Incidental Mutation 'R7459:Adgre1'
ID |
578358 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adgre1
|
Ensembl Gene |
ENSMUSG00000004730 |
Gene Name |
adhesion G protein-coupled receptor E1 |
Synonyms |
DD7A5-7, EGF-TM7, Emr1, Ly71, F4/80, TM7LN3 |
MMRRC Submission |
045533-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.190)
|
Stock # |
R7459 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
57665691-57790527 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 57756933 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Glutamic Acid
at position 730
(V730E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000004850
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000004850]
[ENSMUST00000086763]
|
AlphaFold |
Q61549 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000004850
AA Change: V730E
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000004850 Gene: ENSMUSG00000004730 AA Change: V730E
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
32 |
N/A |
INTRINSIC |
EGF
|
35 |
80 |
1.43e-1 |
SMART |
EGF_CA
|
81 |
122 |
3.59e-7 |
SMART |
EGF_CA
|
133 |
172 |
4.56e-9 |
SMART |
EGF_CA
|
173 |
221 |
1.29e-8 |
SMART |
EGF_CA
|
222 |
271 |
2.31e-10 |
SMART |
EGF_CA
|
272 |
318 |
1.06e-9 |
SMART |
EGF_CA
|
319 |
367 |
1.18e-7 |
SMART |
GPS
|
591 |
641 |
2.57e-19 |
SMART |
Pfam:7tm_2
|
644 |
885 |
2.1e-63 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000086763
AA Change: V730E
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000083971 Gene: ENSMUSG00000004730 AA Change: V730E
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
32 |
N/A |
INTRINSIC |
EGF
|
35 |
80 |
1.43e-1 |
SMART |
EGF_CA
|
81 |
122 |
3.59e-7 |
SMART |
EGF_CA
|
133 |
172 |
4.56e-9 |
SMART |
EGF_CA
|
173 |
221 |
1.29e-8 |
SMART |
EGF_CA
|
222 |
271 |
2.31e-10 |
SMART |
EGF_CA
|
272 |
318 |
1.06e-9 |
SMART |
EGF_CA
|
319 |
367 |
1.18e-7 |
SMART |
GPS
|
591 |
641 |
2.57e-19 |
SMART |
Pfam:7tm_2
|
644 |
885 |
2.1e-63 |
PFAM |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that has a domain resembling seven transmembrane G protein-coupled hormone receptors (7TM receptors) at its C-terminus. The N-terminus of the encoded protein has six EGF-like modules, separated from the transmembrane segments by a serine/threonine-rich domain, a feature reminiscent of mucin-like, single-span, integral membrane glycoproteins with adhesive properties. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012] PHENOTYPE: Homozygous null mice fail to develop peripheral tolerance after inoculation with antigen because of a lack of efferent regulatory T cell development. [provided by MGI curators]
|
Allele List at MGI |
All alleles(4) : Targeted(3) Chemically induced(1)
|
Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl1 |
G |
A |
7: 76,069,814 (GRCm39) |
D449N |
not run |
Het |
Agr2 |
A |
T |
12: 36,047,452 (GRCm39) |
E96V |
probably benign |
Het |
Atp1a2 |
A |
C |
1: 172,114,862 (GRCm39) |
S308A |
probably benign |
Het |
Birc7 |
T |
C |
2: 180,571,150 (GRCm39) |
S71P |
possibly damaging |
Het |
Brme1 |
T |
G |
8: 84,893,981 (GRCm39) |
S383A |
probably benign |
Het |
Camk2g |
T |
C |
14: 20,829,275 (GRCm39) |
I73V |
probably damaging |
Het |
Carf |
C |
A |
1: 60,167,198 (GRCm39) |
T177K |
possibly damaging |
Het |
Ccdc191 |
C |
T |
16: 43,767,820 (GRCm39) |
Q665* |
probably null |
