Incidental Mutation 'R0139:Cfap44'
| ID |
22215 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cfap44
|
| Ensembl Gene |
ENSMUSG00000071550 |
| Gene Name |
cilia and flagella associated protein 44 |
| Synonyms |
Wdr52, 6330444M21Rik, D16Ertd642e |
| MMRRC Submission |
038424-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0139 (G1)
|
| Quality Score |
203 |
|
Status
|
Validated
(trace)
|
| Chromosome |
16 |
| Chromosomal Location |
44215159-44302791 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to C
at 44253785 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glycine to Arginine
at position 893
(G893R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000113908
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099742]
[ENSMUST00000120049]
|
| AlphaFold |
E9Q5M6 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000099742
AA Change: G893R
PolyPhen 2
Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000097331
Gene: ENSMUSG00000071550
AA Change: G893R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
42 |
64 |
N/A |
INTRINSIC |
|
low complexity region
|
76 |
92 |
N/A |
INTRINSIC |
|
Blast:WD40
|
161 |
201 |
1e-7 |
BLAST |
|
WD40
|
204 |
246 |
4.58e1 |
SMART |
|
WD40
|
249 |
288 |
4.62e-1 |
SMART |
|
Blast:WD40
|
292 |
337 |
2e-15 |
BLAST |
|
WD40
|
342 |
381 |
4.8e-2 |
SMART |
|
WD40
|
447 |
486 |
4.95e-4 |
SMART |
|
WD40
|
491 |
532 |
2.64e2 |
SMART |
|
WD40
|
552 |
591 |
2.98e-7 |
SMART |
|
Blast:WD40
|
595 |
634 |
1e-19 |
BLAST |
|
coiled coil region
|
669 |
711 |
N/A |
INTRINSIC |
|
WD40
|
780 |
820 |
3.82e1 |
SMART |
|
WD40
|
830 |
872 |
2.4e-2 |
SMART |
|
coiled coil region
|
907 |
955 |
N/A |
INTRINSIC |
|
coiled coil region
|
1101 |
1122 |
N/A |
INTRINSIC |
|
low complexity region
|
1266 |
1295 |
N/A |
INTRINSIC |
|
low complexity region
|
1312 |
1325 |
N/A |
INTRINSIC |
|
coiled coil region
|
1402 |
1459 |
N/A |
INTRINSIC |
|
low complexity region
|
1476 |
1488 |
N/A |
INTRINSIC |
|
low complexity region
|
1489 |
1523 |
N/A |
INTRINSIC |
|
coiled coil region
|
1543 |
1607 |
N/A |
INTRINSIC |
|
coiled coil region
|
1630 |
1731 |
N/A |
INTRINSIC |
|
coiled coil region
|
1795 |
1822 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000120049
AA Change: G893R
PolyPhen 2
Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000113908
Gene: ENSMUSG00000071550
AA Change: G893R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
42 |
64 |
N/A |
INTRINSIC |
|
low complexity region
|
76 |
92 |
N/A |
INTRINSIC |
|
Blast:WD40
|
161 |
201 |
1e-7 |
BLAST |
|
WD40
|
204 |
246 |
4.58e1 |
SMART |
|
WD40
|
249 |
288 |
4.62e-1 |
SMART |
|
Blast:WD40
|
292 |
337 |
2e-15 |
BLAST |
|
WD40
|
342 |
381 |
4.8e-2 |
SMART |
|
WD40
|
447 |
486 |
4.95e-4 |
SMART |
|
WD40
|
491 |
532 |
2.64e2 |
