Incidental Mutation 'R1919:Arhgef4'
ID |
212793 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arhgef4
|
Ensembl Gene |
ENSMUSG00000037509 |
Gene Name |
Rho guanine nucleotide exchange factor 4 |
Synonyms |
Asef, 9330140K16Rik, C230030N03Rik |
MMRRC Submission |
039937-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1919 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
34717263-34851819 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 34850221 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Arginine
at position 1798
(Q1798R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124213
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047534]
[ENSMUST00000047664]
[ENSMUST00000159021]
[ENSMUST00000159747]
[ENSMUST00000160855]
[ENSMUST00000162599]
[ENSMUST00000167518]
|
AlphaFold |
Q7TNR9 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000047534
|
SMART Domains |
Protein: ENSMUSP00000042212 Gene: ENSMUSG00000037503
Domain | Start | End | E-Value | Type |
Pfam:TCRP1
|
1 |
194 |
1e-108 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000047664
AA Change: Q427R
PolyPhen 2
Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
|
SMART Domains |
Protein: ENSMUSP00000035980 Gene: ENSMUSG00000037509 AA Change: Q427R
Domain | Start | End | E-Value | Type |
SH3
|
1 |
45 |
6.97e-7 |
SMART |
RhoGEF
|
82 |
261 |
3.86e-56 |
SMART |
PH
|
294 |
402 |
2.33e-14 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159021
|
SMART Domains |
Protein: ENSMUSP00000124467 Gene: ENSMUSG00000037509
Domain | Start | End | E-Value | Type |
SH3
|
1 |
45 |
6.97e-7 |
SMART |
Pfam:RhoGEF
|
82 |
190 |
3.4e-29 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159059
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000159747
AA Change: Q1798R
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000124213 Gene: ENSMUSG00000037509 AA Change: Q1798R
Domain | Start | End | E-Value | Type |
low complexity region
|
15 |
28 |
N/A |
INTRINSIC |
low complexity region
|
573 |
584 |
N/A |
INTRINSIC |
low complexity region
|
686 |
712 |
N/A |
INTRINSIC |
low complexity region
|
915 |
926 |
N/A |
INTRINSIC |
low complexity region
|
1119 |
1137 |
N/A |
INTRINSIC |
low complexity region
|
1240 |
1254 |
N/A |
INTRINSIC |
SH3
|
1361 |
1416 |
3.73e-16 |
SMART |
RhoGEF
|
1453 |
1632 |
3.86e-56 |
SMART |
PH
|
1665 |
1773 |
2.33e-14 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000160855
|
SMART Domains |
Protein: ENSMUSP00000124207 Gene: ENSMUSG00000037509
Domain | Start | End | E-Value | Type |
SH3
|
1 |
45 |
6.97e-7 |
SMART |
Pfam:RhoGEF
|
82 |
187 |
1.2e-21 |
PFAM |
low complexity region
|
194 |
211 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000193040
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000162599
AA Change: Q571R
PolyPhen 2
Score 0.831 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000124906 Gene: ENSMUSG00000037509 AA Change: Q571R
Domain | Start | End | E-Value | Type |
low complexity region
|
73 |
87 |
N/A |
INTRINSIC |
SH3
|
194 |
249 |
3.73e-16 |
SMART |
Pfam:RhoGEF
|
304 |
405 |
1.2e-25 |
PFAM |
PH
|
438 |
546 |
