Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
A |
C |
3: 59,840,161 (GRCm39) |
T78P |
probably damaging |
Het |
Abcc8 |
T |
C |
7: 45,800,291 (GRCm39) |
K497R |
probably damaging |
Het |
Aldh1a3 |
C |
T |
7: 66,068,927 (GRCm39) |
R19Q |
possibly damaging |
Het |
Bmp2k |
A |
G |
5: 97,234,944 (GRCm39) |
|
probably benign |
Het |
Ccni |
A |
T |
5: 93,335,553 (GRCm39) |
L195Q |
possibly damaging |
Het |
Cdkl4 |
C |
A |
17: 80,832,764 (GRCm39) |
G327* |
probably null |
Het |
Cdsn |
T |
C |
17: 35,866,326 (GRCm39) |
V285A |
possibly damaging |
Het |
Cfap20dc |
A |
G |
14: 8,518,736 (GRCm38) |
V240A |
probably benign |
Het |
Chtf18 |
T |
C |
17: 25,943,540 (GRCm39) |
E352G |
possibly damaging |
Het |
Clasp2 |
T |
A |
9: 113,732,984 (GRCm39) |
I961N |
probably damaging |
Het |
Cpsf2 |
A |
G |
12: 101,949,752 (GRCm39) |
Q128R |
probably damaging |
Het |
Cttnbp2 |
C |
A |
6: 18,406,525 (GRCm39) |
Q1055H |
possibly damaging |
Het |
Cyld |
T |
G |
8: 89,433,860 (GRCm39) |
F216L |
probably benign |
Het |
Cyp3a41a |
A |
G |
5: 145,656,858 (GRCm39) |
M1T |
probably null |
Het |
Disp3 |
C |
T |
4: 148,328,673 (GRCm39) |
R1097H |
possibly damaging |
Het |
Dmap1 |
T |
C |
4: 117,538,233 (GRCm39) |
D67G |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 30,875,959 (GRCm39) |
F529L |
probably benign |
Het |
Ergic3 |
T |
C |
2: 155,859,638 (GRCm39) |
|
probably null |
Het |
Fkbp14 |
A |
G |
6: 54,569,943 (GRCm39) |
I29T |
probably benign |
Het |
Gm4845 |
T |
A |
1: 141,184,623 (GRCm39) |
|
noncoding transcript |
Het |
Gm7135 |
A |
T |
1: 97,281,801 (GRCm39) |
|
noncoding transcript |
Het |
Gpbar1 |
TACCAC |
TAC |
1: 74,318,704 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,424,481 (GRCm39) |
I57F |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,809,280 (GRCm39) |
V1722A |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,283,037 (GRCm39) |
D1971G |
possibly damaging |
Het |
Il21 |
C |
A |
3: 37,286,653 (GRCm39) |
S21I |
probably damaging |
Het |
Itih4 |
T |
A |
14: 30,614,244 (GRCm39) |
I398N |
probably damaging |
Het |
Kansl1 |
A |
T |
11: 104,226,390 (GRCm39) |
S922R |
probably damaging |
Het |
Krt27 |
G |
A |
11: 99,237,722 (GRCm39) |
Q339* |
probably null |
Het |
Lama1 |
C |
A |
17: 68,045,829 (GRCm39) |
L245I |
possibly damaging |
Het |
Lmo2 |
T |
A |
2: 103,806,488 (GRCm39) |
C60* |
probably null |
Het |
Med16 |
A |
G |
10: 79,738,839 (GRCm39) |
S316P |
possibly damaging |
Het |
Mia3 |
T |
C |
1: 183,111,970 (GRCm39) |
N529S |
probably benign |
Het |
Msi2 |
T |
C |
11: 88,285,481 (GRCm39) |
K188E |
probably damaging |
Het |
Myh7 |
T |
C |
14: 55,209,128 (GRCm39) |
K1870R |
probably damaging |
Het |
Nhlrc1 |
A |
G |
13: 47,167,216 (GRCm39) |
V347A |
probably benign |
Het |
Nol6 |
C |
T |
4: 41,120,167 (GRCm39) |
R487H |
probably benign |
Het |
Or4c117 |
T |
C |
2: 88,955,682 (GRCm39) |
Y131C |