SMART |
|
WD40
|
552 |
591 |
2.98e-7 |
SMART |
|
Blast:WD40
|
595 |
634 |
1e-19 |
BLAST |
|
coiled coil region
|
669 |
711 |
N/A |
INTRINSIC |
|
WD40
|
780 |
820 |
3.82e1 |
SMART |
|
WD40
|
830 |
872 |
2.4e-2 |
SMART |
|
coiled coil region
|
907 |
955 |
N/A |
INTRINSIC |
|
coiled coil region
|
1101 |
1122 |
N/A |
INTRINSIC |
|
low complexity region
|
1266 |
1295 |
N/A |
INTRINSIC |
|
low complexity region
|
1312 |
1325 |
N/A |
INTRINSIC |
|
coiled coil region
|
1402 |
1459 |
N/A |
INTRINSIC |
|
low complexity region
|
1476 |
1488 |
N/A |
INTRINSIC |
|
low complexity region
|
1489 |
1523 |
N/A |
INTRINSIC |
|
coiled coil region
|
1543 |
1607 |
N/A |
INTRINSIC |
|
coiled coil region
|
1630 |
1731 |
N/A |
INTRINSIC |
|
coiled coil region
|
1795 |
1822 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128916
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142648
|
| Meta Mutation Damage Score |
0.1450 |
| Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.1%
- 10x: 95.9%
- 20x: 91.2%
|
| Validation Efficiency |
97% (89/92) |
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele exhibit complete male sterility, asthenozoospermia, and teratozoospermia characterized by multiple sperm axonemal defects. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A230072I06Rik |
C |
T |
8: 12,329,899 (GRCm39) |
S118L |
unknown |
Het |
| Adprs |
A |
G |
4: 126,211,947 (GRCm39) |
Y122H |
probably damaging |
Het |
| Ankrd52 |
T |
C |
10: 128,222,007 (GRCm39) |
S544P |
probably benign |
Het |
| Aopep |
A |
G |
13: 63,338,298 (GRCm39) |
N558S |
probably benign |
Het |
| Arhgef7 |
A |
G |
8: 11,850,503 (GRCm39) |
E111G |
probably damaging |
Het |
| Atp11a |
A |
G |
8: 12,896,054 (GRCm39) |
M755V |
probably benign |
Het |
| Atp2a2 |
A |
G |
5: 122,629,778 (GRCm39) |
I97T |
probably damaging |
Het |
| Bmp3 |
G |
A |
5: 99,027,768 (GRCm39) |
D463N |
possibly damaging |
Het |
| Cacna2d4 |
T |
C |
6: 119,255,230 (GRCm39) |
|
probably benign |
Het |
| Ccdc28a |
G |
A |
10: 18,106,188 (GRCm39) |
S46F |
possibly damaging |
Het |
| Ccdc40 |
G |
A |
11: 119,155,125 (GRCm39) |
G1122S |
probably benign |
Het |
| Cenpw |
T |
G |
10: 30,076,455 (GRCm39) |
T8P |
probably benign |
Het |
| Cimap3 |
A |
T |
3: 105,906,886 (GRCm39) |
M171K |
possibly damaging |
Het |
| Cops7a |
A |
T |
6: 124,938,323 (GRCm39) |
C110S |
probably damaging |
Het |
| Cstl1 |
A |
G |
2: 148,597,245 (GRCm39) |
N134S |
probably damaging |
Het |
| Cyp2s1 |
G |
T |
7: 25,511,114 (GRCm39) |
|
probably null |
Het |
| Dio2 |
T |
A |
12: 90,696,617 (GRCm39) |
N124Y |
probably damaging |
Het |
| Ecel1 |
C |
A |
1: 87,082,248 (GRCm39) |
G155V |
possibly damaging |
Het |
| Efr3a |
G |
T |
15: 65,717,830 (GRCm39) |
V337F |
possibly damaging |
Het |
| Eva1b |
A |
C |
