Incidental Mutation 'R5302:Grip1'
ID |
404305 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Grip1
|
Ensembl Gene |
ENSMUSG00000034813 |
Gene Name |
glutamate receptor interacting protein 1 |
Synonyms |
4931400F03Rik, eb |
MMRRC Submission |
042885-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R5302 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
10 |
Chromosomal Location |
119289810-119923172 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 119855982 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Proline
at position 236
(L236P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000122349
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041962]
[ENSMUST00000077871]
[ENSMUST00000081260]
[ENSMUST00000105261]
[ENSMUST00000105262]
[ENSMUST00000130387]
[ENSMUST00000138410]
[ENSMUST00000144959]
[ENSMUST00000147356]
[ENSMUST00000147454]
[ENSMUST00000148954]
[ENSMUST00000154238]
[ENSMUST00000144825]
|
AlphaFold |
Q925T6 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000041962
AA Change: L600P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000042436 Gene: ENSMUSG00000034813 AA Change: L600P
Domain | Start | End | E-Value | Type |
PDZ
|
63 |
137 |
4.86e-13 |
SMART |
PDZ
|
161 |
239 |
6.4e-22 |
SMART |
PDZ
|
262 |
337 |
1.97e-13 |
SMART |
low complexity region
|
354 |
367 |
N/A |
INTRINSIC |
low complexity region
|
388 |
405 |
N/A |
INTRINSIC |
low complexity region
|
413 |
424 |
N/A |
INTRINSIC |
PDZ
|
429 |
509 |
6.36e-17 |
SMART |
PDZ
|
530 |
606 |
1.11e-16 |
SMART |
PDZ
|
629 |
703 |
1.73e-18 |
SMART |
PDZ
|
947 |
1019 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000077871
AA Change: L573P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000077033 Gene: ENSMUSG00000034813 AA Change: L573P
Domain | Start | End | E-Value | Type |
PDZ
|
36 |
110 |
4.86e-13 |
SMART |
PDZ
|
134 |
212 |
6.4e-22 |
SMART |
PDZ
|
235 |
310 |
1.97e-13 |
SMART |
low complexity region
|
327 |
340 |
N/A |
INTRINSIC |
low complexity region
|
361 |
378 |
N/A |
INTRINSIC |
low complexity region
|
386 |
397 |
N/A |
INTRINSIC |
PDZ
|
402 |
482 |
6.36e-17 |
SMART |
PDZ
|
503 |
579 |
1.11e-16 |
SMART |
PDZ
|
602 |
676 |
1.73e-18 |
SMART |
PDZ
|
920 |
992 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000081260
AA Change: L236P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000080016 Gene: ENSMUSG00000034813 AA Change: L236P
Domain | Start | End | E-Value | Type |
low complexity region
|
49 |
60 |
N/A |
INTRINSIC |
PDZ
|
65 |
145 |
3e-19 |
SMART |
PDZ
|
166 |
242 |
5.2e-19 |
SMART |
PDZ
|
265 |
339 |
8.4e-21 |
SMART |
PDZ
|
518 |
590 |
1.4e-15 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105261
AA Change: L236P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000100896 Gene: ENSMUSG00000034813 AA Change: L236P
Domain | Start | End | E-Value | Type |
low complexity region
|
49 |
60 |
N/A |
INTRINSIC |
PDZ
|
65 |
145 |
6.36e-17 |
SMART |
PDZ
|
166 |
242 |
1.11e-16 |
SMART |
PDZ
|
265 |
339 |
1.73e-18 |
SMART |
PDZ
|
518 |
590 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105262
AA Change: L599P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000100897 Gene: ENSMUSG00000034813 AA Change: L599P
Domain | Start | End | E-Value | Type |
PDZ
|
62 |
136 |
4.86e-13 |
SMART |
PDZ
|
160 |
238 |
6.4e-22 |
SMART |
PDZ
|
261 |
336 |
1.97e-13 |
SMART |
low complexity region
|
353 |
366 |
N/A |
INTRINSIC |
low complexity region
|
387 |
404 |
N/A |
INTRINSIC |
