ZMP
slc22a18
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 22 member 18 [Source:RefSeq peptide;Acc:NP_001032462]
Human Orthologue:
SLC22A18
Human Description:
solute carrier family 22, member 18 [Source:HGNC Symbol;Acc:10964]
Mouse Orthologue:
Slc22a18
Mouse Description:
solute carrier family 22 (organic cation transporter), member 18 Gene [Source:MGI Symbol;Acc:MGI:133
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21035 | Essential Splice Site | Available for shipment | Available now |
sa34132 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21035
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 |
---|---|---|---|---|---|
ENSDART00000074093 | Essential Splice Site | 299 | 400 | 8 | 10 |
ENSDART00000134174 | None | None | 136 | None | 5 |
ENSDART00000143040 | Essential Splice Site | 300 | 401 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 40934153)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 39270410 |
GRCz11 | 7 | 39541427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTACTGCTGCTATCTGTTGGGGTTTCTAGTCTAGTGGGCCTTGCACAG[G/A]TAAACTGCTATCGGGCTCCTTACTTTTTCTTTTTTTTTACAGTAGTGTCT
Long Flanking Sequence:
AGTTCATTTAAGCGAAGACCGAGCTACTTGTGGCGACCACCATCTATGCAAGCGGCAACAACCGTTGACGACCAGGTGAGCGTGTTGAGCGATGCAAATAAAAGAGCGGCTCTCTTGAGTGACAGCCAATAGGAGCACCTATAGAGCTCACATCATCCTCTCTCAGCTCACTCAGAGGCTGGATGTATTCTCTTGTGCTGTAGACCTACACAGACCTGCACACTGTTTGCAGCAGATCGCCACCCAGATCGACAGGCACCTACAAAGTCACTGCTAGTGTGAATGAGGCAACTGTTTTGATCCACTTCAAATGTTGACTACTGTACATTGTTTTACATTTGAGAACAGATGGTGTAGCTTTGTGAATAAATGACACTAATGTCTTACTGTTTTTTAAGGTGATCCAAGGGGCTGTAATCGGGCGTCTGACGTCTAGCTTTTCAGAGAATTCTTTACTGCTGCTATCTGTTGGGGTTTCTAGTCTAGTGGGCCTTGCACAG[G/A]TAAACTGCTATCGGGCTCCTTACTTTTTCTTTTTTTTTACAGTAGTGTCTGTCAAACAGGATTAGGTAGCATGTCTTCTATTAGTGTATTTCCTAATTATATTTGTTTTGTGTGTTTTTCAGGCATTGATGACAAATGTGTTTCAGTTTTGCTTCATCGTTATACCAATGATGTTTTCTCTAAGTGTCTTCAATGTCATCACAGACAGCATGCTGACCAAGAGTGTGTCTCCGGCTGACACAGGTAATCCACAAACATGCACATTAGGGCTGCACAGTATATTTTTCTAGACCAGCATTAACATTGCAATATGCACCATAACACAGGATGCACAATGTCGAGTTGGGATTATAATTGACCTGACACCACTGTTCACAACACCTGACTTGTGGACTCATCACATAGTTTAACCACAATAAAATGAAAGTTTATAATTTTCATGTGTTTTTACCACCTGTAACTGGAAGCATTCCAAGTGAGTTCGAAGAATTGTGGCTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34132
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074093 | Essential Splice Site | 299 | 400 | 8 | 10 |
ENSDART00000134174 | None | None | 136 | None | 5 |
ENSDART00000143040 | Essential Splice Site | 300 | 401 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 40934152)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 39270409 |
GRCz11 | 7 | 39541426 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACTGCTGCTATCTGTTGGGGTTTCTAGTCTAGTGGGCCTTGCACAGG[T/C]AAACTGCTATCGGGCTCCTTACTTTTTCTTTTTTTTTACAGTAGTGTCTG
Long Flanking Sequence:
GTTCATTTAAGCGAAGACCGAGCTACTTGTGGCGACCACCATCTATGCAAGCGGCAACAACCGTTGACGACCAGGTGAGCGTGTTGAGCGATGCAAATAAAAGAGCGGCTCTCTTGAGTGACAGCCAATAGGAGCACCTATAGAGCTCACATCATCCTCTCTCAGCTCACTCAGAGGCTGGATGTATTCTCTTGTGCTGTAGACCTACACAGACCTGCACACTGTTTGCAGCAGATCGCCACCCAGATCGACAGGCACCTACAAAGTCACTGCTAGTGTGAATGAGGCAACTGTTTTGATCCACTTCAAATGTTGACTACTGTACATTGTTTTACATTTGAGAACAGATGGTGTAGCTTTGTGAATAAATGACACTAATGTCTTACTGTTTTTTAAGGTGATCCAAGGGGCTGTAATCGGGCGTCTGACGTCTAGCTTTTCAGAGAATTCTTTACTGCTGCTATCTGTTGGGGTTTCTAGTCTAGTGGGCCTTGCACAGG[T/C]AAACTGCTATCGGGCTCCTTACTTTTTCTTTTTTTTTACAGTAGTGTCTGTCAAACAGGATTAGGTAGCATGTCTTCTATTAGTGTATTTCCTAATTATATTTGTTTTGTGTGTTTTTCAGGCATTGATGACAAATGTGTTTCAGTTTTGCTTCATCGTTATACCAATGATGTTTTCTCTAAGTGTCTTCAATGTCATCACAGACAGCATGCTGACCAAGAGTGTGTCTCCGGCTGACACAGGTAATCCACAAACATGCACATTAGGGCTGCACAGTATATTTTTCTAGACCAGCATTAACATTGCAATATGCACCATAACACAGGATGCACAATGTCGAGTTGGGATTATAATTGACCTGACACCACTGTTCACAACACCTGACTTGTGGACTCATCACATAGTTTAACCACAATAAAATGAAAGTTTATAATTTTCATGTGTTTTTACCACCTGTAACTGGAAGCATTCCAAGTGAGTTCGAAGAATTGTGGCTCAAA
Associated Phenotype:
Not determined