Incidental Mutation 'R0326:Dab2'
ID |
25909 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dab2
|
Ensembl Gene |
ENSMUSG00000022150 |
Gene Name |
disabled 2, mitogen-responsive phosphoprotein |
Synonyms |
5730435J12Rik, D15Wsu122e, D630005B22Rik, p96 |
MMRRC Submission |
038536-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.914)
|
Stock # |
R0326 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
15 |
Chromosomal Location |
6329269-6470193 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 6447797 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Methionine
at position 60
(V60M)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000125696
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078019]
[ENSMUST00000080880]
[ENSMUST00000110663]
[ENSMUST00000110664]
[ENSMUST00000159046]
[ENSMUST00000159490]
[ENSMUST00000162094]
[ENSMUST00000161812]
[ENSMUST00000160134]
[ENSMUST00000161040]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000078019
AA Change: V60M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000077166 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
PTB
|
45 |
179 |
1.16e-27 |
SMART |
low complexity region
|
270 |
288 |
N/A |
INTRINSIC |
low complexity region
|
292 |
306 |
N/A |
INTRINSIC |
low complexity region
|
335 |
355 |
N/A |
INTRINSIC |
low complexity region
|
378 |
394 |
N/A |
INTRINSIC |
PDB:3H8D|H
|
465 |
493 |
2e-12 |
PDB |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000080880
AA Change: V60M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000079689 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
PTB
|
45 |
179 |
1.16e-27 |
SMART |
low complexity region
|
488 |
506 |
N/A |
INTRINSIC |
low complexity region
|
510 |
524 |
N/A |
INTRINSIC |
low complexity region
|
553 |
573 |
N/A |
INTRINSIC |
low complexity region
|
596 |
612 |
N/A |
INTRINSIC |
PDB:3H8D|H
|
683 |
711 |
3e-12 |
PDB |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000110663
AA Change: V60M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106291 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
PTB
|
45 |
179 |
1.16e-27 |
SMART |
low complexity region
|
270 |
288 |
N/A |
INTRINSIC |
low complexity region
|
292 |
306 |
N/A |
INTRINSIC |
low complexity region
|
335 |
355 |
N/A |
INTRINSIC |
low complexity region
|
378 |
394 |
N/A |
INTRINSIC |
PDB:3H8D|H
|
465 |
493 |
2e-12 |
PDB |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000110664
AA Change: V60M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106292 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
PTB
|
45 |
179 |
1.16e-27 |
SMART |
low complexity region
|
467 |
485 |
N/A |
INTRINSIC |
low complexity region
|
489 |
503 |
N/A |
INTRINSIC |
low complexity region
|
532 |
552 |
N/A |
INTRINSIC |
low complexity region
|
575 |
591 |
N/A |
INTRINSIC |
PDB:3H8D|H
|
662 |
690 |
3e-12 |
PDB |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159046
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000159490
AA Change: V60M
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000124145 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
PDB:1P3R|C
|
35 |
60 |
4e-11 |
PDB |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159552
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000162094
AA Change: V60M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000125696 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
Pfam:PID
|
50 |
110 |
2.8e-9 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000161812
AA Change: V60M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000124589 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
PTB
|
45 |
179 |
1.16e-27 |
SMART |
low complexity region
|
249 |
