Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
T |
A |
5: 88,120,438 (GRCm39) |
D398E |
possibly damaging |
Het |
Adam34 |
T |
C |
8: 44,105,303 (GRCm39) |
Y114C |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,004,896 (GRCm39) |
D156E |
probably benign |
Het |
Apba1 |
T |
A |
19: 23,889,825 (GRCm39) |
S408T |
probably benign |
Het |
Asb14 |
C |
T |
14: 26,625,412 (GRCm39) |
H256Y |
probably benign |
Het |
Atf6 |
A |
T |
1: 170,627,181 (GRCm39) |
|
probably null |
Het |
Atp6v1b2 |
T |
A |
8: 69,541,548 (GRCm39) |
V35E |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,255,289 (GRCm39) |
|
probably null |
Het |
Ccdc170 |
C |
A |
10: 4,432,597 (GRCm39) |
P12Q |
unknown |
Het |
Cdh23 |
C |
T |
10: 60,167,567 (GRCm39) |
E1810K |
probably damaging |
Het |
Cdo1 |
A |
T |
18: 46,853,475 (GRCm39) |
F94L |
probably damaging |
Het |
Cfap96 |
T |
G |
8: 46,409,474 (GRCm39) |
S282R |
probably damaging |
Het |
Chdh |
C |
T |
14: 29,758,809 (GRCm39) |
P585S |
possibly damaging |
Het |
Clasp2 |
A |
G |
9: 113,683,391 (GRCm39) |
N407S |
probably benign |
Het |
Clca3a1 |
T |
A |
3: 144,453,329 (GRCm39) |
S465C |
probably benign |
Het |
Clip2 |
C |
A |
5: 134,551,484 (GRCm39) |
V213L |
probably damaging |
Het |
Col6a6 |
A |
G |
9: 105,644,707 (GRCm39) |
S1194P |
probably damaging |
Het |
Cyp7a1 |
T |
C |
4: 6,268,463 (GRCm39) |
T421A |
possibly damaging |
Het |
Dhh |
C |
T |
15: 98,791,907 (GRCm39) |
G367E |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,326,796 (GRCm39) |
N2002D |
probably damaging |
Het |
Epn2 |
T |
A |
11: 61,437,528 (GRCm39) |
N15Y |
probably damaging |
Het |
Evi5 |
A |
C |
5: 107,936,147 (GRCm39) |
V647G |
probably benign |
Het |
Eya1 |
T |
C |
1: 14,353,424 (GRCm39) |
|
probably null |
Het |
Fam120a |
A |
G |
13: 49,102,589 (GRCm39) |
V222A |
probably benign |
Het |
Fastkd5 |
A |
T |
2: 130,457,864 (GRCm39) |
I242K |
possibly damaging |
Het |
Hnrnpul1 |
A |
G |
7: 25,450,319 (GRCm39) |
M131T |
probably benign |
Het |
Ice1 |
T |
C |
13: 70,744,283 (GRCm39) |
N2100S |
probably damaging |
Het |
Ifi205 |
T |
A |
1: 173,855,916 (GRCm39) |
D38V |
possibly damaging |
Het |
Klhl9 |
G |
A |
4: 88,639,843 (GRCm39) |
Q133* |
probably null |
Het |
Krt84 |
T |
C |
15: 101,436,924 (GRCm39) |
E370G |
probably benign |
Het |
Lrrc4c |
T |
C |
2: 97,459,410 (GRCm39) |
I12T |
probably benign |
Het |
Lrriq4 |
T |
A |
3: 30,709,850 (GRCm39) |
L398* |
probably null |
Het |
Ltf |
G |
A |
9: 110,855,198 (GRCm39) |
|
probably null |
Het |
Macf1 |
C |
T |
4: 123,366,101 (GRCm39) |
V1322I |
probably benign |
Het |
Mark2 |
T |
A |
19: 7,264,698 (GRCm39) |
I112L |
probably damaging |
Het |
Mettl25b |
A |
G |
3: 87,831,649 (GRCm39) |
|
probably null |
Het |
Mterf2 |
A |
T |
10: 84,956,527 (GRCm39) |
C32* |
probably null |
Het |
Myo3b |
C |
T |
2: 69,925,608 (GRCm39) |
T25I |
probably damaging |
Het |
Nsun7 |
A |
C |
5: 66,421,378 (GRCm39) |
I115L |
probably benign |
Het |
Olfm3 |
G |
A |
3: 114,883,805 (GRCm39) |
V36M |
probably damaging |
Het |
Or1p1c |
T |
C |
11: 74,160,428 (GRCm39) |
I71T |
possibly damaging |
Het |
Or5d44 |
T |
C |
2: 88,141,373 (GRCm39) |
T256A |
probably benign |
Het |
Or8b3 |
A |
T |
9: 38,314,965 (GRCm39) |
Y262F |
possibly damaging |
Het |
Or8g18 |
A |
T |
9: 39,148,983 (GRCm39) |
S246T |
possibly damaging |
Het |
Pcdhgb8 |
A |
T |
18: 37,896,962 (GRCm39) |
R677S |
probably benign |
Het |
Prrt4 |
A |
C |
6: 29,170,538 (GRCm39) |
L638R |
possibly damaging |
Het |
Ptk2 |
G |
A |
