Incidental Mutation 'R0360:Iqgap2'
| ID |
65688 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Iqgap2
|
| Ensembl Gene |
ENSMUSG00000021676 |
| Gene Name |
IQ motif containing GTPase activating protein 2 |
| Synonyms |
4933417J23Rik |
| MMRRC Submission |
038566-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0360 (G1)
|
| Quality Score |
208 |
|
Status
|
Validated
|
| Chromosome |
13 |
| Chromosomal Location |
95627177-95891922 bp(-) (GRCm38) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to C
at 95731275 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000067685
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000068603]
|
| AlphaFold |
Q3UQ44 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000068603
|
| SMART Domains |
Protein: ENSMUSP00000067685
Gene: ENSMUSG00000021676
| Domain | Start | End | E-Value | Type |
|---|
|
CH
|
43 |
152 |
3.32e-16 |
SMART |
|
coiled coil region
|
253 |
276 |
N/A |
INTRINSIC |
|
low complexity region
|
469 |
480 |
N/A |
INTRINSIC |
|
IQ
|
689 |
711 |
1.38e-4 |
SMART |
|
IQ
|
719 |
741 |
7.36e0 |
SMART |
|
IQ
|
749 |
771 |
2.43e1 |
SMART |
|
coiled coil region
|
799 |
828 |
N/A |
INTRINSIC |
|
RasGAP
|
905 |
1258 |
2.6e-120 |
SMART |
|
Pfam:RasGAP_C
|
1367 |
1498 |
3.2e-40 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.3%
- 10x: 96.2%
- 20x: 92.6%
|
| Validation Efficiency |
98% (93/95) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the IQGAP family. The protein contains three IQ domains, one calponin homology domain, one Ras-GAP domain and one WW domain. It interacts with components of the cytoskeleton, with cell adhesion molecules, and with several signaling molecules to regulate cell morphology and motility. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null mutation display reduced survival with increased incidence of hepatocellular carcinomas, increased hepatocyte apoptosis, and hepatocyte mitochondrial abnormalities. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 95 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acp7 |
G |
A |
7: 28,611,128 (GRCm38) |
|
probably benign |
Het |
| Adcyap1r1 |
G |
T |
6: 55,475,523 (GRCm38) |
|
probably benign |
Het |
| Ankrd6 |
T |
C |
4: 32,836,424 (GRCm38) |
T44A |
probably damaging |
Het |
| Ano7 |
A |
G |
1: 93,388,658 (GRCm38) |
D221G |
probably benign |
Het |
| Bhlhe40 |
C |
A |
6: 108,664,750 (GRCm38) |
N218K |
probably damaging |
Het |
| Bms1 |
A |
G |
6: 118,405,290 (GRCm38) |
V429A |
probably benign |
Het |
| C7 |
T |
A |
15: 4,988,962 (GRCm38) |
T800S |
probably benign |
Het |
| Camta2 |
G |
A |
11: 70,683,310 (GRCm38) |
T127I |
probably damaging |
Het |
| Ccdc13 |
T |
A |
9: 121,798,216 (GRCm38) |
N665I |
probably damaging |
Het |
| Ccdc157 |
T |
C |
11: 4,146,663 (GRCm38) |
E362G |
probably damaging |
Het |
| Ccdc73 |
T |
A |
2: 104,981,007 (GRCm38) |
N310K |
probably damaging |
Het |
| Cmklr1 |
A |
T |
5: 113,614,517 (GRCm38) |
L141H |
probably damaging |
Het |
| Cnst |
C |
A |
1: 179,579,535 (GRCm38) |
A49E |
probably benign |
Het |
| Col5a3 |
C |
T |
9: 20,772,466 (GRCm38) |
R1498Q |
unknown |
Het |
| Crybb3 |
T |
A |
5: 113,075,953 (GRCm38) |
I197F |
probably damaging |
Het |
| Cryzl1 |
G |
A |
16: 91,707,267 (GRCm38) |
P97S |
probably benign |
Het |
| Cubn |
T |
C |
2: 13,310,507 (GRCm38) |
|
probably benign |
Het |
| Cyp2d37-ps |
T |
C |
15: 82,690,052 (GRCm38) |
|
noncoding transcript |
Het |
| Cyp4a12b |
C |
A |
4: 115,432,920 (GRCm38) |
N223K |
probably benign |
Het |