4: 126,043,446 (GRCm39) |
H162P |
probably damaging |
Het |
| Exoc5 |
C |
T |
14: 49,273,493 (GRCm39) |
E301K |
probably damaging |
Het |
| F13b |
G |
A |
1: 139,435,941 (GRCm39) |
S249N |
probably damaging |
Het |
| Fam120b |
C |
T |
17: 15,646,446 (GRCm39) |
|
probably benign |
Het |
| Gbf1 |
T |
C |
19: 46,250,231 (GRCm39) |
L396S |
probably damaging |
Het |
| Gck |
T |
A |
11: 5,859,139 (GRCm39) |
K143* |
probably null |
Het |
| Gck |
C |
A |
11: 5,860,370 (GRCm39) |
V91L |
probably damaging |
Het |
| Glt8d2 |
T |
C |
10: 82,496,644 (GRCm39) |
N138S |
probably damaging |
Het |
| Gm4884 |
T |
C |
7: 40,692,387 (GRCm39) |
F119L |
probably benign |
Het |
| Igsf11 |
T |
C |
16: 38,829,240 (GRCm39) |
S45P |
probably damaging |
Het |
| Iho1 |
T |
C |
9: 108,289,695 (GRCm39) |
T176A |
probably damaging |
Het |
| Il10 |
G |
A |
1: 130,950,271 (GRCm39) |
V142M |
probably damaging |
Het |
| Insc |
A |
T |
7: 114,368,237 (GRCm39) |
H9L |
probably damaging |
Het |
| Iqsec1 |
G |
T |
6: 90,786,740 (GRCm39) |
|
probably benign |
Het |
| Katnb1 |
A |
G |
8: 95,825,050 (GRCm39) |
S611G |
possibly damaging |
Het |
| Kcnb1 |
A |
G |
2: 166,947,459 (GRCm39) |
I463T |
possibly damaging |
Het |
| Lao1 |
A |
G |
4: 118,821,399 (GRCm39) |
N90S |
probably benign |
Het |
| Med16 |
T |
A |
10: 79,732,635 (GRCm39) |
M710L |
probably benign |
Het |
| Mroh2a |
G |
C |
1: 88,185,524 (GRCm39) |
E1510D |
probably damaging |
Het |
| Mtus1 |
G |
A |
8: 41,469,233 (GRCm39) |
|
probably benign |
Het |
| Mybpc3 |
A |
G |
2: 90,950,682 (GRCm39) |
|
probably benign |
Het |
| Ndor1 |
C |
T |
2: 25,138,366 (GRCm39) |
V405M |
possibly damaging |
Het |
| Nell2 |
A |
G |
15: 95,330,782 (GRCm39) |
V213A |
probably benign |
Het |
| Nme8 |
T |
C |
13: 19,862,018 (GRCm39) |
I204V |
probably benign |
Het |
| Nup133 |
A |
T |
8: 124,656,082 (GRCm39) |
N466K |
probably benign |
Het |
| Nxt1 |
A |
G |
2: 148,517,390 (GRCm39) |
T44A |
probably benign |
Het |
| Or14c46 |
T |
C |
7: 85,918,187 (GRCm39) |
E270G |
probably benign |
Het |
| Or2ag15 |
A |
T |
7: 106,340,832 (GRCm39) |
I103N |
probably benign |
Het |
| Or2y12 |
C |
T |
11: 49,426,401 (GRCm39) |
L130F |
probably benign |
Het |
| Or4e1 |
T |
C |
14: 52,700,669 (GRCm39) |
T239A |
probably damaging |
Het |
| Or4f7 |
A |
T |
2: 111,644,699 (GRCm39) |
I124K |
possibly damaging |
Het |
| Or7e168 |
C |
T |
9: 19,720,165 (GRCm39) |
L184F |
probably damaging |
Het |
| Pced1a |
T |
C |
2: 130,263,827 (GRCm39) |
K275R |
probably benign |
Het |
| Pdcd11 |
A |
G |
19: 47,099,398 (GRCm39) |
|
probably null |
Het |
| Phldb2 |
A |
C |
16: 45,591,029 (GRCm39) |
|
probably benign |
Het |
| Piwil1 |
C |
A |
5: 128,824,387 (GRCm39) |
S490Y |
probably damaging |
Het |
| Plekhh3 |
T |
C |
11: 101,054,501 (GRCm39) |
|
