Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahdc1 |
A |
T |
4: 132,792,313 (GRCm39) |
S1185C |
possibly damaging |
Het |
Akap9 |
C |
G |
5: 4,018,745 (GRCm39) |
H1109D |
probably benign |
Het |
Alpk2 |
T |
C |
18: 65,439,887 (GRCm39) |
D502G |
possibly damaging |
Het |
Bcl2 |
A |
G |
1: 106,640,153 (GRCm39) |
V153A |
possibly damaging |
Het |
Brinp3 |
A |
T |
1: 146,777,301 (GRCm39) |
S583C |
probably damaging |
Het |
Calr4 |
A |
T |
4: 109,096,161 (GRCm39) |
Q113L |
probably benign |
Het |
Carm1 |
T |
G |
9: 21,497,832 (GRCm39) |
|
probably null |
Het |
Ccdc30 |
A |
G |
4: 119,207,063 (GRCm39) |
L353P |
probably damaging |
Het |
Ccdc91 |
C |
G |
6: 147,491,957 (GRCm39) |
Q280E |
unknown |
Het |
Cdk5rap2 |
T |
C |
4: 70,185,109 (GRCm39) |
T1114A |
probably benign |
Het |
Ciao3 |
A |
C |
17: 25,997,944 (GRCm39) |
T154P |
probably damaging |
Het |
Dync2i2 |
C |
T |
2: 29,938,790 (GRCm39) |
R31Q |
probably benign |
Het |
Enpep |
T |
A |
3: 129,077,740 (GRCm39) |
T626S |
probably benign |
Het |
Epcam |
T |
C |
17: 87,947,721 (GRCm39) |
S64P |
probably damaging |
Het |
Erc1 |
G |
T |
6: 119,801,721 (GRCm39) |
P99T |
possibly damaging |
Het |
Fastkd1 |
A |
G |
2: 69,524,988 (GRCm39) |
L636S |
probably damaging |
Het |
Fmn1 |
A |
G |
2: 113,195,353 (GRCm39) |
D351G |
unknown |
Het |
Fndc8 |
T |
G |
11: 82,788,400 (GRCm39) |
S77A |
probably damaging |
Het |
Gbp10 |
G |
A |
5: 105,384,015 (GRCm39) |
|
probably benign |
Het |
Gemin6 |
T |
A |
17: 80,533,155 (GRCm39) |
Y29* |
probably null |
Het |
Gja8 |
T |
C |
3: 96,827,209 (GRCm39) |
E151G |
probably benign |
Het |
Gje1 |
A |
G |
10: 14,592,501 (GRCm39) |
Y94H |
probably damaging |
Het |
Glt6d1 |
A |
G |
2: 25,704,134 (GRCm39) |
F26S |
probably benign |
Het |
Gltpd2 |
T |
A |
11: 70,410,306 (GRCm39) |
|
probably null |
Het |
Gm10153 |
A |
C |
7: 141,743,859 (GRCm39) |
C70G |
unknown |
Het |
Gm28729 |
G |
A |
9: 96,376,410 (GRCm39) |
T368M |
probably damaging |
Het |
Gm4559 |
A |
G |
7: 141,827,677 (GRCm39) |
C142R |
unknown |
Het |
Golm1 |
T |
C |
13: 59,792,920 (GRCm39) |
N195S |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,487,522 (GRCm39) |
S3506C |
possibly damaging |
Het |
Hnrnpll |
G |
A |
17: 80,351,943 (GRCm39) |
S334L |
possibly damaging |
Het |
Ighv7-3 |
A |
T |
12: 114,116,865 (GRCm39) |
I99N |
possibly damaging |
Het |
Igkv8-24 |
A |
G |
6: 70,194,002 (GRCm39) |
S69P |
not run |
Het |
Ilvbl |
A |
T |
10: 78,419,531 (GRCm39) |
H537L |
possibly damaging |
Het |
Lama1 |
G |
A |
17: 68,089,036 (GRCm39) |
G1569D |
|
Het |
Lin7b |
A |
T |
7: 45,018,649 (GRCm39) |
Y118* |
probably null |
Het |
Mansc1 |
T |
A |
6: 134,587,674 (GRCm39) |
S168C |
possibly damaging |
Het |
Mast3 |
A |
G |
8: 71,233,838 (GRCm39) |
V969A |
probably damaging |
Het |
Muc4 |
C |
T |
16: 32,754,500 (GRCm38) |
T1458I |
probably benign |
Het |
Myh10 |
A |
G |
11: 68,692,992 (GRCm39) |
E1429G |
probably damaging |
Het |
Neurod1 |
G |
T |
2: 79,284,689 (GRCm39) |
Y231* |
probably null |
Het |
Nrxn2 |
G |
T |
19: 6,581,540 (GRCm39) |
E1492* |
probably null |
Het |
Nwd2 |
A |
G |
5: 63,964,736 (GRCm39) |
Q1440R |
probably benign |
Het |
Or10j3b |
A |
G |
1: 173,043,538 (GRCm39) |
T107A |
probably benign |
Het |
Or6z7 |
T |
A |
7: 6,483,330 (GRCm39) |
N275I |
probably damaging |
Het |
Or8u3-ps |
A |
G |
