Incidental Mutation 'R7034:Tmem131'
ID |
546493 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tmem131
|
Ensembl Gene |
ENSMUSG00000026116 |
Gene Name |
transmembrane protein 131 |
Synonyms |
Rw1, CC28, YR-23, Neg, D1Bwg0491e, 2610524E03Rik |
MMRRC Submission |
045135-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.885)
|
Stock # |
R7034 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
36831270-36978714 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 36832054 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glycine to Glutamic Acid
at position 1861
(G1861E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000142307
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027290]
[ENSMUST00000194563]
|
AlphaFold |
O70472 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000027290
AA Change: G1861E
PolyPhen 2
Score 0.795 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000027290 Gene: ENSMUSG00000026116 AA Change: G1861E
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
44 |
N/A |
INTRINSIC |
low complexity region
|
77 |
89 |
N/A |
INTRINSIC |
Pfam:TMEM131_like
|
106 |
189 |
1.7e-32 |
PFAM |
transmembrane domain
|
1081 |
1103 |
N/A |
INTRINSIC |
transmembrane domain
|
1116 |
1138 |
N/A |
INTRINSIC |
low complexity region
|
1232 |
1258 |
N/A |
INTRINSIC |
low complexity region
|
1283 |
1315 |
N/A |
INTRINSIC |
low complexity region
|
1369 |
1382 |
N/A |
INTRINSIC |
low complexity region
|
1384 |
1433 |
N/A |
INTRINSIC |
low complexity region
|
1460 |
1471 |
N/A |
INTRINSIC |
low complexity region
|
1595 |
1610 |
N/A |
INTRINSIC |
low complexity region
|
1613 |
1626 |
N/A |
INTRINSIC |
low complexity region
|
1628 |
1646 |
N/A |
INTRINSIC |
low complexity region
|
1675 |
1684 |
N/A |
INTRINSIC |
low complexity region
|
1693 |
1701 |
N/A |
INTRINSIC |
low complexity region
|
1738 |
1748 |
N/A |
INTRINSIC |
low complexity region
|
1760 |
1779 |
N/A |
INTRINSIC |
low complexity region
|
1799 |
1810 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000194563
AA Change: G1861E
PolyPhen 2
Score 0.795 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000142307 Gene: ENSMUSG00000026116 AA Change: G1861E
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
44 |
N/A |
INTRINSIC |
low complexity region
|
77 |
89 |
N/A |
INTRINSIC |
Pfam:DUF3651
|
170 |
243 |
1.9e-27 |
PFAM |
Pfam:DUF3651
|
500 |
580 |
4.5e-16 |
PFAM |
Pfam:DUF3651
|
631 |
706 |
5.2e-15 |
PFAM |
transmembrane domain
|
1081 |
1103 |
N/A |
INTRINSIC |
transmembrane domain
|
1116 |
1138 |
N/A |
INTRINSIC |
low complexity region
|
1232 |
1258 |
N/A |
INTRINSIC |
low complexity region
|
1283 |
1315 |
N/A |
INTRINSIC |
low complexity region
|
1369 |
1382 |
N/A |
INTRINSIC |
low complexity region
|
1384 |
1433 |
N/A |
INTRINSIC |
low complexity region
|
1460 |
1471 |
N/A |
INTRINSIC |
low complexity region
|
1595 |
1610 |
N/A |
INTRINSIC |
low complexity region
|
1613 |
1626 |
N/A |
INTRINSIC |
low complexity region
|
1628 |
1646 |
N/A |
INTRINSIC |
low complexity region
|
1675 |
1684 |
N/A |
INTRINSIC |
low complexity region
|
1693 |
1701 |
N/A |
INTRINSIC |
low complexity region
|
1738 |
1748 |
N/A |
INTRINSIC |
low complexity region
|
1760 |
1779 |
N/A |
INTRINSIC |
low complexity region
|
1799 |
1810 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
A |
10: 100,445,118 (GRCm39) |
|
probably null |
Het |
Adamts1 |
T |
A |
