Incidental Mutation 'R4684:Trpm3'
| ID |
353573 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Trpm3
|
| Ensembl Gene |
ENSMUSG00000052387 |
| Gene Name |
transient receptor potential cation channel, subfamily M, member 3 |
| Synonyms |
6330504P12Rik, LTRPC3, melastatin 2, B930001P07Rik, MLSN2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.082)
|
| Stock # |
R4684 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
19 |
| Chromosomal Location |
22116410-22972774 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 22965145 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Threonine
at position 1547
(A1547T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097164
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037901]
[ENSMUST00000074770]
[ENSMUST00000087576]
[ENSMUST00000099569]
|
| AlphaFold |
J9S314 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000037901
|
| SMART Domains |
Protein: ENSMUSP00000042184
Gene: ENSMUSG00000052387
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:ANK
|
485 |
514 |
1e-6 |
BLAST |
|
low complexity region
|
619 |
631 |
N/A |
INTRINSIC |
|
low complexity region
|
674 |
689 |
N/A |
INTRINSIC |
|
low complexity region
|
788 |
800 |
N/A |
INTRINSIC |
|
low complexity region
|
821 |
840 |
N/A |
INTRINSIC |
|
Pfam:Ion_trans
|
883 |
1136 |
1.7e-19 |
PFAM |
|
Pfam:TRPM_tetra
|
1227 |
1282 |
1.5e-26 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000074770
AA Change: A1537T
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000074328
Gene: ENSMUSG00000052387
AA Change: A1537T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
16 |
33 |
N/A |
INTRINSIC |
|
Blast:ANK
|
487 |
516 |
5e-7 |
BLAST |
|
low complexity region
|
611 |
623 |
N/A |
INTRINSIC |
|
low complexity region
|
666 |
681 |
N/A |
INTRINSIC |
|
low complexity region
|
780 |
792 |
N/A |
INTRINSIC |
|
low complexity region
|
813 |
832 |
N/A |
INTRINSIC |
|
transmembrane domain
|
874 |
896 |
N/A |
INTRINSIC |
|
Pfam:Ion_trans
|
908 |
1116 |
5.1e-14 |
PFAM |
|
low complexity region
|
1378 |
1388 |
N/A |
INTRINSIC |
|
low complexity region
|
1433 |
1455 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000087576
AA Change: A1547T
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000084857
Gene: ENSMUSG00000052387
AA Change: A1547T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
16 |
33 |
N/A |
INTRINSIC |
|
Blast:ANK
|
487 |
516 |
5e-7 |
BLAST |
|
low complexity region
|
621 |
633 |
N/A |
INTRINSIC |
|
low complexity region
|
676 |
691 |
N/A |
INTRINSIC |
|
low complexity region
|
790 |
802 |
N/A |
INTRINSIC |
|
low complexity region
|
823 |
842 |
N/A |
INTRINSIC |
|
transmembrane domain
|
884 |
906 |
N/A |
INTRINSIC |
|
Pfam:Ion_trans
|
918 |
1126 |
5.1e-14 |
PFAM |
|
low complexity region
|
1388 |
1398 |
N/A |
INTRINSIC |
|
low complexity region
|
1443 |
1465 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099569
AA Change: A1547T
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000097164
Gene: ENSMUSG00000052387
AA Change: A1547T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
16 |
33 |
N/A |
INTRINSIC |
|
Blast:ANK
|
487 |
516 |
6e-7 |
BLAST |
|
low complexity region
|
609 |
621 |
N/A |
INTRINSIC |
|
low complexity region
|
664 |
679 |
N/A |
INTRINSIC |
|
low complexity region
|
778 |
790 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
830 |
N/A |
INTRINSIC |
|
Pfam:Ion_trans
|
873 |
1138 |
3.2e-19 |
PFAM |
|
Pfam:TRPM_tetra
|
1229 |
1284 |
4.4e-26 |
PFAM |
|
low complexity region
|
1388 |
1398 |
N/A |
INTRINSIC |
|
low complexity region
|
1443 |
1465 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.0%
