Incidental Mutation 'R1470:Trank1'
ID |
197976 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Trank1
|
Ensembl Gene |
ENSMUSG00000062296 |
Gene Name |
tetratricopeptide repeat and ankyrin repeat containing 1 |
Synonyms |
LOC235639, C030048J01Rik, A230061D21Rik, Lba1 |
MMRRC Submission |
039523-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1470 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
9 |
Chromosomal Location |
111140807-111224843 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 111172300 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Leucine
at position 96
(F96L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000143534
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078626]
[ENSMUST00000197049]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000078626
AA Change: F225L
PolyPhen 2
Score 0.778 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000077697 Gene: ENSMUSG00000062296 AA Change: F225L
Domain | Start | End | E-Value | Type |
low complexity region
|
4 |
30 |
N/A |
INTRINSIC |
low complexity region
|
34 |
52 |
N/A |
INTRINSIC |
low complexity region
|
113 |
129 |
N/A |
INTRINSIC |
Blast:TPR
|
144 |
177 |
1e-15 |
BLAST |
Blast:TPR
|
178 |
209 |
8e-13 |
BLAST |
Blast:ANK
|
332 |
361 |
1e-6 |
BLAST |
ANK
|
369 |
405 |
5.29e0 |
SMART |
ANK
|
538 |
567 |
2.11e2 |
SMART |
ANK
|
572 |
609 |
7.29e2 |
SMART |
ANK
|
621 |
652 |
1.21e2 |
SMART |
low complexity region
|
887 |
895 |
N/A |
INTRINSIC |
low complexity region
|
1152 |
1172 |
N/A |
INTRINSIC |
Blast:AAA
|
1351 |
1569 |
1e-6 |
BLAST |
low complexity region
|
2166 |
2177 |
N/A |
INTRINSIC |
low complexity region
|
2395 |
2411 |
N/A |
INTRINSIC |
low complexity region
|
2636 |
2649 |
N/A |
INTRINSIC |
low complexity region
|
2966 |
2983 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000197049
AA Change: F96L
PolyPhen 2
Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000143534 Gene: ENSMUSG00000062296 AA Change: F96L
Domain | Start | End | E-Value | Type |
Blast:TPR
|
15 |
48 |
3e-17 |
BLAST |
SCOP:d1ihga1
|
15 |
84 |
8e-10 |
SMART |
Blast:TPR
|
49 |
82 |
4e-14 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000200151
|
Meta Mutation Damage Score |
0.1451 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.5%
- 20x: 93.0%
|
Validation Efficiency |
97% (125/129) |
Allele List at MGI |
All alleles(2) : Targeted, other(2)
|
Other mutations in this stock |
Total: 142 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
A |
6: 86,944,337 (GRCm39) |
S749T |
unknown |
Het |
Abcb4 |
A |
T |
5: 8,990,968 (GRCm39) |
I843F |
probably damaging |
Het |
Abcb6 |
A |
T |
1: 75,149,323 (GRCm39) |
|
probably benign |
Het |
AC238840.1 |
A |
T |
7: 38,467,377 (GRCm39) |
|
noncoding transcript |
Het |
Actr8 |
T |
A |
14: 29,708,926 (GRCm39) |
H244Q |
possibly damaging |
Het |
Acyp2 |
A |
G |
11: 30,456,452 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,530,417 (GRCm39) |
Y5886H |
probably benign |
Het |
Afap1 |
C |
T |
5: 36,119,081 (GRCm39) |
|
probably benign |
Het |
Agk |
T |
A |
6: 40,363,751 (GRCm39) |
W244R |
probably damaging |
Het |
Akirin1 |
T |
A |
4: 123,631,883 (GRCm39) |
|
probably benign |
Het |
Ankrd11 |
C |
A |
8: 123,626,463 (GRCm39) |
V161L |
probably damaging |
Het |
Arap3 |
T |
C |
18: 38,122,249 (GRCm39) |
|
probably null |
Het |
Arhgap29 |
A |
G |
3: 121,785,968 (GRCm39) |
|
probably benign |
Het |
Armc3 |
A |
G |
2: 19,243,547 (GRCm39) |
M88V |
