Incidental Mutation 'R1789:Trappc9'
ID |
201668 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Trappc9
|
Ensembl Gene |
ENSMUSG00000047921 |
Gene Name |
trafficking protein particle complex 9 |
Synonyms |
TRS130, Nibp, 2900005P22Rik, 4632408O18Rik, 1810044A24Rik |
MMRRC Submission |
039820-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1789 (G1)
|
Quality Score |
188 |
Status
|
Not validated
|
Chromosome |
15 |
Chromosomal Location |
72461469-72933053 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 72897816 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Tryptophan
at position 377
(R377W)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000131997
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023276]
[ENSMUST00000089770]
[ENSMUST00000168191]
[ENSMUST00000170633]
[ENSMUST00000228960]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000023276
AA Change: R189W
PolyPhen 2
Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000023276 Gene: ENSMUSG00000047921 AA Change: R189W
Domain | Start | End | E-Value | Type |
Pfam:TRAPPC9-Trs120
|
2 |
920 |
3.6e-239 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000089770
AA Change: R368W
PolyPhen 2
Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000087202 Gene: ENSMUSG00000047921 AA Change: R368W
Domain | Start | End | E-Value | Type |
Pfam:TRAPPC9-Trs120
|
182 |
350 |
4.1e-20 |
PFAM |
Pfam:TRAPPC9-Trs120
|
434 |
664 |
2.2e-16 |
PFAM |
low complexity region
|
993 |
1004 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000168191
AA Change: R368W
PolyPhen 2
Score 0.973 (Sensitivity: 0.76; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000131295 Gene: ENSMUSG00000047921 AA Change: R368W
Domain | Start | End | E-Value | Type |
Pfam:TRAPPC9-Trs120
|
1 |
810 |
3.7e-222 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000170633
AA Change: R377W
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000131997 Gene: ENSMUSG00000047921 AA Change: R377W
Domain | Start | End | E-Value | Type |
Pfam:TRAPPC9-Trs120
|
1 |
820 |
7.6e-224 |
PFAM |
coiled coil region
|
857 |
885 |
N/A |
INTRINSIC |
low complexity region
|
906 |
929 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000228960
AA Change: R368W
PolyPhen 2
Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000230025
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000230270
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.2%
- 20x: 92.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive mental retardation. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
G |
A |
16: 20,184,701 (GRCm39) |
P986L |
probably damaging |
Het |
Acad10 |
A |
T |
5: 121,769,456 (GRCm39) |
Y667N |
possibly damaging |
Het |
Ahi1 |
G |
A |
10: 20,839,014 (GRCm39) |
G121D |
probably benign |
Het |
Ampd1 |
T |
A |
3: 103,006,442 (GRCm39) |
I690N |
possibly damaging |
Het |
Amy1 |
C |
A |
3: 113,351,814 (GRCm39) |
W425L |
possibly damaging |
Het |
Arhgap27 |
A |
T |
11: 103,223,831 (GRCm39) |
V823E |
probably damaging |
Het |
Arhgef17 |
A |
G |
7: 100,579,077 (GRCm39) |
S624P |
probably damaging |
Het |
Arid5b |
T |
C |
10: 68,021,897 (GRCm39) |
H231R |
probably damaging |
Het |
Aspscr1 |
C |
A |
11: 120,579,386 (GRCm39) |
T78N |
probably damaging |
Het |
Auts2 |
T |
A |
5: 131,501,288 (GRCm39) |
T42S |
probably damaging |
Het |
Ccdc171 |
A |
G |
4: 83,473,045 (GRCm39) |
D158G |
probably damaging |
Het |
Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
Cfap61 |
T |
C |
2: 145,781,913 (GRCm39) |
|
probably null |
Het |
Chrna5 |
T |
C |
9: 54,911,935 (GRCm39) |
V245A |
possibly damaging |
Het |
Cntnap5c |
G |
A |
17: 58,320,916 (GRCm39) |
G163R |
probably damaging |
