Incidental Mutation 'IGL00467:Mta3'
ID |
5739 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Mta3
|
Ensembl Gene |
ENSMUSG00000055817 |
Gene Name |
metastasis associated 3 |
Synonyms |
1110002J22Rik |
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.506)
|
Stock # |
IGL00467
|
Quality Score |
|
Status
|
|
Chromosome |
17 |
Chromosomal Location |
84013592-84128945 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to A
at 84063113 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000135064
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000067826]
[ENSMUST00000112349]
[ENSMUST00000112350]
[ENSMUST00000112352]
[ENSMUST00000176816]
[ENSMUST00000177069]
|
AlphaFold |
Q924K8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000067826
|
SMART Domains |
Protein: ENSMUSP00000068931 Gene: ENSMUSG00000055817
Domain | Start | End | E-Value | Type |
BAH
|
4 |
147 |
2.62e-30 |
SMART |
ELM2
|
150 |
203 |
3.49e-16 |
SMART |
SANT
|
266 |
315 |
7.94e-8 |
SMART |
ZnF_GATA
|
371 |
425 |
8.33e-15 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000112349
|
SMART Domains |
Protein: ENSMUSP00000107968 Gene: ENSMUSG00000055817
Domain | Start | End | E-Value | Type |
BAH
|
4 |
147 |
2.62e-30 |
SMART |
ELM2
|
150 |
204 |
2.5e-17 |
SMART |
SANT
|
267 |
316 |
7.94e-8 |
SMART |
ZnF_GATA
|
373 |
427 |
8.33e-15 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000112350
|
SMART Domains |
Protein: ENSMUSP00000107969 Gene: ENSMUSG00000055817
Domain | Start | End | E-Value | Type |
BAH
|
4 |
147 |
2.62e-30 |
SMART |
ELM2
|
150 |
204 |
2.5e-17 |
SMART |
SANT
|
267 |
316 |
7.94e-8 |
SMART |
ZnF_GATA
|
372 |
426 |
8.33e-15 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000112352
|
SMART Domains |
Protein: ENSMUSP00000107971 Gene: ENSMUSG00000055817
Domain | Start | End | E-Value | Type |
BAH
|
4 |
147 |
2.62e-30 |
SMART |
ELM2
|
150 |
204 |
2.5e-17 |
SMART |
SANT
|
267 |
316 |
7.94e-8 |
SMART |
ZnF_GATA
|
372 |
426 |
8.33e-15 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176816
|
SMART Domains |
Protein: ENSMUSP00000135752 Gene: ENSMUSG00000055817
Domain | Start | End | E-Value | Type |
ELM2
|
1 |
52 |
3.23e-11 |
SMART |
SANT
|
115 |
164 |
7.94e-8 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000177069
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177416
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
C |
11: 110,036,496 (GRCm39) |
|
probably benign |
Het |
Acvrl1 |
C |
A |
15: 101,041,221 (GRCm39) |
|
probably null |
Het |
Ahnak |
T |
A |
19: 8,984,587 (GRCm39) |
M1957K |
probably damaging |
Het |
Brinp3 |
A |
G |
1: 146,777,512 (GRCm39) |
D653G |
probably damaging |
Het |
Dcstamp |
T |
A |
15: 39,617,812 (GRCm39) |
C74S |
probably benign |
Het |
Esrrg |
A |
G |
1: 187,943,107 (GRCm39) |
E360G |
probably damaging |
Het |
Fam13a |
C |
T |
6: 58,917,098 (GRCm39) |
|
probably benign |
Het |
Glipr1l1 |
A |
G |
10: 111,914,286 (GRCm39) |
T216A |
probably benign |
Het |
Lama2 |
T |
A |
10: 27,343,193 (GRCm39) |
|
probably benign |
Het |
Men1 |
G |
A |
19: 6,387,237 (GRCm39) |
|
probably null |
Het |
Nfu1 |
A |
G |
6: 86,997,755 (GRCm39) |
M213V |
possibly damaging |
Het |
Pam |
A |
T |
1: 97,852,152 (GRCm39) |
|
probably benign |
Het |
Pcca |
A |
T |
14: 122,820,041 (GRCm39) |
M62L |
probably benign |
Het |
Phf6 |
A |
G |
X: 52,020,523 (GRCm39) |
Y25C |
probably damaging |
Het |
Phlpp2 |
C |
T |
8: 110,652,422 (GRCm39) |
H589Y |
probably benign |
Het |
Ppp1r13b |
A |
G |
12: 111,795,804 (GRCm39) |
I956T |
probably damaging |
Het |
Prkcd |
G |
A |
14: 30,324,379 (GRCm39) |
|
probably benign |
Het |
Rapgef4 |
A |
T |
2: 72,086,656 (GRCm39) |
N973I |
possibly damaging |
Het |
Rnf20 |
G |
T |
4: 49,655,480 (GRCm39) |
E905* |
probably null |
Het |
Slc26a6 |
T |
A |
9: 108,733,088 (GRCm39) |
D22E |
probably benign |
Het |
Sp2 |
C |
