Incidental Mutation 'R2022:Tnr'
ID |
224070 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tnr
|
Ensembl Gene |
ENSMUSG00000015829 |
Gene Name |
tenascin R |
Synonyms |
J1-tenascin, restrictin, janusin, TN-R |
MMRRC Submission |
040031-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R2022 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
159351339-159759299 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 159679592 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Valine
at position 189
(I189V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000141553
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000111669]
[ENSMUST00000192069]
[ENSMUST00000193325]
|
AlphaFold |
Q8BYI9 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000111669
AA Change: I189V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000107298 Gene: ENSMUSG00000015829 AA Change: I189V
Domain | Start | End | E-Value | Type |
EGF_like
|
203 |
231 |
3.87e1 |
SMART |
EGF_like
|
234 |
262 |
3.16e1 |
SMART |
EGF_like
|
265 |
293 |
2.8e1 |
SMART |
EGF
|
296 |
324 |
2.43e1 |
SMART |
FN3
|
326 |
404 |
4.77e-8 |
SMART |
FN3
|
415 |
493 |
3.1e-7 |
SMART |
FN3
|
504 |
583 |
2.01e-6 |
SMART |
FN3
|
594 |
675 |
1.98e-5 |
SMART |
FN3
|
686 |
763 |
3.29e-11 |
SMART |
FN3
|
774 |
851 |
3.32e-7 |
SMART |
FN3
|
864 |
942 |
3.73e-10 |
SMART |
FN3
|
953 |
1031 |
2.28e-5 |
SMART |
FN3
|
1041 |
1118 |
8.56e-10 |
SMART |
FBG
|
1133 |
1343 |
2.69e-133 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000192069
AA Change: I189V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000141553 Gene: ENSMUSG00000015829 AA Change: I189V
Domain | Start | End | E-Value | Type |
EGF_like
|
203 |
231 |
3.87e1 |
SMART |
EGF_like
|
234 |
262 |
3.16e1 |
SMART |
EGF_like
|
265 |
293 |
2.8e1 |
SMART |
EGF
|
296 |
324 |
2.43e1 |
SMART |
FN3
|
326 |
404 |
4.77e-8 |
SMART |
FN3
|
415 |
493 |
3.1e-7 |
SMART |
FN3
|
504 |
583 |
2.01e-6 |
SMART |
FN3
|
594 |
675 |
1.98e-5 |
SMART |
FN3
|
686 |
763 |
3.29e-11 |
SMART |
FN3
|
774 |
851 |
3.32e-7 |
SMART |
FN3
|
864 |
942 |
3.73e-10 |
SMART |
FN3
|
953 |
1031 |
2.28e-5 |
SMART |
FN3
|
1041 |
1118 |
8.56e-10 |
SMART |
FBG
|
1133 |
1343 |
2.69e-133 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000192457
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000193325
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.7%
|
Validation Efficiency |
|
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 tenascin family of extracellular matrix glycoproteins. The encoded protein is restricted to the central nervous system. The protein may play a role in neurite outgrowth, neural cell adhesion and modulation of sodium channel function. It is a constituent of perineuronal nets. [provided by RefSeq, Aug 2013] PHENOTYPE: In spite of having decreased conduction velocity in the optic nerve and ultrastrucural alterations within the hippocampus, homozygous null mice are viable, fertile, and display normal behavior. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34l |
A |
T |
8: 44,078,954 (GRCm39) |
C423* |
probably null |
Het |
Akr1cl |
T |
A |
1: 65,053,857 (GRCm39) |
Y271F |
probably benign |
Het |
Asnsd1 |
A |
G |
1: 53,386,386 (GRCm39) |
S414P |
possibly damaging |
Het |
Atp12a |
T |
A |
14: 56,602,739 (GRCm39) |
M1K |
probably null |
Het |
Atp4b |
A |
C |
8: 13,437,477 (GRCm39) |
N225K |
possibly damaging |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Cactin |