16: 85,599,634 (GRCm39) |
|
probably benign |
Het |
Aff4 |
A |
G |
11: 53,299,236 (GRCm39) |
K979E |
probably damaging |
Het |
Aftph |
A |
T |
11: 20,642,498 (GRCm39) |
M845K |
probably damaging |
Het |
Akt2 |
T |
C |
7: 27,336,437 (GRCm39) |
|
probably null |
Het |
Aldh1a7 |
A |
T |
19: 20,685,542 (GRCm39) |
L336Q |
possibly damaging |
Het |
Ank3 |
C |
T |
10: 69,835,209 (GRCm39) |
T680M |
probably damaging |
Het |
Apeh |
T |
C |
9: 107,971,470 (GRCm39) |
E59G |
possibly damaging |
Het |
Armc8 |
C |
T |
9: 99,366,018 (GRCm39) |
|
probably null |
Het |
Armh3 |
A |
G |
19: 45,953,688 (GRCm39) |
I195T |
probably damaging |
Het |
Atp2b1 |
C |
T |
10: 98,823,172 (GRCm39) |
T244I |
probably damaging |
Het |
Btaf1 |
C |
A |
19: 36,981,869 (GRCm39) |
T1633K |
probably benign |
Het |
Cacng8 |
A |
G |
7: 3,463,819 (GRCm39) |
S324G |
probably benign |
Het |
Calcr |
T |
A |
6: 3,692,543 (GRCm39) |
Q400L |
probably damaging |
Het |
Caprin2 |
G |
A |
6: 148,749,703 (GRCm39) |
P536S |
possibly damaging |
Het |
Ccdc54 |
A |
T |
16: 50,410,951 (GRCm39) |
M105K |
probably benign |
Het |
Ccna1 |
T |
C |
3: 54,953,460 (GRCm39) |
E381G |
possibly damaging |
Het |
Cd2ap |
A |
T |
17: 43,109,490 (GRCm39) |
L623Q |
probably damaging |
Het |
Cdkl3 |
A |
G |
11: 51,918,042 (GRCm39) |
E415G |
probably benign |
Het |
Chd5 |
C |
A |
4: 152,445,398 (GRCm39) |
L430I |
possibly damaging |
Het |
Clspn |
G |
A |
4: 126,474,775 (GRCm39) |
E975K |
possibly damaging |
Het |
Cobl |
C |
A |
11: 12,204,177 (GRCm39) |
V835F |
probably damaging |
Het |
D430041D05Rik |
C |
A |
2: 104,022,883 (GRCm39) |
R1037L |
probably damaging |
Het |
Derl1 |
A |
G |
15: 57,742,443 (GRCm39) |
|
probably null |
Het |
Dhrs9 |
T |
G |
2: 69,223,520 (GRCm39) |
N89K |
probably benign |
Het |
Erich1 |
A |
G |
8: 14,114,330 (GRCm39) |
I60T |
probably benign |
Het |
Fam184a |
A |
T |
10: 53,570,910 (GRCm39) |
S408T |
possibly damaging |
Het |
Fcgr4 |
T |
A |
1: 170,847,657 (GRCm39) |
M85K |
probably benign |
Het |
Foxj3 |
A |
G |
4: 119,476,497 (GRCm39) |
E259G |
probably damaging |
Het |
Galnt11 |
T |
C |
5: 25,463,811 (GRCm39) |
I361T |
probably damaging |
Het |
Gck |
A |
G |
11: 5,851,747 (GRCm39) |
S441P |
probably damaging |
Het |
Gdap1l1 |
G |
T |
2: 163,288,065 (GRCm39) |
V98F |
probably damaging |
Het |
Gramd1a |
A |
G |
7: 30,832,181 (GRCm39) |
|
probably null |
Het |
H2ac21 |
C |
T |
3: 96,127,304 (GRCm39) |
Q25* |
probably null |
Het |
Herc3 |
A |
T |
6: 58,853,840 (GRCm39) |
M629L |
probably benign |
Het |
Hoxc12 |
G |
A |
15: 102,846,795 (GRCm39) |
G229D |
probably damaging |
Het |
Hycc2 |
T |
A |
1: 58,574,696 (GRCm39) |
M282L |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,527,433 (GRCm39) |
L528P |
probably benign |
Het |
Krt39 |
A |
C |
11: 99,412,062 (GRCm39) |
V8G |
probably benign |
Het |
Krt71 |
A |
G |
15: 101,646,772 (GRCm39) |
I312T |
probably benign |
Het |
Lrrc37 |
T |
A |
11: 103,506,638 (GRCm39) |
|
probably benign |
Het |
Mllt11 |
A |
G |
3: 95,127,744 (GRCm39) |
Y9H |
probably damaging |
Het |
Mrgpra3 |
G |
T |
7: 47,239,838 (GRCm39) |
N29K |
possibly damaging |
Het |
Mug1 |
A |
G |
6: 121,850,603 (GRCm39) |
T700A |
probably benign |
Het |
Myl1 |
T |
C |
1: 66,969,395 (GRCm39) |
N79S |
probably damaging |
Het |
Myo18b |
G |
A |
5: 112,871,770 (GRCm39) |
Q2104* |
probably null |
Het |
Nalf1 |
G |
A |
8: 9,820,589 (GRCm39) |
P144S |
possibly damaging |
Het |
Ndufs2 |
