Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
G |
12: 71,289,801 (GRCm39) |
C1499G |
probably benign |
Het |
Aldoart1 |
A |
G |
4: 72,770,352 (GRCm39) |
V152A |
possibly damaging |
Het |
Alms1 |
T |
C |
6: 85,673,771 (GRCm39) |
L3591P |
probably benign |
Het |
Ankrd12 |
A |
T |
17: 66,356,843 (GRCm39) |
M58K |
probably damaging |
Het |
Asb3 |
A |
C |
11: 31,051,114 (GRCm39) |
I523L |
probably benign |
Het |
Ascl2 |
T |
C |
7: 142,522,436 (GRCm39) |
H4R |
possibly damaging |
Het |
Asic2 |
T |
C |
11: 80,862,413 (GRCm39) |
M246V |
probably damaging |
Het |
Btc |
A |
T |
5: 91,524,779 (GRCm39) |
C53S |
possibly damaging |
Het |
Cdhr5 |
T |
C |
7: 140,856,437 (GRCm39) |
I39M |
probably damaging |
Het |
Cdkn3 |
T |
A |
14: 47,004,807 (GRCm39) |
M123K |
possibly damaging |
Het |
Cebpz |
A |
G |
17: 79,233,542 (GRCm39) |
Y762H |
possibly damaging |
Het |
Ces1g |
T |
A |
8: 94,063,821 (GRCm39) |
|
probably benign |
Het |
Chd7 |
G |
T |
4: 8,844,417 (GRCm39) |
G1537W |
probably damaging |
Het |
Clca3a2 |
A |
T |
3: 144,793,703 (GRCm39) |
D317E |
probably damaging |
Het |
Clec3a |
C |
A |
8: 115,149,712 (GRCm39) |
N56K |
probably damaging |
Het |
Col11a1 |
T |
A |
3: 114,002,011 (GRCm39) |
|
probably null |
Het |
Cox20 |
G |
A |
1: 178,149,598 (GRCm39) |
|
probably benign |
Het |
Cyp2d22 |
A |
G |
15: 82,255,839 (GRCm39) |
V471A |
possibly damaging |
Het |
D630045J12Rik |
A |
G |
6: 38,135,163 (GRCm39) |
V1339A |
probably damaging |
Het |
Duox2 |
T |
C |
2: 122,112,352 (GRCm39) |
D1278G |
probably benign |
Het |
Epc1 |
G |
A |
18: 6,450,614 (GRCm39) |
P284L |
probably benign |
Het |
Evi5l |
G |
T |
8: 4,235,990 (GRCm39) |
R61L |
possibly damaging |
Het |
Fbln2 |
T |
C |
6: 91,243,365 (GRCm39) |
Y914H |
probably damaging |
Het |
Fbxo44 |
A |
G |
4: 148,238,030 (GRCm39) |
S191P |
probably damaging |
Het |
Fign |
A |
G |
2: 63,809,569 (GRCm39) |
I567T |
probably benign |
Het |
Fryl |
C |
T |
5: 73,262,117 (GRCm39) |
R550K |
probably damaging |
Het |
Gpcpd1 |
G |
A |
2: 132,400,597 (GRCm39) |
|
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,481,739 (GRCm39) |
I3096T |
probably benign |
Het |
Hic2 |
T |
A |
16: 17,075,712 (GRCm39) |
D180E |
probably benign |
Het |
Ibtk |
A |
G |
9: 85,617,057 (GRCm39) |
F172L |
possibly damaging |
Het |
Itga1 |
A |
G |
13: 115,138,845 (GRCm39) |
S369P |
possibly damaging |
Het |
Itgb4 |
G |
A |
11: 115,880,575 (GRCm39) |
R675Q |
probably null |
Het |
Lrrc3b |
T |
C |
14: 15,358,591 (GRCm38) |
D5G |
probably damaging |
Het |
Maml3 |
T |
A |
3: 52,011,146 (GRCm39) |
D140V |
probably damaging |
Het |
Med21 |
A |
G |
6: 146,550,683 (GRCm39) |
T65A |
probably benign |
Het |
Mta1 |
T |
C |
12: 113,095,186 (GRCm39) |
|
probably benign |
Het |
Mybpc1 |
T |
C |
10: 88,406,430 (GRCm39) |
D152G |
probably damaging |
Het |
Oas1b |
C |
A |
5: 120,960,269 (GRCm39) |
Q325K |
probably benign |
Het |
Or10j27 |
A |
G |
1: 172,958,673 (GRCm39) |
L37P |
probably benign |
Het |
Or2n1c |
C |
A |
17: 38,519,995 (GRCm39) |
N286K |
probably damaging |
Het |
Or5d44 |
A |
C |
2: 88,141,334 (GRCm39) |
C269G |
probably benign |
Het |
Pclo |
A |
G |
5: 14,726,626 (GRCm39) |
|
probably benign |
Het |
Phactr2 |
C |
T |
10: 13,129,360 (GRCm39) |
V233I |
possibly damaging |
Het |
Plekha2 |
A |
T |
8: 25,533,063 (GRCm39) |
|
probably null |
Het |
Reg3b |
A |
G |
6: 78,349,843 (GRCm39) |
M128V |
probably benign |
Het |
Rnaseh2a |
A |
G |
8: 85,684,735 (GRCm39) |
