Incidental Mutation 'R4910:Dop1a'
ID |
379418 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dop1a
|
Ensembl Gene |
ENSMUSG00000034973 |
Gene Name |
DOP1 leucine zipper like protein A |
Synonyms |
D9Ertd809e, B130005I07Rik, Dopey1 |
MMRRC Submission |
042512-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.338)
|
Stock # |
R4910 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
9 |
Chromosomal Location |
86349194-86436683 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 86374114 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Isoleucine
at position 191
(T191I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000140740
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034987]
[ENSMUST00000185919]
[ENSMUST00000188675]
[ENSMUST00000190957]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000034987
AA Change: T191I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000034987 Gene: ENSMUSG00000034973 AA Change: T191I
Domain | Start | End | E-Value | Type |
Pfam:Dopey_N
|
11 |
300 |
1e-117 |
PFAM |
low complexity region
|
631 |
649 |
N/A |
INTRINSIC |
low complexity region
|
961 |
973 |
N/A |
INTRINSIC |
low complexity region
|
1073 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1105 |
1118 |
N/A |
INTRINSIC |
low complexity region
|
1268 |
1281 |
N/A |
INTRINSIC |
low complexity region
|
1296 |
1318 |
N/A |
INTRINSIC |
low complexity region
|
1335 |
1344 |
N/A |
INTRINSIC |
low complexity region
|
1362 |
1373 |
N/A |
INTRINSIC |
low complexity region
|
1575 |
1589 |
N/A |
INTRINSIC |
low complexity region
|
2217 |
2227 |
N/A |
INTRINSIC |
low complexity region
|
2351 |
2362 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000185919
AA Change: T191I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000140040 Gene: ENSMUSG00000034973 AA Change: T191I
Domain | Start | End | E-Value | Type |
Pfam:Dopey_N
|
10 |
306 |
1.9e-106 |
PFAM |
low complexity region
|
629 |
647 |
N/A |
INTRINSIC |
low complexity region
|
959 |
971 |
N/A |
INTRINSIC |
low complexity region
|
1071 |
1082 |
N/A |
INTRINSIC |
low complexity region
|
1103 |
1116 |
N/A |
INTRINSIC |
low complexity region
|
1266 |
1279 |
N/A |
INTRINSIC |
low complexity region
|
1294 |
1316 |
N/A |
INTRINSIC |
low complexity region
|
1333 |
1342 |
N/A |
INTRINSIC |
low complexity region
|
1360 |
1371 |
N/A |
INTRINSIC |
low complexity region
|
1573 |
1587 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186290
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186841
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000187607
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000188675
AA Change: T191I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000139413 Gene: ENSMUSG00000034973 AA Change: T191I
Domain | Start | End | E-Value | Type |
Pfam:Dopey_N
|
10 |
306 |
3e-106 |
PFAM |
low complexity region
|
622 |
640 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190407
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000190957
AA Change: T191I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000140740 Gene: ENSMUSG00000034973 AA Change: T191I
Domain | Start | End | E-Value | Type |
