Incidental Mutation 'R4687:Sipa1l2'
ID |
353769 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sipa1l2
|
Ensembl Gene |
ENSMUSG00000001995 |
Gene Name |
signal-induced proliferation-associated 1 like 2 |
Synonyms |
|
MMRRC Submission |
041938-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.312)
|
Stock # |
R4687 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
126144802-126296547 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 126217984 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Tyrosine
at position 451
(C451Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000148536
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108775]
[ENSMUST00000212168]
[ENSMUST00000212987]
|
AlphaFold |
Q80TE4 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000108775
AA Change: C451Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000104405 Gene: ENSMUSG00000001995 AA Change: C451Y
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
64 |
N/A |
INTRINSIC |
low complexity region
|
163 |
172 |
N/A |
INTRINSIC |
low complexity region
|
261 |
272 |
N/A |
INTRINSIC |
low complexity region
|
427 |
449 |
N/A |
INTRINSIC |
Pfam:Rap_GAP
|
625 |
807 |
2.6e-67 |
PFAM |
PDZ
|
960 |
1026 |
6.47e-9 |
SMART |
low complexity region
|
1091 |
1103 |
N/A |
INTRINSIC |
low complexity region
|
1120 |
1138 |
N/A |
INTRINSIC |
low complexity region
|
1220 |
1238 |
N/A |
INTRINSIC |
low complexity region
|
1299 |
1312 |
N/A |
INTRINSIC |
low complexity region
|
1321 |
1329 |
N/A |
INTRINSIC |
low complexity region
|
1334 |
1355 |
N/A |
INTRINSIC |
low complexity region
|
1404 |
1418 |
N/A |
INTRINSIC |
Pfam:SPAR_C
|
1421 |
1666 |
2.5e-76 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000212168
AA Change: C451Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000212987
AA Change: C451Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.8%
|
Validation Efficiency |
|
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 signal-induced proliferation-associated 1 like family. Members of this family contain a GTPase activating domain, a PDZ domain and a C-terminal coiled-coil domain with a leucine zipper. A similar protein in rat acts as a GTPases for the small GTPase Rap. [provided by RefSeq, Sep 2015]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
T |
A |
17: 9,210,985 (GRCm39) |
Y45N |
probably damaging |
Het |
Agbl3 |
T |
C |
6: 34,775,261 (GRCm39) |
V189A |
probably damaging |
Het |
Akip1 |
C |
A |
7: 109,304,193 (GRCm39) |
S90* |
probably null |
Het |
Amn |
A |
T |
12: 111,242,502 (GRCm39) |
D439V |
probably benign |
Het |
Arhgap17 |
T |
A |
7: 122,920,826 (GRCm39) |
D149V |
probably damaging |
Het |
Atp6v0a4 |
A |
T |
6: 38,069,400 (GRCm39) |
I76N |
possibly damaging |
Het |
Atp6v1h |
A |
T |
1: 5,203,308 (GRCm39) |
N291I |
probably damaging |
Het |
Baiap2l2 |
G |
T |
15: 79,143,453 (GRCm39) |
P462T |
probably damaging |
Het |
Bves |
C |
T |
10: 45,230,936 (GRCm39) |
|
probably null |
Het |
Cabp7 |
T |
A |
11: 4,689,265 (GRCm39) |
K127* |
probably null |
Het |
Cacna1h |
A |
G |
17: 25,612,884 (GRCm39) |
V313A |
possibly damaging |
Het |
Camkk2 |
T |
C |
5: 122,891,787 (GRCm39) |
H245R |
probably damaging |
Het |
Celsr1 |
T |
A |
15: 85,816,661 (GRCm39) |
S1761C |
possibly damaging |
Het |
Cfap46 |
T |
C |
7: 139,207,372 (GRCm39) |
E1849G |
possibly damaging |
Het |
Ciz1 |
T |
C |
2: 32,257,477 (GRCm39) |
L174P |
probably damaging |
Het |
Crim1 |
G |
T |
17: 78,610,454 (GRCm39) |
C303F |
probably damaging |
Het |
Cyp26c1 |
A |
G |
19: 37,681,385 (GRCm39) |
Q396R |
probably damaging |
