Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsf3 |
T |
C |
8: 123,506,920 (GRCm39) |
L71P |
probably damaging |
Het |
Adamts2 |
A |
T |
11: 50,666,201 (GRCm39) |
D399V |
probably damaging |
Het |
Adck2 |
T |
A |
6: 39,560,752 (GRCm39) |
V380E |
probably benign |
Het |
Alg11 |
T |
A |
8: 22,555,468 (GRCm39) |
V243D |
possibly damaging |
Het |
Ankrd27 |
T |
A |
7: 35,318,864 (GRCm39) |
L585Q |
probably damaging |
Het |
Armh4 |
A |
G |
14: 50,005,859 (GRCm39) |
|
probably benign |
Het |
Atp7a |
T |
A |
X: 105,153,447 (GRCm39) |
N1117K |
probably damaging |
Het |
Bltp3a |
T |
A |
17: 28,114,844 (GRCm39) |
|
probably benign |
Het |
Cacna1b |
G |
A |
2: 24,528,669 (GRCm39) |
|
probably benign |
Het |
Cacna1d |
T |
A |
14: 29,818,926 (GRCm39) |
M1210L |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,001,234 (GRCm39) |
|
probably benign |
Het |
Chd7 |
T |
C |
4: 8,852,670 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
A |
T |
9: 79,559,315 (GRCm39) |
S1858T |
probably benign |
Het |
Cotl1 |
C |
T |
8: 120,567,063 (GRCm39) |
W26* |
probably null |
Het |
Csmd3 |
T |
C |
15: 47,492,635 (GRCm39) |
T3000A |
probably benign |
Het |
Dcp1a |
T |
A |
14: 30,206,551 (GRCm39) |
|
probably benign |
Het |
Ddhd2 |
A |
T |
8: 26,229,617 (GRCm39) |
|
probably null |
Het |
Dnah8 |
T |
C |
17: 30,984,653 (GRCm39) |
I3117T |
probably damaging |
Het |
Dnm3 |
G |
T |
1: 162,181,194 (GRCm39) |
Q162K |
probably benign |
Het |
Dpy19l2 |
G |
T |
9: 24,569,876 (GRCm39) |
A359D |
probably damaging |
Het |
Ece1 |
T |
A |
4: 137,676,746 (GRCm39) |
|
probably benign |
Het |
Eif4g3 |
A |
G |
4: 137,897,873 (GRCm39) |
K1025R |
probably damaging |
Het |
Eml2 |
C |
A |
7: 18,918,797 (GRCm39) |
Y82* |
probably null |
Het |
Eml6 |
A |
G |
11: 29,742,367 (GRCm39) |
V1057A |
possibly damaging |
Het |
Eral1 |
A |
G |
11: 77,966,884 (GRCm39) |
|
probably benign |
Het |
Espl1 |
T |
C |
15: 102,220,976 (GRCm39) |
S911P |
probably benign |
Het |
Fbxo8 |
A |
G |
8: 57,043,296 (GRCm39) |
|
probably benign |
Het |
Flrt1 |
A |
T |
19: 7,074,475 (GRCm39) |
|
probably benign |
Het |
Fndc7 |
A |
G |
3: 108,766,235 (GRCm39) |
|
probably benign |
Het |
G3bp1 |
G |
A |
11: 55,382,854 (GRCm39) |
G139D |
probably damaging |
Het |
Gabra6 |
C |
T |
11: 42,205,774 (GRCm39) |
V351I |
probably benign |
Het |
Galc |
A |
T |
12: 98,218,293 (GRCm39) |
H186Q |
probably damaging |
Het |
Ganab |
A |
G |
19: 8,890,177 (GRCm39) |
D702G |
possibly damaging |
Het |
Hdac10 |
T |
C |
15: 89,010,085 (GRCm39) |
E291G |
possibly damaging |
Het |
Hectd3 |
T |
G |
4: 116,859,810 (GRCm39) |
V749G |
probably damaging |
Het |
Kash5 |
C |
T |
7: 44,849,675 (GRCm39) |
A83T |
probably benign |
Het |
Kcnh1 |
T |
A |
