Incidental Mutation 'R0602:Stil'
| ID |
55480 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Stil
|
| Ensembl Gene |
ENSMUSG00000028718 |
| Gene Name |
Scl/Tal1 interrupting locus |
| Synonyms |
Sil |
| MMRRC Submission |
038791-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R0602 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
114857356-114900393 bp(+) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
T to A
at 114881620 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000118849
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030490]
[ENSMUST00000129957]
[ENSMUST00000141933]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000030490
|
| SMART Domains |
Protein: ENSMUSP00000030490
Gene: ENSMUSG00000028718
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:STIL_N
|
22 |
426 |
5.1e-199 |
PFAM |
|
low complexity region
|
709 |
724 |
N/A |
INTRINSIC |
|
low complexity region
|
1106 |
1118 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000129957
|
| SMART Domains |
Protein: ENSMUSP00000123385
Gene: ENSMUSG00000028718
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:STIL_N
|
22 |
416 |
1.5e-180 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000130401
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000141933
|
| SMART Domains |
Protein: ENSMUSP00000118849
Gene: ENSMUSG00000028718
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:STIL_N
|
22 |
392 |
6.6e-166 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144316
|
| Coding Region Coverage |
- 1x: 99.6%
- 3x: 99.1%
- 10x: 97.5%
- 20x: 94.7%
|
| Validation Efficiency |
95% (58/61) |
| MGI Phenotype |
FUNCTION: This gene encodes a centrosomal protein ubiquitously expressed in proliferating cells and during early embryonic development. Mice lacking the encoded protein die in utero with marked growth retardation, defects in the developing neural fold and randomization of left-right asymmetry. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]
PHENOTYPE: Mice homozygous for disruptions in this gene die as embryos with various neural tube defects. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 55 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9430038I01Rik |
T |
C |
7: 136,978,090 (GRCm39) |
|
probably benign |
Het |
| Arih1 |
A |
G |
9: 59,302,154 (GRCm39) |
|
probably benign |
Het |
| Bcl9 |
T |
C |
3: 97,113,102 (GRCm39) |
I1118V |
probably benign |
Het |
| Cap1 |
T |
C |
4: 122,766,202 (GRCm39) |
E12G |
probably damaging |
Het |
| Ccdc168 |
T |
A |
1: 44,099,127 (GRCm39) |
K657I |
possibly damaging |
Het |
| Ccr2 |
A |
G |
9: 123,906,658 (GRCm39) |
I313V |
probably benign |
Het |
| Cd1d2 |
T |
C |
3: 86,895,110 (GRCm39) |
S161P |
probably benign |
Het |
| Cd226 |
C |
T |
18: 89,287,135 (GRCm39) |
T311I |
probably benign |
Het |
| Col25a1 |
A |
G |
3: 130,369,063 (GRCm39) |
|
probably null |
Het |
| Cspg4 |
T |
C |
9: 56,795,301 (GRCm39) |
F1012S |
probably damaging |
Het |
| Dnah7b |
A |
G |
1: 46,364,002 (GRCm39) |
M3541V |
probably damaging |
Het |
| Erbb2 |
G |
A |
11: 98,325,097 (GRCm39) |
V852M |
probably damaging |
Het |
| Fer1l6 |
A |
C |
15: 58,449,794 (GRCm39) |
T667P |
probably damaging |
Het |
| Gal3st2c |
A |
G |
1: 93,936,901 (GRCm39) |
Y282C |
probably damaging |
Het |
| Glp1r |
T |
C |
17: 31,128,201 (GRCm39) |
L60P |
probably benign |
Het |
| Gtf2h2 |
A |
G |
13: 100,605,533 (GRCm39) |
V358A |
probably benign |
Het |
| H2ac18 |
T |
C |
3: 96,152,866 (GRCm39) |
|
probably benign |
Het |
| Hephl1 |
T |
A |
9: 15,000,347 (GRCm39) |
I302F |
probably damaging |
Het |
| Lgi2 |
T |
C |
5: 52,711,765 (GRCm39) |
D185G |
probably damaging |
Het |
| Lrtm1 |
T |
C |
14: 28,744,179 (GRCm39) |
|
probably benign |
Het |
| Megf10 |
T |
G |
18: 57,395,172 (GRCm39) |
D511E |
probably damaging |
Het |
| Myo5c |
A |
G |
9: 75,173,478 (GRCm39) |
