ZMP
dlx5a
Ensembl ID:
ZFIN IDs:
Description:
Homeobox protein Dlx5a [Source:UniProtKB/Swiss-Prot;Acc:P50576]
Human Orthologue:
DLX5
Human Description:
distal-less homeobox 5 [Source:HGNC Symbol;Acc:2918]
Mouse Orthologue:
Dlx5
Mouse Description:
distal-less homeobox 5 Gene [Source:MGI Symbol;Acc:MGI:101926]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13174 | Nonsense | Available for shipment | Available now |
sa39257 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13174
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062026 | Nonsense | 72 | 281 | 1 | 5 |
ENSDART00000113388 | Nonsense | 72 | 282 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 42443772)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 41886786 |
GRCz11 | 19 | 41471841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTRTTGTTCACCGAACTCGGGCWCCTATGGGAAACCTCTTAATGCCTA[T/G]CAGTACCAATACCACGGAGTCAATGGATCTTCTGGAAATTACTCTGCAAA
Long Flanking Sequence:
GTTTGTAAACATACCATAAATACCTCTATTAAGTTTTTTTGTTCATCTGAAACTGGTTGAACGAGTTGGGGAGTAACTGCCTGTCTGCTGTGCTCCTTGGCCAATGGCACTGGATCCTCCCTGCAGTGCGTAACAGCGCAATTTAGGATTTAACCAAGTCTTTGCTGCGGGGCTTAAAGCAGTCTTCAAGAGAGACGCTTGACGCTTGCACGCACAATGTTAGTGTAGACTCTTTGGACCCCTATAGAGTTAGACTGCCTTTTTTTACGTCGTCTTATCCAAACTATGACTGGAGTATTCGACAGAAGGATTCCGAGTATTAAACCTGCAGATTTTCAAAACCCTTTTCAGCTCTCCACGATGCATCATCCGTCTCAGGAATCTCCAACCCTACCGGAGTCCACAGCCACGGATTCTGGCTATTACAGCCCTGCCGGAGGAGTTCATCATGGCTATTGTTCACCGAACTCGGGCACCTATGGGAAACCTCTTAATGCCTA[T/G]CAGTACCAATACCACGGAGTCAATGGATCTTCTGGAAATTACTCTGCAAAATCCTACCCTGATTACGGCTCATACTCCACAGCGTATCACCAATACGCAGGAACATATAACAGAGTGCAATCACAACCGAGCCCGCAAGGTTAGTTGTTATATAAAATTATTTAAAGCATGTTATTATTATTATTATAGTTGTGGTGGTTGAAGATTATTATTTAACATGTTATATAACACGTGTGTTACTTCTTATAATAAAAATACTTAGGCTACTTGGATTAAACACTGCAGCATTGTGCATTACGCACTGTCGGTTTTTGAAAATAAAAATACACGGAATATGGAATATCAAACTATTATACTTCTGAGCACGTTAAATGCGTAATGAGTTGAGTTTTTTTTTTGTGACAAAAATCAAGCCTGATTATTAAGCACTGTGATATTTAGTTTAAATCACGGTAATTATTACAAACAAAGGCGCATTTCTACTCTCAAGTATTCATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39257
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062026 | Nonsense | 126 | 281 | 2 | 5 |
ENSDART00000113388 | Nonsense | 126 | 282 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 42443231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 41886245 |
GRCz11 | 19 | 41471300 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTCATCTAATTTCTGTTTTATTTGCCAGAAAAAGAAACAGCCGAGCCC[G/T]AAGTAAGGATGGTCAACGGAAAACCCAAAAAAGTCCGGAAGCCCCGAACC
Long Flanking Sequence:
ACTCTGCAAAATCCTACCCTGATTACGGCTCATACTCCACAGCGTATCACCAATACGCAGGAACATATAACAGAGTGCAATCACAACCGAGCCCGCAAGGTTAGTTGTTATATAAAATTATTTAAAGCATGTTATTATTATTATTATAGTTGTGGTGGTTGAAGATTATTATTTAACATGTTATATAACACGTGTGTTACTTCTTATAATAAAAATACTTAGGCTACTTGGATTAAACACTGCAGCATTGTGCATTACGCACTGTCGGTTTTTGAAAATAAAAATACACGGAATATGGAATATCAAACTATTATACTTCTGAGCACGTTAAATGCGTAATGAGTTGAGTTTTTTTTTTGTGACAAAAATCAAGCCTGATTATTAAGCACTGTGATATTTAGTTTAAATCACGGTAATTATTACAAACAAAGGCGCATTTCTACTCTCAAGTATTCATCTAATTTCTGTTTTATTTGCCAGAAAAAGAAACAGCCGAGCCC[G/T]AAGTAAGGATGGTCAACGGAAAACCCAAAAAAGTCCGGAAGCCCCGAACCATTTACTCCAGTTTCCAGCTCGCAGCTTTACAGAGAAGGTTTCAGAACACGCAATACCTCGCGCTTCCAGAAAGAGCCGAGCTCGCCGCATCGCTGGGACTCACACAGACACAGGTTCGCACAATTTCCTGGAATATTTTATTGCAATCTATTTTATGTTTAAAGCTGAACATAAAATTATACCTCTAGATTTGTATTGGTGGTTAAATATTATAATGTTAAATATTCTGCAACATTAAGATTCGTTTGCATGCATGACTTTTTATAGCCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAACACAAGCTGTTAAAATAATGTTGACATTTCTTTGAAGAATTTTCGACAACACACTTTACTCAGGGATTTTCCCCAGAAATTAATAACCCCTTTTTCTTTATCGCAGGTGAAA
Associated Phenotype:
Not determined