- 20x: 94.7%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene belongs to the family of transient receptor potential (TRP) channels. TRP channels are cation-selective channels important for cellular calcium signaling and homeostasis. The protein encoded by this gene mediates calcium entry, and this entry is potentiated by calcium store depletion. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null mutation display impaired thermal and chemical nociception. [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 |
|---|
| 2310039H08Rik |
T |
C |
17: 47,083,872 (GRCm39) |
V45A |
probably benign |
Het |
| 4921509C19Rik |
A |
G |
2: 151,313,791 (GRCm39) |
I629T |
unknown |
Het |
| 4933402N03Rik |
T |
C |
7: 130,740,413 (GRCm39) |
R268G |
probably damaging |
Het |
| Abca13 |
A |
T |
11: 9,384,193 (GRCm39) |
R3882* |
probably null |
Het |
| Adamts3 |
T |
G |
5: 89,850,866 (GRCm39) |
T558P |
probably damaging |
Het |
| Ano2 |
A |
G |
6: 125,767,304 (GRCm39) |
N214S |
probably benign |
Het |
| Arhgef4 |
A |
T |
1: 34,850,866 (GRCm39) |
|
probably null |
Het |
| Boc |
C |
T |
16: 44,320,743 (GRCm39) |
A306T |
probably benign |
Het |
| Capn10 |
T |
C |
1: 92,871,503 (GRCm39) |
F367S |
probably damaging |
Het |
| Ccdc6 |
T |
C |
10: 70,025,086 (GRCm39) |
|
probably benign |
Het |
| Cobll1 |
G |
T |
2: 64,929,372 (GRCm39) |
S688R |
possibly damaging |
Het |
| Cpxm2 |
G |
T |
7: 131,650,767 (GRCm39) |
P631Q |
possibly damaging |
Het |
| Cyp2c68 |
A |
G |
19: 39,687,779 (GRCm39) |
V406A |
possibly damaging |
Het |
| Cyp4a30b |
T |
A |
4: 115,312,200 (GRCm39) |
Y118N |
probably damaging |
Het |
| Dgki |
A |
T |
6: 37,276,781 (GRCm39) |
|
probably benign |
Het |
| Disp2 |
A |
G |
2: 118,623,237 (GRCm39) |
N1323S |
probably damaging |
Het |
| Dock1 |
T |
A |
7: 134,326,138 (GRCm39) |
Y42* |
probably null |
Het |
| Eps8l1 |
C |
A |
7: 4,476,944 (GRCm39) |
P471Q |
probably damaging |
Het |
| Fam20a |
A |
C |
11: 109,612,513 (GRCm39) |
L10R |
unknown |
Het |
| Fpr-rs4 |
T |
A |
17: 18,242,446 (GRCm39) |
I151K |
probably damaging |
Het |
| Gga1 |
C |
A |
15: 78,769,509 (GRCm39) |
P161T |
probably damaging |
Het |
| Gm9923 |
T |
A |
10: 72,145,306 (GRCm39) |
Y52* |
probably null |
Het |
| Gucy2g |
A |
G |
19: 55,194,688 (GRCm39) |
F910L |
probably damaging |
Het |
| H2-T5 |
A |
T |
17: 36,476,750 (GRCm39) |
H241Q |
possibly damaging |
Het |
| Helz |
T |
C |
11: 107,539,971 (GRCm39) |
V315A |
probably damaging |
Het |
| Hk2 |
T |
C |
6: 82,716,629 (GRCm39) |
Y301C |
probably damaging |
Het |
| Htt |
C |
T |
5: 35,010,109 (GRCm39) |
P1521S |
probably damaging |
Het |
| Iah1 |
T |
C |
12: 21,366,434 (GRCm39) |
M1T |
probably null |
Het |
| Ik |
T |
C |
18: 36,885,467 (GRCm39) |
S287P |
probably damaging |
Het |
| Itga1 |
T |
A |
13: 115,185,906 (GRCm39) |
D32V |
probably damaging |
Het |
| Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
| Klk14 |
A |
G |
7: 43,341,392 (GRCm39) |
I15V |
probably benign |
Het |
| Kng2 |
T |
C |
16: 22,806,391 (GRCm39) |
I603V |
possibly damaging |
Het |
| Lama1 |
T |
C |
17: 68,080,773 (GRCm39) |
I1267T |
possibly damaging |
Het |
| Lrp1b |
A |
C |
2: 40,812,316 (GRCm39) |
L2430V |
probably benign |
Het |
| Lrrn3 |
T |
G |
12: 41,504,243 (GRCm39) |
K25Q |
possibly damaging |
Het |
| Lta4h |
T |
A |
10: 93,304,678 (GRCm39) |
N233K |
probably benign |
Het |
| Mapk13 |
T |
C |
17: 28,989,023 (GRCm39) |
I53T |
probably damaging |
Het |
| Mdn1 |
T |
C |
4: 32,666,430 (GRCm39) |
F123L |
probably damaging |
Het |
| Myh4 |
G |
C |
11: 67,136,637 (GRCm39) |
D472H |
probably damaging |
Het |
