Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
A |
10: 78,902,473 (GRCm39) |
K614N |
probably benign |
Het |
2610008E11Rik |
T |
G |
10: 78,902,474 (GRCm39) |
K614T |
probably benign |
Het |
Ahsa1 |
T |
A |
12: 87,317,116 (GRCm39) |
S120R |
probably benign |
Het |
Anapc16 |
G |
A |
10: 59,832,302 (GRCm39) |
T37I |
possibly damaging |
Het |
Arid2 |
C |
A |
15: 96,276,756 (GRCm39) |
P1606H |
probably damaging |
Het |
Ash1l |
TATCTCCTTTTCCAAAAA |
TA |
3: 88,890,764 (GRCm39) |
|
probably null |
Het |
Asic1 |
T |
A |
15: 99,569,968 (GRCm39) |
N96K |
probably damaging |
Het |
Asph |
A |
T |
4: 9,484,575 (GRCm39) |
D582E |
probably benign |
Het |
Astn1 |
A |
G |
1: 158,400,557 (GRCm39) |
D528G |
probably damaging |
Het |
Atp9b |
A |
G |
18: 80,952,871 (GRCm39) |
V164A |
|
Het |
Cbx6 |
C |
T |
15: 79,712,866 (GRCm39) |
G187D |
possibly damaging |
Het |
Clca4a |
A |
T |
3: 144,667,651 (GRCm39) |
L440* |
probably null |
Het |
Crybg2 |
A |
T |
4: 133,792,754 (GRCm39) |
I130F |
probably benign |
Het |
Crybg3 |
T |
C |
16: 59,357,167 (GRCm39) |
E798G |
probably damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,480,995 (GRCm39) |
E81G |
possibly damaging |
Het |
Cwc22 |
C |
T |
2: 77,759,822 (GRCm39) |
R75H |
possibly damaging |
Het |
Cym |
T |
G |
3: 107,121,530 (GRCm39) |
D254A |
probably damaging |
Het |
Dcaf11 |
T |
A |
14: 55,806,383 (GRCm39) |
|
probably null |
Het |
Dctn1 |
A |
T |
6: 83,157,026 (GRCm39) |
|
probably null |
Het |
Dennd5a |
C |
T |
7: 109,495,449 (GRCm39) |
|
probably null |
Het |
Dmpk |
T |
A |
7: 18,821,232 (GRCm39) |
C217S |
probably damaging |
Het |
Dnah1 |
C |
A |
14: 31,008,033 (GRCm39) |
V2125L |
probably benign |
Het |
Exoc4 |
G |
A |
6: 33,415,408 (GRCm39) |
A427T |
probably benign |
Het |
Farp2 |
G |
T |
1: 93,548,956 (GRCm39) |
V1021F |
probably damaging |
Het |
Flg2 |
T |
C |
3: 93,127,069 (GRCm39) |
S1994P |
unknown |
Het |
Fmnl1 |
T |
C |
11: 103,072,610 (GRCm39) |
|
probably null |
Het |
Frem2 |
T |
A |
3: 53,479,760 (GRCm39) |
I1978F |
possibly damaging |
Het |
Gan |
T |
A |
8: 117,913,969 (GRCm39) |
C122* |
probably null |
Het |
Gpr25 |
T |
A |
1: 136,188,559 (GRCm39) |
Y18F |
probably damaging |
Het |
Hoxa7 |
C |
T |
6: 52,192,720 (GRCm39) |
E223K |
probably benign |
Het |
Hypk |
A |
G |
2: 121,283,961 (GRCm39) |
|
probably null |
Het |
Ibsp |
A |
T |
5: 104,450,172 (GRCm39) |
K27* |
probably null |
Het |
Ighv6-5 |
T |
A |
12: 114,380,395 (GRCm39) |
T41S |
probably benign |
Het |
Ighv9-4 |
T |
C |
12: 114,263,757 (GRCm39) |
M59V |
probably benign |
Het |
Il17rb |
T |
C |
14: 29,718,828 (GRCm39) |
D418G |
probably damaging |
Het |
Ints5 |
T |
A |
19: 8,872,923 (GRCm39) |
V294E |
probably damaging |
Het |
Irx6 |
G |
A |
8: 93,405,041 (GRCm39) |
C303Y |
probably damaging |
Het |
Itih3 |
T |
A |
14: 30,639,655 (GRCm39) |
I389F |
probably damaging |
