Busch Lab

ZMP

slc22a18

Ensembl ID:
ENSDARG00000052271
ZFIN ID:
ZDB-GENE-051120-165
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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