Pfam:Dopey_N
|
10 |
305 |
1.3e-108 |
PFAM |
low complexity region
|
631 |
649 |
N/A |
INTRINSIC |
low complexity region
|
961 |
973 |
N/A |
INTRINSIC |
low complexity region
|
1073 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1105 |
1118 |
N/A |
INTRINSIC |
low complexity region
|
1268 |
1281 |
N/A |
INTRINSIC |
low complexity region
|
1296 |
1318 |
N/A |
INTRINSIC |
low complexity region
|
1335 |
1344 |
N/A |
INTRINSIC |
low complexity region
|
1362 |
1373 |
N/A |
INTRINSIC |
low complexity region
|
1575 |
1589 |
N/A |
INTRINSIC |
low complexity region
|
2217 |
2227 |
N/A |
INTRINSIC |
low complexity region
|
2351 |
2362 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190906
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190834
|
Meta Mutation Damage Score |
0.1281 |
Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 94.6%
- 20x: 86.1%
|
Validation Efficiency |
95% (144/151) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm3 |
T |
A |
3: 59,776,435 (GRCm39) |
|
probably null |
Het |
Adam3 |
T |
A |
8: 25,184,321 (GRCm39) |
I560L |
probably benign |
Het |
Agxt |
T |
C |
1: 93,063,436 (GRCm39) |
F113L |
probably benign |
Het |
Aknad1 |
T |
A |
3: 108,688,568 (GRCm39) |
|
probably null |
Het |
Alpk2 |
T |
A |
18: 65,399,357 (GRCm39) |
K2074* |
probably null |
Het |
Apob |
A |
G |
12: 8,057,848 (GRCm39) |
Y2077C |
probably damaging |
Het |
Arhgap17 |
A |
T |
7: 122,907,600 (GRCm39) |
L254Q |
probably damaging |
Het |
Arhgap26 |
T |
A |
18: 39,126,690 (GRCm39) |
|
probably benign |
Het |
Arhgef5 |
A |
G |
6: 43,249,762 (GRCm39) |
D171G |
probably benign |
Het |
Arid1b |
T |
A |
17: 5,392,478 (GRCm39) |
S2003T |
probably damaging |
Het |
Armc5 |
T |
G |
7: 127,839,900 (GRCm39) |
L406R |
possibly damaging |
Het |
Arsb |
T |
C |
13: 93,908,485 (GRCm39) |
V67A |
probably benign |
Het |
Aspm |
A |
G |
1: 139,419,281 (GRCm39) |
Y2982C |
probably damaging |
Het |
Bltp1 |
C |
A |
3: 37,052,348 (GRCm39) |
T3016K |
probably damaging |
Het |
Btbd7 |
A |
G |
12: 102,774,307 (GRCm39) |
L487P |
probably damaging |
Het |
Card11 |
C |
G |
5: 140,860,169 (GRCm39) |
D1063H |
probably damaging |
Het |
Ccdc186 |
G |
A |
19: 56,787,123 (GRCm39) |
T615M |
probably damaging |
Het |
Cd101 |
T |
A |
3: 100,901,205 (GRCm39) |
T960S |
probably benign |
Het |
Cdca7l |
C |
A |
12: 117,837,520 (GRCm39) |
S191* |
probably null |
Het |
Cemip |
A |
T |
7: 83,646,619 (GRCm39) |
I143N |
probably damaging |
Het |
Cep170 |
C |
T |
1: 176,609,829 (GRCm39) |
E161K |
possibly damaging |
Het |
Cfhr4 |
T |
G |
1: 139,702,301 (GRCm39) |
D61A |
probably damaging |
Het |
Chrm2 |
A |
T |
6: 36,501,168 (GRCm39) |
T342S |
probably benign |
Het |
Cib2 |
A |
G |
9: 54,457,163 (GRCm39) |
F34L |
probably benign |
Het |
Cnot1 |
A |
T |
8: 96,459,859 (GRCm39) |
I1836N |
probably benign |
Het |
Col4a3 |
C |
A |
1: 82,650,400 (GRCm39) |
P552Q |
unknown |
Het |
Cp |
T |
A |
3: 20,043,388 (GRCm39) |
|
probably benign |
Het |
Cul3 |
C |
T |
1: 80,267,806 (GRCm39) |
V112I |
probably benign |
Het |
Dcdc5 |
A |
G |
2: 106,195,895 (GRCm39) |
|
noncoding transcript |
Het |
Disp1 |
A |
T |
1: 182,917,027 (GRCm39) |
V133E |
probably damaging |
