ZMP
zgc:165580
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC555262 [Source:RefSeq peptide;Acc:NP_001103169]
Human Orthologue:
SLC22A15
Human Description:
solute carrier family 22, member 15 [Source:HGNC Symbol;Acc:20301]
Mouse Orthologue:
Slc22a15
Mouse Description:
solute carrier family 22 (organic anion/cation transporter), member 15 Gene [Source:MGI Symbol;Acc:M
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9673 | Essential Splice Site | Available for shipment | Available now |
sa36377 | Splice Site, Nonsense | Available for shipment | Available now |
sa8710 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9673
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077804 | Essential Splice Site | 176 | 497 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 17 (position 19333922)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19483933 |
GRCz11 | 17 | 19503769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTACTTTCACAGTAATSGCATGATAMTAAYGYGTTTCTCTGTGYTCC[A/T]GGGACCTTGACTAATATGACCTTTGCAGTGGGCATCTCTCTGTTCGCTGC
Long Flanking Sequence:
CCGAAATAAAACAAATAAGACTTTTCCCAGAAGAAAAAATATAATCTGACATACTGTCAAAATTCTCTTGCTCTATTAAACATCATTTGTAAAATATTTAAAAAAGAAAAAATATGTGTGTGTGTACATTTTATGCGTTCTATAGCTGCTCTGCACTGCAAAGATGTTGCTTCACATGATACACAACCAACTGAAAGCCAAAAGGAAAGAAAAACAATAATTTATCATACAATATTGACTCCTCTTTCTCAGGTCTGTTTTTTGAGGTCTTGTTTGGTTATGGAACCGCATTAGCACCCAGTTATGAGGCGTTCGCTGTGTCTCGGCTGCTGGTTGGTGTGATGAATGGAGGAATGGCGTTGGTCTGCTTTGTTTTGACTCAGGAATATGTGGGAAAGTCCTACTGGGCGATGACAGGTGCACATTTATCTATTATACAAACATTTTCACTGTTTACTTTCACAGTAATCGCATGATACTAACGCGTTTCTCTGTGTTCC[A/T]GGGACCTTGACTAATATGACCTTTGCAGTGGGCATCTCTCTGTTCGCTGCGTTGGGTTATTATGTTCGGCCGTGGCGAAACCTCGCAACTGCTGCCAACTGTCCTGGACTTTTGCTCTTCCTGCTGTGTGTGTGAGTGAGATCACTGCATCCTGTTCAACTATAGCACTGTGAATTTATTTAAAAGTTGCTGTGTAAAGCTGCTTTTGATGTTGCTTCTTGGACACAAAAGTTATACCCCCGCACCTAAAATCTTAAATACTGAACACTATACTACAATACACAACTCTTCAGTAGTTGATGGTTTATGAATTAGTGTTATGCTTTAAGACTCATATGTTCACTTGGATAGCTATATCTTGTAGCATGTTCAAAGTGTTATTCTTGTTTCACACTTAGCTGATGCTTGATAAGGTAAATGCGTATTTGACATGCTGTCCCAAAAGAGAGCCTTGAGCTTAGAGAATCCTCGAGCCTTCGGGGCTCCCTCCTGCTTAGTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36377
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077804 | Splice Site, Nonsense | 338 | 497 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 17 (position 19336817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19486828 |
GRCz11 | 17 | 19506664 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCACACTCTTCTGCTGTATTCATTTGAGTGTGTTTGTTTTTCTTTCAG[G/A]GCAGGCAGGAGAAAGTCAATGGCCAATTTTCTTGCCTTTGCAGGCATATC
Long Flanking Sequence:
