Incidental Mutation 'R1721:Dip2c'
ID |
191489 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dip2c
|
Ensembl Gene |
ENSMUSG00000048264 |
Gene Name |
disco interacting protein 2 homolog C |
Synonyms |
2900024P20Rik |
MMRRC Submission |
039753-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.589)
|
Stock # |
R1721 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
9326564-9718964 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 9709404 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 1415
(T1415A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000133806
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000166299]
[ENSMUST00000169960]
[ENSMUST00000174552]
|
AlphaFold |
E9PWR4 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000166299
AA Change: T1416A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000126827 Gene: ENSMUSG00000048264 AA Change: T1416A
Domain | Start | End | E-Value | Type |
DMAP_binding
|
7 |
120 |
3.55e-43 |
SMART |
low complexity region
|
170 |
187 |
N/A |
INTRINSIC |
low complexity region
|
275 |
287 |
N/A |
INTRINSIC |
Pfam:AMP-binding
|
324 |
801 |
3.6e-23 |
PFAM |
Pfam:AMP-binding
|
977 |
1451 |
1.5e-72 |
PFAM |
low complexity region
|
1514 |
1526 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000169960
AA Change: T1386A
PolyPhen 2
Score 0.955 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000131238 Gene: ENSMUSG00000048264 AA Change: T1386A
Domain | Start | End | E-Value | Type |
DMAP_binding
|
7 |
176 |
3.02e-37 |
SMART |
low complexity region
|
226 |
243 |
N/A |
INTRINSIC |
low complexity region
|
331 |
343 |
N/A |
INTRINSIC |
Pfam:AMP-binding
|
380 |
637 |
5.9e-10 |
PFAM |
SCOP:d1lci__
|
675 |
875 |
2e-8 |
SMART |
Pfam:AMP-binding
|
947 |
1421 |
1.2e-56 |
PFAM |
low complexity region
|
1484 |
1496 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000174552
AA Change: T1415A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000133806 Gene: ENSMUSG00000048264 AA Change: T1415A
Domain | Start | End | E-Value | Type |
DMAP_binding
|
7 |
120 |
3.55e-43 |
SMART |
low complexity region
|
170 |
187 |
N/A |
INTRINSIC |
low complexity region
|
275 |
287 |
N/A |
INTRINSIC |
Pfam:AMP-binding
|
324 |
800 |
2.7e-20 |
PFAM |
Pfam:AMP-binding
|
976 |
1450 |
1.3e-56 |
PFAM |
low complexity region
|
1513 |
1525 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000222280
AA Change: T518A
|
Meta Mutation Damage Score |
0.9212 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.1%
|
Validation Efficiency |
99% (87/88) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the disco-interacting protein homolog 2 family. The protein shares strong similarity with a Drosophila protein which interacts with the transcription factor disco and is expressed in the nervous system. [provided by RefSeq, Oct 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acin1 |
A |
T |
14: 54,901,995 (GRCm39) |
V559E |
probably benign |
Het |
Adamts20 |
A |
G |
15: 94,236,340 (GRCm39) |
F844L |
probably benign |
Het |
Adcy5 |
C |
A |
16: 35,118,794 (GRCm39) |
D1048E |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,259,630 (GRCm39) |
C768* |
probably null |
Het |
Aldh18a1 |
G |
T |
19: 40,553,282 (GRCm39) |
Q487K |
probably damaging |
Het |
Aldh3b1 |
G |
A |
19: 3,971,271 (GRCm39) |
|
probably benign |
Het |
Asb18 |
T |
G |
1: 89,896,302 (GRCm39) |
D246A |
probably benign |
Het |
Atp2b1 |
T |
C |
10: 98,832,750 (GRCm39) |
V417A |
probably damaging |
Het |
Bcl2l15 |
A |
G |
3: 103,745,914 (GRCm39) |
|
probably null |
Het |
Brd10 |
A |
T |
19: 29,720,998 (GRCm39) |
S743T |
probably damaging |
Het |
Cage1 |
T |
A |
13: 38,207,309 (GRCm39) |
