Incidental Mutation 'R0452:Cfap44'
ID |
39722 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cfap44
|
Ensembl Gene |
ENSMUSG00000071550 |
Gene Name |
cilia and flagella associated protein 44 |
Synonyms |
Wdr52, 6330444M21Rik, D16Ertd642e |
MMRRC Submission |
038652-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0452 (G1)
|
Quality Score |
163 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
44215159-44302791 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 44252308 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Leucine
at position 806
(M806L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000113908
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099742]
[ENSMUST00000120049]
|
AlphaFold |
E9Q5M6 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000099742
AA Change: M806L
PolyPhen 2
Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
|
SMART Domains |
Protein: ENSMUSP00000097331 Gene: ENSMUSG00000071550 AA Change: M806L
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 |
probably benign
Transcript: ENSMUST00000120049
AA Change: M806L
PolyPhen 2
Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
|
SMART Domains |
Protein: ENSMUSP00000113908 Gene: ENSMUSG00000071550 AA Change: M806L
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 |
0.0720 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.7%
|
Validation Efficiency |
99% (93/94) |
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: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030452D12Rik |
A |
G |
8: 107,233,822 (GRCm39) |
|
probably benign |
Het |
Acap3 |
C |
A |
4: 155,986,785 (GRCm39) |
S347* |
probably null |
Het |
Acvr1 |
G |
A |
2: 58,390,507 (GRCm39) |
P19L |
probably benign |
Het |
Add2 |
G |
T |
6: 86,081,611 (GRCm39) |
E366* |
probably null |
Het |
Ankrd28 |
C |
A |
14: 31,470,695 (GRCm39) |
A153S |
probably damaging |
Het |
Anxa8 |
A |
T |
14: 33,816,727 (GRCm39) |
I206F |
probably damaging |
Het |
Arhgef4 |
G |
A |
1: 34,771,403 (GRCm39) |
E1237K |
probably damaging |
Het |
Arid1a |
C |
T |
4: 133,416,416 (GRCm39) |
A1120T |
unknown |
Het |
Atad5 |
T |
C |
11: 79,997,247 (GRCm39) |
V857A |
probably damaging |
Het |
Atp2a3 |
T |
A |
11: 72,868,058 (GRCm39) |
|
probably null |
Het |
Atxn1l |
C |
T |
8: 110,459,027 (GRCm39) |
V412I |
possibly damaging |
Het |
Card11 |
A |
G |
5: 140,866,125 (GRCm39) |
S923P |
probably benign |
Het |
Cars1 |
C |
A |
7: 143,146,362 (GRCm39) |
E21* |
probably null |
Het |
Ccdc115 |
A |
G |
1: 34,476,702 (GRCm39) |
|
probably benign |
Het |
Ccnj |
T |
A |
19: 40,833,508 (GRCm39) |
|
probably null |
Het |
Cds2 |
C |
T |
2: 132,140,399 (GRCm39) |
T182I |
probably damaging |
Het |
Ceacam14 |
A |
G |
7: 17,549,248 (GRCm39) |
H213R |
probably benign |
Het |
Chd8 |
A |
T |
14: 52,452,044 (GRCm39) |
