Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl6 |
A |
G |
11: 54,227,961 (GRCm39) |
E327G |
probably damaging |
Het |
Adcy6 |
T |
C |
15: 98,496,260 (GRCm39) |
D593G |
probably benign |
Het |
Ankmy1 |
T |
C |
1: 92,816,370 (GRCm39) |
D248G |
probably damaging |
Het |
Atp2a1 |
T |
C |
7: 126,047,428 (GRCm39) |
I743V |
possibly damaging |
Het |
Axdnd1 |
T |
C |
1: 156,208,456 (GRCm39) |
N396D |
possibly damaging |
Het |
Cacna1e |
C |
T |
1: 154,318,024 (GRCm39) |
A1391T |
probably damaging |
Het |
Ccr8 |
G |
A |
9: 119,923,415 (GRCm39) |
G177S |
probably damaging |
Het |
Clmn |
C |
T |
12: 104,747,276 (GRCm39) |
G757D |
possibly damaging |
Het |
Cntn2 |
T |
A |
1: 132,456,750 (GRCm39) |
I99F |
probably damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,088,650 (GRCm39) |
A271G |
unknown |
Het |
Dnah1 |
A |
T |
14: 30,987,872 (GRCm39) |
C3515* |
probably null |
Het |
Eif2d |
A |
G |
1: 131,082,100 (GRCm39) |
Y64C |
probably damaging |
Het |
Elovl4 |
A |
G |
9: 83,667,162 (GRCm39) |
F65S |
probably damaging |
Het |
F5 |
G |
C |
1: 164,026,486 (GRCm39) |
R1686P |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,209,550 (GRCm39) |
E938G |
probably benign |
Het |
Foxn1 |
T |
C |
11: 78,249,825 (GRCm39) |
T567A |
probably benign |
Het |
Gabrr1 |
T |
C |
4: 33,162,781 (GRCm39) |
M449T |
probably benign |
Het |
Gdf2 |
C |
T |
14: 33,663,178 (GRCm39) |
P24L |
probably damaging |
Het |
Itgb3bp |
T |
C |
4: 99,690,433 (GRCm39) |
I29V |
probably benign |
Het |
Kcnk7 |
C |
T |
19: 5,754,830 (GRCm39) |
|
probably null |
Het |
Klf11 |
T |
C |
12: 24,710,247 (GRCm39) |
S432P |
probably damaging |
Het |
Neo1 |
C |
T |
9: 58,829,160 (GRCm39) |
A580T |
probably benign |
Het |
Nexmif |
G |
T |
X: 103,128,555 (GRCm39) |
Q1121K |
probably benign |
Het |
Or51aa5 |
T |
C |
7: 103,166,931 (GRCm39) |
Y220C |
probably damaging |
Het |
Or51f5 |
T |
C |
7: 102,423,872 (GRCm39) |
I47T |
probably damaging |
Het |
Or5p62 |
T |
C |
7: 107,771,217 (GRCm39) |
T245A |
probably benign |
Het |
Osgepl1 |
G |
T |
1: 53,362,354 (GRCm39) |
E399* |
probably null |
Het |
Parvg |
T |
A |
15: 84,215,222 (GRCm39) |
V197E |
probably damaging |
Het |
Pcyt2 |
A |
G |
11: 120,502,870 (GRCm39) |
L257P |
probably damaging |
Het |
Pou3f2 |
T |
C |
4: 22,486,960 (GRCm39) |
D391G |
possibly damaging |
Het |
Psmd2 |
C |
T |
16: 20,474,079 (GRCm39) |
R261C |
probably benign |
Het |
Ptpn13 |
T |
C |
5: 103,722,998 (GRCm39) |
F1981L |
probably benign |
Het |
Rbp3 |
A |
T |
14: 33,680,604 (GRCm39) |
I1069F |
probably benign |
Het |
Rhbdf2 |
A |
T |
11: 116,490,987 (GRCm39) |
L655Q |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,331,063 (GRCm39) |
N317K |
possibly damaging |
Het |
Serpina3f |
T |
C |
12: 104,184,612 (GRCm39) |
V252A |
probably damaging |
Het |
Slc22a23 |
C |
T |
13: 34,528,366 (GRCm39) |
G139S |
possibly damaging |
Het |
Smyd2 |
T |
C |
1: 189,621,059 (GRCm39) |
T220A |
possibly damaging |
Het |
Snrpb2 |
T |
A |
2: 142,907,281 (GRCm39) |
|
probably benign |
Het |
Spopfm1 |
A |
G |
3: 94,173,102 (GRCm39) |
M37V |
probably benign |
Het |
Sptan1 |
A |
T |
2: 29,903,530 (GRCm39) |
I1502F |
probably damaging |
Het |
Srprb |
A |
T |
9: 103,074,794 (GRCm39) |
L116H |
probably damaging |
Het |
Stradb |
T |
A |
1: 59,016,174 (GRCm39) |
|
probably benign |
Het |
Tm9sf4 |
C |
A |
2: 153,045,734 (GRCm39) |
F535L |
probably damaging |
Het |
Tmprss15 |
A |
T |
16: 78,821,736 (GRCm39) |
S440T |
possibly damaging |
Het |
Usp34 |
C |
T |
11: 23,417,243 (GRCm39) |
T2964I |
possibly damaging |
Het |
Usp35 |
C |
A |
7: 96,960,874 (GRCm39) |
E851* |
probably null |
