Incidental Mutation 'R1171:Cfap43'
| ID |
99509 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cfap43
|
| Ensembl Gene |
ENSMUSG00000044948 |
| Gene Name |
cilia and flagella associated protein 43 |
| Synonyms |
D19Ertd652e, 4632415N18Rik, Wdr96, 4930428C11Rik, 4930463G05Rik |
| MMRRC Submission |
039244-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.111)
|
| Stock # |
R1171 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
19 |
| Chromosomal Location |
47723706-47825893 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 47824150 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Glutamic Acid
at position 74
(K74E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000125007
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000160247]
|
| AlphaFold |
E9Q7R9 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000026048
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159204
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000160247
AA Change: K74E
PolyPhen 2
Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000125007
Gene: ENSMUSG00000044948
AA Change: K74E
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
36 |
N/A |
INTRINSIC |
|
Blast:WD40
|
70 |
111 |
6e-7 |
BLAST |
|
Blast:WD40
|
115 |
156 |
1e-5 |
BLAST |
|
Blast:WD40
|
162 |
197 |
8e-10 |
BLAST |
|
WD40
|
349 |
388 |
1.07e0 |
SMART |
|
Blast:WD40
|
392 |
432 |
3e-13 |
BLAST |
|
WD40
|
435 |
473 |
3.96e1 |
SMART |
|
WD40
|
479 |
518 |
3.82e1 |
SMART |
|
Blast:WD40
|
638 |
683 |
8e-17 |
BLAST |
|
Blast:WD40
|
689 |
728 |
1e-17 |
BLAST |
|
low complexity region
|
766 |
781 |
N/A |
INTRINSIC |
|
coiled coil region
|
855 |
886 |
N/A |
INTRINSIC |
|
coiled coil region
|
925 |
961 |
N/A |
INTRINSIC |
|
low complexity region
|
971 |
981 |
N/A |
INTRINSIC |
|
coiled coil region
|
1170 |
1224 |
N/A |
INTRINSIC |
|
low complexity region
|
1248 |
1259 |
N/A |
INTRINSIC |
|
low complexity region
|
1268 |
1279 |
N/A |
INTRINSIC |
|
low complexity region
|
1524 |
1529 |
N/A |
INTRINSIC |
|
coiled coil region
|
1652 |
1671 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.6%
- 3x: 98.6%
- 10x: 96.2%
- 20x: 91.6%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the cilia- and flagella-associated protein family. [provided by RefSeq, Sep 2016]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit complete male sterility, asthenozoospermia, and teratozoospermia characterized by short, thick, and coiled flagella and sperm axonemal defects. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(4) : Gene trapped(4) |
| Other mutations in this stock |
Total: 92 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acsm5 |
A |
T |
7: 119,140,075 (GRCm39) |
E492V |
probably damaging |
Het |
| Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
| Atr |
T |
C |
9: 95,789,376 (GRCm39) |
F1511L |
probably damaging |
Het |
| Bdkrb2 |
G |
T |
12: 105,558,416 (GRCm39) |
R219L |
probably benign |
Het |
| Bhmt2 |
A |
T |
13: 93,798,837 (GRCm39) |
M328K |
probably benign |
Het |
| Btbd3 |
A |
G |
2: 138,125,881 (GRCm39) |
D286G |
probably benign |
Het |
| Bub1b |
T |
G |
2: 118,437,167 (GRCm39) |
L122V |
probably benign |
Het |
| Caml |
T |
C |
13: 55,772,820 (GRCm39) |
S155P |
probably damaging |
Het |
| Chst4 |
A |
G |
8: 110,757,255 (GRCm39) |
S120P |
probably damaging |
Het |
| Col11a1 |
A |
G |
3: 113,860,213 (GRCm39) |
D213G |
unknown |
Het |
| Cripto |
C |
A |
9: 110,772,235 (GRCm39) |
V54L |
probably benign |
Het |
| Cxcl10 |
TACTCAC |
TACTCACTCAC |
5: 92,495,941 (GRCm39) |
|
probably null |
Het |
