Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
A |
G |
11: 109,982,439 (GRCm39) |
M1T |
probably null |
Het |
Abhd2 |
T |
A |
7: 78,975,194 (GRCm39) |
M128K |
probably benign |
Het |
Adamts12 |
A |
G |
15: 11,317,298 (GRCm39) |
T1333A |
possibly damaging |
Het |
Alg8 |
A |
G |
7: 97,040,131 (GRCm39) |
T438A |
probably benign |
Het |
Ccn3 |
G |
T |
15: 54,609,734 (GRCm39) |
S78I |
possibly damaging |
Het |
Cebpa |
A |
G |
7: 34,819,867 (GRCm39) |
I342V |
possibly damaging |
Het |
Chd9 |
T |
C |
8: 91,778,326 (GRCm39) |
M2779T |
probably damaging |
Het |
Cnot3 |
C |
A |
7: 3,661,221 (GRCm39) |
P577T |
probably benign |
Het |
Col17a1 |
T |
C |
19: 47,649,556 (GRCm39) |
D755G |
probably damaging |
Het |
Col5a3 |
A |
G |
9: 20,685,347 (GRCm39) |
V1443A |
unknown |
Het |
Crygs |
C |
T |
16: 22,624,082 (GRCm39) |
R175H |
probably damaging |
Het |
Fam193a |
A |
G |
5: 34,619,430 (GRCm39) |
D1031G |
probably damaging |
Het |
Fam83b |
T |
A |
9: 76,399,267 (GRCm39) |
H612L |
probably benign |
Het |
Gabrr2 |
A |
G |
4: 33,081,410 (GRCm39) |
T149A |
probably damaging |
Het |
Gm3667 |
T |
C |
14: 18,269,663 (GRCm39) |
N156D |
probably benign |
Het |
Hpcal1 |
T |
A |
12: 17,841,171 (GRCm39) |
L183Q |
probably damaging |
Het |
Ilf2 |
G |
T |
3: 90,394,777 (GRCm39) |
E342* |
probably null |
Het |
Ints13 |
A |
G |
6: 146,452,264 (GRCm39) |
S652P |
probably damaging |
Het |
Klhl6 |
T |
C |
16: 19,768,201 (GRCm39) |
E448G |
probably null |
Het |
Mmp14 |
A |
G |
14: 54,673,707 (GRCm39) |
I124V |
probably benign |
Het |
Morc2b |
A |
T |
17: 33,354,747 (GRCm39) |
D1008E |
probably benign |
Het |
Muc16 |
A |
C |
9: 18,554,767 (GRCm39) |
V3842G |
unknown |
Het |
Myo9b |
A |
T |
8: 71,807,405 (GRCm39) |
I1614F |
probably benign |
Het |
Nipa1 |
A |
T |
7: 55,629,547 (GRCm39) |
C189S |
probably damaging |
Het |
Ntn4 |
T |
C |
10: 93,480,335 (GRCm39) |
|
probably benign |
Het |
Or12k5 |
A |
G |
2: 36,894,972 (GRCm39) |
I218T |
probably benign |
Het |
Or2t29 |
A |
G |
11: 58,433,624 (GRCm39) |
L239P |
probably damaging |
Het |
Or3a4 |
A |
C |
11: 73,944,982 (GRCm39) |
L201R |
probably damaging |
Het |
Or4x13 |
A |
T |
2: 90,231,395 (GRCm39) |
Y130F |
probably damaging |
Het |
Or8g17 |
T |
G |
9: 38,930,349 (GRCm39) |
I163L |
probably benign |
Het |
Pank1 |
T |
A |
19: 34,791,096 (GRCm39) |
H528L |
probably damaging |
Het |
Pappa2 |
A |
T |
1: 158,589,131 (GRCm39) |
L1698* |
probably null |
Het |
Park7 |
A |
G |
4: 150,988,341 (GRCm39) |
S85P |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,564,408 (GRCm39) |
D1334G |
probably damaging |
Het |
Pira1 |
C |
G |
7: 3,740,319 (GRCm39) |
A301P |
probably damaging |
Het |
Rapgef2 |
T |
C |
3: 79,122,276 (GRCm39) |
E30G |
probably benign |
Het |
Rhbdf1 |
A |
G |
11: 32,160,523 (GRCm39) |
F676L |
probably damaging |
Het |
Rsf1 |
GGC |
GGCCACGGCAGC |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Scd4 |
G |
T |
19: 44,329,687 (GRCm39) |
M219I |
probably benign |
Het |