C |
T |
10: 81,158,727 (GRCm39) |
T231I |
possibly damaging |
Het |
Casp8ap2 |
T |
C |
4: 32,644,560 (GRCm39) |
V1211A |
probably benign |
Het |
Ccdc180 |
C |
A |
4: 45,944,418 (GRCm39) |
H1423N |
probably benign |
Het |
Cfap251 |
G |
A |
5: 123,411,853 (GRCm39) |
G495D |
probably benign |
Het |
Chd9 |
T |
C |
8: 91,761,682 (GRCm39) |
Y2256H |
probably benign |
Het |
Chst8 |
A |
G |
7: 34,374,589 (GRCm39) |
Y417H |
possibly damaging |
Het |
Clcn6 |
A |
G |
4: 148,095,109 (GRCm39) |
|
probably null |
Het |
Clec5a |
A |
T |
6: 40,562,128 (GRCm39) |
V12E |
probably damaging |
Het |
Crebbp |
C |
T |
16: 3,903,683 (GRCm39) |
R1852H |
probably damaging |
Het |
Cyp2c40 |
T |
A |
19: 39,801,224 (GRCm39) |
|
probably benign |
Het |
Dip2c |
T |
C |
13: 9,601,836 (GRCm39) |
L265P |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,550,465 (GRCm39) |
Y3274H |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,004,405 (GRCm39) |
T3853S |
probably benign |
Het |
Dnttip2 |
T |
C |
3: 122,069,870 (GRCm39) |
S362P |
probably damaging |
Het |
Dst |
G |
A |
1: 34,205,372 (GRCm39) |
V1025I |
possibly damaging |
Het |
Dym |
T |
C |
18: 75,213,321 (GRCm39) |
V181A |
probably benign |
Het |
Dynlt4 |
A |
G |
4: 116,985,504 (GRCm39) |
E109G |
possibly damaging |
Het |
Elk3 |
T |
A |
10: 93,101,539 (GRCm39) |
I71F |
probably damaging |
Het |
Epb41l4a |
C |
T |
18: 34,054,893 (GRCm39) |
S65N |
probably benign |
Het |
Erap1 |
T |
A |
13: 74,814,627 (GRCm39) |
V451E |
probably benign |
Het |
F830045P16Rik |
T |
A |
2: 129,314,585 (GRCm39) |
I231F |
probably damaging |
Het |
Fahd1 |
T |
C |
17: 25,068,814 (GRCm39) |
I88V |
probably benign |
Het |
Fam120b |
C |
T |
17: 15,644,638 (GRCm39) |
T744I |
possibly damaging |
Het |
Fam83f |
T |
G |
15: 80,576,468 (GRCm39) |
V373G |
possibly damaging |
Het |
Frem1 |
G |
T |
4: 82,831,795 (GRCm39) |
T1988K |
probably benign |
Het |
Gdap1l1 |
A |
T |
2: 163,289,517 (GRCm39) |
T161S |
probably benign |
Het |
Gm6309 |
C |
T |
5: 146,105,121 (GRCm39) |
G264D |
probably benign |
Het |
Hsd11b1 |
T |
C |
1: 192,922,686 (GRCm39) |
T124A |
probably benign |
Het |
Ino80b |
A |
G |
6: 83,101,353 (GRCm39) |
M119T |
probably damaging |
Het |
Kif3a |
G |
A |
11: 53,461,408 (GRCm39) |
V17M |
probably damaging |
Het |
Krt40 |
T |
A |
11: 99,430,818 (GRCm39) |
E285D |
probably damaging |
Het |
Lair1 |
C |
G |
7: 4,066,063 (GRCm39) |
|
probably null |
Het |
Lvrn |
A |
G |
18: 46,999,503 (GRCm39) |
T290A |
possibly damaging |
Het |
Macf1 |
G |
T |
4: 123,366,523 (GRCm39) |
A2746E |
probably damaging |
Het |
Matn4 |
A |
G |
2: 164,242,573 (GRCm39) |
V175A |
probably damaging |
Het |
Mok |
A |
T |
12: 110,778,257 (GRCm39) |
D216E |
probably benign |
Het |
Muc15 |
A |
T |
2: 110,561,821 (GRCm39) |
T86S |
probably benign |
Het |
Myo16 |
A |
G |
8: 10,322,633 (GRCm39) |
K21R |
probably benign |
Het |
Ncl |
A |
G |
1: 86,284,677 (GRCm39) |
|
probably null |
Het |
Nfrkb |
C |
T |
9: 31,322,546 (GRCm39) |
T872I |
probably benign |
Het |
Nhlrc2 |
A |
T |
19: 56,585,710 (GRCm39) |
E648D |
probably benign |
Het |
Nlrp9c |
A |
T |
7: 26,084,221 (GRCm39) |
Y453N |
probably damaging |
Het |
Notch4 |
T |
C |
17: 34,806,502 (GRCm39) |
L1813P |
probably damaging |
Het |
Nrg3 |
T |
A |
14: 38,098,309 (GRCm39) |
D515V |
probably damaging |
Het |
Nsd1 |
T |
C |
13: 55,361,092 (GRCm39) |
V20A |
probably damaging |
Het |
Opn4 |
T |
A |
