Incidental Mutation 'R9328:Tmem131'
| ID |
706615 |
| 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 |
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.885)
|
| Stock # |
R9328 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
36831270-36978714 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to A
at 36858236 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Stop codon
at position 704
(Q704*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000027290
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027290]
[ENSMUST00000186486]
[ENSMUST00000189470]
[ENSMUST00000190442]
[ENSMUST00000194563]
|
| AlphaFold |
O70472 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000027290
AA Change: Q704*
|
| SMART Domains |
Protein: ENSMUSP00000027290
Gene: ENSMUSG00000026116
AA Change: Q704*
| 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 |
probably benign
Transcript: ENSMUST00000186486
|
| SMART Domains |
Protein: ENSMUSP00000142080
Gene: ENSMUSG00000026116
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
31 |
48 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000189470
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000190442
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000194563
AA Change: Q704*
|
| SMART Domains |
Protein: ENSMUSP00000142307
Gene: ENSMUSG00000026116
AA Change: Q704*
| 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: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1600014C10Rik |
A |
G |
7: 37,894,272 (GRCm39) |
T102A |
probably benign |
Het |
| 1700109H08Rik |
A |
G |
5: 3,632,161 (GRCm39) |
K164E |
possibly damaging |
Het |
| 2610042L04Rik |
C |
T |
14: 4,350,013 (GRCm38) |
Q74* |
probably null |
Het |
| Aadacl4fm4 |
T |
A |
4: 144,401,256 (GRCm39) |
H76L |
probably benign |
Het |
| Adgrb2 |
T |
A |
4: 129,915,363 (GRCm39) |
M1381K |
probably damaging |
Het |
| Adgrv1 |
C |
A |
13: 81,620,523 (GRCm39) |
D3975Y |
probably damaging |
Het |
| Ano10 |
C |
T |
9: 122,090,168 (GRCm39) |
E382K |
possibly damaging |
Het |
| Ascc3 |
T |
C |
10: 50,535,015 (GRCm39) |
V636A |
probably damaging |
Het |
| AU040320 |
T |
C |
4: 126,729,332 (GRCm39) |
V498A |
possibly damaging |
Het |
| Bahcc1 |
C |
T |
11: 120,165,885 (GRCm39) |
T1047I |
possibly damaging |
Het |
| BC004004 |
A |
T |
17: 29,501,682 (GRCm39) |
T74S |
possibly damaging |
Het |
| Bend3 |
A |
G |
10: 43,387,419 (GRCm39) |
D604G |
possibly damaging |
Het |
| Brinp3 |
T |
A |
1: 146,707,455 (GRCm39) |
V373E |
probably damaging |
Het |
| Bsph2 |
A |
T |
7: 13,290,764 (GRCm39) |
D38E |
probably benign |
Het |
| Castor1 |
T |
C |
11: 4,170,423 (GRCm39) |
F140L |
probably benign |
Het |
| Catsperd |
A |
G |
17: 56,965,074 (GRCm39) |
I474V |
possibly damaging |
Het |
| Ccdc180 |
A |
G |
4: 45,902,447 (GRCm39) |
N292S |
possibly damaging |
Het |
| Cd1d1 |
A |
T |
3: 86,905,459 (GRCm39) |
V178E |
possibly damaging |
Het |
| Cdca2 |
T |
A |
14: 67,931,131 (GRCm39) |
R521W |
probably damaging |
Het |
| Champ1 |
A |
G |
8: 13,929,392 (GRCm39) |
K517E |
probably damaging |
Het |
| Chrna9 |
T |
C |
5: 66,128,569 (GRCm39) |
F259S |
probably damaging |
Het |
| Chuk |
A |
T |
19: 44,085,422 (GRCm39) |
C241* |
probably null |
Het |
| Clns1a |
A |
G |
7: 97,363,240 (GRCm39) |
Y204C |
probably benign |
Het |
| Cplane1 |
A |
G |
15: 8,215,692 (GRCm39) |
D416G |
probably damaging |
Het |
| Cyp2j7 |
A |
T |
4: 96,115,869 (GRCm39) |
N192K |
probably damaging |
Het |
| Ddr2 |
A |
G |
1: 169,829,504 (GRCm39) |
V250A |
probably benign |
Het |
| Dlgap2 |
A |
G |
8: 14,777,441 (GRCm39) |
S229G |
probably damaging |
Het |
| Dmrt1 |
A |
T |
19: 25,523,231 (GRCm39) |
H194L |
probably damaging |
Het |
| Dock7 |
A |
T |
4: 98,968,064 (GRCm39) |
F138I |
|
Het |
| Dsg2 |
T |
C |
18: 20,715,847 (GRCm39) |
V263A |
possibly damaging |
Het |
| Dusp16 |
A |
G |
6: 134,716,902 (GRCm39) |
L135P |
probably damaging |
Het |
| Dysf |
A |
G |
6: 84,050,895 (GRCm39) |
N414S |
probably damaging |
Het |
| Efhc1 |
A |
G |
1: 21,030,598 (GRCm39) |
Y177C |
