Incidental Mutation 'R1767:Arhgef2'
ID |
194448 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arhgef2
|
Ensembl Gene |
ENSMUSG00000028059 |
Gene Name |
Rho/Rac guanine nucleotide exchange factor 2 |
Synonyms |
Lfc, Lbcl1, LFP40, P40, GEFH1, GEF-H1 |
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.664)
|
Stock # |
R1767 (G1)
|
Quality Score |
99 |
Status
|
Not validated
|
Chromosome |
3 |
Chromosomal Location |
88513273-88555359 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 88551260 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Arginine
at position 778
(Q778R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000135131
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029694]
[ENSMUST00000107510]
[ENSMUST00000170653]
[ENSMUST00000175779]
[ENSMUST00000175903]
[ENSMUST00000175911]
[ENSMUST00000176500]
[ENSMUST00000176804]
[ENSMUST00000177303]
[ENSMUST00000177498]
|
AlphaFold |
Q60875 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000029694
AA Change: Q807R
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000029694 Gene: ENSMUSG00000028059 AA Change: Q807R
Domain | Start | End | E-Value | Type |
C1
|
40 |
86 |
4.22e-9 |
SMART |
low complexity region
|
90 |
95 |
N/A |
INTRINSIC |
low complexity region
|
133 |
146 |
N/A |
INTRINSIC |
RhoGEF
|
240 |
432 |
1.86e-58 |
SMART |
PH
|
474 |
574 |
9.56e-11 |
SMART |
coiled coil region
|
588 |
619 |
N/A |
INTRINSIC |
low complexity region
|
812 |
827 |
N/A |
INTRINSIC |
coiled coil region
|
829 |
866 |
N/A |
INTRINSIC |
low complexity region
|
872 |
888 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000107510
AA Change: Q780R
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000103134 Gene: ENSMUSG00000028059 AA Change: Q780R
Domain | Start | End | E-Value | Type |
C1
|
13 |
59 |
4.22e-9 |
SMART |
low complexity region
|
63 |
68 |
N/A |
INTRINSIC |
low complexity region
|
106 |
119 |
N/A |
INTRINSIC |
RhoGEF
|
213 |
405 |
1.86e-58 |
SMART |
PH
|
447 |
547 |
9.56e-11 |
SMART |
coiled coil region
|
561 |
592 |
N/A |
INTRINSIC |
low complexity region
|
785 |
800 |
N/A |
INTRINSIC |
coiled coil region
|
802 |
839 |
N/A |
INTRINSIC |
low complexity region
|
845 |
861 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000170653
AA Change: Q778R
PolyPhen 2
Score 0.072 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000127843 Gene: ENSMUSG00000028059 AA Change: Q778R
Domain | Start | End | E-Value | Type |
C1
|
13 |
59 |
4.22e-9 |
SMART |
low complexity region
|
63 |
68 |
N/A |
INTRINSIC |
low complexity region
|
104 |
117 |
N/A |
INTRINSIC |
RhoGEF
|
211 |
403 |
1.86e-58 |
SMART |
PH
|
445 |
545 |
9.56e-11 |
SMART |
coiled coil region
|
559 |
590 |
N/A |
INTRINSIC |
low complexity region
|
783 |
798 |
N/A |
INTRINSIC |
coiled coil region
|
800 |
837 |
N/A |
INTRINSIC |
low complexity region
|
843 |
859 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000175779
AA Change: Q792R
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000135177 Gene: ENSMUSG00000028059 AA Change: Q792R
Domain | Start | End | E-Value | Type |