14: 34,319,028 (GRCm39) |
T186S |
probably benign |
Het |
Or9k2 |
T |
C |
10: 129,999,049 (GRCm39) |
M49V |
probably benign |
Het |
Pcdh15 |
T |
G |
10: 74,467,025 (GRCm39) |
S1684A |
possibly damaging |
Het |
Phf11a |
T |
A |
14: 59,532,363 (GRCm39) |
E24V |
possibly damaging |
Het |
Pigg |
A |
T |
5: 108,460,788 (GRCm39) |
|
probably benign |
Het |
Plscr2 |
A |
G |
9: 92,177,647 (GRCm39) |
D136G |
probably damaging |
Het |
Ppp3r2 |
T |
C |
4: 49,681,723 (GRCm39) |
I76V |
probably benign |
Het |
Prdm6 |
A |
G |
18: 53,598,031 (GRCm39) |
|
probably benign |
Het |
Prex1 |
A |
G |
2: 166,417,534 (GRCm39) |
W1188R |
possibly damaging |
Het |
Prmt2 |
T |
A |
10: 76,061,292 (GRCm39) |
R65* |
probably null |
Het |
Prom1 |
G |
T |
5: 44,187,068 (GRCm39) |
D396E |
probably benign |
Het |
Ptcd3 |
C |
T |
6: 71,862,537 (GRCm39) |
C466Y |
probably damaging |
Het |
Ptk2 |
A |
G |
15: 73,114,255 (GRCm39) |
V701A |
possibly damaging |
Het |
Rab36 |
T |
C |
10: 74,888,306 (GRCm39) |
I250T |
probably benign |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Scn11a |
G |
T |
9: 119,640,274 (GRCm39) |
A207E |
possibly damaging |
Het |
Serpinb3d |
A |
G |
1: 107,006,182 (GRCm39) |
V302A |
probably benign |
Het |
Slc22a16 |
T |
C |
10: 40,467,873 (GRCm39) |
Y469H |
probably damaging |
Het |
Smo |
A |
G |
6: 29,754,715 (GRCm39) |
N262D |
possibly damaging |
Het |
Spata31e5 |
A |
T |
1: 28,817,234 (GRCm39) |
V266D |
probably damaging |
Het |
Sptan1 |
C |
T |
2: 29,897,573 (GRCm39) |
A1212V |
probably damaging |
Het |
Ssr1 |
C |
T |
13: 38,173,525 (GRCm39) |
A79T |
probably damaging |
Het |
Tiam1 |
T |
A |
16: 89,674,075 (GRCm39) |
T479S |
probably benign |
Het |
Tm9sf3 |
A |
G |
19: 41,227,231 (GRCm39) |
F280S |
probably damaging |
Het |
Tmem72 |
T |
C |
6: 116,673,800 (GRCm39) |
H106R |
probably damaging |
Het |
Tpbpa |
T |
A |
13: 61,088,036 (GRCm39) |
N50I |
probably benign |
Het |
Tshz1 |
T |
A |
18: 84,031,987 (GRCm39) |
Y807F |
probably damaging |
Het |
Tspo2 |
C |
T |
17: 48,755,750 (GRCm39) |
A131T |
possibly damaging |
Het |
Usp16 |
T |
C |
16: 87,270,014 (GRCm39) |
L322P |
probably damaging |
Het |
Vmn1r185 |
A |
G |
7: 26,310,935 (GRCm39) |
V190A |
possibly damaging |
Het |
Vmn1r34 |
T |
C |
6: 66,614,385 (GRCm39) |
K118E |
possibly damaging |
Het |
Vmn1r68 |
A |
G |
7: 10,261,918 (GRCm39) |
L60P |
probably damaging |
Het |
Vmn2r-ps158 |
A |
G |
7: 42,673,454 (GRCm39) |
N171D |
probably benign |
Het |
Vps51 |
T |
C |
19: 6,121,612 (GRCm39) |
E162G |
probably benign |
Het |
Yy1 |
CGGG |
CGGGGGG |
12: 108,759,916 (GRCm39) |
|
probably benign |
Het |
Zdhhc4 |
C |
T |
5: 143,307,538 (GRCm39) |
R161H |
probably damaging |
Het |
Zfp456 |
A |
T |
13: 67,514,616 (GRCm39) |
C363* |
probably null |
Het |
Zfp541 |
T |
A |
7: 15,816,110 (GRCm39) |
S866T |
probably damaging |
Het |
|
Other mutations in Tnr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00432:Tnr
|
APN |
1 |
159,688,815 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00905:Tnr
|
APN |
1 |
159,679,752 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01396:Tnr
|
APN |
1 |
159,724,594 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01550:Tnr
|
APN |
1 |
159,701,828 (GRCm39) |
missense |
probably benign |
|
IGL01803:Tnr
|
APN |
1 |
159,695,813 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01845:Tnr
|
APN |
1 |
159,695,576 (GRCm39) |
unclassified |
probably benign |
|
IGL01983:Tnr