Het |
Dlg4 |
A |
G |
11: 69,921,751 (GRCm39) |
D30G |
probably damaging |
Het |
Enam |
T |
G |
5: 88,650,173 (GRCm39) |
S561A |
probably benign |
Het |
Fbxw8 |
G |
T |
5: 118,263,092 (GRCm39) |
|
probably null |
Het |
Filip1 |
A |
G |
9: 79,725,214 (GRCm39) |
V1135A |
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,614,059 (GRCm39) |
T81A |
probably benign |
Het |
Ghdc |
T |
C |
11: 100,657,814 (GRCm39) |
K472E |
probably benign |
Het |
Gm10568 |
T |
G |
1: 3,751,164 (GRCm39) |
|
noncoding transcript |
Het |
Gm4953 |
T |
A |
1: 158,995,929 (GRCm39) |
|
noncoding transcript |
Het |
Gm6871 |
T |
A |
7: 41,223,016 (GRCm39) |
H24L |
probably benign |
Het |
Gpr155 |
G |
A |
2: 73,197,882 (GRCm39) |
Q413* |
probably null |
Het |
Grhl2 |
A |
G |
15: 37,291,920 (GRCm39) |
|
probably null |
Het |
Ighv1-31 |
G |
C |
12: 114,793,128 (GRCm39) |
S36* |
probably null |
Het |
Ighv8-5 |
A |
G |
12: 115,031,462 (GRCm39) |
S26P |
probably damaging |
Het |
Igkv17-134 |
A |
C |
6: 67,697,910 (GRCm39) |
|
probably benign |
Het |
Igkv5-48 |
A |
C |
6: 69,703,833 (GRCm39) |
L24R |
probably damaging |
Het |
Isg20l2 |
T |
A |
3: 87,846,570 (GRCm39) |
V340E |
probably damaging |
Het |
Lrrtm1 |
A |
G |
6: 77,221,884 (GRCm39) |
Y447C |
probably damaging |
Het |
Ltbp1 |
T |
C |
17: 75,634,287 (GRCm39) |
S855P |
probably damaging |
Het |
Mgat4e |
A |
T |
1: 134,469,602 (GRCm39) |
N147K |
probably damaging |
Het |
Mlc1 |
A |
G |
15: 88,842,415 (GRCm39) |
L315P |
possibly damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,076,292 (GRCm39) |
V322A |
probably benign |
Het |
Mroh7 |
T |
C |
4: 106,567,152 (GRCm39) |
|
probably null |
Het |
Mybpc1 |
T |
A |
10: 88,391,586 (GRCm39) |
K304* |
probably null |
Het |
Nlrp14 |
A |
C |
7: 106,785,790 (GRCm39) |
D622A |
possibly damaging |
Het |
Nlrp1b |
T |
A |
11: 71,108,103 (GRCm39) |
H466L |
probably benign |
Het |
Nlrp4d |
T |
A |
7: 10,112,336 (GRCm39) |
|
noncoding transcript |
Het |
Nrxn3 |
A |
G |
12: 89,227,130 (GRCm39) |
E628G |
possibly damaging |
Het |
Nup133 |
T |
C |
8: 124,653,870 (GRCm39) |
R530G |
possibly damaging |
Het |
Nup98 |
A |
G |
7: 101,845,007 (GRCm39) |
S21P |
unknown |
Het |
Or2h2b-ps1 |
T |
C |
17: 37,480,934 (GRCm39) |
I202V |
probably benign |
Het |
Or2l13b |
T |
C |
16: 19,348,768 (GRCm39) |
T301A |
probably benign |
Het |
Or4f14b |
A |
T |
2: 111,775,423 (GRCm39) |
I126K |
possibly damaging |
Het |
Or52e8 |
G |
A |
7: 104,624,686 (GRCm39) |
P169S |
possibly damaging |
Het |
Or5k1 |
T |
A |
16: 58,617,805 (GRCm39) |
T135S |
probably benign |
Het |
Or6c66 |
T |
C |
10: 129,461,676 (GRCm39) |
T85A |
probably damaging |
Het |
Or8c11 |
T |
A |
9: 38,290,038 (GRCm39) |
V287E |
probably null |
Het |
Otog |
A |
T |
7: 45,913,486 (GRCm39) |
Y773F |
probably damaging |
Het |
Otog |
A |
T |
7: 45,947,958 (GRCm39) |
I2320F |
probably damaging |
Het |
Otogl |
T |
C |
10: 107,715,378 (GRCm39) |
S433G |
probably benign |
Het |
Pcdhb17 |
A |
T |
18: 37,618,212 (GRCm39) |
M1L |
possibly damaging |
Het |
Pde7b |
T |
A |
10: 20,600,480 (GRCm39) |
|
probably benign |
Het |
Pgm1 |
T |
C |
4: 99,820,724 (GRCm39) |
V207A |
probably damaging |
Het |
Pkd1 |
T |