Het |
Cd79a |
A |
T |
7: 24,598,567 (GRCm39) |
T39S |
possibly damaging |
Het |
Ces5a |
C |
A |
8: 94,262,369 (GRCm39) |
|
probably benign |
Het |
Dkk2 |
C |
A |
3: 131,880,790 (GRCm39) |
T145N |
probably benign |
Het |
Dot1l |
C |
T |
10: 80,609,007 (GRCm39) |
A188V |
probably damaging |
Het |
Egfr |
T |
A |
11: 16,846,967 (GRCm39) |
V788D |
probably damaging |
Het |
Esyt3 |
T |
A |
9: 99,240,117 (GRCm39) |
H109L |
probably benign |
Het |
Fam234b |
C |
T |
6: 135,188,899 (GRCm39) |
T168I |
probably benign |
Het |
Fan1 |
G |
T |
7: 63,998,714 (GRCm39) |
S936Y |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,194,745 (GRCm39) |
E1098G |
probably damaging |
Het |
Fcgbp |
A |
G |
7: 27,806,710 (GRCm39) |
D2226G |
possibly damaging |
Het |
Flacc1 |
T |
G |
1: 58,730,911 (GRCm39) |
E48D |
possibly damaging |
Het |
Flvcr2 |
T |
C |
12: 85,793,831 (GRCm39) |
V69A |
probably benign |
Het |
Foxb2 |
T |
A |
19: 16,850,436 (GRCm39) |
H190L |
unknown |
Het |
Fut4 |
C |
T |
9: 14,662,602 (GRCm39) |
V231M |
possibly damaging |
Het |
Gtf2a1 |
G |
A |
12: 91,542,426 (GRCm39) |
A91V |
probably benign |
Het |
Hip1 |
A |
G |
5: 135,443,151 (GRCm39) |
S961P |
probably damaging |
Het |
Hsf2bp |
C |
T |
17: 32,165,708 (GRCm39) |
V296M |
probably benign |
Het |
Hspbp1 |
G |
T |
7: 4,687,577 (GRCm39) |
H11Q |
probably benign |
Het |
Ighv1-84 |
C |
T |
12: 115,944,432 (GRCm39) |
E81K |
probably benign |
Het |
Isg20l2 |
T |
C |
3: 87,839,485 (GRCm39) |
L232P |
possibly damaging |
Het |
Isx |
A |
G |
8: 75,619,392 (GRCm39) |
Y181C |
probably benign |
Het |
Kif9 |
A |
G |
9: 110,348,109 (GRCm39) |
Y644C |
probably damaging |
Het |
Lin7c |
T |
A |
2: 109,727,682 (GRCm39) |
V177D |
probably benign |
Het |
Lpin3 |
T |
C |
2: 160,739,220 (GRCm39) |
S343P |
probably benign |
Het |
Mat1a |
A |
T |
14: 40,842,141 (GRCm39) |
Q246L |
probably benign |
Het |
Mlkl |
T |
C |
8: 112,060,162 (GRCm39) |
I75V |
probably benign |
Het |
Ndufa7 |
T |
A |
17: 34,057,140 (GRCm39) |
S107T |
probably damaging |
Het |
Niban3 |
T |
A |
8: 72,057,671 (GRCm39) |
C516S |
possibly damaging |
Het |
Nip7 |
T |
A |
8: 107,783,968 (GRCm39) |
C69* |
probably null |
Het |
Nipa2 |
A |
T |
7: 55,583,089 (GRCm39) |
W219R |
probably damaging |
Het |
Oas2 |
A |
C |
5: 120,887,775 (GRCm39) |
S22A |
unknown |
Het |
Obscn |
A |
G |
11: 59,022,483 (GRCm39) |
V754A |
probably benign |
Het |
Or4a76 |
G |
A |
2: 89,461,012 (GRCm39) |
P77S |
probably damaging |
Het |
Osbpl1a |
C |
T |
18: 13,066,642 (GRCm39) |
C39Y |
probably damaging |
Het |
Pcdhb16 |
A |
T |
18: 37,612,606 (GRCm39) |
Y522F |
probably benign |
Het |
Pced1a |
T |
G |
2: 130,261,744 (GRCm39) |
D303A |
possibly damaging |
Het |
Peli1 |
T |
A |
11: 21,098,190 (GRCm39) |
Y308* |
probably null |
Het |
Pfas |
T |
A |
11: 68,879,481 (GRCm39) |
R243W |
|
Het |
Pik3r5 |
C |
A |
11: 68,383,416 (GRCm39) |
Q412K |
probably benign |
Het |
Pkd1l1 |
A |
T |
11: 8,852,428 (GRCm39) |
I1135N |
|
Het |
Prune1 |
C |
A |
3: 95,189,021 (GRCm39) |
|
probably benign |
Het |
Ptpn4 |
T |
A |
1: 119,587,564 (GRCm39) |
K926N |
probably damaging |
Het |
Ptpre |
A |
G |
7: 135,269,329 (GRCm39) |
N277S |
probably benign |
Het |
Raver2 |
A |
T |
4: 100,964,410 (GRCm39) |
D255V |
possibly damaging |
Het |
Rgs20 |
A |
G |
1: 4,980,857 (GRCm39) |
V187A |
probably benign |
Het |
Rgs3 |
A |
G |
4: 62,543,391 (GRCm39) |
