Incidental Mutation 'R4716:Abi3bp'
| ID |
354078 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Abi3bp
|
| Ensembl Gene |
ENSMUSG00000035258 |
| Gene Name |
ABI family member 3 binding protein |
| Synonyms |
D930038M13Rik, TARSH, 5033411B22Rik, eratin |
| MMRRC Submission |
041983-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.090)
|
| Stock # |
R4716 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
16 |
| Chromosomal Location |
56298241-56510498 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 56471088 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Stop codon
at position 578
(R578*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000156180
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048471]
[ENSMUST00000096012]
[ENSMUST00000096013]
[ENSMUST00000171000]
[ENSMUST00000231781]
[ENSMUST00000231832]
[ENSMUST00000231870]
|
| AlphaFold |
A0A338P6S8 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000048471
AA Change: R658*
|
| SMART Domains |
Protein: ENSMUSP00000036257
Gene: ENSMUSG00000035258
AA Change: R658*
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
|
FN3
|
114 |
203 |
3.08e-2 |
SMART |
|
low complexity region
|
433 |
446 |
N/A |
INTRINSIC |
|
low complexity region
|
516 |
528 |
N/A |
INTRINSIC |
|
low complexity region
|
579 |
591 |
N/A |
INTRINSIC |
|
low complexity region
|
734 |
747 |
N/A |
INTRINSIC |
|
low complexity region
|
751 |
764 |
N/A |
INTRINSIC |
|
FN3
|
941 |
1024 |
6.29e-8 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000096012
|
| SMART Domains |
Protein: ENSMUSP00000093711
Gene: ENSMUSG00000035258
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
|
FN3
|
114 |
203 |
3.08e-2 |
SMART |
|
low complexity region
|
433 |
446 |
N/A |
INTRINSIC |
|
low complexity region
|
634 |
647 |
N/A |
INTRINSIC |
|
low complexity region
|
651 |
664 |
N/A |
INTRINSIC |
|
FN3
|
841 |
924 |
6.29e-8 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000096013
AA Change: R578*
|
| SMART Domains |
Protein: ENSMUSP00000093712
Gene: ENSMUSG00000035258
AA Change: R578*
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
|
FN3
|
114 |
203 |
3.08e-2 |
SMART |
|
low complexity region
|
433 |
446 |
N/A |
INTRINSIC |
|
low complexity region
|
670 |
683 |
N/A |
INTRINSIC |
|
low complexity region
|
687 |
700 |
N/A |
INTRINSIC |
|
FN3
|
877 |
960 |
6.29e-8 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000171000
|
| SMART Domains |
Protein: ENSMUSP00000128818
Gene: ENSMUSG00000035258
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
|
FN3
|
114 |
203 |
3.08e-2 |
SMART |
|
low complexity region
|
464 |
477 |
N/A |
INTRINSIC |
|
low complexity region
|
481 |
494 |
N/A |
INTRINSIC |
|
FN3
|
671 |
754 |
6.29e-8 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000231781
AA Change: R1100*
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231832
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000231870
AA Change: R578*
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam8 |
T |
A |
7: 139,563,851 (GRCm39) |
D717V |
probably benign |
Het |
| Aknad1 |
T |
C |
3: 108,682,417 (GRCm39) |
|
probably null |
Het |
| Alk |
A |
T |
17: 72,512,937 (GRCm39) |
W341R |
probably damaging |
Het |
| Ankdd1b |
G |
A |
13: 96,591,091 (GRCm39) |
Q101* |
probably null |
Het |
| Anpep |
A |
C |
7: 79,476,380 (GRCm39) |
S829A |
probably benign |
Het |
| Armh3 |
A |
G |
19: 45,948,781 (GRCm39) |
S233P |
probably damaging |
Het |
| Ate1 |
A |
T |
7: 130,115,511 (GRCm39) |
C72S |
probably damaging |
Het |
| Atp6v0a4 |
G |
A |
6: 38,037,999 (GRCm39) |