T |
C |
1: 171,065,877 (GRCm39) |
D256G |
probably benign |
Het |
Nek5 |
T |
C |
8: 22,597,739 (GRCm39) |
N280S |
probably benign |
Het |
Nwd2 |
A |
T |
5: 63,962,258 (GRCm39) |
N614I |
probably damaging |
Het |
Or6c88 |
G |
A |
10: 129,406,941 (GRCm39) |
C139Y |
possibly damaging |
Het |
Parp1 |
G |
T |
1: 180,425,817 (GRCm39) |
K849N |
possibly damaging |
Het |
Pcnx2 |
T |
C |
8: 126,512,041 (GRCm39) |
T1422A |
probably damaging |
Het |
Plce1 |
A |
G |
19: 38,727,801 (GRCm39) |
N1520S |
probably damaging |
Het |
Ppcdc |
T |
C |
9: 57,322,453 (GRCm39) |
T149A |
probably damaging |
Het |
Ppl |
A |
G |
16: 4,905,366 (GRCm39) |
V1643A |
probably benign |
Het |
Pramel23 |
A |
T |
4: 143,423,898 (GRCm39) |
I297N |
probably damaging |
Het |
Prrx1 |
T |
A |
1: 163,075,907 (GRCm39) |
M220L |
probably benign |
Het |
Pspc1 |
A |
C |
14: 56,996,085 (GRCm39) |
|
probably null |
Het |
Ptpn20 |
A |
G |
14: 33,336,392 (GRCm39) |
*44W |
probably null |
Het |
Qars1 |
T |
A |
9: 108,391,976 (GRCm39) |
V83E |
probably damaging |
Het |
Rbm33 |
T |
C |
5: 28,599,496 (GRCm39) |
M956T |
unknown |
Het |
Sash1 |
C |
A |
10: 8,605,847 (GRCm39) |
E848* |
probably null |
Het |
Scai |
T |
A |
2: 39,011,147 (GRCm39) |
Y163F |
probably damaging |
Het |
Serpinf2 |
A |
T |
11: 75,329,244 (GRCm39) |
|
probably benign |
Het |
Sgo2b |
T |
A |
8: 64,379,868 (GRCm39) |
H988L |
probably benign |
Het |
Sh2b2 |
G |
A |
5: 136,247,739 (GRCm39) |
T604I |
probably benign |
Het |
Skint4 |
A |
T |
4: 112,015,281 (GRCm39) |
I449F |
possibly damaging |
Het |
Slc30a2 |
A |
G |
4: 134,074,653 (GRCm39) |
I88V |
possibly damaging |
Het |
Smug1 |
A |
G |
15: 103,064,369 (GRCm39) |
L184P |
probably damaging |
Het |
Spatc1 |
A |
G |
15: 76,168,080 (GRCm39) |
T180A |
probably benign |
Het |
Ssr1 |
A |
T |
13: 38,178,001 (GRCm39) |
L20Q |
probably null |
Het |
Supt4a |
A |
G |
11: 87,634,084 (GRCm39) |
E100G |
probably damaging |
Het |
Teddm2 |
T |
C |
1: 153,726,320 (GRCm39) |
I132V |
probably benign |
Het |
Tpr |
A |
T |
1: 150,299,358 (GRCm39) |
H1186L |
probably benign |
Het |
Trim34b |
A |
T |
7: 103,978,743 (GRCm39) |
|
probably benign |
Het |
Trpm2 |
T |
C |
10: 77,748,426 (GRCm39) |
M1415V |
probably benign |
Het |
Ttll12 |
A |
G |
15: 83,471,086 (GRCm39) |
F264S |
probably benign |
Het |
Vmn2r59 |
T |
C |
7: 41,695,644 (GRCm39) |
E256G |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,546,672 (GRCm39) |
H848L |
probably benign |
Het |
Vps35l |
T |
C |
7: 118,372,315 (GRCm39) |
S290P |
probably damaging |
Het |
Wdfy3 |
G |
A |
5: 102,055,384 (GRCm39) |
T1562I |
probably damaging |
Het |
Ybey |
T |
C |
10: 76,304,197 (GRCm39) |
S2G |
possibly damaging |
Het |
Zfp346 |
A |
T |
13: 55,280,200 (GRCm39) |
Q308L |
probably benign |
Het |
|
Other mutations in Tmem131 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00561:Tmem131
|
APN |
1 |
36,850,508 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00945:Tmem131
|
APN |
1 |
36,866,086 (GRCm39) |
splice site |
probably benign |
|
IGL01107:Tmem131
|
APN |
1 |
36,868,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01401:Tmem131
|
APN |
1 |
36,838,468 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01533:Tmem131
|
APN |
1 |
36,857,803 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01701:Tmem131
|
APN |
1 |
36,847,318 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01784:Tmem131
|
APN |
1 |