C1
|
25 |
71 |
4.22e-9 |
SMART |
low complexity region
|
75 |
80 |
N/A |
INTRINSIC |
low complexity region
|
118 |
131 |
N/A |
INTRINSIC |
RhoGEF
|
225 |
417 |
1.86e-58 |
SMART |
PH
|
459 |
559 |
9.56e-11 |
SMART |
coiled coil region
|
573 |
604 |
N/A |
INTRINSIC |
low complexity region
|
797 |
812 |
N/A |
INTRINSIC |
coiled coil region
|
814 |
851 |
N/A |
INTRINSIC |
low complexity region
|
857 |
873 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000175903
AA Change: Q790R
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000135168 Gene: ENSMUSG00000028059 AA Change: Q790R
Domain | Start | End | E-Value | Type |
C1
|
25 |
71 |
4.22e-9 |
SMART |
low complexity region
|
75 |
80 |
N/A |
INTRINSIC |
low complexity region
|
118 |
131 |
N/A |
INTRINSIC |
RhoGEF
|
223 |
415 |
1.86e-58 |
SMART |
PH
|
457 |
557 |
9.56e-11 |
SMART |
coiled coil region
|
571 |
602 |
N/A |
INTRINSIC |
low complexity region
|
795 |
810 |
N/A |
INTRINSIC |
coiled coil region
|
812 |
849 |
N/A |
INTRINSIC |
low complexity region
|
855 |
871 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000175911
|
SMART Domains |
Protein: ENSMUSP00000135428 Gene: ENSMUSG00000028059
Domain | Start | End | E-Value | Type |
C1
|
32 |
78 |
4.22e-9 |
SMART |
low complexity region
|
82 |
87 |
N/A |
INTRINSIC |
low complexity region
|
125 |
138 |
N/A |
INTRINSIC |
RhoGEF
|
232 |
424 |
1.86e-58 |
SMART |
PH
|
466 |
566 |
9.56e-11 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000176272
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000176500
AA Change: Q792R
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000134834 Gene: ENSMUSG00000028059 AA Change: Q792R
Domain | Start | End | E-Value | Type |
C1
|
25 |
71 |
4.22e-9 |
SMART |
low complexity region
|
75 |
80 |
N/A |
INTRINSIC |
low complexity region
|
118 |
131 |
N/A |
INTRINSIC |
RhoGEF
|
225 |
417 |
1.86e-58 |
SMART |
PH
|
459 |
559 |
9.56e-11 |
SMART |
coiled coil region
|
573 |
604 |
N/A |
INTRINSIC |
low complexity region
|
797 |
812 |
N/A |
INTRINSIC |
coiled coil region
|
814 |
851 |
N/A |
INTRINSIC |
low complexity region
|
857 |
873 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000176804
AA Change: Q805R
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000135397 Gene: ENSMUSG00000028059 AA Change: Q805R
Domain | Start | End | E-Value | Type |
C1
|
40 |
86 |
4.22e-9 |
SMART |
low complexity region
|
90 |
95 |
N/A |
INTRINSIC |
low complexity region
|
133 |
146 |
N/A |
INTRINSIC |
RhoGEF
|
238 |
430 |
1.86e-58 |
SMART |
PH
|
472 |
572 |
9.56e-11 |
SMART |
coiled coil region
|
586 |
617 |
N/A |
INTRINSIC |
low complexity region
|
810 |
825 |
N/A |
INTRINSIC |
coiled coil region
|
827 |
864 |
N/A |
INTRINSIC |
low complexity region
|
870 |
886 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000177303
AA Change: Q778R
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000135131 Gene: ENSMUSG00000028059 AA Change: Q778R
Domain | Start | End | E-Value | Type |
C1
|
13 |
59 |
4.22e-9 |
SMART |
low complexity region
|
63 |
68 |
N/A |
INTRINSIC |
