Incidental Mutation 'RF009:Trappc9'
| ID |
603084 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Trappc9
|
| Ensembl Gene |
ENSMUSG00000047921 |
| Gene Name |
trafficking protein particle complex 9 |
| Synonyms |
TRS130, Nibp, 2900005P22Rik, 4632408O18Rik, 1810044A24Rik |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
RF009 (G1)
|
| Quality Score |
132.467 |
|
Status
|
Not validated
|
| Chromosome |
15 |
| Chromosomal Location |
72461469-72933053 bp(-) (GRCm39) |
| Type of Mutation |
small insertion (5 aa in frame mutation) |
| DNA Base Change (assembly) |
GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT to GCTGCTGCTGCTGCTTCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT
at 72673136 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000131997
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023276]
[ENSMUST00000089770]
[ENSMUST00000170633]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000023276
|
| SMART Domains |
Protein: ENSMUSP00000023276
Gene: ENSMUSG00000047921
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TRAPPC9-Trs120
|
2 |
920 |
3.6e-239 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000089770
|
| SMART Domains |
Protein: ENSMUSP00000087202
Gene: ENSMUSG00000047921
| 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 benign
Transcript: ENSMUST00000170633
|
| SMART Domains |
Protein: ENSMUSP00000131997
Gene: ENSMUSG00000047921
| 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 |
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.3%
- 20x: 98.5%
|
| Validation Efficiency |
96% (53/55) |
| 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: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 6030445D17Rik |
ACACACACCCGC |
AC |
4: 136,189,661 (GRCm39) |
|
probably null |
Het |
| AI182371 |
A |
G |
2: 34,979,209 (GRCm39) |
V153A |
possibly damaging |
Het |
| AI837181 |
CGG |
CGGTGG |
19: 5,475,262 (GRCm39) |
|
probably benign |
Het |
| Ankhd1 |
GCGGCG |
GCGGCGTCGGCG |
18: 36,693,975 (GRCm39) |
|
probably benign |
Het |
| Apoc2 |
C |
T |
7: 19,405,767 (GRCm39) |
M71I |
probably benign |
Het |
| Arhgap17 |
CTGTTGTTG |
CTGTTG |
7: 122,886,085 (GRCm39) |
|
probably benign |
Het |
| Atrn |
C |
A |
2: 130,748,842 (GRCm39) |
T121K |
probably benign |
Het |
| Btnl12 |
T |
C |
16: 37,674,841 (GRCm39) |
D207G |
probably benign |
Het |
| Ccdc170 |
C |
CCAG |
10: 4,511,030 (GRCm39) |
|
probably benign |
Het |
| Cckbr |
GCA |
G |
7: 105,083,893 (GRCm39) |
|
probably null |
Het |
| Cdk13 |
T |
C |
13: 17,978,329 (GRCm39) |
D303G |
unknown |
Het |
| Cfap65 |
C |
A |
1: 74,944,806 (GRCm39) |
R1477L |
probably damaging |
Het |
| Chd2 |
A |
G |
7: 73,169,410 (GRCm39) |
S37P |
possibly damaging |
Het |
| Chga |
AGC |
AGCCGC |
12: 102,527,679 (GRCm39) |
|
probably benign |
Het |
| Csf2rb2 |
T |
C |
15: 78,176,127 (GRCm39) |
I259V |
probably benign |
Het |
| Csnk1d |
A |
T |
11: 120,862,453 (GRCm39) |
N275K |
possibly damaging |
Het |
| Dmxl1 |
A |
C |
18: 50,026,461 (GRCm39) |
R1856S |
probably damaging |
Het |
| Dnah5 |
T |
C |
15: 28,204,165 (GRCm39) |
V14A |
