Incidental Mutation 'R1572:Dop1b'
ID |
170909 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dop1b
|
Ensembl Gene |
ENSMUSG00000022946 |
Gene Name |
DOP1 leucine zipper like protein B |
Synonyms |
Dopey2, 0610038M01Rik, 2610510B01Rik |
MMRRC Submission |
039611-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1572 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
93508795-93607476 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 93567041 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Serine
at position 1274
(N1274S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000044437
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045004]
[ENSMUST00000227156]
|
AlphaFold |
Q3UHQ6 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000045004
AA Change: N1274S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000044437 Gene: ENSMUSG00000022946 AA Change: N1274S
Domain | Start | End | E-Value | Type |
Pfam:Dopey_N
|
11 |
308 |
3.9e-104 |
PFAM |
low complexity region
|
651 |
666 |
N/A |
INTRINSIC |
low complexity region
|
709 |
719 |
N/A |
INTRINSIC |
low complexity region
|
747 |
759 |
N/A |
INTRINSIC |
low complexity region
|
1186 |
1199 |
N/A |
INTRINSIC |
low complexity region
|
1436 |
1451 |
N/A |
INTRINSIC |
low complexity region
|
1893 |
1908 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000226215
AA Change: N484S
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000226535
|
Predicted Effect |
unknown
Transcript: ENSMUST00000226836
AA Change: N436S
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000227156
AA Change: N1156S
PolyPhen 2
Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
|
Meta Mutation Damage Score |
0.1392 |
Coding Region Coverage |
- 1x: 98.7%
- 3x: 97.5%
- 10x: 92.9%
- 20x: 80.7%
|
Validation Efficiency |
97% (130/134) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310030G06Rik |
G |
A |
9: 50,651,973 (GRCm39) |
T85M |
probably damaging |
Het |
Actn1 |
A |
G |
12: 80,219,731 (GRCm39) |
|
probably benign |
Het |
Afap1l1 |
A |
T |
18: 61,870,570 (GRCm39) |
S603T |
probably damaging |
Het |
Ahcy |
T |
C |
2: 154,910,851 (GRCm39) |
Y39C |
probably benign |
Het |
Ankmy2 |
T |
C |
12: 36,236,941 (GRCm39) |
|
probably null |
Het |
Anxa13 |
A |
T |
15: 58,220,655 (GRCm39) |
|
noncoding transcript |
Het |
Aoc1 |
T |
C |
6: 48,882,720 (GRCm39) |
S221P |
possibly damaging |
Het |
Arhgef10 |
C |
A |
8: 15,041,211 (GRCm39) |
A770D |
possibly damaging |
Het |
Arhgef19 |
A |
G |
4: 140,982,065 (GRCm39) |
D707G |
probably benign |
Het |
Arhgef3 |
G |
A |
14: 27,123,692 (GRCm39) |
R444H |
probably damaging |
Het |
Asphd1 |
T |
C |
7: 126,548,271 (GRCm39) |
I11V |
probably benign |
Het |
Atp2b1 |
A |
G |
10: 98,830,537 (GRCm39) |
M333V |
probably benign |
Het |
BC051665 |
T |
C |
13: 60,932,841 (GRCm39) |
Y40C |
probably damaging |
Het |
Ccdc87 |
T |
A |
19: 4,890,341 (GRCm39) |
S278T |
probably benign |
Het |
Ccn3 |
T |
A |
15: 54,612,648 (GRCm39) |
M219K |
possibly damaging |
Het |
Cdcp3 |
T |
A |
7: 130,846,560 (GRCm39) |
Y777* |
probably null |
Het |
Chaf1b |
G |
A |
16: 93,698,118 (GRCm39) |
G463D |
possibly damaging |
Het |
Chrna4 |
T |
C |
2: 180,671,100 (GRCm39) |
T219A |
possibly damaging |
Het |
Clcnkb |
T |
G |
4: 141,134,406 (GRCm39) |
T584P |
possibly damaging |
Het |
Clptm1l |
T |
C |
13: 73,755,866 (GRCm39) |
S161P |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,230,777 (GRCm39) |
E1437G |
possibly damaging |
Het |
Col13a1 |
A |
T |
