Incidental Mutation 'IGL01309:Grip1'
ID |
73598 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Grip1
|
Ensembl Gene |
ENSMUSG00000034813 |
Gene Name |
glutamate receptor interacting protein 1 |
Synonyms |
4931400F03Rik, eb |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL01309
|
Quality Score |
|
Status
|
|
Chromosome |
10 |
Chromosomal Location |
119289810-119923172 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
A to T
at 119767207 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Stop codon
at position 111
(K111*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118397
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041962]
[ENSMUST00000077871]
[ENSMUST00000105262]
[ENSMUST00000138410]
[ENSMUST00000144825]
[ENSMUST00000144959]
[ENSMUST00000147356]
[ENSMUST00000148954]
[ENSMUST00000147454]
|
AlphaFold |
Q925T6 |
Predicted Effect |
probably null
Transcript: ENSMUST00000041962
AA Change: K112*
|
SMART Domains |
Protein: ENSMUSP00000042436 Gene: ENSMUSG00000034813 AA Change: K112*
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 null
Transcript: ENSMUST00000077871
AA Change: K85*
|
SMART Domains |
Protein: ENSMUSP00000077033 Gene: ENSMUSG00000034813 AA Change: K85*
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 null
Transcript: ENSMUST00000105262
AA Change: K111*
|
SMART Domains |
Protein: ENSMUSP00000100897 Gene: ENSMUSG00000034813 AA Change: K111*
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 null
Transcript: ENSMUST00000138410
AA Change: K111*
|
SMART Domains |
Protein: ENSMUSP00000123234 Gene: ENSMUSG00000034813 AA Change: K111*
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 null
Transcript: ENSMUST00000144825
AA Change: K84*
|
SMART Domains |
Protein: ENSMUSP00000121670 Gene: ENSMUSG00000034813 AA Change: K84*
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 |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000144959
AA Change: K111*
|
SMART Domains |
Protein: ENSMUSP00000122323 Gene: ENSMUSG00000034813 AA Change: K111*
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 null
Transcript: ENSMUST00000147356
AA Change: K112*
|
SMART Domains |
Protein: ENSMUSP00000115478 Gene: ENSMUSG00000034813 AA Change: K112*
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 null
Transcript: ENSMUST00000148954
AA Change: K111*
|
SMART Domains |
Protein: ENSMUSP00000118397 Gene: ENSMUSG00000034813 AA Change: K111*
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 null
Transcript: ENSMUST00000147454
AA Change: K111*
|
SMART Domains |
Protein: ENSMUSP00000118073 Gene: ENSMUSG00000034813 AA Change: K111*
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 |
noncoding transcript
Transcript: ENSMUST00000147598
|
Coding Region Coverage |
|
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: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
A |
G |
16: 16,931,410 (GRCm39) |
V275A |
possibly damaging |
Het |
Adamts2 |
A |
G |
11: 50,694,528 (GRCm39) |
D1105G |
probably benign |
Het |
Adgrb3 |
T |
A |
1: 25,151,352 (GRCm39) |
M195L |
possibly damaging |
Het |
Adrm1 |
A |
G |
2: 179,817,756 (GRCm39) |
|
probably benign |
Het |
Atg13 |
T |
A |
2: 91,509,176 (GRCm39) |
I457F |
possibly damaging |
Het |
BC034090 |
T |
C |
1: 155,102,130 (GRCm39) |
N45D |
probably damaging |
Het |
C3 |
C |
T |
17: 57,516,652 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
G |
A |
8: 85,249,657 (GRCm39) |
G221D |
probably damaging |
Het |
Calr |
A |
G |
8: 85,573,335 (GRCm39) |
|
probably null |
Het |
Chd3 |
C |
T |
11: 69,248,557 (GRCm39) |
V825I |
probably damaging |
Het |
Chdh |
T |
G |
