (GRCm39) |
A644D |
probably damaging |
Het |
Fbp2 |
A |
T |
13: 63,001,862 (GRCm39) |
F118I |
probably damaging |
Het |
Foxp1 |
A |
G |
6: 98,921,684 (GRCm39) |
|
probably benign |
Het |
Gm10801 |
G |
T |
2: 98,494,185 (GRCm39) |
S109I |
probably benign |
Het |
Il17rd |
G |
A |
14: 26,804,690 (GRCm39) |
C88Y |
probably damaging |
Het |
Il17rd |
C |
A |
14: 26,804,691 (GRCm39) |
C88* |
probably null |
Het |
Ino80c |
A |
G |
18: 24,239,681 (GRCm39) |
F160S |
probably damaging |
Het |
Ints8 |
T |
C |
4: 11,252,857 (GRCm39) |
N75S |
probably damaging |
Het |
Irf2bp1 |
C |
T |
7: 18,739,772 (GRCm39) |
R471C |
possibly damaging |
Het |
Irs1 |
T |
A |
1: 82,266,580 (GRCm39) |
E545D |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,661,762 (GRCm39) |
|
probably benign |
Het |
Mast4 |
C |
A |
13: 103,470,723 (GRCm39) |
|
probably benign |
Het |
Mcc |
C |
G |
18: 44,652,583 (GRCm39) |
|
probably benign |
Het |
Nat8f2 |
A |
T |
6: 85,844,815 (GRCm39) |
S182R |
possibly damaging |
Het |
Nrcam |
G |
T |
12: 44,596,811 (GRCm39) |
V343F |
possibly damaging |
Het |
Opn5 |
T |
C |
17: 42,907,517 (GRCm39) |
S120G |
probably damaging |
Het |
Pdk2 |
T |
C |
11: 94,923,306 (GRCm39) |
H106R |
probably benign |
Het |
Pkhd1 |
G |
A |
1: 20,282,174 (GRCm39) |
T2889I |
probably benign |
Het |
Pkhd1l1 |
T |
A |
15: 44,392,633 (GRCm39) |
L1656H |
probably damaging |
Het |
Plxna2 |
A |
T |
1: 194,327,247 (GRCm39) |
T394S |
probably benign |
Het |
Pnpla8 |
T |
A |
12: 44,329,615 (GRCm39) |
C56S |
probably damaging |
Het |
Prdm8 |
G |
T |
5: 98,332,453 (GRCm39) |
R118L |
probably damaging |
Het |
Prkce |
T |
C |
17: 86,789,539 (GRCm39) |
|
probably benign |
Het |
Ptprk |
T |
A |
10: 28,139,763 (GRCm39) |
Y163N |
probably damaging |
Het |
Rbbp8 |
T |
A |
18: 11,867,614 (GRCm39) |
|
probably benign |
Het |
Rnh1 |
A |
T |
7: 140,744,109 (GRCm39) |
|
probably null |
Het |
Rtn4 |
T |
A |
11: 29,655,527 (GRCm39) |
|
probably benign |
Het |
Sephs1 |
A |
G |
2: 4,904,371 (GRCm39) |
T250A |
probably benign |
Het |
Slc2a2 |
T |
C |
3: 28,771,589 (GRCm39) |
M173T |
probably damaging |
Het |
Slc2a8 |
T |
A |
2: 32,870,011 (GRCm39) |
|
probably null |
Het |
Tdpoz1 |
A |
T |
3: 93,578,121 (GRCm39) |
M221K |
probably benign |
Het |
Tgm7 |
G |
T |
2: 120,924,577 (GRCm39) |
H533Q |
probably benign |
Het |
Timm29 |
C |
A |
9: 21,504,304 (GRCm39) |
A17E |
probably benign |
Het |
Tmem131 |
C |
T |
1: 36,858,209 (GRCm39) |
V713I |
probably benign |
Het |
Tmem89 |
A |
G |
9: 108,743,880 (GRCm39) |
N60S |
probably benign |
Het |
Tpx2 |
A |
G |
2: 152,722,043 (GRCm39) |
T212A |
probably damaging |
Het |
Trio |
G |
T |
15: 27,881,523 (GRCm39) |
|
probably benign |
Het |
Tulp2 |
T |
C |
7: 45,170,284 (GRCm39) |
|
probably benign |
Het |
Uggt2 |
A |
G |
14: 119,244,542 (GRCm39) |
|
probably benign |
Het |
Vmn2r5 |
T |
A |
3: 64,411,221 (GRCm39) |
E449V |
probably benign |
Het |
Vwa8 |
A |
G |
14: 79,401,656 (GRCm39) |
|
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,339,427 (GRCm39) |
D556G |
probably damaging |
Het |
Xrn1 |
T |
C |
9: 95,851,588 (GRCm39) |
L202P |
probably damaging |
Het |
Zfp354a |
A |
T |
11: 50,960,398 (GRCm39) |
H203L |
probably damaging |
Het |