Het |
Zc3h14 |
T |
A |
12: 98,723,460 (GRCm39) |
V250D |
probably damaging |
Het |
Zfp568 |
T |
A |
7: 29,722,746 (GRCm39) |
C564S |
probably damaging |
Het |
|
Other mutations in Tpr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Tpr
|
APN |
1 |
150,299,447 (GRCm39) |
splice site |
probably benign |
|
IGL00424:Tpr
|
APN |
1 |
150,274,346 (GRCm39) |
splice site |
probably benign |
|
IGL01095:Tpr
|
APN |
1 |
150,285,891 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01347:Tpr
|
APN |
1 |
150,302,738 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01519:Tpr
|
APN |
1 |
150,306,919 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01768:Tpr
|
APN |
1 |
150,320,199 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01939:Tpr
|
APN |
1 |
150,289,496 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01988:Tpr
|
APN |
1 |
150,302,750 (GRCm39) |
splice site |
probably null |
|
IGL02065:Tpr
|
APN |
1 |
150,289,525 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02110:Tpr
|
APN |
1 |
150,311,493 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02311:Tpr
|
APN |
1 |
150,274,404 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02454:Tpr
|
APN |
1 |
150,306,943 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02569:Tpr
|
APN |
1 |
150,301,382 (GRCm39) |
unclassified |
probably benign |
|
IGL03168:Tpr
|
APN |
1 |
150,284,508 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03193:Tpr
|
APN |
1 |
150,315,831 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03333:Tpr
|
APN |
1 |
150,302,718 (GRCm39) |
missense |
probably benign |
0.04 |
gridiron
|
UTSW |
1 |
150,299,267 (GRCm39) |
missense |
probably damaging |
1.00 |
Pouch
|
UTSW |
1 |
150,309,523 (GRCm39) |
missense |
probably damaging |
1.00 |
punt
|
UTSW |
1 |
150,293,790 (GRCm39) |
missense |
probably benign |
0.02 |
Turf
|
UTSW |
1 |
150,317,996 (GRCm39) |
critical splice donor site |
probably null |
|
F6893:Tpr
|
UTSW |
1 |
150,269,313 (GRCm39) |
missense |
possibly damaging |
0.84 |
PIT4305001:Tpr
|
UTSW |
1 |
150,315,888 (GRCm39) |
missense |
possibly damaging |
0.85 |
PIT4469001:Tpr
|
UTSW |
1 |
150,279,707 (GRCm39) |
missense |
probably benign |
0.41 |
R0085:Tpr
|
UTSW |
1 |
150,293,164 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0101:Tpr
|
UTSW |
1 |
150,285,053 (GRCm39) |
splice site |
probably benign |
|
R0116:Tpr
|
UTSW |
1 |
150,285,898 (GRCm39) |
missense |
probably damaging |
0.98 |
R0136:Tpr
|
UTSW |
1 |
150,306,346 (GRCm39) |
missense |
probably benign |
0.01 |
R0207:Tpr
|
UTSW |
1 |
150,293,178 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0219:Tpr
|
UTSW |
1 |
150,319,009 (GRCm39) |
splice site |
probably null |
|
R0380:Tpr
|
UTSW |
1 |
150,288,698 (GRCm39) |
missense |
probably benign |
0.27 |
R0403:Tpr
|
UTSW |
1 |
150,283,165 (GRCm39) |
splice site |
probably benign |
|
R0469:Tpr
|
UTSW |
1 |
150,299,418 (GRCm39) |
frame shift |
probably null |
|
R0480:Tpr
|
UTSW |
1 |
150,303,992 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0514:Tpr
|
UTSW |
1 |
150,278,024 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0563:Tpr
|
UTSW |
1 |
150,284,609 (GRCm39) |
missense |
probably benign |
0.13 |
R0631:Tpr
|
UTSW |
1 |
150,298,282 (GRCm39) |
missense |
probably damaging |
0.98 |
R0685:Tpr
|
UTSW |
1 |
150,309,476 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0730:Tpr
|
UTSW |
1 |
150,269,158 (GRCm39) |
utr 5 prime |
probably benign |
|
R0780:Tpr
|
UTSW |
1 |
150,307,092 (GRCm39) |
missense |
probably benign |
0.00 |
R1018:Tpr
|
UTSW |
1 |
150,317,934 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1084:Tpr