1: 192,187,648 (GRCm39) |
I703N |
probably benign |
Het |
Kcnma1 |
G |
A |
14: 23,544,647 (GRCm39) |
T505I |
probably damaging |
Het |
Kctd11 |
A |
G |
11: 69,770,640 (GRCm39) |
C133R |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,672,880 (GRCm39) |
|
probably null |
Het |
Lamb3 |
T |
C |
1: 193,017,335 (GRCm39) |
L842P |
probably damaging |
Het |
Ldlr |
T |
C |
9: 21,649,295 (GRCm39) |
|
probably benign |
Het |
Lipk |
G |
A |
19: 34,024,210 (GRCm39) |
R336H |
probably benign |
Het |
Lrrc24 |
T |
A |
15: 76,607,409 (GRCm39) |
D58V |
probably damaging |
Het |
Lrsam1 |
A |
G |
2: 32,845,197 (GRCm39) |
L106P |
probably damaging |
Het |
Milr1 |
G |
A |
11: 106,645,722 (GRCm39) |
W88* |
probably null |
Het |
Mmp10 |
A |
G |
9: 7,506,544 (GRCm39) |
D340G |
probably damaging |
Het |
Mybpc1 |
T |
A |
10: 88,391,600 (GRCm39) |
Y285F |
possibly damaging |
Het |
Ncoa3 |
A |
G |
2: 165,896,320 (GRCm39) |
T408A |
probably benign |
Het |
Nefm |
T |
A |
14: 68,358,583 (GRCm39) |
K484* |
probably null |
Het |
Nfasc |
A |
G |
1: 132,529,721 (GRCm39) |
S814P |
probably damaging |
Het |
Nlrp4a |
T |
C |
7: 26,161,941 (GRCm39) |
V863A |
probably benign |
Het |
Nos1 |
C |
T |
5: 118,005,948 (GRCm39) |
P223S |
probably benign |
Het |
Nr2f2 |
G |
C |
7: 70,009,923 (GRCm39) |
P52R |
probably damaging |
Het |
Or13c7 |
T |
A |
4: 43,854,512 (GRCm39) |
S68T |
probably damaging |
Het |
Or4c108 |
A |
T |
2: 88,803,740 (GRCm39) |
L165Q |
probably damaging |
Het |
Or5an6 |
A |
T |
19: 12,372,327 (GRCm39) |
E233D |
probably benign |
Het |
Or8k41 |
A |
G |
2: 86,313,730 (GRCm39) |
S119P |
possibly damaging |
Het |
Osbpl5 |
T |
C |
7: 143,295,406 (GRCm39) |
|
probably null |
Het |
Otog |
C |
A |
7: 45,913,456 (GRCm39) |
|
probably null |
Het |
Pacs1 |
A |
T |
19: 5,206,402 (GRCm39) |
I261N |
possibly damaging |
Het |
Pbx1 |
G |
A |
1: 168,031,051 (GRCm39) |
T189I |
possibly damaging |
Het |
Pcnx1 |
T |
C |
12: 81,993,792 (GRCm39) |
I908T |
possibly damaging |
Het |
Pdxdc1 |
A |
T |
16: 13,697,309 (GRCm39) |
W124R |
probably damaging |
Het |
Phex |
C |
A |
X: 155,969,214 (GRCm39) |
D587Y |
probably damaging |
Het |
Plcb3 |
A |
T |
19: 6,940,363 (GRCm39) |
D435E |
probably benign |
Het |
Plce1 |
A |
C |
19: 38,717,330 (GRCm39) |
K1373T |
probably damaging |
Het |
Prkcd |
G |
A |
14: 30,324,045 (GRCm39) |
A311V |
probably damaging |
Het |
Ptpn3 |
A |
T |
4: 57,232,374 (GRCm39) |
S421T |
probably benign |
Het |
Ptprs |
T |
C |
17: 56,743,087 (GRCm39) |
|
probably null |
Het |
Qrich1 |
A |
G |
9: 108,411,333 (GRCm39) |
D286G |
probably damaging |
Het |
Rcc1 |
C |
A |
4: 132,060,226 (GRCm39) |
G393V |
probably damaging |
Het |
Reln |
T |
C |
5: 22,311,043 (GRCm39) |
N290S |
probably benign |
Het |