| D16Ertd472e |
A |
T |
16: 78,547,885 (GRCm38) |
C112S |
probably benign |
Het |
| Dennd2a |
T |
C |
6: 39,508,299 (GRCm38) |
T349A |
probably benign |
Het |
| Dock5 |
G |
A |
14: 67,822,680 (GRCm38) |
|
probably benign |
Het |
| Dpp6 |
T |
C |
5: 27,652,269 (GRCm38) |
L404P |
probably damaging |
Het |
| Dsc3 |
T |
A |
18: 19,971,582 (GRCm38) |
T563S |
possibly damaging |
Het |
| Dync2h1 |
T |
A |
9: 7,113,182 (GRCm38) |
E214D |
possibly damaging |
Het |
| Elac2 |
A |
G |
11: 64,979,310 (GRCm38) |
Y67C |
probably damaging |
Het |
| Elmo1 |
A |
T |
13: 20,564,493 (GRCm38) |
K503* |
probably null |
Het |
| Eng |
T |
C |
2: 32,679,137 (GRCm38) |
S559P |
probably benign |
Het |
| Epc2 |
T |
A |
2: 49,537,133 (GRCm38) |
V563E |
possibly damaging |
Het |
| Fancm |
A |
G |
12: 65,075,950 (GRCm38) |
Y82C |
probably damaging |
Het |
| Flt4 |
A |
T |
11: 49,636,991 (GRCm38) |
M924L |
probably benign |
Het |
| Gabpa |
T |
A |
16: 84,857,387 (GRCm38) |
N317K |
possibly damaging |
Het |
| Gchfr |
T |
G |
2: 119,167,846 (GRCm38) |
Y3* |
probably null |
Het |
| Gli3 |
G |
T |
13: 15,724,764 (GRCm38) |
G912V |
probably benign |
Het |
| Gm10295 |
C |
A |
7: 71,350,613 (GRCm38) |
C73F |
unknown |
Het |
| Gm10382 |
G |
T |
5: 125,389,664 (GRCm38) |
|
probably benign |
Het |
| Gm6614 |
A |
C |
6: 141,982,327 (GRCm38) |
|
probably benign |
Het |
| Gp1ba |
T |
C |
11: 70,640,458 (GRCm38) |
|
probably benign |
Het |
| Gpr146 |
G |
A |
5: 139,379,178 (GRCm38) |
|
probably benign |
Het |
| Hexdc |
T |
A |
11: 121,212,143 (GRCm38) |
H62Q |
probably benign |
Het |
| Hgd |
T |
A |
16: 37,611,184 (GRCm38) |
|
probably benign |
Het |
| Hs6st1 |
G |
A |
1: 36,069,185 (GRCm38) |
|
probably null |
Het |
| Icam4 |
A |
G |
9: 21,029,821 (GRCm38) |
Y123C |
probably damaging |
Het |
| Il24 |
A |
G |
1: 130,883,937 (GRCm38) |
V134A |
probably damaging |
Het |
| Iqcb1 |
G |
T |
16: 36,872,308 (GRCm38) |
A562S |
probably damaging |
Het |
| Islr2 |
T |
C |
9: 58,199,744 (GRCm38) |
T78A |
possibly damaging |
Het |
| Kif1b |
A |
G |
4: 149,262,729 (GRCm38) |
I330T |
probably damaging |
Het |
| Kirrel |
T |
C |
3: 87,089,799 (GRCm38) |
Y287C |
probably damaging |
Het |
| Klf10 |
C |
T |
15: 38,296,846 (GRCm38) |
V317M |
probably benign |
Het |
| Klhl9 |
T |
G |
4: 88,720,290 (GRCm38) |
K571N |
probably benign |
Het |
| Lin37 |
T |
C |
7: 30,557,013 (GRCm38) |
I97V |
possibly damaging |
Het |
| Lrrc37a |
C |
T |
11: 103,500,640 (GRCm38) |
V1320I |
possibly damaging |
Het |
| Lrrc74a |
A |
G |
12: 86,737,795 (GRCm38) |
H99R |
probably damaging |
Het |
| Maats1 |
T |
A |
16: 38,298,297 (GRCm38) |
|
probably null |
Het |
| Me3 |
T |
A |
7: 89,786,414 (GRCm38) |
|
probably null |
Het |
| Med13 |
T |
C |
11: 86,329,161 (GRCm38) |
|
probably benign |
Het |
| Myh6 |
A |
T |
14: 54,948,347 (GRCm38) |
Y1490* |
probably null |
Het |
| Myo10 |
T |
C |
15: 25,804,368 (GRCm38) |
L1583P |
probably damaging |
Het |
| Nkx6-3 |
A |
G |
8: 23,157,706 (GRCm38) |
E227G |
possibly damaging |
Het |
| Nlrp1a |
T |
A |
11: 71,114,004 (GRCm38) |
|
probably benign |
Het |
| Nlrp5-ps |
A |
C |
7: 14,583,091 (GRCm38) |
|
noncoding transcript |
Het |
| Nup188 |
T |
G |
2: 30,326,479 (GRCm38) |
I765S |
probably null |
Het |
| Obscn |
G |
A |
11: 59,128,281 (GRCm38) |
A969V |
probably benign |
Het |
| Olfr1080 |
A |
T |
2: 86,553,779 (GRCm38) |
L115Q |
probably damaging |
Het |
| Olfr348 |
T |
A |
2: 36,787,440 (GRCm38) |
M305K |
probably benign |
Het |
| Olfr76 |
G |
T |
19: 12,119,853 (GRCm38) |
