Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acyp1 |
T |
A |
12: 85,325,786 (GRCm39) |
Y71F |
unknown |
Het |
Akap11 |
A |
T |
14: 78,748,543 (GRCm39) |
H1281Q |
|
Het |
Amz1 |
T |
C |
5: 140,737,975 (GRCm39) |
Y412H |
probably benign |
Het |
Anxa10 |
C |
T |
8: 62,545,545 (GRCm39) |
M62I |
probably benign |
Het |
Arhgap25 |
T |
C |
6: 87,469,184 (GRCm39) |
K109E |
probably damaging |
Het |
Arhgap31 |
T |
A |
16: 38,460,683 (GRCm39) |
E43D |
probably damaging |
Het |
Atf6 |
T |
C |
1: 170,574,708 (GRCm39) |
M577V |
probably damaging |
Het |
Auts2 |
C |
A |
5: 131,505,620 (GRCm39) |
A82S |
unknown |
Het |
Bcl3 |
T |
C |
7: 19,556,602 (GRCm39) |
M1V |
probably null |
Het |
Cblb |
T |
C |
16: 51,959,993 (GRCm39) |
|
probably null |
Het |
Cc2d2b |
T |
C |
19: 40,797,840 (GRCm39) |
V820A |
unknown |
Het |
Clint1 |
T |
G |
11: 45,797,194 (GRCm39) |
M425R |
possibly damaging |
Het |
Clvs1 |
A |
G |
4: 9,429,834 (GRCm39) |
D279G |
probably damaging |
Het |
Colec11 |
A |
C |
12: 28,645,302 (GRCm39) |
I123S |
probably damaging |
Het |
Crebbp |
C |
T |
16: 3,911,355 (GRCm39) |
E1460K |
probably damaging |
Het |
Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
Dcaf8 |
C |
G |
1: 171,999,909 (GRCm39) |
S22R |
possibly damaging |
Het |
Dmxl1 |
T |
C |
18: 50,011,271 (GRCm39) |
S1143P |
probably damaging |
Het |
Dnhd1 |
T |
C |
7: 105,353,709 (GRCm39) |
I2954T |
probably benign |
Het |
Dop1b |
C |
T |
16: 93,607,171 (GRCm39) |
P2275L |
probably benign |
Het |
Drc3 |
A |
G |
11: 60,261,334 (GRCm39) |
S162G |
probably benign |
Het |
Ehd2 |
T |
C |
7: 15,686,077 (GRCm39) |
I332V |
possibly damaging |
Het |
Eml1 |
T |
A |
12: 108,493,958 (GRCm39) |
D584E |
probably damaging |
Het |
Eogt |
T |
C |
6: 97,096,992 (GRCm39) |
T339A |
probably benign |
Het |
Gbf1 |
A |
G |
19: 46,258,389 (GRCm39) |
T949A |
probably benign |
Het |
Gm11568 |
GCTGCTGCCAGCCCTGCTGCCAGCCC |
GCTGCTGCCAGCCCTGCTGCCAGCCCTGCTGCCAGCCC |
11: 99,749,044 (GRCm39) |
|
probably benign |
Het |
Gm11568 |
AGCCC |
AGCCCTGCTGCCTGCCC |
11: 99,749,065 (GRCm39) |
|
probably benign |
Het |
Gtpbp10 |
A |
T |
5: 5,606,120 (GRCm39) |
C88* |
probably null |
Het |
Ifit1bl2 |
A |
T |
19: 34,596,508 (GRCm39) |
Y369* |
probably null |
Het |
Igsf6 |
A |
G |
7: 120,673,697 (GRCm39) |
L11P |
probably benign |
Het |
Lars1 |
A |
T |
18: 42,361,726 (GRCm39) |
I627N |
probably damaging |
Het |
Lmo3 |
G |
T |
6: 138,393,621 (GRCm39) |
Q11K |
|
Het |
Mical2 |
A |
T |
7: 111,936,054 (GRCm39) |
|
probably null |
Het |
Mmp23 |
A |
G |
4: 155,736,567 (GRCm39) |
V158A |
probably benign |
Het |
Mmp24 |
T |
C |
2: 155,654,195 (GRCm39) |
I391T |
probably damaging |
Het |
Mrgpra3 |
A |
T |
7: 47,239,400 (GRCm39) |
Y175* |
probably null |
Het |
Mrpl23 |
G |
A |
7: 142,089,859 (GRCm39) |
V65M |
probably damaging |
Het |
Mup1 |
A |
G |
4: 60,456,488 (GRCm39) |
L85S |
possibly damaging |
Het |
Myo15b |
T |
C |
11: 115,777,466 (GRCm39) |
L747S |
probably damaging |
Het |
Nanog |
G |
T |
6: 122,690,219 (GRCm39) |
W208L |
probably damaging |
Het |
Nkg7 |
A |
G |
7: 43,087,229 (GRCm39) |
Y112C |
probably damaging |
Het |
Nup155 |
A |
G |
15: 8,141,800 (GRCm39) |
D64G |
probably damaging |
Het |
Or13p4 |
A |
G |
4: 118,546,930 (GRCm39) |
S240P |
possibly damaging |
Het |
Palm3 |
T |
C |
8: 84,753,636 (GRCm39) |
S108P |
probably damaging |
Het |
Pam |
T |
C |
1: 97,772,325 (GRCm39) |
N579D |
probably benign |
Het |
Pclo |
A |
G |
5: 14,725,648 (GRCm39) |
E1502G |
unknown |
Het |
Pde4dip |
A |
G |
3: 97,795,896 (GRCm39) |
S31P |
unknown |
Het |
Peg10 |
A |
T |
6: 4,756,871 (GRCm39) |
K482N |
unknown |
Het |
Phf19 |
A |
T |
2: 34,801,708 (GRCm39) |
L34* |
probably null |
Het |
Pla2g2c |
A |
T |
4: 138,461,689 (GRCm39) |
K53* |
probably null |
Het |
Pla2g4f |
T |
A |
2: 120,142,713 (GRCm39) |
|
probably null |
Het |
Polk |
G |
T |
13: 96,630,349 (GRCm39) |
T404K |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,657,079 (GRCm39) |
