Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
A |
G |
4: 144,400,361 (GRCm39) |
V139A |
probably benign |
Het |
Aass |
A |
T |
6: 23,097,195 (GRCm39) |
Y41* |
probably null |
Het |
AI429214 |
G |
A |
8: 37,461,268 (GRCm39) |
V139I |
probably benign |
Het |
Cacna1a |
G |
A |
8: 85,365,426 (GRCm39) |
A2190T |
probably benign |
Het |
Cstpp1 |
A |
G |
2: 91,107,343 (GRCm39) |
Y320H |
probably benign |
Het |
Cutc |
T |
C |
19: 43,744,113 (GRCm39) |
V38A |
probably benign |
Het |
Cxcl10 |
G |
T |
5: 92,495,230 (GRCm39) |
P98H |
probably damaging |
Het |
Dop1a |
T |
C |
9: 86,396,003 (GRCm39) |
S822P |
possibly damaging |
Het |
Dusp19 |
T |
C |
2: 80,454,631 (GRCm39) |
L117P |
probably damaging |
Het |
Emc3 |
A |
G |
6: 113,492,868 (GRCm39) |
F261S |
probably damaging |
Het |
Ephx2 |
T |
C |
14: 66,344,725 (GRCm39) |
T200A |
probably benign |
Het |
Eri1 |
A |
C |
8: 35,945,792 (GRCm39) |
D164E |
probably damaging |
Het |
Ethe1 |
T |
C |
7: 24,305,727 (GRCm39) |
I158T |
probably damaging |
Het |
Fancm |
C |
T |
12: 65,167,331 (GRCm39) |
R1547C |
probably damaging |
Het |
Fer1l4 |
T |
A |
2: 155,890,143 (GRCm39) |
T261S |
probably damaging |
Het |
Fyb2 |
A |
G |
4: 104,802,652 (GRCm39) |
R185G |
probably benign |
Het |
Gabrp |
A |
T |
11: 33,504,464 (GRCm39) |
S284T |
possibly damaging |
Het |
Gga2 |
G |
A |
7: 121,590,845 (GRCm39) |
R488* |
probably null |
Het |
Gm9758 |
A |
G |
5: 14,962,230 (GRCm39) |
L126S |
probably damaging |
Het |
Gse1 |
T |
C |
8: 121,294,542 (GRCm39) |
F290L |
probably damaging |
Het |
Hdgfl1 |
A |
G |
13: 26,954,068 (GRCm39) |
S2P |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,499 (GRCm39) |
S206F |
probably damaging |
Het |
Huwe1 |
A |
G |
X: 150,669,993 (GRCm39) |
K1482R |
probably benign |
Het |
Lama2 |
A |
T |
10: 27,063,869 (GRCm39) |
W1307R |
probably damaging |
Het |
Map3k6 |
A |
G |
4: 132,974,071 (GRCm39) |
K517E |
probably benign |
Het |
Mbl1 |
T |
A |
14: 40,875,555 (GRCm39) |
L3Q |
unknown |
Het |
Mepe |
G |
T |
5: 104,485,151 (GRCm39) |
R97L |
probably benign |
Het |
Minpp1 |
T |
A |
19: 32,463,747 (GRCm39) |
M136K |
possibly damaging |
Het |
Mrgprb1 |
T |
A |
7: 48,097,070 (GRCm39) |
I281F |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,349,207 (GRCm39) |
I1374V |
probably benign |
Het |
Or14j8 |
A |
G |
17: 38,263,273 (GRCm39) |
I214T |
probably damaging |
Het |
Or4c12 |
A |
G |
2: 89,773,790 (GRCm39) |
L223S |
probably damaging |
Het |
Or52e19b |
A |
T |
7: 103,032,825 (GRCm39) |
I128N |
probably damaging |
Het |
Or8g34 |
C |
T |
9: 39,373,387 (GRCm39) |
S217F |
probably damaging |
Het |
Or8g37 |
G |
T |
9: 39,730,939 (GRCm39) |
M1I |
probably null |
Het |
Pamr1 |
T |
G |
2: 102,464,766 (GRCm39) |
V305G |
probably benign |
Het |
Pcbp3 |
T |
C |
10: 76,625,670 (GRCm39) |
T125A |
probably benign |
Het |
Peli2 |
G |
A |
14: 48,490,130 (GRCm39) |
E201K |
possibly damaging |
Het |
Pitpnm3 |
T |
C |
11: 71,941,894 (GRCm39) |
E971G |
possibly damaging |
Het |
Pkdrej |
A |
G |
15: 85,702,774 (GRCm39) |
V1054A |
probably damaging |
Het |
Plcb1 |
G |
A |
2: 135,175,429 (GRCm39) |
|
probably benign |
Het |
Prpf40a |
T |
C |
2: 53,042,971 (GRCm39) |
K480E |
probably damaging |
Het |
Psd3 |
A |
G |
8: 68,413,135 (GRCm39) |
I465T |
possibly damaging |
Het |
Pskh1 |
C |
T |
8: 106,656,352 (GRCm39) |
R343W |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 23,007,371 (GRCm39) |
T1645S |
probably damaging |
Het |
Rasal1 |
T |
C |
5: 120,808,416 (GRCm39) |
F483L |
probably damaging |
Het |
Rbm28 |
T |
C |
6: 29,155,023 (GRCm39) |
|
probably benign |
Het |
Recql |
G |
A |
6: 142,304,612 (GRCm39) |
|
probably benign |
Het |
Rnf40 |
T |
C |
7: 127,196,332 (GRCm39) |
V760A |
probably damaging |
Het |
Rp1l1 |
A |
T |
14: 64,268,085 (GRCm39) |
R1224W |
probably benign |
Het |
Rpgrip1 |
T |
C |
14: 52,378,056 (GRCm39) |
V468A |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,750,509 (GRCm39) |
I1921F |
possibly damaging |
Het |
Sirpa |
G |
A |
2: 129,435,558 (GRCm39) |
G9D |
unknown |
Het |
Slc28a2b |
A |
T |
2: 122,348,988 (GRCm39) |
T305S |
possibly damaging |
Het |
Slc40a1 |
A |
C |
1: 45,948,699 (GRCm39) |
V527G |
probably damaging |
Het |
Smarca4 |
