Incidental Mutation 'R1982:Dqx1'
| ID |
219927 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dqx1
|
| Ensembl Gene |
ENSMUSG00000009145 |
| Gene Name |
DEAQ RNA-dependent ATPase |
| Synonyms |
2310066E11Rik |
| MMRRC Submission |
039994-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.058)
|
| Stock # |
R1982 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
83034825-83044299 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 83035558 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Asparagine
at position 24
(D24N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000144697
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077502]
[ENSMUST00000089645]
[ENSMUST00000092618]
[ENSMUST00000113962]
[ENSMUST00000113963]
[ENSMUST00000122955]
[ENSMUST00000134606]
[ENSMUST00000204803]
|
| AlphaFold |
Q924H9 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000077502
AA Change: D24N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000076708
Gene: ENSMUSG00000009145
AA Change: D24N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
19 |
N/A |
INTRINSIC |
|
DEXDc
|
30 |
236 |
5.01e-4 |
SMART |
|
low complexity region
|
268 |
280 |
N/A |
INTRINSIC |
|
low complexity region
|
288 |
301 |
N/A |
INTRINSIC |
|
HA2
|
441 |
530 |
4e-19 |
SMART |
|
Pfam:OB_NTP_bind
|
555 |
674 |
2.2e-11 |
PFAM |
|
low complexity region
|
695 |
708 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000089645
|
| SMART Domains |
Protein: ENSMUSP00000087073
Gene: ENSMUSG00000068329
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
39 |
N/A |
INTRINSIC |
|
transmembrane domain
|
106 |
125 |
N/A |
INTRINSIC |
|
low complexity region
|
128 |
143 |
N/A |
INTRINSIC |
|
Pfam:Trypsin
|
170 |
341 |
1.1e-14 |
PFAM |
|
Pfam:Trypsin_2
|
182 |
320 |
1.2e-34 |
PFAM |
|
PDZ
|
371 |
445 |
2.86e-10 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000092618
|
| SMART Domains |
Protein: ENSMUSP00000090281
Gene: ENSMUSG00000068328
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
10 |
40 |
N/A |
INTRINSIC |
|
transmembrane domain
|
52 |
74 |
N/A |
INTRINSIC |
|
PlsC
|
119 |
222 |
1.04e-1 |
SMART |
|
low complexity region
|
307 |
322 |
N/A |
INTRINSIC |
|
CUE
|
325 |
366 |
1.3e-9 |
SMART |
|
low complexity region
|
378 |
392 |
N/A |
INTRINSIC |
|
low complexity region
|
421 |
439 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000113962
|
| SMART Domains |
Protein: ENSMUSP00000109595
Gene: ENSMUSG00000068329
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
39 |
N/A |
INTRINSIC |
|
transmembrane domain
|
106 |
125 |
N/A |
INTRINSIC |
|
low complexity region
|
128 |
143 |
N/A |
INTRINSIC |
|
Pfam:Trypsin_2
|
182 |
237 |
2.7e-12 |
PFAM |
|
Pfam:Trypsin
|
212 |
277 |
4.5e-6 |
PFAM |
|
PDZ
|
285 |
348 |
4.89e-1 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000113963
|
| SMART Domains |
Protein: ENSMUSP00000109596
Gene: ENSMUSG00000068329
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
39 |
N/A |
INTRINSIC |
|
transmembrane domain
|
106 |
125 |
N/A |
INTRINSIC |
|
low complexity region
|
128 |
143 |
N/A |
INTRINSIC |
|
Pfam:Trypsin
|
170 |
342 |
6.8e-15 |
PFAM |
|
Pfam:Trypsin_2
|
182 |
320 |
7.1e-24 |
PFAM |
|
PDZ
|
350 |
413 |
4.89e-1 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000122955
|
| SMART Domains |
Protein: ENSMUSP00000138153
Gene: ENSMUSG00000068329
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