probably damaging |
Het |
Or4k41 |
T |
C |
2: 111,280,028 (GRCm39) |
I181T |
probably benign |
Het |
Or52h1 |
A |
T |
7: 103,828,736 (GRCm39) |
V293D |
probably damaging |
Het |
Or5d18 |
T |
C |
2: 87,865,005 (GRCm39) |
I159M |
probably benign |
Het |
Or6c205 |
T |
C |
10: 129,087,141 (GRCm39) |
I246T |
probably damaging |
Het |
Otog |
T |
C |
7: 45,937,415 (GRCm39) |
V1708A |
probably benign |
Het |
Ptprv |
A |
G |
1: 135,046,586 (GRCm39) |
|
noncoding transcript |
Het |
Pus7l |
A |
G |
15: 94,427,369 (GRCm39) |
V471A |
possibly damaging |
Het |
Rab11fip4 |
A |
G |
11: 79,510,497 (GRCm39) |
R68G |
probably damaging |
Het |
Ralgapb |
A |
G |
2: 158,277,428 (GRCm39) |
D264G |
possibly damaging |
Het |
Reln |
A |
G |
5: 22,165,424 (GRCm39) |
S2045P |
probably damaging |
Het |
Rgs22 |
A |
C |
15: 36,055,022 (GRCm39) |
Y593* |
probably null |
Het |
Ror2 |
C |
T |
13: 53,285,954 (GRCm39) |
D87N |
probably damaging |
Het |
Rttn |
T |
A |
18: 89,082,209 (GRCm39) |
|
probably null |
Het |
Runx3 |
A |
G |
4: 134,898,446 (GRCm39) |
T206A |
probably benign |
Het |
Setx |
A |
G |
2: 29,054,562 (GRCm39) |
E2158G |
probably damaging |
Het |
Siglece |
C |
T |
7: 43,308,396 (GRCm39) |
|
probably null |
Het |
Slco1a8 |
T |
C |
6: 141,926,599 (GRCm39) |
S576G |
probably benign |
Het |
Snx1 |
A |
T |
9: 66,012,187 (GRCm39) |
L96* |
probably null |
Het |
Srrm1 |
A |
G |
4: 135,074,031 (GRCm39) |
|
probably benign |
Het |
Stk39 |
A |
T |
2: 68,051,336 (GRCm39) |
|
probably benign |
Het |
Sun3 |
G |
A |
11: 8,988,311 (GRCm39) |
R4* |
probably null |
Het |
Svil |
A |
G |
18: 5,054,025 (GRCm39) |
K347E |
possibly damaging |
Het |
Sybu |
T |
A |
15: 44,541,063 (GRCm39) |
E333V |
probably damaging |
Het |
Tet2 |
A |
G |
3: 133,192,520 (GRCm39) |
|
probably benign |
Het |
Tfip11 |
G |
T |
5: 112,483,613 (GRCm39) |
|
probably benign |
Het |
Tmc1 |
A |
C |
19: 20,884,319 (GRCm39) |
D40E |
probably damaging |
Het |
Twf2 |
G |
T |
9: 106,089,539 (GRCm39) |
G121W |
probably damaging |
Het |
Vpreb3 |
A |
G |
10: 75,775,636 (GRCm39) |
V50A |
probably damaging |
Het |
Vps8 |
T |
A |
16: 21,285,219 (GRCm39) |
L400Q |
probably damaging |
Het |
Xylt1 |
A |
T |
7: 117,266,565 (GRCm39) |
Y861F |
probably damaging |
Het |
Zfp608 |
T |
G |
18: 55,022,962 (GRCm39) |
T1485P |
probably damaging |
Het |
Zfp619 |
T |
G |
7: 39,186,504 (GRCm39) |
S845A |
possibly damaging |
Het |
Zscan4d |
A |
T |
7: 10,899,274 (GRCm39) |
M1K |
probably null |
Het |
|
Other mutations in Rps6ka4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01146:Rps6ka4
|
APN |
19 |
6,808,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01548:Rps6ka4
|
APN |
19 |
6,809,691 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02536:Rps6ka4
|
APN |
19 |
6,809,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02902:Rps6ka4
|
APN |
19 |
6,809,623 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03299:Rps6ka4