36,854,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01890:Tmem131
|
APN |
1 |
36,862,237 (GRCm39) |
splice site |
probably benign |
|
IGL01969:Tmem131
|
APN |
1 |
36,864,541 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02327:Tmem131
|
APN |
1 |
36,838,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02707:Tmem131
|
APN |
1 |
36,864,560 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02743:Tmem131
|
APN |
1 |
36,832,232 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03111:Tmem131
|
APN |
1 |
36,867,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Tmem131
|
UTSW |
1 |
36,858,209 (GRCm39) |
missense |
probably benign |
0.09 |
R0063:Tmem131
|
UTSW |
1 |
36,858,209 (GRCm39) |
missense |
probably benign |
0.09 |
R0238:Tmem131
|
UTSW |
1 |
36,867,131 (GRCm39) |
splice site |
probably benign |
|
R0239:Tmem131
|
UTSW |
1 |
36,867,131 (GRCm39) |
splice site |
probably benign |
|
R0499:Tmem131
|
UTSW |
1 |
36,880,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R0548:Tmem131
|
UTSW |
1 |
36,877,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0845:Tmem131
|
UTSW |
1 |
36,855,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R0975:Tmem131
|
UTSW |
1 |
36,893,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Tmem131
|
UTSW |
1 |
36,833,900 (GRCm39) |
missense |
probably damaging |
0.98 |
R1170:Tmem131
|
UTSW |
1 |
36,873,979 (GRCm39) |
nonsense |
probably null |
|
R1443:Tmem131
|
UTSW |
1 |
36,864,559 (GRCm39) |
missense |
probably damaging |
0.98 |
R1448:Tmem131
|
UTSW |
1 |
36,866,439 (GRCm39) |
missense |
probably benign |
0.16 |
R1472:Tmem131
|
UTSW |
1 |
36,855,322 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1530:Tmem131
|
UTSW |
1 |
36,866,090 (GRCm39) |
critical splice donor site |
probably null |
|
R1672:Tmem131
|
UTSW |
1 |
36,863,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Tmem131
|
UTSW |
1 |
36,847,008 (GRCm39) |
missense |
probably benign |
0.05 |
R1914:Tmem131
|
UTSW |
1 |
36,835,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1915:Tmem131
|
UTSW |
1 |
36,835,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Tmem131
|
UTSW |
1 |
36,851,352 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1971:Tmem131
|
UTSW |
1 |
36,843,680 (GRCm39) |
nonsense |
probably null |
|
R2146:Tmem131
|
UTSW |
1 |
36,851,690 (GRCm39) |
missense |
probably benign |
0.13 |
R2148:Tmem131
|
UTSW |
1 |
36,851,690 (GRCm39) |
missense |
probably benign |
0.13 |
R2149:Tmem131
|
UTSW |
1 |
36,851,690 (GRCm39) |
missense |
probably benign |
0.13 |
R2150:Tmem131
|
UTSW |
1 |
36,851,690 (GRCm39) |
missense |
probably benign |
0.13 |
R2386:Tmem131
|
UTSW |
1 |
36,868,716 (GRCm39) |
missense |
probably benign |
0.00 |
R2879:Tmem131
|
UTSW |
1 |
36,880,788 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2903:Tmem131
|
UTSW |
1 |
36,864,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Tmem131
|
UTSW |
1 |
36,847,902 (GRCm39) |
splice site |
probably benign |
|
R3821:Tmem131
|
UTSW |
1 |
36,847,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R3961:Tmem131
|
UTSW |
1 |
36,858,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R4153:Tmem131
|
UTSW |
1 |
36,847,874 (GRCm39) |
intron |
probably benign |
|
R4154:Tmem131
|
UTSW |
1 |
36,847,874 (GRCm39) |
intron |
probably benign |
|
R4502:Tmem131
|
UTSW |
1 |
36,864,560 (GRCm39) |
missense |
probably benign |
0.03 |
R4503:Tmem131
|
UTSW |