2.33e-14 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162760
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000167518
|
SMART Domains |
Protein: ENSMUSP00000131720 Gene: ENSMUSG00000037503
Domain | Start | End | E-Value | Type |
Pfam:TCRP1
|
1 |
62 |
3.3e-26 |
PFAM |
Pfam:TCRP1
|
54 |
206 |
1.1e-89 |
PFAM |
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.7%
- 20x: 93.3%
|
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 protein encoded by this gene may form complex with G proteins and stimulate Rho-dependent signals. Multiple alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of some variants has not been determined. [provided by RefSeq, Jun 2013] PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased angiogenesis, vascular endothelial cell migration, tumor growth, and tumor vascularization. [provided by MGI curators]
|
Allele List at MGI |
All alleles(1) : Targeted, other(1) |
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,773,031 (GRCm39) |
E740G |
probably damaging |
Het |
4930474N05Rik |
G |
T |
14: 35,817,414 (GRCm39) |
V105F |
possibly damaging |
Het |
Actr10 |
A |
G |
12: 70,989,104 (GRCm39) |
I74M |
probably benign |
Het |
Aen |
T |
C |
7: 78,555,660 (GRCm39) |
Y108H |
probably damaging |
Het |
Afm |
A |
T |
5: 90,672,779 (GRCm39) |
K205* |
probably null |
Het |
Ankrd27 |
T |
A |
7: 35,332,410 (GRCm39) |
S846T |
probably benign |
Het |
Ano3 |
A |
G |
2: 110,715,352 (GRCm39) |
S29P |
probably benign |
Het |
Apaf1 |
C |
T |
10: 90,913,476 (GRCm39) |
W138* |
probably null |
Het |
Arfgef1 |
C |
T |
1: 10,270,103 (GRCm39) |
A349T |
probably benign |
Het |
Astn1 |
G |
A |
1: 158,337,541 (GRCm39) |
V416I |
probably damaging |
Het |
Atxn2l |
G |
A |
7: 126,092,340 (GRCm39) |
T70I |
probably damaging |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,061,132 (GRCm39) |
|
probably null |
Het |
Bspry |
T |
A |
4: 62,413,034 (GRCm39) |
C256S |
probably damaging |
Het |
C3 |
C |
A |
17: 57,527,135 (GRCm39) |
W771C |
probably damaging |
Het |
Camkv |
A |
G |
9: 107,824,287 (GRCm39) |
D233G |
possibly damaging |
Het |
Catsperd |
T |
A |
17: 56,942,548 (GRCm39) |
V109E |
probably damaging |
Het |
Cd101 |
A |
G |
3: 100,926,233 (GRCm39) |
L162P |
probably damaging |
Het |
Cdr2l |
A |
G |
11: 115,283,603 (GRCm39) |
T154A |
probably damaging |
Het |
Clca3a2 |
G |
C |
3: 144,516,457 (GRCm39) |
Q380E |
probably benign |
Het |
Col6a3 |
T |
C |
1: 90,750,081 (GRCm39) |
N251S |
possibly damaging |
Het |
Cttnbp2nl |
A |
G |
3: 104,918,594 (GRCm39) |
V82A |
possibly damaging |
Het |
Cux1 |
G |
A |
5: 136,392,173 (GRCm39) |
Q194* |
probably null |
Het |
Daam2 |
T |
C |
17: 49,792,485 (GRCm39) |
E361G |
probably benign |
Het |
Dcaf17 |
A |
T |
2: 70,908,516 (GRCm39) |
|
probably null |
Het |
Dnai1 |
T |
C |
4: 41,570,020 (GRCm39) |
|
probably null |
Het |
Eml5 |
T |
C |
12: 98,765,098 (GRCm39) |
Y1617C |
probably damaging |
Het |
Epb41l4b |
T |
C |
4: 57,040,993 (GRCm39) |
E490G |
probably damaging |
Het |
Epha7 |
T |
C |
4: 28,963,969 (GRCm39) |
M988T |
possibly damaging |
Het |
Fancm |
T |
C |
12: 65,152,294 (GRCm39) |
C917R |
possibly damaging |
Het |
Fnip1 |
C |
T |