low complexity region
|
412 |
423 |
N/A |
INTRINSIC |
PDZ
|
428 |
508 |
6.36e-17 |
SMART |
PDZ
|
529 |
605 |
1.11e-16 |
SMART |
PDZ
|
628 |
702 |
1.73e-18 |
SMART |
PDZ
|
946 |
1018 |
2.79e-13 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127787
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000130387
AA Change: L236P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000123288 Gene: ENSMUSG00000034813 AA Change: L236P
Domain | Start | End | E-Value | Type |
low complexity region
|
49 |
60 |
N/A |
INTRINSIC |
PDZ
|
65 |
145 |
6.36e-17 |
SMART |
PDZ
|
166 |
242 |
1.11e-16 |
SMART |
PDZ
|
265 |
339 |
1.73e-18 |
SMART |
PDZ
|
583 |
655 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000138410
AA Change: L651P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000123234 Gene: ENSMUSG00000034813 AA Change: L651P
Domain | Start | End | E-Value | Type |
PDZ
|
62 |
136 |
4.86e-13 |
SMART |
PDZ
|
160 |
238 |
6.4e-22 |
SMART |
PDZ
|
261 |
336 |
1.97e-13 |
SMART |
low complexity region
|
393 |
421 |
N/A |
INTRINSIC |
low complexity region
|
439 |
456 |
N/A |
INTRINSIC |
low complexity region
|
464 |
475 |
N/A |
INTRINSIC |
PDZ
|
480 |
560 |
6.36e-17 |
SMART |
PDZ
|
581 |
657 |
1.11e-16 |
SMART |
PDZ
|
680 |
754 |
1.73e-18 |
SMART |
PDZ
|
1013 |
1085 |
2.79e-13 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139352
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000144959
AA Change: L651P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000122323 Gene: ENSMUSG00000034813 AA Change: L651P
Domain | Start | End | E-Value | Type |
PDZ
|
62 |
136 |
4.86e-13 |
SMART |
PDZ
|
160 |
238 |
6.4e-22 |
SMART |
PDZ
|
261 |
336 |
1.97e-13 |
SMART |
low complexity region
|
393 |
421 |
N/A |
INTRINSIC |
low complexity region
|
439 |
456 |
N/A |
INTRINSIC |
low complexity region
|
464 |
475 |
N/A |
INTRINSIC |
PDZ
|
480 |
560 |
6.36e-17 |
SMART |
PDZ
|
581 |
657 |
1.11e-16 |
SMART |
PDZ
|
680 |
754 |
1.73e-18 |
SMART |
PDZ
|
998 |
1070 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000147356
AA Change: L652P
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000115478 Gene: ENSMUSG00000034813 AA Change: L652P
Domain | Start | End | E-Value | Type |
PDZ
|
63 |
137 |
4.86e-13 |
SMART |
PDZ
|
161 |
239 |
6.4e-22 |
SMART |
PDZ
|
262 |
337 |
1.97e-13 |
SMART |
low complexity region
|
394 |
422 |
N/A |
INTRINSIC |
low complexity region
|
440 |
457 |
N/A |
INTRINSIC |
low complexity region
|
465 |
476 |
N/A |
INTRINSIC |
PDZ
|
481 |
561 |
6.36e-17 |
SMART |
PDZ
|
582 |
658 |
1.11e-16 |
SMART |
PDZ
|
681 |
755 |
1.73e-18 |
SMART |
PDZ
|
999 |
1071 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000147454
AA Change: L651P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000118073 Gene: ENSMUSG00000034813 AA Change: L651P
Domain | Start | End | E-Value | Type |
PDZ
|
62 |
136 |
4.86e-13 |
SMART |
PDZ
|
160 |
238 |
6.4e-22 |
SMART |
PDZ
|
261 |
336 |
1.97e-13 |
SMART |
low complexity region
|
393 |
421 |
N/A |
INTRINSIC |
low complexity region
|
439 |
456 |
N/A |
INTRINSIC |
low complexity region
|
464 |
475 |
N/A |
INTRINSIC |
PDZ
|
480 |
560 |
6.36e-17 |
SMART |
PDZ
|
581 |
657 |
1.11e-16 |
SMART |
PDZ
|
680 |
754 |
1.73e-18 |
SMART |
PDZ
|
998 |
1070 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000148954
AA Change: L599P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000118397 Gene: ENSMUSG00000034813 AA Change: L599P
Domain | Start | End | E-Value | Type |
PDZ
|
62 |
136 |
4.86e-13 |