K285* |
probably null |
Het |
Ccn2 |
A |
C |
10: 24,472,695 (GRCm39) |
T202P |
probably damaging |
Het |
Cldn17 |
A |
G |
16: 88,303,444 (GRCm39) |
L95P |
probably damaging |
Het |
Cldn20 |
A |
T |
17: 3,583,157 (GRCm39) |
D110V |
probably damaging |
Het |
Cnot10 |
T |
C |
9: 114,444,067 (GRCm39) |
T443A |
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,310,858 (GRCm39) |
|
probably benign |
Het |
Col23a1 |
T |
C |
11: 51,418,716 (GRCm39) |
Y135H |
unknown |
Het |
Cse1l |
T |
C |
2: 166,768,331 (GRCm39) |
S210P |
probably damaging |
Het |
Cspg4 |
T |
G |
9: 56,796,027 (GRCm39) |
V1254G |
probably damaging |
Het |
Epc2 |
A |
G |
2: 49,422,117 (GRCm39) |
Y337C |
probably damaging |
Het |
Epha2 |
A |
G |
4: 141,049,963 (GRCm39) |
S799G |
probably damaging |
Het |
Fndc10 |
A |
G |
4: 155,779,355 (GRCm39) |
Y133C |
probably damaging |
Het |
Gli3 |
G |
T |
13: 15,900,882 (GRCm39) |
S1423I |
probably benign |
Het |
Gm6034 |
A |
T |
17: 36,354,045 (GRCm39) |
|
probably benign |
Het |
Gmip |
A |
G |
8: 70,263,882 (GRCm39) |
S109G |
probably damaging |
Het |
Grik2 |
C |
A |
10: 49,399,842 (GRCm39) |
W296L |
possibly damaging |
Het |
Gucy2d |
T |
A |
7: 98,103,268 (GRCm39) |
L504H |
probably damaging |
Het |
Il6 |
T |
A |
5: 30,218,490 (GRCm39) |
Y46N |
possibly damaging |
Het |
Ints8 |
C |
A |
4: 11,241,684 (GRCm39) |
C253F |
probably damaging |
Het |
Itga9 |
A |
G |
9: 118,527,374 (GRCm39) |
|
probably benign |
Het |
Kcna7 |
T |
C |
7: 45,056,345 (GRCm39) |
V187A |
possibly damaging |
Het |
Kdm5b |
G |
T |
1: 134,540,919 (GRCm39) |
|
probably benign |
Het |
Knl1 |
T |
G |
2: 118,906,815 (GRCm39) |
S1635A |
probably damaging |
Het |
Lce1b |
A |
G |
3: 92,563,318 (GRCm39) |
S72P |
unknown |
Het |
Lox |
T |
G |
18: 52,653,983 (GRCm39) |
|
probably null |
Het |
Mdc1 |
A |
G |
17: 36,158,718 (GRCm39) |
D366G |
possibly damaging |
Het |
Meiob |
T |
C |
17: 25,053,021 (GRCm39) |
C344R |
probably damaging |
Het |
Mier2 |
A |
G |
10: 79,384,664 (GRCm39) |
V150A |
probably damaging |
Het |
Mon2 |
A |
T |
10: 122,867,002 (GRCm39) |
M551K |
probably damaging |
Het |
Mrps15 |
A |
G |
4: 125,945,187 (GRCm39) |
T125A |
probably benign |
Het |
Mtmr14 |
A |
G |
6: 113,230,693 (GRCm39) |
H99R |
probably damaging |
Het |
Mup4 |
A |
G |
4: 59,960,598 (GRCm39) |
M1T |
probably null |
Het |
Mup5 |
G |
A |
4: 61,750,607 (GRCm39) |
R179* |
probably null |
Het |
Ncoa3 |
T |
G |
2: 165,911,221 (GRCm39) |
V1326G |
possibly damaging |
Het |
Noa1 |
A |
T |
5: 77,455,428 (GRCm39) |
N429K |
probably benign |
Het |
Nrxn1 |
C |
T |
17: 90,469,832 (GRCm39) |
A241T |
probably damaging |
Het |
Or1p1 |
A |
T |
11: 74,180,126 (GRCm39) |
Y218F |
probably damaging |
Het |
Or2t49 |
C |
T |
11: 58,392,765 (GRCm39) |
V206M |
probably damaging |
Het |
Pcdh9 |
G |
A |
14: 94,125,471 (GRCm39) |
S233L |
probably damaging |
Het |
Peg3 |
C |
A |
7: 6,712,900 (GRCm39) |
S774I |
possibly damaging |
Het |
Phyh |
A |
G |
2: 4,942,620 (GRCm39) |
K321R |
probably null |
Het |
Plcg1 |
T |
A |
2: 160,573,840 (GRCm39) |
M35K |
probably damaging |
Het |
Pnisr |
C |
T |
4: 21,874,086 (GRCm39) |
|
probably benign |
Het |
Ppargc1b |
T |
A |
18: 61,440,275 (GRCm39) |
|
probably null |
Het |
Prcd |
A |
C |
11: 116,548,371 (GRCm39) |
S27R |
probably benign |
Het |
Prx |
T |
A |
7: 27,216,948 (GRCm39) |
M622K |
probably benign |
Het |
Psmd1 |
T |
A |
1: 85,999,567 (GRCm39) |
D51E |
probably damaging |
Het |
Psmd13 |
C |
T |
7: 140,463,430 (GRCm39) |
T38I |
probably damaging |
Het |
Ptprf |
A |
C |
4: 118,082,096 (GRCm39) |
D1047E |
possibly damaging |
Het |
Rai14 |
C |
A |
15: 10,633,314 (GRCm39) |
Q25H |
probably damaging |
Het |
Riiad1 |
G |
A |