39 |
N/A |
INTRINSIC |
|
transmembrane domain
|
106 |
125 |
N/A |
INTRINSIC |
|
low complexity region
|
128 |
143 |
N/A |
INTRINSIC |
|
Pfam:Trypsin
|
170 |
321 |
2.1e-10 |
PFAM |
|
Pfam:Trypsin_2
|
182 |
317 |
9.5e-21 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000132099
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000203915
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000203180
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000203331
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154829
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204209
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000203123
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144058
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000203339
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204281
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000203749
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204383
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000204343
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000134606
|
| SMART Domains |
Protein: ENSMUSP00000115547
Gene: ENSMUSG00000068329
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Trypsin
|
7 |
180 |
2.7e-15 |
PFAM |
|
Pfam:Trypsin_2
|
20 |
158 |
3.1e-24 |
PFAM |
|
PDZ
|
209 |
283 |
2.86e-10 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000150217
|
| SMART Domains |
Protein: ENSMUSP00000118234
Gene: ENSMUSG00000068329
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
11 |
N/A |
INTRINSIC |
|
Pfam:Trypsin
|
41 |
215 |
1.6e-11 |
PFAM |
|
Pfam:Trypsin_2
|
53 |
190 |
1.8e-31 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000204803
AA Change: D24N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000144697
Gene: ENSMUSG00000009145
AA Change: D24N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
19 |
N/A |
INTRINSIC |
|
DEXDc
|
30 |
236 |
2.1e-6 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000204719
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204761
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204510
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205152
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204752
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204385
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204895
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205042
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 89 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aatk |
G |
T |
11: 119,904,340 (GRCm39) |
P252Q |
probably damaging |
Het |
| Adamts4 |
T |
C |
1: 171,086,503 (GRCm39) |
V765A |
probably benign |
Het |
| Agfg2 |
A |
T |
5: 137,662,515 (GRCm39) |
V184E |
possibly damaging |
Het |
| Alas1 |
A |
T |
9: 106,115,384 (GRCm39) |
I48N |
probably damaging |
Het |
| Anks1 |
T |
C |
17: 28,204,095 (GRCm39) |
V181A |
probably damaging |
Het |
| Anxa8 |
A |
T |
14: 33,818,527 (GRCm39) |
R261S |
probably damaging |
Het |
| Aqp4 |
T |
C |
18: 15,526,608 (GRCm39) |
D291G |
probably damaging |
Het |
| Atrn |
A |
G |
2: 130,812,142 (GRCm39) |
R696G |
probably benign |
Het |
| Barx2 |
A |
C |
9: 31,824,308 (GRCm39) |
I27S |
probably damaging |
Het |
| Btnl1 |
A |
T |
17: 34,598,725 (GRCm39) |
I114L |
possibly damaging |
Het |
| Casq1 |
C |
T |
1: 172,043,097 (GRCm39) |
A200T |
probably damaging |
