Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
A |
G |
15: 11,285,987 (GRCm39) |
D732G |
probably benign |
Het |
Agpat4 |
A |
G |
17: 12,370,637 (GRCm39) |
|
probably benign |
Het |
AI182371 |
T |
C |
2: 34,985,829 (GRCm39) |
D140G |
possibly damaging |
Het |
Apol11b |
T |
A |
15: 77,519,133 (GRCm39) |
T316S |
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Bard1 |
T |
C |
1: 71,114,333 (GRCm39) |
E216G |
probably benign |
Het |
Bdp1 |
C |
A |
13: 100,186,376 (GRCm39) |
R1692L |
probably damaging |
Het |
Capn10 |
T |
C |
1: 92,871,141 (GRCm39) |
I101T |
probably damaging |
Het |
Ccdc175 |
C |
T |
12: 72,158,979 (GRCm39) |
M653I |
probably benign |
Het |
Ccdc9b |
C |
A |
2: 118,590,058 (GRCm39) |
R262L |
probably damaging |
Het |
Ccr8 |
G |
A |
9: 119,923,530 (GRCm39) |
C215Y |
probably damaging |
Het |
Cct3 |
T |
A |
3: 88,219,092 (GRCm39) |
L241* |
probably null |
Het |
Cd2ap |
A |
T |
17: 43,163,350 (GRCm39) |
I25N |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,820,990 (GRCm39) |
K583E |
probably benign |
Het |
Cela3a |
A |
G |
4: 137,129,986 (GRCm39) |
S212P |
unknown |
Het |
Cfap44 |
T |
A |
16: 44,236,246 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
A |
T |
3: 144,455,473 (GRCm39) |
L440Q |
probably damaging |
Het |
Crybg2 |
A |
G |
4: 133,816,663 (GRCm39) |
Y1676C |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,445,188 (GRCm39) |
D1501G |
probably benign |
Het |
Eml6 |
C |
A |
11: 29,755,757 (GRCm39) |
L832F |
probably benign |
Het |
Enpp3 |
A |
G |
10: 24,649,825 (GRCm39) |
L867P |
probably damaging |
Het |
Erbb3 |
A |
G |
10: 128,422,107 (GRCm39) |
Y46H |
possibly damaging |
Het |
Fads3 |
T |
C |
19: 10,033,384 (GRCm39) |
I342T |
possibly damaging |
Het |
Flvcr1 |
A |
T |
1: 190,753,303 (GRCm39) |
S290T |
probably benign |
Het |
Fut9 |
A |
G |
4: 25,799,191 (GRCm39) |
|
probably benign |
Het |
Gad2 |
C |
T |
2: 22,512,679 (GRCm39) |
A2V |
probably damaging |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Gm10715 |
T |
G |
9: 3,038,073 (GRCm39) |
|
probably benign |
Het |
Herc1 |
T |
G |
9: 66,349,211 (GRCm39) |
D2023E |
probably benign |
Het |
Hsd3b3 |
A |
G |
3: 98,649,801 (GRCm39) |
L174P |
probably damaging |
Het |
Impg2 |
TACCACCACCACCACCACCACCACCA |
TACCACCACCACCACCACCACCA |
16: 56,078,302 (GRCm39) |
|
probably benign |
Het |
Iqcf3 |
A |
G |
9: 106,438,148 (GRCm39) |
|
probably null |
Het |
Kcna4 |
G |
A |
2: 107,126,888 (GRCm39) |
V541M |
probably damaging |
Het |
Kcnj11 |
T |
C |
7: 45,749,240 (GRCm39) |
T28A |
probably benign |
Het |
Kcnmb2 |
T |
A |
3: 32,236,016 (GRCm39) |
N88K |
probably damaging |
Het |
Kdm2a |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
19: 4,374,535 (GRCm39) |
|
probably benign |
Het |
Krt1c |
T |
C |
15: 101,722,395 (GRCm39) |
E430G |
probably damaging |
Het |
Lins1 |
C |
T |
7: 66,360,389 (GRCm39) |
L384F |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mfge8 |
T |
C |
7: 78,784,273 (GRCm39) |
N389D |
probably damaging |
Het |
Mug1 |
C |
T |
6: 121,861,213 (GRCm39) |
T1278I |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,692,077 (GRCm39) |
M161V |
probably damaging |
Het |
Myl7 |
T |
A |
