Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
A |
11: 110,169,982 (GRCm39) |
T1341S |
possibly damaging |
Het |
Abcc12 |
T |
C |
8: 87,293,149 (GRCm39) |
D13G |
possibly damaging |
Het |
Adam24 |
T |
C |
8: 41,134,071 (GRCm39) |
V513A |
probably benign |
Het |
Adgrg6 |
C |
T |
10: 14,314,163 (GRCm39) |
|
probably null |
Het |
Ankrd11 |
T |
C |
8: 123,617,805 (GRCm39) |
T1995A |
probably benign |
Het |
Apoh |
G |
T |
11: 108,302,843 (GRCm39) |
K269N |
probably damaging |
Het |
Bahcc1 |
C |
T |
11: 120,175,319 (GRCm39) |
L1798F |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,464,597 (GRCm39) |
C1454S |
probably benign |
Het |
Cpa5 |
T |
C |
6: 30,615,115 (GRCm39) |
V84A |
probably damaging |
Het |
Ctsh |
T |
C |
9: 89,946,621 (GRCm39) |
I116T |
probably damaging |
Het |
Dlg5 |
T |
A |
14: 24,199,515 (GRCm39) |
E1463V |
probably damaging |
Het |
Dnah11 |
C |
T |
12: 118,046,166 (GRCm39) |
|
probably null |
Het |
Dstyk |
G |
A |
1: 132,384,717 (GRCm39) |
R737Q |
probably damaging |
Het |
Galr1 |
A |
G |
18: 82,411,982 (GRCm39) |
S295P |
probably damaging |
Het |
Gpx2 |
A |
G |
12: 76,839,653 (GRCm39) |
V115A |
probably damaging |
Het |
Hhipl2 |
A |
G |
1: 183,207,597 (GRCm39) |
I219V |
possibly damaging |
Het |
Hkdc1 |
T |
C |
10: 62,244,445 (GRCm39) |
M214V |
possibly damaging |
Het |
Lrfn2 |
T |
C |
17: 49,377,291 (GRCm39) |
V124A |
possibly damaging |
Het |
Lrrcc1 |
T |
G |
3: 14,627,186 (GRCm39) |
S704R |
possibly damaging |
Het |
Marveld2 |
T |
C |
13: 100,748,176 (GRCm39) |
Y301C |
probably damaging |
Het |
Mcpt8 |
T |
C |
14: 56,319,740 (GRCm39) |
I237V |
probably damaging |
Het |
Mtus1 |
A |
T |
8: 41,536,534 (GRCm39) |
V394D |
possibly damaging |
Het |
Ncapd3 |
T |
A |
9: 26,978,265 (GRCm39) |
D821E |
probably benign |
Het |
Pcdh9 |
T |
C |
14: 93,564,156 (GRCm39) |
D1058G |
probably damaging |
Het |
Pld2 |
G |
A |
11: 70,446,888 (GRCm39) |
|
probably null |
Het |
Prdm2 |
A |
G |
4: 142,861,290 (GRCm39) |
S667P |
probably damaging |
Het |
Ptgdr2 |
A |
T |
19: 10,918,352 (GRCm39) |
|
probably null |
Het |
Rfx7 |
C |
T |
9: 72,524,538 (GRCm39) |
T576I |
probably benign |
Het |
Safb |
T |
C |
17: 56,907,349 (GRCm39) |
C426R |
unknown |
Het |
Serpina9 |
G |
A |
12: 103,975,130 (GRCm39) |
R8* |
probably null |
Het |
Shank3 |
G |
A |
15: 89,387,593 (GRCm39) |
R254Q |
probably damaging |
Het |
Simc1 |
T |
C |
13: 54,694,837 (GRCm39) |
V306A |
probably damaging |
Het |
Srfbp1 |
A |
G |
18: 52,621,853 (GRCm39) |
T305A |
probably benign |
Het |
Tdrd5 |
A |
T |
1: 156,105,005 (GRCm39) |
C463* |
probably null |
Het |
Tmem132d |
A |
T |
5: 128,346,336 (GRCm39) |
L62Q |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,220,784 (GRCm39) |
L2507H |
probably damaging |
Het |
Usp45 |
T |
C |
4: 21,830,451 (GRCm39) |
V702A |
probably damaging |
Het |
Wnk2 |
A |
G |
13: 49,256,308 (GRCm39) |
I271T |
probably damaging |
Het |
Zfp292 |
A |
T |
4: 34,805,125 (GRCm39) |
L2640I |
probably damaging |
Het |
Znrf3 |
G |
T |
11: 5,232,110 (GRCm39) |
H468N |
probably damaging |
Het |
|
Other mutations in Clip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00500:Clip2
|
APN |
5 |
134,529,011 (GRCm39) |
splice site |
probably benign |
|
IGL01024:Clip2
|
APN |
5 |
134,539,066 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01103:Clip2
|
APN |
5 |
134,521,204 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01726:Clip2
|
APN |
5 |
134,551,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01833:Clip2
|
APN |
5 |
134,526,938 (GRCm39) |
splice site |
probably benign |
|
IGL02174:Clip2
|
APN |
5 |
134,523,118 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Clip2
|
APN |
5 |
134,531,984 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02271:Clip2
|
APN |
5 |
134,531,425 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02471:Clip2
|
APN |
5 |
134,546,876 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02690:Clip2
|
APN |
5 |
134,539,013 (GRCm39) |
splice site |
probably benign |
|
IGL03198:Clip2
|
APN |
5 |
134,526,936 (GRCm39) |
splice site |
probably benign |
|
IGL03269:Clip2
|
APN |
5 |
134,545,748 (GRCm39) |
missense |
probably damaging |
1.00 |
scissors
|
UTSW |
5 |
134,546,853 (GRCm39) |
nonsense |
probably null |
|
R0335:Clip2
|
UTSW |