267 |
N/A |
INTRINSIC |
low complexity region
|
271 |
285 |
N/A |
INTRINSIC |
low complexity region
|
314 |
334 |
N/A |
INTRINSIC |
low complexity region
|
357 |
373 |
N/A |
INTRINSIC |
PDB:3H8D|H
|
444 |
472 |
2e-12 |
PDB |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000160134
AA Change: V60M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000125021 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
PTB
|
45 |
179 |
1.16e-27 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000161040
AA Change: V60M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000124478 Gene: ENSMUSG00000022150 AA Change: V60M
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
34 |
N/A |
INTRINSIC |
PTB
|
45 |
179 |
1.16e-27 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161558
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000163082
|
SMART Domains |
Protein: ENSMUSP00000124996 Gene: ENSMUSG00000022150
Domain | Start | End | E-Value | Type |
Blast:PTB
|
2 |
59 |
1e-33 |
BLAST |
PDB:1P3R|C
|
2 |
59 |
2e-34 |
PDB |
SCOP:d1ddma_
|
3 |
59 |
9e-12 |
SMART |
low complexity region
|
60 |
79 |
N/A |
INTRINSIC |
low complexity region
|
356 |
374 |
N/A |
INTRINSIC |
low complexity region
|
378 |
392 |
N/A |
INTRINSIC |
low complexity region
|
421 |
441 |
N/A |
INTRINSIC |
low complexity region
|
464 |
480 |
N/A |
INTRINSIC |
PDB:3H8D|H
|
551 |
579 |
3e-12 |
PDB |
|
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.0%
- 10x: 95.8%
- 20x: 91.8%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a mitogen-responsive phosphoprotein. It is expressed in normal ovarian epithelial cells, but is down-regulated or absent from ovarian carcinoma cell lines, suggesting its role as a tumor suppressor. This protein binds to the SH3 domains of GRB2, an adaptor protein that couples tyrosine kinase receptors to SOS (a guanine nucleotide exchange factor for Ras), via its C-terminal proline-rich sequences, and may thus modulate growth factor/Ras pathways by competing with SOS for binding to GRB2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] PHENOTYPE: Homozygous null mutants exhibit abnormal primitive endoderm structure and/or function, lack a proamniotic cavity and die prior to embryonic day 9.5. A conditional mutant survives, but shows kidney proximal tubule abnormality. [provided by MGI curators]
|
Allele List at MGI |
All alleles(4) : Targeted, knock-out(1) Targeted, other(2) Gene trapped(1) |
Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
C |
T |
1: 130,670,635 (GRCm39) |
P286S |
possibly damaging |
Het |
Aagab |
T |
A |
9: 63,526,444 (GRCm39) |
S156T |
probably damaging |
Het |
Abca14 |
T |
G |
7: 119,823,642 (GRCm39) |
Y390D |
probably damaging |
Het |
Abcc2 |
T |
A |
19: 43,814,386 (GRCm39) |
I1122N |
possibly damaging |
Het |
Adamts16 |
T |
C |
13: 70,927,730 (GRCm39) |
E503G |
possibly damaging |
Het |
Adamts9 |
A |
T |
6: 92,835,038 (GRCm39) |
C697* |
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,623,112 (GRCm39) |
D3837G |
possibly damaging |
Het |
Ahcyl |
T |
A |
16: 45,974,246 (GRCm39) |
D377V |
probably benign |
Het |
Aire |
T |
A |
10: 77,878,433 (GRCm39) |
R128S |
probably damaging |
Het |
Alkbh2 |
A |
C |
5: 114,262,011 (GRCm39) |
*240E |
probably null |
Het |
Als2 |
T |
C |
1: 59,219,742 (GRCm39) |
Y1191C |
probably damaging |
Het |
Anapc5 |
A |
T |
5: 122,952,667 (GRCm39) |
V186E |
probably benign |
Het |
Apob |
C |
T |
12: 8,040,307 (GRCm39) |
A548V |
probably damaging |
Het |
B3galt4 |
A |
T |
17: 34,169,722 (GRCm39) |
V172E |
probably damaging |
Het |
Bbs7 |
A |
C |
3: 36,646,525 (GRCm39) |
C432G |
possibly damaging |
Het |
Cacna2d3 |
T |
A |
14: 28,767,601 (GRCm39) |
E758V |
probably damaging |
