Incidental Mutation 'R1892:Tnrc6c'
ID |
211632 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tnrc6c
|
Ensembl Gene |
ENSMUSG00000025571 |
Gene Name |
trinucleotide repeat containing 6C |
Synonyms |
9930033H14Rik |
MMRRC Submission |
039912-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1892 (G1)
|
Quality Score |
183 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
117545115-117654265 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 117605188 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Aspartic acid
at position 108
(N108D)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000101951
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000026658]
[ENSMUST00000106344]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000026658
AA Change: N108D
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000026658 Gene: ENSMUSG00000025571 AA Change: N108D
Domain | Start | End | E-Value | Type |
coiled coil region
|
1 |
32 |
N/A |
INTRINSIC |
low complexity region
|
37 |
58 |
N/A |
INTRINSIC |
low complexity region
|
110 |
132 |
N/A |
INTRINSIC |
low complexity region
|
248 |
257 |
N/A |
INTRINSIC |
low complexity region
|
298 |
318 |
N/A |
INTRINSIC |
low complexity region
|
394 |
408 |
N/A |
INTRINSIC |
low complexity region
|
440 |
457 |
N/A |
INTRINSIC |
internal_repeat_1
|
472 |
573 |
2.14e-5 |
PROSPERO |
low complexity region
|
594 |
614 |
N/A |
INTRINSIC |
low complexity region
|
621 |
632 |
N/A |
INTRINSIC |
internal_repeat_2
|
639 |
704 |
5.49e-5 |
PROSPERO |
internal_repeat_1
|
799 |
902 |
2.14e-5 |
PROSPERO |
low complexity region
|
964 |
981 |
N/A |
INTRINSIC |
internal_repeat_2
|
991 |
1051 |
5.49e-5 |
PROSPERO |
low complexity region
|
1063 |
1079 |
N/A |
INTRINSIC |
low complexity region
|
1111 |
1125 |
N/A |
INTRINSIC |
UBA
|
1145 |
1182 |
3.68e-4 |
SMART |
Pfam:M_domain
|
1232 |
1459 |
6.8e-77 |
PFAM |
Pfam:TNRC6-PABC_bdg
|
1468 |
1646 |
4.1e-75 |
PFAM |
Pfam:TNRC6-PABC_bdg
|
1643 |
1722 |
3.7e-33 |
PFAM |
RRM
|
1725 |
1792 |
1.81e-2 |
SMART |
low complexity region
|
1813 |
1823 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000106344
AA Change: N108D
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000101951 Gene: ENSMUSG00000025571 AA Change: N108D
Domain | Start | End | E-Value | Type |
coiled coil region
|
1 |
32 |
N/A |
INTRINSIC |
low complexity region
|
37 |
58 |
N/A |
INTRINSIC |
low complexity region
|
110 |
132 |
N/A |
INTRINSIC |
low complexity region
|
248 |
257 |
N/A |
INTRINSIC |
low complexity region
|
298 |
318 |
N/A |
INTRINSIC |
low complexity region
|
394 |
408 |
N/A |
INTRINSIC |
low complexity region
|
440 |
457 |
N/A |
INTRINSIC |
internal_repeat_1
|
472 |
573 |
2.14e-5 |
PROSPERO |
low complexity region
|
594 |
614 |
N/A |
INTRINSIC |
low complexity region
|
621 |
632 |
N/A |
INTRINSIC |
internal_repeat_2
|
639 |
704 |
5.49e-5 |
PROSPERO |
internal_repeat_1
|
799 |
902 |
2.14e-5 |
PROSPERO |
low complexity region
|
964 |
981 |
N/A |
INTRINSIC |
internal_repeat_2
|
991 |
1051 |
5.49e-5 |
PROSPERO |
low complexity region
|
1063 |
1079 |
N/A |
INTRINSIC |