5 |
134,564,069 (GRCm39) |
start gained |
probably benign |
|
R0422:Clip2
|
UTSW |
5 |
134,526,967 (GRCm39) |
missense |
probably benign |
0.04 |
R0519:Clip2
|
UTSW |
5 |
134,545,005 (GRCm39) |
missense |
probably benign |
0.01 |
R1169:Clip2
|
UTSW |
5 |
134,521,104 (GRCm39) |
missense |
probably benign |
0.36 |
R1642:Clip2
|
UTSW |
5 |
134,532,107 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1718:Clip2
|
UTSW |
5 |
134,531,783 (GRCm39) |
nonsense |
probably null |
|
R1822:Clip2
|
UTSW |
5 |
134,532,081 (GRCm39) |
missense |
probably benign |
0.01 |
R1824:Clip2
|
UTSW |
5 |
134,532,081 (GRCm39) |
missense |
probably benign |
0.01 |
R2011:Clip2
|
UTSW |
5 |
134,531,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R3106:Clip2
|
UTSW |
5 |
134,551,918 (GRCm39) |
missense |
probably benign |
0.12 |
R3890:Clip2
|
UTSW |
5 |
134,551,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R3891:Clip2
|
UTSW |
5 |
134,551,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R3892:Clip2
|
UTSW |
5 |
134,551,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4134:Clip2
|
UTSW |
5 |
134,521,107 (GRCm39) |
missense |
probably benign |
0.08 |
R4237:Clip2
|
UTSW |
5 |
134,564,051 (GRCm39) |
start gained |
probably benign |
|
R4239:Clip2
|
UTSW |
5 |
134,564,051 (GRCm39) |
start gained |
probably benign |
|
R4294:Clip2
|
UTSW |
5 |
134,521,167 (GRCm39) |
missense |
probably benign |
0.09 |
R4450:Clip2
|
UTSW |
5 |
134,531,807 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4741:Clip2
|
UTSW |
5 |
134,545,123 (GRCm39) |
missense |
probably benign |
0.02 |
R5186:Clip2
|
UTSW |
5 |
134,551,645 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5235:Clip2
|
UTSW |
5 |
134,551,645 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5409:Clip2
|
UTSW |
5 |
134,551,645 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5410:Clip2
|
UTSW |
5 |
134,551,645 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5448:Clip2
|
UTSW |
5 |
134,542,902 (GRCm39) |
missense |
probably benign |
0.01 |
R6464:Clip2
|
UTSW |
5 |
134,520,779 (GRCm39) |
missense |
probably benign |
0.00 |
R7032:Clip2
|
UTSW |
5 |
134,551,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R7152:Clip2
|
UTSW |
5 |
134,525,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R7216:Clip2
|
UTSW |
5 |
134,531,771 (GRCm39) |
missense |
probably benign |
0.01 |
R7358:Clip2
|
UTSW |
5 |
134,531,484 (GRCm39) |
nonsense |
probably null |
|
R7725:Clip2
|
UTSW |
5 |
134,546,853 (GRCm39) |
nonsense |
probably null |
|
R8380:Clip2
|
UTSW |
5 |
134,531,651 (GRCm39) |
missense |
probably damaging |
0.96 |
R8680:Clip2
|
UTSW |
5 |
134,531,462 (GRCm39) |
missense |
probably benign |
|
R9095:Clip2
|
UTSW |
5 |
134,532,254 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9158:Clip2
|
UTSW |
5 |
134,521,251 (GRCm39) |
missense |
probably benign |
0.00 |
R9277:Clip2
|
UTSW |
5 |
134,528,963 (GRCm39) |
missense |
probably benign |
|
R9300:Clip2
|
UTSW |
5 |
134,526,942 (GRCm39) |
critical splice donor site |
probably null |
|
R9457:Clip2
|
UTSW |
5 |
134,531,584 (GRCm39) |
missense |
probably benign |
0.00 |
R9491:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9605:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9630:Clip2
|
UTSW |
5 |
134,531,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R9657:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9660:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9661:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9662:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9663:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9730:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9731:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9732:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9773:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9787:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
R9788:Clip2
|
UTSW |
5 |
134,533,616 (GRCm39) |
missense |
probably benign |
0.04 |
X0062:Clip2
|
UTSW |
5 |
134,531,990 (GRCm39) |
missense |
probably benign |
0.12 |
Z1177:Clip2
|
UTSW |
5 |
134,551,853 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Clip2
|
UTSW |
5 |
134,545,689 (GRCm39) |
missense |
probably damaging |
0.98 |
|