ZMP
mta3
Ensembl ID:
ZFIN ID:
Description:
metastasis-associated protein MTA3 [Source:RefSeq peptide;Acc:NP_956206]
Human Orthologue:
MTA3
Human Description:
metastasis associated 1 family, member 3 [Source:HGNC Symbol;Acc:23784]
Mouse Orthologue:
Mta3
Mouse Description:
metastasis associated 3 Gene [Source:MGI Symbol;Acc:MGI:2151172]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31877 | Essential Splice Site | Available for shipment | Available now |
sa13464 | Nonsense | Available for shipment | Available now |
sa9628 | Nonsense | Available for shipment | Available now |
sa35301 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22102 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31877
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077180 | Essential Splice Site | 9 | 517 | 2 | 15 |
ENSDART00000122665 | Essential Splice Site | 9 | 709 | 1 | 19 |
ENSDART00000127454 | Essential Splice Site | 9 | 517 | 1 | 14 |
The following transcripts of ENSDARG00000054903 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 26751798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 25132786 |
GRCz11 | 12 | 25224146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAACACTCCGGGAGGGCAGAAATGGCGGCCAACATGTACCGGGTCGGAG[G/A]TATGTCCGTCTATATTCTGAATTAACGCAAGTCAAAACACAGGCACCACC
Long Flanking Sequence:
TTCCACAATTGACAGCTTTTAAAAGACACTTATTGTCATAACAAAAAAACTGGCAAAATATGAAAACGTTATTTTAAATGATTTAAATGCACATCAGAACCATGATTAATTGAATTCTGTGGGTAAAACAGTCATGAGTGTCGTGTTGAGGTTGCAGTCTGTAGACTTCATTCACCCTCCTTCTTCCTTCCCTCCTCTTTTCTCTCCTCCTCTCATCTCATCATCAGGAAGCTGCTGCGCTCGAGCCTTTTCTAGCGCGTGAGTGAGTTACTGTATTGTACTGTGAATCTCGGGAGGGGGGCTGCAAAAAAATCTCCTATTCTTACTGAGGTCCACCCCCCTTATTTAAAACTTCTTAAGCCAGATTGCTTTCCAACAGGTCACAGGACGTAGATGCCTTCTTGATTCACATATTTATTTTGTTTTTATTTTAGTTTATGGTTTGGTTTTTTAACACTCCGGGAGGGCAGAAATGGCGGCCAACATGTACCGGGTCGGAG[G/A]TATGTCCGTCTATATTCTGAATTAACGCAAGTCAAAACACAGGCACCACCGTAAGACCTGACTGGAAGGCAGGGACTCATTTCAAGCGAATTCCCGAAACCGGCCGCTCACTTTTAAACTCTTTTAACACGTGCAGTGTCCTTGCAAAAGAAAACGATAACGTGGATGCAGAATATTTTGGGTTCTGATTTGGGTCAGGCCTCTTAAACTATCATAGCCGCACTAGCATTTTAGCAAGCAGGCTATGTTGCTAGCTAGCCACATCATAAACAAATAATCACTACTATATGTAAAACAATCGGAAACGCGCACTTAGAGCACGTTTCTCTTAGATTTACCCACATAGGTTAAAAGCGAGATATGCTTGCTATTTAACCATTGCAATTTTAGACGCCGATGTTTTTCTTTGTGATCATTTGTCTCATTTTTTGGCACGTATCCATTAGTTACGGGTTCTCATTCGGCATGCAAGGTAGCAAAGCGAGCTAGCATTTAACACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13464
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077180 | Nonsense | 246 | 517 | 10 | 15 |
ENSDART00000122665 | Nonsense | 246 | 709 | 9 | 19 |
ENSDART00000127454 | Nonsense | 246 | 517 | 9 | 14 |
The following transcripts of ENSDARG00000054903 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 26782549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 25163537 |
GRCz11 | 12 | 25254897 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WCTGGCTTTCTGAAGTTTCAMGCTATGGACACACTGCATCGGCAYGGCTA[T/A]GACCTGTCCAGTGCTCTCAGCGTTCTTGTTCCTCAAGGTGGGCCAGTCCT
Long Flanking Sequence:
