Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
T |
G |
16: 20,368,484 (GRCm39) |
|
probably null |
Het |
Acap1 |
C |
A |
11: 69,776,343 (GRCm39) |
V219L |
probably benign |
Het |
Arpp21 |
G |
A |
9: 111,955,550 (GRCm39) |
P530S |
probably damaging |
Het |
Atp6v1b1 |
T |
C |
6: 83,731,792 (GRCm39) |
V224A |
probably damaging |
Het |
Brd3 |
T |
C |
2: 27,344,371 (GRCm39) |
D453G |
probably damaging |
Het |
Btbd10 |
A |
T |
7: 112,951,150 (GRCm39) |
|
probably null |
Het |
Ccdc148 |
T |
C |
2: 58,713,657 (GRCm39) |
H498R |
probably damaging |
Het |
Cga |
A |
T |
4: 34,905,171 (GRCm39) |
Y65F |
possibly damaging |
Het |
Chd7 |
A |
T |
4: 8,856,797 (GRCm39) |
H136L |
probably damaging |
Het |
Chit1 |
T |
C |
1: 134,071,022 (GRCm39) |
Y34H |
probably damaging |
Het |
Cimap2 |
C |
G |
4: 106,467,596 (GRCm39) |
|
probably null |
Het |
Dapk2 |
C |
G |
9: 66,161,904 (GRCm39) |
R271G |
probably benign |
Het |
Dnhd1 |
T |
G |
7: 105,362,895 (GRCm39) |
V3819G |
probably damaging |
Het |
Dsg3 |
A |
T |
18: 20,658,216 (GRCm39) |
I276F |
possibly damaging |
Het |
Dusp1 |
T |
C |
17: 26,726,577 (GRCm39) |
S162G |
probably benign |
Het |
Entrep1 |
A |
T |
19: 23,962,082 (GRCm39) |
M307K |
possibly damaging |
Het |
Gga2 |
C |
A |
7: 121,598,111 (GRCm39) |
A328S |
probably benign |
Het |
Gpr183 |
A |
G |
14: 122,191,897 (GRCm39) |
I208T |
possibly damaging |
Het |
Haspin |
T |
C |
11: 73,026,971 (GRCm39) |
D706G |
possibly damaging |
Het |
Hdac5 |
T |
C |
11: 102,095,786 (GRCm39) |
I338V |
probably benign |
Het |
Ik |
C |
T |
18: 36,886,613 (GRCm39) |
R362C |
probably damaging |
Het |
Kdm4c |
T |
G |
4: 74,275,587 (GRCm39) |
C754W |
probably damaging |
Het |
Limk1 |
T |
A |
5: 134,699,332 (GRCm39) |
I142F |
possibly damaging |
Het |
Mccc2 |
T |
C |
13: 100,104,234 (GRCm39) |
E305G |
probably benign |
Het |
Mdm1 |
A |
G |
10: 118,003,962 (GRCm39) |
D639G |
probably damaging |
Het |
Mefv |
T |
G |
16: 3,528,744 (GRCm39) |
T566P |
probably damaging |
Het |
Mep1b |
G |
A |
18: 21,221,727 (GRCm39) |
V226I |
probably benign |
Het |
Mgmt |
T |
C |
7: 136,553,064 (GRCm39) |
M19T |
probably benign |
Het |
Mrgpra6 |
A |
T |
7: 46,835,693 (GRCm39) |
S243T |
probably benign |
Het |
Myh7 |
C |
T |
14: 55,229,197 (GRCm39) |
R169Q |
probably damaging |
Het |
Myo1b |
T |
C |
1: 51,801,668 (GRCm39) |
I917V |
probably damaging |
Het |
Or4a80 |
A |
T |
2: 89,582,971 (GRCm39) |
M67K |
possibly damaging |
Het |
Phlpp1 |
T |
C |
1: 106,100,209 (GRCm39) |
L159P |
probably benign |
Het |
Plekhh3 |
T |
C |
11: 101,056,482 (GRCm39) |
E371G |
probably damaging |
Het |
Rps6ka2 |
C |
A |
17: 7,495,377 (GRCm39) |
D21E |
probably benign |
Het |
Slc47a1 |
T |
A |
11: 61,235,280 (GRCm39) |
M518L |
probably benign |
Het |
Slitrk6 |
T |
C |
14: 110,987,974 (GRCm39) |
T578A |
probably benign |
Het |
Syne2 |
A |
T |
12: 75,974,205 (GRCm39) |
K1133N |
possibly damaging |
Het |
Taco1 |
T |
C |
11: 105,963,942 (GRCm39) |
S234P |
probably benign |
Het |
Trpv4 |
G |
A |
5: 114,771,263 (GRCm39) |
S422F |
probably damaging |
Het |
Vmn1r37 |
A |
T |
6: 66,708,523 (GRCm39) |
I13L |
probably benign |
Het |
Vrk2 |
T |
A |
11: 26,485,597 (GRCm39) |
K130N |
probably damaging |
Het |
Wdfy4 |
C |
T |
14: 32,681,923 (GRCm39) |
R3016Q |
probably damaging |
Het |
Zfp383 |
T |
C |
7: 29,614,380 (GRCm39) |
S212P |
probably benign |
Het |
|
Other mutations in Tvp23b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00863:Tvp23b
|
APN |
11 |
62,774,464 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00901:Tvp23b
|
APN |
11 |
62,774,606 (GRCm39) |
splice site |
probably benign |
|
IGL02004:Tvp23b
|
APN |
11 |
62,782,826 (GRCm39) |
missense |
probably damaging |
1.00 |
Chipotle
|
UTSW |
11 |
62,770,424 (GRCm39) |
splice site |
probably null |
|
R0117:Tvp23b
|
UTSW |
11 |
62,770,430 (GRCm39) |
unclassified |
probably benign |
|
R3838:Tvp23b
|
UTSW |
11 |
62,774,455 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4596:Tvp23b
|
UTSW |
11 |
62,774,544 (GRCm39) |
missense |
probably benign |
|
R4840:Tvp23b
|
UTSW |
11 |
62,770,424 (GRCm39) |
splice site |
probably null |
|
R7499:Tvp23b
|
UTSW |
11 |
62,770,289 (GRCm39) |
unclassified |
probably benign |
|
R7516:Tvp23b
|
UTSW |
11 |
62,782,867 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8511:Tvp23b
|
UTSW |
11 |
62,774,563 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9206:Tvp23b
|
UTSW |
11 |
62,772,842 (GRCm39) |
missense |
possibly damaging |
0.49 |
Z1186:Tvp23b
|
UTSW |
11 |
62,772,769 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1187:Tvp23b
|
UTSW |
11 |
62,772,769 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1188:Tvp23b
|
UTSW |
11 |
62,772,769 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1189:Tvp23b
|
UTSW |
11 |
62,772,769 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1190:Tvp23b
|
UTSW |
11 |
62,772,769 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1191:Tvp23b
|
UTSW |
11 |
62,772,769 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1192:Tvp23b
|
UTSW |
11 |
62,772,769 (GRCm39) |
missense |
possibly damaging |
0.77 |
|