|
probably null |
Het |
| Nrbf2 |
G |
A |
10: 67,103,605 (GRCm39) |
T166M |
probably damaging |
Het |
| Nrm |
C |
A |
17: 36,175,156 (GRCm39) |
Y61* |
probably null |
Het |
| Ola1 |
A |
G |
2: 72,924,056 (GRCm39) |
Y368H |
probably damaging |
Het |
| Or52s1 |
A |
C |
7: 102,861,787 (GRCm39) |
H229P |
possibly damaging |
Het |
| Or9i1b |
A |
G |
19: 13,897,145 (GRCm39) |
T254A |
probably benign |
Het |
| Or9q2 |
T |
C |
19: 13,772,026 (GRCm39) |
|
probably null |
Het |
| Panx1 |
A |
G |
9: 14,921,500 (GRCm39) |
L125P |
probably damaging |
Het |
| Pappa2 |
A |
G |
1: 158,590,625 (GRCm39) |
|
probably benign |
Het |
| Parp6 |
A |
G |
9: 59,556,648 (GRCm39) |
|
probably benign |
Het |
| Pomgnt2 |
A |
G |
9: 121,811,339 (GRCm39) |
Y481H |
probably benign |
Het |
| Ppp4c |
A |
G |
7: 126,388,254 (GRCm39) |
|
probably benign |
Het |
| Prl8a8 |
T |
A |
13: 27,692,533 (GRCm39) |
|
probably benign |
Het |
| Prpf40b |
C |
A |
15: 99,202,352 (GRCm39) |
A70E |
unknown |
Het |
| Ptgfr |
G |
A |
3: 151,540,839 (GRCm39) |
T223M |
probably damaging |
Het |
| Ptprc |
C |
T |
1: 138,017,223 (GRCm39) |
|
probably benign |
Het |
| Rgs22 |
T |
C |
15: 36,140,018 (GRCm39) |
|
probably benign |
Het |
| Rpgrip1 |
A |
G |
14: 52,371,313 (GRCm39) |
E344G |
possibly damaging |
Het |
| Sgca |
A |
T |
11: 94,854,061 (GRCm39) |
I383N |
possibly damaging |
Het |
| Sgms2 |
T |
A |
3: 131,118,756 (GRCm39) |
|
probably null |
Het |
| Slc9b1 |
C |
A |
3: 135,103,516 (GRCm39) |
Q549K |
probably benign |
Het |
| Smc4 |
G |
C |
3: 68,916,871 (GRCm39) |
A187P |
probably damaging |
Het |
| Smco1 |
A |
G |
16: 32,092,062 (GRCm39) |
S47G |
probably damaging |
Het |
| Sobp |
T |
A |
10: 42,898,385 (GRCm39) |
E400V |
probably damaging |
Het |
| Sp140l1 |
C |
G |
1: 85,077,226 (GRCm39) |
K113N |
probably benign |
Het |
| Sult3a2 |
A |
T |
10: 33,658,044 (GRCm39) |
M23K |
probably benign |
Het |
| Syne2 |
AGAGTGAG |
AGAGTGAGTGAG |
12: 76,144,734 (GRCm39) |
|
probably null |
Het |
| Tcam1 |
G |
A |
11: 106,174,904 (GRCm39) |
E120K |
probably benign |
Het |
| Tcof1 |
C |
A |
18: 60,966,605 (GRCm39) |
G329W |
probably damaging |
Het |
| Ttc13 |
A |
T |
8: 125,401,105 (GRCm39) |
S624T |
probably damaging |
Het |
| Vmn1r171 |
G |
T |
7: 23,332,602 (GRCm39) |
V276L |
probably benign |
Het |
| Vps13b |
T |
C |
15: 35,422,514 (GRCm39) |
L158P |
probably damaging |
Het |
| Vps54 |
A |
G |
11: 21,256,434 (GRCm39) |
I634M |
possibly damaging |
Het |
| Vwa8 |
T |
G |
14: 79,258,060 (GRCm39) |
S736R |
probably benign |
Het |
|
| Other mutations in Stil |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01506:Stil
|
APN |
4 |
114,881,309 (GRCm39) |
missense |
probably benign |
0.29 |
|
IGL01672:Stil
|
APN |
4 |
114,889,986 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02058:Stil
|
APN |
4 |
114,871,359 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02076:Stil
|
APN |
4 |
114,880,834 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02104:Stil
|
APN |
4 |
114,898,679 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02355:Stil
|
APN |
4 |
114,867,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02362:Stil
|
APN |
4 |
114,867,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02612:Stil
|
APN |
4 |
114,880,893 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL02695:Stil
|
APN |
4 |
114,873,372 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02696:Stil
|
APN |
4 |
114,898,692 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02826:Stil
|
APN |
4 |
114,881,295 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02946:Stil
|
APN |
4 |
114,887,110 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL03146:Stil
|
APN |
4 |
114,881,612 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB005:Stil
|
UTSW |
4 |
114,887,198 (GRCm39) |
missense |
probably damaging |
0.98 |
|