Het |
Cactin |
T |
G |
10: 81,158,496 (GRCm39) |
L154R |
probably benign |
Het |
Ccdc88a |
A |
C |
11: 29,411,021 (GRCm39) |
R502S |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,450,784 (GRCm39) |
I398N |
possibly damaging |
Het |
Chd1 |
A |
T |
17: 15,988,828 (GRCm39) |
D1527V |
probably damaging |
Het |
Chd1 |
A |
T |
17: 15,988,830 (GRCm39) |
M1528L |
probably benign |
Het |
Chrac1 |
G |
A |
15: 72,964,675 (GRCm39) |
|
probably null |
Het |
Cln3 |
T |
G |
7: 126,182,217 (GRCm39) |
M1L |
probably damaging |
Het |
Cnot6 |
T |
C |
11: 49,568,263 (GRCm39) |
Y442C |
probably damaging |
Het |
Col19a1 |
A |
T |
1: 24,324,132 (GRCm39) |
|
probably null |
Het |
Col1a2 |
T |
C |
6: 4,537,838 (GRCm39) |
F1116L |
unknown |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Cops4 |
T |
G |
5: 100,676,408 (GRCm39) |
V53G |
probably damaging |
Het |
Crnkl1 |
A |
G |
2: 145,761,875 (GRCm39) |
S561P |
probably benign |
Het |
Ctnnb1 |
C |
A |
9: 120,780,778 (GRCm39) |
Q99K |
probably benign |
Het |
Cxcr5 |
T |
C |
9: 44,424,578 (GRCm39) |
S360G |
probably benign |
Het |
Ddx3y |
A |
T |
Y: 1,263,321 (GRCm39) |
Y648* |
probably null |
Het |
Dennd2a |
T |
A |
6: 39,474,044 (GRCm39) |
D430V |
probably damaging |
Het |
Dsp |
G |
T |
13: 38,376,846 (GRCm39) |
E1544* |
probably null |
Het |
Efcab7 |
A |
T |
4: 99,719,631 (GRCm39) |
M38L |
possibly damaging |
Het |
Fto |
A |
G |
8: 92,136,155 (GRCm39) |
N141S |
probably damaging |
Het |
Gabrp |
A |
G |
11: 33,504,362 (GRCm39) |
F318L |
probably damaging |
Het |
Gmeb1 |
A |
C |
4: 131,969,663 (GRCm39) |
C103W |
probably damaging |
Het |
Heatr9 |
T |
C |
11: 83,405,365 (GRCm39) |
D365G |
probably damaging |
Het |
Hif3a |
G |
A |
7: 16,778,325 (GRCm39) |
R436W |
probably benign |
Het |
Hint2 |
A |
G |
4: 43,654,378 (GRCm39) |
V145A |
probably damaging |
Het |
Hmcn2 |
T |
A |
2: 31,313,237 (GRCm39) |
L3482* |
probably null |
Het |
Hsd3b1 |
A |
T |
3: 98,760,590 (GRCm39) |
Y134N |
probably damaging |
Het |
Impg2 |
T |
A |
16: 56,080,848 (GRCm39) |
V775E |
probably damaging |
Het |
Ipo5 |
A |
G |
14: 121,159,635 (GRCm39) |
I154M |
probably benign |
Het |
Itgad |
T |
A |
7: 127,797,550 (GRCm39) |
F893Y |
probably benign |
Het |
Itprid1 |
A |
T |
6: 55,875,228 (GRCm39) |
M393L |
possibly damaging |
Het |
Kdm4a |
T |
C |
4: 118,018,903 (GRCm39) |
R438G |
probably benign |
Het |
Klk1b11 |
T |
A |
7: 43,425,943 (GRCm39) |
M1K |
probably null |
Het |
Lama5 |
A |
T |
2: 179,824,219 (GRCm39) |
V2602D |
possibly damaging |
Het |
Lrch3 |
T |
C |
16: 32,799,870 (GRCm39) |
S35P |
probably damaging |
Het |
Mfn2 |
A |
G |
4: 147,967,745 (GRCm39) |
L441P |
probably damaging |
Het |
Mgat4c |
A |
T |
10: 102,224,565 (GRCm39) |
I260F |
probably damaging |
Het |
Mon1b |
T |
A |
8: 114,364,375 (GRCm39) |
S51T |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,036,744 (GRCm39) |
D993G |
probably benign |
Het |
Myo1a |
A |
G |
10: 127,552,166 (GRCm39) |
N762D |
probably benign |
Het |
Nacc2 |
A |
T |
2: 25,950,345 (GRCm39) |
Y464N |
probably damaging |
Het |
Nckap1 |
A |
G |
2: 80,383,714 (GRCm39) |
I150T |
probably benign |
Het |
Ndufv2 |
G |
T |
17: 66,387,816 (GRCm39) |
P119T |
probably damaging |
Het |
Noc4l |
G |
A |
5: 110,800,241 (GRCm39) |
R95* |
probably null |
Het |
Ntng1 |
A |
T |
3: 110,042,819 (GRCm39) |
Y2* |
probably null |
Het |
Oog4 |
T |
C |
4: 143,165,773 (GRCm39) |
N53D |
probably benign |
Het |
Or10ak11 |
A |
T |
4: 118,687,022 (GRCm39) |
V205D |
possibly damaging |
Het |
Or4d11 |
C |
T |
19: 12,013,525 (GRCm39) |
V194I |
probably benign |
Het |
Or6c6c |
A |
G |
10: 129,541,638 (GRCm39) |
E297G |
possibly damaging |
Het |
Or9i1b |
C |
T |
19: 13,896,873 (GRCm39) |
T163I |
probably benign |