|
APN |
19 |
6,809,615 (GRCm39) |
splice site |
probably benign |
|
R0510:Rps6ka4
|
UTSW |
19 |
6,817,866 (GRCm39) |
missense |
probably benign |
0.13 |
R1104:Rps6ka4
|
UTSW |
19 |
6,808,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R1620:Rps6ka4
|
UTSW |
19 |
6,815,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Rps6ka4
|
UTSW |
19 |
6,816,730 (GRCm39) |
missense |
probably benign |
0.15 |
R1648:Rps6ka4
|
UTSW |
19 |
6,816,730 (GRCm39) |
missense |
probably benign |
0.15 |
R1939:Rps6ka4
|
UTSW |
19 |
6,816,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R2370:Rps6ka4
|
UTSW |
19 |
6,807,468 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2412:Rps6ka4
|
UTSW |
19 |
6,807,309 (GRCm39) |
makesense |
probably null |
|
R2571:Rps6ka4
|
UTSW |
19 |
6,815,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2698:Rps6ka4
|
UTSW |
19 |
6,814,720 (GRCm39) |
missense |
probably benign |
0.08 |
R3427:Rps6ka4
|
UTSW |
19 |
6,815,123 (GRCm39) |
critical splice donor site |
probably null |
|
R3721:Rps6ka4
|
UTSW |
19 |
6,816,645 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3844:Rps6ka4
|
UTSW |
19 |
6,815,171 (GRCm39) |
nonsense |
probably null |
|
R4092:Rps6ka4
|
UTSW |
19 |
6,809,623 (GRCm39) |
critical splice donor site |
probably null |
|
R4169:Rps6ka4
|
UTSW |
19 |
6,809,188 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4677:Rps6ka4
|
UTSW |
19 |
6,816,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:Rps6ka4
|
UTSW |
19 |
6,815,467 (GRCm39) |
missense |
probably benign |
0.02 |
R5631:Rps6ka4
|
UTSW |
19 |
6,808,345 (GRCm39) |
splice site |
probably benign |
|
R6462:Rps6ka4
|
UTSW |
19 |
6,814,957 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6643:Rps6ka4
|
UTSW |
19 |
6,809,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R6939:Rps6ka4
|
UTSW |
19 |
6,815,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7030:Rps6ka4
|
UTSW |
19 |
6,816,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R7902:Rps6ka4
|
UTSW |
19 |
6,808,679 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8021:Rps6ka4
|
UTSW |
19 |
6,807,777 (GRCm39) |
missense |
probably benign |
0.01 |
R8166:Rps6ka4
|
UTSW |
19 |
6,814,811 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8988:Rps6ka4
|
UTSW |
19 |
6,808,667 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9481:Rps6ka4
|
UTSW |
19 |
6,809,372 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9664:Rps6ka4
|
UTSW |
19 |
6,809,354 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9723:Rps6ka4
|
UTSW |
19 |
6,816,663 (GRCm39) |
missense |
probably damaging |
0.99 |
U24488:Rps6ka4
|
UTSW |
19 |
6,809,724 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Rps6ka4
|
UTSW |
19 |
6,815,508 (GRCm39) |
missense |
probably damaging |
0.97 |
X0027:Rps6ka4
|
UTSW |
19 |
6,815,140 (GRCm39) |
missense |
probably benign |
0.37 |
|