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) question?
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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
GeneRefVarChr/LocMutationPredicted EffectZygosity
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
AlleleSourceChrCoordTypePredicted EffectPPH 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