ZMP
zgc:101072
Ensembl ID:
ZFIN ID:
Description:
retinoic acid induced 14-like [Source:RefSeq peptide;Acc:NP_001104687]
Human Orthologue:
RAI14
Human Description:
retinoic acid induced 14 [Source:HGNC Symbol;Acc:14873]
Mouse Orthologue:
Rai14
Mouse Description:
retinoic acid induced 14 Gene [Source:MGI Symbol;Acc:MGI:1922896]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31057 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa37278 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31057
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058485 | Essential Splice Site | 56 | 988 | 3 | 18 |
| ENSDART00000058487 | Essential Splice Site | 56 | 186 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 18398170)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 19533659 |
| GRCz11 | 21 | 19570295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAAAAAGGAGCCTCTCCTACCAAACTTGACAGCGAGGGCAAGTCTGC[G/A]TAAGTATCAGGAACTGAAGCTGTTCTGTTTTCTATTTGATTTGCTCCTTT
Long Flanking Sequence:
TGAACTGCAGCAGATCGTCTTGATCATGTCCACATGCCTAAGTGCATTAAGTTACTGCCATGTGATTGGCTGATTAAAATTTGCATTAATTAGCAGTTGGACAGCTGTACCTAATAATAAGTGGCTGGTAAGTGTATCGTGATGCACCAATTACTGATTTCCCTTTTTTTTTTTTTTTTGGAAAAATATATAACAATTAAATATTATACATGAAAGTGTCAGAATGTCTCATTAATCTTTCTGTCTCCCTTTAATAACATGAGAATTAATTTGCAAGATTGTTTGCTTATGAACCATATTTTCTCTAGAGCTTTGGTTTATCAATGCACTATGTGTATGTTTCTGAATATATATTTTTCTTTTCTTCAGACCCATGAATGGAGCAAGAACGACGAGCGTCTCCTGAGTGCAGTGGAGCATGGAGAGGCAGATAAAGTCACCTCCCTCCTGTCAAAAAAAGGAGCCTCTCCTACCAAACTTGACAGCGAGGGCAAGTCTGC[G/A]TAAGTATCAGGAACTGAAGCTGTTCTGTTTTCTATTTGATTTGCTCCTTTACTGCCTTAATTGCCATTTCAGCCGTGTTTAGAGAGACTTTCTAGACTACATCTTCTGCAACCCACTTGAGATGTGCATAAAAATGAGTTTGTATGTGGGTGTTTACTCTCCAGCCGAGGGAGAGATTTGAGTCATGTGTTTTTTGTGTGCATCTGTTCATCAGGGTGTTTATTTAGGAGGAGAAATCATAATCTAAACCCCAGTCAAACAAATTTAGTCCTTCATTCAACCCTTCAGCCTTTCATATCATGTCATTTATTTTCTCTAATTTACTGCGTTATGCACACAGATGTTCAGATGCGAATGCTCGCCTTGTTTGTGCCAGTCATTCATCCAGCTTTAAAATATGCAACACACATTTTATCCAACAATAACCTAAAGCACTTAAAACCATGAAAAACTGAGATGAGAGCTCAGCATTTTTGGCTTTTTAAGTGTTTAACTTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37278
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058485 | Essential Splice Site | 314 | 988 | 12 | 18 |
| ENSDART00000058487 | None | None | 186 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 18427555)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 19563044 |
| GRCz11 | 21 | 19599680 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCCACTTTCCAGCAACAGTGAATCATCCAAAAGATTTAACTACAAGG[T/G]AAAATACTGAAGGAGTGTTGAGAGATGGCAGTATGAAAGTAAAATACATA
Long Flanking Sequence:
AGACATGCACTGGCGTTTGTCTAACCCTGTAGTGATGATATCCTATTTACCCTAAACTTAAGTGTGCAGTGTGTATTTCACTAACCACTCAATCACTCTCTCCACTCTCCTCATCACGTGCACAATCTCAGCATGGTCAAAAGTTAAATGAGGACAGAAGCTCCACCCCCAAAAAGAGAAAAGCACCTCCTCCTCCCATTAGCCCAATGCAGGTAAAGGCACACAGTGCTGAATCTGTGATCTGCAATCATCTGTGTCTCCACTGTCTGTAAACCTTAGATGCAGTTACTTCATTAATGACTTCTGAAGATTCAGTTCATGGTTGTCTTTAATCTCTACCTATATTGGTTATGCTTGTCTCAACACTAAGCTTTGCTTTAATACTTTTCTCCGTGTATTTTTTTTTTAGTCGCCTGGTTTCACCTCACCACCTTATTTTACTCCTTCTGAAACTCCACTTTCCAGCAACAGTGAATCATCCAAAAGATTTAACTACAAGG[T/G]AAAATACTGAAGGAGTGTTGAGAGATGGCAGTATGAAAGTAAAATACATATGCATGCTAAAATGGAAGAAAACAATAGGTTTATTTTTATCATAATTTTATATTATAATAATATATTTAAGTTTATTTTAACCAATATTTTAAACAGTGAATAATACATTTAAAACATACAGTAAAGTACAAAAATGCAATAAATAAATAAATATATTAAACTAAATGCTAAATAAAAAGACTTCAGTTGCTATTTCCATAGTTTTGCAAACATACTGCACCTATGTGTGCAATTTACTATTAATGGAAGTACAATTCATTAATGCAATACTTACTGTTGAACTATTTATGTATAAATTATGGAAAATTGCATTTGTTTATTATTAGAGATTTTATACAATAATATTGCTTGTATTTGTTGTTCATTTGTTTATTGCATGTTTACTTTAATTATACTTTTGTATAGGCCTGTTATAACACAGCACATAGAGATTACCTTATTAATTTGTA
Associated Phenotype:
Not determined