Het |
| Ccdc33 |
T |
A |
9: 58,024,451 (GRCm39) |
E225D |
probably benign |
Het |
| Cd84 |
C |
A |
1: 171,712,152 (GRCm39) |
|
probably null |
Het |
| Ceacam9 |
T |
G |
7: 16,459,232 (GRCm39) |
L177R |
probably benign |
Het |
| Cenpi |
T |
A |
X: 133,218,782 (GRCm39) |
F161L |
possibly damaging |
Het |
| Cep63 |
T |
C |
9: 102,480,079 (GRCm39) |
K251E |
probably damaging |
Het |
| Cetn3 |
A |
G |
13: 81,932,816 (GRCm39) |
E25G |
probably damaging |
Het |
| Crybg3 |
T |
C |
16: 59,364,488 (GRCm39) |
D2378G |
possibly damaging |
Het |
| Ddx19b |
T |
C |
8: 111,735,975 (GRCm39) |
T357A |
possibly damaging |
Het |
| Dpep2 |
A |
C |
8: 106,716,087 (GRCm39) |
Y266* |
probably null |
Het |
| Dsg4 |
A |
T |
18: 20,604,269 (GRCm39) |
Y912F |
probably damaging |
Het |
| Fezf2 |
G |
T |
14: 12,344,405 (GRCm38) |
P261T |
probably benign |
Het |
| Fmo1 |
T |
C |
1: 162,667,325 (GRCm39) |
I163M |
possibly damaging |
Het |
| Garin1a |
A |
G |
6: 29,285,921 (GRCm39) |
T69A |
probably benign |
Het |
| Gatad2a |
G |
A |
8: 70,365,782 (GRCm39) |
R428* |
probably null |
Het |
| Gfpt1 |
T |
A |
6: 87,031,612 (GRCm39) |
F85I |
possibly damaging |
Het |
| Gimap7 |
A |
T |
6: 48,701,175 (GRCm39) |
I254F |
possibly damaging |
Het |
| Glcci1 |
T |
C |
6: 8,592,980 (GRCm39) |
S261P |
probably damaging |
Het |
| Glis3 |
A |
T |
19: 28,508,674 (GRCm39) |
F437I |
probably damaging |
Het |
| Glp1r |
C |
A |
17: 31,144,601 (GRCm39) |
S258* |
probably null |
Het |
| Gpt2 |
C |
T |
8: 86,242,832 (GRCm39) |
A288V |
possibly damaging |
Het |
| Grin2c |
G |
T |
11: 115,151,731 (GRCm39) |
S76R |
possibly damaging |
Het |
| Guf1 |
T |
A |
5: 69,724,569 (GRCm39) |
Y447* |
probably null |
Het |
| H2-T9 |
T |
A |
17: 36,439,614 (GRCm39) |
D122V |
probably damaging |
Het |
| Hectd1 |
A |
C |
12: 51,832,624 (GRCm39) |
L916V |
probably damaging |
Het |
| Hnf4g |
A |
G |
3: 3,703,268 (GRCm39) |
K96E |
probably damaging |
Het |
| Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
| Ifi207 |
T |
G |
1: 173,562,805 (GRCm39) |
M114L |
probably benign |
Het |
| Ifi35 |
A |
T |
11: 101,349,112 (GRCm39) |
E252V |
probably damaging |
Het |
| Igsf9b |
G |
A |
9: 27,233,535 (GRCm39) |
R345H |
possibly damaging |
Het |
| Itih3 |
T |
C |
14: 30,645,540 (GRCm39) |
|
probably benign |
Het |
| Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
| Kidins220 |
A |
T |
12: 25,101,193 (GRCm39) |
M1252L |
probably benign |
Het |
| Kifap3 |
T |
A |
1: 163,689,591 (GRCm39) |
L525* |
probably null |
Het |
| Limk2 |
A |
T |
11: 3,305,461 (GRCm39) |
D35E |
probably benign |
Het |
| Lrrc37a |
G |
A |
11: 103,389,792 (GRCm39) |
P1878S |
probably benign |
Het |
| Mansc4 |
T |
A |
6: 146,977,173 (GRCm39) |
I148F |
probably benign |
Het |
| Mei1 |
A |
G |
15: 81,987,513 (GRCm39) |
N859S |
probably benign |
Het |
| Mib1 |
A |
G |
18: 10,812,064 (GRCm39) |
D987G |
probably damaging |
Het |
| Mroh8 |
A |
G |
2: 157,113,895 (GRCm39) |
V132A |
possibly damaging |
Het |
| Npnt |
T |
C |
3: 132,653,893 (GRCm39) |
I29M |
probably benign |
Het |
| Nrap |
T |
C |
19: 56,372,537 (GRCm39) |
D138G |
probably damaging |
Het |
| Or10a3m |
A |
G |
7: 108,312,902 (GRCm39) |
Y102C |
probably damaging |
Het |
| Or1e16 |
A |
T |
11: 73,285,918 (GRCm39) |
I310N |
probably benign |
Het |
| Or2h1 |
T |
A |
17: 37,404,700 (GRCm39) |
E22V |
probably damaging |
Het |
| Or6z7 |
T |
C |
7: 6,483,931 (GRCm39) |
