Incidental Mutation 'R0389:Adgre1'
ID |
31541 |
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 |
038595-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.190)
|
Stock # |
R0389 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
57665691-57790527 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 57713839 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Asparagine
at position 175
(D175N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000083971
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000004850]
[ENSMUST00000086763]
|
AlphaFold |
Q61549 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000004850
AA Change: D175N
PolyPhen 2
Score 0.798 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000004850 Gene: ENSMUSG00000004730 AA Change: D175N
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 |
possibly damaging
Transcript: ENSMUST00000086763
AA Change: D175N
PolyPhen 2
Score 0.798 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000083971 Gene: ENSMUSG00000004730 AA Change: D175N
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: 99.1%
- 3x: 98.1%
- 10x: 95.9%
- 20x: 91.5%
|
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: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432M17Rik |
G |
A |
3: 121,465,053 (GRCm39) |
E30K |
unknown |
Het |
Abi3bp |
A |
T |
16: 56,491,670 (GRCm39) |
T1319S |
possibly damaging |
Het |
Adam18 |
T |
C |
8: 25,119,653 (GRCm39) |
|
probably null |
Het |
Adgrf1 |
T |
C |
17: 43,614,679 (GRCm39) |
|
probably null |
Het |
Ankhd1 |
A |
G |
18: 36,777,652 (GRCm39) |
S1612G |
possibly damaging |
Het |
Anks1 |
A |
G |
17: 28,214,926 (GRCm39) |
R458G |
possibly damaging |
Het |
Cacna1g |
C |
T |
11: 94,350,523 (GRCm39) |
V441M |
probably damaging |
Het |
Cadps2 |
A |
T |
6: 23,321,781 (GRCm39) |
V1037E |
possibly damaging |
Het |
Casz1 |
T |
C |
4: 149,033,368 (GRCm39) |
V1380A |
possibly damaging |
Het |
Cenpq |
T |
C |
17: 41,244,085 (GRCm39) |
|
probably benign |
Het |
Chrac1 |
T |
C |
15: 72,965,376 (GRCm39) |
I93T |
possibly damaging |
Het |
Cntnap2 |
T |
A |
6: 45,986,571 (GRCm39) |
S359T |
probably benign |
Het |
Col6a6 |
C |
A |
9: 105,661,403 (GRCm39) |
M235I |
probably benign |
Het |
Crat |
T |
C |
2: 30,293,640 (GRCm39) |
|
probably benign |
Het |
Cyp1a2 |
T |
C |
9: 57,589,308 (GRCm39) |
N169D |
probably benign |
Het |
Dennd1c |
T |
A |
17: 57,374,649 (GRCm39) |
T499S |
probably benign |
Het |
Dst |
A |
G |
1: 34,333,631 (GRCm39) |
|
probably null |
Het |
Dync2h1 |
G |
T |
9: 7,167,244 (GRCm39) |
|
probably null |
Het |
Eif3h |
C |
A |
15: 51,662,660 (GRCm39) |
V129F |
probably damaging |
Het |
Eno2 |
A |
G |
6: 124,739,654 (GRCm39) |
F380L |
probably damaging |
Het |
Ergic2 |
T |
A |
6: 148,084,700 (GRCm39) |
I34F |
probably benign |
Het |
Ergic3 |
G |
A |
2: 155,858,707 (GRCm39) |
V278M |
probably benign |
Het |
Fam185a |
C |
T |
5: 21,664,283 (GRCm39) |
T339M |
probably damaging |
Het |
Fam20b |
A |
T |
1: 156,509,023 (GRCm39) |
D396E |
probably benign |
Het |
Fasn |
G |
T |
11: 120,707,008 (GRCm39) |
D881E |
probably damaging |