Slfn5 |
T |
A |
11: 82,847,613 (GRCm39) |
I166N |
probably benign |
Het |
Smim22 |
A |
T |
16: 4,826,089 (GRCm39) |
D85V |
probably damaging |
Het |
Socs2 |
T |
C |
10: 95,250,812 (GRCm39) |
E7G |
probably benign |
Het |
Thumpd2 |
T |
C |
17: 81,334,157 (GRCm39) |
E477G |
probably benign |
Het |
Tlr12 |
C |
T |
4: 128,510,483 (GRCm39) |
G589D |
probably benign |
Het |
Ttn |
A |
T |
2: 76,595,199 (GRCm39) |
I20317K |
probably damaging |
Het |
Ttyh2 |
A |
G |
11: 114,599,690 (GRCm39) |
|
probably null |
Het |
Ugt2a3 |
T |
A |
5: 87,475,050 (GRCm39) |
D398V |
probably damaging |
Het |
Vmn2r88 |
A |
T |
14: 51,650,589 (GRCm39) |
M101L |
|
Het |
Vmn2r93 |
A |
T |
17: 18,545,954 (GRCm39) |
R609* |
probably null |
Het |
Zfp473 |
C |
T |
7: 44,381,916 (GRCm39) |
E806K |
probably damaging |
Het |
Zfp93 |
T |
C |
7: 23,974,999 (GRCm39) |
L328P |
probably damaging |
Het |
|
Other mutations in Kansl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00822:Kansl2
|
APN |
15 |
98,426,734 (GRCm39) |
splice site |
probably benign |
|
IGL02167:Kansl2
|
APN |
15 |
98,431,396 (GRCm39) |
splice site |
probably benign |
|
IGL02349:Kansl2
|
APN |
15 |
98,427,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Kansl2
|
UTSW |
15 |
98,418,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R1128:Kansl2
|
UTSW |
15 |
98,431,566 (GRCm39) |
nonsense |
probably null |
|
R1129:Kansl2
|
UTSW |
15 |
98,431,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R1311:Kansl2
|
UTSW |
15 |
98,426,797 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2132:Kansl2
|
UTSW |
15 |
98,427,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R2144:Kansl2
|
UTSW |
15 |
98,424,512 (GRCm39) |
missense |
probably benign |
0.00 |
R2232:Kansl2
|
UTSW |
15 |
98,422,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Kansl2
|
UTSW |
15 |
98,426,742 (GRCm39) |
critical splice donor site |
probably null |
|
R3433:Kansl2
|
UTSW |
15 |
98,426,742 (GRCm39) |
critical splice donor site |
probably null |
|
R4125:Kansl2
|
UTSW |
15 |
98,429,636 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4818:Kansl2
|
UTSW |
15 |
98,424,542 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4906:Kansl2
|
UTSW |
15 |
98,429,771 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4962:Kansl2
|
UTSW |
15 |
98,429,724 (GRCm39) |
missense |
probably benign |
0.01 |
R5973:Kansl2
|
UTSW |
15 |
98,427,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Kansl2
|
UTSW |
15 |
98,418,197 (GRCm39) |
critical splice donor site |
probably null |
|
R6077:Kansl2
|
UTSW |
15 |
98,429,312 (GRCm39) |
missense |
probably benign |
0.08 |
R6657:Kansl2
|
UTSW |
15 |
98,422,551 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7168:Kansl2
|
UTSW |
15 |
98,427,425 (GRCm39) |
splice site |
probably null |
|
R7418:Kansl2
|
UTSW |
15 |
98,429,775 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7530:Kansl2
|
UTSW |
15 |
98,426,896 (GRCm39) |
missense |
probably benign |
0.01 |
|