| Cxcl10 |
CAC |
CACTAAC |
5: 92,495,945 (GRCm39) |
|
probably null |
Het |
| Cyp26b1 |
A |
T |
6: 84,553,653 (GRCm39) |
I167N |
possibly damaging |
Het |
| Dchs1 |
A |
G |
7: 105,406,921 (GRCm39) |
S2195P |
probably benign |
Het |
| Ddx25 |
T |
A |
9: 35,458,142 (GRCm39) |
K326* |
probably null |
Het |
| Dip2c |
A |
T |
13: 9,543,162 (GRCm39) |
Y36F |
possibly damaging |
Het |
| Dock2 |
T |
C |
11: 34,586,068 (GRCm39) |
D538G |
probably damaging |
Het |
| E4f1 |
C |
T |
17: 24,670,523 (GRCm39) |
D55N |
probably damaging |
Het |
| Emp1 |
G |
T |
6: 135,358,077 (GRCm39) |
W141L |
probably damaging |
Het |
| Faim2 |
T |
A |
15: 99,398,135 (GRCm39) |
H271L |
probably benign |
Het |
| Fbxw9 |
T |
C |
8: 85,792,707 (GRCm39) |
M352T |
possibly damaging |
Het |
| Fcrl2 |
A |
T |
3: 87,164,167 (GRCm39) |
F321I |
probably benign |
Het |
| Frzb |
C |
T |
2: 80,268,834 (GRCm39) |
|
probably null |
Het |
| Gal3st1 |
G |
T |
11: 3,948,931 (GRCm39) |
K379N |
probably damaging |
Het |
| Gm5519 |
G |
A |
19: 33,800,372 (GRCm39) |
C22Y |
possibly damaging |
Het |
| Gpn3 |
T |
C |
5: 122,516,583 (GRCm39) |
F71L |
probably benign |
Het |
| H2-M9 |
A |
G |
17: 36,952,545 (GRCm39) |
V167A |
probably benign |
Het |
| Hars1 |
A |
G |
18: 36,904,467 (GRCm39) |
F182L |
possibly damaging |
Het |
| Hid1 |
T |
C |
11: 115,243,543 (GRCm39) |
T502A |
probably benign |
Het |
| Hipk3 |
G |
T |
2: 104,302,021 (GRCm39) |
T57K |
probably benign |
Het |
| Iqsec2 |
A |
G |
X: 150,927,727 (GRCm39) |
S87G |
probably benign |
Het |
| Itpk1 |
G |
A |
12: 102,572,378 (GRCm39) |
L112F |
probably damaging |
Het |
| Klk1b9 |
T |
A |
7: 43,443,817 (GRCm39) |
D110E |
possibly damaging |
Het |
| Lemd3 |
A |
T |
10: 120,785,246 (GRCm39) |
M535K |
possibly damaging |
Het |
| Lipg |
A |
T |
18: 75,078,894 (GRCm39) |
S453T |
possibly damaging |
Het |
| Lrrc75a |
A |
T |
11: 62,500,069 (GRCm39) |
W150R |
probably damaging |
Het |
| Lyg1 |
T |
C |
1: 37,986,305 (GRCm39) |
E143G |
probably damaging |
Het |
| Map3k1 |
A |
G |
13: 111,892,177 (GRCm39) |
V1026A |
probably benign |
Het |
| Mgat3 |
T |
A |
15: 80,095,838 (GRCm39) |
F222I |
probably benign |
Het |
| Mindy4 |
A |
T |
6: 55,232,601 (GRCm39) |
N348I |
possibly damaging |
Het |
| Ms4a20 |
T |
C |
19: 11,089,741 (GRCm39) |
Y48C |
probably damaging |
Het |
| Myo1b |
A |
C |
1: 51,817,684 (GRCm39) |
F532C |
probably damaging |
Het |
| Naif1 |
T |
A |
2: 32,342,558 (GRCm39) |
N36K |
probably damaging |
Het |
| Nkpd1 |
C |
A |
7: 19,258,012 (GRCm39) |
A597E |
possibly damaging |
Het |
| Npr2 |
A |
G |
4: 43,647,260 (GRCm39) |
D772G |
possibly damaging |
Het |
| Or52n4 |
T |
G |
7: 104,294,204 (GRCm39) |
D123A |
probably damaging |
Het |
| Or6a2 |
T |
C |
7: 106,600,791 (GRCm39) |
N92S |
probably benign |
Het |
| Pcolce2 |
A |
T |
9: 95,576,793 (GRCm39) |
M355L |
probably benign |
Het |
| Pdgfra |
A |
T |
5: 75,334,108 (GRCm39) |
I394F |
probably damaging |
Het |
| Pdzrn3 |
G |
A |
6: 101,127,838 (GRCm39) |
R943C |
probably damaging |
Het |
| Pml |
A |
G |
9: 58,141,821 (GRCm39) |
V337A |
probably damaging |
Het |
| Pnpla2 |
T |
A |
7: 141,038,794 (GRCm39) |
M321K |
probably benign |
Het |
| Poln |
A |
T |
5: 34,261,284 (GRCm39) |
N546K |
probably damaging |
Het |
| Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
| Prss28 |
T |
A |
17: 25,529,029 (GRCm39) |
F123L |
possibly damaging |
Het |
| Psg18 |
A |
G |
7: 18,080,004 (GRCm39) |
V399A |
probably benign |
Het |
| Rab5a |
T |
C |
17: 53,813,443 (GRCm39) |
C212R |
probably damaging |
Het |
| Ranbp6 |
A |
T |
19: 29,789,679 (GRCm39) |