Het |
Fat1 |
C |
A |
8: 45,403,385 (GRCm39) |
H45Q |
probably benign |
Het |
Fbxw16 |
A |
T |
9: 109,261,550 (GRCm39) |
C439S |
probably benign |
Het |
Garin1a |
T |
A |
6: 29,281,391 (GRCm39) |
V43E |
possibly damaging |
Het |
Gba2 |
A |
T |
4: 43,570,832 (GRCm39) |
F280Y |
probably damaging |
Het |
Gfm1 |
A |
G |
3: 67,365,251 (GRCm39) |
I517V |
probably benign |
Het |
Gng13 |
C |
T |
17: 25,937,696 (GRCm39) |
Q8* |
probably null |
Het |
Golga1 |
A |
T |
2: 38,908,453 (GRCm39) |
S749T |
probably damaging |
Het |
Gphn |
A |
T |
12: 78,637,433 (GRCm39) |
I381F |
probably damaging |
Het |
Grm3 |
T |
C |
5: 9,554,794 (GRCm39) |
N833D |
probably damaging |
Het |
Gstt2 |
G |
T |
10: 75,668,266 (GRCm39) |
T163K |
probably damaging |
Het |
Gusb |
A |
T |
5: 130,026,927 (GRCm39) |
V388E |
probably damaging |
Het |
Hcrtr2 |
A |
T |
9: 76,153,662 (GRCm39) |
Y243* |
probably null |
Het |
Hspg2 |
A |
G |
4: 137,242,734 (GRCm39) |
T650A |
possibly damaging |
Het |
Ints2 |
C |
T |
11: 86,139,677 (GRCm39) |
V306I |
probably damaging |
Het |
Itga1 |
T |
A |
13: 115,128,996 (GRCm39) |
D554V |
probably benign |
Het |
Itgam |
C |
T |
7: 127,680,806 (GRCm39) |
A245V |
probably damaging |
Het |
Kcnk15 |
A |
G |
2: 163,700,243 (GRCm39) |
T161A |
probably benign |
Het |
Klhl18 |
A |
T |
9: 110,257,749 (GRCm39) |
C564S |
probably benign |
Het |
Krt40 |
T |
A |
11: 99,432,540 (GRCm39) |
R159* |
probably null |
Het |
L3mbtl4 |
G |
A |
17: 68,762,775 (GRCm39) |
V103M |
probably damaging |
Het |
Lnx2 |
C |
A |
5: 146,955,850 (GRCm39) |
V649L |
possibly damaging |
Het |
Lpp |
A |
T |
16: 24,426,991 (GRCm39) |
Q39H |
probably damaging |
Het |
Lrpprc |
A |
T |
17: 85,060,540 (GRCm39) |
|
probably null |
Het |
Map3k19 |
A |
T |
1: 127,750,152 (GRCm39) |
N1066K |
probably benign |
Het |
Mbtps2 |
G |
T |
X: 156,351,364 (GRCm39) |
T134K |
probably benign |
Het |
Mfng |
C |
T |
15: 78,648,637 (GRCm39) |
V147M |
possibly damaging |
Het |
Mks1 |
T |
C |
11: 87,748,754 (GRCm39) |
S273P |
probably benign |
Het |
Myh2 |
T |
C |
11: 67,071,647 (GRCm39) |
L488P |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,369,364 (GRCm39) |
N708S |
probably benign |
Het |
Myo6 |
A |
T |
9: 80,199,748 (GRCm39) |
N1019I |
probably damaging |
Het |
Myrf |
G |
C |
19: 10,195,526 (GRCm39) |
T428S |
probably benign |
Het |
Ncoa1 |
T |
G |
12: 4,345,976 (GRCm39) |
N457T |
probably benign |
Het |
Neb |
T |
C |
2: 52,051,489 (GRCm39) |
|
probably null |
Het |
Nlrp4e |
C |
A |
7: 23,054,628 (GRCm39) |
N927K |
probably damaging |
Het |
Npffr2 |
T |
C |
5: 89,730,613 (GRCm39) |
M181T |
probably benign |
Het |
Nxf7 |
A |
T |
X: 134,485,132 (GRCm39) |
C495S |
possibly damaging |
Het |
Oas1g |
T |
C |
5: 121,025,592 (GRCm39) |
T12A |
probably benign |
Het |
Or11g2 |
T |
A |
14: 50,856,036 (GRCm39) |
L119Q |
probably damaging |
Het |
Or1e17 |
T |
A |
11: 73,831,879 (GRCm39) |
V269E |
probably benign |
Het |
Or2g7 |
C |
G |
17: 38,378,562 (GRCm39) |
R167G |
possibly damaging |
Het |
Or52s1b |
A |
T |
7: 102,822,490 (GRCm39) |
V118E |
possibly damaging |
Het |
Or5p60 |