M75V |
probably benign |
Het |
| Osbpl5 |
A |
C |
7: 143,295,408 (GRCm39) |
|
probably null |
Het |
| Pcna-ps2 |
T |
C |
19: 9,261,047 (GRCm39) |
V102A |
possibly damaging |
Het |
| Pik3c2g |
T |
C |
6: 139,599,546 (GRCm39) |
S221P |
probably damaging |
Het |
| Plppr3 |
A |
G |
10: 79,702,259 (GRCm39) |
I271T |
probably damaging |
Het |
| Ppp4r3c1 |
A |
T |
X: 88,975,051 (GRCm39) |
V382E |
probably damaging |
Het |
| Pramel25 |
C |
A |
4: 143,521,720 (GRCm39) |
H445Q |
probably benign |
Het |
| Prkar1b |
C |
T |
5: 139,113,398 (GRCm39) |
A41T |
probably benign |
Het |
| Prkcsh |
A |
G |
9: 21,924,164 (GRCm39) |
D458G |
probably damaging |
Het |
| Prr14 |
G |
T |
7: 127,074,662 (GRCm39) |
R398L |
possibly damaging |
Het |
| Ptafr |
A |
G |
4: 132,307,296 (GRCm39) |
R229G |
probably damaging |
Het |
| Rbp3 |
T |
C |
14: 33,676,502 (GRCm39) |
F150S |
probably damaging |
Het |
| Rel |
C |
T |
11: 23,692,761 (GRCm39) |
G424D |
probably benign |
Het |
| Rlf |
T |
C |
4: 121,007,309 (GRCm39) |
Y557C |
probably damaging |
Het |
| Samt3 |
A |
C |
X: 85,090,740 (GRCm39) |
M211L |
probably benign |
Het |
| Selenop |
A |
T |
15: 3,305,176 (GRCm39) |
I111F |
probably damaging |
Het |
| Slc2a2 |
G |
A |
3: 28,771,590 (GRCm39) |
M173I |
probably benign |
Het |
| Slc43a1 |
G |
T |
2: 84,687,233 (GRCm39) |
G361V |
possibly damaging |
Het |
| Slit2 |
G |
A |
5: 48,407,178 (GRCm39) |
V870M |
probably damaging |
Het |
| Ssxb10 |
A |
G |
X: 8,197,258 (GRCm39) |
D77G |
probably benign |
Het |
| Stk32b |
T |
A |
5: 37,806,458 (GRCm39) |
I29F |
probably damaging |
Het |
| Stra6l |
T |
A |
4: 45,867,237 (GRCm39) |
C161* |
probably null |
Het |
| Tecpr2 |
T |
A |
12: 110,921,219 (GRCm39) |
M1264K |
probably benign |
Het |
| Tfap2c |
A |
T |
2: 172,399,156 (GRCm39) |
I468F |
probably damaging |
Het |
| Ticam1 |
C |
T |
17: 56,578,555 (GRCm39) |
R180H |
probably damaging |
Het |
| Tlr4 |
T |
A |
4: 66,759,272 (GRCm39) |
N688K |
probably benign |
Het |
| Tmem35b |
A |
T |
4: 127,019,846 (GRCm39) |
|
probably benign |
Het |
| Ugt2b34 |
T |
C |
5: 87,054,172 (GRCm39) |
E203G |
probably damaging |
Het |
| Vegfa |
A |
C |
17: 46,329,786 (GRCm39) |
*393G |
probably null |
Het |
| Vmn2r16 |
T |
C |
5: 109,511,890 (GRCm39) |
V699A |
probably benign |
Het |
| Zfp324 |
T |
C |
7: 12,705,145 (GRCm39) |
S445P |
probably damaging |
Het |
| Zfp982 |
T |
A |
4: 147,597,049 (GRCm39) |
C135* |
probably null |
Het |
| Zfp990 |
A |
C |
4: 145,263,439 (GRCm39) |
N146H |
probably damaging |
Het |
| Zfyve26 |
A |
G |
12: 79,302,017 (GRCm39) |
Y431H |
possibly damaging |
Het |
|
| Other mutations in Dqx1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01796:Dqx1
|
APN |
6 |
83,043,408 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02158:Dqx1
|
APN |
6 |
83,035,891 (GRCm39) |
splice site |
probably benign |
|
|
IGL02288:Dqx1
|
APN |
6 |
83,037,309 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02801:Dqx1
|
APN |
6 |
83,037,476 (GRCm39) |
splice site |
probably null |
|
|
IGL02929:Dqx1
|
APN |
6 |
83,037,465 (GRCm39) |
unclassified |
probably benign |
|
|
R0396:Dqx1
|
UTSW |
6 |
83,035,986 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0448:Dqx1
|
UTSW |
6 |
83,037,326 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0471:Dqx1
|
UTSW |
6 |
83,036,407 (GRCm39) |
splice site |
probably benign |
|
|
R1022:Dqx1
|
UTSW |
6 |
