Incidental Mutation 'R7340:Insrr'
ID |
569752 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Insrr
|
Ensembl Gene |
ENSMUSG00000005640 |
Gene Name |
insulin receptor-related receptor |
Synonyms |
|
MMRRC Submission |
045430-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.274)
|
Stock # |
R7340 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
87704258-87723408 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (1 bp from exon) |
DNA Base Change (assembly) |
G to A
at 87721623 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000029711
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029711]
[ENSMUST00000029714]
[ENSMUST00000090981]
[ENSMUST00000107582]
|
AlphaFold |
Q9WTL4 |
Predicted Effect |
probably null
Transcript: ENSMUST00000029711
|
SMART Domains |
Protein: ENSMUSP00000029711 Gene: ENSMUSG00000005640
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:Recep_L_domain
|
47 |
159 |
1.8e-25 |
PFAM |
FU
|
225 |
268 |
9.54e-11 |
SMART |
Pfam:Recep_L_domain
|
346 |
460 |
3.8e-28 |
PFAM |
FN3
|
483 |
586 |
9.19e-1 |
SMART |
FN3
|
605 |
798 |
6.45e-5 |
SMART |
FN3
|
816 |
899 |
6.35e-4 |
SMART |
TyrKc
|
979 |
1246 |
4.61e-128 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000029714
|
SMART Domains |
Protein: ENSMUSP00000029714 Gene: ENSMUSG00000028073
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
low complexity region
|
67 |
78 |
N/A |
INTRINSIC |
EGF
|
102 |
130 |
3.82e-2 |
SMART |
EGF_like
|
132 |
173 |
2.92e1 |
SMART |
EGF_like
|
146 |
185 |
1.92e0 |
SMART |
EGF_like
|
189 |
246 |
1.99e0 |
SMART |
EGF
|
217 |
258 |
1.04e1 |
SMART |
EGF_Lam
|
274 |
313 |
1.21e-4 |
SMART |
EGF
|
312 |
344 |
4.03e-1 |
SMART |
EGF_Lam
|
361 |
402 |
1.33e-1 |
SMART |
EGF
|
401 |
433 |
1.18e-2 |
SMART |
EGF_like
|
449 |
488 |
1.72e0 |
SMART |
EGF
|
487 |
519 |
6.92e0 |
SMART |
EGF_Lam
|
535 |
574 |
2.08e-3 |
SMART |
EGF
|
573 |
605 |
5.49e-3 |
SMART |
EGF_Lam
|
620 |
660 |
1.58e-3 |
SMART |
EGF
|
659 |
691 |
3.1e-2 |
SMART |
EGF
|
702 |
734 |
2.53e1 |
SMART |
transmembrane domain
|
754 |
776 |
N/A |
INTRINSIC |
low complexity region
|
809 |
822 |
N/A |
INTRINSIC |
low complexity region
|
829 |
835 |
N/A |
INTRINSIC |
low complexity region
|
954 |
971 |
N/A |
INTRINSIC |
low complexity region
|
993 |
1002 |
N/A |
INTRINSIC |
low complexity region
|
1019 |
1031 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000090981
|
SMART Domains |
Protein: ENSMUSP00000088503 Gene: ENSMUSG00000028073
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
low complexity region
|
67 |
78 |
N/A |
INTRINSIC |
EGF
|
102 |
130 |
3.82e-2 |
SMART |
EGF_like
|
132 |
173 |
2.92e1 |
SMART |
EGF_like
|
146 |
185 |
1.92e0 |
SMART |
EGF_like
|
189 |
246 |
1.99e0 |
SMART |
EGF
|
217 |
258 |
1.04e1 |
SMART |
EGF_Lam
|
274 |
313 |
1.21e-4 |
SMART |
EGF
|
312 |
344 |
4.03e-1 |
SMART |
EGF_Lam
|
361 |
402 |
1.33e-1 |
SMART |
EGF
|
401 |
433 |
1.18e-2 |
SMART |
EGF_like
|
449 |
488 |
1.72e0 |
SMART |
EGF
|
487 |
519 |
6.92e0 |
SMART |
EGF_Lam
|
535 |
574 |
2.08e-3 |
SMART |
EGF
|
573 |
605 |
5.49e-3 |
SMART |
EGF_Lam
|
620 |
660 |
1.58e-3 |
SMART |
EGF
|
659 |
691 |
3.1e-2 |
SMART |
EGF
|
702 |
734 |
2.53e1 |
SMART |
transmembrane domain
|
754 |
776 |
N/A |
INTRINSIC |
low complexity region
|
809 |
822 |
N/A |
INTRINSIC |
low complexity region
|
829 |
835 |
N/A |
INTRINSIC |
low complexity region
|
954 |
971 |
N/A |
INTRINSIC |
low complexity region
|
993 |
1002 |
N/A |
INTRINSIC |
low complexity region
|
1019 |
1031 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107582
|
SMART Domains |
