Incidental Mutation 'R6895:Dnaaf2'
| ID |
538298 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dnaaf2
|
| Ensembl Gene |
ENSMUSG00000020973 |
| Gene Name |
dynein, axonemal assembly factor 2 |
| Synonyms |
1110034A24Rik, kintoun, 2810020C19Rik, Ktu |
| MMRRC Submission |
044989-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R6895 (G1)
|
| Quality Score |
176.009 |
|
Status
|
Validated
|
| Chromosome |
12 |
| Chromosomal Location |
69235861-69245203 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 69244437 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 208
(V208A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000021356
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021356]
[ENSMUST00000021359]
[ENSMUST00000221411]
[ENSMUST00000222699]
|
| AlphaFold |
Q8BPI1 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000021356
AA Change: V208A
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| SMART Domains |
Protein: ENSMUSP00000021356
Gene: ENSMUSG00000020973
AA Change: V208A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
19 |
N/A |
INTRINSIC |
|
Pfam:PIH1
|
43 |
352 |
2e-99 |
PFAM |
|
low complexity region
|
360 |
373 |
N/A |
INTRINSIC |
|
SCOP:d1keka4
|
398 |
460 |
4e-3 |
SMART |
|
low complexity region
|
672 |
693 |
N/A |
INTRINSIC |
|
low complexity region
|
734 |
743 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000021359
|
| SMART Domains |
Protein: ENSMUSP00000021359
Gene: ENSMUSG00000020974
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Dpoe2NT
|
2 |
74 |
1.9e-32 |
PFAM |
|
Pfam:DNA_pol_E_B
|
287 |
489 |
1.4e-58 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000221411
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000222699
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000223192
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.3%
- 20x: 97.7%
|
| Validation Efficiency |
100% (45/45) |
| MGI Phenotype |
FUNCTION: This gene encodes a highly conserved protein involved in the preassembly of dynein arm complexes which power cilia. These complexes are found in some cilia and are assembled in the cytoplasm prior to transport for cilia formation. Mutations in the human gene have been associated with primary ciliary dyskinesia. [provided by RefSeq, Sep 2015]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit postnatal lethality, reduced body size, situs inversus totalis, hydroencephaly and abnormal brain ependymal and tracheal cilia morphology and motility. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ankrd29 |
A |
G |
18: 12,394,046 (GRCm39) |
V256A |
probably benign |
Het |
| Arid4a |
A |
G |
12: 71,110,076 (GRCm39) |
D139G |
probably benign |
Het |
| AU040320 |
T |
C |
4: 126,685,723 (GRCm39) |
W100R |
probably damaging |
Het |
| C4bp |
T |
C |
1: 130,563,943 (GRCm39) |
*470W |
probably null |
Het |
| Capn8 |
C |
A |
1: 182,456,234 (GRCm39) |
D661E |
possibly damaging |
Het |
| Car14 |
T |
C |
3: 95,805,472 (GRCm39) |
T334A |
probably benign |
Het |
| Cfhr4 |
G |
A |
1: 139,668,210 (GRCm39) |
P308S |
possibly damaging |
Het |
| Chd6 |
T |
A |
2: 160,830,260 (GRCm39) |
T1012S |
probably damaging |
Het |
| Csmd3 |
T |
C |
15: 47,529,910 (GRCm39) |
|
probably null |
Het |
| Dnah11 |
A |
G |
12: 117,958,926 (GRCm39) |
W2986R |
probably damaging |
Het |
| Epb42 |
G |
A |
2: 120,867,104 (GRCm39) |
|
probably benign |
Het |
| Fam120a |
A |
G |
13: 49,045,497 (GRCm39) |
F780L |
probably benign |
Het |
| Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
| Grid2 |
T |
C |
6: 64,372,283 (GRCm39) |
F655S |
probably damaging |
Het |
| Homer3 |
T |
C |
8: 70,737,955 (GRCm39) |
S2P |
probably damaging |
Het |
| Hydin |
T |
C |
8: 111,038,883 (GRCm39) |
V207A |
probably benign |
Het |
| Inpp5j |
T |
C |
11: 3,445,557 (GRCm39) |
|
probably null |
Het |
| Jak1 |
C |
T |
4: 101,011,734 (GRCm39) |
|
probably null |
Het |
| Jmjd1c |
A |
G |
10: 67,052,869 (GRCm39) |
I220V |
probably benign |
Het |
| Kat6a |
T |
G |
8: 23,425,799 (GRCm39) |
S1115A |
possibly damaging |
Het |
| Larp4 |
T |
G |
15: 99,905,611 (GRCm39) |
|
probably null |
Het |
| Lrrc72 |
T |
G |
12: 36,259,717 (GRCm39) |
D43A |
probably damaging |
Het |
| Mptx2 |
A |
C |
1: 173,105,252 (GRCm39) |
V13G |
probably benign |
Het |
| Nmbr |
A |
T |
10: 14,645,704 (GRCm39) |
*258Y |
probably null |
Het |
| Nup210l |
C |
T |
3: 90,067,231 (GRCm39) |