probably benign |
Het |
| Ppargc1b |
A |
T |
18: 61,449,034 (GRCm39) |
|
probably benign |
Het |
| Psg19 |
C |
T |
7: 18,530,942 (GRCm39) |
V71I |
possibly damaging |
Het |
| Ptk6 |
T |
C |
2: 180,838,724 (GRCm39) |
|
probably benign |
Het |
| Pus7 |
A |
G |
5: 23,983,090 (GRCm39) |
S126P |
probably damaging |
Het |
| Rab6b |
T |
A |
9: 103,017,576 (GRCm39) |
|
probably null |
Het |
| Ranbp3 |
G |
A |
17: 57,016,272 (GRCm39) |
R347Q |
possibly damaging |
Het |
| Sanbr |
A |
T |
11: 23,570,214 (GRCm39) |
|
probably benign |
Het |
| Sbf1 |
A |
T |
15: 89,186,701 (GRCm39) |
L866Q |
probably damaging |
Het |
| Slc25a34 |
A |
G |
4: 141,349,663 (GRCm39) |
V164A |
possibly damaging |
Het |
| Smg1 |
A |
G |
7: 117,751,898 (GRCm39) |
|
probably null |
Het |
| Spin1 |
G |
T |
13: 51,303,048 (GRCm39) |
V214L |
probably benign |
Het |
| Spmip2 |
A |
T |
3: 79,313,142 (GRCm39) |
Y72F |
probably damaging |
Het |
| Sptbn1 |
T |
C |
11: 30,092,289 (GRCm39) |
N492S |
probably benign |
Het |
| Stk-ps2 |
A |
G |
1: 46,068,955 (GRCm39) |
|
noncoding transcript |
Het |
| Taar7f |
T |
C |
10: 23,926,312 (GRCm39) |
I302T |
probably benign |
Het |
| Tdrd1 |
C |
A |
19: 56,831,630 (GRCm39) |
H340Q |
probably benign |
Het |
| Thumpd3 |
A |
G |
6: 113,044,762 (GRCm39) |
D498G |
probably benign |
Het |
| Tpgs2 |
A |
G |
18: 25,282,242 (GRCm39) |
L103P |
probably damaging |
Het |
| Trip10 |
A |
G |
17: 57,568,633 (GRCm39) |
|
probably null |
Het |
| Trip6 |
A |
T |
5: 137,310,436 (GRCm39) |
H269Q |
probably benign |
Het |
| Trmt12 |
T |
C |
15: 58,744,743 (GRCm39) |
V47A |
possibly damaging |
Het |
| Trpm7 |
A |
T |
2: 126,654,691 (GRCm39) |
S1416T |
probably benign |
Het |
| Tsks |
G |
A |
7: 44,603,883 (GRCm39) |
A438T |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,727,630 (GRCm39) |
|
probably benign |
Het |
| Twf2 |
G |
A |
9: 106,090,155 (GRCm39) |
V136M |
possibly damaging |
Het |
| Uty |
A |
C |
Y: 1,197,223 (GRCm39) |
Y115D |
probably damaging |
Het |
| Vcan |
A |
G |
13: 89,839,380 (GRCm39) |
S2055P |
probably damaging |
Het |
| Yes1 |
A |
G |
5: 32,842,039 (GRCm39) |
Q521R |
possibly damaging |
Het |
| Zfp114 |
A |
T |
7: 23,880,685 (GRCm39) |
T344S |
possibly damaging |
Het |
| Zfp661 |
A |
T |
2: 127,420,532 (GRCm39) |
V89D |
possibly damaging |
Het |
| Zfp91 |
A |
T |
19: 12,747,834 (GRCm39) |
Y430N |
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 |
|
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 |
|
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 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCTACAGGGCCTCCAACCGC -3'
(R):5'- TCCAGGTACAGAAATGGCATCAGAGAA -3'
Sequencing Primer
(F):5'- ccattcaccactacctccc -3'
(R):5'- TGGCATCAGAGAAAATTAGCATTC -3'
|
| Posted On |
2013-04-16 |
Incidental Mutation