SMART |
PDZ
|
160 |
238 |
6.4e-22 |
SMART |
PDZ
|
261 |
336 |
1.97e-13 |
SMART |
low complexity region
|
353 |
366 |
N/A |
INTRINSIC |
low complexity region
|
387 |
404 |
N/A |
INTRINSIC |
low complexity region
|
412 |
423 |
N/A |
INTRINSIC |
PDZ
|
428 |
508 |
6.36e-17 |
SMART |
PDZ
|
529 |
605 |
1.11e-16 |
SMART |
PDZ
|
628 |
702 |
1.73e-18 |
SMART |
PDZ
|
961 |
1033 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000154238
AA Change: L236P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000122349 Gene: ENSMUSG00000034813 AA Change: L236P
Domain | Start | End | E-Value | Type |
low complexity region
|
49 |
60 |
N/A |
INTRINSIC |
PDZ
|
65 |
145 |
6.36e-17 |
SMART |
PDZ
|
166 |
242 |
1.11e-16 |
SMART |
PDZ
|
265 |
339 |
1.73e-18 |
SMART |
PDZ
|
598 |
670 |
2.79e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000144825
AA Change: L572P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000121670 Gene: ENSMUSG00000034813 AA Change: L572P
Domain | Start | End | E-Value | Type |
PDZ
|
35 |
109 |
4.86e-13 |
SMART |
PDZ
|
133 |
211 |
6.4e-22 |
SMART |
PDZ
|
234 |
309 |
1.97e-13 |
SMART |
low complexity region
|
326 |
339 |
N/A |
INTRINSIC |
low complexity region
|
360 |
377 |
N/A |
INTRINSIC |
low complexity region
|
385 |
396 |
N/A |
INTRINSIC |
PDZ
|
401 |
481 |
6.36e-17 |
SMART |
PDZ
|
502 |
578 |
1.11e-16 |
SMART |
PDZ
|
601 |
675 |
1.73e-18 |
SMART |
PDZ
|
919 |
991 |
2.79e-13 |
SMART |
|
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.8%
- 10x: 97.6%
- 20x: 96.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: This gene encodes a protein containing multiple PDZ (post synaptic density protein, Drosophila disc large tumor suppressor, and zonula occludens-1 protein) domains. The encoded protein acts as a mediator between cytoskeletal and membrane proteins, particularly in neuronal cells, and facilitates complex formation at the cell membrane. Mutation of this gene can cause embryonic lethality resulting from defects of the dermo-epidermal junction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013] PHENOTYPE: Homozygous ablation of gene function results in embryonic lethality and blistering skin lesions. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
G |
1: 71,323,111 (GRCm39) |
V1657A |
possibly damaging |
Het |
Abca8b |
C |
A |
11: 109,868,639 (GRCm39) |
G175V |
probably damaging |
Het |
Acot5 |
A |
G |
12: 84,120,215 (GRCm39) |
Y190C |
probably damaging |
Het |
Ascc3 |
T |
A |
10: 50,583,873 (GRCm39) |
Y941N |
probably benign |
Het |
BC035947 |
A |
T |
1: 78,488,599 (GRCm39) |
M1K |
probably null |
Het |
C2cd5 |
A |
G |
6: 143,019,482 (GRCm39) |
C278R |
probably benign |
Het |
Cd200r1 |
G |
T |
16: 44,613,172 (GRCm39) |
L259F |
possibly damaging |
Het |
Clcn4 |
A |
G |
7: 7,297,050 (GRCm39) |
V136A |
possibly damaging |
Het |
Cntnap5a |
T |
C |
1: 116,085,300 (GRCm39) |
S413P |
probably benign |
Het |
Corin |
T |
A |
5: 72,473,441 (GRCm39) |
E748D |
probably benign |
Het |
Crtc2 |
G |
T |
3: 90,168,325 (GRCm39) |
G356V |
probably damaging |
Het |
D1Pas1 |
T |
A |
1: 186,701,642 (GRCm39) |
Y524N |
probably damaging |
Het |
Dlgap4 |
T |
C |
2: 156,602,818 (GRCm39) |
S147P |
probably damaging |
Het |
Eif1ad16 |
T |
A |
12: 87,985,316 (GRCm39) |
I76F |
probably damaging |
Het |
Enpp1 |
A |
T |
10: 24,527,288 (GRCm39) |
I633N |
probably benign |
Het |
Gm3095 |
A |
G |
14: 15,170,367 (GRCm39) |
D72G |
probably null |
Het |
Gm5449 |
C |
T |
13: 53,679,787 (GRCm39) |
|