probably benign |
Het |
Atp13a5 |
G |
T |
16: 29,167,833 (GRCm39) |
P109T |
probably benign |
Het |
Avpr1b |
T |
A |
1: 131,528,323 (GRCm39) |
V282D |
probably damaging |
Het |
Baz2b |
T |
C |
2: 59,808,890 (GRCm39) |
K120E |
possibly damaging |
Het |
Bltp1 |
T |
C |
3: 37,052,480 (GRCm39) |
M3060T |
probably benign |
Het |
Cacna1a |
T |
A |
8: 85,241,579 (GRCm39) |
|
probably benign |
Het |
Cacng6 |
G |
A |
7: 3,473,404 (GRCm39) |
C76Y |
probably damaging |
Het |
Cactin |
G |
T |
10: 81,158,985 (GRCm39) |
E279* |
probably null |
Het |
Car9 |
A |
G |
4: 43,510,222 (GRCm39) |
Y268C |
probably damaging |
Het |
Ccdc146 |
T |
A |
5: 21,524,564 (GRCm39) |
I263F |
probably damaging |
Het |
Cdc16 |
A |
T |
8: 13,808,992 (GRCm39) |
|
probably benign |
Het |
Cdh16 |
T |
G |
8: 105,345,003 (GRCm39) |
S429R |
probably benign |
Het |
Cep250 |
A |
G |
2: 155,832,995 (GRCm39) |
E1639G |
probably damaging |
Het |
Ces1d |
A |
T |
8: 93,921,649 (GRCm39) |
V38D |
possibly damaging |
Het |
Chd1 |
A |
T |
17: 15,946,545 (GRCm39) |
Q97L |
possibly damaging |
Het |
Ciita |
G |
A |
16: 10,332,332 (GRCm39) |
D898N |
possibly damaging |
Het |
Clstn1 |
A |
G |
4: 149,719,179 (GRCm39) |
N336S |
possibly damaging |
Het |
Cntnap5a |
A |
G |
1: 116,187,249 (GRCm39) |
D607G |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Col20a1 |
C |
T |
2: 180,636,753 (GRCm39) |
H245Y |
probably benign |
Het |
Coq8b |
A |
T |
7: 26,951,734 (GRCm39) |
T399S |
probably benign |
Het |
Cpn2 |
A |
G |
16: 30,079,003 (GRCm39) |
S233P |
probably benign |
Het |
Cryz |
G |
A |
3: 154,312,113 (GRCm39) |
G70D |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 16,207,218 (GRCm39) |
|
probably benign |
Het |
Def6 |
T |
A |
17: 28,444,956 (GRCm39) |
D451E |
possibly damaging |
Het |
Dnah8 |
T |
A |
17: 30,966,251 (GRCm39) |
C2480* |
probably null |
Het |
Dnah9 |
T |
C |
11: 65,818,648 (GRCm39) |
N3230S |
probably benign |
Het |
Dyrk4 |
G |
T |
6: 126,893,337 (GRCm39) |
S15* |
probably null |
Het |
Erc1 |
T |
C |
6: 119,671,563 (GRCm39) |
R917G |
probably damaging |
Het |
Fgd2 |
T |
A |
17: 29,593,082 (GRCm39) |
|
probably benign |
Het |
Frem3 |
G |
T |
8: 81,337,820 (GRCm39) |
V38L |
probably benign |
Het |
Gas2l3 |
T |
C |
10: 89,249,796 (GRCm39) |
I441V |
probably benign |
Het |
Gm14393 |
T |
A |
2: 174,905,774 (GRCm39) |
Y6F |
probably damaging |
Het |
Gm1527 |
A |
G |
3: 28,969,417 (GRCm39) |
K256E |
possibly damaging |
Het |
Gm21905 |
G |
T |
5: 68,103,740 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,424,656 (GRCm39) |
|
probably null |
Het |
Hmces |
C |
A |
6: 87,913,121 (GRCm39) |
T292K |
probably benign |
Het |
Hpse2 |
G |
A |
19: 43,376,692 (GRCm39) |
S20L |
probably benign |
Het |
Ift70b |
G |
T |
2: 75,768,155 (GRCm39) |
S199R |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,204,224 (GRCm39) |
V23E |
probably null |
Het |
Ino80 |
A |
T |
2: 119,210,130 (GRCm39) |
V1387E |
probably damaging |
Het |
Islr |
G |
T |
9: 58,064,589 (GRCm39) |
A306D |
probably damaging |
Het |
Jakmip1 |
G |
A |
5: 37,258,182 (GRCm39) |
G276D |
probably damaging |
Het |
Jchain |
A |
G |
5: 88,673,979 (GRCm39) |
V55A |
probably benign |
Het |
Kalrn |
T |
C |
16: 34,007,841 (GRCm39) |
K1350E |
probably damaging |
Het |
Kansl1l |
T |
C |
1: 66,841,156 (GRCm39) |
Q48R |
possibly damaging |
Het |
Kmt5a |
T |
C |
5: 124,585,334 (GRCm39) |
L23P |
probably damaging |
Het |
Lrba |
C |
T |
3: 86,644,449 (GRCm39) |
H381Y |
probably damaging |
Het |