|
probably benign |
Het |
Scn5a |
T |
C |
9: 119,363,073 (GRCm39) |
S516G |
probably benign |
Het |
Serpina12 |
T |
A |
12: 104,001,807 (GRCm39) |
|
probably null |
Het |
Slc10a1 |
T |
C |
12: 81,000,540 (GRCm39) |
T320A |
possibly damaging |
Het |
Slc26a7 |
A |
T |
4: 14,519,402 (GRCm39) |
D539E |
probably benign |
Het |
Specc1l |
C |
A |
10: 75,082,007 (GRCm39) |
R485S |
possibly damaging |
Het |
Srp54b |
T |
G |
12: 55,302,366 (GRCm39) |
I339S |
probably damaging |
Het |
Tada1 |
G |
A |
1: 166,207,081 (GRCm39) |
|
probably benign |
Het |
Trim16 |
T |
C |
11: 62,711,751 (GRCm39) |
C54R |
probably damaging |
Het |
Trio |
C |
T |
15: 27,735,618 (GRCm39) |
R2824Q |
probably benign |
Het |
Ttpa |
A |
G |
4: 20,021,245 (GRCm39) |
I138V |
probably damaging |
Het |
Ubap2 |
A |
C |
4: 41,251,578 (GRCm39) |
M18R |
possibly damaging |
Het |
Usp38 |
A |
G |
8: 81,712,392 (GRCm39) |
S548P |
possibly damaging |
Het |
Vmn2r73 |
T |
C |
7: 85,525,046 (GRCm39) |
D34G |
probably benign |
Het |
Vps13d |
T |
A |
4: 144,904,904 (GRCm39) |
H74L |
probably damaging |
Het |
Zfp408 |
C |
T |
2: 91,475,588 (GRCm39) |
C622Y |
probably benign |
Het |
Zfp616 |
T |
C |
11: 73,975,321 (GRCm39) |
I530T |
possibly damaging |
Het |
Zfp9 |
C |
A |
6: 118,442,140 (GRCm39) |
C174F |
probably damaging |
Het |
Zfyve16 |
A |
G |
13: 92,658,096 (GRCm39) |
I605T |
possibly damaging |
Het |
Zmym5 |
T |
C |
14: 57,031,519 (GRCm39) |
T530A |
probably damaging |
Het |
|
Other mutations in Cfap44 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Cfap44
|
APN |
16 |
44,227,767 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00952:Cfap44
|
APN |
16 |
44,241,638 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01340:Cfap44
|
APN |
16 |
44,224,493 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01530:Cfap44
|
APN |
16 |
44,269,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02083:Cfap44
|
APN |
16 |
44,257,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Cfap44
|
APN |
16 |
44,271,991 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02142:Cfap44
|
APN |
16 |
44,241,507 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02311:Cfap44
|
APN |
16 |
44,225,134 (GRCm39) |
splice site |
probably benign |
|
IGL02574:Cfap44
|
APN |
16 |
44,301,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02893:Cfap44
|
APN |
16 |
44,237,180 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02959:Cfap44
|
APN |
16 |
44,291,230 (GRCm39) |
splice site |
probably benign |
|
IGL03291:Cfap44
|
APN |
16 |
44,227,674 (GRCm39) |
missense |
possibly damaging |
0.86 |
feldgrau
|
UTSW |
16 |
44,254,029 (GRCm39) |
nonsense |
probably null |
|
I2288:Cfap44
|
UTSW |
16 |
44,269,501 (GRCm39) |
nonsense |
probably null |
|
R0023:Cfap44
|
UTSW |
16 |
44,241,583 (GRCm39) |
missense |
probably benign |
0.01 |
R0023:Cfap44
|
UTSW |
16 |
44,241,583 (GRCm39) |
missense |
probably benign |
0.01 |
R0036:Cfap44
|
UTSW |
16 |
44,259,432 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0139:Cfap44
|
UTSW |
16 |
44,253,785 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0145:Cfap44
|
UTSW |
16 |
44,288,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Cfap44
|
UTSW |
16 |
44,269,573 (GRCm39) |
splice site |
probably null |
|
R0238:Cfap44
|
UTSW |
16 |
44,242,681 (GRCm39) |
missense |
probably benign |
|
R0238:Cfap44
|
UTSW |
16 |
44,242,681 (GRCm39) |
missense |
probably benign |
|