|
UTSW |
1 |
150,317,912 (GRCm39) |
missense |
probably benign |
0.18 |
R1532:Tpr
|
UTSW |
1 |
150,293,751 (GRCm39) |
missense |
probably damaging |
0.99 |
R1551:Tpr
|
UTSW |
1 |
150,312,552 (GRCm39) |
missense |
probably benign |
0.00 |
R1608:Tpr
|
UTSW |
1 |
150,302,644 (GRCm39) |
missense |
probably damaging |
0.96 |
R1759:Tpr
|
UTSW |
1 |
150,305,275 (GRCm39) |
missense |
probably benign |
0.19 |
R1817:Tpr
|
UTSW |
1 |
150,295,654 (GRCm39) |
missense |
probably damaging |
0.98 |
R1932:Tpr
|
UTSW |
1 |
150,297,414 (GRCm39) |
missense |
probably benign |
0.00 |
R1978:Tpr
|
UTSW |
1 |
150,295,658 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2031:Tpr
|
UTSW |
1 |
150,317,870 (GRCm39) |
missense |
probably benign |
|
R2176:Tpr
|
UTSW |
1 |
150,295,691 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2235:Tpr
|
UTSW |
1 |
150,317,843 (GRCm39) |
missense |
probably benign |
0.33 |
R2339:Tpr
|
UTSW |
1 |
150,289,525 (GRCm39) |
missense |
probably benign |
0.01 |
R2367:Tpr
|
UTSW |
1 |
150,309,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R2507:Tpr
|
UTSW |
1 |
150,268,695 (GRCm39) |
start codon destroyed |
probably null |
|
R3931:Tpr
|
UTSW |
1 |
150,311,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R4320:Tpr
|
UTSW |
1 |
150,299,325 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4439:Tpr
|
UTSW |
1 |
150,279,712 (GRCm39) |
missense |
probably benign |
0.01 |
R4568:Tpr
|
UTSW |
1 |
150,268,710 (GRCm39) |
unclassified |
probably benign |
|
R4644:Tpr
|
UTSW |
1 |
150,299,250 (GRCm39) |
missense |
probably benign |
0.01 |
R4665:Tpr
|
UTSW |
1 |
150,320,150 (GRCm39) |
missense |
probably damaging |
0.97 |
R4672:Tpr
|
UTSW |
1 |
150,299,318 (GRCm39) |
missense |
probably benign |
0.45 |
R4673:Tpr
|
UTSW |
1 |
150,299,318 (GRCm39) |
missense |
probably benign |
0.45 |
R4735:Tpr
|
UTSW |
1 |
150,317,947 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4767:Tpr
|
UTSW |
1 |
150,306,280 (GRCm39) |
intron |
probably benign |
|
R4772:Tpr
|
UTSW |
1 |
150,288,864 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4815:Tpr
|
UTSW |
1 |
150,274,359 (GRCm39) |
missense |
probably benign |
0.01 |
R4839:Tpr
|
UTSW |
1 |
150,324,948 (GRCm39) |
nonsense |
probably null |
|
R4844:Tpr
|
UTSW |
1 |
150,321,630 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4925:Tpr
|
UTSW |
1 |
150,308,316 (GRCm39) |
missense |
probably benign |
0.00 |
R4967:Tpr
|
UTSW |
1 |
150,285,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R5017:Tpr
|
UTSW |
1 |
150,274,388 (GRCm39) |
missense |
probably benign |
0.00 |
R5096:Tpr
|
UTSW |
1 |
150,321,953 (GRCm39) |
missense |
probably damaging |
0.99 |
R5353:Tpr
|
UTSW |
1 |
150,321,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Tpr
|
UTSW |
1 |
150,321,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R5484:Tpr
|
UTSW |
1 |
150,302,639 (GRCm39) |
missense |
probably benign |
0.33 |
R5601:Tpr
|
UTSW |
1 |
150,311,604 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5642:Tpr
|
UTSW |
1 |
150,299,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R5779:Tpr
|
UTSW |
1 |
150,299,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R5787:Tpr
|
UTSW |
1 |
150,271,037 (GRCm39) |
missense |
probably benign |
0.01 |
R5892:Tpr
|
UTSW |
1 |
150,283,151 (GRCm39) |
missense |
probably benign |
0.44 |
R5915:Tpr
|
UTSW |
1 |
150,301,400 (GRCm39) |
missense |
probably benign |
0.15 |
R5928:Tpr
|
UTSW |
1 |
150,303,878 (GRCm39) |
missense |
probably benign |
0.30 |
R6146:Tpr
|
UTSW |
1 |
150,298,913 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6154:Tpr