low complexity region
|
1111 |
1125 |
N/A |
INTRINSIC |
UBA
|
1145 |
1182 |
3.68e-4 |
SMART |
Pfam:M_domain
|
1232 |
1459 |
6.8e-77 |
PFAM |
Pfam:TNRC6-PABC_bdg
|
1468 |
1646 |
4.1e-75 |
PFAM |
Pfam:TNRC6-PABC_bdg
|
1643 |
1722 |
3.7e-33 |
PFAM |
RRM
|
1725 |
1792 |
1.81e-2 |
SMART |
low complexity region
|
1813 |
1823 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141115
|
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.4%
- 20x: 93.0%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a gene trap allele exhibit complete neonatal lethality with cyanosis, respiratory distress and thickened mesenchyme in air sacs. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
G |
A |
7: 119,815,561 (GRCm39) |
A270T |
probably benign |
Het |
Abcb7 |
A |
T |
X: 103,386,142 (GRCm39) |
H97Q |
probably damaging |
Het |
Adat3 |
T |
C |
10: 80,442,249 (GRCm39) |
L29P |
probably damaging |
Het |
AI987944 |
A |
T |
7: 41,024,020 (GRCm39) |
C320S |
probably damaging |
Het |
Asic4 |
C |
T |
1: 75,446,126 (GRCm39) |
R285W |
probably damaging |
Het |
Asic5 |
A |
T |
3: 81,928,293 (GRCm39) |
I419L |
probably damaging |
Het |
Batf |
A |
G |
12: 85,736,102 (GRCm39) |
K42E |
probably damaging |
Het |
Bcar3 |
A |
G |
3: 122,301,785 (GRCm39) |
N160S |
probably benign |
Het |
Bco2 |
C |
A |
9: 50,461,863 (GRCm39) |
G47V |
probably damaging |
Het |
Bicc1 |
T |
G |
10: 70,794,614 (GRCm39) |
K181T |
probably damaging |
Het |
Brinp2 |
A |
G |
1: 158,082,542 (GRCm39) |
|
probably null |
Het |
Cacng8 |
A |
G |
7: 3,463,568 (GRCm39) |
D240G |
possibly damaging |
Het |
Calca |
A |
G |
7: 114,232,962 (GRCm39) |
Y96H |
probably damaging |
Het |
Cdh1 |
A |
T |
8: 107,390,882 (GRCm39) |
K666I |
possibly damaging |
Het |
Cdh16 |
A |
T |
8: 105,344,631 (GRCm39) |
I500N |
possibly damaging |
Het |
Chst14 |
A |
G |
2: 118,757,830 (GRCm39) |
Y208C |
probably damaging |
Het |
Chst9 |
T |
C |
18: 15,586,017 (GRCm39) |
H182R |
probably damaging |
Het |
Clk2 |
A |
G |
3: 89,082,502 (GRCm39) |
I367M |
possibly damaging |
Het |
Cobl |
G |
C |
11: 12,203,258 (GRCm39) |
S1066W |
probably damaging |
Het |
Ctcfl |
A |
G |
2: 172,960,478 (GRCm39) |
V35A |
probably benign |
Het |
Dchs1 |
G |
T |
7: 105,413,363 (GRCm39) |
H1151N |
probably benign |
Het |
Dennd1c |
T |
C |
17: 57,374,083 (GRCm39) |
T529A |
probably benign |
Het |
Dnah11 |
A |
T |
12: 118,070,209 (GRCm39) |
V1532D |
possibly damaging |
Het |
Dync1h1 |
A |
G |
12: 110,612,738 (GRCm39) |
Y2871C |
probably damaging |
Het |
Dytn |
T |
C |
1: 63,716,420 (GRCm39) |
E51G |
probably benign |
Het |
Esd |
C |
T |
14: 74,987,113 (GRCm39) |
A266V |
probably damaging |
Het |
Gli1 |
T |
C |
10: 127,165,975 (GRCm39) |
M1093V |
possibly damaging |
Het |
Gm15446 |
A |
G |
5: 110,091,253 (GRCm39) |
K502E |
probably damaging |
Het |
Gm4076 |
T |
A |
13: 85,275,447 (GRCm39) |
|
noncoding transcript |
Het |
Gm9830 |
A |
G |
9: 44,375,825 (GRCm39) |
|
noncoding transcript |
Het |
Gm9938 |
G |
A |
19: 23,701,955 (GRCm39) |
|
probably benign |
Het |
Grhl1 |
G |
A |
12: 24,634,909 (GRCm39) |
R245H |
probably damaging |
Het |
Hnrnpul1 |
A |
T |
