Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3100002H09Rik |
A |
G |
4: 124,504,445 (GRCm39) |
S36P |
probably damaging |
Het |
Agmo |
A |
G |
12: 37,302,538 (GRCm39) |
D125G |
probably damaging |
Het |
Arhgap26 |
A |
T |
18: 39,490,880 (GRCm39) |
S328C |
probably null |
Het |
Arl6 |
T |
C |
16: 59,439,169 (GRCm39) |
D175G |
probably damaging |
Het |
Asb3 |
G |
A |
11: 31,005,559 (GRCm39) |
A192T |
probably damaging |
Het |
Atp10b |
A |
T |
11: 43,126,573 (GRCm39) |
M1110L |
possibly damaging |
Het |
Cacna1i |
T |
C |
15: 80,220,883 (GRCm39) |
I175T |
probably damaging |
Het |
Car15 |
A |
T |
16: 17,655,227 (GRCm39) |
I71N |
probably benign |
Het |
Casq1 |
T |
A |
1: 172,044,407 (GRCm39) |
Y140F |
probably benign |
Het |
Ccdc93 |
C |
T |
1: 121,362,269 (GRCm39) |
T17M |
possibly damaging |
Het |
Cfap46 |
CCTTCTTCT |
CCTTCT |
7: 139,218,816 (GRCm39) |
|
probably benign |
Het |
Ciart |
G |
A |
3: 95,788,323 (GRCm39) |
|
probably benign |
Het |
Cul5 |
A |
T |
9: 53,558,094 (GRCm39) |
V170D |
probably benign |
Het |
Cyb5r3 |
T |
C |
15: 83,038,917 (GRCm39) |
D224G |
probably benign |
Het |
Daam1 |
G |
A |
12: 72,035,723 (GRCm39) |
G964R |
probably damaging |
Het |
Daglb |
T |
A |
5: 143,475,689 (GRCm39) |
L383Q |
probably damaging |
Het |
Dazap2 |
T |
G |
15: 100,514,864 (GRCm39) |
H28Q |
possibly damaging |
Het |
Dnttip2 |
A |
T |
3: 122,068,905 (GRCm39) |
D40V |
probably benign |
Het |
Dynlt2b |
T |
A |
16: 32,245,727 (GRCm39) |
D125E |
possibly damaging |
Het |
Epn1 |
G |
T |
7: 5,098,925 (GRCm39) |
D406Y |
probably damaging |
Het |
Epn1 |
G |
T |
7: 5,098,935 (GRCm39) |
R409L |
probably damaging |
Het |
Evc |
T |
C |
5: 37,457,843 (GRCm39) |
T966A |
probably benign |
Het |
Extl3 |
T |
C |
14: 65,314,375 (GRCm39) |
D269G |
probably damaging |
Het |
Gfra3 |
TGCGC |
TGC |
18: 34,828,864 (GRCm39) |
|
probably null |
Het |
Gpr87 |
A |
T |
3: 59,086,528 (GRCm39) |
F326I |
probably damaging |
Het |
Hivep3 |
C |
A |
4: 119,952,137 (GRCm39) |
P151H |
probably damaging |
Het |
Kcnj14 |
T |
A |
7: 45,467,440 (GRCm39) |
E302V |
probably damaging |
Het |
Kdm5d |
T |
C |
Y: 921,693 (GRCm39) |
Y534H |
probably damaging |
Homo |
Map3k5 |
T |
A |
10: 20,014,006 (GRCm39) |
|
probably null |
Het |
Mdn1 |
A |
G |
4: 32,748,590 (GRCm39) |
T4212A |
probably benign |
Het |
Ms4a6d |
A |
T |
19: 11,564,504 (GRCm39) |
S122R |
probably damaging |
Het |
Mtarc1 |
G |
A |
1: 184,527,648 (GRCm39) |
R271W |
probably damaging |
Het |
Nectin3 |
A |
T |
16: 46,215,513 (GRCm39) |
H76Q |
probably damaging |
Het |
Notch1 |
C |
A |
2: 26,364,182 (GRCm39) |
E846D |
possibly damaging |
Het |
Or1e23 |
A |
G |
11: 73,407,534 (GRCm39) |
S164P |
probably benign |
Het |
Or4a67 |
T |
C |
2: 88,598,632 (GRCm39) |
E9G |
probably damaging |
Het |
Or8b36 |
GTTT |
GTTTGCTTTTT |
9: 37,937,842 (GRCm39) |
|
probably null |
Het |
Or8b36 |
TT |
TTGCTGTGT |
9: 37,937,844 (GRCm39) |
|
probably null |
Het |
Or8b36 |
G |
GGGATTGC |
9: 37,937,833 (GRCm39) |
|
probably null |
Het |
Or8b36 |
TGTTT |
TGTTTGCAGTTT |