D286E |
possibly damaging |
Het |
| Olfr96 |
T |
C |
17: 37,226,043 (GRCm38) |
L306P |
possibly damaging |
Het |
| Otogl |
T |
A |
10: 107,770,650 (GRCm38) |
|
probably benign |
Het |
| Pcnx3 |
G |
A |
19: 5,665,583 (GRCm38) |
R1472W |
probably damaging |
Het |
| Plekha5 |
G |
A |
6: 140,591,747 (GRCm38) |
R646K |
possibly damaging |
Het |
| Plscr4 |
T |
A |
9: 92,488,761 (GRCm38) |
|
probably benign |
Het |
| Pon2 |
G |
A |
6: 5,266,156 (GRCm38) |
Q288* |
probably null |
Het |
| Ptpn13 |
C |
A |
5: 103,533,348 (GRCm38) |
R805S |
probably damaging |
Het |
| Pyroxd2 |
A |
T |
19: 42,747,553 (GRCm38) |
V62D |
probably damaging |
Het |
| Rab37 |
G |
T |
11: 115,156,964 (GRCm38) |
C44F |
probably damaging |
Het |
| Rbm44 |
T |
C |
1: 91,152,347 (GRCm38) |
S52P |
probably benign |
Het |
| Rgl3 |
A |
G |
9: 21,976,857 (GRCm38) |
W454R |
probably damaging |
Het |
| Rita1 |
A |
G |
5: 120,609,772 (GRCm38) |
S154P |
probably benign |
Het |
| Scn5a |
T |
C |
9: 119,522,599 (GRCm38) |
D772G |
probably damaging |
Het |
| Sec23ip |
G |
A |
7: 128,761,405 (GRCm38) |
|
probably benign |
Het |
| Slc23a1 |
T |
A |
18: 35,622,979 (GRCm38) |
|
probably benign |
Het |
| Sparcl1 |
T |
A |
5: 104,089,637 (GRCm38) |
D444V |
probably damaging |
Het |
| Taar6 |
C |
A |
10: 23,985,148 (GRCm38) |
V167L |
probably benign |
Het |
| Tmcc3 |
T |
A |
10: 94,578,545 (GRCm38) |
N36K |
probably benign |
Het |
| Tmem200c |
T |
A |
17: 68,840,548 (GRCm38) |
V42E |
probably damaging |
Het |
| Trhde |
T |
C |
10: 114,502,982 (GRCm38) |
|
probably benign |
Het |
| Tshz3 |
A |
G |
7: 36,770,533 (GRCm38) |
E649G |
probably benign |
Het |
| Utp4 |
T |
C |
8: 106,898,537 (GRCm38) |
|
probably benign |
Het |
| Vmn1r30 |
A |
G |
6: 58,435,277 (GRCm38) |
V190A |
probably benign |
Het |
| Vmn1r35 |
A |
G |
6: 66,678,843 (GRCm38) |
I281T |
probably damaging |
Het |
| Vmn1r58 |
G |
T |
7: 5,410,330 (GRCm38) |
H300Q |
probably benign |
Het |
| Vmn1r84 |
A |
G |
7: 12,361,872 (GRCm38) |
L286P |
probably damaging |
Het |
| Vmn2r54 |
A |
T |
7: 12,615,649 (GRCm38) |
C669S |
probably damaging |
Het |
| Wdr61 |
A |
T |
9: 54,727,578 (GRCm38) |
|
probably benign |
Het |
| Zfp623 |
T |
C |
15: 75,948,661 (GRCm38) |
S489P |
probably benign |
Het |
|
| Other mutations in Iqgap2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00799:Iqgap2
|
APN |
13 |
95,657,944 (GRCm38) |
splice site |
probably benign |
|
|
IGL01968:Iqgap2
|
APN |
13 |
95,635,582 (GRCm38) |
missense |
possibly damaging |
0.80 |
|
IGL02049:Iqgap2
|
APN |
13 |
95,675,405 (GRCm38) |
splice site |
probably benign |
|
|
IGL02195:Iqgap2
|
APN |
13 |
95,661,734 (GRCm38) |
splice site |
probably benign |
|
|
IGL02387:Iqgap2
|
APN |
13 |
95,689,701 (GRCm38) |
missense |
probably benign |
0.00 |
|
IGL02634:Iqgap2
|
APN |
13 |
95,628,114 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02666:Iqgap2
|
APN |
13 |
95,628,056 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02685:Iqgap2
|
APN |
13 |
95,671,404 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02927:Iqgap2
|
APN |
13 |
95,724,676 (GRCm38) |
missense |
possibly damaging |
0.62 |
|
IGL02943:Iqgap2
|
APN |
13 |
95,661,735 (GRCm38) |
splice site |
probably benign |
|
|
IGL03167:Iqgap2
|
APN |
13 |
95,684,898 (GRCm38) |
missense |
probably benign |
0.34 |
|
IGL03169:Iqgap2
|
APN |
13 |
95,731,277 (GRCm38) |
splice site |
probably null |
|
|
IGL03293:Iqgap2
|
APN |
13 |
95,731,434 (GRCm38) |
missense |
probably damaging |
1.00 |
|
G1Funyon:Iqgap2
|