AATATACTCCAAATCAATTAATTCGAGAGTTTGTGAATTTGCATCCAGCCACGAAATATGCATCTCATCCCAGTCCAAAAAATACATTTGCAATAAACGGATGCATCATGTTTTCCATGCTTTTTGTGAGCCCATCAGATCAGACCGGTGACCCCTTTTCGGGCTTTGACCCATGAGTTGGGAATCTCTGGTGTAGAAGCCACTGGAAAGTGTGTCAGCGAGGAAACCGATGGCATAATTAAATTTGCATGATGAAACTGTGTGCAGAGCGGTTGGTACGTTTGCCCGGGCGTTGGACTGCAGCAGCTCCGTCAGACAGCCCAGCTTACACATGAGCGCCGCGGCAGCCTCACGAGACATCACACTGGTACCCGTCCCATCAGCACCATCTGTCTCTCACTCTCTCTATATCCACCAGAGATGTGAAAACCCTGATTAATTCTTTTCCTGTCTGGCTTTCTGAAGTTTCACGCTATGGACACACTGCATCGGCATGGCTA[T/A]GACCTGTCCAGTGCTCTCAGCGTTCTTGTTCCTCAAGGTGGGCCAGTCCTGTGCCGGGATGAGATGGAGGAGTGGAGCTCGTCAGAGGCCAATCTGTTTGAAGAGGCCCTGGAGAAATACGGCAAAGACTTCAACGATATACGGCAAGATTTTGTGAGTAAAATCAGAAAGTGACAGTTTACTGCATTGATTCACTGATGTAATTTTGCTAGCACTTTATTTTACAGTAGAGGGCGGTGTTTTTCAAAAGCATTGTAAGCCTAAGTTGACCTTACAATCATTGTCACTAGTACACGTCTGTGCACTTTTCATAGATATTACCTAGTGGGTAATAACTACGTACTCTATCTAAACCTACCCCTGTACCTAATCTTAACTTGCATATTACATTACTTTCTTACACAGTTAAGTACTTATTAATTTCACATTACATTATAAAGTGCATTATTTAAAAAAACAAACCTTATTATTTTTTAAAGAAATCTGTAAAGTTCTCCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9628
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077180 | Nonsense | 515 | 517 | 15 | 15 |
ENSDART00000122665 | None | None | 709 | None | 19 |
ENSDART00000127454 | Nonsense | 515 | 517 | 14 | 14 |
The following transcripts of ENSDARG00000054903 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 26794560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 25175548 |
GRCz11 | 12 | 25266908 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGTGCCCATTAACTGTGGTGCCATAAAGGCGGAGTGTAAGAGCTCTT[T/A]AAATTCCTAACTTCAGCGTCGCGTACAAACACACACACATCCCACATTGT
Long Flanking Sequence:
AAAAACACACTTATTGTGAGCTGCTCAGTTAAAAAGATCAGTGCTGCACATAGCATTAAAAATTTATAGAGTATAATTACAGTGCAATGTCTTGTGCTTTAACAATTGGGAAAAACTGTAATGCATTCTCAGATATTTTAAGAAGAATATAAGCTACCTTACAAGTACTTTCTGAAAATTGTCCTCCTTGTATTTCCCTGTTCTGATACTCTTGCTGTTGTTTTTCCAATATCAATCCAACATTTCCTCACCTGTCTCCTCACAGGAATCACGTTCTCGTGGCCACTGTGCCCGTCAGTCTTCCCACATGGTCCCCATCCGGAACAGTGGTAGCCCAAAATCCTCCATGAAGACCAAGCAGGCGTTCCTCCTGCAGGCAACGCGCCTCACCAAGCTGGCGCGTCACATGTGCCGCGATCTCATCAGGCTGCGCCGGGCCGCGCGCCGCCCCTTTGTGCCCATTAACTGTGGTGCCATAAAGGCGGAGTGTAAGAGCTCTT[T/A]AAATTCCTAACTTCAGCGTCGCGTACAAACACACACACATCCCACATTGTCCCACCCGCTCTGTTCCCCGACCACACCTGTCCACATCTCGCTGTCATCCCCCCCCTCCCTCCATCTTCCTGTCTTGTACTGTTTTTATTATTATAATTATTGCTATTATATTTTATTTTGTTTTTTGTATTCTCCCCACCCCATTTCCAATAAAGACTGCCTGTCCTCCATATTTTGCGTTTCAATCATCTTTTCAGTTCAGATTCACTTTCTTTCCCCCCACATTTAATTGACTTGGTTTAAGGGTGTCATGAGGGCTGTTTAAATTTGACAAGAACATTTTTAGCACTTCTCTCAGTTTGTTGAAGAGAGCTTTTTTATGTGCGCACTACACACACACACATACACACAAATGCCCTATTATGCTTGCTTCACCTTAAATTGTAATTATACTTGAATTGCATATCATAGTCTGAGCCTTATATTTATTAAAGCTTCAGAAAGACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35301
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077180 | None | None | 517 | None | 15 |
ENSDART00000122665 | Nonsense | 582 | 709 | 16 | 19 |
ENSDART00000127454 | None | None | 517 | None | 14 |
The following transcripts of ENSDARG00000054903 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 26799290)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 25180278 |
