Incidental Mutation 'R0118:Odad3'
| ID |
20931 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Odad3
|
| Ensembl Gene |
ENSMUSG00000039632 |
| Gene Name |
outer dynein arm docking complex subunit 3 |
| Synonyms |
Ccdc151, C330001K17Rik, b2b1885Clo |
| MMRRC Submission |
038404-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.067)
|
| Stock # |
R0118 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
(trace)
|
| Chromosome |
9 |
| Chromosomal Location |
21901167-21913930 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 21906353 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Lysine
at position 224
(N224K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000041117
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044926]
[ENSMUST00000115336]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000044926
AA Change: N224K
PolyPhen 2
Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000041117
Gene: ENSMUSG00000039632
AA Change: N224K
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
88 |
286 |
N/A |
INTRINSIC |
|
low complexity region
|
334 |
345 |
N/A |
INTRINSIC |
|
coiled coil region
|
378 |
420 |
N/A |
INTRINSIC |
|
low complexity region
|
495 |
514 |
N/A |
INTRINSIC |
|
low complexity region
|
550 |
565 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115336
AA Change: N224K
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000110993
Gene: ENSMUSG00000039632
AA Change: N224K
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
88 |
286 |
N/A |
INTRINSIC |
|
low complexity region
|
335 |
346 |
N/A |
INTRINSIC |
|
coiled coil region
|
379 |
421 |
N/A |
INTRINSIC |
|
low complexity region
|
496 |
515 |
N/A |
INTRINSIC |
|
low complexity region
|
551 |
566 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000214420
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.2%
- 10x: 89.3%
- 20x: 67.4%
|
| Validation Efficiency |
98% (50/51) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing coiled-coil domains. The encoded protein functions in outer dynein arm assembly and is required for motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]
PHENOTYPE: Mico homozygous for an ENU-induced allele exhibit dextrocardia associated with situs inversus totalis and hypoplastic spleen, adrenal anomalies and immotile/dyskinetic tracheal airway cilia. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 49 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts15 |
T |
C |
9: 30,823,040 (GRCm39) |
R343G |
probably damaging |
Het |
| Asxl2 |
T |
G |
12: 3,546,923 (GRCm39) |
V569G |
probably damaging |
Het |
| Azin2 |
A |
C |
4: 128,843,430 (GRCm39) |
H85Q |
probably damaging |
Het |
| Cacna1a |
C |
T |
8: 85,262,712 (GRCm39) |
R324C |
probably damaging |
Het |
| Ccr3 |
C |
A |
9: 123,829,647 (GRCm39) |
Y327* |
probably null |
Het |
| Cers2 |
T |
C |
3: 95,227,537 (GRCm39) |
F55S |
probably benign |
Het |
| Cic |
C |
T |
7: 24,985,459 (GRCm39) |
S301L |
probably damaging |
Het |
| Cntnap2 |
T |
C |
6: 45,037,326 (GRCm39) |
|
probably null |
Het |
| Cpn2 |
T |
C |
16: 30,079,186 (GRCm39) |
R172G |
probably benign |
Het |
| Ctdnep1 |
T |
C |
11: 69,879,557 (GRCm39) |
|
probably null |
Het |
| Dennd3 |
T |
A |
15: 73,436,925 (GRCm39) |
Y1051N |
probably damaging |
Het |
| Dmap1 |
T |
G |
4: 117,533,680 (GRCm39) |
Y196S |
probably damaging |
Het |
| Entpd7 |
G |
A |
19: 43,692,751 (GRCm39) |
W102* |
probably null |
Het |
| Frem2 |
A |
T |
3: 53,442,664 (GRCm39) |
C2624* |
probably null |
Het |
| Gdpd3 |
A |
G |
7: 126,370,165 (GRCm39) |
Y238C |
probably damaging |
Het |
| Gjb3 |
A |
G |
4: 127,220,451 (GRCm39) |
V27A |
probably damaging |
Het |
| Kat6b |
T |
C |
14: 21,720,042 (GRCm39) |
F1465L |
probably damaging |
Het |
| Klra17 |
A |
T |
6: 129,808,552 (GRCm39) |
M227K |
probably benign |
Het |
| Map6 |
A |
G |
7: 98,966,824 (GRCm39) |
D348G |
possibly damaging |
Het |
| Mapkbp1 |
T |
C |
2: 119,855,696 (GRCm39) |
S1472P |
probably benign |
Het |
| Megf6 |
C |
A |
4: 154,339,098 (GRCm39) |
P545Q |
probably damaging |
Het |
| Mertk |
C |
T |
2: 128,601,086 (GRCm39) |
R357W |
probably damaging |
Het |
| Mesd |
T |
A |
7: 83,544,835 (GRCm39) |
I104N |
probably damaging |
Het |
| Mrm3 |
T |
A |
11: 76,140,781 (GRCm39) |
V263E |
possibly damaging |
Het |
| Ndst4 |
T |
A |
3: 125,405,210 (GRCm39) |
Y488* |
probably null |
Het |