15: 73,093,658 (GRCm39) |
P854S |
possibly damaging |
Het |
Rab44 |
T |
C |
17: 29,359,438 (GRCm39) |
F542S |
unknown |
Het |
Rhobtb3 |
T |
A |
13: 76,020,513 (GRCm39) |
E596D |
probably benign |
Het |
Rpl36 |
T |
C |
17: 56,920,944 (GRCm39) |
I44T |
probably benign |
Het |
Rptor |
A |
G |
11: 119,737,762 (GRCm39) |
I112V |
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,993,813 (GRCm39) |
I611T |
probably damaging |
Het |
Slc12a4 |
G |
T |
8: 106,675,865 (GRCm39) |
N553K |
probably damaging |
Het |
Spata31d1d |
T |
A |
13: 59,876,046 (GRCm39) |
R496S |
probably benign |
Het |
Strbp |
T |
C |
2: 37,493,125 (GRCm39) |
D387G |
possibly damaging |
Het |
Tas2r107 |
A |
T |
6: 131,636,153 (GRCm39) |
C299S |
possibly damaging |
Het |
Tbc1d21 |
A |
T |
9: 58,274,134 (GRCm39) |
|
probably null |
Het |
Tdrd12 |
A |
T |
7: 35,180,471 (GRCm39) |
Y847* |
probably null |
Het |
Tlr2 |
A |
T |
3: 83,745,212 (GRCm39) |
N290K |
probably benign |
Het |
Tnks1bp1 |
C |
A |
2: 84,892,297 (GRCm39) |
H741Q |
probably benign |
Het |
Trpc6 |
G |
A |
9: 8,609,951 (GRCm39) |
V140M |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,641,932 (GRCm39) |
D13427G |
probably damaging |
Het |
Uba7 |
C |
A |
9: 107,853,371 (GRCm39) |
L106I |
possibly damaging |
Het |
Unc5b |
T |
G |
10: 60,614,587 (GRCm39) |
T237P |
probably damaging |
Het |
Vit |
A |
C |
17: 78,932,294 (GRCm39) |
D467A |
probably damaging |
Het |
Vmn1r103 |
T |
C |
7: 20,243,780 (GRCm39) |
Y227C |
possibly damaging |
Het |
Vmn1r77 |
T |
A |
7: 11,776,017 (GRCm39) |
Y196* |
probably null |
Het |
Zhx3 |
A |
G |
2: 160,622,898 (GRCm39) |
V423A |
probably damaging |
Het |
|
Other mutations in Tmppe |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01823:Tmppe
|
APN |
9 |
114,234,175 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02274:Tmppe
|
APN |
9 |
114,234,499 (GRCm39) |
missense |
probably benign |
|
IGL02349:Tmppe
|
APN |
9 |
114,234,268 (GRCm39) |
missense |
probably benign |
|
R0201:Tmppe
|
UTSW |
9 |
114,233,707 (GRCm39) |
frame shift |
probably null |
|
R1668:Tmppe
|
UTSW |
9 |
114,233,968 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2206:Tmppe
|
UTSW |
9 |
114,234,640 (GRCm39) |
missense |
probably benign |
|
R5026:Tmppe
|
UTSW |
9 |
114,234,887 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5054:Tmppe
|
UTSW |
9 |
114,235,026 (GRCm39) |
missense |
probably benign |
0.41 |
R5118:Tmppe
|
UTSW |
9 |
114,234,549 (GRCm39) |
missense |
probably benign |
0.02 |
R5623:Tmppe
|
UTSW |
9 |
114,234,964 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6307:Tmppe
|
UTSW |
9 |
114,233,812 (GRCm39) |
missense |
probably benign |
0.00 |
R6502:Tmppe
|
UTSW |
9 |
114,234,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R6597:Tmppe
|
UTSW |
9 |
114,234,312 (GRCm39) |
missense |
probably benign |
0.00 |
R6627:Tmppe
|
UTSW |
9 |
114,234,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:Tmppe
|
UTSW |
9 |
114,233,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Tmppe
|
UTSW |
9 |
114,234,591 (GRCm39) |
missense |
probably benign |
0.06 |
R7141:Tmppe
|
UTSW |
9 |
114,234,036 (GRCm39) |
missense |
probably benign |
0.00 |
R7642:Tmppe
|
UTSW |
9 |
114,233,862 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8894:Tmppe
|
UTSW |
9 |
114,230,260 (GRCm39) |
start gained |
probably benign |
|
R9101:Tmppe
|
UTSW |
9 |
114,234,309 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Tmppe
|
UTSW |
9 |
114,234,145 (GRCm39) |
missense |
probably benign |
0.01 |
|