ZMP

slc13a2

Ensembl ID:

ENSDARG00000053853

ZFIN ID:

ZDB-GENE-040426-2389

Description:

solute carrier family 13 member 2 [Source:RefSeq peptide;Acc:NP_998617]

Human Orthologue:

SLC13A2

Human Description:

solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2 [Source:HGNC Symbol;

Mouse Orthologue:

Slc13a2

Mouse Description:

solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2 Gene [Source:MGI Sym

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13412	Nonsense	Available for shipment	Available now
sa43700	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13412

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
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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075958	Nonsense	14	613	1	12

Genomic Location (Zv9):

Chromosome 21 (position 37935301)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	39055380
GRCz11	21	39100438

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGACACAGRCATGGGGTGCACCAAAGCAAGTTTAGTTCTGCGCTGGCTGT[T/A]GCTTCACAGAAACTACATCCTTATCTTSTGTGTTCCTCTGCTCATTTTMC

Long Flanking Sequence:

GACAGAATTTGGCTGAACTGCCCCTTTATTAGTGAAAACTGATAATAAACCACATTATTCCAATACACATTTCCTCATTTAAGTTCCCAGAAGAGCACAACGAGAAACATTCTCGACATATTTCTGGACATGAATCAGGGCGACACCTGTTCCTCCGTGATGACTTTAGCAGTGTGAAAAGTTCAAATGTGTTTTTAATAAATCCATTACGCACTGCTGCAACAATACAATCAAACTGCTGCTTTAGACAGAGATAACACAAGGGTTTATCTTCTGTGTTTGTCATATACCCCCCTCCTCCTTCATACCCCTGTTTACCCTCCCCTTGTTCACACAGTTAATGTTTAATTTTCCTTATGTGACGATGCCTATAAACGCATTGATCGAGCTGGCTCTCCTCTGCAGTGCTCAAACCATCAGCGCTCCAGCAACAAACACCTGAGGGACCCAGGACACAGACATGGGGTGCACCAAAGCAAGTTTAGTTCTGCGCTGGCTGT[T/A]GCTTCACAGAAACTACATCCTTATCTTCTGTGTTCCTCTGCTCATTTTACCCCTGCCGTTGGTGCTCCCGACTCCAGTAAGTACAGAGGGAATATTTCATTTAAATGTAAAGCAAAGTCTTTGAATGTCTGGTATAAAGTCTTTCTATGTTGTTTGAATGGTCTGAAAATGTACTCTCAAATATCGACATTTTAAAGAAAAATGATAAAAGATGAATGATAACTGAAGTGTGTATTTATTCAGCTTGCGGAGGTCACCATCATGTCACAAATAATGAAAAGGAAGCCCCGTGGCTCACAGTTAGACAGAGCTGACAGATCTTCAGCTGAAAAAATAATGCAGGAATATTTTCTGTTCTAAGCAACCACTGAAGTTAGGAAAACTTCAATATTTTGATCACTCAAACCACATTGAGGGACTTTTATTAAGTGAAACAATCAATCATACTCTTATAACAATGTTTTGGTTTATCTTTTACAGACTGGAAGGGTTTGGAAAGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43700

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075958	Nonsense	81	613	2	12

Genomic Location (Zv9):

Chromosome 21 (position 37938467)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	39058546
GRCz11	21	39103604

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGCCCTGCTGCCCGTCGTCCTCTTCCCTATGATGGGTATCATGGAGTCT[G/T]GAAAGGTACAGTTCATTTCTGCGTCTACACTGTAAAACTTGCAGACACTG

Long Flanking Sequence:

ACTGGATTTACTAAGCATTTACGGGGTCAAACGCATTACACAGCCTTTTCTCTATAGTGATAAAAGCCCTCCATAAAATAGAAGCATCCATAAAAGTAAATCCATTGAAAATTGTTTAGTGTCGTTGATGGTCAAGGGTTACTTTTATCAGCACTTTTTCGAGCGATAGATGAAGATCTGTAAGAGATATAGCAGTGACGCCTTCACCAGATGCAAGAATCCCACCCTTTCATCCCATATGACAGCCTATGATGAGATCTGATGTGTCATGCATTTCATTCACACACAATAATCCTACAGCAGTGTGTCCTACTGCTACTGGAATAGGTGATGTATTCACTGTAGATCTCTTACCCTATGACTGCTCTGTTCATCAGGAGGCAAGATGTGGTTTTGCCATCATCCTGATGGCTCTGTTCTGGTGTACGGAGTGTATGCCGCTGGCCATCACTGCCCTGCTGCCCGTCGTCCTCTTCCCTATGATGGGTATCATGGAGTCT[G/T]GAAAGGTACAGTTCATTTCTGCGTCTACACTGTAAAACTTGCAGACACTGTACACCATACACATGAAGCAATTCTGTGGATGCTGAGTTCAACACAATTGCTTCATGTTGTCCCAACACAAACCGATTAAATTAACTTCATTGTTTTGTTTTTTTACAAATTTATTTTGATTTAACATAAAACAATTAAGTTGTCCCAAAAAAACTGAAGAATTGTGTAGATTCAGCTCAACTTGAAGAAGAAGTTTGAACAAAAAGATTTTTTAGTGTGTGAACTTTTTATTTTTGGTGGAATATTTATACATTTAAAAATACAGAGACATAAAGTTGTGAGATACTAAAATATGCTTTAAGAATAAAGTAAATATTACTAAAAAATGAAGTAGATTCAAATAATTTGAGAAAATATTGTCATAAATAATTAATATTCCTAACAGAGGCAGCAGATATTCTAAAATAGTGTTCTTAAATAAATTTCAGCCTGAATTTACATTGTCAGAT

Associated Phenotype:

Not determined