| Nfat5 |
C |
T |
8: 108,065,707 (GRCm39) |
R156W |
probably damaging |
Het |
| Nfs1 |
T |
C |
2: 155,976,444 (GRCm39) |
H150R |
probably damaging |
Het |
| Or1n1b |
A |
G |
2: 36,780,035 (GRCm39) |
M275T |
probably benign |
Het |
| Or8b56 |
T |
C |
9: 38,739,154 (GRCm39) |
S50P |
possibly damaging |
Het |
| Or8g19 |
T |
A |
9: 39,055,399 (GRCm39) |
M1K |
probably null |
Het |
| Or9q1 |
A |
G |
19: 13,804,929 (GRCm39) |
F277S |
possibly damaging |
Het |
| Pcdh8 |
T |
C |
14: 80,004,848 (GRCm39) |
Y1059C |
probably damaging |
Het |
| Pik3r5 |
T |
A |
11: 68,381,306 (GRCm39) |
L164Q |
probably damaging |
Het |
| Polr3g |
T |
C |
13: 81,824,240 (GRCm39) |
|
probably benign |
Het |
| Ppm1e |
T |
A |
11: 87,122,564 (GRCm39) |
K464N |
probably benign |
Het |
| Rims1 |
T |
C |
1: 22,416,631 (GRCm39) |
T1037A |
probably damaging |
Het |
| Rpgrip1l |
A |
T |
8: 91,996,750 (GRCm39) |
I108N |
probably damaging |
Het |
| Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
| Spem1 |
T |
C |
11: 69,712,371 (GRCm39) |
K98E |
possibly damaging |
Het |
| St7l |
T |
C |
3: 104,796,619 (GRCm39) |
V237A |
probably damaging |
Het |
| Tbc1d16 |
T |
C |
11: 119,048,642 (GRCm39) |
H337R |
probably damaging |
Het |
| Tbc1d32 |
T |
A |
10: 55,893,701 (GRCm39) |
I1291F |
probably benign |
Het |
| Tnfaip6 |
G |
T |
2: 51,933,827 (GRCm39) |
E61* |
probably null |
Het |
| Trib2 |
A |
T |
12: 15,843,929 (GRCm39) |
W102R |
probably damaging |
Het |
| Uimc1 |
G |
T |
13: 55,233,457 (GRCm39) |
N66K |
probably damaging |
Het |
| Vmn1r63 |
T |
A |
7: 5,805,838 (GRCm39) |
T265S |
probably benign |
Het |
| Vps35 |
G |
A |
8: 86,021,582 (GRCm39) |
T3I |
probably benign |
Het |
| Yeats2 |
T |
A |
16: 19,975,692 (GRCm39) |
L63* |
probably null |
Het |
| Zfp282 |
A |
G |
6: 47,869,866 (GRCm39) |
R304G |
probably benign |
Het |
|
| Other mutations in Odad3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01473:Odad3
|
APN |
9 |
21,906,675 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL01922:Odad3
|
APN |
9 |
21,904,826 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02223:Odad3
|
APN |
9 |
21,904,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03161:Odad3
|
APN |
9 |
21,913,611 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03269:Odad3
|
APN |
9 |
21,909,339 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0129:Odad3
|
UTSW |
9 |
21,904,848 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0279:Odad3
|
UTSW |
9 |
21,901,543 (GRCm39) |
unclassified |
probably benign |
|
|
R0390:Odad3
|
UTSW |
9 |
21,903,004 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1349:Odad3
|
UTSW |
9 |
21,904,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1372:Odad3
|
UTSW |
9 |
21,904,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1891:Odad3
|
UTSW |
9 |
21,906,677 (GRCm39) |
splice site |
probably null |
|
|
R2044:Odad3
|
UTSW |
9 |
21,903,154 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5116:Odad3
|
UTSW |
9 |
21,901,424 (GRCm39) |
makesense |
probably null |
|
|
R5147:Odad3
|
UTSW |
9 |
21,906,158 (GRCm39) |
missense |
probably benign |
0.21 |
|
R5929:Odad3
|
UTSW |
9 |
21,913,718 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6182:Odad3
|
UTSW |
9 |
21,901,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7253:Odad3
|
UTSW |
9 |
21,913,767 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7498:Odad3
|
UTSW |
9 |
21,913,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7742:Odad3
|
UTSW |
9 |
21,904,193 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8331:Odad3
|
UTSW |
9 |
21,903,007 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8976:Odad3
|
UTSW |
9 |
21,903,334 (GRCm39) |
unclassified |
probably benign |
|
|
R9319:Odad3
|
UTSW |
9 |
21,906,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9324:Odad3
|
UTSW |
9 |
21,903,207 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9422:Odad3
|
UTSW |
9 |
21,913,628 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R9614:Odad3
|
UTSW |
9 |
21,904,310 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1176:Odad3
|
UTSW |
9 |
21,901,720 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGGCAGGCTAGTACCTTGGCAATG -3'
(R):5'- ACCAGGTAATACTGCGGCAGAAAC -3'
Sequencing Primer
(F):5'- AGTACCTTGGCAATGTCCCG -3'
(R):5'- CTGGAGATGGCAGAGGTCC -3'
|
| Posted On |
2013-04-11 |
Incidental Mutation