Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600014C23Rik |
G |
A |
17: 46,044,583 (GRCm39) |
T46I |
unknown |
Het |
Arhgef1 |
G |
A |
7: 24,616,306 (GRCm39) |
D317N |
probably damaging |
Het |
Atxn7l2 |
T |
C |
3: 108,114,719 (GRCm39) |
D109G |
probably damaging |
Het |
B4galnt3 |
C |
A |
6: 120,195,913 (GRCm39) |
V305L |
probably benign |
Het |
C9 |
T |
A |
15: 6,488,402 (GRCm39) |
N85K |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,305,867 (GRCm39) |
I1941V |
probably benign |
Het |
Capn15 |
A |
G |
17: 26,183,125 (GRCm39) |
V518A |
probably benign |
Het |
Chst10 |
A |
T |
1: 38,905,106 (GRCm39) |
Y200N |
probably damaging |
Het |
Ciao3 |
T |
C |
17: 26,001,226 (GRCm39) |
*493Q |
probably null |
Het |
Cir1 |
A |
G |
2: 73,142,823 (GRCm39) |
S4P |
probably damaging |
Het |
Cish |
G |
A |
9: 107,177,840 (GRCm39) |
R172Q |
probably benign |
Het |
Cnot10 |
A |
T |
9: 114,422,506 (GRCm39) |
N693K |
probably damaging |
Het |
Ddx6 |
A |
G |
9: 44,538,939 (GRCm39) |
D249G |
probably damaging |
Het |
Dennd6b |
T |
C |
15: 89,069,447 (GRCm39) |
D528G |
probably benign |
Het |
Dmtf1 |
T |
A |
5: 9,174,489 (GRCm39) |
T484S |
possibly damaging |
Het |
Dnaaf5 |
T |
C |
5: 139,138,596 (GRCm39) |
V259A |
probably damaging |
Het |
Dzip1l |
A |
T |
9: 99,519,589 (GRCm39) |
S39C |
probably damaging |
Het |
Efcab8 |
T |
A |
2: 153,623,695 (GRCm39) |
M60K |
|
Het |
Eml2 |
T |
A |
7: 18,920,035 (GRCm39) |
V113D |
possibly damaging |
Het |
Fnip1 |
A |
T |
11: 54,406,325 (GRCm39) |
I1141F |
probably benign |
Het |
Gm7298 |
T |
A |
6: 121,712,570 (GRCm39) |
S127R |
probably damaging |
Het |
Hcn2 |
G |
A |
10: 79,570,017 (GRCm39) |
R622Q |
possibly damaging |
Het |
Ift172 |
C |
T |
5: 31,423,723 (GRCm39) |
W746* |
probably null |
Het |
Irs1 |
A |
G |
1: 82,265,412 (GRCm39) |
Y935H |
probably damaging |
Het |
Kctd17 |
CAGCTGGAGGAGC |
CAGC |
15: 78,321,113 (GRCm39) |
|
probably benign |
Het |
Klhl20 |
T |
C |
1: 160,936,827 (GRCm39) |
I183V |
probably benign |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Lalba |
T |
C |
15: 98,379,474 (GRCm39) |
D103G |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,747,210 (GRCm39) |
L822P |
probably damaging |
Het |
Lrrc38 |
G |
A |
4: 143,076,845 (GRCm39) |
C36Y |
probably damaging |
Het |
Ly6e |
T |
C |
15: 74,830,183 (GRCm39) |
S46P |
possibly damaging |
Het |
Nav2 |
T |
C |
7: 49,244,067 (GRCm39) |
I2098T |
probably benign |
Het |
Nipbl |
T |
C |
15: 8,381,010 (GRCm39) |
E594G |
probably benign |
Het |
Or52k2 |
T |
A |
7: 102,253,853 (GRCm39) |
H97Q |
probably benign |
Het |
Parn |
T |
C |
16: 13,425,117 (GRCm39) |
D432G |
probably damaging |
Het |
Pcdh20 |
A |
G |
14: 88,704,793 (GRCm39) |
S836P |
probably damaging |
Het |
Pcmtd2 |
C |
T |
2: 181,496,868 (GRCm39) |
R282C |
probably damaging |
Het |
Ppp2r3c |
A |
G |
12: 55,328,490 (GRCm39) |
I425T |
probably benign |
Het |
Samm50 |
T |
A |
15: 84,085,081 (GRCm39) |
|