10: 61,702,205 (GRCm39) |
|
probably null |
Het |
Col3a1 |
T |
C |
1: 45,385,128 (GRCm39) |
S82P |
possibly damaging |
Het |
Cpeb3 |
A |
T |
19: 37,116,482 (GRCm39) |
M383K |
probably benign |
Het |
Cr2 |
T |
A |
1: 194,845,622 (GRCm39) |
H111L |
probably damaging |
Het |
Cttnbp2 |
T |
C |
6: 18,375,974 (GRCm39) |
S1522G |
possibly damaging |
Het |
Cul3 |
T |
C |
1: 80,260,506 (GRCm39) |
D281G |
possibly damaging |
Het |
Cyp2c70 |
T |
G |
19: 40,172,426 (GRCm39) |
K72T |
probably benign |
Het |
Cyp39a1 |
A |
T |
17: 43,991,020 (GRCm39) |
I110F |
probably damaging |
Het |
Cyp46a1 |
T |
A |
12: 108,318,198 (GRCm39) |
M203K |
probably null |
Het |
Cyp8b1 |
A |
T |
9: 121,744,024 (GRCm39) |
V436D |
possibly damaging |
Het |
Ddx17 |
T |
C |
15: 79,422,766 (GRCm39) |
D324G |
probably damaging |
Het |
Dscaml1 |
G |
A |
9: 45,632,631 (GRCm39) |
V1166I |
probably benign |
Het |
Dsp |
T |
C |
13: 38,379,714 (GRCm39) |
V1554A |
probably damaging |
Het |
Efr3a |
T |
A |
15: 65,726,641 (GRCm39) |
|
probably null |
Het |
Egfem1 |
A |
T |
3: 29,702,420 (GRCm39) |
N223I |
probably benign |
Het |
Egr2 |
T |
C |
10: 67,375,805 (GRCm39) |
S147P |
probably damaging |
Het |
Elmo3 |
A |
G |
8: 106,034,933 (GRCm39) |
T408A |
probably benign |
Het |
Flnb |
A |
G |
14: 7,883,908 (GRCm38) |
D378G |
probably damaging |
Het |
Foxj2 |
T |
A |
6: 122,810,220 (GRCm39) |
M193K |
probably benign |
Het |
Gm6327 |
A |
G |
16: 12,578,020 (GRCm39) |
|
noncoding transcript |
Het |
Gm7694 |
T |
C |
1: 170,130,335 (GRCm39) |
H21R |
probably benign |
Het |
Gpr107 |
A |
G |
2: 31,057,037 (GRCm39) |
D43G |
probably damaging |
Het |
Grid2 |
T |
A |
6: 64,406,678 (GRCm39) |
Y679* |
probably null |
Het |
Grin2c |
G |
A |
11: 115,146,900 (GRCm39) |
P432S |
possibly damaging |
Het |
H2-M10.1 |
A |
G |
17: 36,636,625 (GRCm39) |
F60L |
possibly damaging |
Het |
Hectd4 |
A |
G |
5: 121,439,941 (GRCm39) |
D1147G |
possibly damaging |
Het |
Idua |
G |
T |
5: 108,828,455 (GRCm39) |
A223S |
probably benign |
Het |
Ifi206 |
T |
C |
1: 173,314,419 (GRCm39) |
Q7R |
probably benign |
Het |
Itgad |
T |
A |
7: 127,802,406 (GRCm39) |
V986E |
probably damaging |
Het |
Itsn2 |
G |
A |
12: 4,700,044 (GRCm39) |
R670H |
probably benign |
Het |
Kdm4a |
T |
C |
4: 117,996,146 (GRCm39) |
E961G |
possibly damaging |
Het |
Klra5 |
T |
A |
6: 129,883,585 (GRCm39) |
I91L |
probably damaging |
Het |
Kntc1 |
A |
G |
5: 123,910,176 (GRCm39) |
T525A |
probably damaging |
Het |
Lct |
A |
G |
1: 128,221,932 (GRCm39) |
F1536L |
probably benign |
Het |
Lmod1 |
T |
A |
1: 135,291,671 (GRCm39) |
D175E |
probably benign |
Het |
Lonrf1 |
A |
C |
8: 36,701,126 (GRCm39) |
D361E |
probably benign |
Het |
Lrrc19 |
T |
C |
4: 94,526,666 (GRCm39) |
Y297C |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,873,431 (GRCm39) |
E1787G |
possibly damaging |
Het |
Mpp2 |
G |
A |
11: 101,951,374 (GRCm39) |
A452V |
probably benign |
Het |
Msh2 |
T |
C |
17: 88,026,080 (GRCm39) |
V686A |
possibly damaging |
Het |
Mthfd1 |
C |
T |
12: 76,317,193 (GRCm39) |
Q15* |
probably null |
Het |
Mtnr1b |
A |
T |
9: 15,774,438 (GRCm39) |
I207N |
probably damaging |
Het |
Nid2 |
A |
G |
14: 19,855,480 (GRCm39) |
T1207A |
probably benign |
Het |
Nin |
A |
T |
12: 70,085,524 (GRCm39) |
V1569D |
probably damaging |
Het |
Nrcam |
T |
A |
12: 44,584,147 (GRCm39) |
|
probably benign |
Het |
Nsd1 |
T |
A |
13: 55,394,782 (GRCm39) |
H897Q |
probably damaging |
Het |
Or10g9 |
A |
G |
9: 39,912,490 (GRCm39) |
F11S |
