Incidental Mutation 'R7214:Tiam2'
ID |
561346 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tiam2
|
Ensembl Gene |
ENSMUSG00000023800 |
Gene Name |
T cell lymphoma invasion and metastasis 2 |
Synonyms |
STEF, 3000002F19Rik |
MMRRC Submission |
045286-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7214 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
3376675-3569672 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 3568687 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 1611
(I1611N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000072020
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041003]
[ENSMUST00000072156]
[ENSMUST00000169838]
[ENSMUST00000227405]
|
AlphaFold |
Q6ZPF3 |
PDB Structure |
Crystal structure of the Tiam2 PHCCEx domain [X-RAY DIFFRACTION]
Low-resolution crystal structure of the Tiam2 PHCCEx domain [X-RAY DIFFRACTION]
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000041003
|
SMART Domains |
Protein: ENSMUSP00000035291 Gene: ENSMUSG00000036983
Domain | Start | End | E-Value | Type |
rADc
|
43 |
234 |
5.56e-69 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000072156
AA Change: I1611N
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000072020 Gene: ENSMUSG00000023800 AA Change: I1611N
Domain | Start | End | E-Value | Type |
low complexity region
|
230 |
245 |
N/A |
INTRINSIC |
low complexity region
|
267 |
281 |
N/A |
INTRINSIC |
low complexity region
|
471 |
492 |
N/A |
INTRINSIC |
PH
|
505 |
620 |
7.82e-16 |
SMART |
RBD
|
831 |
902 |
1.32e-26 |
SMART |
PDZ
|
921 |
995 |
2.38e-7 |
SMART |
RhoGEF
|
1124 |
1313 |
2.23e-61 |
SMART |
PH
|
1347 |
1478 |
2.86e0 |
SMART |
low complexity region
|
1522 |
1532 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000169838
AA Change: I1611N
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000125842 Gene: ENSMUSG00000023800 AA Change: I1611N
Domain | Start | End | E-Value | Type |
low complexity region
|
230 |
245 |
N/A |
INTRINSIC |
low complexity region
|
267 |
281 |
N/A |
INTRINSIC |
low complexity region
|
471 |
492 |
N/A |
INTRINSIC |
PH
|
505 |
620 |
7.82e-16 |
SMART |
RBD
|
831 |
902 |
1.32e-26 |
SMART |
PDZ
|
921 |
995 |
2.38e-7 |
SMART |
RhoGEF
|
1124 |
1313 |
2.23e-61 |
SMART |
PH
|
1347 |
1478 |
2.86e0 |
SMART |
low complexity region
|
1522 |
1532 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000227405
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a guanine nucleotide exchange factor. A highly similar mouse protein specifically activates ras-related C3 botulinum substrate 1, converting this Rho-like guanosine triphosphatase (GTPase) from a guanosine diphosphate-bound inactive state to a guanosine triphosphate-bound active state. The encoded protein may play a role in neural cell development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg5 |
C |
T |
8: 95,660,646 (GRCm39) |
T95I |
|
Het |
Arap2 |
C |
T |
5: 62,906,681 (GRCm39) |
V113I |
probably benign |
Het |
Atraid |
C |
T |
5: 31,209,590 (GRCm39) |
Q85* |
probably null |
Het |
Bcdin3d |
T |
C |
15: 99,368,344 (GRCm39) |
D285G |
probably benign |
Het |
Bmal1 |
T |
A |
7: 112,898,610 (GRCm39) |
I346K |
probably benign |
Het |
Carmil3 |
T |
C |
14: 55,736,069 (GRCm39) |
W604R |
probably damaging |
Het |
Ccl6 |
C |
T |
11: 83,480,582 (GRCm39) |
|
probably null |
Het |
Cct4 |
C |
T |
