Incidental Mutation 'R1800:Dab2'
ID |
203083 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dab2
|
Ensembl Gene |
ENSMUSG00000022150 |
Gene Name |
disabled 2, mitogen-responsive phosphoprotein |
Synonyms |
5730435J12Rik, D15Wsu122e, D630005B22Rik, p96 |
MMRRC Submission |
039830-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.914)
|
Stock # |
R1800 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
15 |
Chromosomal Location |
6329269-6470193 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 6464948 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Leucine
at position 361
(M361L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124589
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078019]
[ENSMUST00000080880]
[ENSMUST00000110663]
[ENSMUST00000110664]
[ENSMUST00000161812]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000078019
AA Change: M382L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000077166 Gene: ENSMUSG00000022150 AA Change: M382L
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 benign
Transcript: ENSMUST00000080880
AA Change: M600L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000079689 Gene: ENSMUSG00000022150 AA Change: M600L
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 benign
Transcript: ENSMUST00000110663
AA Change: M382L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000106291 Gene: ENSMUSG00000022150 AA Change: M382L
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 benign
Transcript: ENSMUST00000110664
AA Change: M579L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000106292 Gene: ENSMUSG00000022150 AA Change: M579L
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 |
noncoding transcript
Transcript: ENSMUST00000159552
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161812
AA Change: M361L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000124589 Gene: ENSMUSG00000022150 AA Change: M361L
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 |
unknown
Transcript: ENSMUST00000163082
AA Change: M467L
|
SMART Domains |
Protein: ENSMUSP00000124996 Gene: ENSMUSG00000022150 AA Change: M467L
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: 97.4%
- 3x: 96.8%
- 10x: 95.0%
- 20x: 91.2%
|
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: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,772,479 (GRCm39) |
K556R |
probably damaging |
Het |
4933406P04Rik |
A |
T |
10: 20,186,893 (GRCm39) |
|
probably benign |
Het |
Acmsd |
C |
A |
1: 127,687,493 (GRCm39) |
Y258* |
probably null |
Het |
Adgrf5 |
A |
T |
17: 43,761,973 (GRCm39) |
I1223F |
probably damaging |
Het |
Afp |
C |
T |
5: 90,638,655 (GRCm39) |
P6S |
probably benign |
Het |
Agap2 |
C |
A |
10: 126,927,540 (GRCm39) |
H1120Q |
probably damaging |
Het |
Angpt1 |
A |
G |
15: 42,375,800 (GRCm39) |
V152A |
probably damaging |
Het |
Ankrd1 |
A |
T |
19: 36,096,759 (GRCm39) |
F23I |
probably damaging |
Het |
Armc12 |
T |
C |
17: 28,757,869 (GRCm39) |
S334P |
possibly damaging |
Het |
Arnt2 |
C |
A |
7: 83,924,583 (GRCm39) |
D415Y |
probably damaging |
Het |
Cacna1s |
G |
T |
1: 136,004,592 (GRCm39) |
V131L |
probably benign |
Het |
Cacna2d2 |
T |
C |
9: 107,404,632 (GRCm39) |
V1141A |