UTSW |
13 |
95,682,151 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0257:Iqgap2
|
UTSW |
13 |
95,724,544 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0335:Iqgap2
|
UTSW |
13 |
95,635,633 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R0364:Iqgap2
|
UTSW |
13 |
95,731,275 (GRCm38) |
splice site |
probably benign |
|
|
R0419:Iqgap2
|
UTSW |
13 |
95,689,699 (GRCm38) |
critical splice donor site |
probably null |
|
|
R1229:Iqgap2
|
UTSW |
13 |
95,632,165 (GRCm38) |
missense |
probably benign |
0.32 |
|
R1290:Iqgap2
|
UTSW |
13 |
95,668,513 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1397:Iqgap2
|
UTSW |
13 |
95,632,165 (GRCm38) |
missense |
probably benign |
0.32 |
|
R1498:Iqgap2
|
UTSW |
13 |
95,646,805 (GRCm38) |
missense |
probably benign |
|
|
R1513:Iqgap2
|
UTSW |
13 |
95,630,010 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1630:Iqgap2
|
UTSW |
13 |
95,689,785 (GRCm38) |
missense |
probably benign |
|
|
R2088:Iqgap2
|
UTSW |
13 |
95,891,663 (GRCm38) |
critical splice donor site |
probably null |
|
|
R2928:Iqgap2
|
UTSW |
13 |
95,682,236 (GRCm38) |
missense |
probably benign |
|
|
R3026:Iqgap2
|
UTSW |
13 |
95,673,056 (GRCm38) |
critical splice acceptor site |
probably null |
|
|
R3720:Iqgap2
|
UTSW |
13 |
95,668,528 (GRCm38) |
splice site |
probably null |
|
|
R3846:Iqgap2
|
UTSW |
13 |
95,673,678 (GRCm38) |
splice site |
probably benign |
|
|
R4056:Iqgap2
|
UTSW |
13 |
95,750,033 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4077:Iqgap2
|
UTSW |
13 |
95,657,867 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4353:Iqgap2
|
UTSW |
13 |
95,671,396 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4517:Iqgap2
|
UTSW |
13 |
95,664,061 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4628:Iqgap2
|
UTSW |
13 |
95,763,329 (GRCm38) |
missense |
probably benign |
0.17 |
|
R4686:Iqgap2
|
UTSW |
13 |
95,721,609 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R4724:Iqgap2
|
UTSW |
13 |
95,635,497 (GRCm38) |
missense |
possibly damaging |
0.73 |
|
R4826:Iqgap2
|
UTSW |
13 |
95,763,275 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4847:Iqgap2
|
UTSW |
13 |
95,673,743 (GRCm38) |
missense |
probably benign |
0.19 |
|
R4967:Iqgap2
|
UTSW |
13 |
95,630,006 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4973:Iqgap2
|
UTSW |
13 |
95,657,797 (GRCm38) |
splice site |
probably null |
|
|
R5010:Iqgap2
|
UTSW |
13 |
95,673,743 (GRCm38) |
missense |
probably benign |
0.19 |
|
R5086:Iqgap2
|
UTSW |
13 |
95,635,580 (GRCm38) |
missense |
probably benign |
0.01 |
|
R5496:Iqgap2
|
UTSW |
13 |
95,630,053 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5512:Iqgap2
|
UTSW |
13 |
95,675,376 (GRCm38) |
nonsense |
probably null |
|
|
R5629:Iqgap2
|
UTSW |
13 |
95,632,174 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5824:Iqgap2
|
UTSW |
13 |
95,675,372 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5830:Iqgap2
|
UTSW |
13 |
95,675,372 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5831:Iqgap2
|
UTSW |
13 |
95,675,372 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5832:Iqgap2
|
UTSW |
13 |
95,675,372 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5833:Iqgap2
|
UTSW |
13 |
95,675,372 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5834:Iqgap2
|
UTSW |
13 |
95,675,372 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5852:Iqgap2
|
UTSW |
13 |
95,675,372 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5888:Iqgap2
|
UTSW |
13 |
