Incidental Mutation 'R4962:Nacad'
| ID |
381857 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Nacad
|
| Ensembl Gene |
ENSMUSG00000041073 |
| Gene Name |
NAC alpha domain containing |
| Synonyms |
mKIAA0363 |
| MMRRC Submission |
042559-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4962 (G1)
|
| Quality Score |
223 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
6547823-6556053 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 6549169 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 1294
(D1294V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049490
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000000388]
[ENSMUST00000045713]
[ENSMUST00000109721]
[ENSMUST00000109722]
|
| AlphaFold |
Q5SWP3 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000000388
|
| SMART Domains |
Protein: ENSMUSP00000000388
Gene: ENSMUSG00000000378
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
12 |
N/A |
INTRINSIC |
|
Blast:PTB
|
60 |
230 |
2e-35 |
BLAST |
|
low complexity region
|
242 |
252 |
N/A |
INTRINSIC |
|
Pfam:CCM2_C
|
296 |
396 |
8.9e-50 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000045713
AA Change: D1294V
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000049490
Gene: ENSMUSG00000041073
AA Change: D1294V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
28 |
N/A |
INTRINSIC |
|
low complexity region
|
70 |
87 |
N/A |
INTRINSIC |
|
low complexity region
|
228 |
235 |
N/A |
INTRINSIC |
|
low complexity region
|
266 |
277 |
N/A |
INTRINSIC |
|
low complexity region
|
294 |
306 |
N/A |
INTRINSIC |
|
low complexity region
|
328 |
354 |
N/A |
INTRINSIC |
|
low complexity region
|
391 |
422 |
N/A |
INTRINSIC |
|
low complexity region
|
454 |
479 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
537 |
689 |
6.19e-8 |
PROSPERO |
|
low complexity region
|
692 |
713 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
732 |
889 |
6.19e-8 |
PROSPERO |
|
low complexity region
|
924 |
939 |
N/A |
INTRINSIC |
|
low complexity region
|
1159 |
1170 |
N/A |
INTRINSIC |
|
low complexity region
|
1308 |
1325 |
N/A |
INTRINSIC |
|
Pfam:NAC
|
1357 |
1413 |
2.9e-24 |
PFAM |
|
low complexity region
|
1449 |
1466 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109721
|
| SMART Domains |
Protein: ENSMUSP00000105343
Gene: ENSMUSG00000000378
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:PTB
|
2 |
166 |
2e-32 |
BLAST |
|
low complexity region
|
178 |
188 |
N/A |
INTRINSIC |
|
low complexity region
|
230 |
244 |
N/A |
INTRINSIC |
|
PDB:4FQN|D
|
245 |
324 |
5e-52 |
PDB |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109722
|
| SMART Domains |
Protein: ENSMUSP00000105344
Gene: ENSMUSG00000000378
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:PTB
|
2 |
166 |
2e-32 |
BLAST |
|
low complexity region
|
178 |
188 |
N/A |
INTRINSIC |
|
low complexity region
|
230 |
244 |
N/A |
INTRINSIC |
|
PDB:4FQN|D
|
245 |
324 |
5e-52 |
PDB |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161667
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000177050
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000177391
AA Change: D210V
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.6%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 92 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4921509C19Rik |
A |
G |
2: 151,314,728 (GRCm39) |
F317L |
possibly damaging |
Het |
| Abcc4 |
A |
G |
14: 118,905,811 (GRCm39) |
I85T |
probably benign |
Het |
| Acoxl |
