ZMP
dlx4a
Ensembl ID:
ZFIN ID:
Description:
Homeobox protein Dlx4a [Source:UniProtKB/Swiss-Prot;Acc:Q98879]
Human Orthologues:
DLX1, DLX6
Human Descriptions:
distal-less homeobox 1 [Source:HGNC Symbol;Acc:2914]
distal-less homeobox 6 [Source:HGNC Symbol;Acc:2919]
distal-less homeobox 6 [Source:HGNC Symbol;Acc:2919]
Mouse Orthologues:
Dlx1, Dlx6
Mouse Descriptions:
distal-less homeobox 1 Gene [Source:MGI Symbol;Acc:MGI:94901]
distal-less homeobox 6 Gene [Source:MGI Symbol;Acc:MGI:101927]
distal-less homeobox 6 Gene [Source:MGI Symbol;Acc:MGI:101927]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40108 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2124 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa40108
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000007073 | Nonsense | 55 | 250 | 1 | 4 |
| ENSDART00000133457 | Nonsense | 55 | 250 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 34755711)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 34540907 |
| GRCz11 | 3 | 34670415 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGCGCACTATCCGGTGCACGGTTTGCATCAAGGCGCGCATTCGCAATA[C/A]GACGCGGCCTTCTCTCCTGGCGCTGCGTCTTACAGCCGTCCACTCGCTTA
Long Flanking Sequence:
AAAAAAAAAGAAATATAAACACCCGTCTAAAGGCAAACTGCAATGCTATGCGCATATTACACTGTCGTGACGTCACAGAGAATAAAGAAACGATGCGGTCTGCGCACGCAGCCAATAAGAGCGCATTGCGTTCTCACTGCAGGAATCAACTCAGTATGTGACGACGCTGTTGAGATGAAGTTCTCAGACTTCACACACGGCCAAAACGAAAGCAAACGCACCAGCCCCACGGACATGGATCTCTTTGATGGCCCTCTTTAAGAGATGGAAATTACATGACTTCTAAATAGATGCCACTTTTATGGTGCACCGGTCTAATGGACATAACTCTAAAACATGACTATGACTTCATTGTCTGAAAGTTTGGAGGCTTCAGATCCCTCAAAGTCGGCTTTTCTGGAGTTCAGTCACGGTTACCAGTCTCACCAGCAGCATTCACCCGGTGTGTCTCACGCGCACTATCCGGTGCACGGTTTGCATCAAGGCGCGCATTCGCAATA[C/A]GACGCGGCCTTCTCTCCTGGCGCTGCGTCTTACAGCCGTCCACTCGCTTACCACTATTCCACCGCACACCACCATCCAGGAGCTTACCTACCCTATCAACACAACAGCGCAGTCGGATATTCAAGAGTTGAGGATGCAGGTAAAGTGTGCTCTCATTCACTCACTAAAAATGGCATTGGAAAATTATGATACAAGGCGCTGGATTTCTGACAAATTTTACAATTGTGCAGTTTGGGCTCCATATTATTGTACTTTAAATATCTTTAATCACTTAGCTATTTGATTATTTTTTAAATCAAAAAGTAAAATTGATCCTGTGGAATTTATCGACGTTTTTTGTACGTTTACAAATTTGAAACAAACTGAGAGCCTTAAAAATATATGGAGAAATTAAGAAGTGTCTATATTTATTTAGACATAAAATAGACTTAAAATAATTATTTGTAAAAAAAAAAACAGTAGCTAAACTGACATATAAACGGGTGCATTTTTCATTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2124
Status:
F2 line generated
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000007073 | Nonsense | 228 | 250 | 3 | 4 |
| ENSDART00000133457 | Nonsense | 228 | 250 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 34766381)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 34551577 |
| GRCz11 | 3 | 34681085 |
KASP Assay ID:
554-3326.1 (used for ordering genotyping assays)
KASP Sequence:
TGGGATGTTTCCATGCCCAGCAAAGGTGCTCCCATCCACTCTGGAGGATA[T/A]ATGAACTCTTTCGGACACTGGTACTCGGGTCATCATCAAGACCCAATGGC
Long Flanking Sequence:
GTAATTGCAGCTTGAAATTTGGTTCCAGAACAAACATTTCAATTACAAAAGAAATGTATGAAAATGTATAAAGTTGCATCATGCATGCATATAATAATAATTATAAAATAACAAAAATGTTTTGTTTTTTTTATTTAAAATAAAGGTTACAACTCCCTCACCCTAAACAAATCTATTTTAATTAAATATTTAAACAAATAATACATTTCTGTATTTTAATAAACTGATATTTAAATGAATTCAATTTCTGCATTTTATATTTAATGAGTTTCACAATATTTGTTTCATCAAAGTAAATGATTTTGCATATTGCAGGTCAAGATATGGTTCCAGAACAAGCGTTCCAAGTACAAAAAGATCATGAAACATGGCTCAAGTGGACCTGAAGGAGAACACCTTCAAGCAGCGTCTGCTTCAGGAGCCCCATGTTCACCAGGCATGCCACCCCTATGGGATGTTTCCATGCCCAGCAAAGGTGCTCCCATCCACTCTGGAGGATA[T/A]ATGAACTCTTTCGGACACTGGTACTCGGGTCATCATCAAGACCCAATGGCCAGAACTCAGATGATGTGATGGGACGTTTAGAACAATCTACAGTGTTTCCACGTCCCATCTACTGATTCCAGCAGTTCACACCAGCACTCTTTAGCACTGCGTACTCCGCCAAACATCCTTCCCAGTATTTTCCTCATAAAGATTTACATTGCTGACATTTTGGTTTATTTGCTTGCAGGTTTTTGTGGTGGATTTAAAAAAAAAAGACTGAATAAACAGCCTAACCTGAACTTGGATTTTTGTATGTTCTTGTAAATTTGAATAAAATGCCTTTGTCTGATTGTCATAAATGTCTATTTAATATTTTAATATCCTCAGTTCTCTCTCTGAAATATTTATCGGTCTGTTGCATGATATTTTTCTTTGGTTTAAAGAAAACAGCAGTGTTGAATTTTGCTTTGTTTTTCAATGTTTTCAGTTTGACCCGTTCATTAATATACACTTGAATG
Associated Phenotype:
Not determined