Rgl1 |
T |
C |
1: 152,430,175 (GRCm39) |
|
probably benign |
Het |
Rhpn1 |
C |
T |
15: 75,585,971 (GRCm39) |
T628I |
probably benign |
Het |
Rilp |
A |
G |
11: 75,401,747 (GRCm39) |
R176G |
probably benign |
Het |
Riok3 |
C |
T |
18: 12,288,284 (GRCm39) |
A487V |
probably benign |
Het |
Rnf224 |
T |
C |
2: 25,126,219 (GRCm39) |
T45A |
probably damaging |
Het |
Rpa1 |
A |
G |
11: 75,219,513 (GRCm39) |
V137A |
probably benign |
Het |
Rps6ka1 |
C |
A |
4: 133,575,842 (GRCm39) |
Q693H |
probably benign |
Het |
Scn2a |
G |
T |
2: 65,566,118 (GRCm39) |
V1381F |
probably benign |
Het |
Sdk1 |
T |
C |
5: 141,984,502 (GRCm39) |
W696R |
probably damaging |
Het |
Slc26a7 |
C |
A |
4: 14,532,651 (GRCm39) |
V408F |
probably damaging |
Het |
Slc28a2 |
T |
A |
2: 122,285,008 (GRCm39) |
I332N |
probably benign |
Het |
Slc37a3 |
A |
G |
6: 39,314,172 (GRCm39) |
V480A |
probably benign |
Het |
Slc45a4 |
T |
A |
15: 73,453,755 (GRCm39) |
E674D |
probably benign |
Het |
Smpd3 |
T |
C |
8: 106,991,788 (GRCm39) |
E255G |
probably damaging |
Het |
Snx29 |
C |
T |
16: 11,478,417 (GRCm39) |
R658W |
probably damaging |
Het |
Sppl2a |
A |
T |
2: 126,762,256 (GRCm39) |
M275K |
probably benign |
Het |
Stac |
T |
C |
9: 111,464,089 (GRCm39) |
N59S |
probably damaging |
Het |
Stk25 |
A |
T |
1: 93,554,782 (GRCm39) |
L131Q |
probably damaging |
Het |
Tep1 |
C |
T |
14: 51,100,486 (GRCm39) |
|
probably benign |
Het |
Thbs1 |
C |
A |
2: 117,944,874 (GRCm39) |
N229K |
probably damaging |
Het |
Tmx2 |
A |
T |
2: 84,506,186 (GRCm39) |
H89Q |
probably damaging |
Het |
Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
Tradd |
T |
C |
8: 105,985,924 (GRCm39) |
N209S |
possibly damaging |
Het |
Trappc3l |
A |
T |
10: 33,974,928 (GRCm39) |
R119* |
probably null |
Het |
Trmt1l |
G |
A |
1: 151,333,205 (GRCm39) |
|
probably benign |
Het |
Ublcp1 |
G |
T |
11: 44,349,104 (GRCm39) |
Y243* |
probably null |
Het |
Usp24 |
C |
A |
4: 106,271,601 (GRCm39) |
C2158* |
probably null |
Het |
Usp34 |
A |
T |
11: 23,383,206 (GRCm39) |
K2088N |
probably damaging |
Het |
Vmn1r53 |
G |
C |
6: 90,200,925 (GRCm39) |
S133C |
probably damaging |
Het |
Vmn2r52 |
A |
G |
7: 9,893,327 (GRCm39) |
V604A |
probably damaging |
Het |
Vmn2r93 |
A |
G |
17: 18,525,061 (GRCm39) |
K240E |
probably benign |
Het |
Wdr13 |
T |
G |
X: 7,994,284 (GRCm39) |
D242A |
probably damaging |
Het |
Wwp1 |
C |
T |
4: 19,641,734 (GRCm39) |
|
probably null |
Het |
Zan |
G |
A |
5: 137,396,624 (GRCm39) |
H4311Y |
unknown |
Het |
Zc3h12c |
C |
A |
9: 52,055,383 (GRCm39) |
R123L |
possibly damaging |
Het |
Zfp125 |
A |
T |
12: 20,950,562 (GRCm39) |
|
noncoding transcript |
Het |
Zfp318 |
C |
T |
17: 46,707,739 (GRCm39) |
P266S |
probably benign |