7: 25,426,191 (GRCm39) |
D553E |
probably benign |
Het |
Hpn |
G |
A |
7: 30,798,468 (GRCm39) |
Q415* |
probably null |
Het |
Hsd11b1 |
T |
G |
1: 192,906,068 (GRCm39) |
M175L |
probably benign |
Het |
Htra1 |
G |
A |
7: 130,586,799 (GRCm39) |
V461I |
possibly damaging |
Het |
Il1rl2 |
A |
G |
1: 40,366,694 (GRCm39) |
H76R |
probably damaging |
Het |
Insrr |
G |
A |
3: 87,721,184 (GRCm39) |
V1112M |
probably damaging |
Het |
Ints9 |
T |
C |
14: 65,257,872 (GRCm39) |
S351P |
probably benign |
Het |
Itgav |
T |
A |
2: 83,601,680 (GRCm39) |
N350K |
probably damaging |
Het |
Kdm4d |
C |
A |
9: 14,375,613 (GRCm39) |
V82L |
probably benign |
Het |
Klc1 |
T |
C |
12: 111,748,261 (GRCm39) |
|
probably null |
Het |
Kmt5c |
T |
A |
7: 4,745,714 (GRCm39) |
C69* |
probably null |
Het |
Lgals3 |
T |
G |
14: 47,622,164 (GRCm39) |
N193K |
possibly damaging |
Het |
Morc2b |
T |
A |
17: 33,354,748 (GRCm39) |
D1008V |
probably damaging |
Het |
Mpg |
C |
T |
11: 32,181,720 (GRCm39) |
Q243* |
probably null |
Het |
Muc15 |
C |
T |
2: 110,567,697 (GRCm39) |
R281* |
probably null |
Het |
Ncstn |
CAGCTCCACGAAG |
CAG |
1: 171,899,038 (GRCm39) |
|
probably null |
Het |
Nek5 |
A |
G |
8: 22,597,745 (GRCm39) |
M278T |
probably benign |
Het |
Npas2 |
A |
G |
1: 39,384,503 (GRCm39) |
T599A |
probably benign |
Het |
Nrf1 |
A |
G |
6: 30,144,787 (GRCm39) |
D519G |
probably null |
Het |
Nup43 |
A |
G |
10: 7,549,373 (GRCm39) |
H176R |
probably damaging |
Het |
Nxpe2 |
T |
C |
9: 48,237,914 (GRCm39) |
T114A |
probably damaging |
Het |
Or10j3 |
T |
C |
1: 173,031,795 (GRCm39) |
Y291H |
probably damaging |
Het |
Or5p72 |
A |
T |
7: 108,022,147 (GRCm39) |
Y123F |
possibly damaging |
Het |
Or6c75 |
A |
C |
10: 129,336,902 (GRCm39) |
I50L |
probably benign |
Het |
Perm1 |
C |
T |
4: 156,302,340 (GRCm39) |
R295C |
probably benign |
Het |
Pik3ip1 |
G |
T |
11: 3,283,304 (GRCm39) |
A135S |
probably damaging |
Het |
Pira13 |
A |
C |
7: 3,827,573 (GRCm39) |
C195G |
probably benign |
Het |
Ppp4c |
A |
G |
7: 126,385,452 (GRCm39) |
V119A |
probably damaging |
Het |
Prepl |
A |
G |
17: 85,395,878 (GRCm39) |
Y35H |
possibly damaging |
Het |
Ptpn13 |
A |
G |
5: 103,649,545 (GRCm39) |
Y316C |
possibly damaging |
Het |
Pxk |
C |
T |
14: 8,151,507 (GRCm38) |
R441* |
probably null |
Het |
Ranbp2 |
T |
C |
10: 58,299,921 (GRCm39) |
V491A |
probably benign |
Het |
Ranbp9 |
C |
A |
13: 43,569,933 (GRCm39) |
C495F |
possibly damaging |
Het |
Rfx8 |
A |
T |
1: 39,709,746 (GRCm39) |
|
probably null |
Het |
Rnf111 |
T |
A |
9: 70,383,656 (GRCm39) |
K92N |
probably damaging |
Het |
Rtn1 |
A |
G |
12: 72,259,337 (GRCm39) |
I772T |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,673,844 (GRCm39) |
K72* |
probably null |
Het |
Sergef |
A |
T |
7: 46,264,040 (GRCm39) |
|
probably null |
Het |
Sez6l |
T |
C |
5: 112,620,665 (GRCm39) |
N305S |
probably damaging |
Het |
Slc40a1 |
A |
T |
1: 45,950,302 (GRCm39) |
C383* |
probably null |
Het |
Stab2 |
C |
T |
10: 86,773,913 (GRCm39) |
C806Y |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,524,189 (GRCm39) |
T795A |
probably benign |
Het |
