Other mutations in this stock |
Total: 107 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,349,430 (GRCm39) |
H3668L |
probably damaging |
Het |
Acsbg3 |
A |
T |
17: 57,190,631 (GRCm39) |
I400F |
probably benign |
Het |
Acvr1c |
T |
C |
2: 58,174,850 (GRCm39) |
T313A |
probably damaging |
Het |
Adam28 |
T |
C |
14: 68,855,188 (GRCm39) |
K651R |
probably damaging |
Het |
Adamtsl3 |
A |
T |
7: 82,171,198 (GRCm39) |
D417V |
probably damaging |
Het |
Adgrf4 |
A |
T |
17: 42,978,204 (GRCm39) |
C380S |
probably damaging |
Het |
AI597479 |
T |
G |
1: 43,150,277 (GRCm39) |
L129R |
probably benign |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Anxa7 |
A |
C |
14: 20,519,566 (GRCm39) |
|
probably null |
Het |
Arb2a |
T |
A |
13: 77,910,070 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
A |
G |
14: 33,091,374 (GRCm39) |
R650G |
possibly damaging |
Het |
Atp8a1 |
T |
A |
5: 67,969,416 (GRCm39) |
|
probably benign |
Het |
Bcr |
C |
T |
10: 75,017,466 (GRCm39) |
T1209I |
possibly damaging |
Het |
Bmpr1a |
C |
T |
14: 34,151,734 (GRCm39) |
S185N |
probably benign |
Het |
Calcoco1 |
A |
T |
15: 102,624,198 (GRCm39) |
M246K |
probably benign |
Het |
Casp12 |
T |
A |
9: 5,345,534 (GRCm39) |
|
probably benign |
Het |
Ccno |
T |
A |
13: 113,126,530 (GRCm39) |
L333Q |
probably damaging |
Het |
Cdhr2 |
T |
A |
13: 54,882,614 (GRCm39) |
|
probably benign |
Het |
Cftr |
T |
A |
6: 18,226,096 (GRCm39) |
M318K |
probably null |
Het |
Ckmt2 |
T |
A |
13: 92,011,322 (GRCm39) |
D96V |
possibly damaging |
Het |
Cnnm1 |
C |
T |
19: 43,430,349 (GRCm39) |
P489L |
probably damaging |
Het |
Cntnap1 |
A |
T |
11: 101,079,135 (GRCm39) |
D1175V |
probably damaging |
Het |
Cpne5 |
A |
T |
17: 29,430,634 (GRCm39) |
L92H |
probably damaging |
Het |
Crcp |
C |
A |
5: 130,071,083 (GRCm39) |
Q61K |
possibly damaging |
Het |
Crppa |
C |
T |
12: 36,431,837 (GRCm39) |
A22V |
possibly damaging |
Het |
Dcaf8 |
T |
A |
1: 172,014,978 (GRCm39) |
D414E |
probably benign |
Het |
Ddx28 |
T |
C |
8: 106,736,877 (GRCm39) |
T394A |
probably benign |
Het |
Ddx55 |
T |
C |
5: 124,697,210 (GRCm39) |
F191L |
probably benign |
Het |
Dnaaf1 |
T |
C |
8: 120,322,756 (GRCm39) |
|
probably benign |
Het |
Dnaaf2 |
C |
A |
12: 69,244,518 (GRCm39) |
R181L |
probably damaging |
Het |
Elac2 |
A |
G |
11: 64,870,136 (GRCm39) |
Y67C |
probably damaging |
Het |
Elf5 |
A |
G |
2: 103,260,765 (GRCm39) |
|
probably benign |
Het |
Emcn |
T |
A |
3: 137,122,575 (GRCm39) |
|
probably benign |
Het |
Erbb4 |
T |
C |
1: 68,337,439 (GRCm39) |
|
probably benign |
Het |
Erbin |
C |
A |
13: 104,005,373 (GRCm39) |
C114F |
probably damaging |
Het |
Etfdh |
T |
C |
3: 79,517,151 (GRCm39) |
I353V |
probably benign |
Het |
Fads2b |
T |
A |
2: 85,348,895 (GRCm39) |
R72S |
probably benign |
Het |
Fbxl12 |
C |
T |
9: 20,549,776 (GRCm39) |
G316D |
probably damaging |
Het |
Gbf1 |
G |
A |
19: 46,260,709 (GRCm39) |
|
probably null |
Het |
Gbp2b |
T |
G |
3: 142,313,937 (GRCm39) |