G |
T |
2: 127,917,810 (GRCm39) |
C498F |
probably damaging |
Het |
| Akap13 |
C |
T |
7: 75,399,178 (GRCm39) |
T2752I |
probably damaging |
Het |
| Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
| Ap2a2 |
T |
G |
7: 141,210,061 (GRCm39) |
F836C |
probably damaging |
Het |
| Atp2c1 |
A |
G |
9: 105,320,149 (GRCm39) |
V404A |
probably benign |
Het |
| Atp7b |
G |
T |
8: 22,510,901 (GRCm39) |
A415E |
probably damaging |
Het |
| Babam2 |
A |
T |
5: 31,942,927 (GRCm39) |
I71L |
possibly damaging |
Het |
| Bean1 |
A |
G |
8: 104,943,606 (GRCm39) |
T54A |
probably damaging |
Het |
| Cacna1b |
T |
A |
2: 24,508,330 (GRCm39) |
I1816F |
probably damaging |
Het |
| Cacna1b |
C |
T |
2: 24,547,378 (GRCm39) |
G1202D |
probably damaging |
Het |
| Casp8ap2 |
A |
G |
4: 32,640,554 (GRCm39) |
E536G |
probably damaging |
Het |
| Cfap57 |
A |
G |
4: 118,470,262 (GRCm39) |
V206A |
probably benign |
Het |
| Clca3a2 |
A |
T |
3: 144,783,640 (GRCm39) |
D658E |
probably damaging |
Het |
| Cwc22 |
A |
T |
2: 77,726,653 (GRCm39) |
S809T |
probably benign |
Het |
| Cyp2c54 |
C |
T |
19: 40,060,585 (GRCm39) |
R132Q |
possibly damaging |
Het |
| Ddx20 |
A |
T |
3: 105,587,921 (GRCm39) |
D386E |
possibly damaging |
Het |
| Ddx50 |
T |
C |
10: 62,478,632 (GRCm39) |
T185A |
probably damaging |
Het |
| Decr1 |
G |
A |
4: 15,930,976 (GRCm39) |
R119* |
probably null |
Het |
| Dennd4a |
T |
C |
9: 64,813,285 (GRCm39) |
S1415P |
probably benign |
Het |
| Dnah12 |
A |
T |
14: 26,437,855 (GRCm39) |
I495L |
probably benign |
Het |
| Dnah2 |
G |
A |
11: 69,346,799 (GRCm39) |
Q2596* |
probably null |
Het |
| Dnajb13 |
A |
G |
7: 100,156,707 (GRCm39) |
L123S |
probably benign |
Het |
| Drgx |
G |
T |
14: 32,369,101 (GRCm39) |
|
probably benign |
Het |
| Elavl3 |
G |
A |
9: 21,948,107 (GRCm39) |
P19L |
probably benign |
Het |
| Fer1l6 |
T |
C |
15: 58,443,250 (GRCm39) |
S518P |
probably benign |
Het |
| Fgd3 |
T |
C |
13: 49,420,105 (GRCm39) |
S591G |
probably benign |
Het |
| Galnt18 |
C |
A |
7: 111,071,271 (GRCm39) |
R566L |
probably benign |
Het |
| Galnt6 |
A |
T |
15: 100,594,455 (GRCm39) |
Y525* |
probably null |
Het |
| Gm10036 |
A |
T |
18: 15,966,359 (GRCm39) |
Y170F |
probably benign |
Het |
| Hacd2 |
A |
G |
16: 34,842,921 (GRCm39) |
D24G |
unknown |
Het |
| Idh3a |
T |
C |
9: 54,503,325 (GRCm39) |
M128T |
possibly damaging |
Het |
| Ido1 |
C |
T |
8: 25,074,565 (GRCm39) |
M359I |
probably benign |
Het |
| Ikbkb |
T |
C |
8: 23,171,693 (GRCm39) |
T185A |
probably damaging |
Het |
| Insl6 |
C |
T |
19: 29,299,019 (GRCm39) |
G131D |
probably damaging |
Het |
| Irgm1 |
A |
C |
11: 48,757,159 (GRCm39) |
S217R |
possibly damaging |
Het |
| Itga11 |
T |
A |
9: 62,668,850 (GRCm39) |
Y702* |
probably null |
Het |
| Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
| Kansl2 |
T |
C |
15: 98,429,724 (GRCm39) |
M103V |
probably benign |
Het |
| Kcnq2 |
T |
C |
2: 180,753,836 (GRCm39) |
N258S |
possibly damaging |
Het |
| Kdm5d |
A |
T |
Y: 940,624 (GRCm39) |
D1045V |
probably damaging |
Het |
| Lats2 |
A |
G |
14: 57,937,049 (GRCm39) |
L480P |
probably damaging |
Het |
| Lin28b |
T |
A |
10: 45,296,736 (GRCm39) |
K87N |
possibly damaging |
Het |
| Lpgat1 |
T |
A |
1: 191,451,682 (GRCm39) |
W103R |
probably damaging |
Het |
| Lpl |
G |
T |
8: 69,347,345 (GRCm39) |
G166C |
probably damaging |
Het |
| Ly75 |
A |
T |
2: 60,182,469 (GRCm39) |
Y569N |
probably damaging |
Het |
| Mcm8 |
A |
T |
2: 132,680,689 (GRCm39) |
E564D |
