Incidental Mutation 'R7644:Dennd2b'
ID |
590422 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dennd2b
|
Ensembl Gene |
ENSMUSG00000031024 |
Gene Name |
DENN domain containing 2B |
Synonyms |
Denn2b, 2610305K15Rik, St5, 2010004M01Rik |
MMRRC Submission |
045723-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.390)
|
Stock # |
R7644 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
109123118-109302812 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
A to T
at 109156000 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Stop codon
at position 250
(L250*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000077067
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077909]
[ENSMUST00000079282]
[ENSMUST00000084738]
[ENSMUST00000168005]
[ENSMUST00000207394]
[ENSMUST00000207745]
[ENSMUST00000208583]
|
AlphaFold |
Q924W7 |
Predicted Effect |
probably null
Transcript: ENSMUST00000077909
AA Change: L250*
|
SMART Domains |
Protein: ENSMUSP00000077067 Gene: ENSMUSG00000031024 AA Change: L250*
Domain | Start | End | E-Value | Type |
low complexity region
|
28 |
46 |
N/A |
INTRINSIC |
low complexity region
|
197 |
213 |
N/A |
INTRINSIC |
low complexity region
|
314 |
326 |
N/A |
INTRINSIC |
low complexity region
|
327 |
348 |
N/A |
INTRINSIC |
low complexity region
|
365 |
379 |
N/A |
INTRINSIC |
low complexity region
|
407 |
426 |
N/A |
INTRINSIC |
low complexity region
|
577 |
609 |
N/A |
INTRINSIC |
low complexity region
|
624 |
638 |
N/A |
INTRINSIC |
low complexity region
|
645 |
656 |
N/A |
INTRINSIC |
uDENN
|
690 |
781 |
1.16e-30 |
SMART |
DENN
|
788 |
972 |
7.84e-78 |
SMART |
low complexity region
|
1007 |
1014 |
N/A |
INTRINSIC |
dDENN
|
1019 |
1086 |
3.12e-22 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000079282
AA Change: L250*
|
SMART Domains |
Protein: ENSMUSP00000078264 Gene: ENSMUSG00000031024 AA Change: L250*
Domain | Start | End | E-Value | Type |
low complexity region
|
28 |
46 |
N/A |
INTRINSIC |
low complexity region
|
197 |
213 |
N/A |
INTRINSIC |
low complexity region
|
314 |
326 |
N/A |
INTRINSIC |
low complexity region
|
327 |
348 |
N/A |
INTRINSIC |
low complexity region
|
365 |
379 |
N/A |
INTRINSIC |
low complexity region
|
407 |
426 |
N/A |
INTRINSIC |
low complexity region
|
577 |
609 |
N/A |
INTRINSIC |
low complexity region
|
624 |
638 |
N/A |
INTRINSIC |
low complexity region
|
645 |
656 |
N/A |
INTRINSIC |
uDENN
|
690 |
781 |
1.16e-30 |
SMART |
DENN
|
788 |
972 |
7.84e-78 |
SMART |
low complexity region
|
1007 |
1014 |
N/A |
INTRINSIC |
dDENN
|
1019 |
1086 |
3.12e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000084738
|
SMART Domains |
Protein: ENSMUSP00000081789 Gene: ENSMUSG00000031024
Domain | Start | End | E-Value | Type |
low complexity region
|
160 |
192 |
N/A |
INTRINSIC |
low complexity region
|
207 |
221 |
N/A |
INTRINSIC |
low complexity region
|
228 |
239 |
N/A |
INTRINSIC |
uDENN
|
273 |
364 |
1.16e-30 |
SMART |
DENN
|
371 |
555 |
7.84e-78 |
SMART |
low complexity region
|
590 |
597 |
N/A |
INTRINSIC |
dDENN
|
602 |
669 |
3.12e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000168005
|
SMART Domains |
Protein: ENSMUSP00000130119 Gene: ENSMUSG00000031024
Domain | Start | End | E-Value | Type |
low complexity region
|
160 |
192 |
N/A |
INTRINSIC |
low complexity region
|
207 |
221 |
N/A |
INTRINSIC |