S406A |
probably benign |
Het |
Gli3 |
T |
G |
13: 15,898,143 (GRCm39) |
L741R |
probably damaging |
Het |
Gmip |
G |
T |
8: 70,263,468 (GRCm39) |
S70I |
probably benign |
Het |
Gnptab |
T |
C |
10: 88,276,171 (GRCm39) |
S1153P |
probably damaging |
Het |
Gp1ba |
A |
G |
11: 70,531,235 (GRCm39) |
|
probably benign |
Het |
Gramd1a |
T |
C |
7: 30,837,679 (GRCm39) |
D360G |
possibly damaging |
Het |
Hectd4 |
T |
C |
5: 121,397,927 (GRCm39) |
I285T |
probably benign |
Het |
Hrh4 |
A |
G |
18: 13,140,302 (GRCm39) |
|
probably benign |
Het |
Hsp90b1 |
T |
C |
10: 86,530,019 (GRCm39) |
E226G |
probably damaging |
Het |
Hspa13 |
A |
T |
16: 75,562,018 (GRCm39) |
D60E |
probably damaging |
Het |
Htt |
T |
A |
5: 34,974,478 (GRCm39) |
|
probably benign |
Het |
Iqca1l |
T |
C |
5: 24,750,783 (GRCm39) |
|
probably null |
Het |
Kif14 |
G |
C |
1: 136,423,764 (GRCm39) |
|
probably benign |
Het |
Kit |
T |
G |
5: 75,813,489 (GRCm39) |
V888G |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,747,225 (GRCm39) |
V827A |
probably benign |
Het |
Lrriq4 |
T |
C |
3: 30,709,873 (GRCm39) |
S406P |
probably benign |
Het |
Man2c1 |
T |
C |
9: 57,048,467 (GRCm39) |
V777A |
probably benign |
Het |
Mcm8 |
A |
G |
2: 132,661,914 (GRCm39) |
K83E |
possibly damaging |
Het |
Mep1a |
A |
G |
17: 43,808,789 (GRCm39) |
|
probably null |
Het |
Mtor |
T |
A |
4: 148,568,837 (GRCm39) |
V1119E |
probably benign |
Het |
Mybpc2 |
C |
T |
7: 44,158,453 (GRCm39) |
A710T |
possibly damaging |
Het |
Myo9a |
C |
G |
9: 59,830,960 (GRCm39) |
T2368S |
probably damaging |
Het |
Nbeal1 |
A |
G |
1: 60,307,222 (GRCm39) |
Y1684C |
probably damaging |
Het |
Npm3 |
A |
G |
19: 45,737,965 (GRCm39) |
F11L |
probably benign |
Het |
Nutf2 |
T |
A |
8: 106,602,995 (GRCm39) |
S37T |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,931,267 (GRCm39) |
I5790F |
probably damaging |
Het |
Obscn |
A |
T |
11: 58,943,332 (GRCm39) |
D4833E |
probably damaging |
Het |
Or2g1 |
A |
T |
17: 38,106,880 (GRCm39) |
M182L |
probably benign |
Het |
Or7d9 |
T |
A |
9: 20,197,153 (GRCm39) |
S61T |
possibly damaging |
Het |
Or8g35 |
T |
C |
9: 39,381,852 (GRCm39) |
T57A |
possibly damaging |
Het |
Or9g4b |
T |
A |
2: 85,616,147 (GRCm39) |
C97* |
probably null |
Het |
Pcdhb1 |
A |
G |
18: 37,400,077 (GRCm39) |
D676G |
possibly damaging |
Het |
Pcif1 |
G |
T |
2: 164,731,364 (GRCm39) |
R466L |
probably damaging |
Het |
Pdk1 |
T |
C |
2: 71,726,018 (GRCm39) |
|
probably benign |
Het |
Phxr2 |
T |
C |
10: 98,961,979 (GRCm39) |
|
probably benign |
Het |
Pidd1 |
A |
T |
7: 141,019,474 (GRCm39) |
|
probably benign |
Het |
Plec |
A |
G |
15: 76,075,618 (GRCm39) |
|
probably null |
Het |
Polr1a |
T |
A |
6: 71,943,400 (GRCm39) |
C1212S |
possibly damaging |
Het |
Pot1a |
A |
G |
6: 25,778,830 (GRCm39) |
|
probably benign |
Het |
Prdm5 |
T |
C |
6: 65,839,887 (GRCm39) |
|
probably benign |
Het |
Primpol |
A |
T |
8: 47,063,496 (GRCm39) |
N53K |
probably damaging |
Het |
Pyroxd1 |
A |
G |