3: 94,380,176 (GRCm39) |
P40S |
possibly damaging |
Het |
Rnft1 |
T |
A |
11: 86,377,096 (GRCm39) |
N53K |
probably benign |
Het |
Scn4a |
C |
T |
11: 106,211,646 (GRCm39) |
R1457H |
probably benign |
Het |
Sema6c |
A |
T |
3: 95,078,099 (GRCm39) |
I492F |
probably damaging |
Het |
Shbg |
T |
C |
11: 69,505,798 (GRCm39) |
H403R |
probably damaging |
Het |
Slc15a5 |
A |
T |
6: 138,049,845 (GRCm39) |
|
probably benign |
Het |
Slc38a1 |
G |
A |
15: 96,485,016 (GRCm39) |
T221M |
probably damaging |
Het |
Slc6a16 |
T |
A |
7: 44,910,600 (GRCm39) |
V375E |
possibly damaging |
Het |
Slc6a17 |
T |
A |
3: 107,379,492 (GRCm39) |
M559L |
probably damaging |
Het |
Slmap |
A |
G |
14: 26,181,373 (GRCm39) |
|
probably benign |
Het |
Sorcs2 |
G |
A |
5: 36,184,092 (GRCm39) |
R965W |
probably damaging |
Het |
St8sia4 |
C |
A |
1: 95,581,394 (GRCm39) |
R116L |
probably damaging |
Het |
Tcaf1 |
A |
C |
6: 42,652,272 (GRCm39) |
S737A |
possibly damaging |
Het |
Thbs2 |
T |
A |
17: 14,899,072 (GRCm39) |
Y676F |
probably benign |
Het |
Tmod2 |
A |
G |
9: 75,493,324 (GRCm39) |
|
probably benign |
Het |
Trim75 |
T |
C |
8: 65,435,391 (GRCm39) |
|
probably null |
Het |
Ubr5 |
A |
T |
15: 38,042,090 (GRCm39) |
S169T |
probably benign |
Het |
Usp54 |
A |
T |
14: 20,633,508 (GRCm39) |
Y37* |
probably null |
Het |
Vill |
T |
C |
9: 118,895,082 (GRCm39) |
F100S |
probably damaging |
Het |
Vstm5 |
A |
G |
9: 15,168,663 (GRCm39) |
R76G |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,032,321 (GRCm39) |
T540A |
probably benign |
Het |
Zfp947 |
A |
C |
17: 22,365,184 (GRCm39) |
N163K |
probably benign |
Het |
Zfyve26 |
T |
C |
12: 79,308,573 (GRCm39) |
H228R |
possibly damaging |
Het |
|
Other mutations in Dip2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Dip2c
|
APN |
13 |
9,543,144 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00426:Dip2c
|
APN |
13 |
9,656,551 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00503:Dip2c
|
APN |
13 |
9,617,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00586:Dip2c
|
APN |
13 |
9,660,791 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01306:Dip2c
|
APN |
13 |
9,625,179 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL01580:Dip2c
|
APN |
13 |
9,687,124 (GRCm39) |
splice site |
probably null |
|
IGL01985:Dip2c
|
APN |
13 |
9,603,303 (GRCm39) |
splice site |
probably benign |
|
IGL02060:Dip2c
|
APN |
13 |
9,672,666 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02122:Dip2c
|
APN |
13 |
9,556,695 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02170:Dip2c
|
APN |
13 |
9,656,371 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02211:Dip2c
|
APN |
13 |
9,660,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02755:Dip2c
|
APN |
13 |
9,600,356 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02836:Dip2c
|
APN |
13 |
9,660,826 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02935:Dip2c
|
APN |
13 |
9,712,182 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03032:Dip2c
|
APN |
13 |
9,601,814 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU23:Dip2c
|
UTSW |
13 |
9,625,179 (GRCm39) |
missense |
possibly damaging |
0.72 |
P0038:Dip2c
|
UTSW |
13 |
9,697,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Dip2c
|
UTSW |
13 |
9,671,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Dip2c
|
UTSW |
13 |
9,687,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R0271:Dip2c
|
UTSW |
13 |
9,665,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R0306:Dip2c
|
UTSW |
13 |
9,654,635 (GRCm39) |
missense |
probably benign |
0.09 |
R0415:Dip2c
|
UTSW |
13 |
9,618,325 (GRCm39) |
splice site |
probably benign |
|
R0519:Dip2c
|
