Incidental Mutation 'R4684:Secisbp2l'
| ID |
353492 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Secisbp2l
|
| Ensembl Gene |
ENSMUSG00000035093 |
| Gene Name |
SECIS binding protein 2-like |
| Synonyms |
3110001I20Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.751)
|
| Stock # |
R4684 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
125736986-125782870 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 125745942 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 751
(D751G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000055772
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053699]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000053699
AA Change: D751G
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000055772
Gene: ENSMUSG00000035093
AA Change: D751G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
441 |
459 |
N/A |
INTRINSIC |
|
low complexity region
|
555 |
568 |
N/A |
INTRINSIC |
|
Pfam:Ribosomal_L7Ae
|
700 |
802 |
7.6e-24 |
PFAM |
|
low complexity region
|
821 |
831 |
N/A |
INTRINSIC |
|
low complexity region
|
970 |
978 |
N/A |
INTRINSIC |
|
low complexity region
|
985 |
996 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000136450
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000139944
AA Change: D376G
|
| SMART Domains |
Protein: ENSMUSP00000121529
Gene: ENSMUSG00000035093
AA Change: D376G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
67 |
85 |
N/A |
INTRINSIC |
|
low complexity region
|
181 |
194 |
N/A |
INTRINSIC |
|
Pfam:Ribosomal_L7Ae
|
326 |
427 |
3.5e-24 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.0%
- 20x: 94.7%
|
| Validation Efficiency |
|
| 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: 46,772,946 (GRCm38) |
V45A |
probably benign |
Het |
| 4921509C19Rik |
A |
G |
2: 151,471,871 (GRCm38) |
I629T |
unknown |
Het |
| 4933402N03Rik |
T |
C |
7: 131,138,684 (GRCm38) |
R268G |
probably damaging |
Het |
| Abca13 |
A |
T |
11: 9,434,193 (GRCm38) |
R3882* |
probably null |
Het |
| Adamts3 |
T |
G |
5: 89,703,007 (GRCm38) |
T558P |
probably damaging |
Het |
| Ano2 |
A |
G |
6: 125,790,341 (GRCm38) |
N214S |
probably benign |
Het |
| Arhgef4 |
A |
T |
1: 34,811,785 (GRCm38) |
|
probably null |
Het |
| Boc |
C |
T |
16: 44,500,380 (GRCm38) |
A306T |
probably benign |
Het |
| Capn10 |
T |
C |
1: 92,943,781 (GRCm38) |
F367S |
probably damaging |
Het |
| Ccdc6 |
T |
C |
10: 70,189,256 (GRCm38) |
|
probably benign |
Het |
| Cobll1 |
G |
T |
2: 65,099,028 (GRCm38) |
S688R |
possibly damaging |
Het |
| Cpxm2 |
G |
T |
7: 132,049,038 (GRCm38) |
P631Q |
possibly damaging |
Het |
| Cyp2c68 |
A |
G |
19: 39,699,335 (GRCm38) |
V406A |
possibly damaging |
Het |
| Cyp4a30b |
T |
A |
4: 115,455,003 (GRCm38) |
Y118N |
probably damaging |
Het |
| Dgki |
A |
T |
6: 37,299,846 (GRCm38) |
|
probably benign |
Het |
| Disp2 |
A |
G |
2: 118,792,756 (GRCm38) |
N1323S |
probably damaging |
Het |
| Dock1 |
T |
A |
7: 134,724,409 (GRCm38) |
Y42* |
probably null |
Het |
| Eps8l1 |
C |
A |
7: 4,473,945 (GRCm38) |
P471Q |
probably damaging |
Het |
| Fam20a |
A |
C |
11: 109,721,687 (GRCm38) |
L10R |
unknown |
Het |
| Fpr-rs4 |
T |
A |
17: 18,022,184 (GRCm38) |
I151K |
probably damaging |
Het |
| Gga1 |
C |
A |
15: 78,885,309 (GRCm38) |
P161T |
probably damaging |
Het |
| Gm8909 |
A |
T |
17: 36,165,858 (GRCm38) |
H241Q |
possibly damaging |
Het |
| Gm9923 |
T |
A |
10: 72,309,476 (GRCm38) |
Y52* |
probably null |
Het |
| Gucy2g |
A |
G |
19: 55,206,256 (GRCm38) |
F910L |
probably damaging |
Het |
| Helz |
T |
C |
11: 107,649,145 (GRCm38) |
V315A |
probably damaging |
Het |
| Hk2 |
T |
C |
6: 82,739,648 (GRCm38) |
Y301C |
probably damaging |
Het |
| Htt |
C |
T |
5: 34,852,765 (GRCm38) |
P1521S |
probably damaging |
Het |
| Iah1 |
T |
C |
12: 21,316,433 (GRCm38) |
M1T |
probably null |
Het |
| Ik |
T |
C |
18: 36,752,414 (GRCm38) |
S287P |
probably damaging |
