Incidental Mutation 'IGL03091:Odad4'
ID |
418384 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Odad4
|
Ensembl Gene |
ENSMUSG00000006784 |
Gene Name |
outer dynein arm complex subunit 4 |
Synonyms |
4933404O19Rik, Ttc25 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.089)
|
Stock # |
IGL03091
|
Quality Score |
|
Status
|
|
Chromosome |
11 |
Chromosomal Location |
100436434-100463392 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 100441076 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Stop codon
at position 102
(Y102*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000090355
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000006976]
[ENSMUST00000092684]
|
AlphaFold |
Q9D4B2 |
Predicted Effect |
probably null
Transcript: ENSMUST00000006976
AA Change: Y102*
|
SMART Domains |
Protein: ENSMUSP00000006976 Gene: ENSMUSG00000006784 AA Change: Y102*
Domain | Start | End | E-Value | Type |
TPR
|
11 |
44 |
3.69e1 |
SMART |
TPR
|
45 |
78 |
3.07e1 |
SMART |
TPR
|
79 |
112 |
4.96e0 |
SMART |
low complexity region
|
147 |
158 |
N/A |
INTRINSIC |
low complexity region
|
191 |
208 |
N/A |
INTRINSIC |
TPR
|
318 |
351 |
4.96e0 |
SMART |
TPR
|
358 |
391 |
1.11e1 |
SMART |
Blast:TPR
|
395 |
428 |
7e-14 |
BLAST |
TPR
|
435 |
468 |
2.99e1 |
SMART |
low complexity region
|
493 |
505 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000092684
AA Change: Y102*
|
SMART Domains |
Protein: ENSMUSP00000090355 Gene: ENSMUSG00000006784 AA Change: Y102*
Domain | Start | End | E-Value | Type |
TPR
|
11 |
44 |
3.69e1 |
SMART |
TPR
|
45 |
78 |
3.07e1 |
SMART |
TPR
|
79 |
112 |
4.96e0 |
SMART |
low complexity region
|
147 |
158 |
N/A |
INTRINSIC |
low complexity region
|
191 |
208 |
N/A |
INTRINSIC |
TPR
|
318 |
351 |
4.96e0 |
SMART |
TPR
|
358 |
391 |
1.11e1 |
SMART |
Blast:TPR
|
395 |
428 |
5e-14 |
BLAST |
TPR
|
435 |
468 |
2.99e1 |
SMART |
coiled coil region
|
528 |
548 |
N/A |
INTRINSIC |
low complexity region
|
556 |
567 |
N/A |
INTRINSIC |
coiled coil region
|
599 |
624 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127389
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132143
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150331
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a null allele display partial preweaning lethality, impaired ciliary motility, and a variety of left-right body symmetry defects. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ago1 |
A |
T |
4: 126,352,982 (GRCm39) |
Y314N |
probably damaging |
Het |
Aknad1 |
A |
G |
3: 108,659,219 (GRCm39) |
T78A |
possibly damaging |
Het |
Arhgap33 |
G |
A |
7: 30,227,718 (GRCm39) |
P494S |
probably damaging |
Het |
Babam2 |
T |
A |
5: 31,943,022 (GRCm39) |
|
probably null |
Het |
Ces2g |
T |
C |
8: 105,691,386 (GRCm39) |
V174A |
probably damaging |
Het |
Chd1l |
G |
A |
3: 97,470,863 (GRCm39) |
R811C |
probably damaging |
Het |
Crot |
A |
T |
5: 9,016,897 (GRCm39) |
H598Q |
probably benign |
Het |
Dtx2 |
C |
T |
5: 136,041,228 (GRCm39) |
S211L |
probably damaging |
Het |
Duox2 |
T |
G |
2: 122,119,955 (GRCm39) |
M852L |
probably benign |
Het |
Fmc1 |
G |
T |
6: 38,516,170 (GRCm39) |
S72I |
probably damaging |
Het |
Fut1 |
T |
C |
7: 45,268,951 (GRCm39) |
C302R |
probably damaging |
Het |
Gm6401 |
T |
C |
14: 41,786,615 (GRCm39) |
T184A |
possibly damaging |
Het |
Gsdma2 |
C |
T |
11: 98,542,828 (GRCm39) |
T29I |
probably damaging |
Het |
Lgi2 |
C |
A |
5: 52,721,307 (GRCm39) |
|
probably null |
Het |
Lipe |
A |
G |
7: 25,080,180 (GRCm39) |
L926P |
probably damaging |
Het |
Lrp1 |
T |
A |
10: 127,394,993 (GRCm39) |
I2511F |
probably benign |
Het |
Med10 |
T |
C |
13: 69,963,816 (GRCm39) |
|
probably benign |
Het |
Nbea |
A |
G |
3: 55,992,725 (GRCm39) |
S294P |
probably damaging |
Het |
Neb |
T |
A |
2: 52,161,324 (GRCm39) |
H2156L |