I1317K |
probably damaging |
Het |
Cherp |
A |
T |
8: 73,215,366 (GRCm39) |
|
probably benign |
Het |
Creb5 |
C |
G |
6: 53,581,527 (GRCm39) |
T30S |
possibly damaging |
Het |
Csf2ra |
A |
G |
19: 61,215,333 (GRCm39) |
M94T |
probably benign |
Het |
Cyp2b19 |
A |
C |
7: 26,466,187 (GRCm39) |
D330A |
probably benign |
Het |
Ddost |
G |
A |
4: 138,037,499 (GRCm39) |
V188M |
possibly damaging |
Het |
Dnah7a |
A |
T |
1: 53,644,978 (GRCm39) |
D1019E |
probably benign |
Het |
Dtx1 |
A |
T |
5: 120,833,057 (GRCm39) |
I127N |
possibly damaging |
Het |
Dyrk2 |
T |
C |
10: 118,704,668 (GRCm39) |
T3A |
possibly damaging |
Het |
Elovl5 |
C |
T |
9: 77,868,193 (GRCm39) |
T35M |
probably damaging |
Het |
Emc7 |
T |
C |
2: 112,297,314 (GRCm39) |
|
probably benign |
Het |
Erp27 |
T |
C |
6: 136,886,487 (GRCm39) |
Y182C |
probably damaging |
Het |
Exoc2 |
T |
A |
13: 31,070,310 (GRCm39) |
|
probably benign |
Het |
F5 |
A |
C |
1: 164,012,676 (GRCm39) |
D530A |
probably damaging |
Het |
Fam149a |
A |
T |
8: 45,808,686 (GRCm39) |
V149E |
probably damaging |
Het |
Fbxo41 |
A |
G |
6: 85,455,164 (GRCm39) |
S614P |
probably damaging |
Het |
Fmn1 |
T |
A |
2: 113,467,124 (GRCm39) |
Y1342N |
possibly damaging |
Het |
Gpr22 |
T |
A |
12: 31,758,793 (GRCm39) |
D443V |
possibly damaging |
Het |
Il17rd |
T |
A |
14: 26,813,888 (GRCm39) |
W56R |
probably damaging |
Het |
Itga2b |
A |
T |
11: 102,356,779 (GRCm39) |
|
probably null |
Het |
Jmjd1c |
T |
C |
10: 67,091,261 (GRCm39) |
M2514T |
probably benign |
Het |
Klk1b9 |
T |
C |
7: 43,443,675 (GRCm39) |
|
probably benign |
Het |
Krr1 |
T |
C |
10: 111,811,503 (GRCm39) |
Y66H |
probably damaging |
Het |
Lamb2 |
T |
C |
9: 108,363,553 (GRCm39) |
|
probably benign |
Het |
Lgals3bp |
A |
T |
11: 118,284,290 (GRCm39) |
Y430N |
probably benign |
Het |
Lrp10 |
T |
C |
14: 54,705,036 (GRCm39) |
V113A |
probably benign |
Het |
Mgam |
A |
G |
6: 40,736,024 (GRCm39) |
Y841C |
probably damaging |
Het |
Nisch |
T |
A |
14: 30,899,421 (GRCm39) |
|
probably benign |
Het |
Nlrp4d |
G |
A |
7: 10,112,219 (GRCm39) |
T650I |
probably benign |
Het |
Or4f61 |
T |
A |
2: 111,922,981 (GRCm39) |
K22* |
probably null |
Het |
Or5p78 |
C |
T |
7: 108,211,577 (GRCm39) |
T21I |
possibly damaging |
Het |
Parp4 |
A |
G |
14: 56,886,300 (GRCm39) |
D1793G |
unknown |
Het |
Pcm1 |
A |
G |
8: 41,778,942 (GRCm39) |
D1850G |
probably benign |
Het |
Pgap2 |
G |
A |
7: 101,885,669 (GRCm39) |
A145T |
probably damaging |
Het |
Phc1 |
G |
A |
6: 122,299,995 (GRCm39) |
A583V |
probably damaging |
Het |
Plcd3 |
G |
A |
11: 102,962,085 (GRCm39) |
|
probably benign |
Het |
Ppm1m |
T |
A |
9: 106,074,501 (GRCm39) |
Q214L |
probably damaging |
Het |
Prkg2 |
A |
G |
5: 99,145,379 (GRCm39) |
|
probably benign |
Het |
Prss3l |
A |
G |
6: 41,422,271 (GRCm39) |