83,038,070 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1023:Dqx1
|
UTSW |
6 |
83,038,070 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1024:Dqx1
|
UTSW |
6 |
83,038,070 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1480:Dqx1
|
UTSW |
6 |
83,036,433 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R1804:Dqx1
|
UTSW |
6 |
83,037,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1848:Dqx1
|
UTSW |
6 |
83,043,088 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2064:Dqx1
|
UTSW |
6 |
83,035,524 (GRCm39) |
unclassified |
probably benign |
|
|
R2350:Dqx1
|
UTSW |
6 |
83,036,068 (GRCm39) |
nonsense |
probably null |
|
|
R3110:Dqx1
|
UTSW |
6 |
83,035,953 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3112:Dqx1
|
UTSW |
6 |
83,035,953 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3119:Dqx1
|
UTSW |
6 |
83,043,216 (GRCm39) |
nonsense |
probably null |
|
|
R4179:Dqx1
|
UTSW |
6 |
83,036,460 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4180:Dqx1
|
UTSW |
6 |
83,036,460 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4873:Dqx1
|
UTSW |
6 |
83,037,993 (GRCm39) |
missense |
probably benign |
0.25 |
|
R4875:Dqx1
|
UTSW |
6 |
83,037,993 (GRCm39) |
missense |
probably benign |
0.25 |
|
R4882:Dqx1
|
UTSW |
6 |
83,043,069 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R5015:Dqx1
|
UTSW |
6 |
83,043,092 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5128:Dqx1
|
UTSW |
6 |
83,037,548 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5346:Dqx1
|
UTSW |
6 |
83,036,700 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5480:Dqx1
|
UTSW |
6 |
83,041,784 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6939:Dqx1
|
UTSW |
6 |
83,036,446 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6979:Dqx1
|
UTSW |
6 |
83,037,992 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7059:Dqx1
|
UTSW |
6 |
83,041,790 (GRCm39) |
missense |
probably benign |
0.18 |
|
R7084:Dqx1
|
UTSW |
6 |
83,043,436 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7354:Dqx1
|
UTSW |
6 |
83,037,957 (GRCm39) |
nonsense |
probably null |
|
|
R7389:Dqx1
|
UTSW |
6 |
83,041,775 (GRCm39) |
missense |
probably null |
0.99 |
|
R7497:Dqx1
|
UTSW |
6 |
83,036,028 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7632:Dqx1
|
UTSW |
6 |
83,036,680 (GRCm39) |
missense |
probably benign |
|
|
R7762:Dqx1
|
UTSW |
6 |
83,038,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8002:Dqx1
|
UTSW |
6 |
83,035,558 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8036:Dqx1
|
UTSW |
6 |
83,036,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8147:Dqx1
|
UTSW |
6 |
83,037,222 (GRCm39) |
missense |
probably benign |
0.41 |
|
R8776:Dqx1
|
UTSW |
6 |
83,035,619 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8776-TAIL:Dqx1
|
UTSW |
6 |
83,035,619 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9090:Dqx1
|
UTSW |
6 |
83,036,024 (GRCm39) |
missense |
probably benign |
0.13 |
|
R9139:Dqx1
|
UTSW |
6 |
83,036,759 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R9271:Dqx1
|
UTSW |
6 |
83,036,024 (GRCm39) |
missense |
probably benign |
0.13 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCTTAGAGACACCCAGCACG -3'
(R):5'- CAGAATCTTCCTCCACCTGG -3'
Sequencing Primer
(F):5'- TTAGAGACACCCAGCACGGTTTC -3'
(R):5'- ACCTGGGTGCTCTTGCCAG -3'
|
| Posted On |
2014-08-25 |
Incidental Mutation