Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
G |
9: 44,189,333 (GRCm39) |
D388A |
probably benign |
Het |
Ampd3 |
A |
C |
7: 110,401,730 (GRCm39) |
E408A |
probably damaging |
Het |
Bmp1 |
G |
T |
14: 70,723,606 (GRCm39) |
N743K |
probably benign |
Het |
Brsk1 |
A |
G |
7: 4,709,399 (GRCm39) |
K398E |
probably damaging |
Het |
Ccdc157 |
A |
T |
11: 4,101,888 (GRCm39) |
M11K |
probably damaging |
Het |
Cep295 |
A |
C |
9: 15,252,187 (GRCm39) |
M394R |
probably damaging |
Het |
Col13a1 |
C |
T |
10: 61,679,388 (GRCm39) |
G713R |
unknown |
Het |
Cxcr2 |
A |
T |
1: 74,197,991 (GRCm39) |
K162* |
probably null |
Het |
Cyp3a44 |
C |
T |
5: 145,716,376 (GRCm39) |
D405N |
possibly damaging |
Het |
Exo1 |
G |
T |
1: 175,721,380 (GRCm39) |
D340Y |
possibly damaging |
Het |
Farp2 |
T |
G |
1: 93,456,470 (GRCm39) |
L51R |
probably damaging |
Het |
Fat4 |
A |
T |
3: 38,943,083 (GRCm39) |
I659F |
possibly damaging |
Het |
Gbp2b |
T |
A |
3: 142,304,806 (GRCm39) |
W81R |
probably damaging |
Het |
Gipc2 |
C |
T |
3: 151,871,541 (GRCm39) |
|
probably benign |
Het |
Gm10941 |
G |
T |
10: 77,094,670 (GRCm39) |
|
probably benign |
Het |
Gm1988 |
A |
T |
7: 38,823,229 (GRCm39) |
|
noncoding transcript |
Het |
Hapln3 |
G |
T |
7: 78,767,006 (GRCm39) |
|
probably null |
Het |
Ifi213 |
A |
G |
1: 173,396,629 (GRCm39) |
S482P |
possibly damaging |
Het |
Insc |
A |
G |
7: 114,428,302 (GRCm39) |
T92A |
probably damaging |
Het |
Lrrn1 |
T |
A |
6: 107,544,315 (GRCm39) |
C38S |
probably damaging |
Het |
Mycbpap |
T |
C |
11: 94,396,519 (GRCm39) |
E107G |
probably damaging |
Het |
Neb |
A |
T |
2: 52,067,547 (GRCm39) |
L5848* |
probably null |
Het |
Nrg3 |
A |
T |
14: 38,092,950 (GRCm39) |
M545K |
probably damaging |
Het |
Nudt3 |
A |
G |
17: 27,802,202 (GRCm39) |
L28P |
probably damaging |
Het |
Or8g35 |
T |
A |
9: 39,381,099 (GRCm39) |
M308L |
probably benign |
Het |
Otop1 |
A |
T |
5: 38,460,104 (GRCm39) |
Y557F |
probably damaging |
Het |
Pcare |
T |
A |
17: 72,058,321 (GRCm39) |
D452V |
probably damaging |
Het |
Pdgfra |
G |
A |
5: 75,349,998 (GRCm39) |
|
probably null |
Het |
Pi4kb |
A |
G |
3: 94,891,988 (GRCm39) |
M223V |
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,209,699 (GRCm39) |
T2335A |
probably benign |
Het |
Ppp6c |
A |
G |
2: 39,087,453 (GRCm39) |
V251A |
probably benign |
Het |
Prkg1 |
C |
T |
19: 31,742,162 (GRCm39) |
E21K |
possibly damaging |
Het |
Ptpru |
T |
C |
4: 131,530,691 (GRCm39) |
E521G |
probably null |
Het |
Rasl10b |
G |
T |
11: 83,309,640 (GRCm39) |
R199L |
probably damaging |
Het |
Rhbdf2 |
G |
A |
11: 116,496,203 (GRCm39) |
R111C |
probably damaging |
Het |
Sec23ip |
G |
T |
7: 128,346,707 (GRCm39) |
|
probably benign |
Het |
Sptbn5 |
A |
T |
2: 119,910,273 (GRCm39) |
|
noncoding transcript |
Het |
Srsf11 |
C |
T |
3: 157,728,981 (GRCm39) |
|
probably benign |
Het |
Syne2 |
T |
C |
12: 76,141,886 (GRCm39) |
S6141P |
probably benign |
Het |
Szt2 |
A |
G |
4: 118,230,414 (GRCm39) |
V2653A |
unknown |
Het |
Tex46 |
T |
C |
4: 136,337,925 (GRCm39) |
F39S |
probably damaging |
Het |
Tmem50a |
AACCA |
AA |
4: 134,625,778 (GRCm39) |
|
probably benign |
Het |
Tmem62 |
G |
T |
2: 120,820,874 (GRCm39) |
W180L |
probably damaging |
Het |
Tnxb |
G |
A |
17: 34,904,185 (GRCm39) |
A1232T |
probably benign |
Het |
Tubgcp3 |
T |
C |
8: 12,674,888 (GRCm39) |
H744R |
possibly damaging |
Het |
Uggt2 |
A |
G |
14: 119,315,136 (GRCm39) |
I311T |
probably damaging |
Het |
Usp8 |
C |
T |
2: 126,584,197 (GRCm39) |
R469C |
probably damaging |
Het |
Vmn1r19 |
T |
C |
6: 57,382,281 (GRCm39) |
L278S |
probably damaging |
Het |
Vmn2r129 |
A |
T |
4: 156,686,505 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r59 |
A |
T |
7: 41,695,884 (GRCm39) |
I176N |
probably benign |
Het |
Wdr93 |
A |
G |
7: 79,420,766 (GRCm39) |
T376A |
probably benign |
Het |
Zfp575 |
G |
A |
7: 24,285,077 (GRCm39) |
A188V |
possibly 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 |
|
R5344:Cfap44
|
UTSW |
16 |
44,236,763 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|