Incidental Mutation 'IGL01584:Gm15446'
ID |
91495 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gm15446
|
Ensembl Gene |
ENSMUSG00000090015 |
Gene Name |
predicted gene 15446 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.053)
|
Stock # |
IGL01584
|
Quality Score |
|
Status
|
|
Chromosome |
5 |
Chromosomal Location |
110081429-110089576 bp(+) (GRCm39) |
Type of Mutation |
makesense |
DNA Base Change (assembly) |
T to A
at 110088668 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Stop codon to Lysine
at position 64
(*64K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000127438
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000112544]
[ENSMUST00000170826]
|
AlphaFold |
D3Z5Y8 |
Predicted Effect |
probably null
Transcript: ENSMUST00000112544
|
SMART Domains |
Protein: ENSMUSP00000108163 Gene: ENSMUSG00000090015
Domain | Start | End | E-Value | Type |
KRAB
|
4 |
60 |
1.74e-14 |
SMART |
ZnF_C2H2
|
103 |
125 |
1.1e-2 |
SMART |
ZnF_C2H2
|
131 |
153 |
1.67e-2 |
SMART |
ZnF_C2H2
|
159 |
181 |
4.87e-4 |
SMART |
ZnF_C2H2
|
187 |
209 |
3.39e-3 |
SMART |
ZnF_C2H2
|
215 |
237 |
1.76e-1 |
SMART |
ZnF_C2H2
|
243 |
265 |
1.3e-4 |
SMART |
ZnF_C2H2
|
271 |
293 |
1.1e-2 |
SMART |
ZnF_C2H2
|
299 |
321 |
2.27e-4 |
SMART |
ZnF_C2H2
|
327 |
349 |
6.99e-5 |
SMART |
ZnF_C2H2
|
355 |
377 |
5.21e-4 |
SMART |
ZnF_C2H2
|
383 |
405 |
9.73e-4 |
SMART |
ZnF_C2H2
|
411 |
433 |
3.39e-3 |
SMART |
ZnF_C2H2
|
439 |
461 |
1.58e-3 |
SMART |
ZnF_C2H2
|
467 |
489 |
5.14e-3 |
SMART |
ZnF_C2H2
|
495 |
517 |
2.61e-4 |
SMART |
ZnF_C2H2
|
523 |
545 |
3.21e-4 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146564
|
Predicted Effect |
probably null
Transcript: ENSMUST00000170826
AA Change: *64K
|
SMART Domains |
Protein: ENSMUSP00000127438 Gene: ENSMUSG00000090015 AA Change: *64K
Domain | Start | End | E-Value | Type |
KRAB
|
3 |
59 |
1.74e-14 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,195,749 (GRCm39) |
V570A |
probably damaging |
Het |
Abcb1a |
T |
C |
5: 8,748,637 (GRCm39) |
S323P |
possibly damaging |
Het |
Adcy8 |
C |
T |
15: 64,687,170 (GRCm39) |
D445N |
probably damaging |
Het |
Cdc14a |
A |
T |
3: 116,186,474 (GRCm39) |
Y102* |
probably null |
Het |
Cubn |
A |
G |
2: 13,313,472 (GRCm39) |
|
probably benign |
Het |
Dcaf7 |
T |
C |
11: 105,944,653 (GRCm39) |
S279P |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,511,567 (GRCm39) |
Q1514R |
probably damaging |
Het |
Dtx2 |
G |
A |
5: 136,055,420 (GRCm39) |
S369N |
possibly damaging |
Het |
Dusp11 |
A |
G |
6: 85,930,376 (GRCm39) |
F136S |
probably damaging |
Het |
Fbxo32 |
T |
C |
15: 58,047,632 (GRCm39) |
D227G |
probably damaging |
Het |
Flg2 |
T |
A |
3: 93,120,773 (GRCm39) |
V1215E |
unknown |
Het |
Flg2 |
A |
T |
3: 93,122,777 (GRCm39) |
D1649V |
unknown |
Het |
Gabbr2 |
T |
C |
4: 46,674,524 (GRCm39) |
K821R |
probably damaging |
Het |
Gga2 |
T |
C |
7: 121,590,761 (GRCm39) |
T516A |
probably benign |
Het |
Gm5900 |
T |
C |
7: 104,599,361 (GRCm39) |
|
noncoding transcript |
Het |
Il17rb |
A |
G |
14: 29,725,637 (GRCm39) |
F121S |
probably damaging |
Het |
Ip6k3 |
C |
A |
17: 27,370,034 (GRCm39) |
R128L |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,754,250 (GRCm39) |
|
probably benign |
Het |
Lrrn4 |
A |
G |
2: 132,719,996 (GRCm39) |
L268P |
probably damaging |
Het |
Mthfd1l |
C |
A |
10: 3,966,738 (GRCm39) |
S332R |
probably damaging |
Het |
Or12d12 |
C |
T |
17: 37,610,629 (GRCm39) |
R228H |
probably benign |
Het |
Or5t17 |
G |
A |
2: 86,832,495 (GRCm39) |
V61I |
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,592,569 (GRCm39) |