Het |
Col5a2 |
A |
G |
1: 45,417,465 (GRCm39) |
|
probably null |
Het |
Col5a2 |
T |
C |
1: 45,433,936 (GRCm39) |
Q759R |
probably damaging |
Het |
Comp |
A |
G |
8: 70,829,796 (GRCm39) |
D340G |
probably benign |
Het |
Cyfip1 |
T |
A |
7: 55,576,143 (GRCm39) |
D1104E |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,002,515 (GRCm39) |
S308T |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,270,572 (GRCm39) |
H958R |
probably benign |
Het |
Elp3 |
A |
G |
14: 65,785,368 (GRCm39) |
Y478H |
probably damaging |
Het |
Fam237b |
A |
T |
5: 5,625,652 (GRCm39) |
Q116L |
possibly damaging |
Het |
Fat3 |
T |
C |
9: 16,288,281 (GRCm39) |
Y414C |
probably benign |
Het |
Fbxo10 |
C |
A |
4: 45,046,389 (GRCm39) |
A574S |
probably damaging |
Het |
Fsip2 |
G |
T |
2: 82,807,906 (GRCm39) |
L1408F |
probably benign |
Het |
Fubp3 |
T |
C |
2: 31,501,747 (GRCm39) |
V425A |
possibly damaging |
Het |
Gm7168 |
A |
T |
17: 14,169,846 (GRCm39) |
R404S |
probably benign |
Het |
Gpd1 |
T |
G |
15: 99,621,083 (GRCm39) |
F299C |
probably damaging |
Het |
Gpr137 |
C |
T |
19: 6,919,425 (GRCm39) |
|
probably benign |
Het |
Grin3b |
T |
C |
10: 79,809,242 (GRCm39) |
S331P |
probably benign |
Het |
Grk3 |
T |
A |
5: 113,089,584 (GRCm39) |
I281F |
probably damaging |
Het |
Hoxb7 |
T |
A |
11: 96,177,607 (GRCm39) |
S18R |
probably damaging |
Het |
Igf1r |
C |
T |
7: 67,864,681 (GRCm39) |
R1160* |
probably null |
Het |
Itfg1 |
A |
G |
8: 86,452,141 (GRCm39) |
|
probably null |
Het |
Itgb8 |
T |
C |
12: 119,166,190 (GRCm39) |
I114V |
probably benign |
Het |
Kcnk1 |
A |
G |
8: 126,752,123 (GRCm39) |
E243G |
possibly damaging |
Het |
Kif27 |
A |
G |
13: 58,491,822 (GRCm39) |
L439P |
probably damaging |
Het |
Kif2c |
T |
A |
4: 117,024,558 (GRCm39) |
Q279L |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,749,955 (GRCm39) |
|
probably benign |
Het |
L3mbtl1 |
A |
G |
2: 162,816,422 (GRCm39) |
T821A |
probably benign |
Het |
Lrrc24 |
A |
T |
15: 76,606,778 (GRCm39) |
M206K |
probably benign |
Het |
Mamdc4 |
T |
G |
2: 25,457,634 (GRCm39) |
K460Q |
possibly damaging |
Het |
Maml2 |
C |
G |
9: 13,608,641 (GRCm39) |
L30V |
probably damaging |
Het |
Mc5r |
C |
G |
18: 68,471,741 (GRCm39) |
|
probably null |
Het |
Myo10 |
T |
G |
15: 25,726,611 (GRCm39) |
|
probably null |
Het |
Myo1e |
T |
A |
9: 70,246,066 (GRCm39) |
L419Q |
probably damaging |
Het |
Myo6 |
C |
A |
9: 80,207,854 (GRCm39) |
H1115Q |
probably damaging |
Het |
Myo7a |
A |
G |
7: 97,756,302 (GRCm39) |
V10A |
probably damaging |
Het |
Myoz2 |
C |
T |
3: 122,819,776 (GRCm39) |
R61H |
probably damaging |
Het |
Ncdn |
G |
A |
4: 126,645,796 (GRCm39) |
R38C |
probably damaging |
Het |
Nckap1 |
T |
A |
2: 80,350,900 (GRCm39) |
T736S |
probably benign |
Het |
Ncor2 |
G |
A |
5: 125,096,954 (GRCm39) |
A2325V |
probably damaging |
Het |
Nid2 |
T |
A |
14: 19,802,499 (GRCm39) |
V140E |
possibly damaging |
Het |
Nlrp9c |
C |
A |
7: 26,079,915 (GRCm39) |
D704Y |
probably benign |
Het |
Notch3 |
T |
A |
17: 32,377,699 (GRCm39) |
S126C |
probably damaging |
Het |
Or2g7 |
T |
C |
17: 38,378,839 (GRCm39) |
I259T |
probably damaging |
Het |
Or5p60 |
A |
G |
7: 107,724,122 (GRCm39) |
F116S |
probably benign |
Het |
Or5w10 |
A |
T |
2: 87,375,327 (GRCm39) |
L187H |
probably damaging |
Het |
Or6c219 |
A |
T |
10: 129,781,451 (GRCm39) |
L160* |
probably null |
Het |
Or6c6c |
T |
C |
10: 129,541,476 (GRCm39) |
M243T |
possibly damaging |
Het |
Or6d15 |
A |
C |
6: 116,559,658 (GRCm39) |
F83C |
probably damaging |
Het |
Pdzd7 |
A |
G |
19: 45,027,667 (GRCm39) |
I269T |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,845,287 (GRCm39) |
D1299E |
probably damaging |
Het |
Pitx2 |
T |