11: 22,940,616 (GRCm39) |
|
probably benign |
Het |
Cd2ap |
C |
T |
17: 43,156,285 (GRCm39) |
R84Q |
possibly damaging |
Het |
Cdt1 |
T |
A |
8: 123,295,012 (GRCm39) |
|
probably null |
Het |
Cln3 |
C |
T |
7: 126,181,942 (GRCm39) |
G40D |
probably damaging |
Het |
Crlf3 |
T |
C |
11: 79,955,216 (GRCm39) |
S47G |
possibly damaging |
Het |
Csrp3 |
T |
C |
7: 48,480,385 (GRCm39) |
K193R |
probably benign |
Het |
Cxcl3 |
A |
C |
5: 90,934,219 (GRCm39) |
E33A |
probably damaging |
Het |
Cyp11b1 |
T |
C |
15: 74,708,708 (GRCm39) |
D362G |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,321,935 (GRCm39) |
D3795G |
probably damaging |
Het |
Dnah3 |
G |
A |
7: 119,521,965 (GRCm39) |
A4076V |
probably damaging |
Het |
Dnaja3 |
T |
A |
16: 4,519,046 (GRCm39) |
I380N |
possibly damaging |
Het |
Dock10 |
T |
A |
1: 80,546,246 (GRCm39) |
H785L |
probably benign |
Het |
Dop1b |
T |
G |
16: 93,607,023 (GRCm39) |
F2226V |
possibly damaging |
Het |
Dscaml1 |
A |
T |
9: 45,581,437 (GRCm39) |
I419F |
probably benign |
Het |
Dyrk4 |
T |
A |
6: 126,862,200 (GRCm39) |
I431F |
probably benign |
Het |
Endog |
C |
T |
2: 30,062,902 (GRCm39) |
R181C |
probably damaging |
Het |
Fam90a1a |
A |
T |
8: 22,453,641 (GRCm39) |
Y332F |
probably benign |
Het |
Fastkd3 |
T |
C |
13: 68,737,499 (GRCm39) |
I588T |
probably benign |
Het |
Galnt9 |
G |
A |
5: 110,737,694 (GRCm39) |
V217I |
probably benign |
Het |
Gm973 |
A |
T |
1: 59,601,888 (GRCm39) |
R501* |
probably null |
Het |
Gnptab |
C |
T |
10: 88,215,019 (GRCm39) |
|
probably benign |
Het |
Gpn1 |
T |
C |
5: 31,660,761 (GRCm39) |
F184S |
probably damaging |
Het |
Imp3 |
G |
T |
9: 56,845,007 (GRCm39) |
V73L |
probably benign |
Het |
Ipo11 |
T |
C |
13: 107,032,365 (GRCm39) |
D259G |
probably null |
Het |
Jag1 |
T |
C |
2: 136,948,802 (GRCm39) |
S142G |
probably benign |
Het |
Klhl5 |
A |
T |
5: 65,289,098 (GRCm39) |
E120V |
probably benign |
Het |
Lct |
C |
A |
1: 128,228,197 (GRCm39) |
V1099L |
probably benign |
Het |
Lrba |
G |
C |
3: 86,235,633 (GRCm39) |
W912C |
probably damaging |
Het |
Lss |
C |
T |
10: 76,383,305 (GRCm39) |
T535I |
probably damaging |
Het |
Mcts2 |
T |
C |
2: 152,529,297 (GRCm39) |
I36T |
probably benign |
Het |
Meikin |
T |
A |
11: 54,302,738 (GRCm39) |
N383K |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,461,055 (GRCm39) |
Y663C |
probably damaging |
Het |
Nadk2 |
T |
A |
15: 9,108,342 (GRCm39) |
M419K |
probably damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nfat5 |
T |
C |
8: 108,020,515 (GRCm39) |
S20P |
probably damaging |
Het |
Nlrp1a |
C |
T |
11: 71,014,119 (GRCm39) |
C377Y |
probably damaging |
Het |
Nlrp9a |
T |
C |
7: 26,250,463 (GRCm39) |
V76A |
probably damaging |
Het |
Nrap |
C |
A |
19: 56,366,567 (GRCm39) |
A341S |
probably benign |
Het |
Ntng2 |
T |
C |
2: 29,117,732 (GRCm39) |
S239G |
probably damaging |
Het |
Nup188 |
T |
A |
2: 30,197,566 (GRCm39) |
C207S |
possibly damaging |
Het |
Or10a4 |
T |
C |
7: 106,697,619 (GRCm39) |
*316R |
probably null |
Het |
Or10ak7 |
T |
A |
4: 118,791,146 (GRCm39) |
I300F |
possibly damaging |
Het |
Or1j17 |
T |
C |
2: 36,578,107 (GRCm39) |
I31T |
probably benign |
Het |
Or2ag1 |
T |
C |
7: 106,473,474 (GRCm39) |
|
probably benign |
Het |
Or5b118 |
T |
A |
19: 13,448,337 (GRCm39) |
M1K |
probably null |
Het |
Or8c13 |
A |
C |
9: 38,091,318 (GRCm39) |
V267G |
probably damaging |