R0288:Cfap44
|
UTSW |
16 |
44,236,257 (GRCm39) |
splice site |
probably benign |
|
R0367:Cfap44
|
UTSW |
16 |
44,253,839 (GRCm39) |
critical splice donor site |
probably null |
|
R0452:Cfap44
|
UTSW |
16 |
44,252,308 (GRCm39) |
missense |
probably benign |
0.01 |
R0531:Cfap44
|
UTSW |
16 |
44,221,789 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R0722:Cfap44
|
UTSW |
16 |
44,225,039 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0801:Cfap44
|
UTSW |
16 |
44,242,849 (GRCm39) |
missense |
probably benign |
0.41 |
R1209:Cfap44
|
UTSW |
16 |
44,242,780 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1215:Cfap44
|
UTSW |
16 |
44,239,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1385:Cfap44
|
UTSW |
16 |
44,291,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Cfap44
|
UTSW |
16 |
44,241,575 (GRCm39) |
missense |
probably benign |
0.01 |
R1415:Cfap44
|
UTSW |
16 |
44,301,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R1475:Cfap44
|
UTSW |
16 |
44,254,175 (GRCm39) |
splice site |
probably benign |
|
R1901:Cfap44
|
UTSW |
16 |
44,242,737 (GRCm39) |
missense |
probably benign |
0.00 |
R1902:Cfap44
|
UTSW |
16 |
44,242,737 (GRCm39) |
missense |
probably benign |
0.00 |
R1903:Cfap44
|
UTSW |
16 |
44,242,737 (GRCm39) |
missense |
probably benign |
0.00 |
R2023:Cfap44
|
UTSW |
16 |
44,236,375 (GRCm39) |
missense |
probably benign |
0.01 |
R2126:Cfap44
|
UTSW |
16 |
44,230,838 (GRCm39) |
missense |
probably benign |
0.40 |
R2147:Cfap44
|
UTSW |
16 |
44,272,047 (GRCm39) |
missense |
probably benign |
0.31 |
R2233:Cfap44
|
UTSW |
16 |
44,271,888 (GRCm39) |
missense |
probably benign |
0.01 |
R2439:Cfap44
|
UTSW |
16 |
44,301,609 (GRCm39) |
unclassified |
probably benign |
|
R3015:Cfap44
|
UTSW |
16 |
44,230,832 (GRCm39) |
missense |
probably benign |
0.40 |
R4178:Cfap44
|
UTSW |
16 |
44,272,216 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4421:Cfap44
|
UTSW |
16 |
44,242,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4516:Cfap44
|
UTSW |
16 |
44,294,227 (GRCm39) |
nonsense |
probably null |
|
R4742:Cfap44
|
UTSW |
16 |
44,269,615 (GRCm39) |
splice site |
probably null |
|
R4766:Cfap44
|
UTSW |
16 |
44,236,246 (GRCm39) |
splice site |
probably null |
|
R4810:Cfap44
|
UTSW |
16 |
44,271,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R4955:Cfap44
|
UTSW |
16 |
44,295,640 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5058:Cfap44
|
UTSW |
16 |
44,240,567 (GRCm39) |
splice site |
probably null |
|
R5164:Cfap44
|
UTSW |
16 |
44,301,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R5172:Cfap44
|
UTSW |
16 |
44,269,556 (GRCm39) |
missense |
probably benign |
|
R5519:Cfap44
|
UTSW |
16 |
44,224,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R5572:Cfap44
|
UTSW |
16 |
44,301,668 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5601:Cfap44
|
UTSW |
16 |
44,280,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R5625:Cfap44
|
UTSW |
16 |
44,280,710 (GRCm39) |
splice site |
probably null |
|
R5638:Cfap44
|
UTSW |
16 |
44,275,894 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5727:Cfap44
|
UTSW |
16 |
44,255,805 (GRCm39) |
missense |
probably damaging |
0.98 |
R5950:Cfap44
|
UTSW |
16 |
44,300,210 (GRCm39) |
missense |
probably damaging |
0.99 |
R6057:Cfap44
|
UTSW |
16 |
44,269,460 (GRCm39) |
missense |
probably benign |
0.03 |
R6063:Cfap44
|
UTSW |
16 |
44,250,255 (GRCm39) |
missense |
probably benign |