A757V |
probably damaging |
Het |
| Nup62 |
A |
G |
7: 44,479,157 (GRCm39) |
K391E |
possibly damaging |
Het |
| Nup93 |
T |
A |
8: 94,970,314 (GRCm39) |
I71K |
probably damaging |
Het |
| Or14a256 |
A |
T |
7: 86,265,323 (GRCm39) |
C177S |
probably damaging |
Het |
| Or8b51 |
A |
C |
9: 38,569,385 (GRCm39) |
L101R |
probably damaging |
Het |
| Pik3cg |
A |
G |
12: 32,254,346 (GRCm39) |
M547T |
possibly damaging |
Het |
| Ropn1 |
A |
T |
16: 34,497,668 (GRCm39) |
I187F |
possibly damaging |
Het |
| Rtp3 |
T |
C |
9: 110,816,264 (GRCm39) |
R96G |
possibly damaging |
Het |
| Sfrp5 |
A |
T |
19: 42,188,227 (GRCm39) |
S197R |
probably damaging |
Het |
| Slc12a6 |
A |
G |
2: 112,185,440 (GRCm39) |
H903R |
probably damaging |
Het |
| Slc26a3 |
G |
T |
12: 31,513,523 (GRCm39) |
A482S |
probably damaging |
Het |
| Slc2a12 |
G |
T |
10: 22,568,084 (GRCm39) |
A504S |
probably damaging |
Het |
| Slitrk5 |
C |
A |
14: 111,919,085 (GRCm39) |
P903Q |
probably damaging |
Het |
| Tas2r123 |
A |
T |
6: 132,824,133 (GRCm39) |
H10L |
probably benign |
Het |
| Tex46 |
T |
C |
4: 136,340,212 (GRCm39) |
V99A |
probably benign |
Het |
| Top2b |
T |
C |
14: 16,413,604 (GRCm38) |
V1024A |
probably benign |
Het |
| Ugt2b36 |
G |
A |
5: 87,240,157 (GRCm39) |
T76I |
probably benign |
Het |
| Usp31 |
G |
T |
7: 121,252,399 (GRCm39) |
T747K |
probably benign |
Het |
| Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
|
| Other mutations in Dnaaf2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00230:Dnaaf2
|
APN |
12 |
69,243,540 (GRCm39) |
missense |
probably benign |
0.23 |
|
IGL01321:Dnaaf2
|
APN |
12 |
69,243,376 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01880:Dnaaf2
|
APN |
12 |
69,236,811 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0329:Dnaaf2
|
UTSW |
12 |
69,244,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0330:Dnaaf2
|
UTSW |
12 |
69,244,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1051:Dnaaf2
|
UTSW |
12 |
69,244,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1668:Dnaaf2
|
UTSW |
12 |
69,243,465 (GRCm39) |
missense |
probably benign |
0.04 |
|
R2011:Dnaaf2
|
UTSW |
12 |
69,243,559 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2179:Dnaaf2
|
UTSW |
12 |
69,245,071 (GRCm39) |
unclassified |
probably benign |
|
|
R2243:Dnaaf2
|
UTSW |
12 |
69,243,418 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R2356:Dnaaf2
|
UTSW |
12 |
69,244,992 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4120:Dnaaf2
|
UTSW |
12 |
69,244,812 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R5086:Dnaaf2
|
UTSW |
12 |
69,244,060 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5205:Dnaaf2
|
UTSW |
12 |
69,239,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5300:Dnaaf2
|
UTSW |
12 |
69,245,002 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5399:Dnaaf2
|
UTSW |
12 |
69,243,516 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5739:Dnaaf2
|
UTSW |
12 |
69,243,715 (GRCm39) |
missense |
probably benign |
|
|
R5765:Dnaaf2
|
UTSW |
12 |
69,239,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5872:Dnaaf2
|
UTSW |
12 |
69,244,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6043:Dnaaf2
|
UTSW |
12 |
69,244,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6338:Dnaaf2
|
UTSW |
12 |
69,244,896 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6503:Dnaaf2
|
UTSW |
12 |
69,244,285 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6524:Dnaaf2
|
UTSW |
12 |
69,237,159 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7490:Dnaaf2
|
UTSW |
12 |
69,244,380 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7971:Dnaaf2
|
UTSW |
12 |
69,244,119 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8209:Dnaaf2
|
UTSW |
12 |
69,244,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8790:Dnaaf2
|
UTSW |
12 |
69,244,068 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9210:Dnaaf2
|
UTSW |
12 |
69,244,602 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9548:Dnaaf2
|
UTSW |
12 |
69,244,776 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Dnaaf2
|
UTSW |
12 |
69,244,624 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TAATCCTGGAGGTCTACGTGG -3'
(R):5'- TGTGCAGCAACTCACTGGTAG -3'
Sequencing Primer
(F):5'- AGGTCTACGTGGTGGCGC -3'
(R):5'- AGCAACTCACTGGTAGGCGTAC -3'
|
| Posted On |
2018-11-06 |
Incidental Mutation