Het |
Or8k31-ps1 |
C |
T |
2: 86,356,150 (GRCm39) |
V124I |
probably damaging |
Het |
Pcdhgb2 |
C |
A |
18: 37,823,159 (GRCm39) |
A50E |
probably damaging |
Het |
Pgap1 |
A |
T |
1: 54,582,220 (GRCm39) |
M209K |
possibly damaging |
Het |
Plbd1 |
T |
A |
6: 136,589,829 (GRCm39) |
D463V |
probably damaging |
Het |
Plcg2 |
T |
A |
8: 118,310,288 (GRCm39) |
I380N |
probably damaging |
Het |
Pnpt1 |
T |
C |
11: 29,087,285 (GRCm39) |
W184R |
probably damaging |
Het |
Pptc7 |
G |
A |
5: 122,451,840 (GRCm39) |
V202I |
probably benign |
Het |
Prpf6 |
C |
T |
2: 181,282,389 (GRCm39) |
A510V |
probably damaging |
Het |
Prr5l |
T |
C |
2: 101,559,777 (GRCm39) |
Y235C |
probably benign |
Het |
Ptprk |
T |
C |
10: 28,450,905 (GRCm39) |
V1022A |
probably benign |
Het |
Rbl2 |
T |
C |
8: 91,810,057 (GRCm39) |
|
probably null |
Het |
Rmnd1 |
T |
C |
10: 4,360,753 (GRCm39) |
K348E |
probably benign |
Het |
Rsf1 |
CGGCGGC |
CGGCGGCGGGGGCGGC |
7: 97,229,136 (GRCm39) |
|
probably benign |
Het |
Sacs |
T |
A |
14: 61,429,241 (GRCm39) |
N433K |
probably benign |
Het |
Scyl1 |
T |
C |
19: 5,810,057 (GRCm39) |
T590A |
probably benign |
Het |
Sdhd |
A |
G |
9: 50,508,533 (GRCm39) |
V111A |
possibly damaging |
Het |
Sec24b |
G |
T |
3: 129,827,509 (GRCm39) |
P330Q |
probably benign |
Het |
Serpinb6d |
C |
T |
13: 33,848,128 (GRCm39) |
P31S |
probably damaging |
Het |
Slc26a9 |
A |
T |
1: 131,687,211 (GRCm39) |
R457W |
probably damaging |
Het |
Slc5a8 |
G |
A |
10: 88,755,364 (GRCm39) |
M490I |
probably benign |
Het |
Slx4 |
A |
G |
16: 3,806,844 (GRCm39) |
I533T |
probably benign |
Het |
Slx4ip |
T |
A |
2: 136,888,650 (GRCm39) |
F110L |
probably benign |
Het |
Smchd1 |
T |
C |
17: 71,652,359 (GRCm39) |
R2000G |
probably benign |
Het |
Snx8 |
T |
C |
5: 140,346,008 (GRCm39) |
E75G |
possibly damaging |
Het |
Stab2 |
C |
A |
10: 86,735,705 (GRCm39) |
C1292F |
probably damaging |
Het |
Swt1 |
A |
T |
1: 151,270,364 (GRCm39) |
M617K |
possibly damaging |
Het |
Thoc2l |
A |
G |
5: 104,670,229 (GRCm39) |
T1584A |
probably benign |
Het |
Tmem63b |
T |
G |
17: 45,972,748 (GRCm39) |
N682T |
probably benign |
Het |
Trio |
C |
T |
15: 27,871,273 (GRCm39) |
V674M |
probably damaging |
Het |
Trpc3 |
G |
A |
3: 36,704,286 (GRCm39) |
T557M |
possibly damaging |
Het |
Vac14 |
T |
G |
8: 111,397,674 (GRCm39) |
L463R |
probably damaging |
Het |
Vmn2r43 |
C |
T |
7: 8,256,379 (GRCm39) |
|
probably null |
Het |
Wdr49 |
A |
T |
3: 75,265,751 (GRCm39) |
Y232N |
possibly damaging |
Het |
Wdr90 |
T |
C |
17: 26,064,367 (GRCm39) |
M1835V |
probably benign |
Het |
Xpc |
T |
C |
6: 91,469,320 (GRCm39) |
E809G |
probably damaging |
Het |
Zfhx3 |
A |
T |
8: 109,675,493 (GRCm39) |
Q2181L |
probably damaging |
Het |
Zfp442 |
T |
C |
2: 150,251,201 (GRCm39) |
T234A |
probably benign |
Het |
Zfp764 |
A |
T |
7: 127,004,450 (GRCm39) |
M227K |
probably benign |
Het |
Zfp764l1 |
A |
G |
7: 126,990,695 (GRCm39) |
S431P |
probably benign |
Het |
Zfp957 |
A |
G |
14: 79,450,750 (GRCm39) |
S350P |
unknown |
Het |
Zscan29 |
T |
A |
2: 120,999,761 (GRCm39) |
K147* |
probably null |
Het |
|
Other mutations in Tiam2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Tiam2
|
APN |
17 |
3,465,303 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01320:Tiam2
|
APN |
17 |
3,556,020 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01384:Tiam2
