Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
T |
C |
11: 58,312,533 (GRCm39) |
S4P |
probably benign |
Het |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Acsl6 |
A |
G |
11: 54,225,880 (GRCm39) |
N307D |
probably benign |
Het |
Atxn1 |
A |
G |
13: 45,721,433 (GRCm39) |
V154A |
probably benign |
Het |
Bltp3a |
A |
G |
17: 28,112,414 (GRCm39) |
D1201G |
probably damaging |
Het |
Cacna2d4 |
T |
C |
6: 119,213,611 (GRCm39) |
L10S |
probably benign |
Het |
Cd33 |
A |
T |
7: 43,182,150 (GRCm39) |
H98Q |
probably benign |
Het |
Cenpk |
T |
G |
13: 104,370,682 (GRCm39) |
C103G |
probably benign |
Het |
Cep97 |
T |
A |
16: 55,726,093 (GRCm39) |
Q670L |
probably benign |
Het |
Cfap65 |
C |
T |
1: 74,945,468 (GRCm39) |
|
probably null |
Het |
Cir1 |
A |
G |
2: 73,142,781 (GRCm39) |
S18P |
probably damaging |
Het |
Coprs |
T |
C |
8: 13,935,081 (GRCm39) |
Y158C |
probably damaging |
Het |
Creld1 |
T |
C |
6: 113,469,765 (GRCm39) |
F389S |
probably damaging |
Het |
Dimt1 |
T |
C |
13: 107,093,636 (GRCm39) |
I276T |
possibly damaging |
Het |
Dok1 |
T |
C |
6: 83,009,972 (GRCm39) |
K46E |
probably damaging |
Het |
Dsp |
T |
A |
13: 38,371,781 (GRCm39) |
C911S |
probably benign |
Het |
Egr3 |
A |
G |
14: 70,314,978 (GRCm39) |
I29V |
probably benign |
Het |
Fam186a |
A |
G |
15: 99,844,766 (GRCm39) |
S493P |
unknown |
Het |
Fam83a |
G |
A |
15: 57,849,765 (GRCm39) |
G103D |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,175,808 (GRCm39) |
Q1635L |
probably damaging |
Het |
Figla |
A |
C |
6: 85,997,689 (GRCm39) |
H139P |
probably benign |
Het |
Fryl |
T |
C |
5: 73,262,115 (GRCm39) |
K551E |
probably damaging |
Het |
Galr2 |
A |
G |
11: 116,174,452 (GRCm39) |
T361A |
probably benign |
Het |
Gart |
A |
T |
16: 91,427,596 (GRCm39) |
S467R |
probably benign |
Het |
Ggps1 |
T |
C |
13: 14,229,742 (GRCm39) |
K45R |
probably benign |
Het |
Ghsr |
G |
C |
3: 27,426,630 (GRCm39) |
V229L |
possibly damaging |
Het |
H2ac21 |
A |
G |
3: 96,127,401 (GRCm39) |
E57G |
probably damaging |
Het |
Hectd2 |
A |
T |
19: 36,582,689 (GRCm39) |
H473L |
possibly damaging |
Het |
Hic2 |
T |
C |
16: 17,076,293 (GRCm39) |
V374A |
possibly damaging |
Het |
Hivep2 |
T |
A |
10: 14,005,523 (GRCm39) |
I707N |
probably benign |
Het |
Il17rc |
T |
C |
6: 113,449,741 (GRCm39) |
S116P |
probably damaging |
Het |
Krt34 |
A |
T |
11: 99,929,226 (GRCm39) |
I328N |
probably damaging |
Het |
Krt79 |
G |
A |
15: 101,840,288 (GRCm39) |
R303C |
probably damaging |
Het |
Lama2 |
T |
C |
10: 27,100,015 (GRCm39) |
E830G |
probably benign |
Het |
Lamb2 |
C |
T |
9: 108,358,006 (GRCm39) |
T149I |
probably damaging |
Het |
Mau2 |
T |
C |
8: 70,480,153 (GRCm39) |
Y318C |
probably damaging |
Het |
Mier2 |
T |
C |
10: 79,377,496 (GRCm39) |
S486G |
probably benign |
Het |
Mllt10 |
A |
G |
2: 18,164,322 (GRCm39) |
D284G |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,937,366 (GRCm39) |
S748R |
probably damaging |
Het |
Ncoa6 |
A |
G |
2: 155,248,133 (GRCm39) |
S1724P |
probably benign |
Het |
Nipal4 |
T |
A |
11: 46,052,922 (GRCm39) |
|
probably null |
Het |
Nlrc4 |
G |
C |
17: 74,753,736 (GRCm39) |
L216V |
probably benign |
Het |
Ogfr |
A |
G |
2: 180,235,417 (GRCm39) |
M164V |
possibly damaging |
Het |
Or1o4 |
G |
T |
17: 37,591,386 (GRCm39) |
|
probably benign |
Het |
Or4b12 |
G |
A |
2: 90,096,709 (GRCm39) |
Q22* |
probably null |
Het |
Pcdha12 |
G |
T |
18: 37,155,526 (GRCm39) |
W748C |
probably damaging |
Het |
Pkd1l3 |
T |
C |
8: 110,395,849 (GRCm39) |
V2083A |
probably damaging |
Het |
Plin3 |
C |
A |