L533F |
probably damaging |
Het |
| Bach1 |
T |
C |
16: 87,512,267 (GRCm39) |
|
probably benign |
Het |
| Baz2b |
T |
C |
2: 59,799,599 (GRCm39) |
D240G |
probably benign |
Het |
| Cdc14b |
C |
T |
13: 64,357,014 (GRCm39) |
S21N |
probably damaging |
Het |
| Cdh3 |
A |
G |
8: 107,270,520 (GRCm39) |
I466V |
probably benign |
Het |
| Cog1 |
A |
G |
11: 113,547,923 (GRCm39) |
E137G |
probably damaging |
Het |
| Col4a2 |
A |
G |
8: 11,452,224 (GRCm39) |
D180G |
probably damaging |
Het |
| Cyp2c40 |
A |
T |
19: 39,791,105 (GRCm39) |
|
probably null |
Het |
| Dclk2 |
C |
T |
3: 86,827,188 (GRCm39) |
R97H |
probably damaging |
Het |
| Ddx52 |
T |
C |
11: 83,846,031 (GRCm39) |
|
probably null |
Het |
| Dhx58 |
C |
T |
11: 100,587,797 (GRCm39) |
|
probably null |
Het |
| Dmp1 |
T |
A |
5: 104,360,427 (GRCm39) |
S368T |
probably damaging |
Het |
| Dnah17 |
C |
A |
11: 117,964,474 (GRCm39) |
V2435L |
probably benign |
Het |
| Dnajc7 |
A |
G |
11: 100,510,402 (GRCm39) |
V10A |
probably benign |
Het |
| Dscam |
G |
T |
16: 96,420,771 (GRCm39) |
T1705K |
possibly damaging |
Het |
| Dscaml1 |
G |
A |
9: 45,361,890 (GRCm39) |
V217M |
probably damaging |
Het |
| Dync2h1 |
A |
G |
9: 7,142,648 (GRCm39) |
|
probably null |
Het |
| F5 |
A |
G |
1: 164,021,488 (GRCm39) |
D1321G |
probably damaging |
Het |
| Fam174a |
C |
T |
1: 95,241,770 (GRCm39) |
P77S |
probably benign |
Het |
| Fars2 |
G |
A |
13: 36,389,051 (GRCm39) |
R180H |
probably damaging |
Het |
| Fnbp1 |
T |
C |
2: 30,945,532 (GRCm39) |
T154A |
probably benign |
Het |
| Fsip2 |
T |
A |
2: 82,805,203 (GRCm39) |
N507K |
probably damaging |
Het |
| Glg1 |
G |
T |
8: 111,887,407 (GRCm39) |
Y449* |
probably null |
Het |
| Gm15130 |
A |
T |
2: 110,964,560 (GRCm39) |
Y187* |
probably null |
Het |
| Gm973 |
A |
T |
1: 59,591,713 (GRCm39) |
K366* |
probably null |
Het |
| H2bc11 |
T |
A |
13: 22,227,533 (GRCm39) |
V45E |
possibly damaging |
Het |
| Hao1 |
A |
G |
2: 134,347,540 (GRCm39) |
I255T |
probably damaging |
Het |
| Herc6 |
T |
A |
6: 57,575,423 (GRCm39) |
V148E |
probably damaging |
Het |
| Insm2 |
T |
A |
12: 55,647,677 (GRCm39) |
C474S |
possibly damaging |
Het |
| Itch |
T |
C |
2: 155,052,502 (GRCm39) |
|
probably null |
Het |
| Itga2 |
A |
G |
13: 114,993,909 (GRCm39) |
V748A |
probably damaging |
Het |
| Itga9 |
T |
A |
9: 118,510,826 (GRCm39) |
S452T |
probably damaging |
Het |
| Kdm4b |
C |
A |
17: 56,693,178 (GRCm39) |
D338E |
probably benign |
Het |
| Krt40 |
G |
A |
11: 99,431,045 (GRCm39) |
R155C |
probably damaging |
Het |
| Krtap16-1 |
A |
G |
11: 99,876,000 (GRCm39) |
V468A |
probably damaging |
Het |
| Lactb2 |
G |
A |
1: 13,708,619 (GRCm39) |
P143L |
probably damaging |
Het |
| Lrba |
C |
A |
3: 86,550,021 (GRCm39) |
T2330K |
probably damaging |
Het |
| Lrp2bp |
A |
T |
8: 46,466,208 (GRCm39) |
I106F |
probably benign |
Het |
| Luzp2 |
A |
G |
7: 54,485,710 (GRCm39) |
K2E |
probably damaging |
Het |
| Lypd6 |
T |
C |
2: 50,078,855 (GRCm39) |
|
probably null |
Het |
| Maml1 |
A |
T |
11: 50,148,694 (GRCm39) |
D1015E |
probably benign |
Het |
| Mdfi |
T |
G |
17: 48,131,906 (GRCm39) |
D106A |
possibly damaging |
Het |
| Olfm3 |
T |
C |
3: 114,874,755 (GRCm39) |
M17T |
probably benign |
Het |
| Or2n1d |
A |
C |
17: 38,646,731 (GRCm39) |
I228L |
possibly damaging |
Het |
| Or2o1 |
A |
G |
11: 49,051,717 (GRCm39) |
Y292C |
probably damaging |
Het |
| Or8c16 |
T |
A |
9: 38,130,714 (GRCm39) |
N198K |
probably damaging |
Het |
| Or8g30 |
A |
G |
9: 39,230,725 (GRCm39) |
F62L |
probably benign |
Het |
| Otud7b |
T |
G |