noncoding transcript |
Het |
Gpx7 |
T |
C |
4: 108,258,111 (GRCm39) |
T161A |
probably benign |
Het |
H2-Q2 |
G |
T |
17: 35,563,885 (GRCm39) |
R255S |
probably damaging |
Het |
Il17rc |
G |
T |
6: 113,459,997 (GRCm39) |
A648S |
possibly damaging |
Het |
Klhl12 |
A |
G |
1: 134,417,189 (GRCm39) |
E540G |
possibly damaging |
Het |
Mcm10 |
T |
C |
2: 5,012,181 (GRCm39) |
I135V |
probably benign |
Het |
Mrps26 |
C |
A |
2: 130,406,087 (GRCm39) |
T100K |
probably benign |
Het |
Nid2 |
A |
G |
14: 19,829,769 (GRCm39) |
T687A |
probably benign |
Het |
Npas3 |
A |
T |
12: 54,115,619 (GRCm39) |
D829V |
probably damaging |
Het |
Ocln |
T |
C |
13: 100,642,807 (GRCm39) |
D176G |
probably damaging |
Het |
Or11h6 |
A |
G |
14: 50,879,776 (GRCm39) |
|
probably null |
Het |
Pax3 |
A |
C |
1: 78,098,249 (GRCm39) |
M380R |
possibly damaging |
Het |
Pcdha3 |
A |
G |
18: 37,081,208 (GRCm39) |
E650G |
probably damaging |
Het |
Pdcd11 |
C |
A |
19: 47,096,083 (GRCm39) |
H668N |
probably damaging |
Het |
Polr3b |
T |
C |
10: 84,535,264 (GRCm39) |
Y858H |
possibly damaging |
Het |
Pus10 |
T |
C |
11: 23,617,416 (GRCm39) |
|
probably null |
Het |
Raver1 |
T |
C |
9: 20,986,677 (GRCm39) |
D739G |
probably damaging |
Het |
Skic3 |
G |
A |
13: 76,295,886 (GRCm39) |
E1050K |
possibly damaging |
Het |
Slc26a11 |
T |
C |
11: 119,254,276 (GRCm39) |
L198P |
probably damaging |
Het |
Slc44a3 |
A |
G |
3: 121,303,962 (GRCm39) |
V258A |
probably damaging |
Het |
Socs7 |
T |
A |
11: 97,280,025 (GRCm39) |
I524N |
probably damaging |
Het |
Steap4 |
T |
A |
5: 8,025,547 (GRCm39) |
L36* |
probably null |
Het |
Svep1 |
G |
C |
4: 58,096,183 (GRCm39) |
T1479S |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,547,619 (GRCm39) |
V32184F |
probably damaging |
Het |
Vmn1r22 |
T |
C |
6: 57,877,960 (GRCm39) |
N6D |
possibly damaging |
Het |
|
Other mutations in Grip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01309:Grip1
|
APN |
10 |
119,767,207 (GRCm39) |
nonsense |
probably null |
|
IGL01374:Grip1
|
APN |
10 |
119,885,273 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01592:Grip1
|
APN |
10 |
119,765,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02207:Grip1
|
APN |
10 |
119,911,214 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02222:Grip1
|
APN |
10 |
119,835,714 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02225:Grip1
|
APN |
10 |
119,885,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02447:Grip1
|
APN |
10 |
119,855,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02492:Grip1
|
APN |
10 |
119,765,945 (GRCm39) |
splice site |
probably benign |
|
IGL02522:Grip1
|
APN |
10 |
119,767,154 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02574:Grip1
|
APN |
10 |
119,778,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02718:Grip1
|
APN |
10 |
119,911,420 (GRCm39) |
makesense |
probably null |
|
IGL02751:Grip1
|
APN |
10 |
119,814,482 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03221:Grip1
|
APN |
10 |
119,822,299 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03377:Grip1
|
APN |
10 |
119,890,937 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4403001:Grip1
|
UTSW |
10 |
119,765,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R0304:Grip1
|
UTSW |
10 |
119,911,376 (GRCm39) |
missense |
probably benign |
0.31 |
R0681:Grip1
|
UTSW |
10 |
119,846,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R0760:Grip1
|
UTSW |
10 |
119,853,983 (GRCm39) |
missense |