probably damaging |
Het |
| Fam83e |
A |
T |
7: 45,372,912 (GRCm39) |
R174S |
probably benign |
Het |
| Fgf4 |
C |
T |
7: 144,416,664 (GRCm39) |
L199F |
probably damaging |
Het |
| Fignl2 |
A |
G |
15: 100,951,271 (GRCm39) |
L337P |
unknown |
Het |
| Gm4353 |
T |
C |
7: 115,682,724 (GRCm39) |
R286G |
probably damaging |
Het |
| Gm5142 |
T |
C |
14: 59,416,126 (GRCm39) |
S11G |
probably benign |
Het |
| Gpr151 |
A |
G |
18: 42,712,270 (GRCm39) |
V136A |
probably damaging |
Het |
| Ift80 |
T |
A |
3: 68,847,483 (GRCm39) |
I338F |
probably damaging |
Het |
| Itgb4 |
A |
G |
11: 115,880,625 (GRCm39) |
S693G |
probably benign |
Het |
| Kif13a |
T |
A |
13: 46,951,838 (GRCm39) |
I812F |
probably damaging |
Het |
| Krit1 |
T |
C |
5: 3,862,577 (GRCm39) |
|
probably null |
Het |
| Mapk6 |
T |
C |
9: 75,305,252 (GRCm39) |
D55G |
possibly damaging |
Het |
| Matn3 |
A |
G |
12: 9,002,033 (GRCm39) |
I82V |
possibly damaging |
Het |
| Mecom |
T |
A |
3: 30,063,994 (GRCm39) |
D32V |
unknown |
Het |
| Nacad |
T |
C |
11: 6,552,417 (GRCm39) |
H258R |
possibly damaging |
Het |
| Ndufaf5 |
T |
A |
2: 140,030,752 (GRCm39) |
S213T |
possibly damaging |
Het |
| Nphp1 |
C |
T |
2: 127,582,892 (GRCm39) |
D674N |
possibly damaging |
Het |
| Nsmaf |
A |
G |
4: 6,426,412 (GRCm39) |
L250P |
probably damaging |
Het |
| Ogdh |
T |
C |
11: 6,297,838 (GRCm39) |
S571P |
probably benign |
Het |
| Or1e31 |
T |
C |
11: 73,690,478 (GRCm39) |
Y35C |
probably damaging |
Het |
| Or51i2 |
T |
A |
7: 103,689,268 (GRCm39) |
D88E |
|
Het |
| Or8g27 |
T |
C |
9: 39,129,175 (GRCm39) |
I174T |
probably damaging |
Het |
| Osbpl11 |
A |
G |
16: 33,047,245 (GRCm39) |
I403V |
probably damaging |
Het |
| Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
| Pira13 |
T |
A |
7: 3,827,580 (GRCm39) |
R192S |
unknown |
Het |
| Plat |
A |
G |
8: 23,268,133 (GRCm39) |
R300G |
probably damaging |
Het |
| Ppid |
T |
C |
3: 79,505,059 (GRCm39) |
I134T |
probably damaging |
Het |
| Rad51ap2 |
A |
G |
12: 11,507,772 (GRCm39) |
I565V |
probably benign |
Het |
| Rasa1 |
T |
C |
13: 85,403,575 (GRCm39) |
|
probably null |
Het |
| Sema4a |
C |
T |
3: 88,345,613 (GRCm39) |
W490* |
probably null |
Het |
| Septin3 |
A |
G |
15: 82,173,439 (GRCm39) |
Y257C |
probably damaging |
Het |
| Sh3rf2 |
C |
A |
18: 42,274,161 (GRCm39) |
F442L |
probably benign |
Het |
| Sipa1l1 |
A |
G |
12: 82,388,792 (GRCm39) |
I339M |
possibly damaging |
Het |
| Six2 |
T |
C |
17: 85,995,196 (GRCm39) |
N62S |
possibly damaging |
Het |
| Slc44a5 |
T |
C |
3: 153,964,678 (GRCm39) |
I526T |
probably benign |
Het |
| Smarca5 |
T |
C |
8: 81,447,378 (GRCm39) |
S402G |
probably benign |
Het |
| Son |
T |
A |
16: 91,452,645 (GRCm39) |
V464E |
possibly damaging |
Het |
| Sorcs3 |
A |
G |
19: 48,785,950 (GRCm39) |
K1144E |
probably damaging |
Het |
| Stxbp6 |
A |
G |
12: 44,902,659 (GRCm39) |
L204P |
probably damaging |
Het |
| Tchh |
A |
G |
3: 93,351,570 (GRCm39) |
R337G |
unknown |
Het |
| Tgm4 |
T |
C |
9: 122,885,697 (GRCm39) |
V413A |
possibly damaging |
Het |
| Tmpo |
T |
C |
10: 90,998,825 (GRCm39) |
K321E |
probably damaging |
Het |
| Trim75 |
G |
T |
8: 65,435,315 (GRCm39) |
N378K |
probably benign |
Het |
| Tspan18 |
T |
A |
2: 93,036,065 (GRCm39) |
I227F |
probably benign |
Het |
| Ttn |
C |
T |
2: 76,541,526 (GRCm39) |
W33820* |
probably null |
Het |
| Urb2 |
T |
A |
8: 124,774,034 (GRCm39) |
Y1522N |
probably damaging |
Het |
| Zbtb40 |
T |
C |
4: 136,745,620 (GRCm39) |
N138D |
probably benign |
Het |
| Zfp715 |
A |
T |
7: 42,947,328 (GRCm39) |
H877Q |
possibly damaging |
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 |
|
R7034:Tmem131
|
UTSW |
1 |
36,832,054 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
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 |
|
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'- ACACAGGACGACCATGAGTG -3'
(R):5'- CAGTACTTCTGTAACATGCACGATG -3'
Sequencing Primer
(F):5'- CGACCATGAGTGCCGAGAAC -3'
(R):5'- AAAAGCTGGCCTGTGATCTC -3'
|
| Posted On |
2022-04-18 |
Incidental Mutation