A |
17: 24,791,661 (GRCm39) |
V1116E |
probably damaging |
Het |
Pkd1l1 |
T |
A |
11: 8,879,360 (GRCm39) |
Y497F |
possibly damaging |
Het |
Pomgnt2 |
T |
C |
9: 121,812,013 (GRCm39) |
N256S |
probably benign |
Het |
Pot1a |
A |
T |
6: 25,746,020 (GRCm39) |
|
probably benign |
Het |
Prdm9 |
T |
C |
17: 15,764,585 (GRCm39) |
T732A |
probably benign |
Het |
Prg4 |
T |
A |
1: 150,331,574 (GRCm39) |
|
probably benign |
Het |
Ptpro |
T |
C |
6: 137,345,336 (GRCm39) |
V114A |
probably damaging |
Het |
Pyurf |
A |
G |
6: 57,668,933 (GRCm39) |
S20P |
unknown |
Het |
Rasgrf1 |
A |
G |
9: 89,858,805 (GRCm39) |
T488A |
probably benign |
Het |
Rassf8 |
A |
T |
6: 145,761,006 (GRCm39) |
K111* |
probably null |
Het |
Reps1 |
A |
T |
10: 17,983,436 (GRCm39) |
E426D |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,730,666 (GRCm39) |
K982R |
probably damaging |
Het |
Rps23 |
T |
C |
13: 91,071,871 (GRCm39) |
|
probably null |
Het |
Scamp4 |
T |
A |
10: 80,445,505 (GRCm39) |
V56E |
probably damaging |
Het |
Serpina1c |
C |
T |
12: 103,861,291 (GRCm39) |
V408I |
probably benign |
Het |
Sigirr |
A |
G |
7: 140,673,701 (GRCm39) |
W49R |
probably damaging |
Het |
Slc17a6 |
A |
T |
7: 51,308,489 (GRCm39) |
H271L |
possibly damaging |
Het |
Slc7a5 |
G |
T |
8: 122,611,861 (GRCm39) |
T389K |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,191,999 (GRCm39) |
H945L |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,523,549 (GRCm39) |
S662P |
probably damaging |
Het |
Snta1 |
C |
A |
2: 154,218,938 (GRCm39) |
E466* |
probably null |
Het |
Sowaha |
A |
G |
11: 53,369,272 (GRCm39) |
L488P |
probably damaging |
Het |
Spata17 |
C |
A |
1: 186,926,208 (GRCm39) |
V41F |
probably damaging |
Het |
Spta1 |
T |
A |
1: 174,045,429 (GRCm39) |
|
probably null |
Het |
Srrm2 |
T |
A |
17: 24,034,362 (GRCm39) |
|
probably benign |
Het |
Stard13 |
T |
C |
5: 150,985,992 (GRCm39) |
N388S |
probably benign |
Het |
Stmn3 |
T |
C |
2: 180,950,630 (GRCm39) |
K59E |
probably damaging |
Het |
Sval1 |
A |
G |
6: 41,932,378 (GRCm39) |
N76S |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,096,276 (GRCm39) |
H1448R |
possibly damaging |
Het |
Sycp2 |
A |
T |
2: 178,000,017 (GRCm39) |
D986E |
probably benign |
Het |
Sytl5 |
C |
T |
X: 9,781,841 (GRCm39) |
P181L |
possibly damaging |
Het |
Tbkbp1 |
G |
A |
11: 97,029,956 (GRCm39) |
S400L |
probably benign |
Het |
Tesc |
G |
T |
5: 118,194,531 (GRCm39) |
|
probably benign |
Het |
Tjp1 |
C |
T |
7: 64,993,475 (GRCm39) |
G33R |
probably damaging |
Het |
Tlr11 |
C |
A |
14: 50,600,346 (GRCm39) |
F777L |
probably benign |
Het |
Tmem156 |
A |
G |
5: 65,248,805 (GRCm39) |
|
probably benign |
Het |
Top3a |
A |
G |
11: 60,643,204 (GRCm39) |
|
probably benign |
Het |
Tpcn1 |
A |
G |
5: 120,694,584 (GRCm39) |
W162R |
probably damaging |
Het |
Tpd52l2 |
A |
T |
2: 181,157,005 (GRCm39) |
|
probably benign |
Het |
Trim80 |
G |
A |
11: 115,337,281 (GRCm39) |
G381D |
probably damaging |
Het |
Ugt1a10 |
C |
T |
1: 88,142,845 (GRCm39) |
P113L |
probably damaging |
Het |
Vmn2r117 |
TC |
T |
17: 23,698,487 (GRCm39) |
|
probably null |
Het |
Vmn2r56 |
T |
A |
7: 12,449,462 (GRCm39) |
I259F |