low complexity region
|
106 |
119 |
N/A |
INTRINSIC |
RhoGEF
|
211 |
403 |
1.86e-58 |
SMART |
PH
|
445 |
545 |
9.56e-11 |
SMART |
coiled coil region
|
559 |
590 |
N/A |
INTRINSIC |
low complexity region
|
783 |
798 |
N/A |
INTRINSIC |
coiled coil region
|
800 |
837 |
N/A |
INTRINSIC |
low complexity region
|
843 |
859 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000177498
AA Change: Q790R
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000134840 Gene: ENSMUSG00000028059 AA Change: Q790R
Domain | Start | End | E-Value | Type |
C1
|
25 |
71 |
4.22e-9 |
SMART |
low complexity region
|
75 |
80 |
N/A |
INTRINSIC |
low complexity region
|
116 |
129 |
N/A |
INTRINSIC |
RhoGEF
|
223 |
415 |
1.86e-58 |
SMART |
PH
|
457 |
557 |
9.56e-11 |
SMART |
coiled coil region
|
571 |
602 |
N/A |
INTRINSIC |
low complexity region
|
795 |
810 |
N/A |
INTRINSIC |
coiled coil region
|
812 |
849 |
N/A |
INTRINSIC |
low complexity region
|
855 |
871 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177099
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177418
|
Meta Mutation Damage Score |
0.0834 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.4%
- 20x: 92.8%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The encoded protein may form complex with G proteins and stimulate rho-dependent signals. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Jun 2009] PHENOTYPE: Mice homozygous for a gene trap allele exhibit impaired response to viral infection. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110065P20Rik |
T |
C |
4: 124,743,754 (GRCm39) |
N128S |
possibly damaging |
Het |
Adam26b |
T |
A |
8: 43,972,948 (GRCm39) |
I685F |
probably benign |
Het |
Adgrf5 |
A |
T |
17: 43,761,455 (GRCm39) |
Y1050F |
possibly damaging |
Het |
Alcam |
A |
T |
16: 52,091,077 (GRCm39) |
N480K |
probably damaging |
Het |
Alk |
T |
A |
17: 72,207,693 (GRCm39) |
H1014L |
possibly damaging |
Het |
Arhgef6 |
T |
C |
X: 56,383,922 (GRCm39) |
M5V |
probably benign |
Het |
Ascc3 |
T |
A |
10: 50,594,472 (GRCm39) |
I1189N |
probably damaging |
Het |
AU040320 |
G |
A |
4: 126,734,517 (GRCm39) |
G713D |
probably damaging |
Het |
Bmpr1a |
A |
G |
14: 34,169,727 (GRCm39) |
|
probably null |
Het |
Bpifa6 |
A |
G |
2: 153,829,147 (GRCm39) |
T225A |
possibly damaging |
Het |
Cacna1g |
T |
C |
11: 94,350,628 (GRCm39) |
S406G |
probably benign |
Het |
Ccdc198 |
G |
A |
14: 49,473,341 (GRCm39) |
T128I |
probably benign |
Het |
Ccdc40 |
T |
A |
11: 119,121,522 (GRCm39) |
|
probably null |
Het |
Cckbr |
A |
T |
7: 105,083,758 (GRCm39) |
I229F |
possibly damaging |
Het |
Cers3 |
A |
G |
7: 66,433,151 (GRCm39) |
K156R |
probably damaging |
Het |
Chd1 |
T |
A |
17: 15,990,565 (GRCm39) |
W1706R |
probably damaging |
Het |
Col11a2 |
T |
A |
17: 34,282,869 (GRCm39) |
|
probably benign |
Het |
Coq10b |
A |
G |
1: 55,100,513 (GRCm39) |
R66G |
probably damaging |
Het |
Cpn2 |
A |
T |
16: 30,078,485 (GRCm39) |
Y405* |
probably null |
Het |
Dis3 |
A |
T |
14: 99,321,578 (GRCm39) |
Y590N |
probably damaging |
Het |
Dpy19l1 |
T |
C |