probably benign |
Het |
Or12d2 |
A |
T |
17: 37,624,371 (GRCm39) |
N301K |
probably benign |
Het |
Or2w2 |
T |
A |
13: 21,758,480 (GRCm39) |
I49F |
possibly damaging |
Het |
Or7d10 |
G |
T |
9: 19,832,208 (GRCm39) |
K234N |
probably benign |
Het |
Paip1 |
T |
C |
13: 119,588,320 (GRCm39) |
|
probably benign |
Het |
Pcnx3 |
G |
A |
19: 5,735,375 (GRCm39) |
R484* |
probably null |
Het |
Pdxk |
A |
G |
10: 78,283,814 (GRCm39) |
Y127H |
probably damaging |
Het |
Phf20 |
T |
A |
2: 156,129,754 (GRCm39) |
V442E |
probably benign |
Het |
Phlpp1 |
G |
A |
1: 106,320,519 (GRCm39) |
D1505N |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,417,664 (GRCm39) |
T2496A |
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,406,869 (GRCm39) |
T2369A |
probably benign |
Het |
Plod2 |
T |
A |
9: 92,485,120 (GRCm39) |
|
probably benign |
Het |
Pnpla7 |
T |
A |
2: 24,905,263 (GRCm39) |
M617K |
possibly damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Prkch |
T |
A |
12: 73,696,131 (GRCm39) |
|
probably null |
Het |
Prr12 |
G |
A |
7: 44,678,224 (GRCm39) |
H1974Y |
unknown |
Het |
Prr16 |
A |
G |
18: 51,436,042 (GRCm39) |
I174V |
probably benign |
Het |
Prss45 |
A |
T |
9: 110,667,497 (GRCm39) |
T39S |
probably benign |
Het |
Pum1 |
T |
A |
4: 130,445,515 (GRCm39) |
D161E |
probably damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,113 (GRCm39) |
D345G |
probably damaging |
Het |
Ralgapb |
A |
G |
2: 158,288,119 (GRCm39) |
|
probably benign |
Het |
Rasgrp3 |
A |
G |
17: 75,807,729 (GRCm39) |
H262R |
possibly damaging |
Het |
Rnf213 |
T |
A |
11: 119,327,437 (GRCm39) |
I1809N |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,761,616 (GRCm39) |
L3177P |
probably damaging |
Het |
Scyl2 |
C |
A |
10: 89,486,818 (GRCm39) |
R230L |
probably damaging |
Het |
Sfxn2 |
T |
C |
19: 46,570,915 (GRCm39) |
|
probably benign |
Het |
Slc18b1 |
T |
C |
10: 23,674,639 (GRCm39) |
|
probably benign |
Het |
Spata31d1d |
T |
C |
13: 59,876,005 (GRCm39) |
H510R |
probably benign |
Het |
Stab1 |
A |
T |
14: 30,872,780 (GRCm39) |
N1109K |
probably damaging |
Het |
Styxl2 |
C |
T |
1: 165,927,024 (GRCm39) |
V863M |
possibly damaging |
Het |
Sult3a2 |
A |
G |
10: 33,657,973 (GRCm39) |
S47P |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,682,028 (GRCm39) |
N2518S |
possibly damaging |
Het |
Tex21 |
G |
T |
12: 76,253,665 (GRCm39) |
P416Q |
probably benign |
Het |
Tex38 |
T |
C |
4: 115,637,503 (GRCm39) |
N100S |
probably benign |
Het |
Thsd4 |
A |
C |
9: 60,301,836 (GRCm39) |
|
probably benign |
Het |
Ticrr |
T |
C |
7: 79,331,572 (GRCm39) |
V723A |
probably damaging |
Het |
Tmprss15 |
A |
G |
16: 78,887,717 (GRCm39) |
V30A |
probably benign |
Het |
Uba3 |
A |
G |
6: 97,162,298 (GRCm39) |
|
probably benign |
Het |
Ubr1 |
T |
C |
2: 120,765,800 (GRCm39) |
|
probably benign |
Het |
Uchl4 |
A |
T |
9: 64,143,013 (GRCm39) |
I165L |
probably benign |
Het |
Vmn2r112 |
A |
T |
17: 22,822,125 (GRCm39) |
T268S |
possibly damaging |
Het |
Wfdc3 |
T |
C |
2: 164,586,114 (GRCm39) |
|
probably benign |
Het |
Zfp282 |
T |
A |
6: 47,869,801 (GRCm39) |
L282Q |
probably damaging |
Het |
Zfp422 |
A |
T |
6: 116,603,745 (GRCm39) |
C85S |
probably damaging |
Het |
Zfp790 |
A |
T |
7: 29,527,564 (GRCm39) |
Q83L |
probably benign |
Het |
|
Other mutations in Dop1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Dop1b
|
APN |
16 |
93,596,914 (GRCm39) |
unclassified |
probably benign |
|
IGL00492:Dop1b
|
APN |
16 |