possibly damaging |
Het |
Vmn2r59 |
T |
C |
7: 41,693,077 (GRCm39) |
T508A |
probably benign |
Het |
Wdr73 |
A |
G |
7: 80,541,456 (GRCm39) |
V362A |
probably damaging |
Het |
Zdhhc21 |
G |
T |
4: 82,738,568 (GRCm39) |
T207K |
possibly damaging |
Het |
Zfp120 |
T |
A |
2: 149,959,872 (GRCm39) |
Q150L |
probably damaging |
Het |
Zfp212 |
C |
A |
6: 47,908,433 (GRCm39) |
Q471K |
possibly damaging |
Het |
Zfp804b |
C |
T |
5: 6,820,540 (GRCm39) |
G841D |
possibly damaging |
Het |
Znfx1 |
A |
T |
2: 166,878,724 (GRCm39) |
M1884K |
probably damaging |
Het |
Znfx1 |
G |
T |
2: 166,879,402 (GRCm39) |
A1658D |
probably benign |
Het |
|
Other mutations in Dop1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Dop1a
|
APN |
9 |
86,433,732 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL00427:Dop1a
|
APN |
9 |
86,403,552 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00427:Dop1a
|
APN |
9 |
86,403,551 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00427:Dop1a
|
APN |
9 |
86,403,553 (GRCm39) |
missense |
probably benign |
0.09 |
IGL00577:Dop1a
|
APN |
9 |
86,402,999 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00741:Dop1a
|
APN |
9 |
86,404,859 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL00959:Dop1a
|
APN |
9 |
86,369,484 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Dop1a
|
APN |
9 |
86,433,730 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01608:Dop1a
|
APN |
9 |
86,389,614 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01760:Dop1a
|
APN |
9 |
86,401,976 (GRCm39) |
missense |
probably benign |
|
IGL01788:Dop1a
|
APN |
9 |
86,413,772 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01844:Dop1a
|
APN |
9 |
86,396,138 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01923:Dop1a
|
APN |
9 |
86,404,920 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02036:Dop1a
|
APN |
9 |
86,413,818 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02308:Dop1a
|
APN |
9 |
86,402,141 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02494:Dop1a
|
APN |
9 |
86,408,871 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02698:Dop1a
|
APN |
9 |
86,406,412 (GRCm39) |
splice site |
probably benign |
|
IGL02731:Dop1a
|
APN |
9 |
86,369,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02821:Dop1a
|
APN |
9 |
86,402,209 (GRCm39) |
missense |
probably benign |
|
IGL02952:Dop1a
|
APN |
9 |
86,414,975 (GRCm39) |
splice site |
probably benign |
|
IGL03071:Dop1a
|
APN |
9 |
86,371,668 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03271:Dop1a
|
APN |
9 |
86,386,275 (GRCm39) |
nonsense |
probably null |
|
IGL03344:Dop1a
|
APN |
9 |
86,418,197 (GRCm39) |
missense |
probably damaging |
1.00 |
Beg
|
UTSW |
9 |
86,430,225 (GRCm39) |
nonsense |
probably null |
|
covet
|
UTSW |
9 |
86,397,396 (GRCm39) |
missense |
probably damaging |
1.00 |
crave
|
UTSW |
9 |
86,399,092 (GRCm39) |
missense |
probably benign |
|
desire
|
UTSW |
9 |
86,402,109 (GRCm39) |
missense |
possibly damaging |
0.47 |
groak
|
UTSW |
9 |
86,403,710 (GRCm39) |
missense |
probably damaging |
1.00 |
Querer
|
UTSW |
9 |
86,386,265 (GRCm39) |
missense |
probably damaging |
1.00 |
yearn
|
UTSW |
9 |