A |
3: 129,012,403 (GRCm39) |
Y271N |
probably damaging |
Het |
Polk |
T |
C |
13: 96,633,140 (GRCm39) |
E301G |
probably damaging |
Het |
Prkdc |
C |
A |
16: 15,557,388 (GRCm39) |
N2230K |
probably damaging |
Het |
Prlr |
A |
G |
15: 10,322,622 (GRCm39) |
E170G |
probably benign |
Het |
Prss55 |
A |
G |
14: 64,313,179 (GRCm39) |
I235T |
probably damaging |
Het |
Psd3 |
T |
C |
8: 68,413,217 (GRCm39) |
I724V |
probably benign |
Het |
Rabep2 |
A |
G |
7: 126,037,971 (GRCm39) |
T248A |
possibly damaging |
Het |
Rbm26 |
T |
A |
14: 105,354,509 (GRCm39) |
K949N |
probably benign |
Het |
Rnf213 |
T |
A |
11: 119,331,047 (GRCm39) |
D2085E |
probably damaging |
Het |
Serpinb7 |
A |
T |
1: 107,378,003 (GRCm39) |
H232L |
possibly damaging |
Het |
Slu7 |
A |
G |
11: 43,336,069 (GRCm39) |
Q484R |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,745,021 (GRCm39) |
S3044P |
possibly damaging |
Het |
Snrnp48 |
A |
G |
13: 38,405,336 (GRCm39) |
D248G |
possibly damaging |
Het |
Snrpc |
C |
A |
17: 28,064,193 (GRCm39) |
P66Q |
unknown |
Het |
Snrpn |
T |
A |
7: 59,633,207 (GRCm39) |
|
probably benign |
Het |
Spag17 |
T |
A |
3: 99,846,672 (GRCm39) |
S65R |
possibly damaging |
Het |
Srsf6 |
C |
A |
2: 162,776,408 (GRCm39) |
|
probably benign |
Het |
Stil |
T |
A |
4: 114,898,979 (GRCm39) |
M1203K |
probably benign |
Het |
Syt17 |
T |
C |
7: 118,036,061 (GRCm39) |
T106A |
probably benign |
Het |
Tbx15 |
C |
T |
3: 99,259,562 (GRCm39) |
Q478* |
probably null |
Het |
Tg |
A |
T |
15: 66,609,397 (GRCm39) |
Q319L |
probably benign |
Het |
Thada |
A |
G |
17: 84,755,461 (GRCm39) |
L243P |
probably damaging |
Het |
Thada |
G |
T |
17: 84,755,462 (GRCm39) |
L243I |
probably damaging |
Het |
Tnnt3 |
A |
G |
7: 142,066,101 (GRCm39) |
R211G |
probably damaging |
Het |
Togaram1 |
A |
T |
12: 65,049,409 (GRCm39) |
Q1282L |
possibly damaging |
Het |
Tpm3-rs7 |
T |
G |
14: 113,552,379 (GRCm39) |
M91R |
probably damaging |
Het |
Ttll7 |
T |
G |
3: 146,621,535 (GRCm39) |
L378R |
probably damaging |
Het |
Tyw1 |
T |
G |
5: 130,287,834 (GRCm39) |
I22R |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,846,711 (GRCm39) |
S1645P |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,120,364 (GRCm39) |
L263P |
probably damaging |
Het |
Unc13c |
T |
C |
9: 73,663,621 (GRCm39) |
E1071G |
possibly damaging |
Het |
Vmn2r44 |
G |
T |
7: 8,383,122 (GRCm39) |
D157E |
possibly damaging |
Het |
Vps16 |
C |
T |
2: 130,285,520 (GRCm39) |
T821I |
probably benign |
Het |
Washc4 |
T |
C |
10: 83,415,389 (GRCm39) |
V793A |
possibly damaging |
Het |
Wdr35 |
G |
T |
12: 9,027,435 (GRCm39) |
|
probably null |
Het |
Zfp277 |
A |
G |
12: 40,414,084 (GRCm39) |
F254L |
probably benign |
Het |
|
Other mutations in Trappc9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Trappc9
|
APN |
15 |
72,897,875 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01348:Trappc9
|
APN |
15 |
72,808,858 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01367:Trappc9
|
APN |
15 |
72,462,002 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01521:Trappc9
|
APN |
15 |
72,924,016 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01726:Trappc9
|
APN |
15 |
72,817,971 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01881:Trappc9
|
APN |
15 |
72,871,841 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02214:Trappc9
|
APN |
15 |
72,884,731 (GRCm39) |
nonsense |
probably null |
|
IGL02693:Trappc9
|
APN |
15 |
72,835,542 (GRCm39) |
splice site |
probably benign |
|
IGL03229:Trappc9
|
APN |
15 |
72,930,305 (GRCm39) |
missense |
probably damaging |
1.00 |
basilio
|
UTSW |
15 |
72,930,242 (GRCm39) |
missense |
probably damaging |
1.00 |
Boomboom
|
UTSW |
