ZMP
zgc:171831
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC555979 [Source:RefSeq peptide;Acc:NP_001106807]
Human Orthologue:
SLC22A23
Human Description:
solute carrier family 22, member 23 [Source:HGNC Symbol;Acc:21106]
Mouse Orthologue:
Slc22a23
Mouse Description:
solute carrier family 22, member 23 Gene [Source:MGI Symbol;Acc:MGI:1920352]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19649 | Essential Splice Site | Available for shipment | Available now |
| sa10878 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19649
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 |
|---|---|---|---|---|---|
| ENSDART00000126566 | Essential Splice Site | 134 | 942 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 1897279)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 1752365 |
| GRCz11 | 2 | 2095171 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCCAGCTATAAACTGCAAAACGGATTAGAGCAAAATATTGTCACCAAG[G/A]TAAGTGGAGTCATCCCTGAGCTACAATGTTAGGTGGCATAGGCTAATTTA
Long Flanking Sequence:
AAAAAACCACTCCCTGAGCACTGGATGTCAAGCGCGCTTTTGGAGAGGAGAAAATCACGTTTATTCGGTGTGACGCATCACCGGGACCGGACTGCAGCATGTGCGAGACGGTGATGGCCGTTTCTCAGCTGGACACCGAGTCCCACGCACCGGAGAACGGATTTGTGACCCCCGAAACTAGTAAATCTCCGGGGCTGCTCTCGCAGACTGACGGCGGCGTTTTACCGAGTGTGGGTGGATTTGGGAAGTATCAGAAACAGCTGATCGTTTTAACGTGGATCCCGGCCATTTTTATAGGCTTCAGCCAGTTTTCTGACAATTTTCTCCTGACTAATCCGTGTCCTGAGCCGCATAATAACAGCAGCCAGCTCCTGACTGTTGCTCCGACCGCCGTTAGCACCGTGTTTACCGGTGTAAATACCGAGGCGGCATCGCAATGCAACTGCACGCCGTCCAGCTATAAACTGCAAAACGGATTAGAGCAAAATATTGTCACCAAG[G/A]TAAGTGGAGTCATCCCTGAGCTACAATGTTAGGTGGCATAGGCTAATTTAAAAGGAACCAACTTGAAGGGGTAGTTCACACAGACATGAAAATACTGTCATCAAATTCTGTCACTATCTTGAGCTGTTGTTCTGCTGAACTCAAATGAAGATATTCTGAACAATGTTGGACACCATTGACATCTATATAAGCACATATTATTGAAGTCAATGGTTACCGGTTTCCAACAATATATCTTCATTTTCTCTATGTTCAACACAACAACAACAACAAAAAACTTGAGGCTGAATGAATGATGACAAATCTCAATTTTGGATTAACTTTCCCTTTAAAAGGATATTAAACATGAAAATTCTGTCTGTTCACTCACTATTTCAATAAATAATGAGTGAATGTTCATTTTGGGGTGAACAATTCCTTTAAAATTAACAATATGTCATTGTTTATTCACACAGTTAACTTGTTCCAAGCCAAAAACGAAGATGTTCTGAACAATGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10878
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000126566 | Nonsense | 874 | 942 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 1827766)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 1682852 |
| GRCz11 | 2 | 2025658 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCACCCATAGATTCTGGCACCCCATTGTTACAGTTAGACGCTCCWCCT[G/T]AGCTGAACTCTATTGAATCTGCTCCACCTTCATTAAGTAATGGTAGTACT
Long Flanking Sequence:
TAGACTCGGTCGTTCCTCCTGCTGCTGTAGGATCTCCATTGGAAGTTGGTAATGAAGTAGACTCTATAGAGTCCAAGCGACCAGAATCTCCACCTGATGACGTCCTAGCTGTTTTGTCTTCTCCAATTGAGGACACTTCGTTGACCATCCATCCGGTTCCTTCTGAACTTCCTTCGACTCTGGACACAGTCATTCCTGCAACAGTAGGATCTCCATTGGAAGTAAATAACGAAGAAGACTCTACTGATTCAGTTTCACCCCCTATAGACCTTCCCCTCTGCGCATTGACCCAGTCCAACAACCCATCATCAATTGGACAATCGCCAAATCTTTTAAATGACATCCCTCCCTCTTCCTCAATAGACTCCCACACTCATCCAGTGTCCGAAATCTTACCCCCTTCCCCAACTGAACTCTCAATGCTAGACCCGTCTAGTCAAATGAACGCAGCTCCACCCATAGATTCTGGCACCCCATTGTTACAGTTAGACGCTCCTCCT[G/T]AGCTGAACTCTATTGAATCTGCTCCACCTTCATTAAGTAATGGTAGTACTAGTCTCCTTGCAGCTCACGCCACAAGCACTGACTCTGACTCTGTTACAGAATCCGGCAACCCGCTCATGGTGAACTCCACCGTTTCCTCACCTATTGACTCAGGTTTACCTTCGGACGTTGATATACCGAATACTGCCAATGGGGGAACGTCTTCATGACGGAAACATTGTTGGTGCACAGGCATACTTGCTATTCCGACTGCGTGATATCAAAATTAAAGGGATTGTACACGCAAGAATTCAATTTCTCTCATTGATTACGCACTCGAATGTCATTCCAAACCTGAGATCTTCATTCATATTTGAATTGAATTGGGTTGAAGATGTTTTCAATCAGGGGTGCCCCTTCCCTGTTTCTAAAAACTGATTGAATGTTTCAGGACCCTTGCTGTCTTTGGAGGGTCGGAGAGCTCCAGGATTTCATCTAAAATGGCTTAATTTGCATTTCTA
Associated Phenotype:
Not determined