Stk31 |
T |
C |
6: 49,415,408 (GRCm39) |
I536T |
probably damaging |
Het |
Stox1 |
T |
A |
10: 62,501,178 (GRCm39) |
T461S |
possibly damaging |
Het |
Suv39h2 |
T |
C |
2: 3,460,805 (GRCm39) |
Y219C |
probably damaging |
Het |
Tap1 |
T |
G |
17: 34,413,915 (GRCm39) |
D643E |
probably damaging |
Het |
Tbc1d2b |
T |
A |
9: 90,100,996 (GRCm39) |
I665F |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,935,696 (GRCm39) |
N1784S |
probably benign |
Het |
Tmem14c |
T |
C |
13: 41,174,633 (GRCm39) |
F81L |
possibly damaging |
Het |
Tox3 |
A |
T |
8: 90,996,869 (GRCm39) |
N131K |
probably benign |
Het |
Tspear |
T |
A |
10: 77,706,308 (GRCm39) |
D359E |
probably benign |
Het |
Ttc9 |
A |
G |
12: 81,678,551 (GRCm39) |
I125V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,728,531 (GRCm39) |
|
probably benign |
Het |
Ubn2 |
C |
T |
6: 38,468,226 (GRCm39) |
S980F |
probably damaging |
Het |
Vcf1 |
G |
T |
11: 113,554,212 (GRCm39) |
P161H |
probably damaging |
Het |
Zfp362 |
T |
A |
4: 128,684,057 (GRCm39) |
T30S |
probably benign |
Het |
Zfp385c |
A |
C |
11: 100,528,630 (GRCm39) |
H32Q |
probably damaging |
Het |
Zfp870 |
A |
T |
17: 33,102,863 (GRCm39) |
H156Q |
possibly damaging |
Het |
Zfp873 |
T |
C |
10: 81,897,080 (GRCm39) |
C641R |
probably damaging |
Het |
Zfp950 |
A |
T |
19: 61,107,549 (GRCm39) |
H511Q |
probably benign |
Het |
|
Other mutations in Tnrc6c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00839:Tnrc6c
|
APN |
11 |
117,605,011 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01013:Tnrc6c
|
APN |
11 |
117,612,855 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01092:Tnrc6c
|
APN |
11 |
117,612,811 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01383:Tnrc6c
|
APN |
11 |
117,605,083 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01395:Tnrc6c
|
APN |
11 |
117,613,939 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01726:Tnrc6c
|
APN |
11 |
117,640,161 (GRCm39) |
splice site |
probably benign |
|
IGL01869:Tnrc6c
|
APN |
11 |
117,646,274 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02108:Tnrc6c
|
APN |
11 |
117,612,025 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02457:Tnrc6c
|
APN |
11 |
117,613,803 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02612:Tnrc6c
|
APN |
11 |
117,633,826 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02748:Tnrc6c
|
APN |
11 |
117,622,996 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03160:Tnrc6c
|
APN |
11 |
117,640,651 (GRCm39) |
splice site |
probably benign |
|
rodion
|
UTSW |
11 |
117,629,176 (GRCm39) |
critical splice donor site |
probably null |
|
F5770:Tnrc6c
|
UTSW |
11 |
117,614,152 (GRCm39) |
missense |
probably damaging |
1.00 |
K3955:Tnrc6c
|
UTSW |
11 |
117,651,564 (GRCm39) |
missense |
probably damaging |
0.99 |
R0015:Tnrc6c
|
UTSW |
11 |
117,612,284 (GRCm39) |
missense |
probably damaging |
0.98 |
R0143:Tnrc6c
|
UTSW |
11 |
117,643,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R0277:Tnrc6c
|
UTSW |
11 |
117,630,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R0323:Tnrc6c
|
UTSW |
11 |