| Nipa2 |
A |
T |
7: 55,585,574 (GRCm39) |
N121K |
probably benign |
Het |
| Nostrin |
C |
T |
2: 69,014,268 (GRCm39) |
T408M |
probably benign |
Het |
| Oosp2 |
C |
T |
19: 11,627,017 (GRCm39) |
R102H |
probably damaging |
Het |
| Or1j18 |
A |
G |
2: 36,624,686 (GRCm39) |
M118V |
probably damaging |
Het |
| Or4k15b |
T |
C |
14: 50,272,287 (GRCm39) |
D191G |
probably damaging |
Het |
| Osgin2 |
T |
A |
4: 16,001,946 (GRCm39) |
I202L |
probably benign |
Het |
| Pbld2 |
C |
A |
10: 62,893,476 (GRCm39) |
R271S |
probably damaging |
Het |
| Pex6 |
C |
T |
17: 47,023,027 (GRCm39) |
T201I |
probably benign |
Het |
| Pilra |
T |
C |
5: 137,833,777 (GRCm39) |
I96M |
probably damaging |
Het |
| Pllp |
T |
A |
8: 95,403,906 (GRCm39) |
D47V |
possibly damaging |
Het |
| Plxna2 |
A |
G |
1: 194,444,902 (GRCm39) |
S765G |
probably benign |
Het |
| Prkca |
A |
T |
11: 107,852,434 (GRCm39) |
Y100N |
probably damaging |
Het |
| Prkg1 |
T |
A |
19: 31,641,579 (GRCm39) |
K35* |
probably null |
Het |
| Psmc2 |
A |
G |
5: 22,008,263 (GRCm39) |
D389G |
possibly damaging |
Het |
| Rnf213 |
A |
G |
11: 119,331,951 (GRCm39) |
T2387A |
probably damaging |
Het |
| Ros1 |
T |
C |
10: 52,005,192 (GRCm39) |
N914S |
probably damaging |
Het |
| Ruvbl1 |
C |
A |
6: 88,468,581 (GRCm39) |
T367K |
probably benign |
Het |
| Scube2 |
C |
T |
7: 109,409,920 (GRCm39) |
R525H |
probably damaging |
Het |
| Sec14l4 |
T |
C |
11: 3,985,200 (GRCm39) |
|
probably null |
Het |
| Secisbp2l |
T |
C |
2: 125,587,862 (GRCm39) |
D751G |
probably damaging |
Het |
| Setd3 |
T |
C |
12: 108,074,949 (GRCm39) |
D402G |
probably benign |
Het |
| Slc15a2 |
T |
A |
16: 36,578,211 (GRCm39) |
K359N |
probably damaging |
Het |
| Slc25a21 |
A |
G |
12: 57,243,721 (GRCm39) |
S2P |
probably benign |
Het |
| Slfn8 |
A |
T |
11: 82,908,332 (GRCm39) |
H70Q |
probably benign |
Het |
| Spef2 |
T |
C |
15: 9,647,576 (GRCm39) |
I944V |
probably benign |
Het |
| Spg11 |
A |
G |
2: 121,895,557 (GRCm39) |
F1887S |
probably damaging |
Het |
| Sptbn4 |
A |
T |
7: 27,066,160 (GRCm39) |
D649E |
possibly damaging |
Het |
| Sptbn4 |
T |
C |
7: 27,063,844 (GRCm39) |
E879G |
probably damaging |
Het |
| Stx5a |
C |
A |
19: 8,720,725 (GRCm39) |
R121S |
probably damaging |
Het |
| Tbcd |
T |
C |
11: 121,384,597 (GRCm39) |
L26P |
probably damaging |
Het |
| Tecpr1 |
T |
C |
5: 144,144,255 (GRCm39) |
D649G |
probably benign |
Het |
| Tfam |
A |
G |
10: 71,073,677 (GRCm39) |
S32P |
probably benign |
Het |
| Tmt1b |
G |
T |
10: 128,796,571 (GRCm39) |
C79* |
probably null |
Het |
| Trmt44 |
C |
T |
5: 35,715,387 (GRCm39) |
R642H |
probably benign |
Het |
| Ttll6 |
T |
C |
11: 96,044,003 (GRCm39) |
V519A |
probably benign |
Het |
| Umodl1 |
T |
C |
17: 31,217,088 (GRCm39) |
F1107L |
probably benign |
Het |
| Usp5 |
A |
T |
6: 124,794,919 (GRCm39) |
V677E |
probably damaging |
Het |
| Utp20 |
A |
T |
10: 88,643,307 (GRCm39) |
L605* |
probably null |
Het |
| Utrn |
T |
C |
10: 12,620,984 (GRCm39) |
D229G |
probably damaging |
Het |
| Uty |
A |
T |
Y: 1,176,502 (GRCm39) |
L178* |
probably null |
Het |
| Vmn2r88 |
A |
T |
14: 51,650,791 (GRCm39) |
D168V |
possibly damaging |
Het |
| Vps13b |
T |
C |
15: 35,646,324 (GRCm39) |
V1476A |
probably damaging |
Het |
| Vps13b |
C |
A |
15: 35,879,967 (GRCm39) |
T3014K |
probably benign |
Het |
| Vps13b |
C |
T |
15: 35,841,487 (GRCm39) |
H2506Y |
probably benign |
Het |
| Vps37c |
T |
C |
19: 10,690,132 (GRCm39) |
V198A |
probably benign |
Het |
| Zfc3h1 |
T |
C |
10: 115,259,290 (GRCm39) |
Y1621H |
probably benign |
Het |
| Zfp251 |
T |
C |
15: 76,738,607 (GRCm39) |
D162G |
possibly damaging |