Het |
Phkg2 |
T |
G |
7: 127,173,075 (GRCm39) |
L11R |
probably damaging |
Het |
Pogz |
A |
G |
3: 94,777,424 (GRCm39) |
D368G |
probably damaging |
Het |
Prex2 |
T |
A |
1: 11,355,289 (GRCm39) |
L1530Q |
probably damaging |
Het |
Prmt1 |
C |
T |
7: 44,628,878 (GRCm39) |
E144K |
probably damaging |
Het |
Prss8 |
T |
A |
7: 127,526,348 (GRCm39) |
I121F |
probably benign |
Het |
Psmd13 |
T |
C |
7: 140,477,624 (GRCm39) |
L314P |
probably damaging |
Het |
Ptch2 |
G |
A |
4: 116,966,081 (GRCm39) |
G467D |
probably damaging |
Het |
Rbm20 |
C |
A |
19: 53,852,596 (GRCm39) |
P1192Q |
probably damaging |
Het |
Rpl19 |
T |
A |
11: 97,919,200 (GRCm39) |
D45E |
probably benign |
Het |
Rsph10b |
C |
T |
5: 143,903,946 (GRCm39) |
A219V |
probably damaging |
Het |
Rtraf |
C |
T |
14: 19,864,600 (GRCm39) |
|
probably null |
Het |
Scaf1 |
T |
A |
7: 44,658,175 (GRCm39) |
T235S |
probably damaging |
Het |
Shank1 |
T |
A |
7: 43,968,594 (GRCm39) |
C296S |
unknown |
Het |
Slc39a7 |
A |
T |
17: 34,247,924 (GRCm39) |
V426D |
probably damaging |
Het |
Slc41a2 |
A |
T |
10: 83,119,610 (GRCm39) |
V384D |
probably damaging |
Het |
Slco1c1 |
T |
C |
6: 141,505,499 (GRCm39) |
L475P |
probably benign |
Het |
Slco6d1 |
A |
C |
1: 98,418,359 (GRCm39) |
K515T |
probably benign |
Het |
Sos2 |
T |
C |
12: 69,682,459 (GRCm39) |
E253G |
probably damaging |
Het |
Sp6 |
G |
T |
11: 96,912,361 (GRCm39) |
D25Y |
possibly damaging |
Het |
Syt11 |
A |
C |
3: 88,669,855 (GRCm39) |
D12E |
possibly damaging |
Het |
Taf2 |
A |
G |
15: 54,910,856 (GRCm39) |
L606P |
probably damaging |
Het |
Tbc1d5 |
A |
G |
17: 51,273,764 (GRCm39) |
Y116H |
probably damaging |
Het |
Tnfrsf8 |
A |
G |
4: 145,015,029 (GRCm39) |
I243T |
possibly damaging |
Het |
Tnxb |
A |
G |
17: 34,917,153 (GRCm39) |
S2183G |
probably benign |
Het |
Trim66 |
T |
C |
7: 109,059,379 (GRCm39) |
Y853C |
probably benign |
Het |
Ttn |
T |
A |
2: 76,567,839 (GRCm39) |
T27685S |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,573,466 (GRCm39) |
E25809G |
probably damaging |
Het |
Uvssa |
G |
A |
5: 33,566,191 (GRCm39) |
G445S |
probably benign |
Het |
Zfp326 |
T |
C |
5: 106,058,141 (GRCm39) |
S427P |
probably damaging |
Het |
Zfp592 |
A |
G |
7: 80,674,637 (GRCm39) |
T534A |
possibly damaging |
Het |
Zfp672 |
A |
G |
11: 58,207,173 (GRCm39) |
S383P |
possibly damaging |
Het |
Zfp799 |
A |
G |
17: 33,039,700 (GRCm39) |
S188P |
possibly damaging |
Het |
Zyg11b |
A |
C |
4: 108,129,450 (GRCm39) |
V54G |
possibly damaging |
Het |
|
Other mutations in Dab2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00586:Dab2
|
APN |
15 |
6,459,306 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00731:Dab2
|
APN |
15 |
6,465,191 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02382:Dab2
|
APN |
15 |
6,466,468 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02598:Dab2
|
APN |
15 |
6,458,847 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03054:Dab2
|
APN |
15 |
6,447,707 (GRCm39) |
unclassified |
probably benign |
|
IGL03093:Dab2
|
APN |
15 |
6,465,892 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03369:Dab2
|
APN |
15 |
6,464,790 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03372:Dab2
|
APN |
15 |
6,459,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R0157:Dab2
|
UTSW |
15 |
6,459,308 (GRCm39) |
missense |
probably benign |
0.00 |
R0488:Dab2
|
UTSW |
15 |
6,454,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Dab2
|
UTSW |
15 |
6,464,895 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0938:Dab2
|
UTSW |
15 |
6,464,865 (GRCm39) |
missense |
probably benign |
0.04 |
R1433:Dab2
|
UTSW |
15 |
6,459,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Dab2
|
UTSW |
15 |
