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
sa34133	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa21035	Essential Splice Site	Available for shipment	Available now
sa34132	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa34133

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074093	None	None	400	None	10
ENSDART00000134174	Essential Splice Site	None	136	1	5
ENSDART00000143040	None	None	401	None	10

Genomic Location (Zv9):

Chromosome 7 (position 40944837)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	39281094
GRCz11	7	39552111

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCCGTGTTCTTGTTCGGGGATGAAACGATAACATCTTTTATTGAGTACC[G/T]TAAGTCTTTGCAAATATCAATACGTTAGTGTAAATAATATAAAGACTATA

Long Flanking Sequence:

CATCACCAGATTGGAACTGCACATGTCTTACCAGAGTAAGTCACAGAAAATAACAGATTTTAATACAGTATTTTGTATTTCAAAATATTTCTTATCTCCCAAAAGTATTGCTTTTAATTGGTAAAGTCACCTTTCGGACATTCTCCACGCAAAAGCTCCCTCAATCTACACAATGAACTTATTTTCCGTTTAGTCACATTACACGTGTATTGCATTGTAGTAACGTTAGTCACGCCTCTAATGGTCACGACACGCAGAGGAGGAGGTATTTCCTCTATGTTATCTGCAACAAAATGGCGAGTACTTTGCATTTATGATATTATGTTGCACTTTAGAAACATCTATACGTTTATTTTTATTGTTTCATAACCTGAAGCGGTTATGCATATGCGTCACAGCGTTTGTAGGCTACTCGGTCAGGGTAAACAGACTCCGACGGTAAACATCACCAGCCGTGTTCTTGTTCGGGGATGAAACGATAACATCTTTTATTGAGTACC[G/T]TAAGTCTTTGCAAATATCAATACGTTAGTGTAAATAATATAAAGACTATATTATGTTGTAAAGCTTTTCTGTCGCCGCTAGAGCAAGCAGCTCAAATCCTTTAACCTGCTGAGAGTTTGAGGACTGGTCGAAGTTCAGCTCGGCTGTTAACCTTTACCTCACATTAATGTGCTTTGTCACTTAAATCGGTTTGTTATACAGTAGGCACCTGTGTGTGATCTTCAGAGACCGACACTTTGGAACAGATGCACTTGTTTACCTGTTTGAGGAGGTGATCCAGCGGAAGGAGAACTGTCAGAGAATAAAAACATAAAGCTGGTAAATCTACTTCAGTGATCTGGGTGATGATGGATCCTGCAGCAAAGCAGAAAGTGATTTACATCACCTACCTCATAGCGGCTCTGGAAATCACCTGGATGTTCCTCCAGTTCTCCATAACACCGGTTTGTCTGCTTTTTTCCTTATTCATTTACGATCAGATGTTAAATAAATAAAACCAC

Associated Phenotype:

Not determined

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