|
APN |
1 |
159,691,349 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01985:Tnr
|
APN |
1 |
159,746,607 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02210:Tnr
|
APN |
1 |
159,679,671 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02486:Tnr
|
APN |
1 |
159,679,664 (GRCm39) |
splice site |
probably null |
|
IGL03210:Tnr
|
APN |
1 |
159,715,880 (GRCm39) |
missense |
probably benign |
0.00 |
Assiduous
|
UTSW |
1 |
159,719,593 (GRCm39) |
missense |
probably benign |
|
Grip
|
UTSW |
1 |
159,713,680 (GRCm39) |
missense |
possibly damaging |
0.68 |
Persistent
|
UTSW |
1 |
159,679,856 (GRCm39) |
missense |
probably benign |
|
Tenacious
|
UTSW |
1 |
159,701,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0002:Tnr
|
UTSW |
1 |
159,701,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0002:Tnr
|
UTSW |
1 |
159,701,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Tnr
|
UTSW |
1 |
159,679,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R0042:Tnr
|
UTSW |
1 |
159,714,595 (GRCm39) |
missense |
probably benign |
0.01 |
R0594:Tnr
|
UTSW |
1 |
159,677,905 (GRCm39) |
missense |
probably benign |
|
R0617:Tnr
|
UTSW |
1 |
159,695,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R0637:Tnr
|
UTSW |
1 |
159,677,905 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0682:Tnr
|
UTSW |
1 |
159,679,877 (GRCm39) |
nonsense |
probably null |
|
R1171:Tnr
|
UTSW |
1 |
159,685,780 (GRCm39) |
missense |
probably damaging |
0.97 |
R1185:Tnr
|
UTSW |
1 |
159,679,856 (GRCm39) |
missense |
probably benign |
|
R1185:Tnr
|
UTSW |
1 |
159,679,856 (GRCm39) |
missense |
probably benign |
|
R1185:Tnr
|
UTSW |
1 |
159,679,856 (GRCm39) |
missense |
probably benign |
|
R1335:Tnr
|
UTSW |
1 |
159,695,600 (GRCm39) |
missense |
probably benign |
0.18 |
R1540:Tnr
|
UTSW |
1 |
159,677,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R1697:Tnr
|
UTSW |
1 |
159,679,600 (GRCm39) |
missense |
probably benign |
0.00 |
R1938:Tnr
|
UTSW |
1 |
159,722,607 (GRCm39) |
nonsense |
probably null |
|
R1941:Tnr
|
UTSW |
1 |
159,677,704 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2021:Tnr
|
UTSW |
1 |
159,679,592 (GRCm39) |
missense |
probably benign |
|
R2051:Tnr
|
UTSW |
1 |
159,719,603 (GRCm39) |
missense |
probably benign |
|
R2157:Tnr
|
UTSW |
1 |
159,685,840 (GRCm39) |
missense |
probably damaging |
0.98 |
R2319:Tnr
|
UTSW |
1 |
159,677,618 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R2936:Tnr
|
UTSW |
1 |
159,715,932 (GRCm39) |
missense |
probably damaging |
0.96 |
R3015:Tnr
|
UTSW |
1 |
159,715,829 (GRCm39) |
missense |
probably benign |
0.00 |
R3417:Tnr
|
UTSW |
1 |
159,722,612 (GRCm39) |
missense |
probably benign |
0.00 |
R3739:Tnr
|
UTSW |
1 |
159,750,983 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3977:Tnr
|
UTSW |
1 |
159,719,593 (GRCm39) |
missense |
probably benign |
|
R4232:Tnr
|
UTSW |
1 |
159,713,785 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4478:Tnr
|
UTSW |
1 |
159,712,326 (GRCm39) |
splice site |
probably null |
|
R4774:Tnr
|
UTSW |
1 |
159,724,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Tnr
|
UTSW |
1 |
159,685,974 (GRCm39) |
missense |
probably benign |
0.24 |
R4837:Tnr
|
UTSW |
1 |
159,512,358 (GRCm39) |
intron |
probably benign |
|
R5111:Tnr
|
UTSW |
1 |
159,713,798 (GRCm39) |
missense |
probably benign |
0.04 |
R5224:Tnr
|
UTSW |
1 |
159,750,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R5249:Tnr