Het |
| Zfp292 |
T |
C |
4: 34,807,078 (GRCm39) |
T1994A |
probably benign |
Het |
| Zfp791 |
A |
G |
8: 85,837,559 (GRCm39) |
Y102H |
probably benign |
Het |
|
| Other mutations in Trpm3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00514:Trpm3
|
APN |
19 |
22,965,023 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00773:Trpm3
|
APN |
19 |
22,877,523 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL00852:Trpm3
|
APN |
19 |
22,964,435 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL01597:Trpm3
|
APN |
19 |
22,692,610 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01607:Trpm3
|
APN |
19 |
22,964,491 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01818:Trpm3
|
APN |
19 |
22,891,838 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01890:Trpm3
|
APN |
19 |
22,689,083 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02016:Trpm3
|
APN |
19 |
22,879,433 (GRCm39) |
nonsense |
probably null |
|
|
IGL02324:Trpm3
|
APN |
19 |
22,676,143 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL02947:Trpm3
|
APN |
19 |
22,878,483 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03037:Trpm3
|
APN |
19 |
22,866,776 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
IGL03128:Trpm3
|
APN |
19 |
22,891,829 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03335:Trpm3
|
APN |
19 |
22,903,435 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03354:Trpm3
|
APN |
19 |
22,834,082 (GRCm39) |
missense |
probably damaging |
1.00 |
|
bit
|
UTSW |
19 |
22,965,233 (GRCm39) |
missense |
probably benign |
0.00 |
|
G1patch:Trpm3
|
UTSW |
19 |
22,903,392 (GRCm39) |
missense |
probably damaging |
1.00 |
|
P0041:Trpm3
|
UTSW |
19 |
22,875,050 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0001:Trpm3
|
UTSW |
19 |
22,692,695 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R0007:Trpm3
|
UTSW |
19 |
22,964,893 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0007:Trpm3
|
UTSW |
19 |
22,964,893 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0009:Trpm3
|
UTSW |
19 |
22,891,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0009:Trpm3
|
UTSW |
19 |
22,891,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0142:Trpm3
|
UTSW |
19 |
22,965,280 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0194:Trpm3
|
UTSW |
19 |
22,692,720 (GRCm39) |
splice site |
probably null |
|
|
R0268:Trpm3
|
UTSW |
19 |
22,874,885 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0299:Trpm3
|
UTSW |
19 |
22,964,237 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R0449:Trpm3
|
UTSW |
19 |
22,965,418 (GRCm39) |
missense |
probably benign |
|
|
R0481:Trpm3
|
UTSW |
19 |
22,878,435 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R0496:Trpm3
|
UTSW |
19 |
22,676,142 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0499:Trpm3
|
UTSW |
19 |
22,964,237 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R0550:Trpm3
|
UTSW |
19 |
22,965,176 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0729:Trpm3
|
UTSW |
19 |
22,965,153 (GRCm39) |
missense |
probably benign |
|
|
R0883:Trpm3
|
UTSW |
19 |
22,956,018 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0926:Trpm3
|
UTSW |
19 |
22,965,407 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1185:Trpm3
|
UTSW |
19 |
22,891,781 (GRCm39) |
splice site |
probably benign |
|
|
R1185:Trpm3
|
UTSW |
19 |
22,891,781 (GRCm39) |
splice site |
probably benign |
|
|
R1513:Trpm3
|
UTSW |
19 |
22,964,236 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R1521:Trpm3
|
UTSW |
19 |
22,878,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1522:Trpm3
|
UTSW |
19 |