3: 96,058,227 (GRCm39) |
L261V |
probably damaging |
Het |
| P2ry1 |
A |
G |
3: 60,910,893 (GRCm39) |
N11D |
probably damaging |
Het |
| Pate2 |
T |
C |
9: 35,596,978 (GRCm39) |
|
probably benign |
Het |
| Pcdhb16 |
A |
T |
18: 37,612,458 (GRCm39) |
T473S |
probably benign |
Het |
| Per1 |
A |
G |
11: 68,992,057 (GRCm39) |
E137G |
probably damaging |
Het |
| Phf11d |
T |
C |
14: 59,590,791 (GRCm39) |
T189A |
probably benign |
Het |
| Pik3r5 |
C |
A |
11: 68,386,030 (GRCm39) |
S738R |
possibly damaging |
Het |
| Pikfyve |
A |
G |
1: 65,285,635 (GRCm39) |
Y913C |
possibly damaging |
Het |
| Pkd1 |
T |
G |
17: 24,795,107 (GRCm39) |
S2265A |
probably damaging |
Het |
| Pkhd1l1 |
C |
A |
15: 44,419,428 (GRCm39) |
N2964K |
probably damaging |
Het |
| Plch1 |
T |
G |
3: 63,688,967 (GRCm39) |
D79A |
probably damaging |
Het |
| Pnliprp1 |
A |
C |
19: 58,728,901 (GRCm39) |
T363P |
possibly damaging |
Het |
| Ppp1r10 |
T |
A |
17: 36,240,352 (GRCm39) |
D547E |
probably benign |
Het |
| Prkdc |
T |
A |
16: 15,628,701 (GRCm39) |
I3482K |
probably benign |
Het |
| Ptpn4 |
A |
G |
1: 119,649,598 (GRCm39) |
Y333H |
probably damaging |
Het |
| Ptpru |
T |
A |
4: 131,548,279 (GRCm39) |
M73L |
probably benign |
Het |
| Rrp12 |
A |
G |
19: 41,865,867 (GRCm39) |
Y698H |
probably damaging |
Het |
| Scaf8 |
T |
C |
17: 3,227,398 (GRCm39) |
F338L |
unknown |
Het |
| Slc17a1 |
G |
T |
13: 24,064,576 (GRCm39) |
V347L |
probably benign |
Het |
| Slc1a2 |
T |
A |
2: 102,578,883 (GRCm39) |
V263E |
probably damaging |
Het |
| Slc29a4 |
T |
C |
5: 142,704,327 (GRCm39) |
V327A |
probably benign |
Het |
| Slc6a3 |
A |
C |
13: 73,705,195 (GRCm39) |
I229L |
probably benign |
Het |
| Sos2 |
T |
C |
12: 69,654,145 (GRCm39) |
I703V |
probably benign |
Het |
| Srpk1 |
T |
C |
17: 28,840,982 (GRCm39) |
T15A |
probably benign |
Het |
| St6gal2 |
A |
T |
17: 55,817,367 (GRCm39) |
Q510L |
probably benign |
Het |
| Stk24 |
T |
C |
14: 121,532,130 (GRCm39) |
D289G |
possibly damaging |
Het |
| Taf2 |
T |
G |
15: 54,929,364 (GRCm39) |
K64T |
probably benign |
Het |
| Tbx3 |
A |
G |
5: 119,813,735 (GRCm39) |
E257G |
possibly damaging |
Het |
| Tmem102 |
A |
T |
11: 69,695,022 (GRCm39) |
F317I |
probably damaging |
Het |
| Trav10 |
A |
G |
14: 53,743,497 (GRCm39) |
S33G |
possibly damaging |
Het |
| Ttn |
T |
A |
2: 76,745,408 (GRCm39) |
I5214F |
probably damaging |
Het |
| Ube2f |
T |
A |
1: 91,182,002 (GRCm39) |
L2Q |
probably damaging |
Het |
| Ube4b |
A |
G |
4: 149,429,069 (GRCm39) |
F857L |
probably damaging |
Het |
| Vmn2r18 |
T |
A |
5: 151,485,602 (GRCm39) |
I631F |
possibly damaging |
Het |
| Zfp280d |
T |
A |
9: 72,219,947 (GRCm39) |
S241T |
possibly damaging |
Het |
| Zfp638 |
T |
A |
6: 83,956,544 (GRCm39) |
L1717* |
probably null |
Het |
| Zfp719 |
A |
G |
7: 43,240,535 (GRCm39) |
N708D |
possibly damaging |
Het |
|
| Other mutations in Abi3bp |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00780:Abi3bp
|
APN |
16 |
56,423,168 (GRCm39) |
missense |
probably null |
0.99 |
|
IGL01580:Abi3bp
|
APN |
16 |
56,495,573 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01633:Abi3bp
|
APN |
16 |
56,498,163 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01783:Abi3bp
|
APN |
16 |
56,353,332 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL01866:Abi3bp
|
APN |
16 |
56,492,336 (GRCm39) |
missense |
probably benign |
0.19 |
|
IGL02022:Abi3bp
|
APN |
16 |
56,412,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02086:Abi3bp
|
APN |
16 |
56,462,930 (GRCm39) |
splice site |
probably benign |
|
|
IGL02122:Abi3bp