Protein: ENSMUSP00000103208 Gene: ENSMUSG00000005640
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:Recep_L_domain
|
47 |
159 |
7.7e-25 |
PFAM |
FU
|
225 |
268 |
9.54e-11 |
SMART |
Pfam:Recep_L_domain
|
346 |
460 |
1.6e-28 |
PFAM |
FN3
|
483 |
586 |
9.19e-1 |
SMART |
FN3
|
605 |
798 |
6.45e-5 |
SMART |
FN3
|
816 |
899 |
6.35e-4 |
SMART |
TyrKc
|
979 |
1246 |
4.61e-128 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
99% (83/84) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for a targeted null mutation exhibit no anomalies in pancreatic islet morphology, beta-cell mass or pancreatic secretory function. This mutation in combination with Insr mutant mice does not affect the diabetes predisposition of Insr mutant mice. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
C |
T |
2: 69,130,211 (GRCm39) |
D282N |
probably damaging |
Het |
Adam30 |
A |
T |
3: 98,069,637 (GRCm39) |
N490I |
probably benign |
Het |
Ankrd55 |
A |
T |
13: 112,492,497 (GRCm39) |
I223F |
probably damaging |
Het |
Ano8 |
T |
A |
8: 71,935,655 (GRCm39) |
E321V |
probably damaging |
Het |
Apc2 |
A |
G |
10: 80,149,316 (GRCm39) |
K1457E |
probably benign |
Het |
Asb15 |
T |
A |
6: 24,558,513 (GRCm39) |
V38E |
probably benign |
Het |
Atp4a |
T |
C |
7: 30,416,155 (GRCm39) |
S417P |
possibly damaging |
Het |
AY358078 |
A |
G |
14: 52,063,716 (GRCm39) |
N454S |
probably damaging |
Het |
Cables2 |
A |
G |
2: 179,903,450 (GRCm39) |
Y245H |
|
Het |
Cactin |
CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG |
CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG |
10: 81,157,152 (GRCm39) |
|
probably benign |
Het |
Camsap3 |
G |
A |
8: 3,637,960 (GRCm39) |
|
probably null |
Het |
Ccdc178 |
A |
T |
18: 22,150,518 (GRCm39) |
V705E |
probably benign |
Het |
Ccdc47 |
T |
C |
11: 106,091,799 (GRCm39) |
Q472R |
possibly damaging |
Het |
Ccdc62 |
A |
G |
5: 124,089,283 (GRCm39) |
D307G |
probably damaging |
Het |
Cdcp3 |
A |
G |
7: 130,879,344 (GRCm39) |
T1788A |
unknown |
Het |
Cdh23 |
A |
G |
10: 60,366,775 (GRCm39) |
I235T |
probably benign |
Het |
Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
Cfap65 |
T |
C |
1: 74,960,742 (GRCm39) |
N743D |
probably benign |
Het |
Cimap1b |
T |
A |
15: 89,262,610 (GRCm39) |
T116S |
probably benign |
Het |
Clec16a |
A |
G |
16: 10,398,827 (GRCm39) |
N329S |
probably null |
Het |
Col25a1 |
A |
G |
3: 130,340,006 (GRCm39) |
|
probably null |
Het |
Daam1 |
T |
G |
12: 72,035,713 (GRCm39) |
D969E |
probably benign |
Het |
Dntt |
A |
C |
19: 41,047,004 (GRCm39) |
|
probably null |
Het |
Dsel |
C |
T |
1: 111,789,303 (GRCm39) |
G411S |
probably damaging |
Het |
Dst |
T |
A |
1: 34,229,810 (GRCm39) |
Y2468N |
probably benign |
Het |
Exosc9 |
A |
G |
3: 36,615,297 (GRCm39) |
T262A |
possibly damaging |
Het |
Exph5 |
G |
A |
9: 53,288,309 (GRCm39) |
A1797T |
probably damaging |
Het |
Fbp2 |
A |
T |
13: 62,985,061 (GRCm39) |
Y287N |
probably damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Fus |
T |
A |
7: 127,581,123 (GRCm39) |
|
probably null |
Het |
Galnt9 |
T |
A |
5: 110,762,054 (GRCm39) |
N397K |
probably damaging |
Het |
Gdi1 |
G |
A |
X: 73,350,461 (GRCm39) |
R55H |
probably benign |
Het |
Gga1 |
A |
G |
15: 78,775,651 (GRCm39) |
T369A |
probably benign |
Het |
Gp1ba |
T |
C |
11: 70,531,119 (GRCm39) |
I295T |
unknown |
Het |
Hk2 |
T |
C |
6: 82,705,873 (GRCm39) |
E810G |
probably benign |
Het |
Igsf10 |
A |
G |
3: 59,233,189 (GRCm39) |
V1848A |
probably damaging |
Het |
Ip6k3 |
T |
A |
17: 27,367,504 (GRCm39) |
M231L |
probably benign |
Het |
Itgb8 |
T |
C |