Lrch3 |
T |
C |
16: 32,808,865 (GRCm39) |
|
probably benign |
Het |
Lrrc32 |
T |
C |
7: 98,148,564 (GRCm39) |
V448A |
probably benign |
Het |
Mapkbp1 |
T |
C |
2: 119,848,301 (GRCm39) |
M617T |
probably damaging |
Het |
Megf6 |
C |
T |
4: 154,336,876 (GRCm39) |
|
probably benign |
Het |
Mfap1a |
T |
C |
2: 121,333,282 (GRCm39) |
M50V |
probably benign |
Het |
Mgam |
G |
T |
6: 40,736,062 (GRCm39) |
A854S |
probably damaging |
Het |
Myh3 |
A |
C |
11: 66,988,885 (GRCm39) |
|
probably benign |
Het |
Myo18b |
C |
A |
5: 112,840,899 (GRCm39) |
R2298L |
probably damaging |
Het |
Myo1h |
T |
A |
5: 114,457,765 (GRCm39) |
M92K |
probably damaging |
Het |
Nfkbib |
T |
C |
7: 28,461,447 (GRCm39) |
|
probably null |
Het |
Nlrp2 |
T |
A |
7: 5,303,950 (GRCm39) |
T192S |
probably benign |
Het |
Nr2f1 |
A |
T |
13: 78,346,284 (GRCm39) |
Y137N |
possibly damaging |
Het |
Nup98 |
T |
A |
7: 101,796,513 (GRCm39) |
D841V |
probably damaging |
Het |
Nvl |
A |
G |
1: 180,966,827 (GRCm39) |
V59A |
probably damaging |
Het |
Ogdhl |
C |
A |
14: 32,068,745 (GRCm39) |
N948K |
probably damaging |
Het |
Or11g27 |
T |
C |
14: 50,771,159 (GRCm39) |
S97P |
possibly damaging |
Het |
Or12j3 |
A |
G |
7: 139,953,026 (GRCm39) |
S166P |
probably benign |
Het |
Or13a24 |
A |
G |
7: 140,154,662 (GRCm39) |
T199A |
probably benign |
Het |
Or51g1 |
A |
C |
7: 102,633,530 (GRCm39) |
Y280* |
probably null |
Het |
Orc2 |
A |
C |
1: 58,520,317 (GRCm39) |
|
probably benign |
Het |
Osgin1 |
G |
A |
8: 120,171,704 (GRCm39) |
R166H |
probably damaging |
Het |
Palb2 |
A |
T |
7: 121,706,746 (GRCm39) |
F741I |
probably benign |
Het |
Palb2 |
G |
T |
7: 121,706,747 (GRCm39) |
Y740* |
probably null |
Het |
Parvb |
G |
A |
15: 84,155,453 (GRCm39) |
G46D |
probably damaging |
Het |
Parvb |
G |
A |
15: 84,155,509 (GRCm39) |
D65N |
probably benign |
Het |
Pcsk2 |
A |
T |
2: 143,388,438 (GRCm39) |
K10* |
probably null |
Het |
Pde3a |
C |
T |
6: 141,411,932 (GRCm39) |
A502V |
probably benign |
Het |
Pfas |
T |
C |
11: 68,882,185 (GRCm39) |
I893V |
probably benign |
Het |
Pla2g4a |
A |
T |
1: 149,716,471 (GRCm39) |
D663E |
probably damaging |
Het |
Prickle2 |
G |
A |
6: 92,435,583 (GRCm39) |
P6L |
probably damaging |
Het |
Prx |
T |
A |
7: 27,217,026 (GRCm39) |
M648K |
probably benign |
Het |
Ptpn21 |
T |
C |
12: 98,654,735 (GRCm39) |
N744S |
probably benign |
Het |
Ptprq |
C |
T |
10: 107,554,435 (GRCm39) |
V97M |
probably damaging |
Het |
Pvr |
T |
C |
7: 19,652,549 (GRCm39) |
E122G |
possibly damaging |
Het |
Racgap1 |
T |
C |
15: 99,537,656 (GRCm39) |
K15E |
probably damaging |
Het |
Rock1 |
C |
T |
18: 10,136,091 (GRCm39) |
|
probably null |
Het |
Rorc |
T |
A |
3: 94,304,609 (GRCm39) |
Y331* |
probably null |
Het |
Rpl37 |
T |
C |
15: 5,148,096 (GRCm39) |
V91A |
probably benign |
Het |
Rrp36 |
T |
A |
17: 46,983,306 (GRCm39) |
K103* |
probably null |
Het |
Ryr3 |
T |
A |
2: 112,483,352 (GRCm39) |
M4142L |
probably benign |
Het |
Sash1 |
A |
T |
10: 8,665,357 (GRCm39) |
L125H |
probably damaging |
Het |
Scn5a |
T |
C |
9: 119,365,541 (GRCm39) |
M369V |
possibly damaging |
Het |
Siglec1 |
A |
T |
2: 130,912,307 (GRCm39) |
N1678K |
probably benign |
Het |
Slc15a5 |
A |
T |
6: 138,049,992 (GRCm39) |
V141E |
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,690,020 (GRCm39) |
|
probably benign |
Het |
Slc8a3 |
A |
T |
12: 81,246,484 (GRCm39) |
H856Q |
probably benign |
Het |
Spmip11 |
T |
C |
15: 98,483,142 (GRCm39) |
|