1 |
36,864,560 (GRCm39) |
missense |
probably benign |
0.03 |
R4795:Tmem131
|
UTSW |
1 |
36,880,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Tmem131
|
UTSW |
1 |
36,866,255 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5068:Tmem131
|
UTSW |
1 |
36,893,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Tmem131
|
UTSW |
1 |
36,893,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Tmem131
|
UTSW |
1 |
36,911,639 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5507:Tmem131
|
UTSW |
1 |
36,928,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Tmem131
|
UTSW |
1 |
36,838,419 (GRCm39) |
missense |
probably benign |
0.02 |
R5913:Tmem131
|
UTSW |
1 |
36,858,209 (GRCm39) |
missense |
probably benign |
0.01 |
R6044:Tmem131
|
UTSW |
1 |
36,920,422 (GRCm39) |
nonsense |
probably null |
|
R6125:Tmem131
|
UTSW |
1 |
36,847,387 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6259:Tmem131
|
UTSW |
1 |
36,858,209 (GRCm39) |
missense |
probably benign |
0.09 |
R6392:Tmem131
|
UTSW |
1 |
36,920,423 (GRCm39) |
missense |
probably benign |
0.10 |
R6704:Tmem131
|
UTSW |
1 |
36,835,261 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6828:Tmem131
|
UTSW |
1 |
36,843,724 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6964:Tmem131
|
UTSW |
1 |
36,835,373 (GRCm39) |
missense |
probably damaging |
0.99 |
R7036:Tmem131
|
UTSW |
1 |
36,832,054 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7081:Tmem131
|
UTSW |
1 |
36,928,376 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7278:Tmem131
|
UTSW |
1 |
36,835,382 (GRCm39) |
missense |
probably damaging |
0.99 |
R7282:Tmem131
|
UTSW |
1 |
36,880,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7294:Tmem131
|
UTSW |
1 |
36,893,928 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7635:Tmem131
|
UTSW |
1 |
36,911,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7916:Tmem131
|
UTSW |
1 |
36,862,167 (GRCm39) |
missense |
probably benign |
0.00 |
R7948:Tmem131
|
UTSW |
1 |
36,833,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Tmem131
|
UTSW |
1 |
36,847,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R8244:Tmem131
|
UTSW |
1 |
36,847,974 (GRCm39) |
missense |
probably benign |
0.08 |
R8461:Tmem131
|
UTSW |
1 |
36,833,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Tmem131
|
UTSW |
1 |
36,838,186 (GRCm39) |
splice site |
probably benign |
|
R8902:Tmem131
|
UTSW |
1 |
36,848,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Tmem131
|
UTSW |
1 |
36,868,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R8984:Tmem131
|
UTSW |
1 |
36,867,228 (GRCm39) |
missense |
probably benign |
0.05 |
R8994:Tmem131
|
UTSW |
1 |
36,854,538 (GRCm39) |
missense |
probably benign |
0.29 |
R9105:Tmem131
|
UTSW |
1 |
36,854,591 (GRCm39) |
missense |
probably benign |
0.44 |
R9156:Tmem131
|
UTSW |
1 |
36,880,767 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9328:Tmem131
|
UTSW |
1 |
36,858,236 (GRCm39) |
nonsense |
probably null |
|
R9501:Tmem131
|
UTSW |
1 |
36,858,265 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9633:Tmem131
|
UTSW |
1 |
36,847,069 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Tmem131
|
UTSW |
1 |
36,835,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGTGAGAGAAGCCAGTGCAC -3'
(R):5'- TCGTAGTCCATCCTTGGCAAC -3'
Sequencing Primer
(F):5'- AGTGCACCAAGCCTGCC -3'
(R):5'- ATTCAGCAGCTCCATCTGG -3'
|
Posted On |
2019-05-13 |