9: 37,937,841 (GRCm39) |
|
probably null |
Het |
Or8g18 |
T |
A |
9: 39,149,514 (GRCm39) |
I72F |
possibly damaging |
Het |
Pfkl |
C |
T |
10: 77,825,399 (GRCm39) |
|
probably null |
Het |
Pigz |
T |
C |
16: 31,764,424 (GRCm39) |
V494A |
possibly damaging |
Het |
Pik3r4 |
T |
C |
9: 105,531,247 (GRCm39) |
V516A |
probably benign |
Het |
Polr2b |
G |
A |
5: 77,496,141 (GRCm39) |
R1104K |
probably benign |
Het |
Rap1a |
A |
T |
3: 105,639,311 (GRCm39) |
L116* |
probably null |
Het |
Rnf114 |
T |
C |
2: 167,356,649 (GRCm39) |
*230R |
probably null |
Het |
Serpinb5 |
G |
T |
1: 106,802,795 (GRCm39) |
R110I |
possibly damaging |
Het |
Spink6 |
T |
C |
18: 44,207,498 (GRCm39) |
|
probably null |
Het |
Spopfm1 |
G |
T |
3: 94,173,208 (GRCm39) |
S72I |
probably damaging |
Het |
Stk39 |
A |
T |
2: 68,137,383 (GRCm39) |
|
probably null |
Het |
Tcstv2a |
T |
C |
13: 120,724,907 (GRCm39) |
|
probably benign |
Het |
Tcte1 |
A |
T |
17: 45,846,085 (GRCm39) |
T230S |
probably benign |
Het |
Tecpr1 |
C |
A |
5: 144,135,394 (GRCm39) |
V1020L |
probably damaging |
Het |
Tmc7 |
T |
C |
7: 118,160,261 (GRCm39) |
Y192C |
possibly damaging |
Het |
Trim63 |
A |
T |
4: 134,050,537 (GRCm39) |
T274S |
probably benign |
Het |
Wdr43 |
G |
A |
17: 71,957,048 (GRCm39) |
|
probably null |
Het |
Zfr |
T |
C |
15: 12,160,677 (GRCm39) |
I750T |
probably benign |
Het |
|
Other mutations in Rtl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00672:Rtl1
|
APN |
12 |
109,559,434 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01981:Rtl1
|
APN |
12 |
109,558,369 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02418:Rtl1
|
APN |
12 |
109,556,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03164:Rtl1
|
APN |
12 |
109,559,367 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Rtl1
|
UTSW |
12 |
109,557,632 (GRCm39) |
small deletion |
probably benign |
|
R0109:Rtl1
|
UTSW |
12 |
109,561,841 (GRCm39) |
start gained |
probably benign |
|
R0141:Rtl1
|
UTSW |
12 |
109,559,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Rtl1
|
UTSW |
12 |
109,556,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R0389:Rtl1
|
UTSW |
12 |
109,556,797 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0390:Rtl1
|
UTSW |
12 |
109,557,820 (GRCm39) |
missense |
unknown |
|
R0548:Rtl1
|
UTSW |
12 |
109,558,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R0561:Rtl1
|
UTSW |
12 |
109,560,363 (GRCm39) |
missense |
probably damaging |
0.99 |
R0624:Rtl1
|
UTSW |
12 |
109,559,153 (GRCm39) |
missense |
probably damaging |
0.97 |
R0746:Rtl1
|
UTSW |
12 |
109,559,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R1353:Rtl1
|
UTSW |
12 |
109,558,633 (GRCm39) |
missense |
probably benign |
0.00 |
R1868:Rtl1
|
UTSW |
12 |
109,556,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Rtl1
|
UTSW |
12 |
109,558,354 (GRCm39) |
missense |
probably benign |
0.42 |
R2000:Rtl1
|
UTSW |
12 |
109,560,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R2094:Rtl1
|
UTSW |
12 |
109,557,831 (GRCm39) |
missense |
unknown |
|
R2125:Rtl1