low complexity region
|
228 |
239 |
N/A |
INTRINSIC |
uDENN
|
273 |
364 |
1.16e-30 |
SMART |
DENN
|
371 |
555 |
7.84e-78 |
SMART |
low complexity region
|
590 |
597 |
N/A |
INTRINSIC |
dDENN
|
602 |
669 |
3.12e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000207394
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000207745
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000208583
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.9%
|
Validation Efficiency |
100% (86/86) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene was identified by its ability to suppress the tumorigenicity of Hela cells in nude mice. The protein encoded by this gene contains a C-terminal region that shares similarity with the Rab 3 family of small GTP binding proteins. This protein preferentially binds to the SH3 domain of c-Abl kinase, and acts as a regulator of MAPK1/ERK2 kinase, which may contribute to its ability to reduce the tumorigenic phenotype in cells. Three alternatively spliced transcript variants of this gene encoding distinct isoforms are identified. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001O22Rik |
C |
T |
2: 30,687,966 (GRCm39) |
R209Q |
possibly damaging |
Het |
Abl2 |
A |
G |
1: 156,443,563 (GRCm39) |
D24G |
probably benign |
Het |
Adar |
C |
T |
3: 89,652,826 (GRCm39) |
A754V |
probably benign |
Het |
Adcy8 |
C |
T |
15: 64,571,218 (GRCm39) |
V1172I |
possibly damaging |
Het |
Adgrl2 |
C |
T |
3: 148,544,789 (GRCm39) |
V769M |
probably damaging |
Het |
Akna |
T |
A |
4: 63,313,634 (GRCm39) |
Q163L |
possibly damaging |
Het |
Alox15 |
C |
T |
11: 70,236,368 (GRCm39) |
A511T |
probably null |
Het |
Ano8 |
C |
T |
8: 71,937,474 (GRCm39) |
G90D |
probably damaging |
Het |
Aqp5 |
G |
A |
15: 99,492,107 (GRCm39) |
R235H |
probably damaging |
Het |
B3galt4 |
A |
T |
17: 34,169,419 (GRCm39) |
V273E |
probably damaging |
Het |
Ccdc125 |
C |
T |
13: 100,814,884 (GRCm39) |
|
probably null |
Het |
Ccdc90b |
A |
G |
7: 92,216,868 (GRCm39) |
R47G |
possibly damaging |
Het |
Celsr2 |
G |
T |
3: 108,320,806 (GRCm39) |
L669I |
probably damaging |
Het |
Clasp1 |
T |
G |
1: 118,440,480 (GRCm39) |
|
probably null |
Het |
Clec4a2 |
C |
T |
6: 123,101,974 (GRCm39) |
P43L |
probably benign |
Het |
Cntn1 |
T |
C |
15: 92,207,890 (GRCm39) |
I827T |
probably benign |
Het |
Col9a1 |
G |
T |
1: 24,224,243 (GRCm39) |
V142F |
unknown |
Het |
Cplane1 |
T |
A |
15: 8,252,611 (GRCm39) |
D1944E |
probably benign |
Het |
Cts7 |
G |
T |
13: 61,504,782 (GRCm39) |
Y23* |
probably null |
Het |
Dcdc2a |
T |
A |
13: 25,291,674 (GRCm39) |
Y220N |
probably damaging |
Het |
Dmxl1 |
T |
G |
18: 50,026,619 (GRCm39) |
V1909G |
probably benign |
Het |
Ehd2 |
G |
A |
7: 15,691,474 (GRCm39) |
P286L |
possibly damaging |
Het |
Elf3 |
G |
T |
1: 135,184,244 (GRCm39) |
A208E |
possibly damaging |
Het |
Eml5 |
A |
G |
12: 98,822,203 (GRCm39) |
I775T |
probably benign |
Het |
Ephb1 |
T |
C |
9: 101,813,393 (GRCm39) |
T791A |
probably damaging |
Het |
Fanci |
C |
A |
7: 79,094,219 (GRCm39) |
S1105* |
probably null |
Het |
Fastkd1 |
T |
A |
2: 69,527,184 (GRCm39) |
|
probably null |
Het |
Fat4 |
A |
G |
3: 39,064,390 (GRCm39) |
E4782G |
possibly damaging |
Het |
Fnta |
T |
C |
8: 26,503,516 (GRCm39) |
I90V |
probably damaging |
Het |
Fosl1 |
C |
T |
19: 5,500,332 (GRCm39) |
R84* |
probably null |
Het |