117,630,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R0464:Tnrc6c
|
UTSW |
11 |
117,651,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R0699:Tnrc6c
|
UTSW |
11 |
117,613,447 (GRCm39) |
missense |
probably benign |
0.02 |
R1015:Tnrc6c
|
UTSW |
11 |
117,612,748 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1201:Tnrc6c
|
UTSW |
11 |
117,612,500 (GRCm39) |
missense |
probably damaging |
0.96 |
R1297:Tnrc6c
|
UTSW |
11 |
117,624,529 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1560:Tnrc6c
|
UTSW |
11 |
117,650,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R1596:Tnrc6c
|
UTSW |
11 |
117,648,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1758:Tnrc6c
|
UTSW |
11 |
117,651,556 (GRCm39) |
missense |
probably benign |
0.09 |
R1901:Tnrc6c
|
UTSW |
11 |
117,613,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R1935:Tnrc6c
|
UTSW |
11 |
117,646,849 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1936:Tnrc6c
|
UTSW |
11 |
117,646,849 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1937:Tnrc6c
|
UTSW |
11 |
117,646,849 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1940:Tnrc6c
|
UTSW |
11 |
117,646,849 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3622:Tnrc6c
|
UTSW |
11 |
117,640,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R3711:Tnrc6c
|
UTSW |
11 |
117,613,950 (GRCm39) |
missense |
probably benign |
0.00 |
R3725:Tnrc6c
|
UTSW |
11 |
117,614,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R3775:Tnrc6c
|
UTSW |
11 |
117,614,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R3776:Tnrc6c
|
UTSW |
11 |
117,614,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R3836:Tnrc6c
|
UTSW |
11 |
117,614,055 (GRCm39) |
missense |
probably benign |
0.20 |
R3844:Tnrc6c
|
UTSW |
11 |
117,646,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3852:Tnrc6c
|
UTSW |
11 |
117,614,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R3928:Tnrc6c
|
UTSW |
11 |
117,614,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R3929:Tnrc6c
|
UTSW |
11 |
117,614,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R3937:Tnrc6c
|
UTSW |
11 |
117,614,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R3943:Tnrc6c
|
UTSW |
11 |
117,614,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R4501:Tnrc6c
|
UTSW |
11 |
117,613,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Tnrc6c
|
UTSW |
11 |
117,633,784 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4511:Tnrc6c
|
UTSW |
11 |
117,633,784 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4654:Tnrc6c
|
UTSW |
11 |
117,611,797 (GRCm39) |
missense |
probably benign |
|
R4765:Tnrc6c
|
UTSW |
11 |
117,633,753 (GRCm39) |
missense |
probably benign |
0.09 |
R4824:Tnrc6c
|
UTSW |
11 |
117,613,731 (GRCm39) |
missense |
probably damaging |
0.98 |
R5004:Tnrc6c
|
UTSW |
11 |
117,611,872 (GRCm39) |
missense |
probably benign |
0.44 |
R5094:Tnrc6c
|
UTSW |
11 |
117,611,872 (GRCm39) |
missense |
probably benign |
0.00 |
R5130:Tnrc6c
|
UTSW |
11 |
117,629,176 (GRCm39) |
critical splice donor site |
probably null |
|
R5234:Tnrc6c
|
UTSW |
11 |
117,651,555 (GRCm39) |