Het |
| Itga1 |
T |
A |
13: 115,049,370 (GRCm38) |
D32V |
probably damaging |
Het |
| Itpr2 |
A |
G |
6: 146,373,173 (GRCm38) |
F837S |
probably damaging |
Het |
| Klk14 |
A |
G |
7: 43,691,968 (GRCm38) |
I15V |
probably benign |
Het |
| Kng2 |
T |
C |
16: 22,987,641 (GRCm38) |
I603V |
possibly damaging |
Het |
| Lama1 |
T |
C |
17: 67,773,778 (GRCm38) |
I1267T |
possibly damaging |
Het |
| Lrp1b |
A |
C |
2: 40,922,304 (GRCm38) |
L2430V |
probably benign |
Het |
| Lrrn3 |
T |
G |
12: 41,454,244 (GRCm38) |
K25Q |
possibly damaging |
Het |
| Lta4h |
T |
A |
10: 93,468,816 (GRCm38) |
N233K |
probably benign |
Het |
| Mapk13 |
T |
C |
17: 28,770,049 (GRCm38) |
I53T |
probably damaging |
Het |
| Mdn1 |
T |
C |
4: 32,666,430 (GRCm38) |
F123L |
probably damaging |
Het |
| Myh4 |
G |
C |
11: 67,245,811 (GRCm38) |
D472H |
probably damaging |
Het |
| Nipa2 |
A |
T |
7: 55,935,826 (GRCm38) |
N121K |
probably benign |
Het |
| Nostrin |
C |
T |
2: 69,183,924 (GRCm38) |
T408M |
probably benign |
Het |
| Oosp2 |
C |
T |
19: 11,649,653 (GRCm38) |
R102H |
probably damaging |
Het |
| Or1j18 |
A |
G |
2: 36,734,674 (GRCm38) |
M118V |
probably damaging |
Het |
| Or4k15b |
T |
C |
14: 50,034,830 (GRCm38) |
D191G |
probably damaging |
Het |
| Osgin2 |
T |
A |
4: 16,001,946 (GRCm38) |
I202L |
probably benign |
Het |
| Pbld2 |
C |
A |
10: 63,057,697 (GRCm38) |
R271S |
probably damaging |
Het |
| Pex6 |
C |
T |
17: 46,712,101 (GRCm38) |
T201I |
probably benign |
Het |
| Pilra |
T |
C |
5: 137,835,515 (GRCm38) |
I96M |
probably damaging |
Het |
| Pllp |
T |
A |
8: 94,677,278 (GRCm38) |
D47V |
possibly damaging |
Het |
| Plxna2 |
A |
G |
1: 194,762,594 (GRCm38) |
S765G |
probably benign |
Het |
| Prkca |
A |
T |
11: 107,961,608 (GRCm38) |
Y100N |
probably damaging |
Het |
| Prkg1 |
T |
A |
19: 31,664,179 (GRCm38) |
K35* |
probably null |
Het |
| Psmc2 |
A |
G |
5: 21,803,265 (GRCm38) |
D389G |
possibly damaging |
Het |
| Rnf213 |
A |
G |
11: 119,441,125 (GRCm38) |
T2387A |
probably damaging |
Het |
| Ros1 |
T |
C |
10: 52,129,096 (GRCm38) |
N914S |
probably damaging |
Het |
| Ruvbl1 |
C |
A |
6: 88,491,599 (GRCm38) |
T367K |
probably benign |
Het |
| Scube2 |
C |
T |
7: 109,810,713 (GRCm38) |
R525H |
probably damaging |
Het |
| Sec14l4 |
T |
C |
11: 4,035,200 (GRCm38) |
|
probably null |
Het |
| Setd3 |
T |
C |
12: 108,108,690 (GRCm38) |
D402G |
probably benign |
Het |
| Slc15a2 |
T |
A |
16: 36,757,849 (GRCm38) |
K359N |
probably damaging |
Het |
| Slc25a21 |
A |
G |
12: 57,196,936 (GRCm38) |
S2P |
probably benign |
Het |
| Slfn8 |
A |
T |
11: 83,017,506 (GRCm38) |
H70Q |
probably benign |
Het |
| Spef2 |
T |
C |
15: 9,647,490 (GRCm38) |
I944V |
probably benign |
Het |
| Spg11 |
A |
G |
2: 122,065,076 (GRCm38) |
F1887S |
probably damaging |
Het |
| Sptbn4 |
T |
C |
7: 27,364,419 (GRCm38) |
E879G |
probably damaging |
Het |
| Sptbn4 |
A |
T |
7: 27,366,735 (GRCm38) |
D649E |
possibly damaging |
Het |
| Stx5a |
C |
A |
19: 8,743,361 (GRCm38) |
R121S |
probably damaging |
Het |
| Tbcd |
T |
C |
11: 121,493,771 (GRCm38) |
L26P |
probably damaging |
Het |
| Tecpr1 |
T |
C |
5: 144,207,437 (GRCm38) |
D649G |
probably benign |
Het |
| Tfam |
A |
G |
10: 71,237,847 (GRCm38) |
S32P |
probably benign |
Het |
| Tmt1b |
G |
T |
10: 128,960,702 (GRCm38) |
C79* |
probably null |
Het |
| Trmt44 |
C |
T |
5: 35,558,043 (GRCm38) |
R642H |
probably benign |
Het |
| Trpm3 |
G |
A |
19: 22,987,781 (GRCm38) |
A1547T |
probably benign |
Het |
| Ttll6 |
T |
C |
11: 96,153,177 (GRCm38) |
V519A |
probably benign |
Het |
| Umodl1 |
T |
C |
17: 30,998,114 (GRCm38) |
F1107L |
probably benign |
Het |
| Usp5 |
A |
T |
6: 124,817,956 (GRCm38) |
V677E |
probably damaging |
Het |
| Utp20 |
A |
T |
10: 88,807,445 (GRCm38) |
L605* |
probably null |
Het |
| Utrn |
T |
C |
10: 12,745,240 (GRCm38) |
D229G |
probably damaging |
Het |
| Uty |
A |
T |
Y: 1,176,502 (GRCm38) |