11: 54,371,510 (GRCm39) |
T177I |
probably damaging |
Het |
Gm3604 |
G |
T |
13: 62,517,756 (GRCm39) |
H201N |
probably benign |
Het |
Gnpda1 |
T |
C |
18: 38,466,243 (GRCm39) |
|
probably null |
Het |
Gpatch8 |
A |
G |
11: 102,398,968 (GRCm39) |
|
probably null |
Het |
H2-M3 |
T |
C |
17: 37,582,080 (GRCm39) |
Y179H |
possibly damaging |
Het |
H2-Q10 |
C |
A |
17: 35,781,385 (GRCm39) |
S62R |
probably damaging |
Het |
Hipk2 |
G |
A |
6: 38,795,919 (GRCm39) |
R117* |
probably null |
Het |
Hrg |
A |
T |
16: 22,773,207 (GRCm39) |
Q113H |
probably damaging |
Het |
Kcnj16 |
T |
C |
11: 110,915,779 (GRCm39) |
V147A |
possibly damaging |
Het |
Kif1a |
T |
C |
1: 92,946,753 (GRCm39) |
I1650V |
possibly damaging |
Het |
Kmt2a |
C |
T |
9: 44,731,642 (GRCm39) |
|
probably benign |
Het |
Krt90 |
A |
T |
15: 101,465,665 (GRCm39) |
Y319N |
probably damaging |
Het |
Lipo4 |
T |
C |
19: 33,476,671 (GRCm39) |
N359S |
possibly damaging |
Het |
Lrp1b |
G |
T |
2: 41,618,741 (GRCm39) |
T225K |
probably benign |
Het |
Map1a |
C |
T |
2: 121,137,493 (GRCm39) |
P2532S |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,119,600 (GRCm39) |
D193G |
probably benign |
Het |
Mpped2 |
T |
A |
2: 106,697,377 (GRCm39) |
I284N |
probably damaging |
Het |
Msh6 |
A |
G |
17: 88,292,553 (GRCm39) |
H436R |
probably benign |
Het |
Mterf3 |
A |
T |
13: 67,078,126 (GRCm39) |
S48T |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,399,768 (GRCm39) |
F414L |
unknown |
Het |
Mylk4 |
A |
T |
13: 32,908,836 (GRCm39) |
D90E |
probably benign |
Het |
Nherf4 |
T |
C |
9: 44,161,600 (GRCm39) |
D93G |
possibly damaging |
Het |
Nploc4 |
A |
G |
11: 120,295,055 (GRCm39) |
Y420H |
probably damaging |
Het |
Npr2 |
T |
A |
4: 43,640,578 (GRCm39) |
Y344N |
probably damaging |
Het |
Nsun5 |
A |
G |
5: 135,404,452 (GRCm39) |
T397A |
probably benign |
Het |
Ntsr2 |
A |
T |
12: 16,704,111 (GRCm39) |
Q204L |
probably damaging |
Het |
Nwd2 |
T |
A |
5: 63,963,523 (GRCm39) |
Y1036N |
probably damaging |
Het |
Oacyl |
T |
C |
18: 65,843,618 (GRCm39) |
V105A |
possibly damaging |
Het |
Or6c2 |
T |
A |
10: 129,362,918 (GRCm39) |
V274D |
probably damaging |
Het |
Parp3 |
T |
A |
9: 106,352,316 (GRCm39) |
Q70L |
possibly damaging |
Het |
Parp4 |
T |
C |
14: 56,861,474 (GRCm39) |
S936P |
probably damaging |
Het |
Phkb |
A |
G |
8: 86,648,790 (GRCm39) |
E202G |
probably benign |
Het |
Pink1 |
T |
C |
4: 138,041,331 (GRCm39) |
N530S |
probably benign |
Het |
Pou3f2 |
T |
C |
4: 22,487,119 (GRCm39) |
D338G |
probably damaging |
Het |
Prss8 |
G |
T |
7: 127,529,030 (GRCm39) |
L9I |
probably benign |
Het |
Ptpn22 |
G |
A |
3: 103,784,054 (GRCm39) |
|
probably null |
Het |
Rad54b |
A |
C |
4: 11,601,693 (GRCm39) |
N416T |
probably damaging |
Het |
Rasef |
A |
G |
4: 73,662,351 (GRCm39) |
S200P |
possibly damaging |
Het |
Rb1 |
T |
A |
14: 73,450,430 (GRCm39) |
K645* |
probably null |
Het |
Robo2 |
C |
T |
16: 73,696,042 (GRCm39) |
G1367D |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,422,894 (GRCm39) |
V52A |
probably damaging |
Het |
Samd13 |
T |
C |
3: 146,368,467 (GRCm39) |
T23A |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,530,317 (GRCm39) |
