Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4galt |
G |
A |
15: 83,112,694 (GRCm39) |
R30W |
probably damaging |
Het |
Adam7 |
T |
C |
14: 68,748,305 (GRCm39) |
|
probably null |
Het |
Agl |
A |
T |
3: 116,552,455 (GRCm39) |
L1158Q |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,114,569 (GRCm39) |
S66P |
probably damaging |
Het |
Akr1c20 |
T |
A |
13: 4,537,207 (GRCm39) |
D316V |
probably benign |
Het |
App |
C |
A |
16: 84,853,302 (GRCm39) |
E259* |
probably null |
Het |
Arhgef4 |
A |
G |
1: 34,784,529 (GRCm39) |
|
probably null |
Het |
Armc9 |
G |
A |
1: 86,121,984 (GRCm39) |
|
probably null |
Het |
Ass1 |
A |
T |
2: 31,404,831 (GRCm39) |
N371Y |
probably damaging |
Het |
Btaf1 |
C |
T |
19: 36,964,053 (GRCm39) |
P875S |
probably damaging |
Het |
Cc2d1b |
T |
A |
4: 108,483,013 (GRCm39) |
|
probably null |
Het |
Ccar1 |
C |
T |
10: 62,616,236 (GRCm39) |
V165I |
possibly damaging |
Het |
Ccdc106 |
A |
T |
7: 5,063,244 (GRCm39) |
I250F |
probably damaging |
Het |
Ccny |
T |
C |
18: 9,332,917 (GRCm39) |
I205V |
probably benign |
Het |
Cfap52 |
T |
A |
11: 67,844,914 (GRCm39) |
I52L |
probably benign |
Het |
Chd8 |
T |
A |
14: 52,442,283 (GRCm39) |
T2096S |
possibly damaging |
Het |
Clstn3 |
G |
A |
6: 124,428,372 (GRCm39) |
T423I |
probably damaging |
Het |
Col13a1 |
T |
C |
10: 61,703,262 (GRCm39) |
D440G |
possibly damaging |
Het |
Dclk3 |
G |
A |
9: 111,298,231 (GRCm39) |
V592M |
probably damaging |
Het |
Ddx31 |
A |
T |
2: 28,747,144 (GRCm39) |
I208F |
probably damaging |
Het |
Dlat |
A |
T |
9: 50,556,419 (GRCm39) |
|
probably null |
Het |
Eml4 |
T |
C |
17: 83,753,487 (GRCm39) |
|
probably null |
Het |
Enpp2 |
T |
A |
15: 54,710,633 (GRCm39) |
|
probably benign |
Het |
Fryl |
T |
C |
5: 73,244,315 (GRCm39) |
S38G |
possibly damaging |
Het |
Gcnt1 |
G |
A |
19: 17,307,680 (GRCm39) |
T15I |
probably benign |
Het |
Gm21834 |
T |
C |
17: 58,049,121 (GRCm39) |
T32A |
possibly damaging |
Het |
Golga2 |
A |
G |
2: 32,192,945 (GRCm39) |
D394G |
probably damaging |
Het |
Gtf3c4 |
G |
T |
2: 28,730,181 (GRCm39) |
|
probably null |
Het |
Igkv4-69 |
A |
G |
6: 69,261,253 (GRCm39) |
|
probably benign |
Het |
Inpp5j |
T |
C |
11: 3,451,150 (GRCm39) |
R500G |
possibly damaging |
Het |
Kif5b |
A |
T |
18: 6,226,980 (GRCm39) |
|
probably benign |
Het |
Klhl36 |
A |
G |
8: 120,603,290 (GRCm39) |
E515G |
probably damaging |
Het |
Lifr |
C |
T |
15: 7,186,672 (GRCm39) |
R59* |
probably null |
Het |
Lrif1 |
A |
T |
3: 106,641,714 (GRCm39) |
Q10L |
possibly damaging |
Het |
Lrp8 |
A |
G |
4: 107,726,295 (GRCm39) |
E908G |
probably damaging |
Het |
Lrrc23 |
A |
T |
6: 124,747,667 (GRCm39) |
D307E |
probably benign |
Het |
Mpv17l |
T |
C |
16: 13,762,583 (GRCm39) |
F27L |
probably damaging |
Het |
Mta3 |
C |
T |
17: 84,074,016 (GRCm39) |
A76V |
probably damaging |
Het |
Muc5ac |
T |
A |
7: 141,345,771 (GRCm39) |
Y202* |
probably null |
Het |
Naprt |
A |
G |
15: 75,762,918 (GRCm39) |
|
probably benign |
Het |
Npr2 |
T |
A |
4: 43,650,315 (GRCm39) |
V960D |
probably damaging |
Het |
Oca2 |
A |
T |
7: 56,073,100 (GRCm39) |
Y765F |
probably benign |
Het |
Or2d2 |
A |
T |
7: 106,727,939 (GRCm39) |
H220Q |
probably benign |
Het |
Plxna2 |
T |
A |
1: 194,326,712 (GRCm39) |
Y215* |
probably null |
Het |
Prdm16 |
G |
A |
4: 154,561,084 (GRCm39) |
|
probably benign |
Het |
Ptn |
A |
G |
6: 36,721,432 (GRCm39) |
S3P |
probably benign |
Het |
Pus10 |
T |
C |
11: 23,623,331 (GRCm39) |
|
probably benign |
Het |
Rad21 |
A |
T |
15: 51,831,754 (GRCm39) |
D442E |
probably benign |
Het |
Rmdn2 |
A |
G |
17: 79,975,384 (GRCm39) |
H291R |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,415,863 (GRCm39) |
S1750P |
probably damaging |