95,635,610 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R5889:Iqgap2
|
UTSW |
13 |
95,632,042 (GRCm38) |
missense |
probably benign |
0.00 |
|
R6093:Iqgap2
|
UTSW |
13 |
95,628,963 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R6141:Iqgap2
|
UTSW |
13 |
95,721,686 (GRCm38) |
splice site |
probably null |
|
|
R6404:Iqgap2
|
UTSW |
13 |
95,729,477 (GRCm38) |
missense |
probably benign |
0.28 |
|
R6434:Iqgap2
|
UTSW |
13 |
95,682,933 (GRCm38) |
missense |
possibly damaging |
0.85 |
|
R6648:Iqgap2
|
UTSW |
13 |
95,682,211 (GRCm38) |
missense |
probably benign |
0.27 |
|
R6658:Iqgap2
|
UTSW |
13 |
95,660,332 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6903:Iqgap2
|
UTSW |
13 |
95,661,057 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7223:Iqgap2
|
UTSW |
13 |
95,628,972 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7327:Iqgap2
|
UTSW |
13 |
95,635,655 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7371:Iqgap2
|
UTSW |
13 |
95,700,338 (GRCm38) |
splice site |
probably null |
|
|
R7378:Iqgap2
|
UTSW |
13 |
95,732,890 (GRCm38) |
critical splice donor site |
probably null |
|
|
R7441:Iqgap2
|
UTSW |
13 |
95,628,076 (GRCm38) |
missense |
probably benign |
0.23 |
|
R7575:Iqgap2
|
UTSW |
13 |
95,661,623 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7671:Iqgap2
|
UTSW |
13 |
95,628,119 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R7713:Iqgap2
|
UTSW |
13 |
95,731,444 (GRCm38) |
missense |
probably benign |
0.01 |
|
R7806:Iqgap2
|
UTSW |
13 |
95,682,257 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7893:Iqgap2
|
UTSW |
13 |
95,689,709 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R8052:Iqgap2
|
UTSW |
13 |
95,657,879 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R8121:Iqgap2
|
UTSW |
13 |
95,724,568 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8261:Iqgap2
|
UTSW |
13 |
95,635,570 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8301:Iqgap2
|
UTSW |
13 |
95,682,151 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8369:Iqgap2
|
UTSW |
13 |
95,661,603 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8485:Iqgap2
|
UTSW |
13 |
95,660,151 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R8709:Iqgap2
|
UTSW |
13 |
95,660,205 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R8710:Iqgap2
|
UTSW |
13 |
95,660,248 (GRCm38) |
missense |
probably benign |
0.24 |
|
R8737:Iqgap2
|
UTSW |
13 |
95,665,750 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8845:Iqgap2
|
UTSW |
13 |
95,657,884 (GRCm38) |
missense |
possibly damaging |
0.60 |
|
R8902:Iqgap2
|
UTSW |
13 |
95,682,203 (GRCm38) |
missense |
probably benign |
0.16 |
|
R8957:Iqgap2
|
UTSW |
13 |
95,635,646 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9153:Iqgap2
|
UTSW |
13 |
95,708,039 (GRCm38) |
missense |
probably benign |
|
|
R9259:Iqgap2
|
UTSW |
13 |
95,630,053 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9290:Iqgap2
|
UTSW |
13 |
95,750,015 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9414:Iqgap2
|
UTSW |
13 |
95,646,841 (GRCm38) |
missense |
|
|
|
R9432:Iqgap2
|
UTSW |
13 |
95,637,753 (GRCm38) |
missense |
probably benign |
|
|
R9747:Iqgap2
|
UTSW |
13 |
95,684,997 (GRCm38) |
missense |
probably damaging |
1.00 |
|
X0066:Iqgap2
|
UTSW |
13 |
95,671,383 (GRCm38) |
missense |
probably damaging |
0.98 |
|
Z1176:Iqgap2
|
UTSW |
13 |
95,731,443 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
| Predicted Primers |
|
| Posted On |
2013-08-08 |
Incidental Mutation