probably benign |
Het |
Sptlc2 |
T |
A |
12: 87,402,414 (GRCm39) |
M171L |
probably benign |
Het |
Srcap |
T |
A |
7: 127,158,899 (GRCm39) |
|
probably benign |
Het |
St6gal2 |
A |
G |
17: 55,797,944 (GRCm39) |
D310G |
probably damaging |
Het |
Susd2 |
T |
A |
10: 75,473,888 (GRCm39) |
D689V |
probably damaging |
Het |
Suz12 |
A |
T |
11: 79,910,558 (GRCm39) |
E303V |
possibly damaging |
Het |
Taldo1 |
C |
A |
7: 140,978,500 (GRCm39) |
T150K |
probably damaging |
Het |
Tex14 |
T |
C |
11: 87,440,355 (GRCm39) |
|
probably benign |
Het |
Tg |
T |
A |
15: 66,721,312 (GRCm39) |
F274I |
possibly damaging |
Het |
Tmem151b |
T |
C |
17: 45,856,663 (GRCm39) |
D259G |
probably damaging |
Het |
Tmem179 |
G |
T |
12: 112,468,288 (GRCm39) |
H64Q |
probably benign |
Het |
Tmem236 |
A |
G |
2: 14,223,732 (GRCm39) |
T174A |
probably benign |
Het |
Tmtc1 |
T |
A |
6: 148,207,483 (GRCm39) |
|
probably benign |
Het |
Tnc |
A |
T |
4: 63,884,811 (GRCm39) |
N1821K |
probably damaging |
Het |
Tnfrsf11a |
A |
G |
1: 105,752,773 (GRCm39) |
N261S |
probably damaging |
Het |
Traf6 |
G |
T |
2: 101,526,994 (GRCm39) |
|
probably benign |
Het |
Trim56 |
T |
A |
5: 137,142,017 (GRCm39) |
I500F |
probably damaging |
Het |
Ttll5 |
A |
G |
12: 85,926,168 (GRCm39) |
I321V |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,608,367 (GRCm39) |
W17852L |
probably damaging |
Het |
Twnk |
G |
A |
19: 44,997,820 (GRCm39) |
V450M |
probably damaging |
Het |
Uba52 |
A |
G |
8: 70,962,206 (GRCm39) |
I127T |
possibly damaging |
Het |
Ubr4 |
T |
A |
4: 139,148,537 (GRCm39) |
|
probably null |
Het |
Uggt1 |
A |
T |
1: 36,215,877 (GRCm39) |
M130K |
probably benign |
Het |
Ulk4 |
T |
A |
9: 120,910,722 (GRCm39) |
T1101S |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,548,902 (GRCm39) |
S2269P |
probably benign |
Het |
Ush2a |
G |
T |
1: 188,132,403 (GRCm39) |
R875L |
probably benign |
Het |
Usp9y |
T |
A |
Y: 1,332,471 (GRCm39) |
H1624L |
probably benign |
Homo |
Vipr1 |
T |
C |
9: 121,494,586 (GRCm39) |
L308S |
possibly damaging |
Het |
Vps50 |
G |
A |
6: 3,517,777 (GRCm39) |
|
probably benign |
Het |
Xdh |
T |
G |
17: 74,198,107 (GRCm39) |
K1260T |
probably damaging |
Het |
Yipf4 |
A |
G |
17: 74,800,963 (GRCm39) |
I94V |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,478,206 (GRCm39) |
*3582W |
probably null |
Het |
Zfp58 |
T |
C |
13: 67,640,144 (GRCm39) |
N116D |
possibly damaging |
Het |
Zfp750 |
C |
A |
11: 121,402,819 (GRCm39) |
R643L |
probably benign |
Het |
Znfx1 |
A |
G |
2: 166,884,507 (GRCm39) |
V51A |
possibly damaging |
Het |
|
Other mutations in Trank1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00234:Trank1
|
APN |
9 |
111,221,677 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00467:Trank1
|
APN |
9 |
111,193,734 (GRCm39) |
splice site |
probably benign |
|
IGL00569:Trank1
|
APN |
9 |
111,174,579 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL00585:Trank1
|
APN |
9 |
111,178,358 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01070:Trank1
|
APN |
9 |
111,195,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01134:Trank1
|
APN |
9 |
111,220,849 (GRCm39) |
missense |
probably benign |
|
IGL01154:Trank1
|
APN |
9 |
111,215,468 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01355:Trank1
|
APN |
9 |
111,194,588 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01407:Trank1
|
APN |
9 |
111,193,790 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01410:Trank1
|
APN |
