ZMP

si:ch73-335m24.5

Ensembl ID:

ZFIN ID:

Human Orthologues:

SLC24A3, SLC24A4

Human Descriptions:

solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 [Source:HGNC Symbol;Acc:1097
solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 [Source:HGNC Symbol;Acc:1097

Mouse Orthologues:

Slc24a3, Slc24a4

Mouse Descriptions:

solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 Gene [Source:MGI Symbol;Acc:
solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 Gene [Source:MGI Symbol;Acc:

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa17884	Essential Splice Site	Available for shipment	Available now
sa28338	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa17884

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112438	Essential Splice Site	235	621	8	16

Genomic Location (Zv9):

Chromosome 14 (position 34867874)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	33575863
GRCz11	14	33916177

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGTTTGTTTRTGTGTATTTCAGATCATATATGATGAAAAAGTAATCTGG[T/C]GAGTGTGGYTGAGAAGCTGTAAYAATAATTATTTACATTTWAGTGAAGCG

Long Flanking Sequence:

GGCAGCGGGAAGCTCCGCCCCTGAGCTTTTCACATCGTTGATTGGTCAGTGACATCTAGCAATGCTTTTCAATAAATCTTACTTTATAAATAAGTCACTGATAAACAGTCATCTCTTCATATCAGGCGTCTTCATCACCAAGGGAGATCTGGGTGTAGGAACTATCGTGGGATCTGCTGTCTTCAACATCCTGGTCATCATCGGAGTTTGTGGGATATTTGCTGGACAGGTAGTACAGTACATCGGTATTTAAAACAATAAATGTGAGACTATTAAACTGCTAAATATGAATCGCTTCACAGACCATCACTTTGACCTGGTGGCCGCTCTTCCGGGACTCTATTTTCTACATCCTCTCTGTGCTGGCATTGATTCTGGTAAGCAGGACTGTCGTTTTTCAGGTTCTGTTTGTGTTTTACATTTGTACTCACACTAAATTGAGGCCATTTTGTGTTTGTTTGTGTGTATTTCAGATCATATATGATGAAAAAGTAATCTGG[T/C]GAGTGTGGCTGAGAAGCTGTAACAATAATTATTTACATTTTAGTGAAGCGTGCCATTTTTCATATAACATCACTGTTGCAGGTGGGAGACTATAATCCTCATATCGATGTATGGAGTTTACATCCTTATCATGAAGTGAGTATTTAATTTTTTGTAACATTATTTAACTCATTCATTCATTTTCTTTTTGATTAGTCTCTTTATTAATCCAGGGTCACCACAGTGGAATGAACCGCTTATCCAGCACGTTTTTAGGCAGCAGATGCCTTTCCAGCCGCAACCCATCCCTGGGAAACATCCTCACACACACTCATCCACACACATACACTACGGACAATTTAGCCTACCCAATTCACCTGTAGCACATGTCTTTGGACTGTGGGGGAAAACGGAGCACCCGGAGGAAACCTACACGAACGTAGGGAGAACATGCAAACTTCACATAGAAACGCCAACTGACCCAACAGAGGCTCGAACCAGCGACCTTCTTGCTGTGAGGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28338

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112438	Essential Splice Site	563	621	14	16

Genomic Location (Zv9):

Chromosome 14 (position 34881065)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	33562672
GRCz11	14	33902986

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGTTTTCCATGGGCTTTGCGCACCCTAGTGGTTGATTATGGCTCAACTG[T/A]GAGTTTATATTTGTGTGTATATGCGGTTACTGATATTAATTTCTCTAACG

Long Flanking Sequence:

GTTTTGCCCCGTTGGGAGCGCTGGTTCATGGTTACCTTTGTGGCCTCAACACTCTGGATTGCCGTGTTCTCCTACCTCATGGTGTGGATGGTGAGAGATCTGCTCATTTGTTTTTCAAACATTTGTTAGTAATATTAATAATATGCTATGAAAAAAATACATATTTTTTATTGCAGGTCACCATTATCAGTTTTACACTGGACATTCCAGATGTTGTTATGGGTATTACATTTCTAGCAGCAGGCACCAGTGTCCCAGACTGCATGGCTAGTCTCATTGTGGCCCGTCAAGGTCTCAAGATGACCCTTTTCTTCCTTCTCTTGACCATTTATTCAGCTGTATTGATGAGCGATTGAATGAATAGGTGTTTGTGTGTGGTTCTGCAGGTATGGGAGACATGGCGGTGTCCAACTCTATTGGCAGCAACATCTTTGACATTCTGCTGGGTCTTGGTTTTCCATGGGCTTTGCGCACCCTAGTGGTTGATTATGGCTCAACTG[T/A]GAGTTTATATTTGTGTGTATATGCGGTTACTGATATTAATTTCTCTAACGATTGTGGATCAATTCCCCCATAAAAAAAGATAAATATATGGCACAGTAGGTAGCATGATTGGGTAGCAAGTAGGTCGCTAGTTCAAGCCTCGGCTGTGTCAGTTGCAAATTTTGTGCTAGAAAAATTGTAACATTTAAACTCAGAATTTTGAGTTTAGAAAGACACAATTGCCTTTTTTGACCCATGGTGGAATTGTATCAGATTTTTTCATATATTATATTATTCATTCATACATTTTTCTTCATCTTAGTCCCTTTATTCATCAGAGGTCACCACAGTGGAATGAACCGCCAACCTATCCAGAATGTTTTACACAGTGATGGGTTGCAGCTGGAAGGACATTCGCTGCGTAAAACATGTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGTAACCCCTGTTTAAAAAAGGGACTAAGACGAAATGAAAATGAATGAATAAATGATTA

Associated Phenotype:

Not determined