T |
11: 96,845,387 (GRCm39) |
R578H |
probably damaging |
Het |
Taf6l |
A |
T |
19: 8,760,752 (GRCm39) |
N57K |
probably benign |
Het |
Tas2r109 |
C |
A |
6: 132,956,986 (GRCm39) |
V315L |
probably benign |
Het |
Tasor |
A |
G |
14: 27,170,121 (GRCm39) |
N350S |
probably benign |
Het |
Tex9 |
T |
C |
9: 72,385,117 (GRCm39) |
T240A |
probably benign |
Het |
Trank1 |
G |
A |
9: 111,193,734 (GRCm39) |
|
probably benign |
Het |
Trim30c |
A |
T |
7: 104,031,389 (GRCm39) |
Y475* |
probably null |
Het |
Trim60 |
T |
C |
8: 65,453,371 (GRCm39) |
T293A |
possibly damaging |
Het |
Ttc21b |
T |
C |
2: 66,018,708 (GRCm39) |
Y1233C |
probably damaging |
Het |
Wdr75 |
A |
G |
1: 45,841,235 (GRCm39) |
I106V |
probably benign |
Het |
Zkscan16 |
T |
C |
4: 58,957,709 (GRCm39) |
S664P |
possibly damaging |
Het |
|
Other mutations in Mta3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00433:Mta3
|
APN |
17 |
84,015,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00475:Mta3
|
APN |
17 |
84,015,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00539:Mta3
|
APN |
17 |
84,070,412 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01722:Mta3
|
APN |
17 |
84,063,072 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03355:Mta3
|
APN |
17 |
84,107,474 (GRCm39) |
splice site |
probably benign |
|
container
|
UTSW |
17 |
84,015,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R0440:Mta3
|
UTSW |
17 |
84,074,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Mta3
|
UTSW |
17 |
84,022,056 (GRCm39) |
missense |
probably damaging |
0.98 |
R1848:Mta3
|
UTSW |
17 |
84,062,980 (GRCm39) |
splice site |
probably benign |
|
R1870:Mta3
|
UTSW |
17 |
84,089,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R2358:Mta3
|
UTSW |
17 |
84,070,417 (GRCm39) |
missense |
probably damaging |
0.96 |
R2373:Mta3
|
UTSW |
17 |
84,091,730 (GRCm39) |
nonsense |
probably null |
|
R2447:Mta3
|
UTSW |
17 |
84,111,973 (GRCm39) |
missense |
probably benign |
0.03 |
R3711:Mta3
|
UTSW |
17 |
84,070,417 (GRCm39) |
missense |
probably damaging |
0.96 |
R3712:Mta3
|
UTSW |
17 |
84,070,417 (GRCm39) |
missense |
probably damaging |
0.96 |
R4107:Mta3
|
UTSW |
17 |
84,070,343 (GRCm39) |
missense |
probably benign |
0.00 |
R4771:Mta3
|
UTSW |
17 |
84,063,103 (GRCm39) |
missense |
probably damaging |
0.98 |
R5259:Mta3
|
UTSW |
17 |
84,112,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R5980:Mta3
|
UTSW |
17 |
84,015,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Mta3
|
UTSW |
17 |
84,099,222 (GRCm39) |
missense |
probably benign |
|
R6555:Mta3
|
UTSW |
17 |
84,015,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R6909:Mta3
|
UTSW |
17 |
84,073,980 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7170:Mta3
|
UTSW |
17 |
84,022,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R7350:Mta3
|
UTSW |
17 |
84,015,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Mta3
|
UTSW |
17 |
84,083,011 (GRCm39) |
missense |
probably benign |
0.05 |
R7638:Mta3
|
UTSW |
17 |
84,107,572 (GRCm39) |
missense |
probably benign |
|
R7747:Mta3
|
UTSW |
17 |
84,099,165 (GRCm39) |
nonsense |
probably null |
|
R7894:Mta3
|
UTSW |
17 |
84,070,363 (GRCm39) |
missense |
probably benign |
0.01 |
R8170:Mta3
|
UTSW |
17 |
84,099,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R8799:Mta3
|
UTSW |
17 |
84,096,369 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8944:Mta3
|
UTSW |
17 |
84,083,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Mta3
|
UTSW |
17 |
84,015,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R9212:Mta3
|
UTSW |
17 |
84,015,846 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Mta3
|
UTSW |
17 |
84,070,343 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Mta3
|
UTSW |
17 |
84,089,397 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Posted On |
2012-04-20 |