Het |
Dnajc7 |
G |
A |
11: 100,490,126 (GRCm39) |
P43L |
probably damaging |
Het |
Dpf2 |
T |
C |
19: 5,957,040 (GRCm39) |
H16R |
probably damaging |
Het |
Dsp |
A |
G |
13: 38,375,595 (GRCm39) |
T1127A |
probably damaging |
Het |
Dst |
T |
C |
1: 34,240,204 (GRCm39) |
L1525P |
probably damaging |
Het |
Ehf |
T |
A |
2: 103,097,471 (GRCm39) |
D192V |
probably damaging |
Het |
Frem1 |
G |
T |
4: 82,938,868 (GRCm39) |
N71K |
probably damaging |
Het |
Furin |
T |
A |
7: 80,043,195 (GRCm39) |
T339S |
probably benign |
Het |
Gad1 |
T |
A |
2: 70,431,064 (GRCm39) |
I569N |
possibly damaging |
Het |
Gfi1 |
T |
C |
5: 107,871,676 (GRCm39) |
K10R |
probably damaging |
Het |
Gm20775 |
T |
A |
Y: 10,641,258 (GRCm39) |
|
noncoding transcript |
Homo |
Gpn3 |
A |
C |
5: 122,516,638 (GRCm39) |
D89A |
possibly damaging |
Het |
Gpr18 |
T |
A |
14: 122,149,090 (GRCm39) |
R312* |
probably null |
Het |
Gsap |
T |
C |
5: 21,451,969 (GRCm39) |
|
probably benign |
Het |
H2-Ab1 |
C |
A |
17: 34,483,783 (GRCm39) |
T48K |
probably damaging |
Het |
Hmcn2 |
A |
T |
2: 31,328,297 (GRCm39) |
N4326I |
probably benign |
Het |
Igkv4-51 |
A |
C |
6: 69,658,714 (GRCm39) |
|
probably benign |
Het |
Insr |
T |
C |
8: 3,211,709 (GRCm39) |
H1104R |
probably benign |
Het |
Ipo13 |
A |
T |
4: 117,758,773 (GRCm39) |
N697K |
probably benign |
Het |
Iqcm |
T |
G |
8: 76,489,617 (GRCm39) |
F362V |
probably damaging |
Het |
Irak4 |
T |
C |
15: 94,464,704 (GRCm39) |
S425P |
probably damaging |
Het |
Jakmip2 |
T |
C |
18: 43,710,477 (GRCm39) |
E242G |
possibly damaging |
Het |
Kdm4a |
T |
C |
4: 118,001,280 (GRCm39) |
K829R |
probably damaging |
Het |
Kdr |
T |
C |
5: 76,129,452 (GRCm39) |
N145S |
possibly damaging |
Het |
Klra9 |
A |
T |
6: 130,162,480 (GRCm39) |
D185E |
probably benign |
Het |
Lcn12 |
T |
C |
2: 25,383,333 (GRCm39) |
N15S |
probably benign |
Het |
Mei4 |
T |
A |
9: 81,809,370 (GRCm39) |
M151K |
probably damaging |
Het |
Mmp3 |
T |
A |
9: 7,451,223 (GRCm39) |
S320T |
probably benign |
Het |
Mrps5 |
C |
G |
2: 127,432,690 (GRCm39) |
A37G |
probably benign |
Het |
Mttp |
A |
G |
3: 137,798,496 (GRCm39) |
I800T |
possibly damaging |
Het |
Nags |
A |
T |
11: 102,039,022 (GRCm39) |
Q451L |
probably damaging |
Het |
Nbea |
T |
C |
3: 55,965,486 (GRCm39) |
T476A |
probably damaging |
Het |
Ndufb10 |
T |
C |
17: 24,941,393 (GRCm39) |
E145G |
possibly damaging |
Het |
Neb |
T |
G |
2: 52,194,047 (GRCm39) |
S660R |
possibly damaging |
Het |
Nppb |
A |
G |
4: 148,070,753 (GRCm39) |
K43E |
probably benign |
Het |
Nup188 |
A |
T |
2: 30,220,645 (GRCm39) |
Q906L |
probably benign |
Het |
Or10k2 |
T |
A |
8: 84,268,489 (GRCm39) |
S239T |
probably damaging |
Het |
Or4c12 |
T |
C |
2: 89,774,213 (GRCm39) |
D82G |
probably damaging |
Het |
Or8c17 |
C |
A |
9: 38,180,710 (GRCm39) |
N292K |
probably damaging |
Het |
Or9s23 |
T |
C |
1: 92,501,052 (GRCm39) |
I53T |
possibly damaging |
Het |
Ovch2 |
T |
A |
7: 107,395,755 (GRCm39) |
I88F |
possibly damaging |
Het |
Palm3 |
A |
G |
8: 84,756,564 (GRCm39) |
E692G |
probably benign |
Het |
Pcsk6 |
T |
C |
7: 65,633,501 (GRCm39) |
F578L |
probably damaging |
Het |
Piezo2 |
A |
C |
18: 63,203,034 (GRCm39) |
D1535E |
probably damaging |
Het |
Ppp1r15b |
T |
C |
1: 133,059,873 (GRCm39) |
V130A |
probably benign |
Het |
Proca1 |
T |
C |
11: 78,095,724 (GRCm39) |
Y32H |
probably damaging |
Het |
Prtg |
T |
A |
9: 72,798,080 (GRCm39) |
V682E |
probably damaging |
Het |
Pyroxd1 |
A |
T |
6: 142,307,594 (GRCm39) |
M455L |
probably benign |
Het |
Rasa1 |
T |
C |
13: 85,374,754 (GRCm39) |
D739G |
possibly damaging |