V4058D |
possibly damaging |
Het |
Prox2 |
T |
A |
12: 85,134,851 (GRCm39) |
I477F |
probably damaging |
Het |
Ptk6 |
A |
G |
2: 180,837,566 (GRCm39) |
V451A |
probably benign |
Het |
Ptpn3 |
C |
T |
4: 57,205,914 (GRCm39) |
E693K |
possibly damaging |
Het |
Rag2 |
G |
A |
2: 101,461,217 (GRCm39) |
G509D |
probably damaging |
Het |
Rapgef2 |
A |
G |
3: 78,974,093 (GRCm39) |
C1418R |
probably benign |
Het |
Rev1 |
A |
T |
1: 38,102,214 (GRCm39) |
Y716* |
probably null |
Het |
Rsl1d1 |
T |
A |
16: 11,011,385 (GRCm39) |
T440S |
possibly damaging |
Het |
Samd14 |
T |
A |
11: 94,914,372 (GRCm39) |
Y343* |
probably null |
Het |
Sema3a |
A |
T |
5: 13,615,854 (GRCm39) |
D426V |
possibly damaging |
Het |
Slc7a11 |
G |
A |
3: 50,382,201 (GRCm39) |
T182M |
probably benign |
Het |
Slitrk5 |
A |
G |
14: 111,916,726 (GRCm39) |
I117V |
possibly damaging |
Het |
Son |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,222 (GRCm39) |
|
probably benign |
Het |
Stil |
A |
T |
4: 114,878,716 (GRCm39) |
H384L |
possibly damaging |
Het |
Suclg2 |
C |
A |
6: 95,546,666 (GRCm39) |
R270L |
probably damaging |
Het |
Taf5 |
A |
G |
19: 47,065,771 (GRCm39) |
D492G |
probably damaging |
Het |
Tes3-ps |
T |
A |
13: 49,647,815 (GRCm39) |
Y230* |
probably null |
Het |
Ttc41 |
G |
T |
10: 86,565,726 (GRCm39) |
A427S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,553,994 (GRCm39) |
D30903G |
probably damaging |
Het |
Txndc16 |
A |
T |
14: 45,406,798 (GRCm39) |
L219Q |
probably null |
Het |
Usp34 |
T |
A |
11: 23,331,337 (GRCm39) |
H1098Q |
probably damaging |
Het |
Vmn2r52 |
T |
A |
7: 9,905,281 (GRCm39) |
Y186F |
probably damaging |
Het |
Zbtb41 |
T |
C |
1: 139,359,806 (GRCm39) |
F512S |
probably damaging |
Het |
|
Other mutations in 2310022A10Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02292:2310022A10Rik
|
APN |
7 |
27,263,982 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03261:2310022A10Rik
|
APN |
7 |
27,279,863 (GRCm39) |
nonsense |
probably null |
|
R0305:2310022A10Rik
|
UTSW |
7 |
27,274,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R1080:2310022A10Rik
|
UTSW |
7 |
27,265,109 (GRCm39) |
missense |
probably benign |
|
R1696:2310022A10Rik
|
UTSW |
7 |
27,260,022 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1773:2310022A10Rik
|
UTSW |
7 |
27,280,020 (GRCm39) |
missense |
probably damaging |
0.98 |
R4171:2310022A10Rik
|
UTSW |
7 |
27,265,109 (GRCm39) |
missense |
probably benign |
|
R4583:2310022A10Rik
|
UTSW |
7 |
27,274,017 (GRCm39) |
missense |
unknown |
|
R4781:2310022A10Rik
|
UTSW |
7 |
27,271,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:2310022A10Rik
|
UTSW |
7 |
27,265,070 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4998:2310022A10Rik
|
UTSW |
7 |
27,271,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:2310022A10Rik
|
UTSW |
7 |
27,255,946 (GRCm39) |
missense |
probably benign |
0.04 |
R5007:2310022A10Rik
|
UTSW |
7 |
27,278,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R5008:2310022A10Rik
|
UTSW |
7 |
27,278,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R5364:2310022A10Rik
|
UTSW |
7 |
27,278,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R6119:2310022A10Rik
|
UTSW |
7 |
27,265,138 (GRCm39) |
nonsense |
probably null |
|
R6991:2310022A10Rik
|
UTSW |
7 |
27,279,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:2310022A10Rik
|
UTSW |
7 |
27,278,198 (GRCm39) |
nonsense |
probably null |
|
R7519:2310022A10Rik
|
UTSW |
7 |
27,274,155 (GRCm39) |
missense |
|
|
R7787:2310022A10Rik
|
UTSW |
7 |
27,263,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R8244:2310022A10Rik
|
UTSW |
7 |
27,271,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R8525:2310022A10Rik
|
UTSW |
7 |
27,255,936 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9246:2310022A10Rik
|
UTSW |
7 |
27,279,961 (GRCm39) |
missense |
probably benign |
0.06 |
|