H676R |
probably damaging |
Het |
Serpinb6b |
A |
G |
13: 33,162,223 (GRCm39) |
I222V |
probably benign |
Het |
Slc2a8 |
T |
C |
2: 32,870,091 (GRCm39) |
Y150C |
probably damaging |
Het |
Slc7a6os |
C |
A |
8: 106,937,196 (GRCm39) |
R88L |
probably damaging |
Het |
Slc8a2 |
A |
G |
7: 15,886,845 (GRCm39) |
I657V |
probably benign |
Het |
Slit2 |
C |
A |
5: 48,348,358 (GRCm39) |
|
probably benign |
Het |
Spire2 |
A |
G |
8: 124,089,810 (GRCm39) |
D447G |
probably benign |
Het |
Sptlc3 |
A |
G |
2: 139,408,595 (GRCm39) |
N237D |
possibly damaging |
Het |
Stk3 |
G |
A |
15: 35,073,363 (GRCm39) |
T119I |
probably damaging |
Het |
Suv39h2 |
G |
A |
2: 3,465,353 (GRCm39) |
T334I |
probably damaging |
Het |
Syt5 |
G |
T |
7: 4,543,278 (GRCm39) |
T327N |
probably damaging |
Het |
Tcof1 |
T |
C |
18: 60,949,156 (GRCm39) |
D1253G |
possibly damaging |
Het |
Timd5 |
A |
G |
11: 46,419,358 (GRCm39) |
D58G |
possibly damaging |
Het |
Tnks |
A |
T |
8: 35,342,386 (GRCm39) |
V388D |
probably damaging |
Het |
Ugt2b1 |
T |
C |
5: 87,073,859 (GRCm39) |
T167A |
probably benign |
Het |
Usp40 |
G |
A |
1: 87,923,564 (GRCm39) |
R236C |
possibly damaging |
Het |
Utrn |
T |
C |
10: 12,331,224 (GRCm39) |
D2904G |
probably benign |
Het |
Vmn1r226 |
T |
C |
17: 20,907,842 (GRCm39) |
S25P |
probably damaging |
Het |
Vmn2r23 |
T |
C |
6: 123,689,969 (GRCm39) |
S282P |
possibly damaging |
Het |
Vps45 |
T |
C |
3: 95,953,752 (GRCm39) |
E200G |
probably benign |
Het |
Wnt7b |
T |
A |
15: 85,443,281 (GRCm39) |
I41F |
probably damaging |
Het |
Zmym6 |
T |
A |
4: 126,997,207 (GRCm39) |
N275K |
probably damaging |
Het |
|
Other mutations in Arhgef4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00896:Arhgef4
|
APN |
1 |
34,850,777 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02376:Arhgef4
|
APN |
1 |
34,845,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02604:Arhgef4
|
APN |
1 |
34,850,804 (GRCm39) |
nonsense |
probably null |
|
IGL03240:Arhgef4
|
APN |
1 |
34,845,107 (GRCm39) |
missense |
probably benign |
0.03 |
BB004:Arhgef4
|
UTSW |
1 |
34,846,334 (GRCm39) |
missense |
probably damaging |
1.00 |
BB014:Arhgef4
|
UTSW |
1 |
34,846,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:Arhgef4
|
UTSW |
1 |
34,771,451 (GRCm39) |
nonsense |
probably null |
|
R0157:Arhgef4
|
UTSW |
1 |
34,845,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R0243:Arhgef4
|
UTSW |
1 |
34,846,080 (GRCm39) |
splice site |
probably null |
|
R0383:Arhgef4
|
UTSW |
1 |
34,849,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R0440:Arhgef4
|
UTSW |
1 |
34,784,529 (GRCm39) |
splice site |
probably null |
|
R0452:Arhgef4
|
UTSW |
1 |
34,771,403 (GRCm39) |
missense |
probably damaging |
0.97 |
R0893:Arhgef4
|
UTSW |
1 |
34,846,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1429:Arhgef4
|
UTSW |
1 |
34,849,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Arhgef4
|
UTSW |
1 |
34,763,026 (GRCm39) |
missense |
unknown |
|
R1669:Arhgef4
|
UTSW |
1 |
34,771,239 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1780:Arhgef4
|
UTSW |
1 |
34,763,241 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1809:Arhgef4