|
UTSW |
12 |
109,560,355 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2166:Rtl1
|
UTSW |
12 |
109,556,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R2247:Rtl1
|
UTSW |
12 |
109,561,413 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2274:Rtl1
|
UTSW |
12 |
109,561,101 (GRCm39) |
missense |
unknown |
|
R2919:Rtl1
|
UTSW |
12 |
109,557,582 (GRCm39) |
missense |
unknown |
|
R2998:Rtl1
|
UTSW |
12 |
109,561,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R4554:Rtl1
|
UTSW |
12 |
109,560,762 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4566:Rtl1
|
UTSW |
12 |
109,559,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Rtl1
|
UTSW |
12 |
109,558,138 (GRCm39) |
missense |
probably damaging |
0.96 |
R5399:Rtl1
|
UTSW |
12 |
109,556,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R5512:Rtl1
|
UTSW |
12 |
109,557,805 (GRCm39) |
missense |
unknown |
|
R5616:Rtl1
|
UTSW |
12 |
109,559,173 (GRCm39) |
missense |
unknown |
|
R5644:Rtl1
|
UTSW |
12 |
109,558,013 (GRCm39) |
missense |
probably benign |
0.03 |
R5647:Rtl1
|
UTSW |
12 |
109,561,113 (GRCm39) |
missense |
unknown |
|
R5695:Rtl1
|
UTSW |
12 |
109,560,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R5714:Rtl1
|
UTSW |
12 |
109,560,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R5786:Rtl1
|
UTSW |
12 |
109,559,053 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5917:Rtl1
|
UTSW |
12 |
109,558,087 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5948:Rtl1
|
UTSW |
12 |
109,557,033 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6051:Rtl1
|
UTSW |
12 |
109,559,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R6342:Rtl1
|
UTSW |
12 |
109,558,735 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6433:Rtl1
|
UTSW |
12 |
109,561,630 (GRCm39) |
missense |
unknown |
|
R6815:Rtl1
|
UTSW |
12 |
109,560,937 (GRCm39) |
missense |
probably damaging |
0.98 |
R6968:Rtl1
|
UTSW |
12 |
109,561,113 (GRCm39) |
missense |
unknown |
|
R7002:Rtl1
|
UTSW |
12 |
109,560,381 (GRCm39) |
missense |
probably damaging |
0.97 |
R7020:Rtl1
|
UTSW |
12 |
109,558,749 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7026:Rtl1
|
UTSW |
12 |
109,559,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R7027:Rtl1
|
UTSW |
12 |
109,557,848 (GRCm39) |
small deletion |
probably benign |
|
R7196:Rtl1
|
UTSW |
12 |
109,559,221 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7239:Rtl1
|
UTSW |
12 |
109,558,909 (GRCm39) |
missense |
probably benign |
0.05 |
R7312:Rtl1
|
UTSW |
12 |
109,561,672 (GRCm39) |
missense |
unknown |
|
R7476:Rtl1
|
UTSW |
12 |
109,557,539 (GRCm39) |
missense |
unknown |
|
R7589:Rtl1
|
UTSW |
12 |
109,560,279 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7655:Rtl1
|
UTSW |
12 |
109,557,442 (GRCm39) |
missense |
unknown |
|
R7656:Rtl1
|
UTSW |
12 |
109,557,442 (GRCm39) |
missense |
unknown |
|
R7657:Rtl1
|
UTSW |
12 |
109,561,818 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7720:Rtl1
|
UTSW |
12 |
109,560,864 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7772:Rtl1