missense |
probably benign |
0.42 |
R5235:Tnrc6c
|
UTSW |
11 |
117,651,555 (GRCm39) |
missense |
probably benign |
0.42 |
R5345:Tnrc6c
|
UTSW |
11 |
117,614,113 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5359:Tnrc6c
|
UTSW |
11 |
117,649,731 (GRCm39) |
splice site |
silent |
|
R5428:Tnrc6c
|
UTSW |
11 |
117,591,588 (GRCm39) |
start codon destroyed |
probably null |
|
R5548:Tnrc6c
|
UTSW |
11 |
117,651,669 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5587:Tnrc6c
|
UTSW |
11 |
117,640,097 (GRCm39) |
nonsense |
probably null |
|
R5875:Tnrc6c
|
UTSW |
11 |
117,650,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R5947:Tnrc6c
|
UTSW |
11 |
117,613,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Tnrc6c
|
UTSW |
11 |
117,626,831 (GRCm39) |
missense |
probably damaging |
0.97 |
R6354:Tnrc6c
|
UTSW |
11 |
117,640,440 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6389:Tnrc6c
|
UTSW |
11 |
117,613,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R7027:Tnrc6c
|
UTSW |
11 |
117,624,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R7048:Tnrc6c
|
UTSW |
11 |
117,612,800 (GRCm39) |
missense |
probably benign |
0.41 |
R7098:Tnrc6c
|
UTSW |
11 |
117,604,952 (GRCm39) |
missense |
probably benign |
0.03 |
R7315:Tnrc6c
|
UTSW |
11 |
117,614,354 (GRCm39) |
missense |
probably benign |
0.11 |
R7378:Tnrc6c
|
UTSW |
11 |
117,632,606 (GRCm39) |
missense |
probably benign |
0.03 |
R7386:Tnrc6c
|
UTSW |
11 |
117,612,780 (GRCm39) |
missense |
probably benign |
|
R7515:Tnrc6c
|
UTSW |
11 |
117,632,507 (GRCm39) |
missense |
probably benign |
0.03 |
R7665:Tnrc6c
|
UTSW |
11 |
117,611,777 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7755:Tnrc6c
|
UTSW |
11 |
117,648,912 (GRCm39) |
missense |
probably benign |
0.00 |
R8679:Tnrc6c
|
UTSW |
11 |
117,604,961 (GRCm39) |
missense |
probably benign |
|
R8824:Tnrc6c
|
UTSW |
11 |
117,630,680 (GRCm39) |
splice site |
probably benign |
|
R8971:Tnrc6c
|
UTSW |
11 |
117,640,089 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9261:Tnrc6c
|
UTSW |
11 |
117,605,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R9283:Tnrc6c
|
UTSW |
11 |
117,591,630 (GRCm39) |
missense |
unknown |
|
R9342:Tnrc6c
|
UTSW |
11 |
117,630,720 (GRCm39) |
missense |
probably benign |
0.01 |
R9633:Tnrc6c
|
UTSW |
11 |
117,638,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Tnrc6c
|
UTSW |
11 |
117,623,136 (GRCm39) |
missense |
probably benign |
|
V7580:Tnrc6c
|
UTSW |
11 |
117,614,152 (GRCm39) |
missense |
probably damaging |
1.00 |
V7581:Tnrc6c
|
UTSW |
11 |
117,614,152 (GRCm39) |
missense |
probably damaging |
1.00 |
V7582:Tnrc6c
|
UTSW |
11 |
117,614,152 (GRCm39) |
missense |
probably damaging |
1.00 |
V7583:Tnrc6c
|
UTSW |
11 |
117,614,152 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tnrc6c
|
UTSW |
11 |
117,623,003 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
Predicted Primers |
PCR Primer
(F):5'- AAGACCTGTTCAAGCCAGC -3'
(R):5'- AAAGCCTCAGGATTGATGGG -3'
Sequencing Primer
(F):5'- GGTACCAGTCCCAGTACTTCCAC -3'
(R):5'- GACAGCGTAATGGCCACG -3'
|
Posted On |
2014-06-30 |