probably benign |
Het |
Neo1 |
A |
T |
9: 58,885,951 (GRCm39) |
N335K |
probably damaging |
Het |
Nox3 |
G |
T |
17: 3,716,119 (GRCm39) |
Q429K |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,805,564 (GRCm39) |
R1671G |
probably damaging |
Het |
Plec |
T |
C |
15: 76,073,503 (GRCm39) |
T504A |
possibly damaging |
Het |
Pou5f1 |
G |
T |
17: 35,820,939 (GRCm39) |
R127L |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,523,174 (GRCm39) |
|
probably benign |
Het |
Rassf8 |
T |
A |
6: 145,761,536 (GRCm39) |
N287K |
probably benign |
Het |
Rdh16 |
T |
C |
10: 127,649,502 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
G |
A |
7: 28,782,911 (GRCm39) |
A1901V |
possibly damaging |
Het |
Scnn1g |
A |
G |
7: 121,345,906 (GRCm39) |
Y343C |
probably damaging |
Het |
Sema5a |
A |
G |
15: 32,538,880 (GRCm39) |
|
probably benign |
Het |
Slc9b2 |
G |
A |
3: 135,034,791 (GRCm39) |
V310M |
probably damaging |
Het |
Stox2 |
T |
A |
8: 47,646,222 (GRCm39) |
I477F |
possibly damaging |
Het |
Terb1 |
A |
T |
8: 105,195,786 (GRCm39) |
H548Q |
probably benign |
Het |
Tsks |
G |
A |
7: 44,607,319 (GRCm39) |
M547I |
possibly damaging |
Het |
Tuba8 |
G |
A |
6: 121,197,403 (GRCm39) |
E22K |
probably damaging |
Het |
Wee2 |
T |
C |
6: 40,438,968 (GRCm39) |
F364L |
probably benign |
Het |
Zfp644 |
A |
G |
5: 106,784,724 (GRCm39) |
Y608H |
probably damaging |
Het |
|
Other mutations in Odad4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02027:Odad4
|
APN |
11 |
100,460,728 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02379:Odad4
|
APN |
11 |
100,457,809 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02991:Odad4
|
UTSW |
11 |
100,444,698 (GRCm39) |
missense |
probably benign |
0.01 |
R0044:Odad4
|
UTSW |
11 |
100,457,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R0137:Odad4
|
UTSW |
11 |
100,454,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R0280:Odad4
|
UTSW |
11 |
100,441,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Odad4
|
UTSW |
11 |
100,436,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Odad4
|
UTSW |
11 |
100,460,679 (GRCm39) |
splice site |
probably null |
|
R2097:Odad4
|
UTSW |
11 |
100,454,408 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2121:Odad4
|
UTSW |
11 |
100,457,837 (GRCm39) |
critical splice donor site |
probably null |
|
R2509:Odad4
|
UTSW |
11 |
100,444,361 (GRCm39) |
missense |
probably damaging |
0.99 |
R2655:Odad4
|
UTSW |
11 |
100,444,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4635:Odad4
|
UTSW |
11 |
100,442,333 (GRCm39) |
nonsense |
probably null |
|
R4773:Odad4
|
UTSW |
11 |
100,440,742 (GRCm39) |
missense |
probably benign |
0.05 |
R4858:Odad4
|
UTSW |
11 |
100,441,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R5164:Odad4
|
UTSW |
11 |
100,462,346 (GRCm39) |
nonsense |
probably null |
|
R5181:Odad4
|
UTSW |
11 |
100,440,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Odad4
|
UTSW |
11 |
100,444,887 (GRCm39) |
missense |
probably damaging |
0.99 |
R5742:Odad4
|
UTSW |
11 |
100,436,699 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7634:Odad4
|
UTSW |
11 |
100,452,731 (GRCm39) |
critical splice donor site |
probably null |
|
R7851:Odad4
|
UTSW |
11 |
100,436,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R8186:Odad4
|
UTSW |
11 |
100,454,505 (GRCm39) |
missense |
probably benign |
0.27 |
R8194:Odad4
|
UTSW |
11 |
100,454,502 (GRCm39) |
missense |
probably benign |
0.06 |
R8444:Odad4
|
UTSW |
11 |
100,452,731 (GRCm39) |
critical splice donor site |
probably null |
|
R8879:Odad4
|
UTSW |
11 |
100,457,752 (GRCm39) |
nonsense |
probably null |
|
X0018:Odad4
|
UTSW |
11 |
100,444,424 (GRCm39) |
missense |
probably damaging |
0.99 |
X0028:Odad4
|
UTSW |
11 |
100,436,724 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Posted On |
2016-08-02 |