Incidental Mutation 'R5249:Tnr'
| ID |
398731 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Tnr
|
| Ensembl Gene |
ENSMUSG00000015829 |
| Gene Name |
tenascin R |
| Synonyms |
J1-tenascin, restrictin, janusin, TN-R |
| MMRRC Submission |
042820-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R5249 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
159351339-159759299 bp(+) (GRCm39) |
| Type of Mutation |
intron |
| DNA Base Change (assembly) |
C to T
at 159512226 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000141553
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000192069]
|
| AlphaFold |
Q8BYI9 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000097514
|
| SMART Domains |
Protein: ENSMUSP00000095121
Gene: ENSMUSG00000073528
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
27 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192069
|
| SMART Domains |
Protein: ENSMUSP00000141553
Gene: ENSMUSG00000015829
| 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 |
noncoding transcript
Transcript: ENSMUST00000194909
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000195199
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.8%
|
| 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 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 |
|---|
| A4gnt |
A |
G |
9: 99,502,284 (GRCm39) |
H148R |
probably damaging |
Het |
| Acrbp |
A |
G |
6: 125,037,885 (GRCm39) |
D394G |
probably damaging |
Het |
| Adam18 |
T |
C |
8: 25,115,868 (GRCm39) |
T609A |
probably benign |
Het |
| Adam25 |
T |
A |
8: 41,208,991 (GRCm39) |
N752K |
probably benign |
Het |
| Ano6 |
A |
C |
15: 95,811,469 (GRCm39) |
S176R |
probably benign |
Het |
| Ano7 |
T |
C |
1: 93,302,918 (GRCm39) |
S19P |
probably benign |
Het |
| Ap1b1 |
A |
G |
11: 4,976,364 (GRCm39) |
E437G |
probably damaging |
Het |
| Arfgap2 |
T |
A |
2: 91,095,982 (GRCm39) |
C46* |
probably null |
Het |
| Arhgef26 |
T |
A |
3: 62,247,981 (GRCm39) |
L355Q |
probably damaging |
Het |
| B4galnt4 |
C |
T |
7: 140,644,983 (GRCm39) |
T219I |
probably damaging |
Het |
| Bap1 |
C |
T |
14: 30,979,243 (GRCm39) |
|
probably benign |
Het |
| Catip |
T |
G |
1: 74,401,954 (GRCm39) |
L43R |
probably damaging |
Het |
| Ccdc177 |
G |
A |
12: 80,805,282 (GRCm39) |
R331C |
unknown |
Het |
| Cep85l |
T |
C |
10: 53,195,690 (GRCm39) |
|
probably null |
Het |
| Cfap206 |
T |
A |
4: 34,714,502 (GRCm39) |
Q398L |
probably benign |
Het |
| Clec18a |
A |
G |
8: 111,800,368 (GRCm39) |
C352R |
probably damaging |
Het |
| Clic6 |
A |
T |
16: 92,336,339 (GRCm39) |
Y549F |
probably damaging |
Het |
| Cpne9 |
C |
T |
6: 113,270,034 (GRCm39) |
|
probably benign |
Het |
| Cyb5r3 |
A |
C |
15: 83,042,836 (GRCm39) |
|
probably benign |
Het |
| Dnah6 |
C |
T |
6: 73,090,471 (GRCm39) |
R2293K |