9 |
111,194,117 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01410:Trank1
|
APN |
9 |
111,194,327 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01504:Trank1
|
APN |
9 |
111,202,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01744:Trank1
|
APN |
9 |
111,178,431 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02043:Trank1
|
APN |
9 |
111,193,028 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02104:Trank1
|
APN |
9 |
111,219,780 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02193:Trank1
|
APN |
9 |
111,196,344 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02581:Trank1
|
APN |
9 |
111,212,193 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02630:Trank1
|
APN |
9 |
111,202,143 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02839:Trank1
|
APN |
9 |
111,193,824 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02897:Trank1
|
APN |
9 |
111,196,585 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03065:Trank1
|
APN |
9 |
111,219,361 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03123:Trank1
|
APN |
9 |
111,196,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03143:Trank1
|
APN |
9 |
111,195,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03323:Trank1
|
APN |
9 |
111,181,184 (GRCm39) |
missense |
probably damaging |
1.00 |
1mM(1):Trank1
|
UTSW |
9 |
111,222,049 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4486001:Trank1
|
UTSW |
9 |
111,219,175 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4812001:Trank1
|
UTSW |
9 |
111,176,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Trank1
|
UTSW |
9 |
111,195,844 (GRCm39) |
missense |
probably benign |
0.00 |
R0064:Trank1
|
UTSW |
9 |
111,172,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Trank1
|
UTSW |
9 |
111,172,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Trank1
|
UTSW |
9 |
111,221,978 (GRCm39) |
missense |
probably benign |
0.00 |
R0207:Trank1
|
UTSW |
9 |
111,195,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R0255:Trank1
|
UTSW |
9 |
111,195,092 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0334:Trank1
|
UTSW |
9 |
111,222,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Trank1
|
UTSW |
9 |
111,194,421 (GRCm39) |
missense |
probably benign |
0.00 |
R0383:Trank1
|
UTSW |
9 |
111,220,545 (GRCm39) |
missense |
probably benign |
0.08 |
R0421:Trank1
|
UTSW |
9 |
111,220,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Trank1
|
UTSW |
9 |
111,220,361 (GRCm39) |
missense |
probably benign |
0.19 |
R0518:Trank1
|
UTSW |
9 |
111,162,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R0560:Trank1
|
UTSW |
9 |
111,220,154 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0637:Trank1
|
UTSW |
9 |
111,219,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Trank1
|
UTSW |
9 |
111,194,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Trank1
|
UTSW |
9 |
111,195,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Trank1
|
UTSW |
9 |
111,176,537 (GRCm39) |
missense |
probably benign |
0.45 |
R0827:Trank1
|
UTSW |
9 |
111,178,485 (GRCm39) |
unclassified |
probably benign |
|
R1005:Trank1
|
UTSW |
9 |
111,162,789 (GRCm39) |
missense |
probably benign |
0.13 |
R1108:Trank1
|
UTSW |
9 |
111,194,375 (GRCm39) |
missense |
probably benign |
0.00 |
R1155:Trank1
|
UTSW |
9 |
111,196,038 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1470:Trank1
|
UTSW |
9 |
111,172,300 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1596:Trank1