UTSW |
13 |
9,613,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Dip2c
|
UTSW |
13 |
9,603,495 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0964:Dip2c
|
UTSW |
13 |
9,618,699 (GRCm39) |
missense |
probably benign |
0.43 |
R0973:Dip2c
|
UTSW |
13 |
9,626,944 (GRCm39) |
missense |
probably damaging |
0.99 |
R0973:Dip2c
|
UTSW |
13 |
9,626,944 (GRCm39) |
missense |
probably damaging |
0.99 |
R0974:Dip2c
|
UTSW |
13 |
9,626,944 (GRCm39) |
missense |
probably damaging |
0.99 |
R1101:Dip2c
|
UTSW |
13 |
9,684,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R1171:Dip2c
|
UTSW |
13 |
9,543,162 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1403:Dip2c
|
UTSW |
13 |
9,603,300 (GRCm39) |
splice site |
probably null |
|
R1403:Dip2c
|
UTSW |
13 |
9,603,300 (GRCm39) |
splice site |
probably null |
|
R1432:Dip2c
|
UTSW |
13 |
9,603,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R1481:Dip2c
|
UTSW |
13 |
9,601,902 (GRCm39) |
critical splice donor site |
probably null |
|
R1588:Dip2c
|
UTSW |
13 |
9,715,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Dip2c
|
UTSW |
13 |
9,625,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R1867:Dip2c
|
UTSW |
13 |
9,671,985 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1909:Dip2c
|
UTSW |
13 |
9,583,386 (GRCm39) |
missense |
probably benign |
0.00 |
R2013:Dip2c
|
UTSW |
13 |
9,617,882 (GRCm39) |
nonsense |
probably null |
|
R2022:Dip2c
|
UTSW |
13 |
9,601,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R2517:Dip2c
|
UTSW |
13 |
9,659,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R3746:Dip2c
|
UTSW |
13 |
9,651,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R3794:Dip2c
|
UTSW |
13 |
9,654,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R3884:Dip2c
|
UTSW |
13 |
9,601,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R4019:Dip2c
|
UTSW |
13 |
9,664,401 (GRCm39) |
missense |
probably damaging |
0.99 |
R4110:Dip2c
|
UTSW |
13 |
9,687,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R4111:Dip2c
|
UTSW |
13 |
9,687,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R4113:Dip2c
|
UTSW |
13 |
9,687,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R4256:Dip2c
|
UTSW |
13 |
9,659,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R4300:Dip2c
|
UTSW |
13 |
9,660,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4494:Dip2c
|
UTSW |
13 |
9,621,098 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4739:Dip2c
|
UTSW |
13 |
9,583,375 (GRCm39) |
missense |
probably damaging |
0.98 |
R4812:Dip2c
|
UTSW |
13 |
9,687,166 (GRCm39) |
nonsense |
probably null |
|
R4814:Dip2c
|
UTSW |
13 |
9,586,896 (GRCm39) |
missense |
probably benign |
0.07 |
R4816:Dip2c
|
UTSW |
13 |
9,625,186 (GRCm39) |
missense |
probably benign |
0.37 |
R4828:Dip2c
|
UTSW |
13 |
9,610,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Dip2c
|
UTSW |
13 |
9,671,905 (GRCm39) |
splice site |
probably null |
|
R4917:Dip2c
|
UTSW |
13 |
9,671,905 (GRCm39) |
splice site |
probably null |
|
R4932:Dip2c
|
UTSW |
13 |
9,674,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R4993:Dip2c
|
UTSW |
13 |
9,625,259 (GRCm39) |
nonsense |
probably null |
|
R5043:Dip2c
|
UTSW |
13 |
9,601,863 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5349:Dip2c
|
UTSW |
13 |
9,672,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Dip2c
|
UTSW |
13 |
9,618,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R5840:Dip2c
|
UTSW |
13 |
9,556,712 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6110:Dip2c
|
UTSW |
13 |
9,673,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R6160:Dip2c
|
UTSW |
13 |
9,583,290 (GRCm39) |
missense |