2: 85,952,720 (GRCm39) |
Y151C |
probably damaging |
Het |
Pacs1 |
T |
A |
19: 5,195,148 (GRCm39) |
T479S |
probably benign |
Het |
Pds5b |
A |
G |
5: 150,701,726 (GRCm39) |
K786E |
probably damaging |
Het |
Pigp |
A |
G |
16: 94,171,264 (GRCm39) |
L9P |
probably benign |
Het |
Plec |
C |
T |
15: 76,071,946 (GRCm39) |
R707Q |
unknown |
Het |
Ppef2 |
T |
A |
5: 92,400,993 (GRCm39) |
H9L |
possibly damaging |
Het |
Ppid |
T |
A |
3: 79,507,698 (GRCm39) |
C296S |
probably damaging |
Het |
Ppp2r5b |
T |
G |
19: 6,278,514 (GRCm39) |
E465A |
possibly damaging |
Het |
Ppp4r4 |
A |
G |
12: 103,562,708 (GRCm39) |
N559S |
probably damaging |
Het |
Ptprt |
T |
C |
2: 161,449,225 (GRCm39) |
T873A |
possibly damaging |
Het |
Rbpms |
A |
G |
8: 34,356,416 (GRCm39) |
V28A |
probably damaging |
Het |
Retreg2 |
A |
G |
1: 75,121,332 (GRCm39) |
M203V |
probably damaging |
Het |
Robo1 |
C |
T |
16: 72,767,069 (GRCm39) |
P414S |
probably damaging |
Het |
Sac3d1 |
T |
A |
19: 6,166,178 (GRCm39) |
E410D |
probably damaging |
Het |
Scgb2b19 |
A |
T |
7: 32,979,211 (GRCm39) |
C24S |
possibly damaging |
Het |
She |
T |
C |
3: 89,738,919 (GRCm39) |
F37L |
probably damaging |
Het |
Slc5a2 |
G |
A |
7: 127,864,977 (GRCm39) |
V37I |
probably damaging |
Het |
Smyd4 |
T |
A |
11: 75,281,032 (GRCm39) |
D168E |
probably benign |
Het |
Ssc5d |
C |
A |
7: 4,931,572 (GRCm39) |
P260T |
probably damaging |
Het |
Steap2 |
A |
G |
5: 5,727,406 (GRCm39) |
F310L |
probably benign |
Het |
Tctn1 |
A |
T |
5: 122,386,071 (GRCm39) |
I347N |
probably damaging |
Het |
Tmtc2 |
A |
G |
10: 105,206,482 (GRCm39) |
L271P |
probably damaging |
Het |
Tns3 |
T |
A |
11: 8,491,192 (GRCm39) |
M122L |
possibly damaging |
Het |
Ubr7 |
T |
G |
12: 102,735,398 (GRCm39) |
C286G |
probably damaging |
Het |
Usp16 |
T |
C |
16: 87,276,188 (GRCm39) |
S509P |
probably benign |
Het |
Usp44 |
A |
G |
10: 93,682,290 (GRCm39) |
T247A |
probably damaging |
Het |
Vmn2r92 |
A |
C |
17: 18,387,621 (GRCm39) |
M209L |
probably benign |
Het |
Zc3h6 |
C |
T |
2: 128,856,473 (GRCm39) |
P518S |
probably damaging |
Het |
Zfp229 |
A |
G |
17: 21,964,280 (GRCm39) |
H170R |
probably damaging |
Het |
Zfp960 |
A |
G |
17: 17,308,227 (GRCm39) |
T314A |
probably benign |
Het |
|
Other mutations in Rfx4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Rfx4
|
APN |
10 |
84,676,063 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00334:Rfx4
|
APN |
10 |
84,615,917 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00928:Rfx4
|
APN |
10 |
84,675,978 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01063:Rfx4
|
APN |
10 |
84,704,246 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01490:Rfx4
|
APN |
10 |
84,676,715 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02390:Rfx4
|
APN |
10 |
84,676,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02454:Rfx4
|
APN |
10 |
84,675,970 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0099:Rfx4
|
UTSW |
10 |
84,730,168 (GRCm39) |
missense |
probably benign |
|
R0503:Rfx4
|
UTSW |
10 |
84,730,196 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0924:Rfx4
|
UTSW |
10 |
84,704,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R0930:Rfx4
|
UTSW |
10 |
84,704,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R1386:Rfx4
|
UTSW |
10 |