GAGGACATCCTGCAGGATTTCGCATTGAGGAATGGGAAAGGCAGAATTGTGGTGAAGCTCCGGCGGGCCTTCAGCTCTCCAAACTCATCCAGTCCCGGGGTCTTCCAGCTGGTCACACATCCCGTACTACGCTGGAGGACTGTGGTGCTCATGTATGTGTGGTGAGTGTTTCACAAAACCACTATAAGCTAACGAGAGATGATCTAGATGCCCATTTTTGTATTTCTTTAAAACTTTTGTATTCTTATGTACAAGTTTTATGTGTATATTACAGGTATGCCTGTAGCCTCGTTTATTACGGCCTCACTCTCAGTGCCGGTGAAGATAAAGGTAATCGTTACCTTAGTGTTGCCATGTATGGCTTGGTGGAACTGCCTGCTTATCCTCTCTGCATGTACTTCATTAACAAACAGTGGTAAATACACTCACAGCCACATCAACACCCTGACCTATCACACTCTTCTGCTGTATTCATTTGAGTGTGTTTGTTTTTCTTTCAG[G/A]GCAGGCAGGAGAAAGTCAATGGCCAATTTTCTTGCCTTTGCAGGCATATCTTGTCTGCTCACAATGGTTGTACCTGTATCAGGTAATCACTTTTCTTTCACAATTCTAACAGAAAAATTGTAAAACGTGTCATTTGGGTTTGTTTATTAGCAGTCTGGTAAATAATGCTAGCAGTGTGTTAAAAGGAGTTAAACCTGTAGCATATATTCAAAATCTAGTTCCCTAAAGTCTGTTTCTCTTTCCGCAGGGTCTTTATTAAGTGCCACATCGCTGGCTCTAGTGGGAAAACTGATGGTCAGTGCTGCTTTTAATATTGTGTATGTGTATACATCAGAACTCTACCCAACCGTGATCAGGTACAGCCAGCACCTTTGCTGCATGTTTTGTTTGGTGCTTTTTTTACACTTACAATTTTCCATAGAAAAAAATAAGTTTGAAAGGGTAATTATTTACTCGTTTGTTATCGTCATTCTTTCTTTGAACACACATTAAGCTATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8710
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077804 | Nonsense | 409 | 497 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 17 (position 19338894)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19488905 |
GRCz11 | 17 | 19508741 |
KASP Assay ID:
2261-0870.1 (used for ordering genotyping assays)
KASP Sequence:
ACTGTNNNNNNTGTGTGTGTGTGTTCGTGTTAGGAATGCAGGTTTGGGAGTGTG[T/A]TCAATGTCTTGTAGRGTTGGGGGAATTCTGGCACCATTTGTACCAAGTAT
Long Flanking Sequence:
CTGGGATGCAGTTCAACAGATACTTTTGTCAGGTAGTGTAGTAAACGCATACTCTGACTTGCGAGACACAGTTGAAGTCATTTGTAAAGGTTTTCTTTTGGCAAACAAAAGTCTTCATATGATTACAATTAAACCCCTGAGTCACATGAAAGGTTTTGACAATGTTTTTCTGGTTACTTTCCTCTTTCTTTCTGTAACCGTTGCTGTTTATGGGGGGTCAGAGAGCTCACGCATTTAATCCAATATATCTTAATTTGCGTTCTTATAATGAAAGAAGGCCTCAGGGGTTTGGAACAACATTAGTGAGCGATTAATGAAATCTTTTTCATTTTTGAGTGAACTAACCCTTAAATTTAATGTCACTAATAAAATATTCTATGCTTGAGCTAACGGTGTCCTCTAGTGGAGACTATAATGTAATTCATGAAAGTCTCAGTATGAACAGGTTAAACTGTTGTGTGTGTGTGTGTTCGTGTTAGGAATGCAGGTTTGGGAGTGTG[T/A]TCAATGTCTTGTAGAGTTGGGGGAATTCTGGCACCATTTGTACCAAGTATGGTAAGTCACTAAAGGAAATGGTAATTTTCTAATGCTTTTTTTTTTTTTTTGCATCATTATACATTTGCAATAATGAATGAATTGATATACTGCCAAGCTGCTCTTACCATGAAGCAAATTTTATTGACATAAAAGTGTCAAAGTGATGGACATTTTTAAAAAGGTACCACCAGGAAGAATCTTAAGATATATATCAAAAATTGGACTGAGAAAATCATATATAACTTTGAATATGTTTATTGGGTGAAAAATTCTATATTTGTCTATTTAACTTGTTATTGTAATATGAATTTGTTTTTATTATGTAATATTTTAATGTATATCCATTTAGCCATGAAATAGTCATAAGTTGCTGATGTGGCAATACATTAATTGATTCATGCAATAAAATACATTTAGTTAAGAAAAAGTGTGTTTATTGATTATGTACTGACTTGTTTGTTATTGTT
Associated Phenotype:
Not determined