probably benign |
0.01 |
R6161:Dip2c
|
UTSW |
13 |
9,697,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R6477:Dip2c
|
UTSW |
13 |
9,673,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R6522:Dip2c
|
UTSW |
13 |
9,625,264 (GRCm39) |
critical splice donor site |
probably null |
|
R6603:Dip2c
|
UTSW |
13 |
9,704,624 (GRCm39) |
splice site |
probably null |
|
R6658:Dip2c
|
UTSW |
13 |
9,543,213 (GRCm39) |
critical splice donor site |
probably null |
|
R6672:Dip2c
|
UTSW |
13 |
9,617,866 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6697:Dip2c
|
UTSW |
13 |
9,671,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6991:Dip2c
|
UTSW |
13 |
9,684,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6991:Dip2c
|
UTSW |
13 |
9,601,896 (GRCm39) |
nonsense |
probably null |
|
R7018:Dip2c
|
UTSW |
13 |
9,709,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R7053:Dip2c
|
UTSW |
13 |
9,660,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Dip2c
|
UTSW |
13 |
9,654,572 (GRCm39) |
missense |
probably benign |
0.01 |
R7171:Dip2c
|
UTSW |
13 |
9,556,684 (GRCm39) |
missense |
probably benign |
0.34 |
R7371:Dip2c
|
UTSW |
13 |
9,642,785 (GRCm39) |
missense |
probably benign |
0.02 |
R7395:Dip2c
|
UTSW |
13 |
9,664,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7489:Dip2c
|
UTSW |
13 |
9,583,348 (GRCm39) |
missense |
probably damaging |
0.99 |
R7575:Dip2c
|
UTSW |
13 |
9,678,048 (GRCm39) |
missense |
probably damaging |
0.97 |
R7642:Dip2c
|
UTSW |
13 |
9,672,741 (GRCm39) |
critical splice donor site |
probably null |
|
R7687:Dip2c
|
UTSW |
13 |
9,654,617 (GRCm39) |
missense |
probably benign |
0.00 |
R7699:Dip2c
|
UTSW |
13 |
9,709,347 (GRCm39) |
missense |
probably benign |
0.00 |
R7700:Dip2c
|
UTSW |
13 |
9,709,347 (GRCm39) |
missense |
probably benign |
0.00 |
R7715:Dip2c
|
UTSW |
13 |
9,664,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Dip2c
|
UTSW |
13 |
9,656,569 (GRCm39) |
critical splice donor site |
probably null |
|
R7845:Dip2c
|
UTSW |
13 |
9,659,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Dip2c
|
UTSW |
13 |
9,671,918 (GRCm39) |
missense |
probably benign |
0.05 |
R8685:Dip2c
|
UTSW |
13 |
9,687,161 (GRCm39) |
missense |
probably benign |
0.01 |
R8779:Dip2c
|
UTSW |
13 |
9,660,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R8786:Dip2c
|
UTSW |
13 |
9,665,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R8815:Dip2c
|
UTSW |
13 |
9,673,834 (GRCm39) |
nonsense |
probably null |
|
R8833:Dip2c
|
UTSW |
13 |
9,625,519 (GRCm39) |
critical splice donor site |
probably null |
|
R8868:Dip2c
|
UTSW |
13 |
9,625,503 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8873:Dip2c
|
UTSW |
13 |
9,625,182 (GRCm39) |
missense |
probably benign |
0.03 |
R8887:Dip2c
|
UTSW |
13 |
9,673,989 (GRCm39) |
splice site |
probably benign |
|
R8923:Dip2c
|
UTSW |
13 |
9,673,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R9112:Dip2c
|
UTSW |
13 |
9,660,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R9424:Dip2c
|
UTSW |
13 |
9,709,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R9474:Dip2c
|
UTSW |
13 |
9,544,963 (GRCm39) |
missense |
unknown |
|
R9527:Dip2c
|
UTSW |
13 |
9,544,875 (GRCm39) |
missense |
unknown |
|
R9593:Dip2c
|
UTSW |
13 |
9,704,683 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9615:Dip2c
|
UTSW |
13 |
9,625,191 (GRCm39) |
missense |
probably benign |
0.03 |
R9801:Dip2c
|
UTSW |
13 |
9,626,936 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGAGTGGACAAAGTAGCTCATGCAC -3'
(R):5'- GCTCTTGGTTCTCAGGAAGGCAAAG -3'
Sequencing Primer
(F):5'- GACAAAGTAGCTCATGCACAATAATG -3'
(R):5'- gaagccagaaatcagcatcag -3'
|
Posted On |
2014-05-14 |