L178* |
probably null |
Het |
| Vmn2r88 |
A |
T |
14: 51,413,334 (GRCm38) |
D168V |
possibly damaging |
Het |
| Vps13b |
T |
C |
15: 35,646,178 (GRCm38) |
V1476A |
probably damaging |
Het |
| Vps13b |
C |
T |
15: 35,841,341 (GRCm38) |
H2506Y |
probably benign |
Het |
| Vps13b |
C |
A |
15: 35,879,821 (GRCm38) |
T3014K |
probably benign |
Het |
| Vps37c |
T |
C |
19: 10,712,768 (GRCm38) |
V198A |
probably benign |
Het |
| Zfc3h1 |
T |
C |
10: 115,423,385 (GRCm38) |
Y1621H |
probably benign |
Het |
| Zfp251 |
T |
C |
15: 76,854,407 (GRCm38) |
D162G |
possibly damaging |
Het |
| Zfp292 |
T |
C |
4: 34,807,078 (GRCm38) |
T1994A |
probably benign |
Het |
| Zfp791 |
A |
G |
8: 85,110,930 (GRCm38) |
Y102H |
probably benign |
Het |
|
| Other mutations in Secisbp2l |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00421:Secisbp2l
|
APN |
2 |
125,743,856 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL00644:Secisbp2l
|
APN |
2 |
125,743,844 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01093:Secisbp2l
|
APN |
2 |
125,740,325 (GRCm38) |
missense |
probably benign |
|
|
IGL01621:Secisbp2l
|
APN |
2 |
125,773,211 (GRCm38) |
missense |
probably benign |
|
|
IGL01955:Secisbp2l
|
APN |
2 |
125,743,812 (GRCm38) |
critical splice donor site |
probably null |
|
|
IGL02036:Secisbp2l
|
APN |
2 |
125,758,207 (GRCm38) |
missense |
probably benign |
|
|
IGL02045:Secisbp2l
|
APN |
2 |
125,775,578 (GRCm38) |
missense |
possibly damaging |
0.82 |
|
IGL02182:Secisbp2l
|
APN |
2 |
125,747,577 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02408:Secisbp2l
|
APN |
2 |
125,740,869 (GRCm38) |
nonsense |
probably null |
|
|
IGL02455:Secisbp2l
|
APN |
2 |
125,773,478 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
IGL02953:Secisbp2l
|
APN |
2 |
125,760,274 (GRCm38) |
missense |
probably benign |
0.36 |
|
Rift
|
UTSW |
2 |
125,768,193 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Seismic
|
UTSW |
2 |
125,745,909 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0097:Secisbp2l
|
UTSW |
2 |
125,771,456 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R0097:Secisbp2l
|
UTSW |
2 |
125,771,456 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R1415:Secisbp2l
|
UTSW |
2 |
125,740,365 (GRCm38) |
missense |
probably benign |
0.00 |
|
R1626:Secisbp2l
|
UTSW |
2 |
125,775,686 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R1926:Secisbp2l
|
UTSW |
2 |
125,740,677 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R1940:Secisbp2l
|
UTSW |
2 |
125,740,339 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1970:Secisbp2l
|
UTSW |
2 |
125,747,510 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2100:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R2240:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R2252:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R2253:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R2472:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R2474:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R2475:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R2990:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R2993:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3113:Secisbp2l
|
UTSW |
2 |
125,750,286 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3696:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3749:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3750:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3800:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3810:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3812:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3815:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3816:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3817:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R3880:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4077:Secisbp2l
|
UTSW |
2 |