D224E |
probably benign |
Het |
| Recql4 |
T |
C |
15: 76,588,239 (GRCm39) |
I1104M |
possibly damaging |
Het |
| Rev1 |
A |
T |
1: 38,127,581 (GRCm39) |
N226K |
possibly damaging |
Het |
| Rhbdl3 |
T |
A |
11: 80,244,418 (GRCm39) |
V375E |
possibly damaging |
Het |
| Senp6 |
T |
A |
9: 80,024,007 (GRCm39) |
N423K |
possibly damaging |
Het |
| Sertad2 |
C |
G |
11: 20,598,091 (GRCm39) |
L96V |
probably benign |
Het |
| Slc33a1 |
T |
A |
3: 63,861,315 (GRCm39) |
T296S |
probably benign |
Het |
| Smurf2 |
G |
A |
11: 106,743,444 (GRCm39) |
P188S |
possibly damaging |
Het |
| Spta1 |
T |
A |
1: 174,039,180 (GRCm39) |
Y1174* |
probably null |
Het |
| Stra6l |
A |
T |
4: 45,864,982 (GRCm39) |
T103S |
probably benign |
Het |
| Swt1 |
C |
T |
1: 151,281,272 (GRCm39) |
A352T |
probably damaging |
Het |
| Thoc2l |
T |
C |
5: 104,668,769 (GRCm39) |
V1097A |
possibly damaging |
Het |
| Tigd2 |
T |
A |
6: 59,188,361 (GRCm39) |
N409K |
possibly damaging |
Het |
| Tlr6 |
G |
T |
5: 65,112,593 (GRCm39) |
H105N |
probably benign |
Het |
| Tmprss9 |
A |
C |
10: 80,715,692 (GRCm39) |
T15P |
possibly damaging |
Het |
| Tnik |
C |
T |
3: 28,587,089 (GRCm39) |
T120M |
probably damaging |
Het |
| Tnr |
T |
A |
1: 159,685,780 (GRCm39) |
I337N |
probably damaging |
Het |
| Top3a |
A |
G |
11: 60,641,419 (GRCm39) |
Y422H |
probably benign |
Het |
| Trim67 |
A |
G |
8: 125,555,820 (GRCm39) |
N768S |
probably damaging |
Het |
| Ttn |
A |
G |
2: 76,536,310 (GRCm39) |
V35016A |
probably benign |
Het |
| Utrn |
A |
C |
10: 12,357,052 (GRCm39) |
S312R |
probably damaging |
Het |
| Vdac2 |
A |
G |
14: 21,887,879 (GRCm39) |
Y62C |
probably damaging |
Het |
| Vwa5b2 |
A |
G |
16: 20,423,734 (GRCm39) |
T1216A |
probably benign |
Het |
| Wfdc16 |
T |
C |
2: 164,480,403 (GRCm39) |
K31E |
possibly damaging |
Het |
| Wtip |
C |
T |
7: 33,824,921 (GRCm39) |
C221Y |
probably damaging |
Het |
| Xrn1 |
A |
G |
9: 95,873,064 (GRCm39) |
D640G |
possibly damaging |
Het |
| Zdhhc5 |
T |
C |
2: 84,522,685 (GRCm39) |
R293G |
probably benign |
Het |
| Zfp536 |
T |
C |
7: 37,269,059 (GRCm39) |
D119G |
probably damaging |
Het |
| Zfp81 |
T |
C |
17: 33,554,254 (GRCm39) |
T187A |
probably benign |
Het |
| Zfp810 |
C |
T |
9: 22,190,122 (GRCm39) |
G262D |
possibly damaging |
Het |
| Zfp963 |
A |
C |
8: 70,195,669 (GRCm39) |
I203M |
possibly damaging |
Het |
| Zfpm2 |
T |
C |
15: 40,965,075 (GRCm39) |
M520T |
probably damaging |
Het |
| Zswim8 |
G |
A |
14: 20,763,181 (GRCm39) |
R360Q |
possibly damaging |
Het |
| Zwilch |
T |
A |
9: 64,065,999 (GRCm39) |
H254L |
possibly damaging |
Het |
|
| Other mutations in Cfap43 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00158:Cfap43
|
APN |
19 |
47,818,914 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL00325:Cfap43
|
APN |
19 |
47,811,627 (GRCm39) |
splice site |
probably benign |
|
|
IGL00918:Cfap43
|
APN |
19 |
47,885,100 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01402:Cfap43
|
APN |
19 |
47,784,105 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL01404:Cfap43
|
APN |
19 |
47,784,105 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL01656:Cfap43
|
APN |
19 |
47,740,339 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL01738:Cfap43
|
APN |
19 |
47,785,624 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02168:Cfap43
|
APN |
19 |
47,740,362 (GRCm39) |
splice site |
probably benign |
|
|
IGL02225:Cfap43
|
APN |
19 |
47,800,616 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02308:Cfap43
|
APN |
19 |
47,736,463 (GRCm39) |
missense |
