Incidental Mutation 'R0364:Iqgap2'
| ID |
65562 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Iqgap2
|
| Ensembl Gene |
ENSMUSG00000021676 |
| Gene Name |
IQ motif containing GTPase activating protein 2 |
| Synonyms |
4933417J23Rik |
| MMRRC Submission |
038570-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0364 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
13 |
| Chromosomal Location |
95763685-96028788 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to C
at 95867783 bp (GRCm39)
|
| 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: 99.0%
- 3x: 98.0%
- 10x: 95.3%
- 20x: 89.3%
|
| Validation Efficiency |
99% (86/87) |
| 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: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acp7 |
G |
A |
7: 28,310,553 (GRCm39) |
|
probably benign |
Het |
| Ano7 |
A |
G |
1: 93,316,380 (GRCm39) |
D221G |
probably benign |
Het |
| Arhgef12 |
A |
T |
9: 42,929,697 (GRCm39) |
N199K |
probably damaging |
Het |
| Arpc2 |
A |
G |
1: 74,276,046 (GRCm39) |
N26S |
probably null |
Het |
| Camta2 |
G |
A |
11: 70,574,136 (GRCm39) |
T127I |
probably damaging |
Het |
| Ccdc13 |
T |
A |
9: 121,627,282 (GRCm39) |
N665I |
probably damaging |
Het |
| Ccdc178 |
C |
T |
18: 22,048,119 (GRCm39) |
R757H |
probably damaging |
Het |
| Cfap52 |
A |
C |
11: 67,844,436 (GRCm39) |
I93S |
possibly damaging |
Het |
| Cmklr1 |
A |
T |
5: 113,752,578 (GRCm39) |
L141H |
probably damaging |
Het |
| Crybb3 |
T |
A |
5: 113,223,819 (GRCm39) |
I197F |
probably damaging |
Het |
| Cryzl1 |
G |
A |
16: 91,504,155 (GRCm39) |
P97S |
probably benign |
Het |
| Cubn |
T |
C |
2: 13,315,318 (GRCm39) |
|
probably benign |
Het |
| Cyp2d37-ps |
T |
C |
15: 82,574,253 (GRCm39) |
|
noncoding transcript |
Het |
| Cyp4a12b |
C |
A |
4: 115,290,117 (GRCm39) |
N223K |
probably benign |
Het |
| Dennd2a |
T |
C |
6: 39,485,233 (GRCm39) |
T349A |
probably benign |
Het |
| Dnah12 |
A |
G |
14: 26,445,628 (GRCm39) |
T730A |
probably benign |
Het |
| Dock5 |
G |
A |
14: 68,060,129 (GRCm39) |
|
probably benign |
Het |
| Dync2i1 |
A |
G |
12: 116,221,097 (GRCm39) |
|
probably benign |
Het |
| Elac2 |
A |
G |
11: 64,870,136 (GRCm39) |
Y67C |
probably damaging |
Het |
| Elmo1 |
A |
T |
13: 20,748,663 (GRCm39) |
K503* |
probably null |
Het |
| Endou |
A |
T |
15: 97,616,854 (GRCm39) |
|
probably benign |
Het |
| Eng |
T |
C |
2: 32,569,149 (GRCm39) |
S559P |
probably benign |
Het |
| Epc2 |
T |
A |
2: 49,427,145 (GRCm39) |
V563E |
possibly damaging |
Het |
| Fbxw17 |
T |
C |
13: 50,586,477 (GRCm39) |
S40P |
possibly damaging |
Het |
| Flt4 |
A |
T |
11: 49,527,818 (GRCm39) |
M924L |
probably benign |
Het |
| Fyb1 |
A |
G |
15: 6,610,272 (GRCm39) |
K282E |
probably damaging |
Het |
| Gabpa |
T |
A |
16: 84,654,275 (GRCm39) |
N317K |
possibly damaging |
Het |
| Gli3 |
G |
T |
13: 15,899,349 (GRCm39) |
G912V |
probably benign |
Het |
| Gm10295 |
C |
A |
7: 71,000,361 (GRCm39) |
C73F |
unknown |
Het |
| Gm10382 |
G |
T |
5: 125,466,728 (GRCm39) |
|
probably benign |
Het |
| Gp1ba |
T |
C |
11: 70,531,284 (GRCm39) |
|
probably benign |
Het |
