Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd3 |
T |
C |
18: 10,645,121 (GRCm39) |
D391G |
probably benign |
Het |
Arhgdia |
A |
C |
11: 120,470,068 (GRCm39) |
W202G |
probably damaging |
Het |
Atp2a3 |
A |
T |
11: 72,871,131 (GRCm39) |
D575V |
probably benign |
Het |
Cep350 |
C |
A |
1: 155,744,457 (GRCm39) |
V2121L |
probably benign |
Het |
Clcn2 |
CCCGCCGCCGCCGCCGC |
CCCGCCGCCGCCGC |
16: 20,534,702 (GRCm39) |
|
probably benign |
Het |
Cldn9 |
A |
T |
17: 23,902,556 (GRCm39) |
V23E |
probably damaging |
Het |
Cltc |
G |
A |
11: 86,593,237 (GRCm39) |
S1542F |
probably benign |
Het |
Cmbl |
A |
G |
15: 31,589,948 (GRCm39) |
D226G |
probably damaging |
Het |
Dennd4b |
C |
T |
3: 90,178,515 (GRCm39) |
T537I |
probably damaging |
Het |
Dnah7b |
C |
A |
1: 46,165,953 (GRCm39) |
D539E |
possibly damaging |
Het |
Fam219a |
T |
C |
4: 41,521,871 (GRCm39) |
T70A |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,942,571 (GRCm39) |
V488E |
possibly damaging |
Het |
Gm3336 |
A |
G |
8: 71,174,740 (GRCm39) |
*96W |
probably null |
Het |
Hectd1 |
A |
G |
12: 51,832,584 (GRCm39) |
I930T |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,506,053 (GRCm39) |
C3824* |
probably null |
Het |
Ift140 |
T |
C |
17: 25,254,758 (GRCm39) |
F413L |
probably benign |
Het |
Itfg1 |
A |
G |
8: 86,565,566 (GRCm39) |
V90A |
probably benign |
Het |
Jph4 |
A |
T |
14: 55,351,090 (GRCm39) |
W309R |
probably damaging |
Het |
Kdm2a |
C |
T |
19: 4,393,141 (GRCm39) |
D405N |
|
Het |
Klhl5 |
T |
C |
5: 65,305,939 (GRCm39) |
F302S |
probably damaging |
Het |
Klk1b8 |
T |
C |
7: 43,453,177 (GRCm39) |
M256T |
probably benign |
Het |
Klre1 |
A |
T |
6: 129,559,368 (GRCm39) |
R99S |
probably benign |
Het |
Krt79 |
T |
C |
15: 101,839,904 (GRCm39) |
T364A |
probably benign |
Het |
Lin7a |
C |
T |
10: 107,218,483 (GRCm39) |
P131L |
possibly damaging |
Het |
Lrrc49 |
A |
G |
9: 60,594,699 (GRCm39) |
Y9H |
probably benign |
Het |
Lrrc8a |
T |
A |
2: 30,145,663 (GRCm39) |
I159N |
probably damaging |
Het |
Mdga2 |
T |
C |
12: 66,615,532 (GRCm39) |
S692G |
probably benign |
Het |
Myo15a |
G |
A |
11: 60,392,668 (GRCm39) |
V1017M |
|
Het |
Nol4 |
T |
C |
18: 23,172,897 (GRCm39) |
D68G |
probably benign |
Het |
Or4f53 |
T |
C |
2: 111,088,348 (GRCm39) |
V296A |
probably benign |
Het |
Or6c75 |
T |
C |
10: 129,337,515 (GRCm39) |
V254A |
probably damaging |
Het |
Pigw |
C |
A |
11: 84,768,040 (GRCm39) |
A430S |
probably benign |
Het |
Pla2g4c |
T |
C |
7: 13,077,900 (GRCm39) |
L356P |
probably damaging |
Het |
Prorp |
T |
C |
12: 55,385,015 (GRCm39) |
V410A |
probably damaging |
Het |
Prr5 |
A |
G |
15: 84,585,682 (GRCm39) |
T226A |
probably benign |
Het |
Pygo1 |
C |
T |
9: 72,833,056 (GRCm39) |
|
probably benign |
Het |
Rnf214 |
A |
G |
9: 45,779,286 (GRCm39) |
I333T |
possibly damaging |
Het |
Septin3 |
A |
G |
15: 82,167,352 (GRCm39) |
I86V |
probably benign |
Het |
Slc30a3 |
AGGGCTTACCTGAGCGG |
AGG |
5: 31,246,889 (GRCm39) |
|
probably null |
Het |
Socs5 |
C |
A |
17: 87,442,266 (GRCm39) |
T402K |
probably damaging |
Het |
Speer3 |
T |
A |
5: 13,846,368 (GRCm39) |
N229K |
|
Het |
Stk16 |
T |
C |
1: 75,187,804 (GRCm39) |
|
probably benign |
Het |
Tmprss2 |
C |
T |
16: 97,392,669 (GRCm39) |
V93I |
probably benign |
Het |
Tnpo2 |
G |
A |
8: 85,774,015 (GRCm39) |
E350K |
probably benign |
Het |
Tor1aip2 |
C |
T |
1: 155,937,525 (GRCm39) |
P87S |
possibly damaging |
Het |
Trgv7 |
A |
T |
13: 19,362,385 (GRCm39) |
R25* |
probably null |
Het |
Ush2a |
A |
G |
1: 188,558,589 (GRCm39) |
E3606G |
probably benign |
Het |
Zeb1 |
C |
T |
18: 5,766,709 (GRCm39) |
Q407* |
probably null |
Het |
Zfp609 |
A |
G |
9: 65,611,125 (GRCm39) |
S613P |
|
Het |
Zfp735 |
A |
G |
11: 73,602,403 (GRCm39) |
N449S |
possibly damaging |
Het |
|
Other mutations in Taar7d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01719:Taar7d
|
APN |
10 |
23,903,865 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02070:Taar7d
|
APN |
10 |
23,904,152 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02280:Taar7d
|
APN |
10 |
23,904,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02525:Taar7d
|
APN |
10 |
23,903,994 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03115:Taar7d
|
APN |
10 |
23,903,539 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03339:Taar7d
|
APN |
10 |
23,903,204 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1509:Taar7d
|
UTSW |
10 |
23,904,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R1826:Taar7d
|
UTSW |
10 |
23,903,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R2016:Taar7d
|
UTSW |
10 |
23,903,642 (GRCm39) |
missense |
probably benign |
0.11 |
R2051:Taar7d
|
UTSW |
10 |
23,903,904 (GRCm39) |
missense |
probably benign |
0.00 |
R6075:Taar7d
|
UTSW |
10 |
23,903,558 (GRCm39) |
missense |
probably benign |
0.21 |
R6541:Taar7d
|
UTSW |
10 |
23,904,129 (GRCm39) |
missense |
probably benign |
0.01 |
R8165:Taar7d
|
UTSW |
10 |
23,903,495 (GRCm39) |
missense |
probably benign |
0.07 |
R9222:Taar7d
|
UTSW |
10 |
23,904,124 (GRCm39) |
missense |
probably benign |
0.08 |
R9481:Taar7d
|
UTSW |
10 |
23,903,739 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Taar7d
|
UTSW |
10 |
23,903,906 (GRCm39) |
missense |
probably damaging |
1.00 |
|