|
APN |
17 |
3,477,477 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01575:Tiam2
|
APN |
17 |
3,504,591 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01769:Tiam2
|
APN |
17 |
3,477,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02395:Tiam2
|
APN |
17 |
3,471,756 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02652:Tiam2
|
APN |
17 |
3,489,971 (GRCm39) |
splice site |
probably benign |
|
IGL03102:Tiam2
|
APN |
17 |
3,559,823 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03222:Tiam2
|
APN |
17 |
3,488,983 (GRCm39) |
missense |
probably damaging |
0.97 |
Feste_burg
|
UTSW |
17 |
3,464,897 (GRCm39) |
frame shift |
probably null |
|
R0257:Tiam2
|
UTSW |
17 |
3,501,088 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0420:Tiam2
|
UTSW |
17 |
3,553,193 (GRCm39) |
missense |
probably benign |
0.01 |
R0528:Tiam2
|
UTSW |
17 |
3,561,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Tiam2
|
UTSW |
17 |
3,471,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R0551:Tiam2
|
UTSW |
17 |
3,479,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R0554:Tiam2
|
UTSW |
17 |
3,488,956 (GRCm39) |
nonsense |
probably null |
|
R0645:Tiam2
|
UTSW |
17 |
3,564,973 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0726:Tiam2
|
UTSW |
17 |
3,563,108 (GRCm39) |
unclassified |
probably benign |
|
R1139:Tiam2
|
UTSW |
17 |
3,527,542 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1392:Tiam2
|
UTSW |
17 |
3,464,472 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1392:Tiam2
|
UTSW |
17 |
3,464,472 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1529:Tiam2
|
UTSW |
17 |
3,566,978 (GRCm39) |
missense |
probably benign |
0.00 |
R1671:Tiam2
|
UTSW |
17 |
3,557,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Tiam2
|
UTSW |
17 |
3,568,698 (GRCm39) |
missense |
probably damaging |
0.98 |
R1759:Tiam2
|
UTSW |
17 |
3,566,278 (GRCm39) |
missense |
probably damaging |
0.98 |
R1850:Tiam2
|
UTSW |
17 |
3,487,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Tiam2
|
UTSW |
17 |
3,465,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R1855:Tiam2
|
UTSW |
17 |
3,465,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R1931:Tiam2
|
UTSW |
17 |
3,565,000 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1932:Tiam2
|
UTSW |
17 |
3,565,000 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1993:Tiam2
|
UTSW |
17 |
3,465,401 (GRCm39) |
nonsense |
probably null |
|
R2211:Tiam2
|
UTSW |
17 |
3,465,193 (GRCm39) |
nonsense |
probably null |
|
R2217:Tiam2
|
UTSW |
17 |
3,465,389 (GRCm39) |
missense |
probably benign |
0.34 |
R2278:Tiam2
|
UTSW |
17 |
3,477,495 (GRCm39) |
missense |
probably damaging |
0.96 |
R2407:Tiam2
|
UTSW |
17 |
3,527,536 (GRCm39) |
missense |
probably benign |
0.14 |
R2516:Tiam2
|
UTSW |
17 |
3,503,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R2991:Tiam2
|
UTSW |
17 |
3,568,525 (GRCm39) |
missense |
probably benign |
|
R3086:Tiam2
|
UTSW |
17 |
3,471,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R3121:Tiam2
|
UTSW |
17 |
3,489,977 (GRCm39) |
missense |
probably benign |
0.01 |
R3686:Tiam2
|
UTSW |
17 |
3,471,959 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3740:Tiam2
|
UTSW |
17 |
3,464,388 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3742:Tiam2
|
UTSW |
17 |
3,464,388 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3826:Tiam2