|
APN |
16 |
56,507,491 (GRCm39) |
splice site |
probably benign |
|
|
IGL02155:Abi3bp
|
APN |
16 |
56,408,327 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02351:Abi3bp
|
APN |
16 |
56,474,418 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL02358:Abi3bp
|
APN |
16 |
56,474,418 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL02418:Abi3bp
|
APN |
16 |
56,424,479 (GRCm39) |
splice site |
probably benign |
|
|
IGL02559:Abi3bp
|
APN |
16 |
56,507,433 (GRCm39) |
nonsense |
probably null |
|
|
IGL02617:Abi3bp
|
APN |
16 |
56,394,807 (GRCm39) |
nonsense |
probably null |
|
|
IGL02810:Abi3bp
|
APN |
16 |
56,498,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03057:Abi3bp
|
APN |
16 |
56,488,754 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03174:Abi3bp
|
APN |
16 |
56,435,110 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R0389:Abi3bp
|
UTSW |
16 |
56,491,670 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0485:Abi3bp
|
UTSW |
16 |
56,424,375 (GRCm39) |
splice site |
probably null |
|
|
R0557:Abi3bp
|
UTSW |
16 |
56,488,750 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0616:Abi3bp
|
UTSW |
16 |
56,474,433 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0685:Abi3bp
|
UTSW |
16 |
56,353,316 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0783:Abi3bp
|
UTSW |
16 |
56,415,601 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R0828:Abi3bp
|
UTSW |
16 |
56,498,193 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0841:Abi3bp
|
UTSW |
16 |
56,488,639 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1078:Abi3bp
|
UTSW |
16 |
56,474,444 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1101:Abi3bp
|
UTSW |
16 |
56,426,521 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1116:Abi3bp
|
UTSW |
16 |
56,506,792 (GRCm39) |
splice site |
probably benign |
|
|
R1145:Abi3bp
|
UTSW |
16 |
56,488,639 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1145:Abi3bp
|
UTSW |
16 |
56,488,639 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1317:Abi3bp
|
UTSW |
16 |
56,488,672 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R1384:Abi3bp
|
UTSW |
16 |
56,394,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1460:Abi3bp
|
UTSW |
16 |
56,382,780 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1730:Abi3bp
|
UTSW |
16 |
56,488,642 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R1761:Abi3bp
|
UTSW |
16 |
56,488,672 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R1830:Abi3bp
|
UTSW |
16 |
56,408,348 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1873:Abi3bp
|
UTSW |
16 |
56,394,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1875:Abi3bp
|
UTSW |
16 |
56,394,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1996:Abi3bp
|
UTSW |
16 |
56,491,720 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R2018:Abi3bp
|
UTSW |
16 |
56,498,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2019:Abi3bp
|
UTSW |
16 |
56,498,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2035:Abi3bp
|
UTSW |
16 |
56,480,581 (GRCm39) |
missense |
probably benign |
0.21 |
|
R2118:Abi3bp
|
UTSW |
16 |
56,298,227 (GRCm39) |
unclassified |
probably benign |
|
|
R2202:Abi3bp
|
UTSW |
16 |
56,433,566 (GRCm39) |
missense |
probably benign |
0.06 |
|
R2202:Abi3bp
|
UTSW |
16 |
56,471,088 (GRCm39) |
nonsense |
probably null |
|
|
R2203:Abi3bp
|
UTSW |
16 |
56,433,566 (GRCm39) |
missense |
probably benign |
0.06 |
|
R3030:Abi3bp
|
UTSW |
16 |
56,477,682 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R3952:Abi3bp
|
UTSW |
16 |