GRCz11 | 12 | 25271638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGCTTTCCTCTCTTCCAAGTCATGGCCCGCTTGGAATGTTGGGAAAA[C/T]GAAGCTACCATCACCACAGCAGGGTTGAATCTGCAGAAAGGAGGGCTGGT
Long Flanking Sequence:
CAAATGAGATTTGACTCTGCCTGCTGCTTCCATGAAAATCGTTGTCCGGTCAGAAAGATTTGTCACCGCAGGGTTGGTGTTACGCTGCAACATCCATCAAGCCAGCCTGTTCAGAATGCCTCATGTTGGTGTCTAAGTGTGAATGTCTCTTTCATGCTCTTTGACTTGCTTCTATCTCCGTTTGTCTGTTCTGTACTGCTGGTTGATAAATAGATATGATCCGGGTGTCCGAGGGCATGACAGGGAGACCTTTGAAGCCCAAATCTTCTCCCAGGAGCACCCTGACCAGCGTCTTGCAGTATCTTGGTGAGCGACAAGAGATCTGATTTGTCTCCACTGAGTTGTACCTCTCAGATCACAGTGAATCTTCTGTCATTTCAGAGTCCCGTCCAGCAACTCATGTTCAACGGCCTCATCGCACCCCTGGCCTACAGGTGCAGCCTCCACGACGCCTGCTTTCCTCTCTTCCAAGTCATGGCCCGCTTGGAATGTTGGGAAAA[C/T]GAAGCTACCATCACCACAGCAGGGTTGAATCTGCAGAAAGGAGGGCTGGTGCTACAGGACAAGGTGGGTTTACTGTTAAAATGGAAACTAAAATGGAAAGAAAATGTGTAGATTTCTTACTACATACCTCTTTTTTGTCATAGAAAATCCAGCTCATATTGTGGGGCCCATTCTGGTAAGTATCAGACTTTATTTATTGGTAACATTGGGATTGACTGAAGCCAGTTTCTGGAATTTGCTGGTGCTTTTTATTTCTCTTAAAATTGAAAGGTTACATATTAGATAACATCTTACTGGCTTTTGTGTTGTAACCAGGCAACAAGGCCACAGAATGATCGTTTGTGGGAACATCATAGCATGTTGAGGACATGACATGGTAGCTCGTGACCACAAGATCTTAGAGTAGGAACATATTCACATCCAGAGCAATCAGAACAGGCAGGAAATTGCCAGGGCCCCTTATTTTGAGGGTGCCCCCTTGGGATTAGCATTGTGCCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22102
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077180 | None | None | 517 | None | 15 |
ENSDART00000122665 | Essential Splice Site | 602 | 709 | 16 | 19 |
ENSDART00000127454 | None | None | 517 | None | 14 |
The following transcripts of ENSDARG00000054903 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 26799354)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 25180342 |
GRCz11 | 12 | 25271702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACAGCAGGGTTGAATCTGCAGAAAGGAGGGCTGGTGCTACAGGACAAG[G/A]TGGGTTTACTGTTAAAATGGAAACTAAAATGGAAAGAAAATGTGTAGATT
Long Flanking Sequence:
ACCGCAGGGTTGGTGTTACGCTGCAACATCCATCAAGCCAGCCTGTTCAGAATGCCTCATGTTGGTGTCTAAGTGTGAATGTCTCTTTCATGCTCTTTGACTTGCTTCTATCTCCGTTTGTCTGTTCTGTACTGCTGGTTGATAAATAGATATGATCCGGGTGTCCGAGGGCATGACAGGGAGACCTTTGAAGCCCAAATCTTCTCCCAGGAGCACCCTGACCAGCGTCTTGCAGTATCTTGGTGAGCGACAAGAGATCTGATTTGTCTCCACTGAGTTGTACCTCTCAGATCACAGTGAATCTTCTGTCATTTCAGAGTCCCGTCCAGCAACTCATGTTCAACGGCCTCATCGCACCCCTGGCCTACAGGTGCAGCCTCCACGACGCCTGCTTTCCTCTCTTCCAAGTCATGGCCCGCTTGGAATGTTGGGAAAACGAAGCTACCATCACCACAGCAGGGTTGAATCTGCAGAAAGGAGGGCTGGTGCTACAGGACAAG[G/A]TGGGTTTACTGTTAAAATGGAAACTAAAATGGAAAGAAAATGTGTAGATTTCTTACTACATACCTCTTTTTTGTCATAGAAAATCCAGCTCATATTGTGGGGCCCATTCTGGTAAGTATCAGACTTTATTTATTGGTAACATTGGGATTGACTGAAGCCAGTTTCTGGAATTTGCTGGTGCTTTTTATTTCTCTTAAAATTGAAAGGTTACATATTAGATAACATCTTACTGGCTTTTGTGTTGTAACCAGGCAACAAGGCCACAGAATGATCGTTTGTGGGAACATCATAGCATGTTGAGGACATGACATGGTAGCTCGTGACCACAAGATCTTAGAGTAGGAACATATTCACATCCAGAGCAATCAGAACAGGCAGGAAATTGCCAGGGCCCCTTATTTTGAGGGTGCCCCCTTGGGATTAGCATTGTGCCTAGAGGGGTAATAAATGGTAATTCTACTCAGGGGGACCCACCCTGGAATGTGATCATACTGTACCAA
Associated Phenotype:
Not determined