probably benign |
Het |
| Edc4 |
G |
A |
8: 106,615,812 (GRCm39) |
S729N |
probably benign |
Het |
| Emilin3 |
T |
C |
2: 160,751,012 (GRCm39) |
S246G |
probably benign |
Het |
| Epc2 |
T |
G |
2: 49,422,249 (GRCm39) |
|
probably null |
Het |
| Exoc6 |
T |
A |
19: 37,560,068 (GRCm39) |
F101I |
probably benign |
Het |
| Fam171b |
GCAGCA |
GCAGCACCAGCA |
2: 83,643,224 (GRCm39) |
|
probably benign |
Het |
| Fam81b |
CTGTT |
CTGTTGTT |
13: 76,419,435 (GRCm39) |
|
probably benign |
Het |
| Flywch1 |
CTCACCCACTCCTGGTGT |
CTCACCCACTCCTGGTGTGGGGAGGCTACGTAGTCACCCACTCCTGGTGT |
17: 23,981,135 (GRCm39) |
|
probably null |
Het |
| Gab3 |
TTC |
TTCCTC |
X: 74,043,598 (GRCm39) |
|
probably benign |
Het |
| Gab3 |
CTT |
CTTATT |
X: 74,043,630 (GRCm39) |
|
probably null |
Het |
| Gabpa |
C |
A |
16: 84,641,224 (GRCm39) |
Q93K |
probably benign |
Het |
| Gabre |
GGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCTGGCTCAGGCTC |
GGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCAGGCTCTGGCTCAGGCTC |
X: 71,314,318 (GRCm39) |
|
probably benign |
Het |
| Gabre |
GGCTCA |
GGCTCAAGCTCA |
X: 71,314,319 (GRCm39) |
|
probably benign |
Het |
| H2-T3 |
TCCCGAAGAAC |
TC |
17: 36,500,294 (GRCm39) |
|
probably benign |
Het |
| Htr5a |
A |
G |
5: 28,047,859 (GRCm39) |
D138G |
probably damaging |
Het |
| Ifi207 |
G |
A |
1: 173,556,558 (GRCm39) |
P727S |
probably benign |
Het |
| Ifna13 |
T |
A |
4: 88,562,145 (GRCm39) |
S160C |
probably damaging |
Het |
| Kcnh8 |
G |
A |
17: 53,285,267 (GRCm39) |
R1079H |
probably benign |
Het |
| Klri2 |
GGAG |
GG |
6: 129,710,737 (GRCm39) |
|
probably null |
Het |
| Lce1m |
GTTGCTGCCACTG |
GTTGCTGCCACTGTTGCTGCCACTG |
3: 92,925,438 (GRCm39) |
|
probably benign |
Het |
| Lrch1 |
TTGGTGGTGCTGGTGG |
TTGGTGG |
14: 75,185,014 (GRCm39) |
|
probably benign |
Het |
| Lrch4 |
A |
G |
5: 137,635,805 (GRCm39) |
|
probably null |
Het |
| Lrrc2 |
TTGATTCGGTTCACC |
T |
9: 110,810,744 (GRCm39) |
|
probably null |
Het |
| Map1a |
GCTCCAGC |
GCTCCAGCCCCAGCTCCAGCTCCAGCTCCACCTCCAGC |
2: 121,136,782 (GRCm39) |
|
probably benign |
Het |
| Mettl25 |
T |
C |
10: 105,669,100 (GRCm39) |
|
probably benign |
Het |
| Mex3b |
A |
G |
7: 82,516,968 (GRCm39) |
D37G |
probably damaging |
Het |
| Mon1a |
T |
A |
9: 107,778,433 (GRCm39) |
V219E |
probably damaging |
Het |
| Myh3 |
TTACG |
TTACGTACG |
11: 66,977,183 (GRCm39) |
|
probably null |
Het |
| Myh3 |
GATTA |
GATTAATTA |
11: 66,977,181 (GRCm39) |
|
probably null |
Het |
| Myh3 |
ATTAC |
ATTACTTAC |
11: 66,977,182 (GRCm39) |
|
probably null |
Het |
| Myo5b |
T |
A |
18: 74,777,070 (GRCm39) |
C377S |
probably damaging |
Het |
| Nefh |
ACTTGGCCTCAGCTGGGG |
ACTTGGCCTCAGCTGGGGCCTTGGCCTCAGCTGGGG |
11: 4,890,997 (GRCm39) |
|
probably benign |
Het |
| Nos1ap |
T |
C |
1: 170,146,150 (GRCm39) |
D468G |
probably damaging |
Het |
| Ntn5 |
T |
C |
7: 45,342,684 (GRCm39) |
|
probably null |
Het |
| Oog2 |
T |
C |
4: 143,921,855 (GRCm39) |
V255A |
probably benign |
Het |
| Or5ac15 |
T |
A |
16: 58,940,274 (GRCm39) |
H53L |
probably damaging |
Het |
| Or8b37 |
A |
T |
9: 37,959,043 (GRCm39) |