86,386,220 (GRCm39) |
splice site |
probably null |
|
R0055:Dop1a
|
UTSW |
9 |
86,394,705 (GRCm39) |
missense |
probably benign |
0.08 |
R0285:Dop1a
|
UTSW |
9 |
86,394,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0415:Dop1a
|
UTSW |
9 |
86,388,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R0427:Dop1a
|
UTSW |
9 |
86,389,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Dop1a
|
UTSW |
9 |
86,402,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Dop1a
|
UTSW |
9 |
86,367,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R1118:Dop1a
|
UTSW |
9 |
86,397,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1158:Dop1a
|
UTSW |
9 |
86,367,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R1272:Dop1a
|
UTSW |
9 |
86,403,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Dop1a
|
UTSW |
9 |
86,424,785 (GRCm39) |
splice site |
probably null |
|
R1584:Dop1a
|
UTSW |
9 |
86,430,225 (GRCm39) |
nonsense |
probably null |
|
R1601:Dop1a
|
UTSW |
9 |
86,418,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R1674:Dop1a
|
UTSW |
9 |
86,418,213 (GRCm39) |
missense |
probably damaging |
0.98 |
R1706:Dop1a
|
UTSW |
9 |
86,436,133 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1856:Dop1a
|
UTSW |
9 |
86,374,057 (GRCm39) |
missense |
probably damaging |
0.99 |
R1926:Dop1a
|
UTSW |
9 |
86,405,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Dop1a
|
UTSW |
9 |
86,376,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Dop1a
|
UTSW |
9 |
86,403,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Dop1a
|
UTSW |
9 |
86,403,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Dop1a
|
UTSW |
9 |
86,403,652 (GRCm39) |
missense |
probably benign |
0.00 |
R2271:Dop1a
|
UTSW |
9 |
86,376,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2312:Dop1a
|
UTSW |
9 |
86,403,495 (GRCm39) |
nonsense |
probably null |
|
R2379:Dop1a
|
UTSW |
9 |
86,403,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R2507:Dop1a
|
UTSW |
9 |
86,395,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R3737:Dop1a
|
UTSW |
9 |
86,376,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R3804:Dop1a
|
UTSW |
9 |
86,403,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R3916:Dop1a
|
UTSW |
9 |
86,403,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3921:Dop1a
|
UTSW |
9 |
86,402,324 (GRCm39) |
missense |
probably benign |
0.06 |
R4035:Dop1a
|
UTSW |
9 |
86,376,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4392:Dop1a
|
UTSW |
9 |
86,385,196 (GRCm39) |
intron |
probably benign |
|
R4404:Dop1a
|
UTSW |
9 |
86,404,866 (GRCm39) |
nonsense |
probably null |
|
R4513:Dop1a
|
UTSW |
9 |
86,402,612 (GRCm39) |
missense |
probably benign |
0.39 |
R4624:Dop1a
|
UTSW |
9 |
86,403,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R4659:Dop1a
|
UTSW |
9 |
86,384,085 (GRCm39) |
intron |
probably benign |
|
R4919:Dop1a
|
UTSW |
9 |
86,402,109 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5061:Dop1a
|
UTSW |
9 |
86,385,161 (GRCm39) |
splice site |
probably benign |
|
R5079:Dop1a
|
UTSW |
9 |
86,369,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R5118:Dop1a
|
UTSW |
9 |
