Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat1 |
C |
T |
9: 53,498,831 (GRCm39) |
D285N |
probably damaging |
Het |
Aldh3a1 |
G |
A |
11: 61,106,304 (GRCm39) |
|
probably benign |
Het |
Alms1 |
A |
G |
6: 85,600,015 (GRCm39) |
T2083A |
possibly damaging |
Het |
Atrip |
C |
T |
9: 108,890,241 (GRCm39) |
M143I |
possibly damaging |
Het |
Aup1 |
T |
A |
6: 83,033,842 (GRCm39) |
V344D |
probably damaging |
Het |
Baiap2 |
G |
A |
11: 119,891,405 (GRCm39) |
V511M |
probably benign |
Het |
Bnip2 |
T |
A |
9: 69,910,955 (GRCm39) |
|
probably null |
Het |
Cacna1i |
A |
T |
15: 80,256,855 (GRCm39) |
Y1083F |
probably damaging |
Het |
Cbr4 |
T |
C |
8: 61,943,740 (GRCm39) |
|
probably benign |
Het |
Ces2b |
C |
T |
8: 105,561,237 (GRCm39) |
|
probably benign |
Het |
Chd1 |
A |
G |
17: 15,962,550 (GRCm39) |
N769S |
possibly damaging |
Het |
Clca3b |
A |
T |
3: 144,533,701 (GRCm39) |
V558D |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,564,017 (GRCm39) |
D1736G |
probably benign |
Het |
Cpne8 |
C |
A |
15: 90,532,824 (GRCm39) |
C61F |
probably damaging |
Het |
Cxcr1 |
A |
G |
1: 74,231,998 (GRCm39) |
I8T |
probably benign |
Het |
D630003M21Rik |
T |
G |
2: 158,037,327 (GRCm39) |
|
probably benign |
Het |
Dcaf17 |
T |
A |
2: 70,890,763 (GRCm39) |
D99E |
probably damaging |
Het |
Fbf1 |
C |
T |
11: 116,050,880 (GRCm39) |
|
probably benign |
Het |
Fgfr2 |
T |
A |
7: 129,773,354 (GRCm39) |
H570L |
possibly damaging |
Het |
Gars1 |
G |
A |
6: 55,046,472 (GRCm39) |
|
probably null |
Het |
Gm10309 |
A |
G |
17: 86,806,463 (GRCm39) |
|
probably benign |
Het |
Gm17333 |
AAGAAGAGAAGAGAAGAGAAGAGAAGAGAAGAGAA |
AAGAAGAGAAGAGAAGAGAAGAGAAGAGAAGAGAAGAGAA |
16: 77,649,766 (GRCm39) |
|
noncoding transcript |
Het |
Gm9892 |
G |
A |
8: 52,649,860 (GRCm39) |
Q78* |
probably null |
Het |
Has1 |
A |
G |
17: 18,064,125 (GRCm39) |
Y505H |
possibly damaging |
Het |
Hivep3 |
T |
A |
4: 119,989,738 (GRCm39) |
L2063* |
probably null |
Het |
Il1rl1 |
CTTGTTGTTGTTGTTGTTG |
CTTGTTGTTGTTGTTGTTGTTG |
1: 40,481,734 (GRCm39) |
|
probably benign |
Het |
Itgb3 |
T |
C |
11: 104,549,702 (GRCm39) |
V614A |
probably benign |
Het |
Lrrc23 |
A |
G |
6: 124,755,321 (GRCm39) |
|
probably benign |
Het |
Lrrc63 |
A |
T |
14: 75,335,660 (GRCm39) |
|
probably benign |
Het |
Mfhas1 |
C |
T |
8: 36,057,180 (GRCm39) |
R357* |
probably null |
Het |
Mink1 |
C |
A |
11: 70,492,502 (GRCm39) |
N123K |
probably damaging |
Het |
Mtmr4 |
A |
G |
11: 87,501,890 (GRCm39) |
H591R |
probably benign |
Het |
Nav3 |
T |
C |
10: 109,606,058 (GRCm39) |
T923A |
probably benign |
Het |
Ncapg |
A |
G |
5: 45,844,666 (GRCm39) |
T554A |
probably damaging |
Het |
Nfe2l1 |
T |
C |
11: 96,718,514 (GRCm39) |
Y7C |
probably damaging |
Het |
Nol8 |
C |
T |
13: 49,815,923 (GRCm39) |
A677V |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,942,470 (GRCm39) |
M4904K |
probably damaging |
Het |
Obscn |
G |
T |
11: 58,973,602 (GRCm39) |
L1910I |
probably damaging |
Het |
Or8b41 |
T |
C |
9: 38,055,178 (GRCm39) |
F244S |
probably benign |
Het |
Pcdhb15 |
T |
A |
18: 37,608,619 (GRCm39) |
V617E |
probably damaging |
Het |
Pelp1 |
T |
C |
11: 70,286,530 (GRCm39) |
T533A |
possibly damaging |
Het |
Pgrmc1 |
T |
C |
X: 35,865,924 (GRCm39) |
F160S |
probably damaging |
Het |
Pink1 |
G |
T |
4: 138,045,357 (GRCm39) |
P239Q |
probably damaging |
Het |
Pramel25 |
A |
T |
4: 143,520,479 (GRCm39) |
Y77F |
probably benign |
Het |
Prr27 |
A |
G |
5: 87,999,005 (GRCm39) |
|
probably benign |
Het |
Rbpms |
G |
A |
8: 34,296,864 (GRCm39) |
P138S |
probably damaging |
Het |
Rgs3 |
T |
C |
4: 62,564,910 (GRCm39) |