15 |
72,608,718 (GRCm39) |
nonsense |
probably null |
|
bronto
|
UTSW |
15 |
72,930,087 (GRCm39) |
nonsense |
probably null |
|
Earl
|
UTSW |
15 |
72,608,626 (GRCm39) |
nonsense |
probably null |
|
Sotto_aceto
|
UTSW |
15 |
72,557,188 (GRCm39) |
missense |
probably damaging |
0.99 |
P0026:Trappc9
|
UTSW |
15 |
72,824,931 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4453001:Trappc9
|
UTSW |
15 |
72,903,447 (GRCm39) |
frame shift |
probably null |
|
PIT4519001:Trappc9
|
UTSW |
15 |
72,824,943 (GRCm39) |
missense |
probably benign |
|
R0001:Trappc9
|
UTSW |
15 |
72,835,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Trappc9
|
UTSW |
15 |
72,894,929 (GRCm38) |
intron |
probably benign |
|
R0745:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R0747:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R0800:Trappc9
|
UTSW |
15 |
72,824,981 (GRCm39) |
splice site |
probably benign |
|
R0816:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R0819:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R0820:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R0893:Trappc9
|
UTSW |
15 |
72,461,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R0976:Trappc9
|
UTSW |
15 |
72,871,823 (GRCm39) |
missense |
probably damaging |
0.99 |
R1119:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1266:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1453:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1454:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1531:Trappc9
|
UTSW |
15 |
72,565,397 (GRCm39) |
nonsense |
probably null |
|
R1543:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1600:Trappc9
|
UTSW |
15 |
72,808,958 (GRCm39) |
nonsense |
probably null |
|
R1712:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1756:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1978:Trappc9
|
UTSW |
15 |
72,871,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R2001:Trappc9
|
UTSW |
15 |
72,929,885 (GRCm39) |
missense |
probably damaging |
0.99 |
R2312:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R2334:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R2926:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R3123:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R3124:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R3125:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R3813:Trappc9
|
UTSW |
15 |
72,930,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R4012:Trappc9
|
UTSW |
15 |
72,903,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4080:Trappc9
|
UTSW |
15 |
72,813,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R4282:Trappc9
|
UTSW |
15 |
72,462,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R4572:Trappc9
|
UTSW |
15 |
72,808,916 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4739:Trappc9
|
UTSW |
15 |
72,808,909 (GRCm39) |
missense |
probably damaging |
0.97 |
R4959:Trappc9
|
UTSW |
15 |
72,808,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Trappc9
|
UTSW |
15 |
72,808,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R5123:Trappc9
|
UTSW |
15 |
72,785,215 (GRCm39) |
intron |
probably benign |
|
R5128:Trappc9
|
UTSW |
15 |
72,930,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R5228:Trappc9
|
UTSW |
15 |
72,929,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Trappc9
|
UTSW |
15 |
72,930,066 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5802:Trappc9
|
UTSW |
15 |
72,557,188 (GRCm39) |
missense |
probably damaging |
0.99 |
R6032:Trappc9
|
UTSW |
15 |
72,797,379 (GRCm39) |
missense |
probably benign |
0.43 |
R6032:Trappc9
|
UTSW |
15 |
72,797,379 (GRCm39) |
missense |
probably benign |
0.43 |