Het |
Lama1 |
C |
T |
17: 68,089,141 (GRCm39) |
T1604I |
|
Het |
Lama3 |
C |
A |
18: 12,672,843 (GRCm39) |
Q873K |
probably benign |
Het |
Lhx1 |
T |
G |
11: 84,410,746 (GRCm39) |
S284R |
probably benign |
Het |
Lrba |
T |
A |
3: 86,302,238 (GRCm39) |
|
probably null |
Het |
Lrg1 |
C |
T |
17: 56,427,592 (GRCm39) |
G127R |
possibly damaging |
Het |
Macir |
G |
A |
1: 97,573,645 (GRCm39) |
P140L |
probably benign |
Het |
Mapre1 |
T |
A |
2: 153,606,883 (GRCm39) |
L205H |
probably benign |
Het |
Meltf |
A |
G |
16: 31,711,617 (GRCm39) |
N581S |
probably damaging |
Het |
Mgat5 |
A |
C |
1: 127,292,926 (GRCm39) |
M149L |
probably benign |
Het |
Myh1 |
A |
G |
11: 67,093,412 (GRCm39) |
T168A |
probably benign |
Het |
Naalad2 |
C |
T |
9: 18,238,673 (GRCm39) |
V681I |
probably benign |
Het |
Or51e2 |
A |
G |
7: 102,391,524 (GRCm39) |
S229P |
probably damaging |
Het |
Or52r1c |
T |
A |
7: 102,735,205 (GRCm39) |
L155Q |
probably damaging |
Het |
Pcnx2 |
T |
C |
8: 126,528,243 (GRCm39) |
T1326A |
probably benign |
Het |
Peg3 |
A |
T |
7: 6,711,944 (GRCm39) |
C1093S |
probably damaging |
Het |
Pidd1 |
T |
C |
7: 141,019,813 (GRCm39) |
S650G |
probably benign |
Het |
Pik3c2b |
T |
C |
1: 133,017,972 (GRCm39) |
S945P |
possibly damaging |
Het |
Plec |
T |
C |
15: 76,060,227 (GRCm39) |
T3237A |
possibly damaging |
Het |
Prpf3 |
A |
T |
3: 95,741,052 (GRCm39) |
|
probably null |
Het |
Prpf4b |
C |
A |
13: 35,085,477 (GRCm39) |
H974Q |
probably benign |
Het |
Ptpn3 |
T |
C |
4: 57,225,863 (GRCm39) |
T451A |
probably benign |
Het |
Ptprs |
A |
G |
17: 56,724,429 (GRCm39) |
Y1577H |
probably damaging |
Het |
Rgr |
C |
T |
14: 36,770,882 (GRCm39) |
M1I |
probably null |
Het |
Rxrg |
A |
T |
1: 167,458,678 (GRCm39) |
N257I |
probably benign |
Het |
Sbno2 |
T |
C |
10: 79,922,146 (GRCm39) |
D9G |
probably damaging |
Het |
Scd1 |
T |
C |
19: 44,395,034 (GRCm39) |
K64E |
probably damaging |
Het |
Serpinb1a |
T |
A |
13: 33,034,308 (GRCm39) |
I28F |
possibly damaging |
Het |
Sfmbt2 |
A |
T |
2: 10,406,818 (GRCm39) |
E39V |
probably damaging |
Het |
Slc29a1 |
A |
G |
17: 45,900,897 (GRCm39) |
M89T |
possibly damaging |
Het |
Slco4a1 |
T |
A |
2: 180,113,856 (GRCm39) |
V431E |
possibly damaging |
Het |
Smg1 |
C |
T |
7: 117,752,131 (GRCm39) |
C2698Y |
unknown |
Het |
Sptlc2 |
C |
T |
12: 87,397,151 (GRCm39) |
D212N |
probably benign |
Het |
St6galnac1 |
T |
C |
11: 116,657,899 (GRCm39) |
T334A |
possibly damaging |
Het |
Stim2 |
A |
T |
5: 54,156,263 (GRCm39) |
D13V |
possibly damaging |
Het |
Syne1 |
A |
G |
10: 5,181,592 (GRCm39) |
W4248R |
probably damaging |
Het |
Tanc1 |
T |
C |
2: 59,627,953 (GRCm39) |
Y584H |
probably benign |
Het |
Thoc6 |
C |
A |
17: 23,892,634 (GRCm39) |
|
probably null |
Het |
Trim30a |
T |
A |
7: 104,078,533 (GRCm39) |
N181I |
possibly damaging |
Het |
Trip11 |
T |
A |