93,577,670 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00753:Dop1b
|
APN |
16 |
93,566,512 (GRCm39) |
missense |
probably benign |
|
IGL00832:Dop1b
|
APN |
16 |
93,560,289 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00939:Dop1b
|
APN |
16 |
93,570,971 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01019:Dop1b
|
APN |
16 |
93,607,117 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01288:Dop1b
|
APN |
16 |
93,536,181 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01505:Dop1b
|
APN |
16 |
93,554,004 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01535:Dop1b
|
APN |
16 |
93,566,846 (GRCm39) |
nonsense |
probably null |
|
IGL01696:Dop1b
|
APN |
16 |
93,567,128 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02077:Dop1b
|
APN |
16 |
93,577,648 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02163:Dop1b
|
APN |
16 |
93,559,315 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02234:Dop1b
|
APN |
16 |
93,549,039 (GRCm39) |
missense |
probably benign |
|
IGL02302:Dop1b
|
APN |
16 |
93,607,005 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02485:Dop1b
|
APN |
16 |
93,567,710 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02563:Dop1b
|
APN |
16 |
93,574,293 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02733:Dop1b
|
APN |
16 |
93,536,079 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02792:Dop1b
|
APN |
16 |
93,598,460 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02941:Dop1b
|
APN |
16 |
93,552,361 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03143:Dop1b
|
APN |
16 |
93,556,543 (GRCm39) |
missense |
probably benign |
|
PIT4519001:Dop1b
|
UTSW |
16 |
93,558,942 (GRCm39) |
missense |
probably benign |
|
R0320:Dop1b
|
UTSW |
16 |
93,607,035 (GRCm39) |
missense |
probably benign |
0.02 |
R0499:Dop1b
|
UTSW |
16 |
93,567,325 (GRCm39) |
missense |
probably benign |
0.00 |
R0501:Dop1b
|
UTSW |
16 |
93,549,750 (GRCm39) |
missense |
probably benign |
0.00 |
R0534:Dop1b
|
UTSW |
16 |
93,559,393 (GRCm39) |
missense |
probably benign |
0.04 |
R0583:Dop1b
|
UTSW |
16 |
93,552,374 (GRCm39) |
missense |
probably benign |
0.30 |
R0626:Dop1b
|
UTSW |
16 |
93,560,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0724:Dop1b
|
UTSW |
16 |
93,559,213 (GRCm39) |
missense |
probably benign |
0.01 |
R0907:Dop1b
|
UTSW |
16 |
93,598,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R1263:Dop1b
|
UTSW |
16 |
93,574,274 (GRCm39) |
missense |
probably benign |
|
R1378:Dop1b
|
UTSW |
16 |
93,567,280 (GRCm39) |
missense |
probably benign |
|
R1604:Dop1b
|
UTSW |
16 |
93,559,458 (GRCm39) |
missense |
probably benign |
|
R1642:Dop1b
|
UTSW |
16 |
93,559,203 (GRCm39) |
missense |
probably benign |
0.00 |
R1668:Dop1b
|
UTSW |
16 |
93,562,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1669:Dop1b
|
UTSW |
16 |
93,566,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Dop1b
|
UTSW |
16 |
93,544,509 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1711:Dop1b
|
UTSW |
16 |
93,596,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Dop1b
|
UTSW |
16 |
93,513,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Dop1b
|
UTSW |
16 |
93,579,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Dop1b
|
UTSW |
16 |
93,563,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Dop1b
|
UTSW |
16 |
93,566,323 (GRCm39) |
missense |
probably benign |
0.36 |
R2139:Dop1b
|
UTSW |
16 |
93,567,895 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2355:Dop1b
|
UTSW |
16 |