6: 142,307,702 (GRCm39) |
I491V |
probably benign |
Het |
Serpinb3b |
G |
T |
1: 107,087,433 (GRCm39) |
N25K |
probably damaging |
Het |
Slc9b1 |
C |
T |
3: 135,078,996 (GRCm39) |
R218* |
probably null |
Het |
Ssbp2 |
T |
A |
13: 91,828,698 (GRCm39) |
|
probably null |
Het |
Stat4 |
A |
G |
1: 52,130,029 (GRCm39) |
|
probably benign |
Het |
Steap4 |
T |
C |
5: 8,025,829 (GRCm39) |
V130A |
possibly damaging |
Het |
Stoml2 |
A |
G |
4: 43,030,238 (GRCm39) |
|
probably null |
Het |
Syne2 |
G |
T |
12: 76,013,727 (GRCm39) |
G2974C |
probably benign |
Het |
Tfdp2 |
T |
G |
9: 96,188,946 (GRCm39) |
F200V |
probably damaging |
Het |
Tgm4 |
T |
C |
9: 122,877,622 (GRCm39) |
|
probably null |
Het |
Tie1 |
C |
A |
4: 118,341,924 (GRCm39) |
R175L |
probably benign |
Het |
Tmem145 |
A |
G |
7: 25,008,099 (GRCm39) |
|
probably benign |
Het |
Tsacc |
A |
G |
3: 88,190,169 (GRCm39) |
S94P |
possibly damaging |
Het |
Tshz3 |
T |
A |
7: 36,469,458 (GRCm39) |
D482E |
probably benign |
Het |
Tspan33 |
T |
C |
6: 29,711,091 (GRCm39) |
|
probably null |
Het |
Unc80 |
T |
C |
1: 66,713,246 (GRCm39) |
L2788P |
possibly damaging |
Het |
Usp10 |
T |
A |
8: 120,663,296 (GRCm39) |
C39* |
probably null |
Het |
Utp20 |
T |
A |
10: 88,653,841 (GRCm39) |
T260S |
probably benign |
Het |
Vmn2r118 |
G |
T |
17: 55,917,717 (GRCm39) |
T265K |
probably damaging |
Het |
Vmn2r7 |
C |
A |
3: 64,598,439 (GRCm39) |
C797F |
probably damaging |
Het |
Vmn2r98 |
A |
C |
17: 19,286,609 (GRCm39) |
H369P |
probably benign |
Het |
Vps39 |
A |
T |
2: 120,169,268 (GRCm39) |
Y245N |
possibly damaging |
Het |
Wdr27 |
A |
G |
17: 15,154,721 (GRCm39) |
|
probably benign |
Het |
Ythdc2 |
A |
G |
18: 44,998,127 (GRCm39) |
|
probably benign |
Het |
Zcwpw2 |
C |
A |
9: 117,843,123 (GRCm39) |
|
noncoding transcript |
Het |
Zdhhc1 |
C |
A |
8: 106,210,175 (GRCm39) |
A81S |
probably benign |
Het |
Zfp729a |
G |
T |
13: 67,768,473 (GRCm39) |
H585Q |
probably damaging |
Het |
|
Other mutations in Ugt2b35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00703:Ugt2b35
|
APN |
5 |
87,156,051 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01109:Ugt2b35
|
APN |
5 |
87,156,165 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01586:Ugt2b35
|
APN |
5 |
87,159,250 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02151:Ugt2b35
|
APN |
5 |
87,151,141 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02225:Ugt2b35
|
APN |
5 |
87,155,264 (GRCm39) |
splice site |
probably benign |
|
IGL02483:Ugt2b35
|
APN |
5 |
87,149,004 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02504:Ugt2b35
|
APN |
5 |
87,149,400 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02690:Ugt2b35
|
APN |
5 |
87,149,096 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02954:Ugt2b35
|
APN |
5 |
87,159,180 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03242:Ugt2b35
|
APN |
5 |
87,155,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R0513:Ugt2b35
|
UTSW |
5 |
87,151,271 (GRCm39) |