probably benign |
|
|
IGL02354:Cfap43
|
APN |
19 |
47,885,852 (GRCm39) |
nonsense |
probably null |
|
|
IGL02361:Cfap43
|
APN |
19 |
47,885,852 (GRCm39) |
nonsense |
probably null |
|
|
IGL03283:Cfap43
|
APN |
19 |
47,779,851 (GRCm39) |
splice site |
probably benign |
|
|
3-1:Cfap43
|
UTSW |
19 |
47,740,294 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03046:Cfap43
|
UTSW |
19 |
47,804,302 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4495001:Cfap43
|
UTSW |
19 |
47,885,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0270:Cfap43
|
UTSW |
19 |
47,785,642 (GRCm39) |
splice site |
probably benign |
|
|
R0421:Cfap43
|
UTSW |
19 |
47,824,014 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0433:Cfap43
|
UTSW |
19 |
47,814,210 (GRCm39) |
missense |
probably benign |
0.44 |
|
R0576:Cfap43
|
UTSW |
19 |
47,785,579 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0646:Cfap43
|
UTSW |
19 |
47,752,115 (GRCm39) |
missense |
probably benign |
0.25 |
|
R0740:Cfap43
|
UTSW |
19 |
47,824,243 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0836:Cfap43
|
UTSW |
19 |
47,804,285 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0899:Cfap43
|
UTSW |
19 |
47,736,433 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1271:Cfap43
|
UTSW |
19 |
47,736,387 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1271:Cfap43
|
UTSW |
19 |
47,728,183 (GRCm39) |
missense |
probably benign |
0.22 |
|
R1371:Cfap43
|
UTSW |
19 |
47,824,045 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1469:Cfap43
|
UTSW |
19 |
47,885,314 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1541:Cfap43
|
UTSW |
19 |
47,752,291 (GRCm39) |
splice site |
probably null |
|
|
R1625:Cfap43
|
UTSW |
19 |
47,739,527 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1679:Cfap43
|
UTSW |
19 |
47,761,553 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1690:Cfap43
|
UTSW |
19 |
47,739,505 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1820:Cfap43
|
UTSW |
19 |
47,885,655 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1891:Cfap43
|
UTSW |
19 |
47,802,380 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1956:Cfap43
|
UTSW |
19 |
47,885,649 (GRCm39) |
missense |
probably benign |
0.19 |
|
R1958:Cfap43
|
UTSW |
19 |
47,885,649 (GRCm39) |
missense |
probably benign |
0.19 |
|
R2110:Cfap43
|
UTSW |
19 |
47,824,197 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2118:Cfap43
|
UTSW |
19 |
47,758,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2290:Cfap43
|
UTSW |
19 |
47,761,574 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3691:Cfap43
|
UTSW |
19 |
47,885,512 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3765:Cfap43
|
UTSW |
19 |
47,824,014 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3917:Cfap43
|
UTSW |
19 |
47,886,189 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3924:Cfap43
|
UTSW |
19 |
47,785,555 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3925:Cfap43
|
UTSW |
19 |
47,785,555 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3947:Cfap43
|
UTSW |
19 |
47,754,418 (GRCm39) |
missense |
probably benign |
0.28 |
|
R4256:Cfap43
|
UTSW |
19 |
47,770,844 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4385:Cfap43
|
UTSW |
19 |
47,785,568 (GRCm39) |
missense |
probably benign |
0.28 |
|
R4395:Cfap43
|
UTSW |
19 |
47,740,352 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4405:Cfap43
|
UTSW |
19 |
47,728,236 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R4541:Cfap43
|
UTSW |
19 |
47,736,454 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4583:Cfap43