probably damaging |
Het |
| Dnmbp |
C |
A |
19: 43,890,879 (GRCm39) |
R296L |
probably damaging |
Het |
| Dtwd1 |
C |
A |
2: 125,996,694 (GRCm39) |
Q60K |
probably benign |
Het |
| Esyt1 |
C |
A |
10: 128,352,443 (GRCm39) |
V723L |
probably benign |
Het |
| Fbxo42 |
T |
C |
4: 140,926,335 (GRCm39) |
L339P |
probably damaging |
Het |
| Furin |
A |
T |
7: 80,043,169 (GRCm39) |
N347K |
probably damaging |
Het |
| Fzd7 |
T |
C |
1: 59,522,522 (GRCm39) |
M135T |
probably damaging |
Het |
| Garin1b |
A |
G |
6: 29,323,896 (GRCm39) |
D207G |
probably damaging |
Het |
| Hlf |
A |
G |
11: 90,278,632 (GRCm39) |
M144T |
probably benign |
Het |
| Hyal5 |
C |
T |
6: 24,876,648 (GRCm39) |
Q174* |
probably null |
Het |
| Kcnb1 |
T |
A |
2: 166,947,103 (GRCm39) |
M582L |
possibly damaging |
Het |
| Kdm5d |
T |
C |
Y: 916,692 (GRCm39) |
Y391H |
probably damaging |
Het |
| Khdc4 |
T |
A |
3: 88,604,032 (GRCm39) |
I283N |
probably damaging |
Het |
| Kif21b |
C |
T |
1: 136,096,966 (GRCm39) |
T1297M |
probably damaging |
Het |
| Krt8 |
T |
G |
15: 101,906,875 (GRCm39) |
N317T |
possibly damaging |
Het |
| Lctl |
G |
T |
9: 64,045,196 (GRCm39) |
V372L |
probably benign |
Het |
| Lig1 |
C |
T |
7: 13,042,432 (GRCm39) |
H822Y |
possibly damaging |
Het |
| Lrrc4b |
A |
G |
7: 44,111,988 (GRCm39) |
D620G |
possibly damaging |
Het |
| Mboat4 |
C |
T |
8: 34,582,275 (GRCm39) |
H10Y |
probably benign |
Het |
| Med1 |
A |
T |
11: 98,048,066 (GRCm39) |
M910K |
probably benign |
Het |
| Mia2 |
A |
T |
12: 59,154,911 (GRCm39) |
D209V |
probably damaging |
Het |
| Mpp4 |
C |
T |
1: 59,184,017 (GRCm39) |
|
probably benign |
Het |
| Mrgprb1 |
A |
T |
7: 48,097,225 (GRCm39) |
V229E |
possibly damaging |
Het |
| Mtor |
T |
A |
4: 148,548,189 (GRCm39) |
C485S |
probably damaging |
Het |
| Mx1 |
T |
C |
16: 97,258,628 (GRCm39) |
D23G |
probably damaging |
Het |
| Myrfl |
T |
C |
10: 116,619,138 (GRCm39) |
D740G |
probably benign |
Het |
| Myt1l |
G |
A |
12: 29,882,331 (GRCm39) |
G509R |
unknown |
Het |
| Nav2 |
G |
A |
7: 49,185,661 (GRCm39) |
V874I |
probably damaging |
Het |
| Ntrk3 |
A |
T |
7: 78,110,914 (GRCm39) |
N262K |
possibly damaging |
Het |
| Opa1 |
A |
T |
16: 29,437,077 (GRCm39) |
D699V |
probably damaging |
Het |
| Or10u4 |
C |
T |
10: 129,802,078 (GRCm39) |
A164T |
probably benign |
Het |
| Or8b51 |
A |
G |
9: 38,569,374 (GRCm39) |
C105R |
possibly damaging |
Het |
| Otud7a |
A |
G |
7: 63,407,181 (GRCm39) |
N495D |
possibly damaging |
Het |
| Pcsk9 |
T |
C |
4: 106,320,950 (GRCm39) |
D53G |
probably benign |
Het |
| Pdcd5 |
A |
G |
7: 35,346,421 (GRCm39) |
|
probably benign |
Het |
| Phf21a |
C |
T |
2: 92,058,822 (GRCm39) |
P28L |
probably damaging |
Het |
| Pitpnm1 |
T |
A |
19: 4,158,130 (GRCm39) |
D573E |
probably damaging |
Het |
| Ppp1r35 |
C |
T |