9: 24,373,880 (GRCm39) |
H270R |
probably benign |
Het |
Dync1h1 |
G |
A |
12: 110,602,943 (GRCm39) |
E2195K |
probably benign |
Het |
Ephx1 |
C |
T |
1: 180,822,242 (GRCm39) |
G101S |
probably damaging |
Het |
Flg |
A |
T |
3: 93,187,220 (GRCm39) |
Y224F |
possibly damaging |
Het |
Focad |
G |
T |
4: 88,275,705 (GRCm39) |
V1105L |
unknown |
Het |
Fzd1 |
A |
G |
5: 4,806,812 (GRCm39) |
Y257H |
probably benign |
Het |
Gm11116 |
T |
C |
5: 88,259,311 (GRCm39) |
|
probably benign |
Het |
Gm11938 |
G |
A |
11: 99,494,071 (GRCm39) |
S8F |
unknown |
Het |
Grin3a |
A |
T |
4: 49,844,423 (GRCm39) |
V220E |
probably damaging |
Het |
Gstt2 |
T |
C |
10: 75,670,098 (GRCm39) |
D8G |
probably damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Hook3 |
A |
G |
8: 26,561,084 (GRCm39) |
|
probably null |
Het |
Itpr2 |
T |
C |
6: 146,251,566 (GRCm39) |
D993G |
possibly damaging |
Het |
Jhy |
T |
C |
9: 40,872,444 (GRCm39) |
R22G |
probably benign |
Het |
Krt13 |
A |
C |
11: 100,011,926 (GRCm39) |
H132Q |
possibly damaging |
Het |
Krtap27-1 |
G |
A |
16: 88,468,199 (GRCm39) |
S115L |
probably damaging |
Het |
L1td1 |
T |
C |
4: 98,625,686 (GRCm39) |
V627A |
probably benign |
Het |
Lrrn4cl |
A |
G |
19: 8,829,135 (GRCm39) |
T38A |
probably benign |
Het |
Ly96 |
A |
G |
1: 16,776,399 (GRCm39) |
T112A |
probably benign |
Het |
Meltf |
G |
T |
16: 31,702,747 (GRCm39) |
C158F |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,485,841 (GRCm39) |
H1040Q |
probably damaging |
Het |
Npas4 |
G |
A |
19: 5,038,211 (GRCm39) |
P199L |
probably benign |
Het |
Or12j3 |
T |
C |
7: 139,953,389 (GRCm39) |
I45V |
possibly damaging |
Het |
Or52r1 |
T |
A |
7: 102,536,833 (GRCm39) |
I176F |
probably damaging |
Het |
Or8k3b |
A |
G |
2: 86,520,728 (GRCm39) |
M197T |
probably benign |
Het |
Pcdh10 |
A |
T |
3: 45,338,612 (GRCm39) |
H923L |
probably damaging |
Het |
Pias3 |
T |
C |
3: 96,608,719 (GRCm39) |
S228P |
probably damaging |
Het |
Pign |
A |
G |
1: 105,580,917 (GRCm39) |
V154A |
probably benign |
Het |
Plod3 |
T |
A |
5: 137,019,030 (GRCm39) |
V305E |
possibly damaging |
Het |
Prkra |
G |
T |
2: 76,477,584 (GRCm39) |
H40Q |
possibly damaging |
Het |
Prss22 |
T |
A |
17: 24,215,331 (GRCm39) |
E148D |
probably benign |
Het |
Psg17 |
A |
G |
7: 18,550,727 (GRCm39) |
V376A |
possibly damaging |
Het |
Retnlg |
A |
T |
16: 48,693,991 (GRCm39) |
D49V |
possibly damaging |
Het |
Rnf26rt |
A |
T |
6: 76,474,588 (GRCm39) |
N9K |
unknown |
Het |
Rtp1 |
A |
G |
16: 23,250,124 (GRCm39) |
E163G |
probably damaging |
Het |
Slc6a20a |
T |
A |
9: 123,466,165 (GRCm39) |
I522F |
probably damaging |
Het |
Slco5a1 |
T |
C |
1: 13,059,839 (GRCm39) |
D294G |
probably damaging |
Het |
Slco6d1 |
A |
G |
1: 98,418,274 (GRCm39) |
T487A |
possibly damaging |
Het |
Smarcc2 |
A |
T |
10: 128,304,951 (GRCm39) |
D262V |
possibly damaging |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Ssbp3 |
G |
T |
4: 106,904,612 (GRCm39) |
D336Y |
probably damaging |
Het |
Sun2 |
A |
G |
15: 79,609,758 (GRCm39) |
S694P |
probably benign |
Het |
Tdp1 |
G |
A |