probably null |
Het |
Sars1 |
C |
T |
3: 108,338,780 (GRCm39) |
|
probably null |
Het |
Senp8 |
A |
G |
9: 59,645,121 (GRCm39) |
Y12H |
possibly damaging |
Het |
Slc13a4 |
T |
C |
6: 35,247,290 (GRCm39) |
I577V |
possibly damaging |
Het |
Srr |
T |
G |
11: 74,803,961 (GRCm39) |
|
probably null |
Het |
Steap2 |
T |
A |
5: 5,732,967 (GRCm39) |
N19I |
possibly damaging |
Het |
Sucla2 |
A |
G |
14: 73,806,433 (GRCm39) |
Y168C |
probably damaging |
Het |
Tha1 |
T |
C |
11: 117,760,281 (GRCm39) |
Q275R |
probably damaging |
Het |
Trim56 |
T |
C |
5: 137,143,510 (GRCm39) |
N2S |
probably benign |
Het |
Tubgcp6 |
T |
A |
15: 88,988,426 (GRCm39) |
H849L |
probably benign |
Het |
Ybx1 |
A |
G |
4: 119,136,164 (GRCm39) |
*323Q |
probably null |
Het |
Zfp354b |
C |
T |
11: 50,819,390 (GRCm39) |
|
probably null |
Het |
Zfp36l2 |
A |
T |
17: 84,494,346 (GRCm39) |
L97Q |
probably benign |
Het |
Zfp729a |
T |
A |
13: 67,771,612 (GRCm39) |
R78S |
possibly damaging |
Het |
|
Other mutations in Uevld |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02858:Uevld
|
APN |
7 |
46,605,377 (GRCm39) |
missense |
probably benign |
0.31 |
IGL03294:Uevld
|
APN |
7 |
46,580,778 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1344:Uevld
|
UTSW |
7 |
46,587,758 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1418:Uevld
|
UTSW |
7 |
46,587,758 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1698:Uevld
|
UTSW |
7 |
46,605,372 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1848:Uevld
|
UTSW |
7 |
46,594,975 (GRCm39) |
unclassified |
probably benign |
|
R2872:Uevld
|
UTSW |
7 |
46,597,693 (GRCm39) |
missense |
probably null |
0.68 |
R2872:Uevld
|
UTSW |
7 |
46,597,693 (GRCm39) |
missense |
probably null |
0.68 |
R4426:Uevld
|
UTSW |
7 |
46,589,890 (GRCm39) |
missense |
probably benign |
0.15 |
R4664:Uevld
|
UTSW |
7 |
46,587,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5861:Uevld
|
UTSW |
7 |
46,576,104 (GRCm39) |
missense |
probably benign |
0.03 |
R6283:Uevld
|
UTSW |
7 |
46,587,729 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7148:Uevld
|
UTSW |
7 |
46,600,724 (GRCm39) |
missense |
probably damaging |
0.99 |
R7718:Uevld
|
UTSW |
7 |
46,587,804 (GRCm39) |
missense |
probably benign |
0.03 |
R7727:Uevld
|
UTSW |
7 |
46,593,553 (GRCm39) |
missense |
probably benign |
0.13 |
R7775:Uevld
|
UTSW |
7 |
46,576,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R7778:Uevld
|
UTSW |
7 |
46,576,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R8349:Uevld
|
UTSW |
7 |
46,595,055 (GRCm39) |
missense |
probably damaging |
0.98 |
R8449:Uevld
|
UTSW |
7 |
46,595,055 (GRCm39) |
missense |
probably damaging |
0.98 |
R9061:Uevld
|
UTSW |
7 |
46,587,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R9170:Uevld
|
UTSW |
7 |
46,587,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9773:Uevld
|
UTSW |
7 |
46,597,659 (GRCm39) |
critical splice donor site |
probably null |
|
|