Y45H |
probably benign |
Het |
Rasal3 |
T |
C |
17: 32,614,791 (GRCm39) |
|
probably benign |
Het |
Rfc1 |
A |
T |
5: 65,421,640 (GRCm39) |
D1086E |
probably benign |
Het |
Rnf145 |
T |
A |
11: 44,452,587 (GRCm39) |
L522H |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,382,168 (GRCm39) |
|
probably null |
Het |
Sik1 |
C |
A |
17: 32,068,055 (GRCm39) |
V377F |
possibly damaging |
Het |
Slc44a4 |
T |
C |
17: 35,147,071 (GRCm39) |
I367T |
possibly damaging |
Het |
Slfn3 |
A |
G |
11: 83,103,954 (GRCm39) |
D275G |
possibly damaging |
Het |
Smarcad1 |
A |
T |
6: 65,051,806 (GRCm39) |
N313I |
possibly damaging |
Het |
Smc4 |
A |
T |
3: 68,915,361 (GRCm39) |
K138* |
probably null |
Het |
Smg6 |
T |
A |
11: 74,821,039 (GRCm39) |
S437T |
probably benign |
Het |
Spaca9 |
G |
T |
2: 28,586,005 (GRCm39) |
Q20K |
probably damaging |
Het |
Spatc1 |
T |
G |
15: 76,152,493 (GRCm39) |
I41S |
probably damaging |
Het |
Spink5 |
A |
T |
18: 44,096,385 (GRCm39) |
T5S |
possibly damaging |
Het |
St3gal1 |
C |
A |
15: 66,981,504 (GRCm39) |
|
probably benign |
Het |
Stat5a |
C |
A |
11: 100,753,961 (GRCm39) |
T97K |
probably benign |
Het |
Stat5b |
A |
T |
11: 100,689,156 (GRCm39) |
I246N |
probably benign |
Het |
Supt6 |
G |
T |
11: 78,117,829 (GRCm39) |
D462E |
probably damaging |
Het |
Swi5 |
A |
T |
2: 32,171,836 (GRCm39) |
|
probably benign |
Het |
Syne1 |
A |
T |
10: 5,355,435 (GRCm39) |
V375E |
probably damaging |
Het |
Tcp1 |
T |
C |
17: 13,143,239 (GRCm39) |
F516S |
probably benign |
Het |
Tdrd7 |
A |
T |
4: 45,965,488 (GRCm39) |
|
probably benign |
Het |
Tgfbr3 |
A |
T |
5: 107,288,289 (GRCm39) |
N457K |
probably benign |
Het |
Tmem209 |
A |
G |
6: 30,487,380 (GRCm39) |
M500T |
probably damaging |
Het |
Tmem44 |
C |
T |
16: 30,336,281 (GRCm39) |
|
probably benign |
Het |
Ttc21a |
T |
A |
9: 119,768,220 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,701,454 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,666,347 (GRCm39) |
I88F |
possibly damaging |
Het |
Ube2w |
T |
C |
1: 16,672,479 (GRCm39) |
|
probably benign |
Het |
Ufc1 |
C |
T |
1: 171,117,527 (GRCm39) |
|
probably benign |
Het |
Uhmk1 |
A |
G |
1: 170,039,971 (GRCm39) |
M132T |
possibly damaging |
Het |
Usp29 |
A |
G |
7: 6,966,181 (GRCm39) |
N675D |
possibly damaging |
Het |
Vmn1r23 |
A |
G |
6: 57,903,469 (GRCm39) |
V103A |
possibly damaging |
Het |
Wdr59 |
G |
T |
8: 112,248,604 (GRCm39) |
R4S |
possibly damaging |
Het |
Zc3hav1 |
T |
A |
6: 38,284,372 (GRCm39) |
E914D |
probably benign |
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 |
|
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'- TTCAGTCCCTCAGATCCACAGTCG -3'
(R):5'- AGCCGTCAGCAAATACTGGTCATC -3'
Sequencing Primer
(F):5'- tgatgggggatggtgagg -3'
(R):5'- CTGGTCATCAAAACTCGAAGTG -3'
|
Posted On |
2013-05-23 |