ZMP
mga
Ensembl ID:
ZFIN ID:
Description:
MAX-interacting protein [Source:RefSeq peptide;Acc:NP_001164210]
Human Orthologue:
TBX6
Human Description:
T-box 6 [Source:HGNC Symbol;Acc:11605]
Mouse Orthologue:
Tbx6
Mouse Description:
T-box 6 Gene [Source:MGI Symbol;Acc:MGI:102539]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa865 | Nonsense | Available for shipment | Available now |
sa18203 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa865
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110593 | Nonsense | 525 | 2735 | 2 | 23 |
ENSDART00000137469 | Nonsense | 525 | 2648 | 3 | 24 |
ENSDART00000144408 | None | None | 23 | None | 2 |
ENSDART00000110593 | Nonsense | 525 | 2735 | 2 | 23 |
ENSDART00000137469 | Nonsense | 525 | 2648 | 3 | 24 |
ENSDART00000144408 | None | None | 23 | None | 2 |
The following transcripts of ENSDARG00000078784 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 10028435)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10416889 |
GRCz11 | 17 | 10572923 |
KASP Assay ID:
554-0767.1 (used for ordering genotyping assays)
KASP Sequence:
ACAAGAGACCTGAACGTGTGCCCCTGCCTCTCCTCGCTAAGTTTCTAAAA[C/T]AGAGAAGACCTATTTTGCCCAAACCTGTCTCTCACAGCTCACTCTCAGAT
Long Flanking Sequence:
ATCTCTCTTTCTCTAACAGTAACAAGAAGCGTCCATCCTCATTGGCATTCTCCGACTTCATTAAAGGTGCTCATGTGAAAGTAAAAAGGTTATCACTTGAGAATATCAACAAAACTGGTGGGGCCACGGAGCCATCTACTGCTTGCACAAGTAAACAAAAGGAGGCAGCTGATATATCATCCATAACAGAAAATTCTTTGCAGGTTGATCAAAAAGATGGAAATGGTGCAGGTGATGTTCTCAGATGTGAAAGCACAGACACGTCTTTAAAAACAGGTGTATTAAAAGCAAACGAGATTAAAAAAGAAATTGATGAACACAGTGCTGACAAGAATACATTGAAATCAAGTGACCAAAATCTATCCTGTTCGGATGAAAAAAAAATGGAGACAGTTTCTTCTCTAAGTACTGAAGCCAAGCCCGAGGCACAAATGAAGAAAACCTTACCACACAAGAGACCTGAACGTGTGCCCCTGCCTCTCCTCGCTAAGTTTCTAAAA[C/T]AGAGAAGACCTATTTTGCCCAAACCTGTCTCTCACAGCTCACTCTCAGATTCTGAAAAGTCCTGTGAACCTGCCCAAACCTCTGAAAGCTCATCTGTCTTAATGTCTTTTGTACCTTGTGTTACCACAAACCTTGATTCACAACCAGCAGTTACCTCATTATCTCAGACAGTTACATCATCAACTACAGATGCAAACAACATGACATCTCTGTCCACAACGTTATCATATTCATCGACAACTGTCCCCCTTATACCATCAGAAACACAATTATGTGATAGATTTTCAGCTTCCCCAGTTGGCAGTGATCCATTCAGTGCCCCAAACACTACCTCTCCCTCGAAACCTAATTCTAACCCAGCACTTGACATTTCTAATAACACTGATGCCATTTTCACACCAGATCATGATAACACACTCAGGTCACAGTCAGACATTTCATCCGATTCAACATGTGATGTTGTGCATGACAGTTGTCCACCAACAGTTAACACTGACACT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa18203
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110593 | Nonsense | 2406 | 2735 | 21 | 23 |
ENSDART00000137469 | Nonsense | 2472 | 2648 | 22 | 24 |
ENSDART00000144408 | None | None | 23 | None | 2 |
The following transcripts of ENSDARG00000078784 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 10015611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10429713 |
GRCz11 | 17 | 10585747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATAACCATAAACAACTCACTTCAACCGATTGGCATCACCTCAGTTGGA[C/T]AACAATCATCTACACCAGGTTTGTCTCCAAACAGGTTAACAATTCTTTTA
Long Flanking Sequence:
TGAGTATTAAAAAACAAAAAAGTCCGGAAATGACTGAAAGTGTTCCTAAATCTACACCATCAGTCTCAGTGCCTGCAGACCTTGATGGTAATAAAAACACTCTTAACGTTCTGGATACTAATACAGTAACAACTACATCAACACCTATTCAACCATCTTTCAACTCCACTTTAGTCATGAAACCAGTCTCTATCCCAAGTCCTATTAAACATCCTCCAATCACACGTGAGAGAATGCGGCCAAACATTCTTTCGCGTGCCTCATCTCAGGCGATGCAAGGATCTCCAGTCAAAGAGTCTCTTTTAACTAATGGTTAGTATGAGAGACATTTACATATATTTGCAATGTAGATGCAACTTGGTTTCGGATGTTCACATATTTTGTTGTTTAATTCAGTGTGTATACCTCAAGTATTACCTCTGATGAATACCATGGTTCCATGCAATCAAATCATAACCATAAACAACTCACTTCAACCGATTGGCATCACCTCAGTTGGA[C/T]AACAATCATCTACACCAGGTTTGTCTCCAAACAGGTTAACAATTCTTTTAAAAGTTCTATAATGAAAAAAAAGTGGTTTGTTGATAAGCATTTGTATTGTTGTTTTTATCTTATTCAACTAGGTGTAGCCTCTGTGTCTATAGTTCCCACAATATCTCACCCGCTTCGAGTGGAAAATACTCTTCCTATGTTGCACCCTCAGTTTATTAAAATCACAAACAGTCCTGTTAATATTAACACAAAAGGTAAGTTACCCGTTTACTCTGATTATGTATATTTAGTAAGTTTCCTTTATTTAAACTTCAGAGATGTTCATTTTGATGAGATGTATTTATTTTTAAATGATTGTAATTTTCAGTGGATTCTGCAAGCCTTCCAAATATCAGCAATGTTATTTCTCTGGCGGAGAATCTAGTAGTACCACGGAAAGTTGTGGAAGATAAACCTGTTTTCCAAGCACAGCCAACATCTGTGGACAATCAGCAGAATTCTTCCAATGA
Associated Phenotype:
Not determined