12: 119,155,939 (GRCm39) |
N171S |
probably benign |
Het |
Ldlrad3 |
T |
C |
2: 101,897,184 (GRCm39) |
|
probably null |
Het |
Ltbp1 |
T |
A |
17: 75,634,223 (GRCm39) |
C886* |
probably null |
Het |
Mettl13 |
T |
C |
1: 162,366,547 (GRCm39) |
D444G |
probably benign |
Het |
Mns1 |
A |
G |
9: 72,356,025 (GRCm39) |
Y224C |
probably damaging |
Het |
Mri1 |
C |
T |
8: 84,983,525 (GRCm39) |
R122Q |
probably benign |
Het |
Ms4a6d |
G |
A |
19: 11,567,437 (GRCm39) |
Q155* |
probably null |
Het |
Myo5c |
A |
C |
9: 75,196,423 (GRCm39) |
K1290Q |
probably benign |
Het |
Nlrp12 |
T |
G |
7: 3,281,755 (GRCm39) |
Q842H |
possibly damaging |
Het |
Oga |
G |
A |
19: 45,755,895 (GRCm39) |
Q583* |
probably null |
Het |
Or14c44 |
T |
C |
7: 86,061,957 (GRCm39) |
L129P |
possibly damaging |
Het |
Or14j8 |
T |
A |
17: 38,263,413 (GRCm39) |
R167S |
probably benign |
Het |
Or2t1 |
A |
T |
14: 14,328,401 (GRCm38) |
T97S |
possibly damaging |
Het |
Or5d39 |
T |
C |
2: 87,979,620 (GRCm39) |
T248A |
possibly damaging |
Het |
Otoa |
A |
G |
7: 120,729,288 (GRCm39) |
T554A |
probably benign |
Het |
Per1 |
A |
G |
11: 68,994,008 (GRCm39) |
D438G |
probably damaging |
Het |
Phactr3 |
G |
A |
2: 177,975,854 (GRCm39) |
R533H |
probably damaging |
Het |
Phykpl |
T |
C |
11: 51,490,370 (GRCm39) |
F417S |
probably damaging |
Het |
Pole |
A |
T |
5: 110,482,330 (GRCm39) |
T2057S |
probably benign |
Het |
Polq |
A |
G |
16: 36,881,288 (GRCm39) |
T1151A |
probably benign |
Het |
Polr1g |
T |
C |
7: 19,093,073 (GRCm39) |
T36A |
probably benign |
Het |
Rbm26 |
A |
T |
14: 105,389,976 (GRCm39) |
V216E |
possibly damaging |
Het |
Ryk |
T |
C |
9: 102,775,737 (GRCm39) |
I449T |
probably damaging |
Het |
Sap25 |
A |
G |
5: 137,640,935 (GRCm39) |
T225A |
probably benign |
Het |
Sart3 |
A |
G |
5: 113,882,728 (GRCm39) |
M864T |
probably benign |
Het |
Sec31b |
T |
C |
19: 44,517,161 (GRCm39) |
S280G |
probably benign |
Het |
Sema4d |
A |
T |
13: 51,877,598 (GRCm39) |
I78N |
probably damaging |
Het |
Sgip1 |
G |
C |
4: 102,778,661 (GRCm39) |
R419S |
unknown |
Het |
Slc13a3 |
T |
C |
2: 165,272,210 (GRCm39) |
I278V |
probably benign |
Het |
Slc2a5 |
A |
G |
4: 150,224,439 (GRCm39) |
D312G |
probably benign |
Het |
Slc39a2 |
A |
T |
14: 52,131,660 (GRCm39) |
Q77L |
possibly damaging |
Het |
Srbd1 |
A |
T |
17: 86,443,782 (GRCm39) |
V148E |
probably benign |
Het |
Syngr2 |
A |
G |
11: 117,703,322 (GRCm39) |
E46G |
probably damaging |
Het |
Taok1 |
A |
G |
11: 77,470,643 (GRCm39) |
V54A |
possibly damaging |
Het |
Tas2r106 |
T |
A |
6: 131,655,185 (GRCm39) |
H222L |
probably damaging |
Het |
Tcaf3 |
A |
G |
6: 42,566,848 (GRCm39) |
I747T |
probably benign |
Het |
Tmem151b |
G |
T |
17: 45,856,195 (GRCm39) |
P415Q |
probably benign |
Het |
Tmf1 |
T |
C |
6: 97,145,061 (GRCm39) |
D659G |
possibly damaging |
Het |
Tnn |
G |
T |
1: 159,973,592 (GRCm39) |
D258E |
probably damaging |
Het |
Traj33 |
A |
G |
14: 54,422,862 (GRCm39) |
I16V |
unknown |
Het |
Ttll13 |
G |
T |
7: 79,906,772 (GRCm39) |
C480F |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,714,415 (GRCm39) |
N8137S |
unknown |
Het |
Vmn1r85 |
T |
C |
7: 12,819,073 (GRCm39) |
N24D |
probably damaging |
Het |
Wdr81 |
T |
C |
11: 75,335,525 (GRCm39) |
Q649R |
probably null |
Het |
Zan |
T |
C |
5: 137,382,092 (GRCm39) |
T5152A |
unknown |
Het |
Zc3h6 |
A |
G |
2: 128,835,110 (GRCm39) |
D82G |
possibly damaging |
Het |
|
Other mutations in Insrr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00718:Insrr
|
APN |
3 |
87,720,981 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00801:Insrr