E25G |
probably damaging |
Het |
Prima1 |
A |
T |
12: 103,169,047 (GRCm39) |
|
probably null |
Het |
Rbm26 |
A |
G |
14: 105,368,968 (GRCm39) |
V737A |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,616,644 (GRCm39) |
|
probably null |
Het |
Sema5b |
G |
T |
16: 35,465,793 (GRCm39) |
C114F |
probably damaging |
Het |
Spata31f1e |
A |
C |
4: 42,794,014 (GRCm39) |
S39R |
probably damaging |
Het |
Speg |
T |
C |
1: 75,407,581 (GRCm39) |
V3196A |
probably damaging |
Het |
Svs3b |
T |
C |
2: 164,097,943 (GRCm39) |
Y126C |
probably benign |
Het |
Tmem171 |
T |
C |
13: 98,828,683 (GRCm39) |
|
probably null |
Het |
Tnrc6b |
T |
A |
15: 80,763,883 (GRCm39) |
W462R |
probably benign |
Het |
Trdmt1 |
T |
C |
2: 13,524,739 (GRCm39) |
R239G |
probably benign |
Het |
Usp5 |
A |
T |
6: 124,796,350 (GRCm39) |
V583E |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,602,111 (GRCm39) |
V639A |
probably benign |
Het |
Vmn1r206 |
T |
C |
13: 22,804,964 (GRCm39) |
K81R |
probably damaging |
Het |
Vwa3a |
A |
G |
7: 120,383,197 (GRCm39) |
I599M |
probably benign |
Het |
|
Other mutations in Gm15446 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0278:Gm15446
|
UTSW |
5 |
110,091,281 (GRCm39) |
missense |
probably benign |
0.14 |
R0606:Gm15446
|
UTSW |
5 |
110,091,347 (GRCm39) |
missense |
probably benign |
|
R1608:Gm15446
|
UTSW |
5 |
110,090,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Gm15446
|
UTSW |
5 |
110,090,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R1892:Gm15446
|
UTSW |
5 |
110,091,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R2000:Gm15446
|
UTSW |
5 |
110,090,677 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2059:Gm15446
|
UTSW |
5 |
110,090,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R3083:Gm15446
|
UTSW |
5 |
110,091,158 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3883:Gm15446
|
UTSW |
5 |
110,088,313 (GRCm39) |
missense |
probably damaging |
0.98 |
R4086:Gm15446
|
UTSW |
5 |
110,091,121 (GRCm39) |
missense |
probably benign |
0.02 |
R4095:Gm15446
|
UTSW |
5 |
110,088,590 (GRCm39) |
splice site |
probably null |
|
R4459:Gm15446
|
UTSW |
5 |
110,091,107 (GRCm39) |
missense |
probably benign |
0.03 |
R4721:Gm15446
|
UTSW |
5 |
110,090,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Gm15446
|
UTSW |
5 |
110,090,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5229:Gm15446
|
UTSW |
5 |
110,091,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Gm15446
|
UTSW |
5 |
110,088,364 (GRCm39) |
nonsense |
probably null |
|
R6116:Gm15446
|
UTSW |
5 |
110,090,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R6166:Gm15446
|
UTSW |
5 |
110,090,646 (GRCm39) |
nonsense |
probably null |
|
R6322:Gm15446
|
UTSW |
5 |
110,091,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R7871:Gm15446
|
UTSW |
5 |
110,091,165 (GRCm39) |
nonsense |
probably null |
|
R7939:Gm15446
|
UTSW |
5 |
110,090,360 (GRCm39) |
missense |
probably benign |
0.22 |
R8045:Gm15446
|
UTSW |
5 |
110,088,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Gm15446
|
UTSW |
5 |
110,088,306 (GRCm39) |
nonsense |
probably null |
|
R8528:Gm15446
|
UTSW |
5 |
110,090,896 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9074:Gm15446
|
UTSW |
5 |
110,091,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9198:Gm15446
|
UTSW |
5 |
110,090,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R9604:Gm15446
|
UTSW |
5 |
110,088,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R9706:Gm15446
|
UTSW |
5 |
110,091,161 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Posted On |
2013-12-09 |