6,459,351 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1713:Dab2
|
UTSW |
15 |
6,459,182 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1757:Dab2
|
UTSW |
15 |
6,359,933 (GRCm39) |
intron |
probably benign |
|
R1800:Dab2
|
UTSW |
15 |
6,464,948 (GRCm39) |
missense |
probably benign |
|
R1837:Dab2
|
UTSW |
15 |
6,365,957 (GRCm39) |
intron |
probably benign |
|
R1999:Dab2
|
UTSW |
15 |
6,446,398 (GRCm39) |
missense |
probably benign |
0.32 |
R2050:Dab2
|
UTSW |
15 |
6,464,696 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2117:Dab2
|
UTSW |
15 |
6,465,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Dab2
|
UTSW |
15 |
6,365,864 (GRCm39) |
nonsense |
probably null |
|
R2150:Dab2
|
UTSW |
15 |
6,446,398 (GRCm39) |
missense |
probably benign |
0.32 |
R2329:Dab2
|
UTSW |
15 |
6,459,044 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2338:Dab2
|
UTSW |
15 |
6,464,733 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2680:Dab2
|
UTSW |
15 |
6,466,474 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3978:Dab2
|
UTSW |
15 |
6,464,644 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3979:Dab2
|
UTSW |
15 |
6,464,644 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3980:Dab2
|
UTSW |
15 |
6,464,644 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4551:Dab2
|
UTSW |
15 |
6,464,775 (GRCm39) |
missense |
probably damaging |
0.97 |
R4795:Dab2
|
UTSW |
15 |
6,459,092 (GRCm39) |
missense |
probably benign |
0.16 |
R4829:Dab2
|
UTSW |
15 |
6,454,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R4830:Dab2
|
UTSW |
15 |
6,457,008 (GRCm39) |
missense |
probably benign |
|
R4832:Dab2
|
UTSW |
15 |
6,366,080 (GRCm39) |
splice site |
probably null |
|
R5168:Dab2
|
UTSW |
15 |
6,365,924 (GRCm39) |
intron |
probably benign |
|
R5620:Dab2
|
UTSW |
15 |
6,447,796 (GRCm39) |
missense |
probably damaging |
0.98 |
R5996:Dab2
|
UTSW |
15 |
6,464,792 (GRCm39) |
nonsense |
probably null |
|
R6159:Dab2
|
UTSW |
15 |
6,465,941 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6998:Dab2
|
UTSW |
15 |
6,454,130 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7002:Dab2
|
UTSW |
15 |
6,464,846 (GRCm39) |
missense |
probably benign |
0.01 |
R7040:Dab2
|
UTSW |
15 |
6,451,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R7138:Dab2
|
UTSW |
15 |
6,458,780 (GRCm39) |
missense |
probably benign |
0.24 |
R7448:Dab2
|
UTSW |
15 |
6,451,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R7548:Dab2
|
UTSW |
15 |
6,459,399 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8062:Dab2
|
UTSW |
15 |
6,456,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R8124:Dab2
|
UTSW |
15 |
6,458,878 (GRCm39) |
nonsense |
probably null |
|
R8164:Dab2
|
UTSW |
15 |
6,460,449 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8171:Dab2
|
UTSW |
15 |
6,453,407 (GRCm39) |
missense |
probably benign |
0.00 |
R8230:Dab2
|
UTSW |
15 |
6,451,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R8372:Dab2
|
UTSW |
15 |
6,446,406 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8427:Dab2
|
UTSW |
15 |
6,458,840 (GRCm39) |
nonsense |
probably null |
|
R8919:Dab2
|
UTSW |
15 |
6,465,271 (GRCm39) |
missense |
|
|
R9363:Dab2
|
UTSW |
15 |
6,460,481 (GRCm39) |
missense |
probably benign |
0.16 |
R9461:Dab2
|
UTSW |
15 |
6,460,435 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9532:Dab2
|
UTSW |
15 |
6,451,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R9779:Dab2
|
UTSW |
15 |
6,460,525 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- ACGAGACTGCACAGCCTGTTTG -3'
(R):5'- GCCCTGGCTTCTCTGAAAAGAGAAC -3'
Sequencing Primer
(F):5'- ACAGTCAGTATTCAATTTTTGGGG -3'
(R):5'- CTTCTCTGAAAAGAGAACACTGG -3'
|
Posted On |
2013-04-16 |