0.00 |
R6221:Cfap44
|
UTSW |
16 |
44,257,549 (GRCm39) |
missense |
probably benign |
0.13 |
R6277:Cfap44
|
UTSW |
16 |
44,257,669 (GRCm39) |
missense |
probably benign |
0.04 |
R6322:Cfap44
|
UTSW |
16 |
44,254,029 (GRCm39) |
nonsense |
probably null |
|
R6836:Cfap44
|
UTSW |
16 |
44,224,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R6854:Cfap44
|
UTSW |
16 |
44,269,391 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6889:Cfap44
|
UTSW |
16 |
44,224,495 (GRCm39) |
missense |
probably benign |
0.03 |
R7233:Cfap44
|
UTSW |
16 |
44,242,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R7294:Cfap44
|
UTSW |
16 |
44,225,256 (GRCm39) |
intron |
probably benign |
|
R7298:Cfap44
|
UTSW |
16 |
44,301,775 (GRCm39) |
missense |
probably benign |
0.04 |
R7332:Cfap44
|
UTSW |
16 |
44,250,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R7410:Cfap44
|
UTSW |
16 |
44,288,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Cfap44
|
UTSW |
16 |
44,225,147 (GRCm39) |
intron |
probably benign |
|
R7456:Cfap44
|
UTSW |
16 |
44,252,305 (GRCm39) |
missense |
probably benign |
0.07 |
R7491:Cfap44
|
UTSW |
16 |
44,291,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R7587:Cfap44
|
UTSW |
16 |
44,224,469 (GRCm39) |
missense |
probably benign |
0.02 |
R7698:Cfap44
|
UTSW |
16 |
44,254,149 (GRCm39) |
missense |
probably damaging |
0.99 |
R7717:Cfap44
|
UTSW |
16 |
44,250,298 (GRCm39) |
missense |
probably damaging |
0.97 |
R7953:Cfap44
|
UTSW |
16 |
44,234,054 (GRCm39) |
missense |
probably benign |
0.00 |
R7994:Cfap44
|
UTSW |
16 |
44,252,501 (GRCm39) |
missense |
probably damaging |
0.97 |
R8043:Cfap44
|
UTSW |
16 |
44,234,054 (GRCm39) |
missense |
probably benign |
0.00 |
R8238:Cfap44
|
UTSW |
16 |
44,235,668 (GRCm39) |
splice site |
probably null |
|
R8338:Cfap44
|
UTSW |
16 |
44,239,698 (GRCm39) |
critical splice donor site |
probably null |
|
R8678:Cfap44
|
UTSW |
16 |
44,295,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Cfap44
|
UTSW |
16 |
44,225,085 (GRCm39) |
missense |
probably damaging |
0.98 |
R8785:Cfap44
|
UTSW |
16 |
44,275,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R8922:Cfap44
|
UTSW |
16 |
44,272,030 (GRCm39) |
missense |
probably benign |
0.23 |
R9005:Cfap44
|
UTSW |
16 |
44,280,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Cfap44
|
UTSW |
16 |
44,257,522 (GRCm39) |
missense |
probably damaging |
0.99 |
R9110:Cfap44
|
UTSW |
16 |
44,255,923 (GRCm39) |
missense |
probably damaging |
0.98 |
R9111:Cfap44
|
UTSW |
16 |
44,252,326 (GRCm39) |
missense |
probably benign |
0.00 |
R9126:Cfap44
|
UTSW |
16 |
44,295,619 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9187:Cfap44
|
UTSW |
16 |
44,225,144 (GRCm39) |
intron |
probably benign |
|
R9194:Cfap44
|
UTSW |
16 |
44,288,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R9251:Cfap44
|
UTSW |
16 |
44,229,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R9334:Cfap44
|
UTSW |
16 |
44,239,654 (GRCm39) |
missense |
probably damaging |
0.98 |
R9336:Cfap44
|
UTSW |
16 |
44,242,807 (GRCm39) |
missense |
probably damaging |
0.97 |
V1662:Cfap44
|
UTSW |
16 |
44,269,501 (GRCm39) |
nonsense |
probably null |
|
X0060:Cfap44
|
UTSW |
16 |
44,269,437 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1088:Cfap44
|
UTSW |
16 |
44,221,829 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Cfap44
|
UTSW |
16 |
44,252,407 (GRCm39) |
missense |
probably benign |
0.04 |
|