|
UTSW |
1 |
159,512,226 (GRCm39) |
intron |
probably benign |
|
R5730:Tnr
|
UTSW |
1 |
159,715,892 (GRCm39) |
missense |
probably benign |
0.02 |
R5807:Tnr
|
UTSW |
1 |
159,714,500 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5832:Tnr
|
UTSW |
1 |
159,713,692 (GRCm39) |
missense |
probably benign |
0.15 |
R5927:Tnr
|
UTSW |
1 |
159,740,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R6049:Tnr
|
UTSW |
1 |
159,740,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R6056:Tnr
|
UTSW |
1 |
159,714,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R6063:Tnr
|
UTSW |
1 |
159,740,254 (GRCm39) |
missense |
probably benign |
0.00 |
R6141:Tnr
|
UTSW |
1 |
159,714,692 (GRCm39) |
missense |
probably benign |
|
R6218:Tnr
|
UTSW |
1 |
159,715,884 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6275:Tnr
|
UTSW |
1 |
159,688,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R6543:Tnr
|
UTSW |
1 |
159,751,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R6626:Tnr
|
UTSW |
1 |
159,677,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Tnr
|
UTSW |
1 |
159,712,432 (GRCm39) |
critical splice donor site |
probably null |
|
R7587:Tnr
|
UTSW |
1 |
159,713,778 (GRCm39) |
missense |
probably benign |
0.27 |
R7766:Tnr
|
UTSW |
1 |
159,715,880 (GRCm39) |
missense |
probably benign |
0.00 |
R8140:Tnr
|
UTSW |
1 |
159,691,265 (GRCm39) |
missense |
probably damaging |
0.99 |
R8215:Tnr
|
UTSW |
1 |
159,715,860 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8248:Tnr
|
UTSW |
1 |
159,719,663 (GRCm39) |
missense |
probably damaging |
0.98 |
R8374:Tnr
|
UTSW |
1 |
159,685,953 (GRCm39) |
missense |
probably benign |
0.24 |
R8427:Tnr
|
UTSW |
1 |
159,713,801 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8465:Tnr
|
UTSW |
1 |
159,713,645 (GRCm39) |
missense |
probably benign |
0.01 |
R8534:Tnr
|
UTSW |
1 |
159,746,585 (GRCm39) |
missense |
probably benign |
0.18 |
R8753:Tnr
|
UTSW |
1 |
159,677,936 (GRCm39) |
missense |
probably benign |
0.28 |
R8804:Tnr
|
UTSW |
1 |
159,685,882 (GRCm39) |
missense |
probably benign |
|
R8857:Tnr
|
UTSW |
1 |
159,713,728 (GRCm39) |
missense |
probably benign |
0.10 |
R8917:Tnr
|
UTSW |
1 |
159,701,692 (GRCm39) |
nonsense |
probably null |
|
R8930:Tnr
|
UTSW |
1 |
159,740,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R8932:Tnr
|
UTSW |
1 |
159,740,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R8940:Tnr
|
UTSW |
1 |
159,685,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R9096:Tnr
|
UTSW |
1 |
159,677,804 (GRCm39) |
missense |
probably benign |
0.10 |
R9127:Tnr
|
UTSW |
1 |
159,713,680 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9205:Tnr
|
UTSW |
1 |
159,722,617 (GRCm39) |
missense |
probably benign |
|
R9311:Tnr
|
UTSW |
1 |
159,677,663 (GRCm39) |
missense |
probably benign |
0.30 |
R9679:Tnr
|
UTSW |
1 |
159,719,608 (GRCm39) |
missense |
probably benign |
0.08 |
X0011:Tnr
|
UTSW |
1 |
159,716,908 (GRCm39) |
missense |
probably benign |
0.02 |
X0028:Tnr
|
UTSW |
1 |
159,701,684 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Tnr
|
UTSW |
1 |
159,722,665 (GRCm39) |
missense |
probably benign |
0.29 |
Z1177:Tnr
|
UTSW |
1 |
159,679,661 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CAGCACCAGTGTGTTCAAGG -3'
(R):5'- ATTGCCCCTTCCCTGAACAG -3'
Sequencing Primer
(F):5'- TTCAAGGAATGAGTGCAGGTCTC -3'
(R):5'- TGTGTAGGGCTCTTCACAGACAC -3'
|
Posted On |
2014-08-25 |