probably damaging |
Het |
| Me2 |
G |
T |
18: 73,918,847 (GRCm39) |
N411K |
probably damaging |
Het |
| Mn1 |
A |
G |
5: 111,602,652 (GRCm39) |
T1297A |
possibly damaging |
Het |
| Mphosph8 |
T |
A |
14: 56,916,046 (GRCm39) |
F447L |
probably benign |
Het |
| Neu3 |
A |
T |
7: 99,472,615 (GRCm39) |
F41I |
probably damaging |
Het |
| Nlrp6 |
G |
T |
7: 140,503,497 (GRCm39) |
L534F |
probably damaging |
Het |
| Nrap |
A |
G |
19: 56,366,575 (GRCm39) |
M338T |
probably damaging |
Het |
| Nuak1 |
T |
C |
10: 84,210,979 (GRCm39) |
K370E |
probably damaging |
Het |
| Or10ab4 |
T |
A |
7: 107,654,647 (GRCm39) |
C153S |
probably benign |
Het |
| Or4d10 |
T |
A |
19: 12,051,639 (GRCm39) |
D119V |
probably damaging |
Het |
| Or5w8 |
A |
G |
2: 87,687,632 (GRCm39) |
T38A |
probably benign |
Het |
| Or6c212 |
C |
T |
10: 129,558,592 (GRCm39) |
V274M |
probably damaging |
Het |
| P3h3 |
T |
C |
6: 124,818,736 (GRCm39) |
S701G |
probably benign |
Het |
| Pdss2 |
T |
C |
10: 43,174,908 (GRCm39) |
M138T |
possibly damaging |
Het |
| Piezo1 |
C |
T |
8: 123,213,220 (GRCm39) |
E1848K |
probably benign |
Het |
| Prmt3 |
T |
G |
7: 49,476,557 (GRCm39) |
S389A |
probably benign |
Het |
| Prune2 |
T |
A |
19: 17,099,637 (GRCm39) |
F1714I |
probably benign |
Het |
| Ptgis |
A |
G |
2: 167,067,194 (GRCm39) |
|
probably null |
Het |
| Ptpn20 |
T |
C |
14: 33,336,416 (GRCm39) |
V85A |
probably benign |
Het |
| Rabepk |
A |
T |
2: 34,670,669 (GRCm39) |
Y264N |
probably damaging |
Het |
| Ralgapa2 |
A |
T |
2: 146,276,754 (GRCm39) |
C495* |
probably null |
Het |
| Satb2 |
A |
G |
1: 56,930,327 (GRCm39) |
I232T |
probably benign |
Het |
| Selenbp2 |
A |
T |
3: 94,610,856 (GRCm39) |
L307F |
probably damaging |
Het |
| Sgpl1 |
T |
G |
10: 60,949,863 (GRCm39) |
Y112S |
probably damaging |
Het |
| Slitrk5 |
T |
C |
14: 111,918,679 (GRCm39) |
S768P |
probably benign |
Het |
| Smc3 |
T |
A |
19: 53,619,948 (GRCm39) |
Y615N |
probably damaging |
Het |
| Spag17 |
A |
G |
3: 99,934,939 (GRCm39) |
N715S |
probably benign |
Het |
| Spats2 |
A |
G |
15: 99,110,157 (GRCm39) |
E518G |
probably benign |
Het |
| Spats2l |
A |
G |
1: 57,924,983 (GRCm39) |
H127R |
possibly damaging |
Het |
| Tenm3 |
T |
A |
8: 48,731,996 (GRCm39) |
K1287* |
probably null |
Het |
| Thoc1 |
T |
A |
18: 9,962,387 (GRCm39) |
S91T |
probably benign |
Het |
| Thoc6 |
C |
T |
17: 23,888,911 (GRCm39) |
G166S |
probably damaging |
Het |
| Tmem107 |
C |
A |
11: 68,962,087 (GRCm39) |
T42N |
possibly damaging |
Het |
| Tmprss11c |
A |
G |
5: 86,385,569 (GRCm39) |
I288T |
probably damaging |
Het |
| Tnrc18 |
A |
G |
5: 142,725,248 (GRCm39) |
F1827S |
unknown |
Het |
| Trmt112 |
C |
A |
19: 6,887,566 (GRCm39) |
T5N |
probably damaging |
Het |
| Trp53bp1 |
A |
T |
2: 121,101,027 (GRCm39) |
M57K |
probably benign |
Het |
| Ttbk2 |
C |
A |
2: 120,575,631 (GRCm39) |
Q1115H |
probably damaging |
Het |
| Ttn |
C |
A |
2: 76,559,989 (GRCm39) |
E27725* |
probably null |
Het |
| Ttn |
A |
G |
2: 76,774,453 (GRCm39) |
M2151T |
probably damaging |
Het |
| Usp9y |
A |
T |
Y: 1,384,336 (GRCm39) |
D727E |
probably damaging |
Het |
| Vps13c |
A |
G |
9: 67,781,173 (GRCm39) |
T221A |
probably damaging |
Het |
| Zbtb20 |
A |
G |
16: 43,439,055 (GRCm39) |
D725G |
probably damaging |
Het |
| Zfp341 |
A |
T |
2: 154,468,734 (GRCm39) |
I126F |
possibly damaging |
Het |
| Zfyve16 |
C |
T |
13: 92,650,402 (GRCm39) |
A861T |
probably damaging |
Het |
|
| Other mutations in Nacad |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00597:Nacad