probably damaging |
0.96 |
R1457:Grip1
|
UTSW |
10 |
119,822,255 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1506:Grip1
|
UTSW |
10 |
119,814,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R1541:Grip1
|
UTSW |
10 |
119,836,448 (GRCm39) |
missense |
probably damaging |
0.99 |
R1553:Grip1
|
UTSW |
10 |
119,890,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Grip1
|
UTSW |
10 |
119,733,620 (GRCm39) |
missense |
probably damaging |
0.98 |
R2055:Grip1
|
UTSW |
10 |
119,885,416 (GRCm39) |
splice site |
probably benign |
|
R2059:Grip1
|
UTSW |
10 |
119,874,603 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2261:Grip1
|
UTSW |
10 |
119,821,489 (GRCm39) |
missense |
probably benign |
0.00 |
R2475:Grip1
|
UTSW |
10 |
119,814,401 (GRCm39) |
missense |
probably benign |
0.01 |
R3777:Grip1
|
UTSW |
10 |
119,821,535 (GRCm39) |
critical splice donor site |
probably null |
|
R3849:Grip1
|
UTSW |
10 |
119,765,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R3956:Grip1
|
UTSW |
10 |
119,765,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R4643:Grip1
|
UTSW |
10 |
119,856,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4693:Grip1
|
UTSW |
10 |
119,836,459 (GRCm39) |
missense |
probably benign |
0.10 |
R4724:Grip1
|
UTSW |
10 |
119,874,588 (GRCm39) |
missense |
probably benign |
0.02 |
R4843:Grip1
|
UTSW |
10 |
119,765,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Grip1
|
UTSW |
10 |
119,911,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R4912:Grip1
|
UTSW |
10 |
119,767,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R5185:Grip1
|
UTSW |
10 |
119,767,164 (GRCm39) |
missense |
probably benign |
0.37 |
R5291:Grip1
|
UTSW |
10 |
119,922,874 (GRCm39) |
missense |
probably benign |
0.04 |
R5293:Grip1
|
UTSW |
10 |
119,733,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R5296:Grip1
|
UTSW |
10 |
119,765,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Grip1
|
UTSW |
10 |
119,908,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R5792:Grip1
|
UTSW |
10 |
119,821,385 (GRCm39) |
missense |
probably benign |
0.07 |
R5861:Grip1
|
UTSW |
10 |
119,765,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Grip1
|
UTSW |
10 |
119,821,397 (GRCm39) |
missense |
probably benign |
0.02 |
R5949:Grip1
|
UTSW |
10 |
119,886,147 (GRCm39) |
missense |
probably benign |
0.00 |
R6112:Grip1
|
UTSW |
10 |
119,829,137 (GRCm39) |
missense |
probably benign |
0.00 |
R6166:Grip1
|
UTSW |
10 |
119,908,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R6167:Grip1
|
UTSW |
10 |
119,733,702 (GRCm39) |
critical splice donor site |
probably null |
|
R6193:Grip1
|
UTSW |
10 |
119,874,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R6218:Grip1
|
UTSW |
10 |
119,822,251 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6267:Grip1
|
UTSW |
10 |
119,911,369 (GRCm39) |
nonsense |
probably null |
|
R6296:Grip1
|
UTSW |
10 |
119,911,369 (GRCm39) |
nonsense |
probably null |
|
R6490:Grip1
|
UTSW |
10 |
119,822,329 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6543:Grip1
|
UTSW |
10 |
119,821,499 (GRCm39) |
missense |
probably benign |
0.00 |
R6558:Grip1
|
UTSW |
10 |
119,290,288 (GRCm39) |
missense |
probably benign |
0.00 |
R6995:Grip1
|
UTSW |
10 |
119,822,375 (GRCm39) |
missense |
probably damaging |
0.99 |
R7122:Grip1
|
UTSW |
10 |
119,871,279 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7157:Grip1
|
UTSW |
10 |
119,781,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R7410:Grip1