17: 56,587,824 (GRCm39) |
G297V |
probably benign |
Het |
Prex1 |
C |
T |
2: 166,419,896 (GRCm39) |
R1260Q |
possibly damaging |
Het |
Prpf38b |
A |
G |
3: 108,818,619 (GRCm39) |
V47A |
probably benign |
Het |
Ptch1 |
T |
C |
13: 63,675,071 (GRCm39) |
T851A |
probably benign |
Het |
Ptk7 |
T |
A |
17: 46,887,744 (GRCm39) |
I563F |
possibly damaging |
Het |
Ptprm |
A |
G |
17: 67,116,466 (GRCm39) |
Y938H |
probably damaging |
Het |
R3hcc1l |
G |
A |
19: 42,507,203 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
T |
C |
11: 54,443,684 (GRCm39) |
V89A |
probably benign |
Het |
Sh2b1 |
CTC |
CTCCGCCACGGGGACCAGTTC |
7: 126,066,770 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
AGCTCAGCCACGGGGACC |
AGCTCAGCCACGGGGACCCGCTCAGCCACGGGGACC |
7: 126,066,750 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
ACCAGCTC |
ACCAGCTCAGCCACGGGGGCCAGCTC |
7: 126,066,765 (GRCm39) |
|
probably benign |
Het |
Slain1 |
T |
A |
14: 103,932,748 (GRCm39) |
V444E |
probably damaging |
Het |
Slc10a5 |
T |
A |
3: 10,400,532 (GRCm39) |
I43F |
possibly damaging |
Het |
Smarca2 |
T |
C |
19: 26,659,452 (GRCm39) |
F914S |
possibly damaging |
Het |
Smarca5 |
A |
C |
8: 81,428,840 (GRCm39) |
L1003V |
probably damaging |
Het |
Spata18 |
A |
T |
5: 73,829,840 (GRCm39) |
I332F |
|
Het |
Spata31d1e |
A |
G |
13: 59,890,806 (GRCm39) |
V338A |
probably damaging |
Het |
Stard9 |
C |
G |
2: 120,534,564 (GRCm39) |
P3607R |
probably damaging |
Het |
Tbx19 |
A |
G |
1: 164,966,546 (GRCm39) |
S443P |
unknown |
Het |
Tktl2 |
C |
G |
8: 66,965,840 (GRCm39) |
A466G |
probably damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmem129 |
A |
G |
5: 33,815,122 (GRCm39) |
V17A |
probably benign |
Het |
Tom1l2 |
T |
C |
11: 60,153,486 (GRCm39) |
T164A |
probably damaging |
Het |
Tor1aip1 |
T |
A |
1: 155,906,177 (GRCm39) |
D205V |
probably damaging |
Het |
Tpp2 |
T |
A |
1: 44,017,648 (GRCm39) |
S751T |
probably benign |
Het |
Trim11 |
G |
T |
11: 58,878,477 (GRCm39) |
A251S |
unknown |
Het |
Trim33 |
T |
C |
3: 103,239,074 (GRCm39) |
V684A |
probably benign |
Het |
Triobp |
C |
T |
15: 78,877,378 (GRCm39) |
R1637C |
probably damaging |
Het |
Trpm3 |
A |
G |
19: 22,960,040 (GRCm39) |
N1225S |
probably benign |
Het |
Usp21 |
T |
C |
1: 171,112,503 (GRCm39) |
Y300C |
probably damaging |
Het |
Usp32 |
T |
C |
11: 84,913,560 (GRCm39) |
T924A |
probably damaging |
Het |
Vmn1r198 |
A |
T |
13: 22,539,015 (GRCm39) |
H167L |
possibly damaging |
Het |
Vmn2r23 |
A |
G |
6: 123,689,672 (GRCm39) |
T183A |
probably benign |
Het |
Zc3h8 |
T |
C |
2: 128,773,223 (GRCm39) |
Y213C |
probably damaging |
Het |
Zcchc17 |
A |
T |
4: 130,232,337 (GRCm39) |
D55E |
probably benign |
Het |
Zfp408 |
A |
T |
2: 91,478,368 (GRCm39) |
W26R |
probably damaging |
Het |
Zfp937 |
G |
T |
2: 150,080,890 (GRCm39) |
A307S |
possibly damaging |
Het |
|
Other mutations in Cebpz |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00817:Cebpz
|
APN |
17 |
79,242,259 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01558:Cebpz
|
APN |
17 |
79,242,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01724:Cebpz
|
APN |
17 |
79,243,342 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01938:Cebpz
|
APN |
17 |
79,242,390 (GRCm39) |
nonsense |
probably null |
|
IGL02165:Cebpz
|
APN |
17 |
79,229,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02397:Cebpz
|
APN |
17 |
79,230,690 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02455:Cebpz
|
APN |
17 |
79,242,465 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02690:Cebpz
|
APN |
17 |