93,567,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R3609:Dop1b
|
UTSW |
16 |
93,536,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Dop1b
|
UTSW |
16 |
93,568,734 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4364:Dop1b
|
UTSW |
16 |
93,567,812 (GRCm39) |
missense |
probably benign |
0.00 |
R4380:Dop1b
|
UTSW |
16 |
93,513,120 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4455:Dop1b
|
UTSW |
16 |
93,563,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R4779:Dop1b
|
UTSW |
16 |
93,553,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Dop1b
|
UTSW |
16 |
93,589,978 (GRCm39) |
missense |
probably benign |
0.00 |
R4834:Dop1b
|
UTSW |
16 |
93,536,892 (GRCm39) |
start codon destroyed |
probably null |
0.70 |
R4866:Dop1b
|
UTSW |
16 |
93,560,318 (GRCm39) |
critical splice donor site |
probably null |
|
R4882:Dop1b
|
UTSW |
16 |
93,549,802 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4900:Dop1b
|
UTSW |
16 |
93,560,318 (GRCm39) |
critical splice donor site |
probably null |
|
R5153:Dop1b
|
UTSW |
16 |
93,570,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R5176:Dop1b
|
UTSW |
16 |
93,536,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5206:Dop1b
|
UTSW |
16 |
93,598,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Dop1b
|
UTSW |
16 |
93,536,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Dop1b
|
UTSW |
16 |
93,567,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Dop1b
|
UTSW |
16 |
93,560,298 (GRCm39) |
missense |
probably damaging |
0.96 |
R5476:Dop1b
|
UTSW |
16 |
93,570,801 (GRCm39) |
splice site |
probably null |
|
R5502:Dop1b
|
UTSW |
16 |
93,590,114 (GRCm39) |
missense |
probably benign |
0.00 |
R5543:Dop1b
|
UTSW |
16 |
93,595,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R5557:Dop1b
|
UTSW |
16 |
93,560,819 (GRCm39) |
missense |
probably damaging |
0.96 |
R5901:Dop1b
|
UTSW |
16 |
93,566,639 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5907:Dop1b
|
UTSW |
16 |
93,598,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R6174:Dop1b
|
UTSW |
16 |
93,563,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R6256:Dop1b
|
UTSW |
16 |
93,604,102 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6383:Dop1b
|
UTSW |
16 |
93,579,136 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6525:Dop1b
|
UTSW |
16 |
93,606,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Dop1b
|
UTSW |
16 |
93,557,346 (GRCm39) |
missense |
probably benign |
0.22 |
R6823:Dop1b
|
UTSW |
16 |
93,552,373 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7036:Dop1b
|
UTSW |
16 |
93,574,378 (GRCm39) |
missense |
probably benign |
0.01 |
R7058:Dop1b
|
UTSW |
16 |
93,573,878 (GRCm39) |
missense |
probably benign |
0.00 |
R7061:Dop1b
|
UTSW |
16 |
93,558,951 (GRCm39) |
missense |
probably benign |
0.00 |
R7209:Dop1b
|
UTSW |
16 |
93,566,733 (GRCm39) |
missense |
probably benign |
|
R7214:Dop1b
|
UTSW |
16 |
93,607,023 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7232:Dop1b
|
UTSW |
16 |
93,557,373 (GRCm39) |
critical splice donor site |
probably null |
|
R7255:Dop1b
|
UTSW |
16 |
93,567,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R7335:Dop1b
|
UTSW |
16 |
93,544,396 (GRCm39) |
missense |
probably benign |
0.04 |
R7535:Dop1b
|
UTSW |
16 |
93,603,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Dop1b
|
UTSW |
16 |
93,595,649 (GRCm39) |
splice site |
probably null |
|
R7763:Dop1b
|
UTSW |
16 |
93,552,402 (GRCm39) |
missense |
probably benign |
0.00 |
R7814:Dop1b