86,388,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R5169:Dop1a
|
UTSW |
9 |
86,415,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R5176:Dop1a
|
UTSW |
9 |
86,403,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R5190:Dop1a
|
UTSW |
9 |
86,369,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Dop1a
|
UTSW |
9 |
86,397,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R5346:Dop1a
|
UTSW |
9 |
86,402,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R5484:Dop1a
|
UTSW |
9 |
86,427,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R5501:Dop1a
|
UTSW |
9 |
86,389,783 (GRCm39) |
missense |
probably benign |
0.04 |
R5554:Dop1a
|
UTSW |
9 |
86,403,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Dop1a
|
UTSW |
9 |
86,385,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5826:Dop1a
|
UTSW |
9 |
86,389,623 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5921:Dop1a
|
UTSW |
9 |
86,383,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R5934:Dop1a
|
UTSW |
9 |
86,424,495 (GRCm39) |
nonsense |
probably null |
|
R5936:Dop1a
|
UTSW |
9 |
86,418,565 (GRCm39) |
nonsense |
probably null |
|
R6046:Dop1a
|
UTSW |
9 |
86,397,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R6053:Dop1a
|
UTSW |
9 |
86,397,347 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6072:Dop1a
|
UTSW |
9 |
86,389,750 (GRCm39) |
missense |
probably benign |
0.00 |
R6104:Dop1a
|
UTSW |
9 |
86,402,860 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6125:Dop1a
|
UTSW |
9 |
86,403,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Dop1a
|
UTSW |
9 |
86,386,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R6930:Dop1a
|
UTSW |
9 |
86,413,825 (GRCm39) |
critical splice donor site |
probably null |
|
R6949:Dop1a
|
UTSW |
9 |
86,382,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R6979:Dop1a
|
UTSW |
9 |
86,403,695 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7035:Dop1a
|
UTSW |
9 |
86,406,355 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7069:Dop1a
|
UTSW |
9 |
86,432,222 (GRCm39) |
critical splice donor site |
probably null |
|
R7101:Dop1a
|
UTSW |
9 |
86,389,722 (GRCm39) |
missense |
probably benign |
|
R7202:Dop1a
|
UTSW |
9 |
86,386,220 (GRCm39) |
splice site |
probably null |
|
R7222:Dop1a
|
UTSW |
9 |
86,404,929 (GRCm39) |
critical splice donor site |
probably null |
|
R7233:Dop1a
|
UTSW |
9 |
86,403,749 (GRCm39) |
missense |
probably benign |
0.00 |
R7236:Dop1a
|
UTSW |
9 |
86,397,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R7252:Dop1a
|
UTSW |
9 |
86,382,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R7268:Dop1a
|
UTSW |
9 |
86,394,830 (GRCm39) |
nonsense |
probably null |
|
R7353:Dop1a
|
UTSW |
9 |
86,394,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R7481:Dop1a
|
UTSW |
9 |
86,417,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Dop1a
|
UTSW |
9 |
86,376,464 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7507:Dop1a
|
UTSW |
9 |
86,418,002 (GRCm39) |
missense |
probably benign |
0.01 |
R7525:Dop1a
|
UTSW |
9 |
86,388,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Dop1a
|
UTSW |
9 |
86,403,626 (GRCm39) |
missense |
probably benign |
0.03 |
R7751:Dop1a
|