|
UTSW |
9 |
111,195,358 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1601:Trank1
|
UTSW |
9 |
111,202,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Trank1
|
UTSW |
9 |
111,220,547 (GRCm39) |
missense |
probably benign |
|
R1754:Trank1
|
UTSW |
9 |
111,221,939 (GRCm39) |
missense |
probably benign |
0.00 |
R1767:Trank1
|
UTSW |
9 |
111,220,547 (GRCm39) |
missense |
probably benign |
|
R1768:Trank1
|
UTSW |
9 |
111,221,995 (GRCm39) |
missense |
probably damaging |
0.96 |
R1809:Trank1
|
UTSW |
9 |
111,221,893 (GRCm39) |
missense |
probably benign |
0.34 |
R1912:Trank1
|
UTSW |
9 |
111,219,777 (GRCm39) |
missense |
probably benign |
0.00 |
R1920:Trank1
|
UTSW |
9 |
111,176,996 (GRCm39) |
critical splice donor site |
probably null |
|
R1960:Trank1
|
UTSW |
9 |
111,220,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Trank1
|
UTSW |
9 |
111,207,900 (GRCm39) |
missense |
probably benign |
0.20 |
R2012:Trank1
|
UTSW |
9 |
111,194,096 (GRCm39) |
missense |
probably benign |
|
R2025:Trank1
|
UTSW |
9 |
111,221,107 (GRCm39) |
missense |
probably benign |
0.01 |
R2050:Trank1
|
UTSW |
9 |
111,193,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Trank1
|
UTSW |
9 |
111,196,001 (GRCm39) |
missense |
probably benign |
0.00 |
R2912:Trank1
|
UTSW |
9 |
111,221,551 (GRCm39) |
missense |
probably damaging |
0.98 |
R2962:Trank1
|
UTSW |
9 |
111,181,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R3030:Trank1
|
UTSW |
9 |
111,220,598 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3821:Trank1
|
UTSW |
9 |
111,207,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3822:Trank1
|
UTSW |
9 |
111,207,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3892:Trank1
|
UTSW |
9 |
111,193,827 (GRCm39) |
missense |
probably benign |
0.03 |
R4105:Trank1
|
UTSW |
9 |
111,181,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Trank1
|
UTSW |
9 |
111,202,592 (GRCm39) |
nonsense |
probably null |
|
R4237:Trank1
|
UTSW |
9 |
111,196,103 (GRCm39) |
missense |
probably benign |
0.04 |
R4239:Trank1
|
UTSW |
9 |
111,196,103 (GRCm39) |
missense |
probably benign |
0.04 |
R4394:Trank1
|
UTSW |
9 |
111,194,265 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4417:Trank1
|
UTSW |
9 |
111,195,036 (GRCm39) |
missense |
probably benign |
0.17 |
R4611:Trank1
|
UTSW |
9 |
111,191,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4694:Trank1
|
UTSW |
9 |
111,221,129 (GRCm39) |
missense |
probably benign |
0.40 |
R4731:Trank1
|
UTSW |
9 |
111,219,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4843:Trank1
|
UTSW |
9 |
111,195,146 (GRCm39) |
missense |
probably benign |
0.00 |
R4852:Trank1
|
UTSW |
9 |
111,220,963 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4859:Trank1
|
UTSW |
9 |
111,194,078 (GRCm39) |
missense |
probably benign |
0.17 |
R4868:Trank1
|
UTSW |
9 |
111,194,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R5080:Trank1
|
UTSW |
9 |
111,218,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R5156:Trank1
|
UTSW |
9 |
111,219,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Trank1
|
UTSW |
9 |
111,194,627 (GRCm39) |
missense |
probably benign |
0.00 |
R5234:Trank1
|
UTSW |
9 |
111,215,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Trank1
|
UTSW |
9 |
111,191,470 (GRCm39) |
missense |
probably benign |
0.12 |
R5419:Trank1
|
UTSW |
9 |
111,220,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5435:Trank1
|
UTSW |
9 |
111,220,958 (GRCm39) |