Zfp53 |
A |
C |
17: 21,728,367 (GRCm39) |
R133S |
probably benign |
Het |
Zfp787 |
C |
T |
7: 6,135,322 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Bcam |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Bcam
|
APN |
7 |
19,490,724 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01433:Bcam
|
APN |
7 |
19,494,107 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01712:Bcam
|
APN |
7 |
19,492,692 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01943:Bcam
|
APN |
7 |
19,499,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01946:Bcam
|
APN |
7 |
19,494,042 (GRCm39) |
nonsense |
probably null |
|
IGL02281:Bcam
|
APN |
7 |
19,492,616 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02714:Bcam
|
APN |
7 |
19,492,732 (GRCm39) |
splice site |
probably benign |
|
IGL02837:Bcam
|
UTSW |
7 |
19,498,111 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4514001:Bcam
|
UTSW |
7 |
19,497,991 (GRCm39) |
missense |
probably benign |
0.06 |
R0063:Bcam
|
UTSW |
7 |
19,500,773 (GRCm39) |
missense |
probably benign |
0.21 |
R1500:Bcam
|
UTSW |
7 |
19,492,889 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1575:Bcam
|
UTSW |
7 |
19,494,307 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1585:Bcam
|
UTSW |
7 |
19,494,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Bcam
|
UTSW |
7 |
19,499,543 (GRCm39) |
missense |
probably null |
1.00 |
R1813:Bcam
|
UTSW |
7 |
19,500,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Bcam
|
UTSW |
7 |
19,500,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R2016:Bcam
|
UTSW |
7 |
19,494,274 (GRCm39) |
missense |
probably benign |
0.38 |
R2117:Bcam
|
UTSW |
7 |
19,492,352 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3713:Bcam
|
UTSW |
7 |
19,498,118 (GRCm39) |
missense |
probably benign |
0.12 |
R3917:Bcam
|
UTSW |
7 |
19,499,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R4596:Bcam
|
UTSW |
7 |
19,498,082 (GRCm39) |
missense |
probably damaging |
0.97 |
R4866:Bcam
|
UTSW |
7 |
19,499,397 (GRCm39) |
missense |
probably benign |
0.00 |
R4874:Bcam
|
UTSW |
7 |
19,503,247 (GRCm39) |
intron |
probably benign |
|
R5054:Bcam
|
UTSW |
7 |
19,490,785 (GRCm39) |
intron |
probably benign |
|
R5062:Bcam
|
UTSW |
7 |
19,494,026 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6783:Bcam
|
UTSW |
7 |
19,500,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R6853:Bcam
|
UTSW |
7 |
19,494,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R7016:Bcam
|
UTSW |
7 |
19,492,368 (GRCm39) |
nonsense |
probably null |
|
R7174:Bcam
|
UTSW |
7 |
19,499,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R7237:Bcam
|
UTSW |
7 |
19,503,232 (GRCm39) |
splice site |
probably null |
|
R7733:Bcam
|
UTSW |
7 |
19,494,313 (GRCm39) |
missense |
probably benign |
0.00 |
R7938:Bcam
|
UTSW |
7 |
19,490,738 (GRCm39) |
missense |
probably benign |
0.08 |
R8474:Bcam
|
UTSW |
7 |
19,494,325 (GRCm39) |
nonsense |
probably null |
|
R8514:Bcam
|
UTSW |
7 |
19,492,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R8880:Bcam
|
UTSW |
7 |
19,492,671 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Bcam
|
UTSW |
7 |
19,494,032 (GRCm39) |
missense |
probably null |
1.00 |
|