79,229,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02698:Cebpz
|
APN |
17 |
79,243,003 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02755:Cebpz
|
APN |
17 |
79,238,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02827:Cebpz
|
APN |
17 |
79,236,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03149:Cebpz
|
APN |
17 |
79,229,982 (GRCm39) |
missense |
probably benign |
0.01 |
cedar_hill
|
UTSW |
17 |
79,244,339 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0125:Cebpz
|
UTSW |
17 |
79,227,317 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0138:Cebpz
|
UTSW |
17 |
79,238,820 (GRCm39) |
missense |
probably benign |
|
R0310:Cebpz
|
UTSW |
17 |
79,233,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R0436:Cebpz
|
UTSW |
17 |
79,243,079 (GRCm39) |
missense |
probably benign |
0.00 |
R0589:Cebpz
|
UTSW |
17 |
79,244,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R0828:Cebpz
|
UTSW |
17 |
79,233,411 (GRCm39) |
missense |
probably benign |
0.04 |
R1355:Cebpz
|
UTSW |
17 |
79,242,753 (GRCm39) |
missense |
probably benign |
0.01 |
R1367:Cebpz
|
UTSW |
17 |
79,230,742 (GRCm39) |
missense |
probably benign |
|
R1583:Cebpz
|
UTSW |
17 |
79,242,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R1639:Cebpz
|
UTSW |
17 |
79,242,035 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1818:Cebpz
|
UTSW |
17 |
79,242,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Cebpz
|
UTSW |
17 |
79,239,545 (GRCm39) |
missense |
probably benign |
0.00 |
R1908:Cebpz
|
UTSW |
17 |
79,242,336 (GRCm39) |
nonsense |
probably null |
|
R1909:Cebpz
|
UTSW |
17 |
79,242,336 (GRCm39) |
nonsense |
probably null |
|
R2094:Cebpz
|
UTSW |
17 |
79,242,983 (GRCm39) |
missense |
probably benign |
0.03 |
R2314:Cebpz
|
UTSW |
17 |
79,227,976 (GRCm39) |
critical splice donor site |
probably null |
|
R2763:Cebpz
|
UTSW |
17 |
79,243,358 (GRCm39) |
missense |
probably benign |
|
R2874:Cebpz
|
UTSW |
17 |
79,239,532 (GRCm39) |
splice site |
probably benign |
|
R3807:Cebpz
|
UTSW |
17 |
79,242,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4012:Cebpz
|
UTSW |
17 |
79,231,896 (GRCm39) |
missense |
probably damaging |
0.98 |
R5344:Cebpz
|
UTSW |
17 |
79,233,542 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5394:Cebpz
|
UTSW |
17 |
79,229,634 (GRCm39) |
missense |
probably benign |
0.34 |
R5711:Cebpz
|
UTSW |
17 |
79,242,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Cebpz
|
UTSW |
17 |
79,233,366 (GRCm39) |
missense |
probably benign |
0.20 |
R6238:Cebpz
|
UTSW |
17 |
79,244,339 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6257:Cebpz
|
UTSW |
17 |
79,243,261 (GRCm39) |
missense |
probably benign |
0.17 |
R6825:Cebpz
|
UTSW |
17 |
79,227,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7735:Cebpz
|
UTSW |
17 |
79,233,342 (GRCm39) |
critical splice donor site |
probably null |
|
R7994:Cebpz
|
UTSW |
17 |
79,242,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R8045:Cebpz
|
UTSW |
17 |
79,239,585 (GRCm39) |
missense |
probably damaging |
0.96 |
R8210:Cebpz
|
UTSW |
17 |
79,230,685 (GRCm39) |
missense |
probably benign |
0.20 |
R8694:Cebpz
|
UTSW |
17 |
79,234,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R8712:Cebpz
|
UTSW |
17 |
79,229,081 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8774:Cebpz
|
UTSW |
17 |
79,229,073 (GRCm39) |
missense |
probably benign |
0.09 |
R8774-TAIL:Cebpz
|
UTSW |
17 |
79,229,073 (GRCm39) |
missense |
probably benign |
0.09 |
R9058:Cebpz
|
UTSW |
17 |
79,243,227 (GRCm39) |
missense |
probably benign |
0.00 |
|