Gdf2 |
T |
C |
14: 33,666,847 (GRCm39) |
F190L |
probably benign |
Het |
Gzmn |
T |
A |
14: 56,404,776 (GRCm39) |
Q88L |
probably damaging |
Het |
Hat1 |
T |
A |
2: 71,240,525 (GRCm39) |
L73Q |
probably damaging |
Het |
Hdhd2 |
G |
A |
18: 77,031,871 (GRCm39) |
G109E |
possibly damaging |
Het |
Il22ra1 |
A |
G |
4: 135,460,346 (GRCm39) |
N34S |
probably damaging |
Het |
Ino80d |
T |
C |
1: 63,097,930 (GRCm39) |
T760A |
probably benign |
Het |
Itga7 |
A |
G |
10: 128,789,370 (GRCm39) |
D971G |
probably benign |
Het |
Kdm6b |
T |
C |
11: 69,291,032 (GRCm39) |
N1574S |
unknown |
Het |
Kel |
T |
C |
6: 41,667,742 (GRCm39) |
E400G |
probably benign |
Het |
Kif22 |
G |
A |
7: 126,632,134 (GRCm39) |
T350I |
probably damaging |
Het |
Kif26b |
A |
G |
1: 178,506,839 (GRCm39) |
N305S |
probably benign |
Het |
Klk12 |
A |
C |
7: 43,419,134 (GRCm39) |
Q33P |
probably damaging |
Het |
Klk1b24 |
G |
A |
7: 43,841,304 (GRCm39) |
|
probably null |
Het |
Krtap31-1 |
T |
A |
11: 99,799,048 (GRCm39) |
C84S |
possibly damaging |
Het |
Ky |
T |
A |
9: 102,414,972 (GRCm39) |
S295T |
probably benign |
Het |
Lpin3 |
T |
A |
2: 160,738,690 (GRCm39) |
M214K |
probably benign |
Het |
Mak |
T |
A |
13: 41,183,586 (GRCm39) |
N565Y |
probably benign |
Het |
Mphosph6 |
T |
C |
8: 118,528,623 (GRCm39) |
T7A |
probably benign |
Het |
Muc6 |
G |
C |
7: 141,217,659 (GRCm39) |
P2338R |
probably damaging |
Het |
Myh11 |
T |
C |
16: 14,039,688 (GRCm39) |
T814A |
|
Het |
Nmbr |
T |
C |
10: 14,636,433 (GRCm39) |
L134P |
probably damaging |
Het |
Nup107 |
C |
T |
10: 117,606,375 (GRCm39) |
V456M |
probably damaging |
Het |
Or56b1b |
A |
G |
7: 108,164,649 (GRCm39) |
S118P |
possibly damaging |
Het |
Or8g22 |
C |
A |
9: 38,958,638 (GRCm39) |
D26Y |
probably damaging |
Het |
Pink1 |
A |
T |
4: 138,044,683 (GRCm39) |
H351Q |
probably damaging |
Het |
Piwil4 |
A |
T |
9: 14,645,711 (GRCm39) |
|
probably null |
Het |
Pkd1l1 |
C |
A |
11: 8,825,758 (GRCm39) |
V1498F |
|
Het |
Polb |
A |
G |
8: 23,130,443 (GRCm39) |
I161T |
probably benign |
Het |
Polg |
A |
T |
7: 79,101,416 (GRCm39) |
L1097Q |
probably damaging |
Het |
Prelp |
T |
C |
1: 133,842,356 (GRCm39) |
N263S |
probably benign |
Het |
Pten |
T |
C |
19: 32,789,234 (GRCm39) |
C211R |
probably damaging |
Het |
Ptprc |
G |
A |
1: 137,995,645 (GRCm39) |
A1012V |
probably benign |
Het |
Ptprr |
T |
A |
10: 115,884,133 (GRCm39) |
H63Q |
probably benign |
Het |
Rapsn |
A |
T |
2: 90,872,299 (GRCm39) |
H211L |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,183,929 (GRCm39) |
N1690S |
probably benign |
Het |
Rpap2 |
A |
G |
5: 107,768,167 (GRCm39) |
E335G |
probably benign |
Het |
Rspry1 |
T |
A |
8: 95,385,396 (GRCm39) |
S567T |
probably benign |
Het |
Sf3b1 |
G |
A |
1: 55,036,302 (GRCm39) |
R924* |
probably null |
Het |
Sftpb |
G |
A |
6: 72,286,818 (GRCm39) |
E241K |
probably benign |
Het |
Smarca4 |
G |
T |
9: 21,566,950 (GRCm39) |
A677S |
probably benign |
Het |
Srrm2 |
G |
A |
17: 24,038,294 (GRCm39) |
R1646Q |
unknown |
Het |
Tex15 |
T |
A |
8: 34,064,445 (GRCm39) |
C1292S |
probably benign |
Het |
Tmem140 |
A |
G |
6: 34,849,708 (GRCm39) |
I75V |
probably benign |
Het |
Trhr2 |
T |
A |
8: 123,084,061 (GRCm39) |
Q313L |
possibly damaging |
Het |
Trim35 |
A |
G |
14: 66,534,546 (GRCm39) |
T10A |
unknown |
Het |
Ttn |
T |
C |
2: 76,750,124 (GRCm39) |
I3642V |