missense |
probably benign |
0.00 |
R5444:Trank1
|
UTSW |
9 |
111,222,026 (GRCm39) |
missense |
probably benign |
0.04 |
R5543:Trank1
|
UTSW |
9 |
111,195,180 (GRCm39) |
missense |
probably damaging |
0.97 |
R5560:Trank1
|
UTSW |
9 |
111,219,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Trank1
|
UTSW |
9 |
111,195,744 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5774:Trank1
|
UTSW |
9 |
111,220,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Trank1
|
UTSW |
9 |
111,194,928 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5858:Trank1
|
UTSW |
9 |
111,221,604 (GRCm39) |
missense |
probably benign |
|
R5878:Trank1
|
UTSW |
9 |
111,195,753 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5900:Trank1
|
UTSW |
9 |
111,220,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R5917:Trank1
|
UTSW |
9 |
111,191,485 (GRCm39) |
missense |
probably benign |
0.38 |
R5954:Trank1
|
UTSW |
9 |
111,194,201 (GRCm39) |
missense |
probably benign |
0.13 |
R6041:Trank1
|
UTSW |
9 |
111,206,864 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6112:Trank1
|
UTSW |
9 |
111,220,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R6165:Trank1
|
UTSW |
9 |
111,220,940 (GRCm39) |
missense |
probably benign |
0.00 |
R6255:Trank1
|
UTSW |
9 |
111,181,314 (GRCm39) |
critical splice donor site |
probably null |
|
R6395:Trank1
|
UTSW |
9 |
111,196,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R6567:Trank1
|
UTSW |
9 |
111,176,589 (GRCm39) |
missense |
probably benign |
0.02 |
R6644:Trank1
|
UTSW |
9 |
111,193,902 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6724:Trank1
|
UTSW |
9 |
111,194,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Trank1
|
UTSW |
9 |
111,219,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6831:Trank1
|
UTSW |
9 |
111,206,967 (GRCm39) |
missense |
probably benign |
0.00 |
R6934:Trank1
|
UTSW |
9 |
111,202,158 (GRCm39) |
missense |
probably damaging |
0.99 |
R7127:Trank1
|
UTSW |
9 |
111,194,864 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7206:Trank1
|
UTSW |
9 |
111,174,583 (GRCm39) |
critical splice donor site |
probably null |
|
R7236:Trank1
|
UTSW |
9 |
111,202,142 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7247:Trank1
|
UTSW |
9 |
111,196,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Trank1
|
UTSW |
9 |
111,206,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7310:Trank1
|
UTSW |
9 |
111,196,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7431:Trank1
|
UTSW |
9 |
111,191,470 (GRCm39) |
missense |
probably benign |
0.12 |
R7448:Trank1
|
UTSW |
9 |
111,195,417 (GRCm39) |
missense |
probably benign |
0.01 |
R7477:Trank1
|
UTSW |
9 |
111,194,025 (GRCm39) |
missense |
probably benign |
0.00 |
R7514:Trank1
|
UTSW |
9 |
111,193,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R7595:Trank1
|
UTSW |
9 |
111,195,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7637:Trank1
|
UTSW |
9 |
111,194,364 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7648:Trank1
|
UTSW |
9 |
111,220,753 (GRCm39) |
missense |
probably benign |
|
R7737:Trank1
|
UTSW |
9 |
111,195,080 (GRCm39) |
nonsense |
probably null |
|
R7784:Trank1
|
UTSW |
9 |
111,193,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:Trank1
|
UTSW |
9 |
111,221,584 (GRCm39) |
missense |
probably benign |
|
R7912:Trank1
|
UTSW |
9 |
111,220,596 (GRCm39) |
missense |
probably benign |
0.04 |
R7938:Trank1
|
UTSW |
9 |
111,194,096 (GRCm39) |