|
UTSW |
10 |
119,855,925 (GRCm39) |
missense |
probably benign |
0.01 |
R7447:Grip1
|
UTSW |
10 |
119,922,871 (GRCm39) |
missense |
probably benign |
0.01 |
R7539:Grip1
|
UTSW |
10 |
119,890,776 (GRCm39) |
missense |
probably benign |
0.17 |
R7586:Grip1
|
UTSW |
10 |
119,913,043 (GRCm39) |
splice site |
probably null |
|
R7768:Grip1
|
UTSW |
10 |
119,874,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R7831:Grip1
|
UTSW |
10 |
119,854,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Grip1
|
UTSW |
10 |
119,814,450 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8103:Grip1
|
UTSW |
10 |
119,814,440 (GRCm39) |
missense |
probably benign |
0.00 |
R8254:Grip1
|
UTSW |
10 |
119,890,810 (GRCm39) |
nonsense |
probably null |
|
R8688:Grip1
|
UTSW |
10 |
119,835,809 (GRCm39) |
missense |
probably benign |
0.12 |
R8823:Grip1
|
UTSW |
10 |
119,811,856 (GRCm39) |
missense |
|
|
R8837:Grip1
|
UTSW |
10 |
119,765,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Grip1
|
UTSW |
10 |
119,290,192 (GRCm39) |
start gained |
probably benign |
|
R8951:Grip1
|
UTSW |
10 |
119,874,509 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9042:Grip1
|
UTSW |
10 |
119,836,438 (GRCm39) |
missense |
probably benign |
0.14 |
R9045:Grip1
|
UTSW |
10 |
119,871,356 (GRCm39) |
missense |
probably damaging |
0.97 |
R9237:Grip1
|
UTSW |
10 |
119,911,310 (GRCm39) |
missense |
probably benign |
0.07 |
R9254:Grip1
|
UTSW |
10 |
119,780,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9259:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9260:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9307:Grip1
|
UTSW |
10 |
119,821,454 (GRCm39) |
missense |
probably benign |
0.01 |
R9379:Grip1
|
UTSW |
10 |
119,780,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9546:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9547:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9548:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9549:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9583:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9584:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9610:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9611:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9612:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9684:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9687:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9690:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9691:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9742:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9744:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9752:Grip1
|
UTSW |
10 |
119,871,256 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9758:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9762:Grip1
|
UTSW |
10 |
119,811,906 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9764:Grip1
|
UTSW |
10 |
119,874,569 (GRCm39) |
missense |
possibly damaging |
0.63 |
RF011:Grip1
|
UTSW |
10 |
119,767,220 (GRCm39) |
missense |
probably null |
0.97 |
Z1176:Grip1
|
UTSW |
10 |
119,655,388 (GRCm39) |
unclassified |
probably benign |
|
Z1177:Grip1
|
UTSW |
10 |
119,822,349 (GRCm39) |
missense |
probably benign |
0.06 |
|
Predicted Primers |
PCR Primer
(F):5'- CCATGTGAACACAAGATTATGCC -3'
(R):5'- ATTCCACTCAAGACTCAGTGC -3'
Sequencing Primer
(F):5'- TGCCTCTAGAAATGGCCTGAGTAC -3'
(R):5'- GACTCAGTGCATAACTCAAAGACTC -3'
|
Posted On |
2016-07-22 |