|
APN |
11 |
6,550,921 (GRCm39) |
missense |
probably benign |
0.24 |
|
IGL00903:Nacad
|
APN |
11 |
6,550,632 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01303:Nacad
|
APN |
11 |
6,548,279 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL01353:Nacad
|
APN |
11 |
6,550,530 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
IGL01833:Nacad
|
APN |
11 |
6,555,700 (GRCm39) |
missense |
unknown |
|
|
IGL02267:Nacad
|
APN |
11 |
6,552,649 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL02531:Nacad
|
APN |
11 |
6,548,580 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02994:Nacad
|
APN |
11 |
6,549,528 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
IGL03121:Nacad
|
APN |
11 |
6,550,933 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL03161:Nacad
|
APN |
11 |
6,550,378 (GRCm39) |
nonsense |
probably null |
|
|
Locusta
|
UTSW |
11 |
6,552,387 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
migratoria
|
UTSW |
11 |
6,551,196 (GRCm39) |
missense |
probably benign |
0.30 |
|
FR4340:Nacad
|
UTSW |
11 |
6,549,761 (GRCm39) |
small insertion |
probably benign |
|
|
FR4342:Nacad
|
UTSW |
11 |
6,549,762 (GRCm39) |
small insertion |
probably benign |
|
|
FR4548:Nacad
|
UTSW |
11 |
6,549,760 (GRCm39) |
small insertion |
probably benign |
|
|
FR4548:Nacad
|
UTSW |
11 |
6,549,752 (GRCm39) |
small insertion |
probably benign |
|
|
FR4589:Nacad
|
UTSW |
11 |
6,549,753 (GRCm39) |
small insertion |
probably benign |
|
|
FR4976:Nacad
|
UTSW |
11 |
6,549,763 (GRCm39) |
small insertion |
probably benign |
|
|
FR4976:Nacad
|
UTSW |
11 |
6,549,756 (GRCm39) |
small insertion |
probably benign |
|
|
FR4976:Nacad
|
UTSW |
11 |
6,549,749 (GRCm39) |
small insertion |
probably benign |
|
|
PIT4402001:Nacad
|
UTSW |
11 |
6,548,621 (GRCm39) |
missense |
probably benign |
0.19 |
|
R0330:Nacad
|
UTSW |
11 |
6,550,903 (GRCm39) |
missense |
probably benign |
|
|
R0331:Nacad
|
UTSW |
11 |
6,549,441 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R0409:Nacad
|
UTSW |
11 |
6,549,810 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0612:Nacad
|
UTSW |
11 |
6,551,382 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0644:Nacad
|
UTSW |
11 |
6,549,486 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R0829:Nacad
|
UTSW |
11 |
6,551,158 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1483:Nacad
|
UTSW |
11 |
6,552,217 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1583:Nacad
|
UTSW |
11 |
6,551,185 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1905:Nacad
|
UTSW |
11 |
6,552,540 (GRCm39) |
missense |
probably benign |
0.15 |
|
R1907:Nacad
|
UTSW |
11 |
6,552,540 (GRCm39) |
missense |
probably benign |
0.15 |
|
R2361:Nacad
|
UTSW |
11 |
6,550,821 (GRCm39) |
missense |
probably benign |
|
|
R2979:Nacad
|
UTSW |
11 |
6,551,424 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4192:Nacad
|
UTSW |
11 |
6,555,534 (GRCm39) |
missense |
probably benign |
0.44 |
|
R4381:Nacad
|
UTSW |
11 |
6,550,204 (GRCm39) |
missense |
probably benign |
0.18 |
|
R4539:Nacad
|
UTSW |
11 |
6,550,677 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4751:Nacad
|
UTSW |
11 |
6,555,726 (GRCm39) |
missense |
unknown |
|
|
R4944:Nacad
|
UTSW |
11 |
6,548,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5102:Nacad
|
UTSW |
11 |
6,548,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5189:Nacad
|
UTSW |
11 |
6,551,611 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5296:Nacad