125,751,865 (GRCm38) |
splice site |
probably benign |
|
|
R4096:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4097:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4164:Secisbp2l
|
UTSW |
2 |
125,751,883 (GRCm38) |
intron |
probably benign |
|
|
R4332:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4418:Secisbp2l
|
UTSW |
2 |
125,752,915 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4598:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4600:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4602:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4603:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4678:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4679:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4741:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4749:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4934:Secisbp2l
|
UTSW |
2 |
125,740,489 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5245:Secisbp2l
|
UTSW |
2 |
125,747,591 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5521:Secisbp2l
|
UTSW |
2 |
125,752,977 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R5547:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R5630:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R5631:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R5632:Secisbp2l
|
UTSW |
2 |
125,740,737 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R6039:Secisbp2l
|
UTSW |
2 |
125,773,216 (GRCm38) |
missense |
probably benign |
0.28 |
|
R6039:Secisbp2l
|
UTSW |
2 |
125,773,216 (GRCm38) |
missense |
probably benign |
0.28 |
|
R6378:Secisbp2l
|
UTSW |
2 |
125,768,325 (GRCm38) |
missense |
possibly damaging |
0.78 |
|
R6616:Secisbp2l
|
UTSW |
2 |
125,768,226 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R6938:Secisbp2l
|
UTSW |
2 |
125,750,352 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7287:Secisbp2l
|
UTSW |
2 |
125,740,369 (GRCm38) |
missense |
probably benign |
|
|
R7373:Secisbp2l
|
UTSW |
2 |
125,757,271 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7403:Secisbp2l
|
UTSW |
2 |
125,760,279 (GRCm38) |
missense |
possibly damaging |
0.73 |
|
R7484:Secisbp2l
|
UTSW |
2 |
125,771,532 (GRCm38) |
nonsense |
probably null |
|
|
R7504:Secisbp2l
|
UTSW |
2 |
125,758,171 (GRCm38) |
missense |
probably benign |
0.30 |
|
R7762:Secisbp2l
|
UTSW |
2 |
125,768,193 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7769:Secisbp2l
|
UTSW |
2 |
125,771,545 (GRCm38) |
critical splice acceptor site |
probably benign |
|
|
R8018:Secisbp2l
|
UTSW |
2 |
125,745,909 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8487:Secisbp2l
|
UTSW |
2 |
125,775,582 (GRCm38) |
nonsense |
probably null |
|
|
R8784:Secisbp2l
|
UTSW |
2 |
125,760,343 (GRCm38) |
nonsense |
probably null |
|
|
R8810:Secisbp2l
|
UTSW |
2 |
125,775,676 (GRCm38) |
missense |
possibly damaging |
0.82 |
|
R8872:Secisbp2l
|
UTSW |
2 |
125,752,972 (GRCm38) |
missense |
probably benign |
|
|
R9111:Secisbp2l
|
UTSW |
2 |
125,760,286 (GRCm38) |
missense |
probably benign |
|
|
R9154:Secisbp2l
|
UTSW |
2 |
125,775,703 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9155:Secisbp2l
|
UTSW |
2 |
125,775,703 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9589:Secisbp2l
|
UTSW |
2 |
125,747,510 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9589:Secisbp2l
|
UTSW |
2 |
125,747,505 (GRCm38) |
missense |
probably benign |
0.03 |
|
R9592:Secisbp2l
|
UTSW |
2 |
125,740,641 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9602:Secisbp2l
|
UTSW |
2 |
125,767,436 (GRCm38) |
missense |
probably benign |
0.19 |
|
R9620:Secisbp2l
|
UTSW |
2 |
125,747,474 (GRCm38) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCACTAACTCACTCCTGGCATG -3'
(R):5'- TGCTTAGCCCTACAGAGAAAC -3'
Sequencing Primer
(F):5'- ACAGCTGTACATAACCTTGCTTGG -3'
(R):5'- CCCTACAGAGAAACTAAAGTACTGGG -3'
|
| Posted On |
2015-10-21 |
Incidental Mutation