|
UTSW |
17 |
3,557,976 (GRCm39) |
splice site |
probably benign |
|
R3829:Tiam2
|
UTSW |
17 |
3,557,976 (GRCm39) |
splice site |
probably benign |
|
R3844:Tiam2
|
UTSW |
17 |
3,471,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R3970:Tiam2
|
UTSW |
17 |
3,479,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R4060:Tiam2
|
UTSW |
17 |
3,479,255 (GRCm39) |
missense |
probably benign |
0.00 |
R4296:Tiam2
|
UTSW |
17 |
3,501,120 (GRCm39) |
missense |
probably benign |
|
R4357:Tiam2
|
UTSW |
17 |
3,501,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4368:Tiam2
|
UTSW |
17 |
3,464,958 (GRCm39) |
missense |
probably benign |
0.01 |
R4369:Tiam2
|
UTSW |
17 |
3,464,242 (GRCm39) |
start gained |
probably benign |
|
R4524:Tiam2
|
UTSW |
17 |
3,564,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R4619:Tiam2
|
UTSW |
17 |
3,568,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Tiam2
|
UTSW |
17 |
3,504,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R4723:Tiam2
|
UTSW |
17 |
3,500,592 (GRCm39) |
missense |
probably benign |
0.00 |
R4979:Tiam2
|
UTSW |
17 |
3,555,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R5182:Tiam2
|
UTSW |
17 |
3,488,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R5451:Tiam2
|
UTSW |
17 |
3,479,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R5728:Tiam2
|
UTSW |
17 |
3,465,231 (GRCm39) |
missense |
probably damaging |
0.99 |
R5827:Tiam2
|
UTSW |
17 |
3,498,764 (GRCm39) |
missense |
probably benign |
0.00 |
R5879:Tiam2
|
UTSW |
17 |
3,487,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5960:Tiam2
|
UTSW |
17 |
3,488,915 (GRCm39) |
missense |
probably benign |
0.24 |
R5974:Tiam2
|
UTSW |
17 |
3,465,084 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6198:Tiam2
|
UTSW |
17 |
3,464,396 (GRCm39) |
missense |
probably benign |
0.06 |
R6222:Tiam2
|
UTSW |
17 |
3,503,613 (GRCm39) |
missense |
probably damaging |
0.96 |
R6295:Tiam2
|
UTSW |
17 |
3,559,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6355:Tiam2
|
UTSW |
17 |
3,464,897 (GRCm39) |
frame shift |
probably null |
|
R6356:Tiam2
|
UTSW |
17 |
3,464,897 (GRCm39) |
frame shift |
probably null |
|
R6454:Tiam2
|
UTSW |
17 |
3,488,938 (GRCm39) |
missense |
probably benign |
0.00 |
R6497:Tiam2
|
UTSW |
17 |
3,557,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R6579:Tiam2
|
UTSW |
17 |
3,464,897 (GRCm39) |
frame shift |
probably null |
|
R6580:Tiam2
|
UTSW |
17 |
3,464,897 (GRCm39) |
frame shift |
probably null |
|
R6581:Tiam2
|
UTSW |
17 |
3,464,897 (GRCm39) |
frame shift |
probably null |
|
R6582:Tiam2
|
UTSW |
17 |
3,464,897 (GRCm39) |
frame shift |
probably null |
|
R6648:Tiam2
|
UTSW |
17 |
3,557,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6705:Tiam2
|
UTSW |
17 |
3,568,518 (GRCm39) |
missense |
probably benign |
0.01 |
R6758:Tiam2
|
UTSW |
17 |
3,568,678 (GRCm39) |
missense |
probably benign |
0.01 |
R6836:Tiam2
|
UTSW |
17 |
3,464,655 (GRCm39) |
missense |
probably benign |
0.17 |
R6924:Tiam2
|
UTSW |
17 |
3,558,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R6977:Tiam2
|
UTSW |
17 |
3,568,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Tiam2
|
UTSW |
17 |
3,498,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R7151:Tiam2
|
UTSW |
17 |
3,498,660 (GRCm39) |
missense |
probably benign |
0.36 |
R7332:Tiam2
|
