ZMP
hoxc3a
Ensembl ID:
ZFIN ID:
Description:
Homeobox protein Hox-C3a [Source:UniProtKB/Swiss-Prot;Acc:P28174]
Human Orthologues:
HOXA3, HOXB3, HOXD3
Human Descriptions:
homeobox A3 [Source:HGNC Symbol;Acc:5104]
homeobox B3 [Source:HGNC Symbol;Acc:5114]
homeobox D3 [Source:HGNC Symbol;Acc:5137]
homeobox B3 [Source:HGNC Symbol;Acc:5114]
homeobox D3 [Source:HGNC Symbol;Acc:5137]
Mouse Orthologues:
Hoxa3, Hoxb3, Hoxd3
Mouse Descriptions:
homeobox A3 Gene [Source:MGI Symbol;Acc:MGI:96175]
homeobox B3 Gene [Source:MGI Symbol;Acc:MGI:96184]
homeobox D3 Gene [Source:MGI Symbol;Acc:MGI:96207]
homeobox B3 Gene [Source:MGI Symbol;Acc:MGI:96184]
homeobox D3 Gene [Source:MGI Symbol;Acc:MGI:96207]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32461 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32461
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082472 | Nonsense | 24 | 254 | 3 | 5 |
ENSDART00000082473 | None | None | 250 | 1 | 2 |
The following transcripts of ENSDARG00000070339 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 36196709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36046362 |
GRCz11 | 23 | 36145165 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGAGTGCGCAAGGCTATTGGAGGAGGCCACCACGTGACTACATTGTTTA[C/A]TCTTGTTGGCAAACAATTAAAGACGCGAGTAAGTGTATTTTTTGGCTTTC
Long Flanking Sequence:
GCAACTGAAGAACATTGGCAAGCGTAAGGAACTGTTGTTAGATCAGCAAAGTGTGAAATGAATAGTTATTTAACCATAAAGCTAAACAAGTCGATCATTTTTAAATACCTACCACAAGAGGACTGAAAAGTCAGTCAAAGATTTAAACATTGTTTTATAAAACATTATCACGGAAATTAAGTCAGTATTCTTCAATCCATTGAAGCAAAAACTAAGACGACGCGATCCCAGACATGTCTTTTCTCTGTCCAAAATGGGTCTCTCTCTCTCTCCCTCCCACCTCACGCTCTCTGAACTCGTGTCAGCACGATGACAGGGTAATGTATGCGCCCTGCTCATGGTTTTTCGTCTGTCCACAGGAAAATCACTCGAAATGGCAAAACAGTCGAAGAATGCGGATGAAAACGGAATCACCGTTTGGCTGCTTACATGCAGTTTACAACTCAAACACCGAGTGCGCAAGGCTATTGGAGGAGGCCACCACGTGACTACATTGTTTA[C/A]TCTTGTTGGCAAACAATTAAAGACGCGAGTAAGTGTATTTTTTGGCTTTCCTACACCTCGAATGAACAATTATATATTTCGGGTGATTAGGACGATTAGAAATGAACAATAACTCGTTTCACGAATATAATTTTAACAGTGAATACTTAAACAAAATATGTTGCAATAAATCTTATGTTTGTTATATGGGGCAACATTTCTCCCCCTGTGCTCTGCAGGAGAACAGTTCTACGTGGAAACGACATGCTGAAGAAAGTTCATCAGAAAATGATAAAGGCAACGTGTGGAACTTTCAAAACCTCTCGAATGTCCAACATCCCTATTCATTCTCTGATGATGGCAACCACTCTTTGGACCCTGCGAATGCATTGGAAAGAGAAAAGGCATGTGAGCTGTCAACTTCCTGCTTATCAACCATGAAGTACCCTTGGATGAGAGAGACACATGCACCCACGCACTTCAGCTCCATTAACGCCATGGAATCAGGTGAGAGAACACGA
Associated Phenotype:
Not determined