|
UTSW |
19 |
47,825,655 (GRCm39) |
missense |
probably null |
0.99 |
|
R4690:Cfap43
|
UTSW |
19 |
47,736,298 (GRCm39) |
missense |
probably benign |
0.45 |
|
R4852:Cfap43
|
UTSW |
19 |
47,885,550 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5185:Cfap43
|
UTSW |
19 |
47,768,833 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5192:Cfap43
|
UTSW |
19 |
47,814,364 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5196:Cfap43
|
UTSW |
19 |
47,814,364 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5197:Cfap43
|
UTSW |
19 |
47,885,811 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5205:Cfap43
|
UTSW |
19 |
47,885,987 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R5425:Cfap43
|
UTSW |
19 |
47,885,371 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5516:Cfap43
|
UTSW |
19 |
47,726,648 (GRCm39) |
splice site |
probably null |
|
|
R5644:Cfap43
|
UTSW |
19 |
47,784,114 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R5844:Cfap43
|
UTSW |
19 |
47,784,135 (GRCm39) |
missense |
probably benign |
|
|
R5901:Cfap43
|
UTSW |
19 |
47,885,538 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5910:Cfap43
|
UTSW |
19 |
47,768,710 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R5920:Cfap43
|
UTSW |
19 |
47,749,335 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R5963:Cfap43
|
UTSW |
19 |
47,734,013 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6817:Cfap43
|
UTSW |
19 |
47,744,524 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R6974:Cfap43
|
UTSW |
19 |
47,773,717 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7219:Cfap43
|
UTSW |
19 |
47,779,912 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7270:Cfap43
|
UTSW |
19 |
47,728,224 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7733:Cfap43
|
UTSW |
19 |
47,886,432 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R7995:Cfap43
|
UTSW |
19 |
47,886,462 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8013:Cfap43
|
UTSW |
19 |
47,761,548 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8176:Cfap43
|
UTSW |
19 |
47,784,114 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8242:Cfap43
|
UTSW |
19 |
47,885,808 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8303:Cfap43
|
UTSW |
19 |
47,754,274 (GRCm39) |
nonsense |
probably null |
|
|
R8333:Cfap43
|
UTSW |
19 |
47,885,765 (GRCm39) |
nonsense |
probably null |
|
|
R8353:Cfap43
|
UTSW |
19 |
47,735,086 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8453:Cfap43
|
UTSW |
19 |
47,735,086 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8474:Cfap43
|
UTSW |
19 |
47,886,363 (GRCm39) |
missense |
probably benign |
0.32 |
|
R8478:Cfap43
|
UTSW |
19 |
47,764,515 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8676:Cfap43
|
UTSW |
19 |
47,736,456 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8928:Cfap43
|
UTSW |
19 |
47,804,399 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9190:Cfap43
|
UTSW |
19 |
47,726,293 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R9426:Cfap43
|
UTSW |
19 |
47,814,237 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9450:Cfap43
|
UTSW |
19 |
47,886,310 (GRCm39) |
missense |
probably benign |
0.23 |
|
R9491:Cfap43
|
UTSW |
19 |
47,800,505 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9515:Cfap43
|
UTSW |
19 |
47,773,814 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9732:Cfap43
|
UTSW |
19 |
47,775,446 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
|
| Posted On |
2014-01-15 |
Incidental Mutation