UTSW |
17 |
3,503,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R7334:Tiam2
|
UTSW |
17 |
3,553,283 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7414:Tiam2
|
UTSW |
17 |
3,464,388 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7660:Tiam2
|
UTSW |
17 |
3,532,880 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
R7743:Tiam2
|
UTSW |
17 |
3,568,431 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7755:Tiam2
|
UTSW |
17 |
3,471,591 (GRCm39) |
missense |
probably benign |
0.01 |
R7805:Tiam2
|
UTSW |
17 |
3,559,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7813:Tiam2
|
UTSW |
17 |
3,487,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Tiam2
|
UTSW |
17 |
3,568,399 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7989:Tiam2
|
UTSW |
17 |
3,568,524 (GRCm39) |
nonsense |
probably null |
|
R8011:Tiam2
|
UTSW |
17 |
3,498,671 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8221:Tiam2
|
UTSW |
17 |
3,568,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R8260:Tiam2
|
UTSW |
17 |
3,568,594 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8292:Tiam2
|
UTSW |
17 |
3,557,142 (GRCm39) |
missense |
probably benign |
0.01 |
R8406:Tiam2
|
UTSW |
17 |
3,558,065 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8424:Tiam2
|
UTSW |
17 |
3,566,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Tiam2
|
UTSW |
17 |
3,566,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R8430:Tiam2
|
UTSW |
17 |
3,568,537 (GRCm39) |
missense |
probably benign |
0.05 |
R8530:Tiam2
|
UTSW |
17 |
3,501,087 (GRCm39) |
missense |
probably benign |
0.03 |
R8692:Tiam2
|
UTSW |
17 |
3,479,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Tiam2
|
UTSW |
17 |
3,527,471 (GRCm39) |
missense |
probably benign |
0.00 |
R9067:Tiam2
|
UTSW |
17 |
3,561,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R9080:Tiam2
|
UTSW |
17 |
3,464,519 (GRCm39) |
missense |
probably benign |
|
R9090:Tiam2
|
UTSW |
17 |
3,465,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Tiam2
|
UTSW |
17 |
3,498,729 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9271:Tiam2
|
UTSW |
17 |
3,465,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R9347:Tiam2
|
UTSW |
17 |
3,471,923 (GRCm39) |
missense |
probably benign |
0.37 |
R9353:Tiam2
|
UTSW |
17 |
3,558,074 (GRCm39) |
nonsense |
probably null |
|
R9407:Tiam2
|
UTSW |
17 |
3,553,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R9460:Tiam2
|
UTSW |
17 |
3,487,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R9550:Tiam2
|
UTSW |
17 |
3,559,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Tiam2
|
UTSW |
17 |
3,561,440 (GRCm39) |
missense |
probably benign |
0.20 |
X0027:Tiam2
|
UTSW |
17 |
3,464,275 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
X0060:Tiam2
|
UTSW |
17 |
3,500,629 (GRCm39) |
splice site |
probably null |
|
X0065:Tiam2
|
UTSW |
17 |
3,555,983 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Tiam2
|
UTSW |
17 |
3,465,294 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Tiam2
|
UTSW |
17 |
3,556,051 (GRCm39) |
missense |
probably null |
1.00 |
Z1177:Tiam2
|
UTSW |
17 |
3,477,538 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GCAACTCACTGGACTCAGATGAG -3'
(R):5'- TGCGCCTTGAGCAAAGTTC -3'
Sequencing Primer
(F):5'- CTCAGATGAGTGCAGCCTGAG -3'
(R):5'- GCCTTGAGCAAAGTTCCTCTG -3'
|
Posted On |
2019-06-26 |