|
UTSW |
12 |
109,559,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Rtl1
|
UTSW |
12 |
109,560,589 (GRCm39) |
missense |
probably benign |
0.08 |
R7890:Rtl1
|
UTSW |
12 |
109,559,251 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7893:Rtl1
|
UTSW |
12 |
109,560,355 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7894:Rtl1
|
UTSW |
12 |
109,561,031 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7909:Rtl1
|
UTSW |
12 |
109,558,914 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7909:Rtl1
|
UTSW |
12 |
109,556,611 (GRCm39) |
missense |
unknown |
|
R7986:Rtl1
|
UTSW |
12 |
109,558,492 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8007:Rtl1
|
UTSW |
12 |
109,558,060 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8146:Rtl1
|
UTSW |
12 |
109,557,145 (GRCm39) |
missense |
probably benign |
0.01 |
R8193:Rtl1
|
UTSW |
12 |
109,558,650 (GRCm39) |
missense |
probably benign |
0.03 |
R8263:Rtl1
|
UTSW |
12 |
109,560,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R8273:Rtl1
|
UTSW |
12 |
109,559,149 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8512:Rtl1
|
UTSW |
12 |
109,561,051 (GRCm39) |
missense |
unknown |
|
R8514:Rtl1
|
UTSW |
12 |
109,560,307 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8748:Rtl1
|
UTSW |
12 |
109,561,492 (GRCm39) |
missense |
probably benign |
0.39 |
R9036:Rtl1
|
UTSW |
12 |
109,559,691 (GRCm39) |
missense |
probably benign |
0.03 |
R9104:Rtl1
|
UTSW |
12 |
109,560,718 (GRCm39) |
missense |
probably benign |
0.21 |
R9151:Rtl1
|
UTSW |
12 |
109,560,007 (GRCm39) |
missense |
|
|
R9238:Rtl1
|
UTSW |
12 |
109,561,017 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9292:Rtl1
|
UTSW |
12 |
109,556,673 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9329:Rtl1
|
UTSW |
12 |
109,556,673 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9332:Rtl1
|
UTSW |
12 |
109,557,291 (GRCm39) |
missense |
probably benign |
0.01 |
R9342:Rtl1
|
UTSW |
12 |
109,558,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9350:Rtl1
|
UTSW |
12 |
109,557,226 (GRCm39) |
nonsense |
probably null |
|
R9446:Rtl1
|
UTSW |
12 |
109,556,604 (GRCm39) |
makesense |
probably null |
|
R9523:Rtl1
|
UTSW |
12 |
109,561,113 (GRCm39) |
missense |
unknown |
|
R9524:Rtl1
|
UTSW |
12 |
109,556,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R9535:Rtl1
|
UTSW |
12 |
109,561,698 (GRCm39) |
missense |
unknown |
|
R9535:Rtl1
|
UTSW |
12 |
109,557,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Rtl1
|
UTSW |
12 |
109,556,713 (GRCm39) |
missense |
probably benign |
0.19 |
R9615:Rtl1
|
UTSW |
12 |
109,556,835 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9661:Rtl1
|
UTSW |
12 |
109,557,346 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9674:Rtl1
|
UTSW |
12 |
109,559,024 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9720:Rtl1
|
UTSW |
12 |
109,559,882 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1088:Rtl1
|
UTSW |
12 |
109,558,753 (GRCm39) |
missense |
probably benign |
0.02 |
|