A |
G |
7: 107,724,023 (GRCm39) |
V149A |
probably benign |
Het |
Papln |
C |
T |
12: 83,830,153 (GRCm39) |
Q1008* |
probably null |
Het |
Pcdhb10 |
A |
C |
18: 37,545,485 (GRCm39) |
D187A |
probably damaging |
Het |
Phf2 |
T |
A |
13: 48,957,965 (GRCm39) |
E1016D |
unknown |
Het |
Phf8 |
T |
A |
X: 150,335,618 (GRCm39) |
D197E |
probably benign |
Het |
Pikfyve |
A |
G |
1: 65,235,865 (GRCm39) |
H179R |
probably damaging |
Het |
Prkcz |
T |
A |
4: 155,353,597 (GRCm39) |
D250V |
probably damaging |
Het |
Prpf4 |
A |
G |
4: 62,340,842 (GRCm39) |
Y419C |
probably damaging |
Het |
Prr15l |
C |
A |
11: 96,825,440 (GRCm39) |
Y23* |
probably null |
Het |
Prr5 |
T |
A |
15: 84,587,152 (GRCm39) |
S301T |
probably benign |
Het |
Psg16 |
T |
A |
7: 16,829,088 (GRCm39) |
I224N |
probably benign |
Het |
Radil |
A |
G |
5: 142,529,226 (GRCm39) |
F186L |
probably damaging |
Het |
Reg3g |
A |
T |
6: 78,445,544 (GRCm39) |
M1K |
probably null |
Het |
Rps6ka3 |
A |
G |
X: 158,100,963 (GRCm39) |
Y76C |
probably damaging |
Het |
Rtl1 |
C |
T |
12: 109,556,797 (GRCm39) |
V1681I |
possibly damaging |
Het |
Sfmbt1 |
C |
T |
14: 30,533,464 (GRCm39) |
R614C |
probably damaging |
Het |
Slc12a4 |
A |
G |
8: 106,678,599 (GRCm39) |
S244P |
probably benign |
Het |
Sp140l2 |
T |
A |
1: 85,247,773 (GRCm39) |
N5Y |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,089,250 (GRCm39) |
T671A |
possibly damaging |
Het |
Supt16 |
A |
T |
14: 52,411,570 (GRCm39) |
N604K |
probably damaging |
Het |
Synj2 |
G |
A |
17: 6,080,058 (GRCm39) |
V1096I |
probably benign |
Het |
Tas2r129 |
G |
T |
6: 132,928,159 (GRCm39) |
C32F |
probably benign |
Het |
Tbc1d25 |
T |
C |
X: 8,039,108 (GRCm39) |
Y140C |
probably damaging |
Het |
Tdrd7 |
A |
G |
4: 46,016,987 (GRCm39) |
D709G |
probably benign |
Het |
Tfap2d |
C |
T |
1: 19,174,591 (GRCm39) |
R15C |
possibly damaging |
Het |
Tgfbi |
C |
A |
13: 56,777,515 (GRCm39) |
T333N |
probably benign |
Het |
Tnk1 |
T |
C |
11: 69,746,508 (GRCm39) |
Y235C |
probably damaging |
Het |
Ttc17 |
A |
G |
2: 94,208,439 (GRCm39) |
F144S |
probably benign |
Het |
Twnk |
G |
T |
19: 44,996,578 (GRCm39) |
G337V |
possibly damaging |
Het |
Unc13a |
A |
G |
8: 72,110,676 (GRCm39) |
F464L |
probably benign |
Het |
Usp17le |
C |
A |
7: 104,417,667 (GRCm39) |
A492S |
probably damaging |
Het |
Vmn1r213 |
A |
T |
13: 23,195,932 (GRCm39) |
M172L |
probably benign |
Het |
Vmn1r71 |
G |
A |
7: 10,482,238 (GRCm39) |
T84I |
probably benign |
Het |
Vmn2r109 |
C |
T |
17: 20,761,336 (GRCm39) |
V674M |
probably damaging |
Het |
Vmn2r19 |
A |
T |
6: 123,312,945 (GRCm39) |
I672F |
possibly damaging |
Het |
Vmn2r77 |
T |
C |
7: 86,450,702 (GRCm39) |
V196A |
probably benign |
Het |
Xdh |
T |
A |
17: 74,205,357 (GRCm39) |
H1036L |
probably damaging |
Het |
Zfp930 |
T |
A |
8: 69,680,948 (GRCm39) |
Y214* |
probably null |
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 |
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 |
R7459:Adgre1
|
UTSW |
17 |
57,756,933 (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 |
|
Posted On |
2013-04-24 |