E242G |
probably benign |
Het |
Rims2 |
T |
G |
15: 39,381,235 (GRCm39) |
S1055R |
probably benign |
Het |
Rnf146 |
T |
C |
10: 29,223,640 (GRCm39) |
D82G |
probably benign |
Het |
Rpgrip1 |
A |
G |
14: 52,378,016 (GRCm39) |
S455G |
probably benign |
Het |
Samm50 |
T |
C |
15: 84,080,057 (GRCm39) |
|
probably null |
Het |
Sh3bgr |
A |
G |
16: 96,007,122 (GRCm39) |
K31E |
probably benign |
Het |
Slc39a8 |
T |
C |
3: 135,592,672 (GRCm39) |
I449T |
probably damaging |
Het |
Slc5a3 |
A |
T |
16: 91,875,905 (GRCm39) |
Y654F |
probably benign |
Het |
Spata1 |
T |
A |
3: 146,181,977 (GRCm39) |
L264F |
possibly damaging |
Het |
Spats2l |
A |
T |
1: 57,838,512 (GRCm39) |
|
probably benign |
Het |
Stard13 |
A |
C |
5: 150,971,064 (GRCm39) |
S848A |
probably damaging |
Het |
Stat2 |
A |
G |
10: 128,112,434 (GRCm39) |
S25G |
possibly damaging |
Het |
Tet2 |
C |
T |
3: 133,186,050 (GRCm39) |
R1129Q |
possibly damaging |
Het |
Tmem232 |
T |
C |
17: 65,563,384 (GRCm39) |
T670A |
probably benign |
Het |
Tmem266 |
T |
C |
9: 55,303,883 (GRCm39) |
L3P |
unknown |
Het |
Tns3 |
A |
T |
11: 8,442,793 (GRCm39) |
D523E |
probably benign |
Het |
Trim3 |
A |
T |
7: 105,267,015 (GRCm39) |
S455T |
probably damaging |
Het |
Trim31 |
T |
C |
17: 37,220,554 (GRCm39) |
V490A |
probably damaging |
Het |
Trmt11 |
A |
C |
10: 30,466,039 (GRCm39) |
N168K |
probably benign |
Het |
Trpc4 |
G |
A |
3: 54,198,653 (GRCm39) |
V526M |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,749,482 (GRCm39) |
D3856Y |
possibly damaging |
Het |
Tulp2 |
G |
A |
7: 45,169,227 (GRCm39) |
D377N |
probably damaging |
Het |
Ubl7 |
A |
G |
9: 57,821,875 (GRCm39) |
T75A |
probably damaging |
Het |
Ugt2b34 |
T |
G |
5: 87,049,134 (GRCm39) |
D297A |
possibly damaging |
Het |
Usp34 |
A |
T |
11: 23,314,458 (GRCm39) |
H800L |
possibly damaging |
Het |
Utp3 |
C |
A |
5: 88,703,412 (GRCm39) |
L314M |
probably damaging |
Het |
Zer1 |
A |
G |
2: 30,003,337 (GRCm39) |
Y27H |
probably damaging |
Het |
|
Other mutations in Adgre1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Adgre1
|
APN |
17 |
57,757,055 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00966:Adgre1
|
APN |
17 |
57,726,335 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01680:Adgre1
|
APN |
17 |
57,709,620 (GRCm39) |
missense |
unknown |
|
IGL01724:Adgre1
|
APN |
17 |
57,751,064 (GRCm39) |
nonsense |
probably null |
|
IGL02172:Adgre1
|
APN |
17 |
57,785,879 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02260:Adgre1
|
APN |
17 |
57,754,891 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02272:Adgre1
|
APN |
17 |
57,757,021 (GRCm39) |
nonsense |
probably null |
|
IGL02336:Adgre1
|
APN |
17 |
57,718,024 (GRCm39) |
nonsense |
probably null |
|
IGL02346:Adgre1
|
APN |
17 |
57,750,919 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02398:Adgre1
|
APN |
17 |
57,709,824 (GRCm39) |
nonsense |
probably null |
|
IGL02618:Adgre1
|
APN |
17 |
57,751,021 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02690:Adgre1
|
APN |
17 |
57,787,921 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02936:Adgre1
|
APN |
17 |
57,785,833 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03112:Adgre1
|
APN |
17 |
57,755,029 (GRCm39) |
splice site |
probably null |
|
IGL03350:Adgre1
|
APN |
17 |
57,708,908 (GRCm39) |
missense |
probably benign |
0.16 |