BB015:Stil
|
UTSW |
4 |
114,887,198 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0058:Stil
|
UTSW |
4 |
114,898,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0256:Stil
|
UTSW |
4 |
114,880,882 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R0324:Stil
|
UTSW |
4 |
114,896,346 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0391:Stil
|
UTSW |
4 |
114,898,369 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R0620:Stil
|
UTSW |
4 |
114,864,356 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R1452:Stil
|
UTSW |
4 |
114,896,392 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1462:Stil
|
UTSW |
4 |
114,881,161 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1462:Stil
|
UTSW |
4 |
114,881,161 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1544:Stil
|
UTSW |
4 |
114,881,049 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1789:Stil
|
UTSW |
4 |
114,898,979 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1878:Stil
|
UTSW |
4 |
114,898,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1895:Stil
|
UTSW |
4 |
114,881,072 (GRCm39) |
missense |
probably benign |
0.40 |
|
R2325:Stil
|
UTSW |
4 |
114,889,904 (GRCm39) |
missense |
probably benign |
0.12 |
|
R2401:Stil
|
UTSW |
4 |
114,873,483 (GRCm39) |
missense |
probably null |
0.81 |
|
R3054:Stil
|
UTSW |
4 |
114,862,163 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3055:Stil
|
UTSW |
4 |
114,871,266 (GRCm39) |
splice site |
probably benign |
|
|
R4097:Stil
|
UTSW |
4 |
114,880,797 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4330:Stil
|
UTSW |
4 |
114,862,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4418:Stil
|
UTSW |
4 |
114,866,574 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4665:Stil
|
UTSW |
4 |
114,898,841 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4688:Stil
|
UTSW |
4 |
114,898,505 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4740:Stil
|
UTSW |
4 |
114,863,979 (GRCm39) |
missense |
probably benign |
0.15 |
|
R4860:Stil
|
UTSW |
4 |
114,895,671 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4860:Stil
|
UTSW |
4 |
114,895,671 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4909:Stil
|
UTSW |
4 |
114,881,422 (GRCm39) |
nonsense |
probably null |
|
|
R6130:Stil
|
UTSW |
4 |
114,887,058 (GRCm39) |
splice site |
probably null |
|
|
R6523:Stil
|
UTSW |
4 |
114,889,911 (GRCm39) |
frame shift |
probably null |
|
|
R7294:Stil
|
UTSW |
4 |
114,864,480 (GRCm39) |
missense |
probably benign |
0.17 |
|
R7357:Stil
|
UTSW |
4 |
114,871,423 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7387:Stil
|
UTSW |
4 |
114,881,233 (GRCm39) |
missense |
probably benign |
0.37 |
|
R7592:Stil
|
UTSW |
4 |
114,881,005 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7776:Stil
|
UTSW |
4 |
114,890,035 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R7908:Stil
|
UTSW |
4 |
114,889,896 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R7928:Stil
|
UTSW |
4 |
114,887,198 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9064:Stil
|
UTSW |
4 |
114,898,932 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9140:Stil
|
UTSW |
4 |
114,864,449 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9500:Stil
|
UTSW |
4 |
114,878,716 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R9695:Stil
|
UTSW |
4 |
114,881,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9697:Stil
|
UTSW |
4 |
114,878,701 (GRCm39) |
missense |
probably benign |
0.45 |
|
Z1088:Stil
|
UTSW |
4 |
114,863,890 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Stil
|
UTSW |
4 |
114,898,576 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGCAATGGAGAACCGTCTCCTGTG -3'
(R):5'- GGAACATCCTGAAGACTCACTGGC -3'
Sequencing Primer
(F):5'- TCCTGTGGCAGGACCTTC -3'
(R):5'- ctcctaaccagcaattatggaac -3'
|
| Posted On |
2013-07-11 |
Incidental Mutation