possibly damaging |
Het |
Cfap61 |
T |
C |
2: 145,884,542 (GRCm39) |
L580P |
probably damaging |
Het |
Chga |
A |
T |
12: 102,522,164 (GRCm39) |
S23C |
probably damaging |
Het |
Chrna5 |
A |
G |
9: 54,912,159 (GRCm39) |
T320A |
probably damaging |
Het |
Col17a1 |
G |
T |
19: 47,639,301 (GRCm39) |
N1081K |
possibly damaging |
Het |
Cox7b2 |
A |
T |
5: 71,600,406 (GRCm39) |
C51S |
possibly damaging |
Het |
Cstdc3 |
T |
A |
16: 36,132,895 (GRCm39) |
D57E |
probably damaging |
Het |
Cwc22 |
A |
T |
2: 77,759,797 (GRCm39) |
D83E |
possibly damaging |
Het |
D130043K22Rik |
A |
C |
13: 25,067,877 (GRCm39) |
D871A |
probably damaging |
Het |
Dnah11 |
A |
C |
12: 117,880,523 (GRCm39) |
Y3866D |
probably damaging |
Het |
Dnmbp |
A |
G |
19: 43,890,159 (GRCm39) |
I536T |
probably benign |
Het |
Ehmt1 |
A |
T |
2: 24,774,302 (GRCm39) |
S43R |
probably damaging |
Het |
Ercc5 |
T |
C |
1: 44,212,540 (GRCm39) |
L666P |
probably benign |
Het |
F5 |
A |
G |
1: 164,010,403 (GRCm39) |
H378R |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,174,718 (GRCm39) |
N1998K |
probably damaging |
Het |
Fbxo28 |
T |
C |
1: 182,169,099 (GRCm39) |
D13G |
unknown |
Het |
Fras1 |
T |
C |
5: 96,857,741 (GRCm39) |
S2012P |
probably benign |
Het |
Gm5624 |
T |
A |
14: 44,799,302 (GRCm39) |
N41I |
probably damaging |
Het |
Gm8104 |
A |
G |
14: 42,959,028 (GRCm39) |
I73V |
possibly damaging |
Het |
Gpr141b |
T |
C |
13: 19,913,849 (GRCm39) |
|
noncoding transcript |
Het |
Gpr68 |
G |
A |
12: 100,845,167 (GRCm39) |
P126S |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,582,685 (GRCm39) |
T156S |
possibly damaging |
Het |
Hacl1 |
T |
A |
14: 31,336,221 (GRCm39) |
Y429F |
probably damaging |
Het |
Haus3 |
A |
C |
5: 34,320,916 (GRCm39) |
L510R |
probably damaging |
Het |
Helq |
C |
T |
5: 100,921,990 (GRCm39) |
G738D |
probably benign |
Het |
Hsd3b2 |
G |
C |
3: 98,619,553 (GRCm39) |
P131A |
probably damaging |
Het |
Il22ra1 |
G |
T |
4: 135,475,471 (GRCm39) |
C247F |
probably benign |
Het |
Ivl |
T |
C |
3: 92,479,891 (GRCm39) |
E58G |
unknown |
Het |
Kcnk9 |
G |
T |
15: 72,417,948 (GRCm39) |
Q61K |
probably benign |
Het |
Kremen1 |
CGGG |
CGGGGGG |
11: 5,151,791 (GRCm39) |
|
probably benign |
Het |
Loxhd1 |
G |
T |
18: 77,490,198 (GRCm39) |
A1314S |
probably damaging |
Het |
Lratd1 |
T |
C |
12: 14,200,226 (GRCm39) |
Y167C |
probably damaging |
Het |
Lrba |
A |
G |
3: 86,259,175 (GRCm39) |
I1397V |
probably benign |
Het |
Lrig3 |
T |
A |
10: 125,832,920 (GRCm39) |
|
probably null |
Het |
Lrrc36 |
A |
G |
8: 106,176,397 (GRCm39) |
D378G |
probably damaging |
Het |
Lrrc49 |
G |
A |
9: 60,505,474 (GRCm39) |
T527I |
probably damaging |
Het |
Map4k4 |
C |
A |
1: 40,062,620 (GRCm39) |
T1195K |
probably damaging |
Het |
Mrps33 |
G |
A |
6: 39,779,429 (GRCm39) |
R89C |
probably damaging |
Het |
Mtor |
T |
C |
4: 148,547,349 (GRCm39) |
V444A |
probably benign |
Het |
Myh2 |
A |
G |
11: 67,079,764 (GRCm39) |
E1046G |
probably damaging |
Het |
Myo15b |
G |
T |
11: 115,771,335 (GRCm39) |
|
probably null |
Het |
Myo5c |
T |
C |
9: 75,153,446 (GRCm39) |
Y111H |
probably damaging |
Het |
Ncoa4-ps |
A |
T |
12: 119,225,506 (GRCm39) |
|
noncoding transcript |
Het |
Ndufv2 |
G |
C |