missense |
probably benign |
|
R7979:Trank1
|
UTSW |
9 |
111,206,967 (GRCm39) |
missense |
probably benign |
0.00 |
R8064:Trank1
|
UTSW |
9 |
111,181,144 (GRCm39) |
nonsense |
probably null |
|
R8100:Trank1
|
UTSW |
9 |
111,221,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Trank1
|
UTSW |
9 |
111,207,995 (GRCm39) |
missense |
probably benign |
0.31 |
R8198:Trank1
|
UTSW |
9 |
111,219,880 (GRCm39) |
missense |
probably benign |
0.09 |
R8219:Trank1
|
UTSW |
9 |
111,193,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Trank1
|
UTSW |
9 |
111,194,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R8316:Trank1
|
UTSW |
9 |
111,178,370 (GRCm39) |
missense |
probably benign |
0.38 |
R8347:Trank1
|
UTSW |
9 |
111,196,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R8436:Trank1
|
UTSW |
9 |
111,220,450 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8489:Trank1
|
UTSW |
9 |
111,219,343 (GRCm39) |
missense |
probably benign |
0.01 |
R8682:Trank1
|
UTSW |
9 |
111,194,412 (GRCm39) |
missense |
probably benign |
0.01 |
R8768:Trank1
|
UTSW |
9 |
111,218,344 (GRCm39) |
missense |
probably benign |
0.00 |
R8770:Trank1
|
UTSW |
9 |
111,219,892 (GRCm39) |
missense |
probably benign |
0.00 |
R8829:Trank1
|
UTSW |
9 |
111,176,591 (GRCm39) |
missense |
probably benign |
|
R8838:Trank1
|
UTSW |
9 |
111,193,973 (GRCm39) |
missense |
probably benign |
0.03 |
R8855:Trank1
|
UTSW |
9 |
111,141,289 (GRCm39) |
missense |
unknown |
|
R8929:Trank1
|
UTSW |
9 |
111,208,003 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9047:Trank1
|
UTSW |
9 |
111,191,500 (GRCm39) |
missense |
probably damaging |
0.99 |
R9090:Trank1
|
UTSW |
9 |
111,174,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R9114:Trank1
|
UTSW |
9 |
111,162,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9133:Trank1
|
UTSW |
9 |
111,220,770 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9177:Trank1
|
UTSW |
9 |
111,221,579 (GRCm39) |
missense |
probably benign |
0.00 |
R9178:Trank1
|
UTSW |
9 |
111,196,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Trank1
|
UTSW |
9 |
111,174,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:Trank1
|
UTSW |
9 |
111,195,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R9373:Trank1
|
UTSW |
9 |
111,194,259 (GRCm39) |
missense |
probably benign |
0.25 |
R9380:Trank1
|
UTSW |
9 |
111,221,738 (GRCm39) |
missense |
probably benign |
0.07 |
R9435:Trank1
|
UTSW |
9 |
111,193,890 (GRCm39) |
missense |
probably benign |
0.04 |
R9501:Trank1
|
UTSW |
9 |
111,176,943 (GRCm39) |
missense |
probably benign |
0.00 |
R9593:Trank1
|
UTSW |
9 |
111,191,365 (GRCm39) |
missense |
probably benign |
0.30 |
R9601:Trank1
|
UTSW |
9 |
111,202,193 (GRCm39) |
missense |
probably benign |
0.18 |
R9729:Trank1
|
UTSW |
9 |
111,220,537 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Trank1
|
UTSW |
9 |
111,172,304 (GRCm39) |
missense |
possibly damaging |
0.57 |
Z1088:Trank1
|
UTSW |
9 |
111,193,778 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Trank1
|
UTSW |
9 |
111,221,938 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Trank1
|
UTSW |
9 |
111,196,445 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Trank1
|
UTSW |
9 |
111,140,970 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- TCCTTTTCCAGGGATACTACCGAGC -3'
(R):5'- TAAGACACAAGGTCCCCTCTGAGC -3'
Sequencing Primer
(F):5'- GGATACTACCGAGCTGGTTATTCC -3'
(R):5'- TGCTGGTTTTACAAAGGCAC -3'
|
Posted On |
2014-05-23 |