11: 5,848,171 (GRCm39) |
Y61F |
probably benign |
Het |
Nlrp4d |
A |
T |
7: 10,096,706 (GRCm39) |
|
unknown |
Het |
Nol3 |
A |
G |
8: 106,008,565 (GRCm39) |
|
probably null |
Het |
Nup85 |
T |
A |
11: 115,468,751 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
A |
11: 58,903,568 (GRCm39) |
T7619S |
probably damaging |
Het |
Or2t49 |
T |
A |
11: 58,392,494 (GRCm39) |
N296I |
probably damaging |
Het |
Or4k48 |
T |
C |
2: 111,476,226 (GRCm39) |
M39V |
probably benign |
Het |
Or52a24 |
C |
T |
7: 103,381,457 (GRCm39) |
T108I |
possibly damaging |
Het |
Or7g26 |
G |
A |
9: 19,230,141 (GRCm39) |
V104I |
probably benign |
Het |
Pax5 |
T |
A |
4: 44,679,494 (GRCm39) |
I184F |
probably damaging |
Het |
Pcdha7 |
T |
A |
18: 37,107,560 (GRCm39) |
V195D |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,853,020 (GRCm39) |
|
probably benign |
Het |
Pla2g15 |
G |
T |
8: 106,889,703 (GRCm39) |
G325V |
probably damaging |
Het |
Ppp1r21 |
T |
C |
17: 88,880,043 (GRCm39) |
F487L |
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,157,016 (GRCm39) |
I965V |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,548,275 (GRCm39) |
V74A |
probably damaging |
Het |
Rif1 |
T |
A |
2: 51,988,946 (GRCm39) |
Y780N |
probably damaging |
Het |
Rps25 |
T |
A |
9: 44,320,046 (GRCm39) |
Y23N |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,785,258 (GRCm39) |
D1811G |
probably damaging |
Het |
Scamp5 |
T |
G |
9: 57,359,319 (GRCm39) |
|
probably null |
Het |
Senp1 |
T |
C |
15: 97,943,777 (GRCm39) |
D602G |
probably damaging |
Het |
Sh2b2 |
T |
G |
5: 136,260,811 (GRCm39) |
D135A |
probably damaging |
Het |
Slc26a8 |
G |
A |
17: 28,857,635 (GRCm39) |
T836M |
probably benign |
Het |
Slfn4 |
T |
G |
11: 83,077,647 (GRCm39) |
I145S |
possibly damaging |
Het |
Spag6l |
G |
A |
16: 16,595,254 (GRCm39) |
T377I |
probably benign |
Het |
Spdye4b |
T |
C |
5: 143,182,089 (GRCm39) |
F129S |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,447,514 (GRCm39) |
G2360E |
probably benign |
Het |
Taar2 |
A |
T |
10: 23,816,669 (GRCm39) |
I70F |
probably damaging |
Het |
Taar7e |
A |
G |
10: 23,914,464 (GRCm39) |
N318S |
probably damaging |
Het |
Tor1a |
C |
A |
2: 30,857,742 (GRCm39) |
R42L |
probably benign |
Het |
Trdn |
A |
T |
10: 33,350,502 (GRCm39) |
Q690H |
probably benign |
Het |
Trim56 |
C |
A |
5: 137,141,579 (GRCm39) |
V646L |
probably benign |
Het |
Tspan15 |
T |
A |
10: 62,027,323 (GRCm39) |
K165I |
probably benign |
Het |
Usp24 |
A |
G |
4: 106,273,245 (GRCm39) |
Y2210C |
probably damaging |
Het |
Usp45 |
A |
G |
4: 21,797,307 (GRCm39) |
T76A |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,785,506 (GRCm39) |
|
probably null |
Het |
Zfp512b |
T |
C |
2: 181,226,888 (GRCm39) |
|
probably benign |
Het |
Zyx |
C |
A |
6: 42,333,093 (GRCm39) |
|
probably null |
Het |
|
Other mutations in 2900026A02Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02810:2900026A02Rik
|
APN |
5 |
113,249,401 (GRCm39) |
missense |
probably damaging |
1.00 |
oyster
|
UTSW |
5 |
113,330,833 (GRCm39) |
missense |
probably benign |
0.14 |
pimento
|
UTSW |
5 |
113,243,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R1394:2900026A02Rik