| Gpr146 |
G |
A |
5: 139,364,933 (GRCm39) |
|
probably benign |
Het |
| Grm5 |
A |
G |
7: 87,723,594 (GRCm39) |
Y628C |
probably damaging |
Het |
| Hexa |
A |
G |
9: 59,471,218 (GRCm39) |
N491D |
probably benign |
Het |
| Hexd |
T |
A |
11: 121,102,969 (GRCm39) |
H62Q |
probably benign |
Het |
| Hpx |
G |
T |
7: 105,245,471 (GRCm39) |
Q101K |
probably benign |
Het |
| Ino80 |
G |
A |
2: 119,213,441 (GRCm39) |
R1249C |
probably damaging |
Het |
| Inpp4b |
A |
T |
8: 82,723,943 (GRCm39) |
T492S |
probably benign |
Het |
| Islr2 |
T |
C |
9: 58,107,027 (GRCm39) |
T78A |
possibly damaging |
Het |
| Itga9 |
A |
G |
9: 118,670,210 (GRCm39) |
T177A |
probably benign |
Het |
| Itpkc |
A |
C |
7: 26,927,174 (GRCm39) |
S247A |
possibly damaging |
Het |
| Kirrel1 |
T |
C |
3: 86,997,106 (GRCm39) |
Y287C |
probably damaging |
Het |
| Kiz |
T |
G |
2: 146,784,076 (GRCm39) |
S536R |
probably benign |
Het |
| Klhl9 |
T |
G |
4: 88,638,527 (GRCm39) |
K571N |
probably benign |
Het |
| Kprp |
A |
T |
3: 92,731,642 (GRCm39) |
Y469* |
probably null |
Het |
| Ksr1 |
A |
T |
11: 78,919,851 (GRCm39) |
|
probably benign |
Het |
| Lrrc37a |
C |
T |
11: 103,391,466 (GRCm39) |
V1320I |
possibly damaging |
Het |
| Ltf |
A |
T |
9: 110,854,235 (GRCm39) |
N350I |
probably benign |
Het |
| Msl3l2 |
G |
A |
10: 55,991,947 (GRCm39) |
R224Q |
possibly damaging |
Het |
| Myh6 |
A |
T |
14: 55,185,804 (GRCm39) |
Y1490* |
probably null |
Het |
| Necap1 |
A |
G |
6: 122,857,728 (GRCm39) |
|
probably benign |
Het |
| Nf1 |
A |
T |
11: 79,332,783 (GRCm39) |
K810* |
probably null |
Het |
| Nkx6-3 |
A |
G |
8: 23,647,722 (GRCm39) |
E227G |
possibly damaging |
Het |
| Nlrp1a |
T |
A |
11: 71,004,830 (GRCm39) |
|
probably benign |
Het |
| Obscn |
G |
A |
11: 59,019,107 (GRCm39) |
A969V |
probably benign |
Het |
| Or11a4 |
T |
C |
17: 37,536,934 (GRCm39) |
L306P |
possibly damaging |
Het |
| Or7g32 |
G |
A |
9: 19,389,268 (GRCm39) |
Q90* |
probably null |
Het |
| Or8b40 |
A |
G |
9: 38,027,325 (GRCm39) |
T78A |
probably benign |
Het |
| Or8k33 |
A |
T |
2: 86,384,123 (GRCm39) |
L115Q |
probably damaging |
Het |
| Pcdhb17 |
C |
A |
18: 37,618,888 (GRCm39) |
A226E |
possibly damaging |
Het |
| Phldb1 |
A |
T |
9: 44,610,632 (GRCm39) |
|
probably benign |
Het |
| Plekha5 |
G |
A |
6: 140,537,473 (GRCm39) |
R646K |
possibly damaging |
Het |
| Pon2 |
G |
A |
6: 5,266,156 (GRCm39) |
Q288* |
probably null |
Het |
| Prr14 |
G |
A |
7: 127,073,751 (GRCm39) |
R205H |
probably benign |
Het |
| Ptpn13 |
C |
A |
5: 103,681,214 (GRCm39) |
R805S |
probably damaging |
Het |
| Pyroxd2 |
A |
T |
19: 42,735,992 (GRCm39) |
V62D |
probably damaging |
Het |
| Rab37 |
G |
T |
11: 115,047,790 (GRCm39) |
C44F |
probably damaging |
Het |
| Rbm44 |
T |
C |
1: 91,080,069 (GRCm39) |
S52P |
probably benign |
Het |
| Rusf1 |
C |
T |
7: 127,889,786 (GRCm39) |
R1H |
probably damaging |
Het |
| Scn5a |
T |
C |
9: 119,351,665 (GRCm39) |
D772G |
probably damaging |
Het |
| Slc7a5 |
A |
G |
8: 122,611,754 (GRCm39) |
F425L |
probably benign |
Het |
| Slk |
T |
A |
19: 47,608,628 (GRCm39) |
L527* |
probably null |
Het |