F480
|
UTSW |
17 |
57,751,063 (GRCm39) |
missense |
probably damaging |
1.00 |
lomax
|
UTSW |
17 |
57,709,811 (GRCm39) |
missense |
unknown |
|
Onion
|
UTSW |
17 |
57,709,841 (GRCm39) |
nonsense |
probably null |
|
Scallion
|
UTSW |
17 |
57,708,977 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0049:Adgre1
|
UTSW |
17 |
57,709,841 (GRCm39) |
nonsense |
probably null |
|
R0153:Adgre1
|
UTSW |
17 |
57,750,939 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0277:Adgre1
|
UTSW |
17 |
57,751,060 (GRCm39) |
missense |
probably benign |
0.00 |
R0278:Adgre1
|
UTSW |
17 |
57,754,872 (GRCm39) |
missense |
probably benign |
0.07 |
R0323:Adgre1
|
UTSW |
17 |
57,751,060 (GRCm39) |
missense |
probably benign |
0.00 |
R0389:Adgre1
|
UTSW |
17 |
57,713,839 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0492:Adgre1
|
UTSW |
17 |
57,709,742 (GRCm39) |
missense |
unknown |
|
R0621:Adgre1
|
UTSW |
17 |
57,748,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R0647:Adgre1
|
UTSW |
17 |
57,718,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1310:Adgre1
|
UTSW |
17 |
57,754,936 (GRCm39) |
missense |
probably benign |
0.00 |
R1601:Adgre1
|
UTSW |
17 |
57,748,353 (GRCm39) |
missense |
probably benign |
0.01 |
R1689:Adgre1
|
UTSW |
17 |
57,756,921 (GRCm39) |
missense |
probably benign |
0.31 |
R1708:Adgre1
|
UTSW |
17 |
57,708,974 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1796:Adgre1
|
UTSW |
17 |
57,748,350 (GRCm39) |
missense |
probably benign |
0.43 |
R1839:Adgre1
|
UTSW |
17 |
57,748,299 (GRCm39) |
missense |
probably benign |
0.00 |
R1860:Adgre1
|
UTSW |
17 |
57,748,363 (GRCm39) |
missense |
probably benign |
0.00 |
R2165:Adgre1
|
UTSW |
17 |
57,726,338 (GRCm39) |
missense |
probably damaging |
0.97 |
R2219:Adgre1
|
UTSW |
17 |
57,708,912 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2519:Adgre1
|
UTSW |
17 |
57,717,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R3874:Adgre1
|
UTSW |
17 |
57,708,925 (GRCm39) |
missense |
probably benign |
0.08 |
R3911:Adgre1
|
UTSW |
17 |
57,754,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R4190:Adgre1
|
UTSW |
17 |
57,709,811 (GRCm39) |
missense |
unknown |
|
R4439:Adgre1
|
UTSW |
17 |
57,754,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R4513:Adgre1
|
UTSW |
17 |
57,717,947 (GRCm39) |
missense |
probably benign |
0.34 |
R4529:Adgre1
|
UTSW |
17 |
57,727,519 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4543:Adgre1
|
UTSW |
17 |
57,713,874 (GRCm39) |
missense |
probably benign |
0.07 |
R4610:Adgre1
|
UTSW |
17 |
57,757,073 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4665:Adgre1
|
UTSW |
17 |
57,787,947 (GRCm39) |
missense |
probably benign |
0.20 |
R4911:Adgre1
|
UTSW |
17 |
57,754,832 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4928:Adgre1
|
UTSW |
17 |
57,751,064 (GRCm39) |
nonsense |
probably null |
|
R4942:Adgre1
|
UTSW |
17 |
57,713,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R4946:Adgre1
|
UTSW |
17 |
57,750,918 (GRCm39) |
missense |
probably benign |
0.33 |
R4953:Adgre1
|
UTSW |
17 |
57,748,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R5107:Adgre1
|
UTSW |
17 |
57,708,977 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5366:Adgre1
|
UTSW |
17 |
57,709,817 (GRCm39) |
missense |
probably benign |
0.39 |
R5590:Adgre1
|
UTSW |
17 |