12: 99,857,602 (GRCm39) |
|
probably null |
Het |
Tfap2a |
A |
T |
13: 40,878,613 (GRCm39) |
I204N |
probably damaging |
Het |
Tfip11 |
T |
A |
5: 112,482,298 (GRCm39) |
W519R |
probably damaging |
Het |
Tie1 |
T |
C |
4: 118,333,373 (GRCm39) |
E831G |
possibly damaging |
Het |
Tjp1 |
A |
G |
7: 64,962,301 (GRCm39) |
|
probably null |
Het |
Tln2 |
C |
T |
9: 67,193,796 (GRCm39) |
A1773T |
probably benign |
Het |
Tmem39b |
A |
C |
4: 129,586,976 (GRCm39) |
I78M |
possibly damaging |
Het |
Trank1 |
T |
C |
9: 111,220,547 (GRCm39) |
V2428A |
probably benign |
Het |
Trim35 |
A |
G |
14: 66,541,617 (GRCm39) |
E247G |
probably damaging |
Het |
Tsc22d1 |
T |
C |
14: 76,655,542 (GRCm39) |
S674P |
probably damaging |
Het |
Tsn |
A |
T |
1: 118,228,618 (GRCm39) |
D201E |
probably damaging |
Het |
Usp42 |
A |
T |
5: 143,700,621 (GRCm39) |
V1134E |
possibly damaging |
Het |
Uvrag |
A |
G |
7: 98,748,601 (GRCm39) |
I117T |
probably damaging |
Het |
Vmn1r192 |
A |
G |
13: 22,371,441 (GRCm39) |
S260P |
probably benign |
Het |
Vmn2r110 |
C |
T |
17: 20,800,840 (GRCm39) |
A531T |
possibly damaging |
Het |
Wdsub1 |
A |
T |
2: 59,689,058 (GRCm39) |
I388N |
probably damaging |
Het |
Wnt10b |
A |
T |
15: 98,670,556 (GRCm39) |
L228Q |
probably damaging |
Het |
Zbtb34 |
A |
C |
2: 33,301,348 (GRCm39) |
S398A |
possibly damaging |
Het |
|
Other mutations in Arhgef2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01913:Arhgef2
|
APN |
3 |
88,539,226 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02165:Arhgef2
|
APN |
3 |
88,553,527 (GRCm39) |
missense |
probably damaging |
1.00 |
monument
|
UTSW |
3 |
88,540,955 (GRCm39) |
critical splice donor site |
probably null |
|
R0090:Arhgef2
|
UTSW |
3 |
88,546,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R0330:Arhgef2
|
UTSW |
3 |
88,549,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R0414:Arhgef2
|
UTSW |
3 |
88,539,575 (GRCm39) |
splice site |
probably benign |
|
R0631:Arhgef2
|
UTSW |
3 |
88,541,743 (GRCm39) |
missense |
probably damaging |
0.99 |
R1635:Arhgef2
|
UTSW |
3 |
88,546,628 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1688:Arhgef2
|
UTSW |
3 |
88,547,607 (GRCm39) |
missense |
probably benign |
0.32 |
R1751:Arhgef2
|
UTSW |
3 |
88,551,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Arhgef2
|
UTSW |
3 |
88,546,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Arhgef2
|
UTSW |
3 |
88,540,222 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1934:Arhgef2
|
UTSW |
3 |
88,537,098 (GRCm39) |
missense |
probably damaging |
0.96 |
R2155:Arhgef2
|
UTSW |
3 |
88,543,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Arhgef2
|
UTSW |
3 |
88,537,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R2360:Arhgef2
|
UTSW |
3 |
88,541,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R3916:Arhgef2
|
UTSW |
3 |
88,540,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R4090:Arhgef2
|
UTSW |
3 |
88,551,185 (GRCm39) |
missense |
probably benign |
0.01 |
R4732:Arhgef2
|
UTSW |
3 |
88,539,247 (GRCm39) |
nonsense |
probably null |
|
R4733:Arhgef2