Het |
Scn3a |
T |
C |
2: 65,295,074 (GRCm39) |
I1550V |
possibly damaging |
Het |
Sepsecs |
T |
C |
5: 52,801,213 (GRCm39) |
D483G |
probably benign |
Het |
Setd7 |
T |
C |
3: 51,457,776 (GRCm39) |
D17G |
probably damaging |
Het |
Slc31a1 |
A |
G |
4: 62,306,939 (GRCm39) |
Y165C |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,249,776 (GRCm39) |
F68L |
possibly damaging |
Het |
Sptbn5 |
A |
G |
2: 119,907,689 (GRCm39) |
|
probably benign |
Het |
Stk3 |
A |
G |
15: 35,114,711 (GRCm39) |
I65T |
probably damaging |
Het |
Tas2r115 |
C |
T |
6: 132,714,247 (GRCm39) |
A235T |
possibly damaging |
Het |
Tenm2 |
C |
T |
11: 35,939,924 (GRCm39) |
A1400T |
probably benign |
Het |
Tet1 |
T |
A |
10: 62,674,570 (GRCm39) |
N1169Y |
probably benign |
Het |
Treml2 |
T |
A |
17: 48,616,425 (GRCm39) |
|
probably null |
Het |
Tspan11 |
A |
G |
6: 127,915,198 (GRCm39) |
E104G |
probably damaging |
Het |
Wdtc1 |
G |
A |
4: 133,023,742 (GRCm39) |
A543V |
probably damaging |
Het |
Zfp148 |
T |
A |
16: 33,317,189 (GRCm39) |
D578E |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,602,682 (GRCm39) |
N542I |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,602,681 (GRCm39) |
N542Y |
probably damaging |
Het |
Zfp869 |
T |
A |
8: 70,160,793 (GRCm39) |
E65D |
probably benign |
Het |
|
Other mutations in Sipa1l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00534:Sipa1l2
|
APN |
8 |
126,218,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00939:Sipa1l2
|
APN |
8 |
126,191,174 (GRCm39) |
splice site |
probably benign |
|
IGL00965:Sipa1l2
|
APN |
8 |
126,174,613 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01321:Sipa1l2
|
APN |
8 |
126,218,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01450:Sipa1l2
|
APN |
8 |
126,149,316 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01753:Sipa1l2
|
APN |
8 |
126,180,031 (GRCm39) |
splice site |
probably benign |
|
IGL01930:Sipa1l2
|
APN |
8 |
126,145,978 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02041:Sipa1l2
|
APN |
8 |
126,218,558 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02215:Sipa1l2
|
APN |
8 |
126,174,576 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02272:Sipa1l2
|
APN |
8 |
126,218,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02370:Sipa1l2
|
APN |
8 |
126,207,008 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02538:Sipa1l2
|
APN |
8 |
126,178,716 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02633:Sipa1l2
|
APN |
8 |
126,174,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03394:Sipa1l2
|
APN |
8 |
126,218,398 (GRCm39) |
missense |
possibly damaging |
0.67 |
Rebellious
|
UTSW |
8 |
126,195,078 (GRCm39) |
missense |
probably benign |
0.01 |
R0144:Sipa1l2
|
UTSW |
8 |
126,176,615 (GRCm39) |
splice site |
probably null |
|
R0153:Sipa1l2
|
UTSW |
8 |
126,148,637 (GRCm39) |
missense |
probably damaging |
0.99 |
R0276:Sipa1l2
|
UTSW |
8 |
126,148,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0318:Sipa1l2
|
UTSW |
8 |
126,174,436 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0373:Sipa1l2
|
UTSW |
8 |
126,191,149 (GRCm39) |
missense |
probably damaging |
0.99 |
R0427:Sipa1l2
|
UTSW |
8 |
126,207,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R0634:Sipa1l2
|
UTSW |
8 |
126,149,363 (GRCm39) |
nonsense |
probably null |
|
R1377:Sipa1l2
|
UTSW |
8 |
126,218,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1404:Sipa1l2
|
UTSW |
8 |
126,176,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R1404:Sipa1l2
|
UTSW |
8 |
126,176,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R1435:Sipa1l2
