ZMP
meox2b
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC566969 [Source:RefSeq peptide;Acc:NP_001038589]
Human Orthologue:
MEOX2
Human Description:
mesenchyme homeobox 2 [Source:HGNC Symbol;Acc:7014]
Mouse Orthologue:
Meox2
Mouse Description:
mesenchyme homeobox 2 Gene [Source:MGI Symbol;Acc:MGI:103219]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23555 | Nonsense | Available for shipment | Available now |
| sa16561 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23555
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088618 | Nonsense | 57 | 289 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 32429061)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 31596350 |
| GRCz11 | 19 | 31183663 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGGACCTTCACCGCCCTGCAGCTACGCCGGGGAGGAGAGCAGTTTTGGA[G/T]GAGCTCATCACAGAGTTCACCCCGCTCCGCAGCATCCACATCACCCGCAG
Long Flanking Sequence:
GCACCGCCGTTCAACCCCCCCTCCCTCGTTCCCTCGTTCCCTCGCTCCAACTCCACTTCTCCAGCAGTGCAGTCTCCACTTGGGCCCCGACAGCTCTGTCTATCTCTCTCTTTCTCTCTCTCTCTCTCTCTCTCTCTACCCTCGTCTGTCACCCGAGCTTCCTCTTTCGCAGGGTGTGTGTGTGCGTGTGTGTTTACCCTCTTTTTCGGCCTGGCAACGGGGCTGCATGCTCAGGATTACCGGAGGCCTTGCCTTTCATCGCCCTCTTCCTTTCGCCTGGACTACGGAGGCCACGGGTGCGAGGCTGTGTGTTTTCTGTGGATCTGTAGATCATGGATCACTCTCTGTTCGGATGCCTTCGAAACCCACATGCCCCGTCTCAAGCTCTGCACCCGGCGTTCACCCAGGCACTCCATGGCCGCTCTGATCACATCTCCTACCCCGACCTCCCGGGACCTTCACCGCCCTGCAGCTACGCCGGGGAGGAGAGCAGTTTTGGA[G/T]GAGCTCATCACAGAGTTCACCCCGCTCCGCAGCATCCACATCACCCGCAGCATCATCAGTGGCACGTCCCACAGATGCCGTCAATAGAGAGTGAGCGGCACGGGCTCTGTCTGCCGCACCCGGACGCTGCTGCTCCAGAACTGTGCGGCACTGGAGCGGGTTCGCAGGGCATGTGCGCCGGTAACCCAACACTCACTGGAAGTGACCCTTCTGGGGTGTCATGCGTGCCTGGAGAGTACGGGAGACAGAACATGTCACCTGTTGAGCCGGAAAGAAGGAGCAGCAAAGGAAAGAGCGACAGTTCAGGTACGTGGACCACAGTGTTGTCTTTCTCGTTCTTTTGCATTCAGAAGAAAAGAAGTGGTTTAGTAAATTTTTAGAAACTTGTTACATTTATTATTTATTATTAGTGTCCAAGTCATGACTCGAGAAGTGAATTTCAATTCTAATTAAACTTGATCAGAATAGTTTATGACTCTCATTTTGGTCAGGAATTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16561
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 |
|---|---|---|---|---|---|
| ENSDART00000088618 | Nonsense | 161 | 289 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 32433940)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 31601229 |
| GRCz11 | 19 | 31188542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGCATTTACAGCGGCTGGAAAGTGATCTGTTTTTCATTTCAGATTCC[C/T]AGGATGGGAGCTATAAGTCAGACRTGAGCAGTAAACCTAGGAAGGAGCGC
Long Flanking Sequence:
TTTTTGCTGAATTTAGTTGTACCTCATAATATGATATATCATAACTATTTCTATAACTATAATAAATGAAGTAAGAAACTTTAGTCAACACGGTTACAGTGAGGGTTGAAGTTGACAATTATTGGACCAATCAGAAATGTTCCTTCAATGAATTCTATTAAAGGAGCCATGTGTGGAAATCGAAGGGTAAATTGATCTGATTGTTGGAGAGTGTGAACGAAGCCCTGGTGATTCAGGCCAGATTTGAGAGCATGTGCTGGGCTTTCTGGCTCCGTCTCTGCTTGCTAAAAAACCCCACCGCCGTATCGCCATAATAAAGCCTGATTGGCAGGCCAAATTGTTCCGCTTTCATTTTTATTTTTGTTCGTTTATTTTATTTCAGAGCCCTGCAGTTTATCACACCATCTTATTTTTTCCCCCCTTTTTTTGCTTTTTCCCCCCCTTCTTTTTCTGTGCATTTACAGCGGCTGGAAAGTGATCTGTTTTTCATTTCAGATTCC[C/T]AGGATGGGAGCTATAAGTCAGACGTGAGCAGTAAACCTAGGAAGGAGCGCACGGCGTTCACCAAGGAACAGATTCGAGAGCTGGAGTCAGAATTCGCTCACCACAACTATCTGACACGGCTTAGACGTTACGAAATCGCTGTCAACCTTGACCTCACAGAGAGACAAGTACGTTGAGCTGCTTTTGCATGTTATCTGGAGACATAACACTGGCACTTCCTTTGGCTTTAAAAATATGGAGGAATAAAATAGGCTGACTCCTGACAATAGGCTGACTTGAAGTGATTAAGTTGTACAAAGTGATAAACACAATGCTTTATGTTATTCTGTAAAAGCAATTGCTTTCAATCGTGAAGTTGGATCAAGTTACCGTTAAACAACTTTTAAATTGCATTGCATTAAACGGACTTATCACCTCTTATATGACTTAAATTGTTAAATTGAATAATGATTAAAGGGATAGTACACCCAAAAATGAAAATTTACTTATTTTCTCACTCT
Associated Phenotype:
Not determined