R6154:Trappc9
|
UTSW |
15 |
72,929,930 (GRCm39) |
missense |
probably benign |
0.03 |
R6372:Trappc9
|
UTSW |
15 |
72,461,923 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6661:Trappc9
|
UTSW |
15 |
72,461,993 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6864:Trappc9
|
UTSW |
15 |
72,809,011 (GRCm39) |
splice site |
probably null |
|
R6893:Trappc9
|
UTSW |
15 |
72,797,499 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7099:Trappc9
|
UTSW |
15 |
72,565,468 (GRCm39) |
missense |
probably benign |
0.00 |
R7276:Trappc9
|
UTSW |
15 |
72,924,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R7349:Trappc9
|
UTSW |
15 |
72,608,718 (GRCm39) |
nonsense |
probably null |
|
R8260:Trappc9
|
UTSW |
15 |
72,813,758 (GRCm39) |
nonsense |
probably null |
|
R8399:Trappc9
|
UTSW |
15 |
72,924,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R8683:Trappc9
|
UTSW |
15 |
72,884,664 (GRCm39) |
missense |
probably benign |
0.26 |
R8839:Trappc9
|
UTSW |
15 |
72,930,087 (GRCm39) |
nonsense |
probably null |
|
R8945:Trappc9
|
UTSW |
15 |
72,929,945 (GRCm39) |
missense |
probably benign |
|
R9083:Trappc9
|
UTSW |
15 |
72,608,626 (GRCm39) |
nonsense |
probably null |
|
R9323:Trappc9
|
UTSW |
15 |
72,565,431 (GRCm39) |
missense |
probably benign |
0.41 |
R9329:Trappc9
|
UTSW |
15 |
72,673,202 (GRCm39) |
missense |
unknown |
|
R9366:Trappc9
|
UTSW |
15 |
72,808,937 (GRCm39) |
missense |
probably benign |
|
R9723:Trappc9
|
UTSW |
15 |
72,461,963 (GRCm39) |
missense |
possibly damaging |
0.87 |
RF008:Trappc9
|
UTSW |
15 |
72,673,138 (GRCm39) |
small insertion |
probably benign |
|
RF009:Trappc9
|
UTSW |
15 |
72,673,136 (GRCm39) |
small insertion |
probably benign |
|
RF014:Trappc9
|
UTSW |
15 |
72,673,132 (GRCm39) |
small insertion |
probably benign |
|
RF016:Trappc9
|
UTSW |
15 |
72,673,138 (GRCm39) |
small insertion |
probably benign |
|
RF023:Trappc9
|
UTSW |
15 |
72,673,180 (GRCm39) |
small insertion |
probably benign |
|
RF023:Trappc9
|
UTSW |
15 |
72,673,173 (GRCm39) |
small insertion |
probably benign |
|
RF028:Trappc9
|
UTSW |
15 |
72,673,139 (GRCm39) |
small insertion |
probably benign |
|
RF029:Trappc9
|
UTSW |
15 |
72,673,172 (GRCm39) |
small insertion |
probably benign |
|
RF030:Trappc9
|
UTSW |
15 |
72,673,174 (GRCm39) |
small insertion |
probably benign |
|
RF034:Trappc9
|
UTSW |
15 |
72,673,147 (GRCm39) |
small insertion |
probably benign |
|
RF036:Trappc9
|
UTSW |
15 |
72,673,169 (GRCm39) |
small insertion |
probably benign |
|
RF038:Trappc9
|
UTSW |
15 |
72,673,172 (GRCm39) |
small insertion |
probably benign |
|
RF040:Trappc9
|
UTSW |
15 |
72,673,141 (GRCm39) |
small insertion |
probably benign |
|
RF042:Trappc9
|
UTSW |
15 |
72,673,132 (GRCm39) |
small insertion |
probably benign |
|
RF043:Trappc9
|
UTSW |
15 |
72,673,154 (GRCm39) |
small insertion |
probably benign |
|
RF049:Trappc9
|
UTSW |
15 |
72,673,155 (GRCm39) |
small insertion |
probably benign |
|
RF049:Trappc9
|
UTSW |
15 |
72,673,150 (GRCm39) |
small insertion |
probably benign |
|
RF053:Trappc9
|
UTSW |
15 |
72,673,177 (GRCm39) |
small insertion |
probably benign |
|
RF057:Trappc9
|
UTSW |
15 |
72,673,144 (GRCm39) |
small insertion |
probably benign |
|
RF063:Trappc9
|
UTSW |
15 |
72,673,173 (GRCm39) |
small insertion |
probably benign |
|
RF063:Trappc9
|
UTSW |
15 |
72,673,169 (GRCm39) |
small insertion |
probably benign |
|
Z1177:Trappc9
|
UTSW |
15 |
72,924,011 (GRCm39) |
missense |
probably null |
0.51 |
|
Predicted Primers |
PCR Primer
(F):5'- AACTGGGAGGAGATGGTGAATTTTC -3'
(R):5'- TGTGCCCGTTAAGACAGACC -3'
Sequencing Primer
(F):5'- GAAAGTCCTGTGTTCAAATCCCAG -3'
(R):5'- GAAATAGCTTTCCCCGAGGGTATC -3'
|
Posted On |
2014-06-23 |