22,955,698 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1569:Trpm3
|
UTSW |
19 |
22,866,809 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1598:Trpm3
|
UTSW |
19 |
22,710,388 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R1600:Trpm3
|
UTSW |
19 |
22,116,519 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1616:Trpm3
|
UTSW |
19 |
22,960,076 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1619:Trpm3
|
UTSW |
19 |
22,689,271 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1923:Trpm3
|
UTSW |
19 |
22,862,776 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1985:Trpm3
|
UTSW |
19 |
22,903,446 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R2002:Trpm3
|
UTSW |
19 |
22,959,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2249:Trpm3
|
UTSW |
19 |
22,710,398 (GRCm39) |
missense |
probably benign |
0.15 |
|
R3719:Trpm3
|
UTSW |
19 |
22,964,354 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3766:Trpm3
|
UTSW |
19 |
22,425,741 (GRCm39) |
missense |
probably benign |
|
|
R3774:Trpm3
|
UTSW |
19 |
22,965,339 (GRCm39) |
missense |
probably benign |
0.03 |
|
R3774:Trpm3
|
UTSW |
19 |
22,955,966 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R3776:Trpm3
|
UTSW |
19 |
22,955,966 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R3820:Trpm3
|
UTSW |
19 |
22,964,813 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3899:Trpm3
|
UTSW |
19 |
22,878,524 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R4204:Trpm3
|
UTSW |
19 |
22,964,928 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4238:Trpm3
|
UTSW |
19 |
22,956,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4301:Trpm3
|
UTSW |
19 |
22,964,656 (GRCm39) |
missense |
probably benign |
0.23 |
|
R4344:Trpm3
|
UTSW |
19 |
22,875,061 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4345:Trpm3
|
UTSW |
19 |
22,875,061 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4365:Trpm3
|
UTSW |
19 |
22,955,694 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4510:Trpm3
|
UTSW |
19 |
22,965,381 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4511:Trpm3
|
UTSW |
19 |
22,965,381 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4565:Trpm3
|
UTSW |
19 |
22,965,233 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4573:Trpm3
|
UTSW |
19 |
22,879,506 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4606:Trpm3
|
UTSW |
19 |
22,955,988 (GRCm39) |
missense |
probably benign |
0.26 |
|
R4677:Trpm3
|
UTSW |
19 |
22,964,752 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4713:Trpm3
|
UTSW |
19 |
22,866,799 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R4745:Trpm3
|
UTSW |
19 |
22,692,659 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R5015:Trpm3
|
UTSW |
19 |
22,689,076 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5030:Trpm3
|
UTSW |
19 |
22,676,130 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5074:Trpm3
|
UTSW |
19 |
22,862,713 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R5089:Trpm3
|
UTSW |
19 |
22,744,120 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5100:Trpm3
|
UTSW |
19 |
22,896,130 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5108:Trpm3
|
UTSW |
19 |
22,882,078 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5204:Trpm3
|
UTSW |
19 |
22,425,705 (GRCm39) |
nonsense |
probably null |
|
|
R5213:Trpm3
|
UTSW |
19 |
22,674,818 (GRCm39) |
nonsense |
probably null |
|
|
R5358:Trpm3
|
UTSW |
19 |
22,903,332 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5374:Trpm3
|
UTSW |
19 |
22,903,548 (GRCm39) |
nonsense |
probably null |
|
|
R5382:Trpm3
|
UTSW |
19 |