|
UTSW |
1 |
34,849,636 (GRCm39) |
critical splice donor site |
probably null |
|
R1879:Arhgef4
|
UTSW |
1 |
34,761,521 (GRCm39) |
missense |
unknown |
|
R1908:Arhgef4
|
UTSW |
1 |
34,763,340 (GRCm39) |
missense |
probably benign |
0.01 |
R2020:Arhgef4
|
UTSW |
1 |
34,762,891 (GRCm39) |
missense |
unknown |
|
R2058:Arhgef4
|
UTSW |
1 |
34,761,458 (GRCm39) |
missense |
unknown |
|
R2213:Arhgef4
|
UTSW |
1 |
34,846,230 (GRCm39) |
splice site |
probably null |
|
R2851:Arhgef4
|
UTSW |
1 |
34,763,129 (GRCm39) |
missense |
unknown |
|
R2852:Arhgef4
|
UTSW |
1 |
34,763,129 (GRCm39) |
missense |
unknown |
|
R2853:Arhgef4
|
UTSW |
1 |
34,763,129 (GRCm39) |
missense |
unknown |
|
R3697:Arhgef4
|
UTSW |
1 |
34,761,521 (GRCm39) |
missense |
unknown |
|
R4012:Arhgef4
|
UTSW |
1 |
34,764,187 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4118:Arhgef4
|
UTSW |
1 |
34,771,428 (GRCm39) |
missense |
probably damaging |
0.98 |
R4133:Arhgef4
|
UTSW |
1 |
34,845,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4534:Arhgef4
|
UTSW |
1 |
34,762,162 (GRCm39) |
missense |
unknown |
|
R4535:Arhgef4
|
UTSW |
1 |
34,762,162 (GRCm39) |
missense |
unknown |
|
R4581:Arhgef4
|
UTSW |
1 |
34,771,205 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4665:Arhgef4
|
UTSW |
1 |
34,845,113 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4678:Arhgef4
|
UTSW |
1 |
34,761,749 (GRCm39) |
missense |
unknown |
|
R4684:Arhgef4
|
UTSW |
1 |
34,850,866 (GRCm39) |
splice site |
probably null |
|
R4706:Arhgef4
|
UTSW |
1 |
34,771,298 (GRCm39) |
missense |
probably benign |
0.00 |
R4745:Arhgef4
|
UTSW |
1 |
34,846,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Arhgef4
|
UTSW |
1 |
34,762,355 (GRCm39) |
missense |
unknown |
|
R4988:Arhgef4
|
UTSW |
1 |
34,762,535 (GRCm39) |
missense |
unknown |
|
R5063:Arhgef4
|
UTSW |
1 |
34,763,296 (GRCm39) |
missense |
probably benign |
0.00 |
R5154:Arhgef4
|
UTSW |
1 |
34,771,455 (GRCm39) |
missense |
probably benign |
0.43 |
R5156:Arhgef4
|
UTSW |
1 |
34,762,355 (GRCm39) |
missense |
unknown |
|
R5263:Arhgef4
|
UTSW |
1 |
34,764,078 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5450:Arhgef4
|
UTSW |
1 |
34,846,405 (GRCm39) |
intron |
probably benign |
|
R5807:Arhgef4
|
UTSW |
1 |
34,846,696 (GRCm39) |
intron |
probably benign |
|
R5863:Arhgef4
|
UTSW |
1 |
34,761,926 (GRCm39) |
missense |
unknown |
|
R6034:Arhgef4
|
UTSW |
1 |
34,760,984 (GRCm39) |
missense |
unknown |
|
R6034:Arhgef4
|
UTSW |
1 |
34,760,984 (GRCm39) |
missense |
unknown |
|
R6311:Arhgef4
|
UTSW |
1 |
34,763,062 (GRCm39) |
missense |
unknown |
|
R6315:Arhgef4
|
UTSW |
1 |
34,762,558 (GRCm39) |
missense |
unknown |
|
R6316:Arhgef4
|
UTSW |
1 |
34,762,558 (GRCm39) |
missense |
unknown |
|
R6318:Arhgef4
|
UTSW |
1 |
34,762,558 (GRCm39) |
missense |
unknown |
|
R6323:Arhgef4
|
UTSW |
1 |
34,762,558 (GRCm39) |
missense |
unknown |
|
R6324:Arhgef4
|
UTSW |
1 |
34,762,558 (GRCm39) |
missense |
unknown |
|
R6325:Arhgef4
|
UTSW |
1 |
34,762,558 (GRCm39) |
missense |
unknown |
|
R6340:Arhgef4
|
UTSW |
1 |
34,771,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6835:Arhgef4