|
UTSW |
11 |
6,555,745 (GRCm39) |
missense |
unknown |
|
|
R5566:Nacad
|
UTSW |
11 |
6,552,136 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5634:Nacad
|
UTSW |
11 |
6,552,387 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R5725:Nacad
|
UTSW |
11 |
6,551,643 (GRCm39) |
missense |
probably benign |
0.15 |
|
R5748:Nacad
|
UTSW |
11 |
6,548,370 (GRCm39) |
nonsense |
probably null |
|
|
R5864:Nacad
|
UTSW |
11 |
6,550,581 (GRCm39) |
missense |
probably benign |
|
|
R5882:Nacad
|
UTSW |
11 |
6,548,568 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6089:Nacad
|
UTSW |
11 |
6,551,331 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6117:Nacad
|
UTSW |
11 |
6,549,810 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6161:Nacad
|
UTSW |
11 |
6,550,902 (GRCm39) |
missense |
probably benign |
|
|
R6351:Nacad
|
UTSW |
11 |
6,550,165 (GRCm39) |
nonsense |
probably null |
|
|
R6351:Nacad
|
UTSW |
11 |
6,549,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6366:Nacad
|
UTSW |
11 |
6,551,196 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6525:Nacad
|
UTSW |
11 |
6,552,255 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6811:Nacad
|
UTSW |
11 |
6,549,400 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6931:Nacad
|
UTSW |
11 |
6,551,877 (GRCm39) |
missense |
probably benign |
0.14 |
|
R6966:Nacad
|
UTSW |
11 |
6,552,634 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7228:Nacad
|
UTSW |
11 |
6,548,412 (GRCm39) |
missense |
probably benign |
0.19 |
|
R7248:Nacad
|
UTSW |
11 |
6,548,589 (GRCm39) |
nonsense |
probably null |
|
|
R7556:Nacad
|
UTSW |
11 |
6,551,272 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7594:Nacad
|
UTSW |
11 |
6,552,457 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7813:Nacad
|
UTSW |
11 |
6,549,071 (GRCm39) |
missense |
probably benign |
0.38 |
|
R7841:Nacad
|
UTSW |
11 |
6,551,031 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8243:Nacad
|
UTSW |
11 |
6,552,643 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8810:Nacad
|
UTSW |
11 |
6,552,853 (GRCm39) |
missense |
probably benign |
0.15 |
|
R9042:Nacad
|
UTSW |
11 |
6,548,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9057:Nacad
|
UTSW |
11 |
6,550,876 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R9114:Nacad
|
UTSW |
11 |
6,552,252 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9328:Nacad
|
UTSW |
11 |
6,552,417 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R9394:Nacad
|
UTSW |
11 |
6,549,390 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9595:Nacad
|
UTSW |
11 |
6,551,790 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9755:Nacad
|
UTSW |
11 |
6,549,374 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9760:Nacad
|
UTSW |
11 |
6,551,662 (GRCm39) |
missense |
probably benign |
0.02 |
|
T0975:Nacad
|
UTSW |
11 |
6,551,632 (GRCm39) |
missense |
probably benign |
0.17 |
|
T0975:Nacad
|
UTSW |
11 |
6,551,622 (GRCm39) |
missense |
probably benign |
0.03 |
|
T0975:Nacad
|
UTSW |
11 |
6,549,750 (GRCm39) |
small insertion |
probably benign |
|
|
X0011:Nacad
|
UTSW |
11 |
6,551,074 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Nacad
|
UTSW |
11 |
6,552,297 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTAAGCATCTGTAGGAGCTGGG -3'
(R):5'- TTCCCAGCTCTTGAACAAAAGG -3'
Sequencing Primer
(F):5'- TAGGAGCTGGGCCGATG -3'
(R):5'- CCCAGCTCTTGAACAAAAGGATGAG -3'
|
| Posted On |
2016-04-27 |
Incidental Mutation