12: 101,850,329 (GRCm39) |
Q1245L |
probably damaging |
Het |
Tshz3 |
A |
G |
7: 36,469,994 (GRCm39) |
D661G |
probably benign |
Het |
Ttll8 |
C |
A |
15: 88,799,630 (GRCm39) |
V604L |
probably damaging |
Het |
Ubtfl1 |
A |
G |
9: 18,320,931 (GRCm39) |
D153G |
probably damaging |
Het |
Ufsp2 |
C |
A |
8: 46,436,661 (GRCm39) |
N137K |
probably benign |
Het |
Ugt2a3 |
A |
G |
5: 87,473,393 (GRCm39) |
I508T |
possibly damaging |
Het |
Uso1 |
G |
A |
5: 92,306,324 (GRCm39) |
E94K |
probably benign |
Het |
Usp54 |
A |
G |
14: 20,611,310 (GRCm39) |
S1169P |
probably benign |
Het |
Vmn1r235 |
C |
T |
17: 21,482,292 (GRCm39) |
P206S |
probably benign |
Het |
Vmn1r69 |
T |
C |
7: 10,314,995 (GRCm39) |
|
probably benign |
Het |
Zfp263 |
T |
A |
16: 3,567,255 (GRCm39) |
C523* |
probably null |
Het |
Zfp799 |
G |
T |
17: 33,039,210 (GRCm39) |
T352K |
probably benign |
Het |
Zfr |
T |
A |
15: 12,180,724 (GRCm39) |
V951E |
probably damaging |
Het |
Zfyve26 |
T |
C |
12: 79,330,926 (GRCm39) |
D431G |
probably benign |
Het |
Zswim9 |
C |
A |
7: 12,993,664 (GRCm39) |
A831S |
probably damaging |
Het |
|
Other mutations in Cct7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02223:Cct7
|
APN |
6 |
85,439,023 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02292:Cct7
|
APN |
6 |
85,438,091 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02724:Cct7
|
APN |
6 |
85,436,131 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02740:Cct7
|
APN |
6 |
85,445,252 (GRCm39) |
missense |
probably benign |
|
PIT4495001:Cct7
|
UTSW |
6 |
85,436,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Cct7
|
UTSW |
6 |
85,438,536 (GRCm39) |
missense |
probably null |
0.55 |
R1363:Cct7
|
UTSW |
6 |
85,443,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1378:Cct7
|
UTSW |
6 |
85,444,545 (GRCm39) |
splice site |
probably null |
|
R2076:Cct7
|
UTSW |
6 |
85,445,122 (GRCm39) |
missense |
probably damaging |
0.98 |
R2210:Cct7
|
UTSW |
6 |
85,436,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R3905:Cct7
|
UTSW |
6 |
85,443,690 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4298:Cct7
|
UTSW |
6 |
85,445,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R4422:Cct7
|
UTSW |
6 |
85,444,127 (GRCm39) |
missense |
probably damaging |
0.98 |
R6519:Cct7
|
UTSW |
6 |
85,439,132 (GRCm39) |
missense |
probably benign |
0.19 |
R6903:Cct7
|
UTSW |
6 |
85,443,675 (GRCm39) |
missense |
probably benign |
0.27 |
R6925:Cct7
|
UTSW |
6 |
85,436,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R7458:Cct7
|
UTSW |
6 |
85,436,978 (GRCm39) |
missense |
probably benign |
0.14 |
R8133:Cct7
|
UTSW |
6 |
85,438,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Cct7
|
UTSW |
6 |
85,444,625 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1177:Cct7
|
UTSW |
6 |
85,443,651 (GRCm39) |
missense |
possibly damaging |
0.91 |
|