17: 66,390,481 (GRCm39) |
T163R |
probably damaging |
Het |
Nf1 |
A |
G |
11: 79,444,794 (GRCm39) |
N373S |
possibly damaging |
Het |
Nwd2 |
A |
G |
5: 63,962,917 (GRCm39) |
M834V |
probably benign |
Het |
Ogfod2 |
T |
C |
5: 124,253,019 (GRCm39) |
V343A |
probably damaging |
Het |
Or11g2 |
C |
T |
14: 50,856,143 (GRCm39) |
L155F |
probably benign |
Het |
Or11j4 |
C |
A |
14: 50,630,786 (GRCm39) |
S191* |
probably null |
Het |
Or3a1b |
A |
T |
11: 74,012,234 (GRCm39) |
T40S |
probably benign |
Het |
Or4c115 |
T |
A |
2: 88,928,050 (GRCm39) |
T74S |
probably benign |
Het |
Or51ag1 |
T |
C |
7: 103,155,248 (GRCm39) |
I302V |
possibly damaging |
Het |
Or52ab2 |
T |
A |
7: 102,969,621 (GRCm39) |
M1K |
probably null |
Het |
Or8g34 |
A |
T |
9: 39,373,410 (GRCm39) |
I228F |
probably damaging |
Het |
Parp1 |
T |
A |
1: 180,428,091 (GRCm39) |
|
probably null |
Het |
Ppp3ca |
A |
T |
3: 136,640,792 (GRCm39) |
I448F |
probably damaging |
Het |
Prss44 |
T |
C |
9: 110,646,272 (GRCm39) |
V333A |
probably damaging |
Het |
Pxk |
C |
T |
14: 8,151,507 (GRCm38) |
R441* |
probably null |
Het |
Rars1 |
A |
C |
11: 35,716,822 (GRCm39) |
D231E |
probably benign |
Het |
Rfc1 |
T |
C |
5: 65,421,722 (GRCm39) |
Y1059C |
probably damaging |
Het |
Rilpl1 |
T |
A |
5: 124,652,719 (GRCm39) |
I2F |
probably damaging |
Het |
Sarm1 |
G |
T |
11: 78,381,820 (GRCm39) |
A221E |
possibly damaging |
Het |
Serpina3f |
A |
G |
12: 104,183,665 (GRCm39) |
T176A |
probably damaging |
Het |
Slc22a20 |
T |
C |
19: 6,035,695 (GRCm39) |
E131G |
probably benign |
Het |
Slc26a11 |
T |
C |
11: 119,263,979 (GRCm39) |
V343A |
probably damaging |
Het |
Slc2a4 |
A |
G |
11: 69,837,133 (GRCm39) |
I9T |
probably benign |
Het |
Slc39a6 |
G |
T |
18: 24,718,259 (GRCm39) |
D599E |
probably damaging |
Het |
Slc5a6 |
G |
T |
5: 31,198,020 (GRCm39) |
S285* |
probably null |
Het |
Spata9 |
A |
G |
13: 76,125,760 (GRCm39) |
H81R |
probably benign |
Het |
St7l |
A |
G |
3: 104,826,812 (GRCm39) |
E436G |
probably damaging |
Het |
Tecrl |
A |
G |
5: 83,427,077 (GRCm39) |
I357T |
probably damaging |
Het |
Thop1 |
C |
T |
10: 80,909,043 (GRCm39) |
R25C |
probably damaging |
Het |
Tmprss12 |
A |
G |
15: 100,190,428 (GRCm39) |
E266G |
probably benign |
Het |
Tpgs1 |
T |
A |
10: 79,511,344 (GRCm39) |
V162D |
possibly damaging |
Het |
Trpa1 |
C |
T |
1: 14,944,648 (GRCm39) |
R1032Q |
probably benign |
Het |
Tspan12 |
A |
G |
6: 21,795,699 (GRCm39) |
Y164H |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,135,274 (GRCm39) |
Y869H |
probably damaging |
Het |
Vmn1r21 |
A |
G |
6: 57,820,799 (GRCm39) |
I215T |
probably benign |
Het |
Zan |
A |
T |
5: 137,384,713 (GRCm39) |
S5104T |
unknown |
Het |
Zfp318 |
T |
C |
17: 46,722,980 (GRCm39) |
V1661A |
probably benign |
Het |
Zfp365 |
C |
T |
10: 67,724,772 (GRCm39) |
R372K |
probably 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 |
R0326:Dab2
|
UTSW |
15 |
6,447,797 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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'- GCCATAATAAGTGGCCAGCCTC -3'
(R):5'- CGCAGCTGGAAGTCCTTAAAC -3'
Sequencing Primer
(F):5'- GGCCAGCCACTCGTTTTTGG -3'
(R):5'- CGCAGCTGGAAGTCCTTAAACATTTC -3'
|
Posted On |
2014-06-23 |