| Stpg4 |
T |
A |
17: 87,697,142 (GRCm39) |
|
probably null |
Het |
| Taar6 |
C |
A |
10: 23,861,046 (GRCm39) |
V167L |
probably benign |
Het |
| Tas2r123 |
T |
A |
6: 132,824,644 (GRCm39) |
S180R |
probably benign |
Het |
| Tmc2 |
C |
T |
2: 130,044,023 (GRCm39) |
R86W |
probably benign |
Het |
| Tmem200c |
T |
A |
17: 69,147,543 (GRCm39) |
V42E |
probably damaging |
Het |
| Trhde |
T |
C |
10: 114,338,887 (GRCm39) |
|
probably benign |
Het |
| Tshz1 |
A |
T |
18: 84,034,249 (GRCm39) |
I53N |
probably benign |
Het |
| Tshz3 |
A |
G |
7: 36,469,958 (GRCm39) |
E649G |
probably benign |
Het |
| Ttll7 |
C |
A |
3: 146,650,936 (GRCm39) |
R719S |
possibly damaging |
Het |
| Utp4 |
T |
C |
8: 107,625,169 (GRCm39) |
|
probably benign |
Het |
| Vmn1r35 |
A |
G |
6: 66,655,827 (GRCm39) |
I281T |
probably damaging |
Het |
| Vps39 |
T |
G |
2: 120,176,119 (GRCm39) |
K76T |
probably damaging |
Het |
| Whamm |
A |
G |
7: 81,243,799 (GRCm39) |
T674A |
probably benign |
Het |
| Zbtb16 |
A |
G |
9: 48,654,876 (GRCm39) |
|
probably benign |
Het |
| Zfp623 |
T |
C |
15: 75,820,510 (GRCm39) |
S489P |
probably benign |
Het |
|
| Other mutations in Iqgap2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00799:Iqgap2
|
APN |
13 |
95,794,452 (GRCm39) |
splice site |
probably benign |
|
|
IGL01968:Iqgap2
|
APN |
13 |
95,772,090 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL02049:Iqgap2
|
APN |
13 |
95,811,913 (GRCm39) |
splice site |
probably benign |
|
|
IGL02195:Iqgap2
|
APN |
13 |
95,798,242 (GRCm39) |
splice site |
probably benign |
|
|
IGL02387:Iqgap2
|
APN |
13 |
95,826,209 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02634:Iqgap2
|
APN |
13 |
95,764,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02666:Iqgap2
|
APN |
13 |
95,764,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02685:Iqgap2
|
APN |
13 |
95,807,912 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02927:Iqgap2
|
APN |
13 |
95,861,184 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL02943:Iqgap2
|
APN |
13 |
95,798,243 (GRCm39) |
splice site |
probably benign |
|
|
IGL03167:Iqgap2
|
APN |
13 |
95,821,406 (GRCm39) |
missense |
probably benign |
0.34 |
|
IGL03169:Iqgap2
|
APN |
13 |
95,867,785 (GRCm39) |
splice site |
probably null |
|
|
IGL03293:Iqgap2
|
APN |
13 |
95,867,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|
G1Funyon:Iqgap2
|
UTSW |
13 |
95,818,659 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0257:Iqgap2
|
UTSW |
13 |
95,861,052 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0335:Iqgap2
|
UTSW |
13 |
95,772,141 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0360:Iqgap2
|
UTSW |
13 |
95,867,783 (GRCm39) |
splice site |
probably benign |
|
|
R0419:Iqgap2
|
UTSW |
13 |
95,826,207 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1229:Iqgap2
|
UTSW |
13 |
95,768,673 (GRCm39) |
missense |
probably benign |
0.32 |
|
R1290:Iqgap2
|
UTSW |
13 |
95,805,021 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1397:Iqgap2
|
UTSW |
13 |
95,768,673 (GRCm39) |
missense |
probably benign |
0.32 |
|
R1498:Iqgap2
|
UTSW |
13 |
