ZMP

slc8a2b

Ensembl ID:

ENSDARG00000040625

ZFIN ID:

ZDB-GENE-050419-209

Description:

sodium/calcium exchanger 2 [Source:RefSeq peptide;Acc:NP_001116756]

Human Orthologue:

SLC8A2

Human Description:

solute carrier family 8 (sodium/calcium exchanger), member 2 [Source:HGNC Symbol;Acc:11069]

Mouse Orthologue:

Slc8a2

Mouse Description:

solute carrier family 8 (sodium/calcium exchanger), member 2 Gene [Source:MGI Symbol;Acc:MGI:107996]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa28535	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa35989	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa28535

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:

A > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000063721	Essential Splice Site	744	961	10	11
ENSDART00000097701	Essential Splice Site	744	961	10	11
ENSDART00000144567	Essential Splice Site	631	848	10	11

Genomic Location (Zv9):

Chromosome 15 (position 41694292)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	43019699
GRCz11	15	42976131

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCATTGGTGGATATAAAAAAAGCTTCCTTTGATTGCCGCCTTTTCTCCTC[A/C]GGTGACGGTGATGAAGATGATGAGGAGGGTCGAGAGGAGCATCCGCCGTC

Long Flanking Sequence:

AAAAAATTTTGTGATGTTCATTCATTTATTCATTCATTTTCCGTCAGCTTAGTCCCTTTATTAATGAGGGGTCGCTACAGTGAAATGAACAGCCAACTTATCCAGCATATGTTTTACACCGCAGATGCCCTTCCTGCTGCAACCCAATACTGGGAAACATCCATACACACTCATTCACACATTCACACTCACACACTACGACCAATTAAGTTTAACGCATTCCTCTATAGAACATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACACCAACAAGGGGAGAACATGCAAACTCCACACAAAAGTGCCAACTGAAGCAGCCGAGACTCGAACCAGCGACCTTCTTGCTGTGAGGCGAAGTGCTAACCACTGATGATCACATAATGTTCAATTTCTTTAAGTATTGCAGGATTAAATGTTTTTTTTGTGCGTGAATTTGCATTGGTGGATATAAAAAAAGCTTCCTTTGATTGCCGCCTTTTCTCCTC[A/C]GGTGACGGTGATGAAGATGATGAGGAGGGTCGAGAGGAGCATCCGCCGTCCTGCTCTGATTACGTCATGCATTTTCTGACGGTCTTCTGGAAGGTTTTGTTTGCGTTCGTTCCTCCCACCGAGTACTGGAACGGCTGGGCCTGTTTCGTGGTTTCCATCACGGTGATCGGGCTCCTGACGGCCGTCATCGGGGATCTGGCGTCGCACTTTGGCTGCACTGTGGGCCTGCGGGACACCGTCACCGCCGTGGTGTTTGTGGCGCTCGGCACTTCCATACCAGGTGCGCTCTCTGCTATTACTACACATGACTGAGTACATTACCGACATATGGTGTTTATTGTAAAGTAGGTTACAGATGAAAATAAGTTTATTTTTGCTCTTCATGAATGCAGAGAAACAGAATATTGAATGAGAAAACAGTGGGCGTGGCTTGTTTTTTCTACTGCGAGCTGATTGGAAGTAGTAAAGTAGGCATTTCATTCAGAAAGATCTTAGGGAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35989

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000063721	Nonsense	946	961	11	11
ENSDART00000097701	Nonsense	946	961	11	11
ENSDART00000144567	Nonsense	833	848	11	11

Genomic Location (Zv9):

Chromosome 15 (position 41699185)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	43024592
GRCz11	15	42981024

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTCCCGACTGCTCACTACACTCCTATTTCTGGGTCTGTGGTTCCTCTA[C/A]ATCCTATTCTCCAGCCTGGAGGCCTACTGCCACATCGAGGGCTTCTGAAC

Long Flanking Sequence:

CCACACAACTGTGTTTAAACCTCATATAAATATGATTTTTGCATAATAGATCCCATTATGCAATGTCTAAGAACTTTCCAAAGCACTTCGTTTTTTGAGAAAATCTGTTGTTGAGCCGTATTGATATGCAACTCTACCACTAATGTTAATTTTTTTTCTTTATTTTTTTCAGACACATTTGCCAGCAAAGTGGCTGCAAAGCAAGATCAGTACGCAGACGCCTCCATCGGAAACGTCACTGGCAGCAATGCCGTCAATGTGTTTCTGGGTATCGGAGTGGCCTGGTCGGTAGCAGCCGTGTACTGGGCCGTCCAGGGAAAGCGATTCAACGTGGACCCTGGCTCTCTGGCCTTCTCCGTCACCCTCTTCACTATCTTTGCCTTCATCTGCATGGCGGTGCTGCTGTTCCGGCGCCGGCCGTCGATCGGAGGAGAGCTGGGCGGCCCTCGAGTCTCCCGACTGCTCACTACACTCCTATTTCTGGGTCTGTGGTTCCTCTA[C/A]ATCCTATTCTCCAGCCTGGAGGCCTACTGCCACATCGAGGGCTTCTGAACAGCTTTCTTTTCCAACATGCACTGATGTTTACCCTCAAATCGAGAGGCTCCGTTTTACGTGACACACAAATTTGCACACACTTTAGGAAAACACGTGAATTGCTGAACGCACTACTAATATCGGTAGAGAATCTGAAGTTGTAGGAATAAAAGATGAGGAAGCAAAGCATGTAGCAAAAGAGGGCAACGATGAGTGTAATGTAGTTAAAAAAGGAACGATGCTGTAAATTAGTCTTACATCTTTTGGTCTCGAGGGAAGAATTGACTTTCAATTTGCATTGTCACTAAACAGTTTTTTATTTATGGTTCAAGGGCACAATTAATCAGAGTAGAGATTTTAAAAAAGAGTCCTCAGAACTATAGTGACGCTAATAAAAATGCACAAGCGTTAACAGATCAGCAGTTTTGCTTCAGCTCTCTGCATCTAAAGCGATCGCTGCTTGAGAGATT

Associated Phenotype:

Not determined