|
UTSW |
5 |
113,249,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R1395:2900026A02Rik
|
UTSW |
5 |
113,249,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R4329:2900026A02Rik
|
UTSW |
5 |
113,243,455 (GRCm39) |
critical splice donor site |
probably null |
|
R6124:2900026A02Rik
|
UTSW |
5 |
113,331,622 (GRCm39) |
missense |
probably benign |
|
R6336:2900026A02Rik
|
UTSW |
5 |
113,331,349 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6365:2900026A02Rik
|
UTSW |
5 |
113,330,510 (GRCm39) |
missense |
probably benign |
0.00 |
R6575:2900026A02Rik
|
UTSW |
5 |
113,330,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6759:2900026A02Rik
|
UTSW |
5 |
113,331,692 (GRCm39) |
missense |
probably benign |
0.00 |
R7117:2900026A02Rik
|
UTSW |
5 |
113,339,250 (GRCm39) |
missense |
probably benign |
0.00 |
R7168:2900026A02Rik
|
UTSW |
5 |
113,285,659 (GRCm39) |
missense |
probably damaging |
0.96 |
R7339:2900026A02Rik
|
UTSW |
5 |
113,330,938 (GRCm39) |
missense |
probably benign |
0.09 |
R7450:2900026A02Rik
|
UTSW |
5 |
113,331,977 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7458:2900026A02Rik
|
UTSW |
5 |
113,338,510 (GRCm39) |
missense |
probably benign |
0.05 |
R7525:2900026A02Rik
|
UTSW |
5 |
113,331,221 (GRCm39) |
missense |
probably damaging |
0.99 |
R7707:2900026A02Rik
|
UTSW |
5 |
113,285,852 (GRCm39) |
start codon destroyed |
probably benign |
0.14 |
R7848:2900026A02Rik
|
UTSW |
5 |
113,340,007 (GRCm39) |
missense |
probably damaging |
0.96 |
R7869:2900026A02Rik
|
UTSW |
5 |
113,332,001 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7871:2900026A02Rik
|
UTSW |
5 |
113,331,092 (GRCm39) |
missense |
probably benign |
0.02 |
R8327:2900026A02Rik
|
UTSW |
5 |
113,331,685 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8411:2900026A02Rik
|
UTSW |
5 |
113,285,588 (GRCm39) |
missense |
probably benign |
|
R8429:2900026A02Rik
|
UTSW |
5 |
113,331,302 (GRCm39) |
missense |
probably benign |
0.29 |
R8940:2900026A02Rik
|
UTSW |
5 |
113,241,068 (GRCm39) |
missense |
probably benign |
0.07 |
R9065:2900026A02Rik
|
UTSW |
5 |
113,323,084 (GRCm39) |
missense |
probably benign |
0.00 |
R9096:2900026A02Rik
|
UTSW |
5 |
113,339,793 (GRCm39) |
missense |
|
|
R9182:2900026A02Rik
|
UTSW |
5 |
113,243,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R9191:2900026A02Rik
|
UTSW |
5 |
113,330,564 (GRCm39) |
missense |
probably benign |
0.34 |
R9330:2900026A02Rik
|
UTSW |
5 |
113,330,833 (GRCm39) |
missense |
probably benign |
0.14 |
R9336:2900026A02Rik
|
UTSW |
5 |
113,240,966 (GRCm39) |
critical splice donor site |
probably null |
|
R9375:2900026A02Rik
|
UTSW |
5 |
113,332,567 (GRCm39) |
missense |
probably benign |
|
R9388:2900026A02Rik
|
UTSW |
5 |
113,338,714 (GRCm39) |
missense |
probably benign |
0.00 |
R9483:2900026A02Rik
|
UTSW |
5 |
113,339,010 (GRCm39) |
missense |
probably benign |
0.01 |
R9529:2900026A02Rik
|
UTSW |
5 |
113,331,682 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9675:2900026A02Rik
|
UTSW |
5 |
113,339,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R9784:2900026A02Rik
|
UTSW |
5 |
113,338,527 (GRCm39) |
missense |
possibly damaging |
0.93 |
|