Het |
|
Other mutations in Scp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01481:Scp2
|
APN |
4 |
107,931,639 (GRCm39) |
splice site |
probably null |
|
IGL02190:Scp2
|
APN |
4 |
107,944,325 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02615:Scp2
|
APN |
4 |
107,964,828 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03006:Scp2
|
APN |
4 |
107,948,477 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03107:Scp2
|
APN |
4 |
107,955,312 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03124:Scp2
|
APN |
4 |
107,921,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R0030:Scp2
|
UTSW |
4 |
107,964,887 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0030:Scp2
|
UTSW |
4 |
107,964,887 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0240:Scp2
|
UTSW |
4 |
107,955,275 (GRCm39) |
missense |
probably benign |
0.01 |
R1507:Scp2
|
UTSW |
4 |
107,944,209 (GRCm39) |
frame shift |
probably null |
|
R1861:Scp2
|
UTSW |
4 |
107,948,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Scp2
|
UTSW |
4 |
107,921,141 (GRCm39) |
missense |
probably benign |
|
R3013:Scp2
|
UTSW |
4 |
107,928,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R4127:Scp2
|
UTSW |
4 |
107,921,181 (GRCm39) |
missense |
probably benign |
0.00 |
R4271:Scp2
|
UTSW |
4 |
107,942,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Scp2
|
UTSW |
4 |
107,928,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R5046:Scp2
|
UTSW |
4 |
107,928,488 (GRCm39) |
missense |
probably benign |
0.07 |
R5345:Scp2
|
UTSW |
4 |
107,912,776 (GRCm39) |
splice site |
probably null |
|
R5401:Scp2
|
UTSW |
4 |
108,001,976 (GRCm39) |
critical splice donor site |
probably null |
|
R6367:Scp2
|
UTSW |
4 |
107,969,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R6415:Scp2
|
UTSW |
4 |
107,962,337 (GRCm39) |
missense |
probably benign |
0.22 |
R6681:Scp2
|
UTSW |
4 |
107,948,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R6910:Scp2
|
UTSW |
4 |
107,962,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6974:Scp2
|
UTSW |
4 |
107,928,475 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R7206:Scp2
|
UTSW |
4 |
107,931,638 (GRCm39) |
missense |
probably benign |
0.00 |
R7342:Scp2
|
UTSW |
4 |
107,948,518 (GRCm39) |
missense |
probably benign |
0.02 |
R8935:Scp2
|
UTSW |
4 |
107,950,072 (GRCm39) |
missense |
probably damaging |
0.98 |
R9035:Scp2
|
UTSW |
4 |
107,912,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R9151:Scp2
|
UTSW |
4 |
107,931,603 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9536:Scp2
|
UTSW |
4 |
107,928,532 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9645:Scp2
|
UTSW |
4 |
107,948,519 (GRCm39) |
missense |
probably benign |
0.01 |
|