|
UTSW |
16 |
93,596,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7839:Dop1b
|
UTSW |
16 |
93,560,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7862:Dop1b
|
UTSW |
16 |
93,546,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R7894:Dop1b
|
UTSW |
16 |
93,607,092 (GRCm39) |
missense |
probably benign |
0.01 |
R7952:Dop1b
|
UTSW |
16 |
93,546,848 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7956:Dop1b
|
UTSW |
16 |
93,567,916 (GRCm39) |
critical splice donor site |
probably null |
|
R8033:Dop1b
|
UTSW |
16 |
93,566,371 (GRCm39) |
missense |
probably benign |
|
R8061:Dop1b
|
UTSW |
16 |
93,546,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8067:Dop1b
|
UTSW |
16 |
93,562,336 (GRCm39) |
nonsense |
probably null |
|
R8146:Dop1b
|
UTSW |
16 |
93,546,827 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8184:Dop1b
|
UTSW |
16 |
93,573,881 (GRCm39) |
missense |
probably benign |
0.13 |
R8221:Dop1b
|
UTSW |
16 |
93,546,847 (GRCm39) |
missense |
probably benign |
0.01 |
R8263:Dop1b
|
UTSW |
16 |
93,559,083 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8329:Dop1b
|
UTSW |
16 |
93,568,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Dop1b
|
UTSW |
16 |
93,568,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R8683:Dop1b
|
UTSW |
16 |
93,570,809 (GRCm39) |
missense |
probably benign |
|
R8683:Dop1b
|
UTSW |
16 |
93,568,699 (GRCm39) |
missense |
probably damaging |
0.98 |
R8716:Dop1b
|
UTSW |
16 |
93,577,673 (GRCm39) |
nonsense |
probably null |
|
R8807:Dop1b
|
UTSW |
16 |
93,558,973 (GRCm39) |
missense |
probably benign |
0.03 |
R8840:Dop1b
|
UTSW |
16 |
93,607,005 (GRCm39) |
missense |
probably benign |
0.08 |
R8851:Dop1b
|
UTSW |
16 |
93,559,398 (GRCm39) |
missense |
probably benign |
0.39 |
R8884:Dop1b
|
UTSW |
16 |
93,556,550 (GRCm39) |
missense |
probably benign |
|
R8976:Dop1b
|
UTSW |
16 |
93,558,969 (GRCm39) |
missense |
probably benign |
0.01 |
R9219:Dop1b
|
UTSW |
16 |
93,567,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9238:Dop1b
|
UTSW |
16 |
93,546,018 (GRCm39) |
missense |
probably benign |
0.14 |
R9284:Dop1b
|
UTSW |
16 |
93,557,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R9289:Dop1b
|
UTSW |
16 |
93,568,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R9298:Dop1b
|
UTSW |
16 |
93,597,087 (GRCm39) |
missense |
probably damaging |
0.96 |
R9338:Dop1b
|
UTSW |
16 |
93,600,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Dop1b
|
UTSW |
16 |
93,577,702 (GRCm39) |
critical splice donor site |
probably null |
|
R9444:Dop1b
|
UTSW |
16 |
93,607,127 (GRCm39) |
missense |
probably benign |
0.00 |
R9500:Dop1b
|
UTSW |
16 |
93,607,171 (GRCm39) |
missense |
probably benign |
|
R9601:Dop1b
|
UTSW |
16 |
93,544,531 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9793:Dop1b
|
UTSW |
16 |
93,598,503 (GRCm39) |
missense |
probably benign |
0.30 |
Z1088:Dop1b
|
UTSW |
16 |
93,560,214 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Dop1b
|
UTSW |
16 |
93,604,756 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1176:Dop1b
|
UTSW |
16 |
93,600,434 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dop1b
|
UTSW |
16 |
93,566,469 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Dop1b
|
UTSW |
16 |
93,560,783 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TTTTCCAGTGACGAGGAGGCTGAC -3'
(R):5'- AATGAGGACCTCCACGCTCTTGAC -3'
Sequencing Primer
(F):5'- ATCACCACATCGAGGCTGTTG -3'
(R):5'- ACGCTCTTGACCTGCACG -3'
|
Posted On |
2014-04-13 |