|
APN |
3 |
87,721,115 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01628:Insrr
|
APN |
3 |
87,708,099 (GRCm39) |
nonsense |
probably null |
|
IGL01755:Insrr
|
APN |
3 |
87,721,493 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02100:Insrr
|
APN |
3 |
87,718,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02261:Insrr
|
APN |
3 |
87,708,029 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02366:Insrr
|
APN |
3 |
87,717,216 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02387:Insrr
|
APN |
3 |
87,720,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02478:Insrr
|
APN |
3 |
87,716,719 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02550:Insrr
|
APN |
3 |
87,711,805 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02555:Insrr
|
APN |
3 |
87,721,124 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02673:Insrr
|
APN |
3 |
87,720,368 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02724:Insrr
|
APN |
3 |
87,716,879 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02798:Insrr
|
APN |
3 |
87,717,824 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02969:Insrr
|
APN |
3 |
87,721,498 (GRCm39) |
nonsense |
probably null |
|
IGL03073:Insrr
|
APN |
3 |
87,717,245 (GRCm39) |
splice site |
probably benign |
|
IGL03178:Insrr
|
APN |
3 |
87,709,848 (GRCm39) |
splice site |
probably null |
|
IGL03389:Insrr
|
APN |
3 |
87,716,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03399:Insrr
|
APN |
3 |
87,716,638 (GRCm39) |
missense |
probably null |
0.99 |
IGL02799:Insrr
|
UTSW |
3 |
87,720,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Insrr
|
UTSW |
3 |
87,716,923 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0053:Insrr
|
UTSW |
3 |
87,707,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Insrr
|
UTSW |
3 |
87,707,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0357:Insrr
|
UTSW |
3 |
87,715,953 (GRCm39) |
splice site |
probably null |
|
R0501:Insrr
|
UTSW |
3 |
87,717,991 (GRCm39) |
missense |
probably benign |
0.12 |
R0504:Insrr
|
UTSW |
3 |
87,720,463 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0522:Insrr
|
UTSW |
3 |
87,708,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Insrr
|
UTSW |
3 |
87,721,744 (GRCm39) |
splice site |
probably benign |
|
R0558:Insrr
|
UTSW |
3 |
87,718,288 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0599:Insrr
|
UTSW |
3 |
87,720,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R1312:Insrr
|
UTSW |
3 |
87,707,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Insrr
|
UTSW |
3 |
87,711,369 (GRCm39) |
missense |
probably benign |
|
R1785:Insrr
|
UTSW |
3 |
87,717,879 (GRCm39) |
splice site |
probably null |
|
R1786:Insrr
|
UTSW |
3 |
87,717,879 (GRCm39) |
splice site |
probably null |
|
R1892:Insrr
|
UTSW |
3 |
87,721,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Insrr
|
UTSW |
3 |
87,721,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Insrr
|
UTSW |
3 |
87,721,598 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2094:Insrr
|
UTSW |
3 |
87,710,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Insrr
|
UTSW |
3 |
87,717,879 (GRCm39) |
splice site |
probably null |
|
R2131:Insrr
|
UTSW |
3 |
87,717,879 (GRCm39) |
splice site |
probably null |
|
R2133:Insrr
|
UTSW |
3 |
87,717,879 (GRCm39) |
splice site |
probably null |
|
R2220:Insrr
|
UTSW |
3 |
87,716,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R2259:Insrr
|
UTSW |
3 |
87,707,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R2404:Insrr
|
UTSW |
3 |
