ZMP

zgc:64076

Ensembl ID:

ENSDARG00000030530

ZFIN ID:

ZDB-GENE-040426-2167

Description:

solute carrier family 22 member 2 [Source:RefSeq peptide;Acc:NP_998315]

Human Orthologues:

SLC22A1, SLC22A2

Human Descriptions:

solute carrier family 22 (organic cation transporter), member 1 [Source:HGNC Symbol;Acc:10963]
solute carrier family 22 (organic cation transporter), member 2 [Source:HGNC Symbol;Acc:10966]

Mouse Orthologues:

Slc22a1, Slc22a2

Mouse Descriptions:

solute carrier family 22 (organic cation transporter), member 1 Gene [Source:MGI Symbol;Acc:MGI:1081
solute carrier family 22 (organic cation transporter), member 2 Gene [Source:MGI Symbol;Acc:MGI:1335

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37131	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43516	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37131

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000048890	Nonsense	49	562	1	11

Genomic Location (Zv9):

Chromosome 20 (position 42700784)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	42771943
GRCz11	20	42669053

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTTTCGTCTATGTGGGGATTGTGTTTCAGGGATTTACTCCTGAGCATTG[G/A]TGCCGTGACCCAGCTGTCAGTGAGATTCGGGAAAGATGCGGATGGAGTCT

Long Flanking Sequence:

TGATATTCATAACAACTATTTAAATTTCACAGCTATTGATAAATCTAAATGTGAAGTCCACCCAGTCTTTCGGAGTTTAGTTAAATTAGTAATAGTTTCAAGCCCTCATTACATCACCGCTTCCCCTACACTCACTTGAATACAAATTATACACTGAAAAACTTACATAACAGCTGTCCCTGGGGCTAAAGTGTAAAACTGTGCCCCCCGTCCCATCGCAGCATGTAATTGGTCAATCGCAGCTGGAATAGATCACGTTTCAGCCTCCTCTGGACTTTAGCTCAGTCAGCTGTCTGTAAATACTCCCCTCTCAACCAAACAGACCTTTTTCTGTTTGTGGCATTCGGCAAAAACATGACCACTTTCGAAGAGATTCTGGAAGAGGCCGGCACATTCGGTCGCAGCCAAATACGCATATTTTGCACTTTCTGTCTGGTCTCCATACCGTTTTCTTTCGTCTATGTGGGGATTGTGTTTCAGGGATTTACTCCTGAGCATTG[G/A]TGCCGTGACCCAGCTGTCAGTGAGATTCGGGAAAGATGCGGATGGAGTCTTCAGGACGCGCGCAGGGCGACCGTACCCTTGATAAACGGATCTTCAGGAGCGTCCTACAGTCAGTGTGGGAGATTTGACGTGGATTGGAACGCAACCGGACTGAGCTGCGAAAATCCAGATGGGGATTTTAACCAGTCCCAGCTCTCTGTAATGCCCATGATGAGTTGTGTGGACGGTTGGGAGTATGACTATGTAGGGAGGCAGTCGTTTGTCACTGAGGTAAGTGGTTGGATTGTAAATGCAATTTTTGTGTGTGTATAAAAGAGGGCTGCATAATATTAAACAAATAAGACATTGGAAAATTTTATTTTTCTGCAATATACAGTTGAAGTCAGAATTATTAGCCCTCCTGTATATTTTTCCCCATTTTTTTCCATCACATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAGCCGATTTCTTTTATCTTTGCCATGATGAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43516

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000048890	Nonsense	223	562	3	11

Genomic Location (Zv9):

Chromosome 20 (position 42708593)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	42779752
GRCz11	20	42676862

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCAGAGCTCTCTTTGGCTTTGGGGTGAAGGGCGGTTGGATGGTTGGATA[T/A]GTGCTAAGTACAAAAACATTTTAAAATAAACAAATTTTATTTTAAAGTAT

Long Flanking Sequence:

GGGTAAAATGTTTAGAAAAATGGTCAGTGATTTTGCTCTGAGAGTGAACATAAATATACATGTATAAGTATTATATTTATTTATTATTATTTTATTTTGCATTAAGTTACTGAAGACTGGGATGATAATGTTTAAAAACAATAATCTTTTTAACAATTATTTAAATATAGCTATAATAATATTTACCTCTTTTTTTATTTTGATCCAGTAAATGCATATACAGTATAGTGACTATTCACAAGGAATGCTACTGACCCCAAATGTAAAAAAAAAATAAATGAATAAATAAAAACAAATGACTCTATTTTTTTAACATTTTTTTCAGCATGAAAGTGATTCATATTTTCTTTTAGATATGGGAGGATGAAGAGTTTCCTGATGACCAACTTCTTCATTGGAGTCACAGGGATTCTGGTGGCCACGTCTCCTAATTACATCTCCCTGCTGGTGTTCAGAGCTCTCTTTGGCTTTGGGGTGAAGGGCGGTTGGATGGTTGGATA[T/A]GTGCTAAGTACAAAAACATTTTAAAATAAACAAATTTTATTTTAAAGTATGTTTGTTTACTTCCTGAAGGAGTGGTATATTAAATGGATAGTTCAGGTCATCCAAGACATATAGTTGAAGTCAAAATGATTAGCCCTCCTGTGAAATTTGAATTCTTTTGAAATTGTTTCTGAAGTGTTGCGTAATGGATTTTTTCAACACAAAATATTTTTTATAAATTTCTAATAACTACATTTTTTATTTTGGTAGCTTTATTTTGATGGTCCATTTGAATATTAGTAGACTGTCTGCTTAATATCTGTTGATACTCCTCTCAACAGACAATCTTAGCAAGTATGTCAACCTACTCTAACCCCAACCCAAACCTCAACCTACAGTCTACTTATAATCCAATCAGAATTAGTTGGCATGTAGATACAATGTAACTTAAATTCAACATACGGACCATCAAAATAAAGTGTGACCTTTATTTTTGCCTAATATTTTACAAGATATTTTTG

Associated Phenotype:

Not determined