84,699,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R1715:Rfx4
|
UTSW |
10 |
84,680,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R1738:Rfx4
|
UTSW |
10 |
84,716,839 (GRCm39) |
critical splice donor site |
probably null |
|
R1987:Rfx4
|
UTSW |
10 |
84,731,952 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3717:Rfx4
|
UTSW |
10 |
84,716,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R4231:Rfx4
|
UTSW |
10 |
84,650,558 (GRCm39) |
missense |
probably benign |
0.03 |
R4300:Rfx4
|
UTSW |
10 |
84,740,966 (GRCm39) |
missense |
probably damaging |
0.98 |
R4581:Rfx4
|
UTSW |
10 |
84,680,164 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4582:Rfx4
|
UTSW |
10 |
84,680,164 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4618:Rfx4
|
UTSW |
10 |
84,716,760 (GRCm39) |
missense |
probably benign |
0.01 |
R5156:Rfx4
|
UTSW |
10 |
84,704,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R5185:Rfx4
|
UTSW |
10 |
84,699,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5377:Rfx4
|
UTSW |
10 |
84,696,406 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5601:Rfx4
|
UTSW |
10 |
84,634,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5879:Rfx4
|
UTSW |
10 |
84,650,625 (GRCm39) |
critical splice donor site |
probably null |
|
R5996:Rfx4
|
UTSW |
10 |
84,675,881 (GRCm39) |
nonsense |
probably null |
|
R6358:Rfx4
|
UTSW |
10 |
84,680,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Rfx4
|
UTSW |
10 |
84,676,092 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7248:Rfx4
|
UTSW |
10 |
84,740,919 (GRCm39) |
missense |
probably benign |
0.05 |
R7427:Rfx4
|
UTSW |
10 |
84,731,876 (GRCm39) |
missense |
probably benign |
0.28 |
R7428:Rfx4
|
UTSW |
10 |
84,731,876 (GRCm39) |
missense |
probably benign |
0.28 |
R7514:Rfx4
|
UTSW |
10 |
84,716,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R8002:Rfx4
|
UTSW |
10 |
84,676,721 (GRCm39) |
missense |
probably damaging |
0.97 |
R8838:Rfx4
|
UTSW |
10 |
84,676,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R8938:Rfx4
|
UTSW |
10 |
84,675,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R9359:Rfx4
|
UTSW |
10 |
84,740,921 (GRCm39) |
missense |
probably benign |
0.00 |
R9513:Rfx4
|
UTSW |
10 |
84,674,050 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
RF010:Rfx4
|
UTSW |
10 |
84,694,351 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF014:Rfx4
|
UTSW |
10 |
84,694,353 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF015:Rfx4
|
UTSW |
10 |
84,694,353 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF023:Rfx4
|
UTSW |
10 |
84,694,349 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF030:Rfx4
|
UTSW |
10 |
84,694,344 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF035:Rfx4
|
UTSW |
10 |
84,694,344 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF046:Rfx4
|
UTSW |
10 |
84,694,345 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF060:Rfx4
|
UTSW |
10 |
84,694,358 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF062:Rfx4
|
UTSW |
10 |
84,694,345 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0024:Rfx4
|
UTSW |
10 |
84,615,938 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1177:Rfx4
|
UTSW |
10 |
84,731,955 (GRCm39) |
missense |
probably benign |
0.30 |
Z1177:Rfx4
|
UTSW |
10 |
84,650,548 (GRCm39) |
missense |
possibly damaging |
0.85 |
|