Het |
Samd4b |
A |
T |
7: 28,107,585 (GRCm39) |
I228N |
probably benign |
Het |
Sdr9c7 |
G |
T |
10: 127,734,822 (GRCm39) |
|
probably benign |
Het |
Slc13a2 |
T |
C |
11: 78,294,001 (GRCm39) |
N254D |
probably benign |
Het |
Slc16a8 |
T |
A |
15: 79,136,807 (GRCm39) |
I132F |
probably damaging |
Het |
Slc18b1 |
T |
A |
10: 23,694,976 (GRCm39) |
Y274N |
probably benign |
Het |
Slc45a2 |
A |
T |
15: 11,000,903 (GRCm39) |
M1L |
probably benign |
Het |
Smc1b |
A |
G |
15: 84,996,874 (GRCm39) |
|
probably benign |
Het |
Stab2 |
T |
C |
10: 86,785,792 (GRCm39) |
S617G |
probably benign |
Het |
Stk10 |
A |
G |
11: 32,554,190 (GRCm39) |
M626V |
probably damaging |
Het |
Synpo2l |
T |
G |
14: 20,711,466 (GRCm39) |
I385L |
possibly damaging |
Het |
Tmprss11d |
T |
C |
5: 86,486,671 (GRCm39) |
Y73C |
probably damaging |
Het |
Ttc21b |
A |
G |
2: 66,066,726 (GRCm39) |
V309A |
probably benign |
Het |
Tubgcp6 |
A |
G |
15: 88,987,268 (GRCm39) |
I1235T |
probably benign |
Het |
Usp8 |
A |
G |
2: 126,567,310 (GRCm39) |
I110V |
probably benign |
Het |
Vps13c |
G |
A |
9: 67,880,143 (GRCm39) |
G3442S |
probably damaging |
Het |
Wdr59 |
GGGTGGTG |
GGGTG |
8: 112,207,172 (GRCm39) |
|
probably benign |
Het |
Zfp207 |
T |
A |
11: 80,286,333 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp748 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02366:Zfp748
|
APN |
13 |
67,693,546 (GRCm39) |
splice site |
probably benign |
|
R0790:Zfp748
|
UTSW |
13 |
67,693,481 (GRCm39) |
missense |
probably benign |
0.03 |
R1760:Zfp748
|
UTSW |
13 |
67,693,540 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2520:Zfp748
|
UTSW |
13 |
67,694,781 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3711:Zfp748
|
UTSW |
13 |
67,688,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R4157:Zfp748
|
UTSW |
13 |
67,690,225 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4288:Zfp748
|
UTSW |
13 |
67,689,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R4289:Zfp748
|
UTSW |
13 |
67,689,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R5091:Zfp748
|
UTSW |
13 |
67,689,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5441:Zfp748
|
UTSW |
13 |
67,688,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R5686:Zfp748
|
UTSW |
13 |
67,690,647 (GRCm39) |
nonsense |
probably null |
|
R5907:Zfp748
|
UTSW |
13 |
67,689,292 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6210:Zfp748
|
UTSW |
13 |
67,688,923 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6268:Zfp748
|
UTSW |
13 |
67,690,705 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6639:Zfp748
|
UTSW |
13 |
67,691,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R6810:Zfp748
|
UTSW |
13 |
67,689,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R7148:Zfp748
|
UTSW |
13 |
67,690,358 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7464:Zfp748
|
UTSW |
13 |
67,690,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Zfp748
|
UTSW |
13 |
67,690,638 (GRCm39) |
missense |
probably benign |
0.20 |
R7644:Zfp748
|
UTSW |
13 |
67,689,568 (GRCm39) |
missense |
probably damaging |
0.99 |
R7799:Zfp748
|
UTSW |
13 |
67,689,608 (GRCm39) |
missense |
probably benign |
0.02 |
R8872:Zfp748
|
UTSW |
13 |
67,689,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R9140:Zfp748
|
UTSW |
13 |
67,689,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Zfp748
|
UTSW |
13 |
67,693,511 (GRCm39) |
missense |
probably benign |
0.33 |
R9649:Zfp748
|
UTSW |
13 |
67,690,647 (GRCm39) |
nonsense |
probably null |
|
R9687:Zfp748
|
UTSW |
13 |
67,690,471 (GRCm39) |
missense |
probably benign |
0.00 |
R9749:Zfp748
|
UTSW |
13 |
67,690,573 (GRCm39) |
missense |
probably benign |
0.00 |
|