ZMP
dmbx1a
Ensembl ID:
ZFIN ID:
Description:
Diencephalon/mesencephalon homeobox protein 1-A [Source:UniProtKB/Swiss-Prot;Acc:Q8JI10]
Human Orthologue:
DMBX1
Human Description:
diencephalon/mesencephalon homeobox 1 [Source:HGNC Symbol;Acc:19026]
Mouse Orthologue:
Dmbx1
Mouse Description:
diencephalon/mesencephalon homeobox 1 Gene [Source:MGI Symbol;Acc:MGI:2153518]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32849 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2052 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32849
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017173 | Essential Splice Site | None | 388 | 2 | 5 |
ENSDART00000128535 | Essential Splice Site | None | 383 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 9977497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 10390780 |
GRCz11 | 2 | 10188600 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTAATCTTCACACTAATAACATACGTGTTTTTCTTTTCTTTTCTTGTAC[A/T]GATAAGTGTGAATCATGCAGCACTACGGAGTGAACGGATACTCTCTCCAC
Long Flanking Sequence:
AAAAGCGTTATACTCTCGCTATAAAGTGACAACCTTTTTGATTGATTGTGTCTCACTAGGCGCATATCCTCCCCCAAAAGTTTATAAAGAAAAATATTTGTTTTAAAAAAACAAACAATGCGTATTTAAAGGCCAAATAAACTGTACCTTGCAGTAAACAATTGAGTTATTTTTTATCTTAGAAATATTTTTAAATCAATACGAATTATTGACAGAAGAAAGCATTTAAACGTTTATCGTGAATTTTGACAATCAGTAAACTATTAAATTTAGCTGTTATAATTAAATTAAACAAACATTCGGGTAAAATAAATCTATGAGTGCAAATGTCATATCTACCCCAAATACCTAACATTTAAAATGCGTTCAAGATGCTGCTATAGCCTATCGAACTTTAGTTTGAAAGCATATTTAAACCACGTTTTTTTTCCAAAAAAACAAAAAATTAAATCTAATCTTCACACTAATAACATACGTGTTTTTCTTTTCTTTTCTTGTAC[A/T]GATAAGTGTGAATCATGCAGCACTACGGAGTGAACGGATACTCTCTCCACGCCATGAACTCACTGAGCGCCATGTACAACCTGCATCAACAGGCGGCGCAGCAAGCGCAGCACGCGCCTGATTACCGGCCGTCCGTTCACGCACTCACCCTGGCAGAGAGGCTGGCTGGTAAGCGCGTTCTCGCCCACTACCTTTACACACTAATCGATGGTTAAAGTACAATGAATTAAATATGCCGTGTCTTTTCTCTTCCAACGGCTGTACATTTCAAGATATCATACTTGAGGCTCGCTACGGCTCTCAGCATCGCAAACAACGGCGCAGTCGCACCGCTTTCACGGCCCAGCAGCTGGAGGCTTTGGAAAAGACTTTCCAGAAGACTCACTACCCAGATGTGGTGATGCGGGAGCGGCTAGCAATGTGCACCAACTTACCCGAGGCACGCGTGCAGGTAACAAACCGCCTTCAAAAATATCTATCCACAAAAATCTTTACAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2052
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 |
---|---|---|---|---|---|
ENSDART00000017173 | Essential Splice Site | 51 | 388 | 2 | 5 |
ENSDART00000128535 | Essential Splice Site | 51 | 383 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 9977328)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 10390611 |
GRCz11 | 2 | 10188431 |
KASP Assay ID:
554-3027.1 (used for ordering genotyping assays)
KASP Sequence:
TGATTACCGGCCGTCCGTTCACGCACTCACCCTGGCAGAGAGGCTGGCTG[G/A]TAAGCGCGTTCTCGCCCACTACCTTTACAMACTAATYGATGGTTAAAGTA
Long Flanking Sequence:
TTTTTTATCTTAGAAATATTTTTAAATCAATACGAATTATTGACAGAAGAAAGCATTTAAACGTTTATCGTGAATTTTGACAATCAGTAAACTATTAAATTTAGCTGTTATAATTAAATTAAACAAACATTCGGGTAAAATAAATCTATGAGTGCAAATGTCATATCTACCCCAAATACCTAACATTTAAAATGCGTTCAAGATGCTGCTATAGCCTATCGAACTTTAGTTTGAAAGCATATTTAAACCACGTTTTTTTTCCAAAAAAACAAAAAATTAAATCTAATCTTCACACTAATAACATACGTGTTTTTCTTTTCTTTTCTTGTACAGATAAGTGTGAATCATGCAGCACTACGGAGTGAACGGATACTCTCTCCACGCCATGAACTCACTGAGCGCCATGTACAACCTGCATCAACAGGCGGCGCAGCAAGCGCAGCACGCGCCTGATTACCGGCCGTCCGTTCACGCACTCACCCTGGCAGAGAGGCTGGCTG[G/A]TAAGCGCGTTCTCGCCCACTACCTTTACACACTAATCGATGGTTAAAGTACAATGAATTAAATATGCCGTGTCTTTTCTCTTCCAACGGCTGTACATTTCAAGATATCATACTTGAGGCTCGCTACGGCTCTCAGCATCGCAAACAACGGCGCAGTCGCACCGCTTTCACGGCCCAGCAGCTGGAGGCTTTGGAAAAGACTTTCCAGAAGACTCACTACCCAGATGTGGTGATGCGGGAGCGGCTAGCAATGTGCACCAACTTACCCGAGGCACGCGTGCAGGTAACAAACCGCCTTCAAAAATATCTATCCACAAAAATCTTTACAATTTTAAAATCTTTTAAAGTTCTCCACAACTTCACATTCATCATGTGCCTACAAATTGACTTTTGGCCATCAGGTATGGTTCAAGAACCGCCGGGCTAAGTTTCGCAAGAAGCAGCGAAGCCTCCAAAAAGAGCAACTTCAAAAGCAGAAAGATGTCTCGACAGATGGAGCCC
Associated Phenotype:
Not determined