14: 29,757,761 (GRCm39) |
|
probably benign |
Het |
Ckap5 |
T |
C |
2: 91,400,529 (GRCm39) |
V627A |
probably damaging |
Het |
Commd3 |
A |
G |
2: 18,677,289 (GRCm39) |
E5G |
probably benign |
Het |
Ddi1 |
T |
C |
9: 6,265,773 (GRCm39) |
R199G |
probably damaging |
Het |
Dennd4c |
A |
G |
4: 86,723,724 (GRCm39) |
|
probably benign |
Het |
Dok7 |
G |
A |
5: 35,236,912 (GRCm39) |
G293D |
possibly damaging |
Het |
Epm2aip1 |
T |
C |
9: 111,102,596 (GRCm39) |
V523A |
probably benign |
Het |
Fam171b |
C |
T |
2: 83,709,791 (GRCm39) |
Q488* |
probably null |
Het |
Gabbr1 |
G |
A |
17: 37,359,499 (GRCm39) |
|
probably null |
Het |
Gm5965 |
T |
G |
16: 88,575,219 (GRCm39) |
S131A |
possibly damaging |
Het |
Gpcpd1 |
T |
C |
2: 132,392,244 (GRCm39) |
D235G |
probably damaging |
Het |
Itih4 |
G |
T |
14: 30,613,706 (GRCm39) |
D308Y |
probably damaging |
Het |
Kcnj6 |
A |
G |
16: 94,633,314 (GRCm39) |
Y266H |
probably damaging |
Het |
Lrrc41 |
T |
C |
4: 115,953,663 (GRCm39) |
L783P |
probably damaging |
Het |
Map4k5 |
T |
C |
12: 69,888,737 (GRCm39) |
D298G |
probably benign |
Het |
Mapkbp1 |
T |
C |
2: 119,849,423 (GRCm39) |
F712L |
probably damaging |
Het |
Mcoln2 |
T |
C |
3: 145,869,282 (GRCm39) |
|
probably benign |
Het |
Megf11 |
T |
A |
9: 64,588,698 (GRCm39) |
S532R |
probably benign |
Het |
Mkx |
T |
C |
18: 6,937,192 (GRCm39) |
D284G |
probably benign |
Het |
Mmp16 |
A |
G |
4: 18,116,185 (GRCm39) |
I596M |
probably damaging |
Het |
Msto1 |
C |
A |
3: 88,820,993 (GRCm39) |
R34L |
probably benign |
Het |
Mtmr9 |
A |
G |
14: 63,764,254 (GRCm39) |
L491P |
probably damaging |
Het |
Or4a66 |
T |
G |
2: 88,531,310 (GRCm39) |
Y121S |
probably damaging |
Het |
Or8b52 |
T |
A |
9: 38,576,289 (GRCm39) |
I284L |
probably benign |
Het |
Or9s13 |
T |
C |
1: 92,548,057 (GRCm39) |
M143T |
probably damaging |
Het |
Otor |
T |
C |
2: 142,920,532 (GRCm39) |
V38A |
possibly damaging |
Het |
Pcdhb12 |
G |
T |
18: 37,569,207 (GRCm39) |
D118Y |
probably damaging |
Het |
Prelp |
T |
C |
1: 133,842,545 (GRCm39) |
H200R |
probably benign |
Het |
Prmt5 |
T |
C |
14: 54,747,334 (GRCm39) |
Y481C |
probably damaging |
Het |
Psg23 |
T |
G |
7: 18,348,465 (GRCm39) |
D114A |
probably damaging |
Het |
Ptger4 |
A |
T |
15: 5,272,239 (GRCm39) |
Y127N |
probably damaging |
Het |
Rabgap1l |
C |
A |
1: 160,528,368 (GRCm39) |
V385L |
probably benign |
Het |
Rergl |
T |
A |
6: 139,470,256 (GRCm39) |
K191* |
probably null |
Het |
Sart3 |
A |
G |
5: 113,897,311 (GRCm39) |
F252S |
probably damaging |
Het |
Sbno1 |
A |
T |
5: 124,519,769 (GRCm39) |
S1169T |
probably benign |
Het |
Serpinb8 |
C |
T |
1: 107,532,448 (GRCm39) |
T180M |
probably damaging |
Het |
Sipa1l1 |
G |
A |
12: 82,434,470 (GRCm39) |
E747K |
probably benign |
Het |
Sptb |
T |
A |
12: 76,634,237 (GRCm39) |
D2158V |
probably benign |
Het |
Sycp2 |
T |
G |
2: 177,999,904 (GRCm39) |
D1024A |
probably benign |
Het |
Tbr1 |
T |
G |
2: 61,636,411 (GRCm39) |
N262K |
possibly damaging |
Het |
Tnrc6a |
A |
T |
7: 122,770,717 (GRCm39) |
I836F |
probably benign |
Het |
Ttn |
T |
C |
2: 76,769,091 (GRCm39) |
E2823G |
probably damaging |
Het |
Uqcrc1 |
T |
A |
9: 108,778,026 (GRCm39) |
L441Q |
possibly damaging |
Het |
Vmn1r180 |
T |
C |
7: 23,652,424 (GRCm39) |
F196L |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,787,997 (GRCm39) |
I451M |
possibly damaging |
Het |
Zcchc7 |
A |
T |
4: 44,926,060 (GRCm39) |
H353L |
probably damaging |
Het |
|
Other mutations in Grip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
R5302:Grip1
|
UTSW |
10 |
119,855,982 (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 |
|
Posted On |
2013-10-07 |