|
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Robo1 |
C |
T |
16: 72,798,839 (GRCm39) |
T933M |
probably benign |
Het |
Sinhcaf |
A |
G |
6: 148,832,163 (GRCm39) |
|
probably benign |
Het |
Steap4 |
T |
C |
5: 8,028,398 (GRCm39) |
|
probably benign |
Het |
Tenm3 |
T |
C |
8: 48,689,560 (GRCm39) |
Y2009C |
probably damaging |
Het |
Tnr |
A |
C |
1: 159,677,905 (GRCm39) |
T97P |
possibly damaging |
Het |
Topaz1 |
T |
A |
9: 122,620,542 (GRCm39) |
L1320* |
probably null |
Het |
Topaz1 |
A |
G |
9: 122,626,727 (GRCm39) |
M1452V |
probably benign |
Het |
Trank1 |
T |
G |
9: 111,219,509 (GRCm39) |
F2082C |
probably damaging |
Het |
Trim24 |
C |
A |
6: 37,935,494 (GRCm39) |
|
probably null |
Het |
Tspoap1 |
T |
A |
11: 87,668,066 (GRCm39) |
|
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,126,926 (GRCm39) |
L483P |
probably damaging |
Het |
Vmn2r2 |
T |
A |
3: 64,033,999 (GRCm39) |
T508S |
probably benign |
Het |
Vps18 |
C |
T |
2: 119,124,386 (GRCm39) |
R438C |
probably damaging |
Het |
Zfp366 |
C |
A |
13: 99,365,474 (GRCm39) |
R212S |
probably damaging |
Het |
Zkscan4 |
T |
A |
13: 21,665,477 (GRCm39) |
C122S |
probably damaging |
Het |
|
Other mutations in Rcc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02040:Rcc2
|
APN |
4 |
140,447,902 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02486:Rcc2
|
APN |
4 |
140,437,673 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4445001:Rcc2
|
UTSW |
4 |
140,448,460 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1856:Rcc2
|
UTSW |
4 |
140,447,915 (GRCm39) |
missense |
probably benign |
0.17 |
R2107:Rcc2
|
UTSW |
4 |
140,448,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Rcc2
|
UTSW |
4 |
140,444,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R4809:Rcc2
|
UTSW |
4 |
140,444,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Rcc2
|
UTSW |
4 |
140,444,977 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5229:Rcc2
|
UTSW |
4 |
140,444,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Rcc2
|
UTSW |
4 |
140,447,877 (GRCm39) |
nonsense |
probably null |
|
R5767:Rcc2
|
UTSW |
4 |
140,443,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R5840:Rcc2
|
UTSW |
4 |
140,439,449 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5909:Rcc2
|
UTSW |
4 |
140,444,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R6056:Rcc2
|
UTSW |
4 |
140,444,335 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6698:Rcc2
|
UTSW |
4 |
140,429,586 (GRCm39) |
missense |
probably benign |
0.00 |
R7086:Rcc2
|
UTSW |
4 |
140,435,280 (GRCm39) |
missense |
probably benign |
0.20 |
R7252:Rcc2
|
UTSW |
4 |
140,429,586 (GRCm39) |
missense |
probably benign |
0.00 |
R7393:Rcc2
|
UTSW |
4 |
140,444,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Rcc2
|
UTSW |
4 |
140,429,586 (GRCm39) |
missense |
probably benign |
0.00 |
R8055:Rcc2
|
UTSW |
4 |
140,429,586 (GRCm39) |
missense |
probably benign |
0.00 |
R8056:Rcc2
|
UTSW |
4 |
140,429,586 (GRCm39) |
missense |
probably benign |
0.00 |
R8057:Rcc2
|
UTSW |
4 |
140,429,586 (GRCm39) |
missense |
probably benign |
0.00 |
R8058:Rcc2
|
UTSW |
4 |
140,429,586 (GRCm39) |
missense |
probably benign |
0.00 |
R8501:Rcc2
|
UTSW |
4 |
140,443,237 (GRCm39) |
missense |
probably damaging |
0.97 |
R9200:Rcc2
|
UTSW |
4 |
140,445,664 (GRCm39) |
missense |
probably benign |
0.00 |
R9337:Rcc2
|
UTSW |
4 |
140,445,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R9380:Rcc2
|
UTSW |
4 |
140,429,702 (GRCm39) |
missense |
probably benign |
0.07 |
R9767:Rcc2
|
UTSW |
4 |
140,435,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|