probably benign |
Het |
Ugt1a2 |
T |
C |
1: 88,128,507 (GRCm39) |
L50P |
probably damaging |
Het |
Unc13a |
C |
A |
8: 72,087,182 (GRCm39) |
V1522L |
probably benign |
Het |
Usp33 |
A |
G |
3: 152,063,589 (GRCm39) |
D21G |
possibly damaging |
Het |
Vmn1r90 |
G |
A |
7: 14,295,616 (GRCm39) |
Q161* |
probably null |
Het |
Vmn2r117 |
A |
T |
17: 23,696,265 (GRCm39) |
W381R |
probably damaging |
Het |
Vmn2r16 |
G |
C |
5: 109,487,837 (GRCm39) |
A237P |
probably damaging |
Het |
Vmn2r74 |
A |
G |
7: 85,606,746 (GRCm39) |
V200A |
probably benign |
Het |
Yjefn3 |
C |
T |
8: 70,340,544 (GRCm39) |
V227M |
probably damaging |
Het |
Zfp652 |
T |
C |
11: 95,640,914 (GRCm39) |
F280L |
probably damaging |
Het |
Zfp748 |
G |
A |
13: 67,689,568 (GRCm39) |
T564I |
probably damaging |
Het |
|
Other mutations in Dennd2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Dennd2b
|
APN |
7 |
109,126,915 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01132:Dennd2b
|
APN |
7 |
109,169,212 (GRCm39) |
splice site |
probably null |
|
IGL01288:Dennd2b
|
APN |
7 |
109,139,029 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01645:Dennd2b
|
APN |
7 |
109,126,841 (GRCm39) |
nonsense |
probably null |
|
IGL01714:Dennd2b
|
APN |
7 |
109,169,269 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02021:Dennd2b
|
APN |
7 |
109,156,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02302:Dennd2b
|
APN |
7 |
109,124,538 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02496:Dennd2b
|
APN |
7 |
109,155,442 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02795:Dennd2b
|
APN |
7 |
109,155,571 (GRCm39) |
missense |
probably damaging |
1.00 |
Bucolic
|
UTSW |
7 |
109,124,755 (GRCm39) |
nonsense |
probably null |
|
Halcyon
|
UTSW |
7 |
109,156,000 (GRCm39) |
nonsense |
probably null |
|
FR4340:Dennd2b
|
UTSW |
7 |
109,156,128 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Dennd2b
|
UTSW |
7 |
109,156,128 (GRCm39) |
unclassified |
probably benign |
|
PIT4466001:Dennd2b
|
UTSW |
7 |
109,130,337 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4469001:Dennd2b
|
UTSW |
7 |
109,130,337 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Dennd2b
|
UTSW |
7 |
109,130,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R0024:Dennd2b
|
UTSW |
7 |
109,123,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R0124:Dennd2b
|
UTSW |
7 |
109,141,718 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0125:Dennd2b
|
UTSW |
7 |
109,155,545 (GRCm39) |
missense |
probably benign |
0.19 |
R0365:Dennd2b
|
UTSW |
7 |
109,138,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Dennd2b
|
UTSW |
7 |
109,156,411 (GRCm39) |
missense |
probably benign |
0.45 |
R0534:Dennd2b
|
UTSW |
7 |
109,140,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R0662:Dennd2b
|
UTSW |
7 |
109,156,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R0743:Dennd2b
|
UTSW |
7 |
109,156,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0772:Dennd2b
|
UTSW |
7 |
109,141,527 (GRCm39) |
splice site |
probably null |
|
R0774:Dennd2b
|
UTSW |
7 |
109,141,527 (GRCm39) |
splice site |
probably null |
|
R0787:Dennd2b
|
UTSW |
7 |
109,124,827 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0884:Dennd2b
|
UTSW |
7 |
109,156,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R1518:Dennd2b
|
UTSW |
7 |