UTSW |
9 |
86,389,783 (GRCm39) |
missense |
probably benign |
0.00 |
R7753:Dop1a
|
UTSW |
9 |
86,371,755 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7839:Dop1a
|
UTSW |
9 |
86,424,818 (GRCm39) |
nonsense |
probably null |
|
R7868:Dop1a
|
UTSW |
9 |
86,384,037 (GRCm39) |
critical splice donor site |
probably null |
|
R8061:Dop1a
|
UTSW |
9 |
86,403,246 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8067:Dop1a
|
UTSW |
9 |
86,400,392 (GRCm39) |
missense |
probably benign |
0.00 |
R8156:Dop1a
|
UTSW |
9 |
86,376,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R8196:Dop1a
|
UTSW |
9 |
86,405,151 (GRCm39) |
missense |
probably benign |
0.12 |
R8223:Dop1a
|
UTSW |
9 |
86,400,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R8267:Dop1a
|
UTSW |
9 |
86,396,054 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8276:Dop1a
|
UTSW |
9 |
86,399,092 (GRCm39) |
missense |
probably benign |
|
R8306:Dop1a
|
UTSW |
9 |
86,402,259 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8353:Dop1a
|
UTSW |
9 |
86,403,639 (GRCm39) |
missense |
probably damaging |
0.97 |
R8362:Dop1a
|
UTSW |
9 |
86,395,941 (GRCm39) |
missense |
probably benign |
0.02 |
R8403:Dop1a
|
UTSW |
9 |
86,382,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Dop1a
|
UTSW |
9 |
86,396,003 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8862:Dop1a
|
UTSW |
9 |
86,406,404 (GRCm39) |
critical splice donor site |
probably null |
|
R8888:Dop1a
|
UTSW |
9 |
86,403,587 (GRCm39) |
missense |
probably benign |
|
R8972:Dop1a
|
UTSW |
9 |
86,403,300 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9001:Dop1a
|
UTSW |
9 |
86,436,374 (GRCm39) |
makesense |
probably null |
|
R9011:Dop1a
|
UTSW |
9 |
86,397,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R9021:Dop1a
|
UTSW |
9 |
86,402,490 (GRCm39) |
missense |
probably benign |
0.35 |
R9039:Dop1a
|
UTSW |
9 |
86,382,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R9128:Dop1a
|
UTSW |
9 |
86,395,208 (GRCm39) |
missense |
probably benign |
|
R9178:Dop1a
|
UTSW |
9 |
86,371,796 (GRCm39) |
nonsense |
probably null |
|
R9238:Dop1a
|
UTSW |
9 |
86,415,027 (GRCm39) |
missense |
probably benign |
|
R9313:Dop1a
|
UTSW |
9 |
86,406,641 (GRCm39) |
makesense |
probably null |
|
R9334:Dop1a
|
UTSW |
9 |
86,403,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9422:Dop1a
|
UTSW |
9 |
86,425,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R9562:Dop1a
|
UTSW |
9 |
86,424,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R9584:Dop1a
|
UTSW |
9 |
86,385,151 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9677:Dop1a
|
UTSW |
9 |
86,425,098 (GRCm39) |
missense |
|
|
RF004:Dop1a
|
UTSW |
9 |
86,436,244 (GRCm39) |
missense |
probably benign |
|
X0019:Dop1a
|
UTSW |
9 |
86,413,803 (GRCm39) |
missense |
probably damaging |
0.98 |
X0019:Dop1a
|
UTSW |
9 |
86,388,280 (GRCm39) |
missense |
probably damaging |
1.00 |
ZE80:Dop1a
|
UTSW |
9 |
86,382,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GTGCTGTGGATGCTGTAAAC -3'
(R):5'- TGCTTGGATGAAAGGTCACAGG -3'
Sequencing Primer
(F):5'- GGATGCTGTAAACTATTTTGGAAGAG -3'
(R):5'- GTCACAGGTATAGACAATAATGCC -3'
|
Posted On |
2016-04-15 |