ZMP
hoxd3a
Ensembl ID:
ZFIN ID:
Description:
Homeobox protein Hox-D3a [Source:UniProtKB/Swiss-Prot;Acc:O42370]
Human Orthologue:
HOXD3
Human Description:
homeobox D3 [Source:HGNC Symbol;Acc:5137]
Mouse Orthologue:
Hoxd3
Mouse Description:
homeobox D3 Gene [Source:MGI Symbol;Acc:MGI:96207]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38720 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21417 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38720
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 |
---|---|---|---|---|---|
ENSDART00000082359 | Nonsense | 14 | 403 | 1 | 2 |
ENSDART00000146131 | Nonsense | 14 | 396 | 1 | 2 |
The following transcripts of ENSDARG00000059280 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 1929850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 1938254 |
GRCz11 | 9 | 1939051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCTTCGCAATGCAGAAAGCCACTTATTATGACAATGCTGGACTTTTC[G/T]GAGGATATTCGTACCCTAAATCTGACTCCTACACGTACGGTCCAACACAC
Long Flanking Sequence:
TTTCCTATAACTTTGCCATCTGTGGTGTAATGCATTATGAAAATATAATTTGTTAAGCAATATTCATGAAATCCTCAATATAAGGAGGAGAAATGGAATCAAGCTTAACATCTGACACCAGTAATTGCAGAATTGGGAGAAATCTTTGTTCATCTGATATTTGAATGGTGAAGAGGCCATGATTTAATTTGCAGTGGGATCCATTTACATGATGTTTAGATTTGCAAAAAGGCATAGTGGTGTATGCATTTATGGAGGTTTTTATTATTTAAATATGAGGTCTCATTCTTTGTGATCTCGTATCCATGATTGTTTCAAGGTCAATGCAATCTTTACTAAAACTGGCTTATTTTCTTAGCAGGTCAAAGGACAGAAAATCTGTGGGAAGCTCCAATCACGTGATTCACAAGTCCATGCTATTGGACAGGAGTTCACAGGATCTCTAAGTTTGAACCTTCGCAATGCAGAAAGCCACTTATTATGACAATGCTGGACTTTTC[G/T]GAGGATATTCGTACCCTAAATCTGACTCCTACACGTACGGTCCAACACACCAGGGCTTCTCATCCTCCAGTATAGAGAATGACTATCAAAGCCCAATTTGTCCAATTCAAACTACATCAGTCCGGCAAGCAACCCATAAAAACGGAGACATCAATGGCAGTTGTATGCGACCAAGTGCCAGTCAGGGCAACAGTCAGCCAGAGAGTATCAGTGAGCAGCAGCAGGCTGCTCCATTAGCGGCCAGCTCTCCCAGCCCCAGCACTAACTCCACACAAAAAAAGAAATCCCCCAGCTCTAATGGATCCAGCACTGCCACCCCAGTCATCTCCAAGCAAATTTTCCCCTGGATGAAAGAGACCCGCCAAAATGCAAAGCAGAAAAGCACCAACTGCCCAGCAGCAGGTATGGGCTTTGCTTGAGTGAGTGTGTGTGCGCGGCTGGAGAGAATAGTTTTATCTACCCAGTATAAGATGAATAACTACAGTCGGAGACAGCTACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21417
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 |
---|---|---|---|---|---|
ENSDART00000082359 | Essential Splice Site | 147 | 403 | 1 | 2 |
ENSDART00000146131 | Essential Splice Site | 147 | 396 | 1 | 2 |
The following transcripts of ENSDARG00000059280 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 1929447)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 1937851 |
GRCz11 | 9 | 1938648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGACCCGCCAAAATGCAAAGCAGAAAAGCACCAACTGCCCAGCAGCAG[G/A]TATGGGCTTTGCTTGAGTGAGTGTGTGTGCGCGGCTGGAGAGAATAGTTT
Long Flanking Sequence:
TCACAAGTCCATGCTATTGGACAGGAGTTCACAGGATCTCTAAGTTTGAACCTTCGCAATGCAGAAAGCCACTTATTATGACAATGCTGGACTTTTCGGAGGATATTCGTACCCTAAATCTGACTCCTACACGTACGGTCCAACACACCAGGGCTTCTCATCCTCCAGTATAGAGAATGACTATCAAAGCCCAATTTGTCCAATTCAAACTACATCAGTCCGGCAAGCAACCCATAAAAACGGAGACATCAATGGCAGTTGTATGCGACCAAGTGCCAGTCAGGGCAACAGTCAGCCAGAGAGTATCAGTGAGCAGCAGCAGGCTGCTCCATTAGCGGCCAGCTCTCCCAGCCCCAGCACTAACTCCACACAAAAAAAGAAATCCCCCAGCTCTAATGGATCCAGCACTGCCACCCCAGTCATCTCCAAGCAAATTTTCCCCTGGATGAAAGAGACCCGCCAAAATGCAAAGCAGAAAAGCACCAACTGCCCAGCAGCAG[G/A]TATGGGCTTTGCTTGAGTGAGTGTGTGTGCGCGGCTGGAGAGAATAGTTTTATCTACCCAGTATAAGATGAATAACTACAGTCGGAGACAGCTACTATCATTATGACCCAGTTCCTTTTGTTTACAGTAGGCTGTCTCGCTTTGGCCTTTAAGTGATGTAATAGGCTGTGTAACACAATTAATCCATTGCACATTTCTGCTCTTTGTGTTCAGGAGAAACCTGCGATGACAAGAGTCCGCCTGGCCCTGCGTCGAAACGAGTGCGCACTGCCTACACCAGCGCCCAGCTAGTCGAGCTGGAGAAGGAGTTTCATTTCAACCGCTACCTGTGTCGCCCCAGAAGAGTGGAGATGGCCAATCTGCTCAACCTCACCGAGCGCCAAATAAAGATCTGGTTTCAAAACAGAAGGATGAAGTACAAAAAAGATCAGAAATCTAAAGGCATAATGCACTCTCCCTTAGGACACTCTCCGGACAGGAGCCCGCCGTTAAGTGGCTCG
Associated Phenotype:
Not determined