H175L |
probably damaging |
Het |
| Pdgfd |
C |
A |
9: 6,288,624 (GRCm39) |
L93M |
probably damaging |
Het |
| Pgls |
G |
T |
8: 72,045,107 (GRCm39) |
V83L |
probably damaging |
Het |
| Pigw |
C |
A |
11: 84,767,987 (GRCm39) |
Q447H |
probably damaging |
Het |
| Pnma8a |
TCATGATGCACCTGCTTCAACATC |
TCATGATGCACCTGCTTCAACATCGCATGATGCACCTGCTTCAACATC |
7: 16,695,352 (GRCm39) |
|
probably benign |
Het |
| Poc1a |
C |
A |
9: 106,172,417 (GRCm39) |
L253M |
possibly damaging |
Het |
| Ppl |
T |
A |
16: 4,915,795 (GRCm39) |
E589D |
probably benign |
Het |
| Prkar1b |
A |
G |
5: 139,094,376 (GRCm39) |
S71P |
probably benign |
Het |
| Prx |
T |
C |
7: 27,218,385 (GRCm39) |
F1101S |
probably damaging |
Het |
| Rffl |
A |
G |
11: 82,736,598 (GRCm39) |
V26A |
probably benign |
Het |
| Scube3 |
T |
A |
17: 28,387,371 (GRCm39) |
L923Q |
probably damaging |
Het |
| Setd2 |
C |
T |
9: 110,379,779 (GRCm39) |
P1198L |
probably damaging |
Het |
| Shank2 |
C |
A |
7: 143,965,308 (GRCm39) |
A972E |
possibly damaging |
Het |
| Slc10a6 |
A |
G |
5: 103,756,858 (GRCm39) |
L302P |
probably damaging |
Het |
| Slc29a3 |
C |
T |
10: 60,586,340 (GRCm39) |
G42D |
probably benign |
Het |
| Spart |
T |
C |
3: 55,035,027 (GRCm39) |
V471A |
probably benign |
Het |
| Srebf1 |
T |
C |
11: 60,094,942 (GRCm39) |
T486A |
probably benign |
Het |
| Sspo |
T |
A |
6: 48,436,919 (GRCm39) |
Y1284* |
probably null |
Het |
| Supt20 |
AGCAGC |
AGCAGCCGCAGC |
3: 54,635,083 (GRCm39) |
|
probably benign |
Het |
| Tcof1 |
GCA |
GCACCA |
18: 60,968,815 (GRCm39) |
|
probably benign |
Het |
| Tff1 |
CTTCCTG |
C |
17: 31,383,901 (GRCm39) |
|
probably benign |
Het |
| Tmprss13 |
ATCTCCAGCAAGGGCACCTCCTCAGGCCTCTCCAGCAAGGACACCTCCTCAGGCCTCTCCAACAAGGACACCTCCTCAGGCCTCTCCAGCAAGGGCACCTCCTC |
ATCTCCAGCAAGGGCACCTCCTCAGGGCTCTCCAGCAAGGGCACCTCCTCAGGCCTCTCCAGCAAGGACACCTCCTCAGGCCTCTCCAACAAGGACACCTCCTCAGGCCTCTCCAGCAAGGGCACCTCCTC |
9: 45,239,762 (GRCm39) |
|
probably benign |
Het |
| Tnfrsf25 |
T |
C |
4: 152,204,081 (GRCm39) |
W341R |
probably damaging |
Het |
| Trav8d-1 |
T |
A |
14: 53,016,207 (GRCm39) |
L31Q |
probably damaging |
Het |
| Ttc23 |
A |
T |
7: 67,375,777 (GRCm39) |
I452F |
possibly damaging |
Het |
| Uimc1 |
T |
C |
13: 55,198,598 (GRCm39) |
E526G |
possibly damaging |
Het |
| Ulbp1 |
T |
A |
10: 7,397,405 (GRCm39) |
K233N |
unknown |
Het |
| Usp17ld |
A |
T |
7: 102,899,495 (GRCm39) |
V479E |
probably damaging |
Het |
| Utrn |
T |
TGTTACCC |
10: 12,509,689 (GRCm39) |
|
probably null |
Het |
| Vmn1r9 |
C |
T |
6: 57,048,465 (GRCm39) |
S180L |
probably benign |
Het |
| Wdr97 |
GAGGAGGA |
G |
15: 76,247,367 (GRCm39) |
|
probably null |
Het |
| Zfp598 |
CACC |
CACCCCTACC |
17: 24,899,761 (GRCm39) |
|
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 |
|
R1789: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 |
|
|
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'- AGGTTGGCAGGGTTTGAAAC -3'
(R):5'- AACTGGAAATGAGTCACCTGGTG -3'
Sequencing Primer
(F):5'- AACATAGGTTCTGCCCCGC -3'
(R):5'- GGCAGCTGTTTAATGTCA -3'
|
| Posted On |
2019-12-04 |
Incidental Mutation