T |
A |
9: 21,547,497 (GRCm39) |
M260K |
probably benign |
Het |
Smarca5 |
A |
T |
8: 81,460,379 (GRCm39) |
M119K |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,758,887 (GRCm39) |
V2206A |
unknown |
Het |
Spata31d1c |
G |
A |
13: 65,182,376 (GRCm39) |
C75Y |
probably damaging |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
Srcap |
T |
C |
7: 127,152,395 (GRCm39) |
S2220P |
probably benign |
Het |
Stra6 |
G |
T |
9: 58,059,265 (GRCm39) |
V543F |
possibly damaging |
Het |
Tenm4 |
T |
A |
7: 96,523,335 (GRCm39) |
F1626I |
probably benign |
Het |
Tjp1 |
T |
C |
7: 64,952,810 (GRCm39) |
N1508S |
probably benign |
Het |
Trrap |
T |
A |
5: 144,782,348 (GRCm39) |
L3298Q |
probably damaging |
Het |
Tsn |
A |
G |
1: 118,232,470 (GRCm39) |
L135P |
probably damaging |
Het |
Ttl |
A |
T |
2: 128,910,778 (GRCm39) |
H54L |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,660,251 (GRCm39) |
T12110S |
unknown |
Het |
Uba6 |
T |
C |
5: 86,296,772 (GRCm39) |
I306V |
probably null |
Het |
Ubap2 |
A |
G |
4: 41,223,425 (GRCm39) |
S204P |
possibly damaging |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 115,958,998 (GRCm39) |
|
probably benign |
Het |
Ush2a |
A |
T |
1: 187,995,231 (GRCm39) |
M1L |
probably benign |
Het |
Vmn1r159 |
C |
A |
7: 22,542,559 (GRCm39) |
V158F |
probably benign |
Het |
Wif1 |
A |
G |
10: 120,932,621 (GRCm39) |
H333R |
possibly damaging |
Het |
Zfp282 |
T |
A |
6: 47,881,760 (GRCm39) |
N482K |
probably benign |
Het |
|
Other mutations in Sp4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02103:Sp4
|
APN |
12 |
118,263,284 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02817:Sp4
|
APN |
12 |
118,263,287 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02833:Sp4
|
APN |
12 |
118,225,616 (GRCm39) |
missense |
probably benign |
0.05 |
Deadloss
|
UTSW |
12 |
118,218,174 (GRCm39) |
missense |
possibly damaging |
0.82 |
Speck
|
UTSW |
12 |
118,264,546 (GRCm39) |
splice site |
probably null |
|
R0128:Sp4
|
UTSW |
12 |
118,264,551 (GRCm39) |
splice site |
probably benign |
|
R0130:Sp4
|
UTSW |
12 |
118,264,551 (GRCm39) |
splice site |
probably benign |
|
R0398:Sp4
|
UTSW |
12 |
118,262,408 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0626:Sp4
|
UTSW |
12 |
118,263,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R1193:Sp4
|
UTSW |
12 |
118,262,981 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1775:Sp4
|
UTSW |
12 |
118,263,335 (GRCm39) |
missense |
probably damaging |
0.99 |
R4724:Sp4
|
UTSW |
12 |
118,225,544 (GRCm39) |
missense |
probably benign |
|
R4861:Sp4
|
UTSW |
12 |
118,264,546 (GRCm39) |
splice site |
probably null |
|
R4861:Sp4
|
UTSW |
12 |
118,264,546 (GRCm39) |
splice site |
probably null |
|
R4969:Sp4
|
UTSW |
12 |
118,263,341 (GRCm39) |
missense |
probably damaging |
0.96 |
R5049:Sp4
|
UTSW |
12 |
118,218,207 (GRCm39) |
missense |
probably benign |
0.04 |
R5178:Sp4
|
UTSW |
12 |
118,225,624 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5208:Sp4
|
UTSW |
12 |
118,263,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R5722:Sp4
|
UTSW |
12 |
118,262,976 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6318:Sp4
|
UTSW |
12 |
118,201,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R6619:Sp4
|
UTSW |
12 |
118,263,077 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6917:Sp4
|
UTSW |
12 |
118,262,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R7195:Sp4
|
UTSW |
12 |
118,263,807 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7614:Sp4
|
UTSW |
12 |
118,218,174 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7747:Sp4
|
UTSW |
12 |
118,218,139 (GRCm39) |
splice site |
probably null |
|
R7983:Sp4
|
UTSW |
12 |
118,264,967 (GRCm39) |
start codon destroyed |
probably null |
|
R8709:Sp4
|
UTSW |
12 |
118,263,189 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9436:Sp4
|
UTSW |
12 |
118,202,000 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9487:Sp4
|
UTSW |
12 |
118,262,859 (GRCm39) |
missense |
probably benign |
0.05 |
R9595:Sp4
|
UTSW |
12 |
118,262,690 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1177:Sp4
|
UTSW |
12 |
118,263,794 (GRCm39) |
missense |
possibly damaging |
0.92 |
|