ZMP
rx3
Ensembl ID:
ZFIN ID:
Description:
Retinal homeobox protein Rx3 [Source:UniProtKB/Swiss-Prot;Acc:O42358]
Human Orthologues:
RAX, RAX2
Human Descriptions:
retina and anterior neural fold homeobox 2 [Source:HGNC Symbol;Acc:18286]
retina and anterior neural fold homeobox [Source:HGNC Symbol;Acc:18662]
retina and anterior neural fold homeobox [Source:HGNC Symbol;Acc:18662]
Mouse Orthologue:
Rax
Mouse Description:
retina and anterior neural fold homeobox Gene [Source:MGI Symbol;Acc:MGI:109632]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29528 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29528
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074833 | Essential Splice Site | 151 | 292 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 9292441)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 10664494 |
GRCz11 | 21 | 10757122 |
KASP Assay ID:
2261-5277.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGAGGAGCTCGCGCTGAAGGTCAACCTGCCCGAAGTCCGAGTACAGG[T/G]GAGAGACACTTTATTCTGTTCAAACTAATACAGCAATAATAAATATTGTA
Long Flanking Sequence:
TTTATGCACGTGTGTTTAGTACATTTTAGATTTCAGTGTTTAAAAAGTAGGTTAAATTTTTTTTTTTTTCAAAATTAAACAATGAAAAATGAACAGAAAATCTTAAGTATGCTATTTTAATTGAAAAGGTAATAAGGCATATAAATATGTGAAATATGGTAATCAAAGTTGTCAAAAATATGTCAGAATTATAAATATGAACATGTTGCACTTTCTCACATATTTCTCACTGTTGGTTTTTTTTTTTTTTTTCTCTCTCTCTCTTTATGCAGGAGTTTGTAGGTCGACTGTAATGGTCAGCCCAGATCTGCCAGACGCGGATGGTGGTAAATTGTCGGATGATGAAAACCCGAAGAAAAAGCACCGGCGGAACCGAACCACGTTCACCACCTTCCAGCTCCACGAGCTCGAGCGCGCCTTCGAGAAGTCGCACTATCCGGATGTCTACAGCAGAGAGGAGCTCGCGCTGAAGGTCAACCTGCCCGAAGTCCGAGTACAGG[T/G]GAGAGACACTTTATTCTGTTCAAACTAATACAGCAATAATAAATATTGTATATATGTATTTATTTGTTTAAAGATGGAGAAGTATAGGCTACTAAAATACAAATTCCACTTCTAACTTTTATGTCACTGAAAAAAATGTTTCATTGGATTTGCTGAATTATTTTAAGGTAAATTGTTGCAAACAATTTATATGGGCTAAAATTAAACAAGTTAAGTTGAAAATTACTAAATTTTTAACTCGTTTGTTTAATTCAGCCCATATAAACTGTTTGCAACTTAAACAAATAAATCCAATTAATAATTTTATTTAGTGTTGGCTATATGAAGTTTACTTGCAAAAAAACGGTTACTCTGTACAGATTTTTATAAATCCTGTTTTATTGTAGTACATTGAAGATATCATTATGAAAAAGAATTGTAAAAAATGATTGATGATAGTATAAAAACATTAATAAAACTAGTATATATTCTTTATTATGCGATTGTTAAATGTAAAGTAT
Associated Phenotype:
Not determined