95,783,313 (GRCm39) |
missense |
probably benign |
|
|
R1513:Iqgap2
|
UTSW |
13 |
95,766,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1630:Iqgap2
|
UTSW |
13 |
95,826,293 (GRCm39) |
missense |
probably benign |
|
|
R2088:Iqgap2
|
UTSW |
13 |
96,028,171 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2928:Iqgap2
|
UTSW |
13 |
95,818,744 (GRCm39) |
missense |
probably benign |
|
|
R3026:Iqgap2
|
UTSW |
13 |
95,809,564 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R3720:Iqgap2
|
UTSW |
13 |
95,805,036 (GRCm39) |
splice site |
probably null |
|
|
R3846:Iqgap2
|
UTSW |
13 |
95,810,186 (GRCm39) |
splice site |
probably benign |
|
|
R4056:Iqgap2
|
UTSW |
13 |
95,886,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4077:Iqgap2
|
UTSW |
13 |
95,794,375 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4353:Iqgap2
|
UTSW |
13 |
95,807,904 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4517:Iqgap2
|
UTSW |
13 |
95,800,569 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4628:Iqgap2
|
UTSW |
13 |
95,899,837 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4686:Iqgap2
|
UTSW |
13 |
95,858,117 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4724:Iqgap2
|
UTSW |
13 |
95,772,005 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R4826:Iqgap2
|
UTSW |
13 |
95,899,783 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4847:Iqgap2
|
UTSW |
13 |
95,810,251 (GRCm39) |
missense |
probably benign |
0.19 |
|
R4967:Iqgap2
|
UTSW |
13 |
95,766,514 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4973:Iqgap2
|
UTSW |
13 |
95,794,305 (GRCm39) |
splice site |
probably null |
|
|
R5010:Iqgap2
|
UTSW |
13 |
95,810,251 (GRCm39) |
missense |
probably benign |
0.19 |
|
R5086:Iqgap2
|
UTSW |
13 |
95,772,088 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5496:Iqgap2
|
UTSW |
13 |
95,766,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5512:Iqgap2
|
UTSW |
13 |
95,811,884 (GRCm39) |
nonsense |
probably null |
|
|
R5629:Iqgap2
|
UTSW |
13 |
95,768,682 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5824:Iqgap2
|
UTSW |
13 |
95,811,880 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5830:Iqgap2
|
UTSW |
13 |
95,811,880 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5831:Iqgap2
|
UTSW |
13 |
95,811,880 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5832:Iqgap2
|
UTSW |
13 |
95,811,880 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5833:Iqgap2
|
UTSW |
13 |
95,811,880 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5834:Iqgap2
|
UTSW |
13 |
95,811,880 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5852:Iqgap2
|
UTSW |
13 |
95,811,880 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5888:Iqgap2
|
UTSW |
13 |
95,772,118 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5889:Iqgap2
|
UTSW |
13 |
95,768,550 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6093:Iqgap2
|
UTSW |
13 |
95,765,471 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6141:Iqgap2
|
UTSW |
13 |
95,858,194 (GRCm39) |
splice site |
probably null |
|
|
R6404:Iqgap2
|
UTSW |
13 |
95,865,985 (GRCm39) |