|
UTSW |
8 |
126,195,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R1523:Sipa1l2
|
UTSW |
8 |
126,174,352 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1577:Sipa1l2
|
UTSW |
8 |
126,219,001 (GRCm39) |
missense |
probably benign |
0.00 |
R1581:Sipa1l2
|
UTSW |
8 |
126,218,356 (GRCm39) |
missense |
probably damaging |
0.96 |
R1583:Sipa1l2
|
UTSW |
8 |
126,148,634 (GRCm39) |
missense |
probably damaging |
0.97 |
R1719:Sipa1l2
|
UTSW |
8 |
126,171,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R1730:Sipa1l2
|
UTSW |
8 |
126,206,880 (GRCm39) |
splice site |
probably null |
|
R1940:Sipa1l2
|
UTSW |
8 |
126,206,887 (GRCm39) |
splice site |
probably benign |
|
R2007:Sipa1l2
|
UTSW |
8 |
126,166,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Sipa1l2
|
UTSW |
8 |
126,218,230 (GRCm39) |
missense |
probably benign |
0.07 |
R2203:Sipa1l2
|
UTSW |
8 |
126,218,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R2764:Sipa1l2
|
UTSW |
8 |
126,219,113 (GRCm39) |
missense |
probably damaging |
0.99 |
R3722:Sipa1l2
|
UTSW |
8 |
126,200,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Sipa1l2
|
UTSW |
8 |
126,177,122 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3787:Sipa1l2
|
UTSW |
8 |
126,149,944 (GRCm39) |
missense |
probably benign |
|
R4106:Sipa1l2
|
UTSW |
8 |
126,219,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R4117:Sipa1l2
|
UTSW |
8 |
126,195,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R4194:Sipa1l2
|
UTSW |
8 |
126,218,411 (GRCm39) |
missense |
probably benign |
0.00 |
R4237:Sipa1l2
|
UTSW |
8 |
126,218,395 (GRCm39) |
missense |
probably benign |
0.44 |
R4240:Sipa1l2
|
UTSW |
8 |
126,218,395 (GRCm39) |
missense |
probably benign |
0.44 |
R4448:Sipa1l2
|
UTSW |
8 |
126,219,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R4515:Sipa1l2
|
UTSW |
8 |
126,218,965 (GRCm39) |
missense |
probably benign |
0.00 |
R4519:Sipa1l2
|
UTSW |
8 |
126,218,965 (GRCm39) |
missense |
probably benign |
0.00 |
R4523:Sipa1l2
|
UTSW |
8 |
126,219,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Sipa1l2
|
UTSW |
8 |
126,191,154 (GRCm39) |
missense |
probably damaging |
0.98 |
R4667:Sipa1l2
|
UTSW |
8 |
126,180,209 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4854:Sipa1l2
|
UTSW |
8 |
126,200,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Sipa1l2
|
UTSW |
8 |
126,218,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R5065:Sipa1l2
|
UTSW |
8 |
126,218,324 (GRCm39) |
missense |
probably benign |
0.19 |
R5194:Sipa1l2
|
UTSW |
8 |
126,166,012 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5266:Sipa1l2
|
UTSW |
8 |
126,218,865 (GRCm39) |
missense |
probably damaging |
0.99 |
R5475:Sipa1l2
|
UTSW |
8 |
126,218,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R5718:Sipa1l2
|
UTSW |
8 |
126,217,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:Sipa1l2
|
UTSW |
8 |
126,218,423 (GRCm39) |
missense |
probably benign |
0.42 |
R5916:Sipa1l2
|
UTSW |
8 |
126,195,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R5941:Sipa1l2
|
UTSW |
8 |
126,200,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R6083:Sipa1l2
|
UTSW |
8 |
126,195,212 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6185:Sipa1l2
|
UTSW |
8 |
126,194,992 (GRCm39) |
nonsense |
probably null |
|
R6235:Sipa1l2
|
UTSW |
8 |
126,201,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Sipa1l2
|
UTSW |
8 |
126,196,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Sipa1l2
|
UTSW |
8 |
126,180,203 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6374:Sipa1l2
|
UTSW |