22,862,705 (GRCm39) |
splice site |
probably null |
|
|
R5509:Trpm3
|
UTSW |
19 |
22,964,622 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5558:Trpm3
|
UTSW |
19 |
22,955,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6154:Trpm3
|
UTSW |
19 |
22,965,178 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6250:Trpm3
|
UTSW |
19 |
22,887,418 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6433:Trpm3
|
UTSW |
19 |
22,878,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6542:Trpm3
|
UTSW |
19 |
22,903,477 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6630:Trpm3
|
UTSW |
19 |
22,965,347 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6640:Trpm3
|
UTSW |
19 |
22,955,946 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6725:Trpm3
|
UTSW |
19 |
22,903,392 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7275:Trpm3
|
UTSW |
19 |
22,956,048 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R7371:Trpm3
|
UTSW |
19 |
22,879,557 (GRCm39) |
missense |
probably benign |
0.27 |
|
R7467:Trpm3
|
UTSW |
19 |
22,955,698 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R7488:Trpm3
|
UTSW |
19 |
22,955,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7495:Trpm3
|
UTSW |
19 |
22,875,160 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7600:Trpm3
|
UTSW |
19 |
22,903,458 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R7710:Trpm3
|
UTSW |
19 |
22,896,154 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7877:Trpm3
|
UTSW |
19 |
22,882,148 (GRCm39) |
missense |
probably benign |
0.25 |
|
R8184:Trpm3
|
UTSW |
19 |
22,896,060 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8234:Trpm3
|
UTSW |
19 |
22,692,640 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R8236:Trpm3
|
UTSW |
19 |
22,964,772 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8443:Trpm3
|
UTSW |
19 |
22,676,226 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R8470:Trpm3
|
UTSW |
19 |
22,887,501 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8784:Trpm3
|
UTSW |
19 |
22,896,040 (GRCm39) |
missense |
probably benign |
0.07 |
|
R8816:Trpm3
|
UTSW |
19 |
22,965,580 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8818:Trpm3
|
UTSW |
19 |
22,955,952 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R8875:Trpm3
|
UTSW |
19 |
22,887,493 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8931:Trpm3
|
UTSW |
19 |
22,744,034 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8969:Trpm3
|
UTSW |
19 |
22,903,308 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8987:Trpm3
|
UTSW |
19 |
22,896,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9300:Trpm3
|
UTSW |
19 |
22,955,745 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R9327:Trpm3
|
UTSW |
19 |
22,896,004 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R9354:Trpm3
|
UTSW |
19 |
22,425,696 (GRCm39) |
missense |
probably benign |
|
|
R9514:Trpm3
|
UTSW |
19 |
22,960,040 (GRCm39) |
missense |
probably benign |
0.42 |
|
R9545:Trpm3
|
UTSW |
19 |
22,878,458 (GRCm39) |
missense |
probably benign |
0.24 |
|
R9712:Trpm3
|
UTSW |
19 |
22,692,716 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R9721:Trpm3
|
UTSW |
19 |
22,866,762 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9750:Trpm3
|
UTSW |
19 |
22,903,495 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Trpm3
|
UTSW |
19 |
22,964,854 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TCACCTCCATGGACACTAGATC -3'
(R):5'- ACTGTCAGAGCTAGGATGGC -3'
Sequencing Primer
(F):5'- GGACACTAGATCTTTTTCTTCAGAC -3'
(R):5'- AGCTAGGATGGCTCAGCTCTG -3'
|
| Posted On |
2015-10-21 |
Incidental Mutation