|
UTSW |
1 |
150,299,567 (GRCm39) |
missense |
probably benign |
0.00 |
R6234:Tpr
|
UTSW |
1 |
150,293,790 (GRCm39) |
missense |
probably benign |
0.02 |
R6263:Tpr
|
UTSW |
1 |
150,317,996 (GRCm39) |
critical splice donor site |
probably null |
|
R6318:Tpr
|
UTSW |
1 |
150,321,639 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6550:Tpr
|
UTSW |
1 |
150,299,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6592:Tpr
|
UTSW |
1 |
150,287,656 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6704:Tpr
|
UTSW |
1 |
150,282,259 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6716:Tpr
|
UTSW |
1 |
150,290,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6836:Tpr
|
UTSW |
1 |
150,312,424 (GRCm39) |
splice site |
probably null |
|
R6886:Tpr
|
UTSW |
1 |
150,299,716 (GRCm39) |
missense |
probably benign |
0.00 |
R6894:Tpr
|
UTSW |
1 |
150,312,598 (GRCm39) |
missense |
probably benign |
0.28 |
R6928:Tpr
|
UTSW |
1 |
150,284,536 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7011:Tpr
|
UTSW |
1 |
150,309,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:Tpr
|
UTSW |
1 |
150,299,358 (GRCm39) |
missense |
probably benign |
0.02 |
R7036:Tpr
|
UTSW |
1 |
150,299,358 (GRCm39) |
missense |
probably benign |
0.02 |
R7183:Tpr
|
UTSW |
1 |
150,282,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7221:Tpr
|
UTSW |
1 |
150,321,929 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7223:Tpr
|
UTSW |
1 |
150,315,007 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7294:Tpr
|
UTSW |
1 |
150,279,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Tpr
|
UTSW |
1 |
150,269,245 (GRCm39) |
missense |
unknown |
|
R7361:Tpr
|
UTSW |
1 |
150,323,372 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7405:Tpr
|
UTSW |
1 |
150,317,878 (GRCm39) |
missense |
probably benign |
0.02 |
R7637:Tpr
|
UTSW |
1 |
150,299,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R7720:Tpr
|
UTSW |
1 |
150,305,283 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7721:Tpr
|
UTSW |
1 |
150,320,180 (GRCm39) |
missense |
probably benign |
|
R7751:Tpr
|
UTSW |
1 |
150,295,646 (GRCm39) |
missense |
probably benign |
0.17 |
R7804:Tpr
|
UTSW |
1 |
150,308,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R7878:Tpr
|
UTSW |
1 |
150,299,411 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7973:Tpr
|
UTSW |
1 |
150,279,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R8013:Tpr
|
UTSW |
1 |
150,274,359 (GRCm39) |
missense |
probably benign |
|
R8220:Tpr
|
UTSW |
1 |
150,308,164 (GRCm39) |
missense |
probably benign |
0.05 |
R8274:Tpr
|
UTSW |
1 |
150,299,230 (GRCm39) |
splice site |
probably benign |
|
R8428:Tpr
|
UTSW |
1 |
150,290,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R8482:Tpr
|
UTSW |
1 |
150,309,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R8699:Tpr
|
UTSW |
1 |
150,293,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R8859:Tpr
|
UTSW |
1 |
150,284,597 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9119:Tpr
|
UTSW |
1 |
150,279,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R9326:Tpr
|
UTSW |
1 |
150,301,407 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9618:Tpr
|
UTSW |
1 |
150,321,979 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9680:Tpr
|
UTSW |
1 |
150,314,887 (GRCm39) |
missense |
probably benign |
0.32 |
R9776:Tpr
|
UTSW |
1 |
150,324,939 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Tpr
|
UTSW |
1 |
150,270,958 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tpr
|
UTSW |
1 |
150,303,986 (GRCm39) |
missense |
probably damaging |
0.99 |
|