57,752,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R5619:Adgre1
|
UTSW |
17 |
57,727,437 (GRCm39) |
missense |
probably benign |
0.15 |
R5699:Adgre1
|
UTSW |
17 |
57,788,007 (GRCm39) |
missense |
probably benign |
0.43 |
R5734:Adgre1
|
UTSW |
17 |
57,750,990 (GRCm39) |
missense |
probably benign |
0.00 |
R5860:Adgre1
|
UTSW |
17 |
57,752,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Adgre1
|
UTSW |
17 |
57,713,859 (GRCm39) |
missense |
probably benign |
0.28 |
R6039:Adgre1
|
UTSW |
17 |
57,713,859 (GRCm39) |
missense |
probably benign |
0.28 |
R6149:Adgre1
|
UTSW |
17 |
57,752,018 (GRCm39) |
missense |
probably benign |
0.08 |
R6478:Adgre1
|
UTSW |
17 |
57,708,955 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6709:Adgre1
|
UTSW |
17 |
57,713,917 (GRCm39) |
missense |
probably benign |
0.10 |
R6864:Adgre1
|
UTSW |
17 |
57,785,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R6945:Adgre1
|
UTSW |
17 |
57,727,399 (GRCm39) |
missense |
probably benign |
0.39 |
R6945:Adgre1
|
UTSW |
17 |
57,717,844 (GRCm39) |
missense |
probably benign |
0.01 |
R6988:Adgre1
|
UTSW |
17 |
57,715,445 (GRCm39) |
missense |
probably benign |
0.00 |
R7019:Adgre1
|
UTSW |
17 |
57,717,945 (GRCm39) |
missense |
probably damaging |
0.98 |
R7154:Adgre1
|
UTSW |
17 |
57,751,087 (GRCm39) |
splice site |
probably null |
|
R7347:Adgre1
|
UTSW |
17 |
57,727,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:Adgre1
|
UTSW |
17 |
57,709,519 (GRCm39) |
missense |
unknown |
|
R7939:Adgre1
|
UTSW |
17 |
57,756,938 (GRCm39) |
missense |
probably damaging |
0.98 |
R7977:Adgre1
|
UTSW |
17 |
57,754,987 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7987:Adgre1
|
UTSW |
17 |
57,754,987 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8187:Adgre1
|
UTSW |
17 |
57,727,349 (GRCm39) |
missense |
probably benign |
0.00 |
R8210:Adgre1
|
UTSW |
17 |
57,752,061 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8223:Adgre1
|
UTSW |
17 |
57,668,692 (GRCm39) |
missense |
probably damaging |
0.99 |
R8344:Adgre1
|
UTSW |
17 |
57,715,459 (GRCm39) |
missense |
probably benign |
0.12 |
R8698:Adgre1
|
UTSW |
17 |
57,709,003 (GRCm39) |
missense |
probably benign |
0.05 |
R9236:Adgre1
|
UTSW |
17 |
57,709,782 (GRCm39) |
nonsense |
probably null |
|
R9262:Adgre1
|
UTSW |
17 |
57,754,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R9303:Adgre1
|
UTSW |
17 |
57,748,275 (GRCm39) |
missense |
probably benign |
0.00 |
R9305:Adgre1
|
UTSW |
17 |
57,748,275 (GRCm39) |
missense |
probably benign |
0.00 |
R9605:Adgre1
|
UTSW |
17 |
57,718,083 (GRCm39) |
missense |
probably benign |
0.00 |
R9661:Adgre1
|
UTSW |
17 |
57,748,368 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9678:Adgre1
|
UTSW |
17 |
57,750,997 (GRCm39) |
missense |
probably damaging |
0.96 |
R9751:Adgre1
|
UTSW |
17 |
57,757,101 (GRCm39) |
missense |
probably null |
0.06 |
R9785:Adgre1
|
UTSW |
17 |
57,785,930 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Adgre1
|
UTSW |
17 |
57,668,729 (GRCm39) |
missense |
possibly damaging |
0.76 |
Z1177:Adgre1
|
UTSW |
17 |
57,726,374 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Predicted Primers |
PCR Primer
(F):5'- TCATCCTAGATGGTGAAGGGG -3'
(R):5'- TGACACTCACCGATTATGCATCC -3'
Sequencing Primer
(F):5'- AAGGGGTGACTCCATCATGCTTAG -3'
(R):5'- TCACCGATTATGCATCCCATAG -3'
|
Posted On |
2019-10-07 |