|
UTSW |
1 |
34,845,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R6981:Arhgef4
|
UTSW |
1 |
34,761,533 (GRCm39) |
missense |
unknown |
|
R7087:Arhgef4
|
UTSW |
1 |
34,850,767 (GRCm39) |
missense |
probably damaging |
0.96 |
R7297:Arhgef4
|
UTSW |
1 |
34,846,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R7525:Arhgef4
|
UTSW |
1 |
34,848,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R7614:Arhgef4
|
UTSW |
1 |
34,771,316 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7693:Arhgef4
|
UTSW |
1 |
34,763,222 (GRCm39) |
missense |
probably benign |
0.01 |
R7892:Arhgef4
|
UTSW |
1 |
34,760,885 (GRCm39) |
missense |
unknown |
|
R7895:Arhgef4
|
UTSW |
1 |
34,845,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R7927:Arhgef4
|
UTSW |
1 |
34,846,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Arhgef4
|
UTSW |
1 |
34,850,762 (GRCm39) |
missense |
probably benign |
|
R7973:Arhgef4
|
UTSW |
1 |
34,763,518 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7979:Arhgef4
|
UTSW |
1 |
34,760,978 (GRCm39) |
missense |
unknown |
|
R8160:Arhgef4
|
UTSW |
1 |
34,762,655 (GRCm39) |
missense |
unknown |
|
R8175:Arhgef4
|
UTSW |
1 |
34,849,455 (GRCm39) |
missense |
probably benign |
|
R8178:Arhgef4
|
UTSW |
1 |
34,761,983 (GRCm39) |
missense |
unknown |
|
R9046:Arhgef4
|
UTSW |
1 |
34,850,846 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9077:Arhgef4
|
UTSW |
1 |
34,760,824 (GRCm39) |
missense |
unknown |
|
R9209:Arhgef4
|
UTSW |
1 |
34,849,576 (GRCm39) |
missense |
probably benign |
|
R9209:Arhgef4
|
UTSW |
1 |
34,764,241 (GRCm39) |
critical splice donor site |
probably null |
|
R9355:Arhgef4
|
UTSW |
1 |
34,849,630 (GRCm39) |
missense |
probably benign |
0.02 |
R9489:Arhgef4
|
UTSW |
1 |
34,761,745 (GRCm39) |
missense |
unknown |
|
R9509:Arhgef4
|
UTSW |
1 |
34,762,772 (GRCm39) |
missense |
unknown |
|
R9605:Arhgef4
|
UTSW |
1 |
34,761,745 (GRCm39) |
missense |
unknown |
|
R9665:Arhgef4
|
UTSW |
1 |
34,849,518 (GRCm39) |
missense |
probably benign |
|
R9675:Arhgef4
|
UTSW |
1 |
34,845,108 (GRCm39) |
missense |
probably benign |
|
R9790:Arhgef4
|
UTSW |
1 |
34,832,445 (GRCm39) |
critical splice donor site |
probably null |
|
R9791:Arhgef4
|
UTSW |
1 |
34,832,445 (GRCm39) |
critical splice donor site |
probably null |
|
RF012:Arhgef4
|
UTSW |
1 |
34,763,565 (GRCm39) |
small deletion |
probably benign |
|
X0062:Arhgef4
|
UTSW |
1 |
34,763,308 (GRCm39) |
missense |
probably benign |
0.35 |
YA93:Arhgef4
|
UTSW |
1 |
34,771,298 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Arhgef4
|
UTSW |
1 |
34,844,007 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Arhgef4
|
UTSW |
1 |
34,762,810 (GRCm39) |
missense |
unknown |
|
Z1177:Arhgef4
|
UTSW |
1 |
34,763,340 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Arhgef4
|
UTSW |
1 |
34,762,447 (GRCm39) |
missense |
unknown |
|
Z1177:Arhgef4
|
UTSW |
1 |
34,762,002 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- AGGCTGTCTCAAGCGTGATAG -3'
(R):5'- AAGCTCTAATTCCTGGTGTCTC -3'
Sequencing Primer
(F):5'- CTGTCTCAAGCGTGATAGGAATG -3'
(R):5'- TCTCCTGGAGGTCAGAGAAGTC -3'
|
Posted On |
2014-07-14 |