splice site |
probably benign |
|
R0571:Ugt2b35
|
UTSW |
5 |
87,148,793 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0827:Ugt2b35
|
UTSW |
5 |
87,155,989 (GRCm39) |
splice site |
probably benign |
|
R1396:Ugt2b35
|
UTSW |
5 |
87,159,389 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1437:Ugt2b35
|
UTSW |
5 |
87,148,890 (GRCm39) |
missense |
probably benign |
0.02 |
R1557:Ugt2b35
|
UTSW |
5 |
87,155,156 (GRCm39) |
splice site |
probably null |
|
R1869:Ugt2b35
|
UTSW |
5 |
87,149,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Ugt2b35
|
UTSW |
5 |
87,149,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R2067:Ugt2b35
|
UTSW |
5 |
87,149,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R2219:Ugt2b35
|
UTSW |
5 |
87,151,191 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3055:Ugt2b35
|
UTSW |
5 |
87,149,457 (GRCm39) |
missense |
probably benign |
0.05 |
R3793:Ugt2b35
|
UTSW |
5 |
87,149,465 (GRCm39) |
missense |
probably benign |
0.15 |
R4452:Ugt2b35
|
UTSW |
5 |
87,151,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R4548:Ugt2b35
|
UTSW |
5 |
87,156,134 (GRCm39) |
nonsense |
probably null |
|
R4902:Ugt2b35
|
UTSW |
5 |
87,151,159 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5311:Ugt2b35
|
UTSW |
5 |
87,159,139 (GRCm39) |
nonsense |
probably null |
|
R6187:Ugt2b35
|
UTSW |
5 |
87,155,181 (GRCm39) |
missense |
probably damaging |
0.98 |
R6332:Ugt2b35
|
UTSW |
5 |
87,149,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R6719:Ugt2b35
|
UTSW |
5 |
87,155,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R7211:Ugt2b35
|
UTSW |
5 |
87,149,177 (GRCm39) |
missense |
probably benign |
0.39 |
R7652:Ugt2b35
|
UTSW |
5 |
87,149,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R7766:Ugt2b35
|
UTSW |
5 |
87,149,061 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7825:Ugt2b35
|
UTSW |
5 |
87,149,218 (GRCm39) |
nonsense |
probably null |
|
R8188:Ugt2b35
|
UTSW |
5 |
87,149,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R8189:Ugt2b35
|
UTSW |
5 |
87,149,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R8191:Ugt2b35
|
UTSW |
5 |
87,149,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R8192:Ugt2b35
|
UTSW |
5 |
87,149,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R8193:Ugt2b35
|
UTSW |
5 |
87,149,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R8220:Ugt2b35
|
UTSW |
5 |
87,149,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R8288:Ugt2b35
|
UTSW |
5 |
87,149,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R8695:Ugt2b35
|
UTSW |
5 |
87,156,064 (GRCm39) |
missense |
probably damaging |
0.97 |
R8898:Ugt2b35
|
UTSW |
5 |
87,159,189 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8924:Ugt2b35
|
UTSW |
5 |
87,152,780 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8944:Ugt2b35
|
UTSW |
5 |
87,149,310 (GRCm39) |
missense |
probably benign |
0.21 |
R9284:Ugt2b35
|
UTSW |
5 |
87,156,140 (GRCm39) |
missense |
probably benign |
|
|