5: 137,777,406 (GRCm39) |
|
probably benign |
Het |
| Ptprq |
T |
C |
10: 107,535,496 (GRCm39) |
Q423R |
probably damaging |
Het |
| Pum1 |
A |
T |
4: 130,490,125 (GRCm39) |
Y699F |
probably benign |
Het |
| Rabgef1 |
A |
G |
5: 130,241,841 (GRCm39) |
D415G |
probably benign |
Het |
| Rapgef6 |
A |
G |
11: 54,413,943 (GRCm39) |
E23G |
probably benign |
Het |
| Rpia |
G |
T |
6: 70,760,563 (GRCm39) |
C121* |
probably null |
Het |
| Sanbr |
A |
G |
11: 23,525,483 (GRCm39) |
*719Q |
probably null |
Het |
| Serpinb13 |
T |
A |
1: 106,926,427 (GRCm39) |
W201R |
probably damaging |
Het |
| Sh3bp4 |
T |
C |
1: 89,065,456 (GRCm39) |
C17R |
probably damaging |
Het |
| Sh3d21 |
A |
G |
4: 126,055,858 (GRCm39) |
|
probably benign |
Het |
| Slamf6 |
A |
C |
1: 171,764,249 (GRCm39) |
N214T |
probably damaging |
Het |
| Slc7a2 |
T |
C |
8: 41,361,130 (GRCm39) |
Y365H |
possibly damaging |
Het |
| Sox18 |
T |
C |
2: 181,312,971 (GRCm39) |
|
probably null |
Het |
| Spink7 |
A |
T |
18: 62,725,507 (GRCm39) |
F79I |
possibly damaging |
Het |
| Srpk3 |
C |
T |
X: 72,818,555 (GRCm39) |
R82* |
probably null |
Het |
| Sspo |
A |
T |
6: 48,470,244 (GRCm39) |
H4561L |
probably damaging |
Het |
| Tcaf1 |
T |
C |
6: 42,653,793 (GRCm39) |
K700R |
probably benign |
Het |
| Tcf25 |
G |
T |
8: 124,115,372 (GRCm39) |
R203L |
probably damaging |
Het |
| Tcp11 |
T |
C |
17: 28,290,757 (GRCm39) |
I201V |
possibly damaging |
Het |
| Tex2 |
T |
C |
11: 106,437,615 (GRCm39) |
D685G |
unknown |
Het |
| Themis |
G |
T |
10: 28,637,195 (GRCm39) |
E100* |
probably null |
Het |
| Tmem52b |
G |
A |
6: 129,491,221 (GRCm39) |
|
probably null |
Het |
| Tox3 |
T |
C |
8: 90,975,444 (GRCm39) |
I396V |
probably benign |
Het |
| Tpm2 |
T |
A |
4: 43,514,828 (GRCm39) |
E269V |
probably benign |
Het |
| Tulp1 |
C |
T |
17: 28,581,651 (GRCm39) |
|
probably benign |
Het |
| Tymp |
GC |
GCC |
15: 89,258,567 (GRCm39) |
|
probably null |
Het |
| Ube2j2 |
A |
C |
4: 156,033,515 (GRCm39) |
K30Q |
possibly damaging |
Het |
| Usp19 |
T |
A |
9: 108,369,807 (GRCm39) |
M1K |
probably null |
Het |
| Vmn2r52 |
C |
A |
7: 9,910,197 (GRCm39) |
R6L |
probably benign |
Het |
| Zbed4 |
G |
A |
15: 88,665,290 (GRCm39) |
V453M |
probably benign |
Het |
| Zfp319 |
T |
C |
8: 96,055,099 (GRCm39) |
E368G |
probably benign |
Het |
| Zfp366 |
A |
C |
13: 99,366,117 (GRCm39) |
E426A |
probably damaging |
Het |
| Zfp687 |
A |
T |
3: 94,916,777 (GRCm39) |
I783N |
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 |
|
|
R2022: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 |
|
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'- ATTGCTGAGCTGACAGAGGC -3'
(R):5'- TGGGAGATAGACTGAGCCAC -3'
Sequencing Primer
(F):5'- AGCTGACAGAGGCTCCCTAC -3'
(R):5'- CTGAGCCACAAAGCAAGGTG -3'
|
| Posted On |
2016-07-06 |
Incidental Mutation