|
UTSW |
3 |
88,539,247 (GRCm39) |
nonsense |
probably null |
|
R4837:Arhgef2
|
UTSW |
3 |
88,540,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4952:Arhgef2
|
UTSW |
3 |
88,549,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R5152:Arhgef2
|
UTSW |
3 |
88,536,875 (GRCm39) |
splice site |
probably null |
|
R5194:Arhgef2
|
UTSW |
3 |
88,542,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Arhgef2
|
UTSW |
3 |
88,540,955 (GRCm39) |
critical splice donor site |
probably null |
|
R5334:Arhgef2
|
UTSW |
3 |
88,553,636 (GRCm39) |
missense |
probably damaging |
0.96 |
R5514:Arhgef2
|
UTSW |
3 |
88,550,304 (GRCm39) |
missense |
probably benign |
0.01 |
R5560:Arhgef2
|
UTSW |
3 |
88,541,744 (GRCm39) |
missense |
probably damaging |
0.97 |
R5595:Arhgef2
|
UTSW |
3 |
88,550,283 (GRCm39) |
missense |
probably benign |
0.00 |
R5879:Arhgef2
|
UTSW |
3 |
88,550,924 (GRCm39) |
splice site |
probably null |
|
R5910:Arhgef2
|
UTSW |
3 |
88,542,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R5914:Arhgef2
|
UTSW |
3 |
88,543,176 (GRCm39) |
missense |
probably benign |
|
R5918:Arhgef2
|
UTSW |
3 |
88,543,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Arhgef2
|
UTSW |
3 |
88,542,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Arhgef2
|
UTSW |
3 |
88,550,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R7167:Arhgef2
|
UTSW |
3 |
88,551,179 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7289:Arhgef2
|
UTSW |
3 |
88,543,192 (GRCm39) |
missense |
probably benign |
|
R7318:Arhgef2
|
UTSW |
3 |
88,539,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R7353:Arhgef2
|
UTSW |
3 |
88,542,993 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7402:Arhgef2
|
UTSW |
3 |
88,540,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Arhgef2
|
UTSW |
3 |
88,551,262 (GRCm39) |
missense |
probably damaging |
0.96 |
R7899:Arhgef2
|
UTSW |
3 |
88,528,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7934:Arhgef2
|
UTSW |
3 |
88,537,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8002:Arhgef2
|
UTSW |
3 |
88,554,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8254:Arhgef2
|
UTSW |
3 |
88,549,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8297:Arhgef2
|
UTSW |
3 |
88,546,739 (GRCm39) |
missense |
probably benign |
0.00 |
R8314:Arhgef2
|
UTSW |
3 |
88,528,600 (GRCm39) |
missense |
probably benign |
0.00 |
R8350:Arhgef2
|
UTSW |
3 |
88,553,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R8450:Arhgef2
|
UTSW |
3 |
88,553,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Arhgef2
|
UTSW |
3 |
88,536,850 (GRCm39) |
missense |
probably benign |
0.00 |
R9632:Arhgef2
|
UTSW |
3 |
88,528,576 (GRCm39) |
missense |
probably benign |
0.43 |
R9710:Arhgef2
|
UTSW |
3 |
88,528,576 (GRCm39) |
missense |
probably benign |
0.43 |
V1662:Arhgef2
|
UTSW |
3 |
88,540,636 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGAAAGACTGATGGAAGCCCTGTTC -3'
(R):5'- AGCTCAAGTATAAAGCGTCGCCC -3'
Sequencing Primer
(F):5'- GAAGCCCTGTTCCCTGAG -3'
(R):5'- AGTGGCTCGTTTTGGCCC -3'
|
Posted On |
2014-05-23 |