87,709,974 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4027:Insrr
|
UTSW |
3 |
87,716,906 (GRCm39) |
missense |
probably benign |
|
R4042:Insrr
|
UTSW |
3 |
87,721,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Insrr
|
UTSW |
3 |
87,715,978 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4511:Insrr
|
UTSW |
3 |
87,715,978 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4571:Insrr
|
UTSW |
3 |
87,708,194 (GRCm39) |
missense |
probably benign |
|
R4870:Insrr
|
UTSW |
3 |
87,718,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Insrr
|
UTSW |
3 |
87,722,572 (GRCm39) |
missense |
probably benign |
0.00 |
R5393:Insrr
|
UTSW |
3 |
87,718,007 (GRCm39) |
splice site |
probably null |
|
R5685:Insrr
|
UTSW |
3 |
87,707,803 (GRCm39) |
splice site |
probably null |
|
R6039:Insrr
|
UTSW |
3 |
87,716,608 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6039:Insrr
|
UTSW |
3 |
87,716,608 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6047:Insrr
|
UTSW |
3 |
87,711,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Insrr
|
UTSW |
3 |
87,707,826 (GRCm39) |
nonsense |
probably null |
|
R6298:Insrr
|
UTSW |
3 |
87,720,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R6726:Insrr
|
UTSW |
3 |
87,720,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R6727:Insrr
|
UTSW |
3 |
87,720,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R6728:Insrr
|
UTSW |
3 |
87,720,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Insrr
|
UTSW |
3 |
87,720,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R7041:Insrr
|
UTSW |
3 |
87,722,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R7169:Insrr
|
UTSW |
3 |
87,715,901 (GRCm39) |
missense |
probably benign |
0.15 |
R7270:Insrr
|
UTSW |
3 |
87,710,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R7398:Insrr
|
UTSW |
3 |
87,716,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R7473:Insrr
|
UTSW |
3 |
87,711,838 (GRCm39) |
splice site |
probably null |
|
R7815:Insrr
|
UTSW |
3 |
87,716,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R8159:Insrr
|
UTSW |
3 |
87,707,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R8289:Insrr
|
UTSW |
3 |
87,721,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R8309:Insrr
|
UTSW |
3 |
87,717,749 (GRCm39) |
missense |
probably benign |
0.00 |
R8312:Insrr
|
UTSW |
3 |
87,707,791 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8445:Insrr
|
UTSW |
3 |
87,720,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R8917:Insrr
|
UTSW |
3 |
87,718,276 (GRCm39) |
missense |
probably benign |
0.00 |
R8960:Insrr
|
UTSW |
3 |
87,720,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R8989:Insrr
|
UTSW |
3 |
87,722,664 (GRCm39) |
missense |
probably damaging |
0.96 |
R9015:Insrr
|
UTSW |
3 |
87,720,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R9202:Insrr
|
UTSW |
3 |
87,720,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R9251:Insrr
|
UTSW |
3 |
87,717,391 (GRCm39) |
missense |
probably benign |
0.08 |
R9327:Insrr
|
UTSW |
3 |
87,721,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9646:Insrr
|
UTSW |
3 |
87,721,805 (GRCm39) |
missense |
probably damaging |
1.00 |
RF022:Insrr
|
UTSW |
3 |
87,711,792 (GRCm39) |
missense |
possibly damaging |
0.51 |
Z1177:Insrr
|
UTSW |
3 |
87,708,134 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1192:Insrr
|
UTSW |
3 |
87,709,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGACTGTCTTCCAGGGAAAC -3'
(R):5'- TGACAAATTTCAGCACCTGC -3'
Sequencing Primer
(F):5'- GGGAAACTAACTTATGACTTCCCTG -3'
(R):5'- TGCTCATTTGATAGACCCTGG -3'
|
Posted On |
2019-09-13 |