56,424,401 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4176:Abi3bp
|
UTSW |
16 |
56,472,563 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4296:Abi3bp
|
UTSW |
16 |
56,488,673 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4301:Abi3bp
|
UTSW |
16 |
56,377,266 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4354:Abi3bp
|
UTSW |
16 |
56,353,314 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4417:Abi3bp
|
UTSW |
16 |
56,474,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4808:Abi3bp
|
UTSW |
16 |
56,414,879 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4814:Abi3bp
|
UTSW |
16 |
56,471,116 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5016:Abi3bp
|
UTSW |
16 |
56,491,631 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5290:Abi3bp
|
UTSW |
16 |
56,462,838 (GRCm39) |
splice site |
probably null |
|
|
R5891:Abi3bp
|
UTSW |
16 |
56,426,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5897:Abi3bp
|
UTSW |
16 |
56,425,032 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R6146:Abi3bp
|
UTSW |
16 |
56,491,628 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6267:Abi3bp
|
UTSW |
16 |
56,414,860 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6905:Abi3bp
|
UTSW |
16 |
56,394,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6908:Abi3bp
|
UTSW |
16 |
56,477,668 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6917:Abi3bp
|
UTSW |
16 |
56,437,684 (GRCm39) |
splice site |
probably null |
|
|
R7071:Abi3bp
|
UTSW |
16 |
56,449,503 (GRCm39) |
nonsense |
probably null |
|
|
R7194:Abi3bp
|
UTSW |
16 |
56,382,734 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7476:Abi3bp
|
UTSW |
16 |
56,435,109 (GRCm39) |
nonsense |
probably null |
|
|
R7554:Abi3bp
|
UTSW |
16 |
56,438,575 (GRCm39) |
splice site |
probably null |
|
|
R7571:Abi3bp
|
UTSW |
16 |
56,451,345 (GRCm39) |
splice site |
probably null |
|
|
R7661:Abi3bp
|
UTSW |
16 |
56,453,263 (GRCm39) |
splice site |
probably null |
|
|
R7662:Abi3bp
|
UTSW |
16 |
56,437,686 (GRCm39) |
splice site |
probably null |
|
|
R7910:Abi3bp
|
UTSW |
16 |
56,498,105 (GRCm39) |
nonsense |
probably null |
|
|
R8121:Abi3bp
|
UTSW |
16 |
56,452,241 (GRCm39) |
missense |
unknown |
|
|
R8781:Abi3bp
|
UTSW |
16 |
56,426,512 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8790:Abi3bp
|
UTSW |
16 |
56,495,437 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8828:Abi3bp
|
UTSW |
16 |
56,507,455 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9094:Abi3bp
|
UTSW |
16 |
56,456,590 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9135:Abi3bp
|
UTSW |
16 |
56,417,173 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9282:Abi3bp
|
UTSW |
16 |
56,440,867 (GRCm39) |
missense |
unknown |
|
|
R9363:Abi3bp
|
UTSW |
16 |
56,438,575 (GRCm39) |
splice site |
probably null |
|
|
R9464:Abi3bp
|
UTSW |
16 |
56,409,046 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R9506:Abi3bp
|
UTSW |
16 |
56,437,773 (GRCm39) |
missense |
unknown |
|
|
RF008:Abi3bp
|
UTSW |
16 |
56,447,952 (GRCm39) |
intron |
probably benign |
|
|
RF016:Abi3bp
|
UTSW |
16 |
56,447,950 (GRCm39) |
frame shift |
probably null |
|
|
RF052:Abi3bp
|
UTSW |
16 |
56,447,948 (GRCm39) |
intron |
probably benign |
|
|
RF061:Abi3bp
|
UTSW |
16 |
56,447,950 (GRCm39) |
frame shift |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GTGCAGCTTCAACATCAACTATG -3'
(R):5'- ATGGCCGAACTTCCTACATAGAAAC -3'
Sequencing Primer
(F):5'- CTGTAACCAGACCCTTCTTCAGGAAG -3'
(R):5'- CATAGCCATACTTTTCTGTATCA -3'
|
| Posted On |
2015-10-21 |
Incidental Mutation