missense |
probably benign |
0.28 |
|
R6434:Iqgap2
|
UTSW |
13 |
95,819,441 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6648:Iqgap2
|
UTSW |
13 |
95,818,719 (GRCm39) |
missense |
probably benign |
0.27 |
|
R6658:Iqgap2
|
UTSW |
13 |
95,796,840 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6903:Iqgap2
|
UTSW |
13 |
95,797,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7223:Iqgap2
|
UTSW |
13 |
95,765,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7327:Iqgap2
|
UTSW |
13 |
95,772,163 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7371:Iqgap2
|
UTSW |
13 |
95,836,846 (GRCm39) |
splice site |
probably null |
|
|
R7378:Iqgap2
|
UTSW |
13 |
95,869,398 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7441:Iqgap2
|
UTSW |
13 |
95,764,584 (GRCm39) |
missense |
probably benign |
0.23 |
|
R7575:Iqgap2
|
UTSW |
13 |
95,798,131 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7671:Iqgap2
|
UTSW |
13 |
95,764,627 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7713:Iqgap2
|
UTSW |
13 |
95,867,952 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7806:Iqgap2
|
UTSW |
13 |
95,818,765 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7893:Iqgap2
|
UTSW |
13 |
95,826,217 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8052:Iqgap2
|
UTSW |
13 |
95,794,387 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8121:Iqgap2
|
UTSW |
13 |
95,861,076 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8261:Iqgap2
|
UTSW |
13 |
95,772,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8301:Iqgap2
|
UTSW |
13 |
95,818,659 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8369:Iqgap2
|
UTSW |
13 |
95,798,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8485:Iqgap2
|
UTSW |
13 |
95,796,659 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8709:Iqgap2
|
UTSW |
13 |
95,796,713 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8710:Iqgap2
|
UTSW |
13 |
95,796,756 (GRCm39) |
missense |
probably benign |
0.24 |
|
R8737:Iqgap2
|
UTSW |
13 |
95,802,258 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8845:Iqgap2
|
UTSW |
13 |
95,794,392 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R8902:Iqgap2
|
UTSW |
13 |
95,818,711 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8957:Iqgap2
|
UTSW |
13 |
95,772,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9153:Iqgap2
|
UTSW |
13 |
95,844,547 (GRCm39) |
missense |
probably benign |
|
|
R9259:Iqgap2
|
UTSW |
13 |
95,766,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9290:Iqgap2
|
UTSW |
13 |
95,886,523 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9414:Iqgap2
|
UTSW |
13 |
95,783,349 (GRCm39) |
missense |
|
|
|
R9432:Iqgap2
|
UTSW |
13 |
95,774,261 (GRCm39) |
missense |
probably benign |
|
|
R9747:Iqgap2
|
UTSW |
13 |
95,821,505 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0066:Iqgap2
|
UTSW |
13 |
95,807,891 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1176:Iqgap2
|
UTSW |
13 |
95,867,951 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
| Predicted Primers |
|
| Posted On |
2013-08-08 |
Incidental Mutation