8 |
126,171,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6459:Sipa1l2
|
UTSW |
8 |
126,171,223 (GRCm39) |
critical splice donor site |
probably null |
|
R6462:Sipa1l2
|
UTSW |
8 |
126,217,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Sipa1l2
|
UTSW |
8 |
126,176,633 (GRCm39) |
missense |
probably benign |
0.00 |
R6543:Sipa1l2
|
UTSW |
8 |
126,177,101 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7154:Sipa1l2
|
UTSW |
8 |
126,195,078 (GRCm39) |
missense |
probably benign |
0.01 |
R7192:Sipa1l2
|
UTSW |
8 |
126,149,348 (GRCm39) |
missense |
probably benign |
0.09 |
R7240:Sipa1l2
|
UTSW |
8 |
126,196,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Sipa1l2
|
UTSW |
8 |
126,180,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R7383:Sipa1l2
|
UTSW |
8 |
126,174,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7417:Sipa1l2
|
UTSW |
8 |
126,208,845 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7604:Sipa1l2
|
UTSW |
8 |
126,146,011 (GRCm39) |
missense |
probably benign |
0.45 |
R7658:Sipa1l2
|
UTSW |
8 |
126,219,029 (GRCm39) |
missense |
probably benign |
0.00 |
R7743:Sipa1l2
|
UTSW |
8 |
126,190,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Sipa1l2
|
UTSW |
8 |
126,218,566 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7812:Sipa1l2
|
UTSW |
8 |
126,218,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7829:Sipa1l2
|
UTSW |
8 |
126,178,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R7880:Sipa1l2
|
UTSW |
8 |
126,191,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:Sipa1l2
|
UTSW |
8 |
126,174,337 (GRCm39) |
missense |
probably benign |
|
R8057:Sipa1l2
|
UTSW |
8 |
126,195,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Sipa1l2
|
UTSW |
8 |
126,218,548 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8092:Sipa1l2
|
UTSW |
8 |
126,145,907 (GRCm39) |
missense |
probably benign |
0.03 |
R8247:Sipa1l2
|
UTSW |
8 |
126,149,372 (GRCm39) |
missense |
probably benign |
0.29 |
R8252:Sipa1l2
|
UTSW |
8 |
126,195,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8386:Sipa1l2
|
UTSW |
8 |
126,218,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R8466:Sipa1l2
|
UTSW |
8 |
126,218,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R8697:Sipa1l2
|
UTSW |
8 |
126,208,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Sipa1l2
|
UTSW |
8 |
126,177,125 (GRCm39) |
missense |
probably benign |
0.28 |
R8727:Sipa1l2
|
UTSW |
8 |
126,177,125 (GRCm39) |
missense |
probably benign |
0.28 |
R9048:Sipa1l2
|
UTSW |
8 |
126,174,465 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9224:Sipa1l2
|
UTSW |
8 |
126,218,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R9279:Sipa1l2
|
UTSW |
8 |
126,208,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R9392:Sipa1l2
|
UTSW |
8 |
126,194,960 (GRCm39) |
missense |
probably benign |
|
R9574:Sipa1l2
|
UTSW |
8 |
126,169,453 (GRCm39) |
missense |
probably benign |
|
R9591:Sipa1l2
|
UTSW |
8 |
126,219,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R9614:Sipa1l2
|
UTSW |
8 |
126,196,565 (GRCm39) |
missense |
probably null |
0.01 |
R9690:Sipa1l2
|
UTSW |
8 |
126,218,996 (GRCm39) |
missense |
probably benign |
|
X0027:Sipa1l2
|
UTSW |
8 |
126,218,875 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sipa1l2
|
UTSW |
8 |
126,174,295 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
Predicted Primers |
PCR Primer
(F):5'- TATCTCGCAGGAAGGCATTAAC -3'
(R):5'- AGGACCTCAACTCCAAGGAG -3'
Sequencing Primer
(F):5'- GTAGTATAGAAGAGTCCCAGAGCCC -3'
(R):5'- TCCAAGGAGAACCCAGATGCTG -3'
|
Posted On |
2015-10-21 |