109,156,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Dennd2b
|
UTSW |
7 |
109,124,533 (GRCm39) |
nonsense |
probably null |
|
R1909:Dennd2b
|
UTSW |
7 |
109,124,533 (GRCm39) |
nonsense |
probably null |
|
R2232:Dennd2b
|
UTSW |
7 |
109,156,414 (GRCm39) |
missense |
probably benign |
|
R2358:Dennd2b
|
UTSW |
7 |
109,155,653 (GRCm39) |
missense |
probably benign |
0.01 |
R2847:Dennd2b
|
UTSW |
7 |
109,124,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2869:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2870:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2870:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2871:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2871:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2873:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2874:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R4534:Dennd2b
|
UTSW |
7 |
109,130,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R4536:Dennd2b
|
UTSW |
7 |
109,130,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R4559:Dennd2b
|
UTSW |
7 |
109,124,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Dennd2b
|
UTSW |
7 |
109,156,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R4846:Dennd2b
|
UTSW |
7 |
109,156,043 (GRCm39) |
nonsense |
probably null |
|
R5110:Dennd2b
|
UTSW |
7 |
109,141,697 (GRCm39) |
missense |
probably benign |
0.02 |
R5181:Dennd2b
|
UTSW |
7 |
109,155,997 (GRCm39) |
missense |
probably benign |
|
R5268:Dennd2b
|
UTSW |
7 |
109,156,519 (GRCm39) |
missense |
probably benign |
|
R5403:Dennd2b
|
UTSW |
7 |
109,156,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R5836:Dennd2b
|
UTSW |
7 |
109,140,552 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5932:Dennd2b
|
UTSW |
7 |
109,169,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R5937:Dennd2b
|
UTSW |
7 |
109,156,478 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6180:Dennd2b
|
UTSW |
7 |
109,156,095 (GRCm39) |
missense |
probably benign |
0.11 |
R6741:Dennd2b
|
UTSW |
7 |
109,144,304 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6781:Dennd2b
|
UTSW |
7 |
109,124,511 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7086:Dennd2b
|
UTSW |
7 |
109,124,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Dennd2b
|
UTSW |
7 |
109,124,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Dennd2b
|
UTSW |
7 |
109,124,755 (GRCm39) |
nonsense |
probably null |
|
R8745:Dennd2b
|
UTSW |
7 |
109,156,279 (GRCm39) |
missense |
probably benign |
0.02 |
R8859:Dennd2b
|
UTSW |
7 |
109,123,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R9016:Dennd2b
|
UTSW |
7 |
109,139,642 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9178:Dennd2b
|
UTSW |
7 |
109,156,291 (GRCm39) |
missense |
probably benign |
0.31 |
R9361:Dennd2b
|
UTSW |
7 |
109,126,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Dennd2b
|
UTSW |
7 |
109,125,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R9595:Dennd2b
|
UTSW |
7 |
109,155,973 (GRCm39) |
missense |
probably damaging |
0.96 |
RF062:Dennd2b
|
UTSW |
7 |
109,156,153 (GRCm39) |
unclassified |
probably benign |
|
X0067:Dennd2b
|
UTSW |
7 |
109,155,447 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGTCTACACTGTAGCAGCTG -3'
(R):5'- CTTCACCCAGGATGAGTCTGTG -3'
Sequencing Primer
(F):5'- GCTAGGGAGCTGGGGGAG -3'
(R):5'- CCCAGGATGAGTCTGTGTGGAG -3'
|
Posted On |
2019-10-24 |