ZMP

slc25a21

Ensembl ID:

ENSDARG00000060564

ZFIN ID:

ZDB-GENE-060929-664

Description:

mitochondrial 2-oxodicarboxylate carrier [Source:RefSeq peptide;Acc:NP_001070100]

Human Orthologue:

SLC25A21

Human Description:

solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 [Source:HGNC Symbol;Acc

Mouse Orthologue:

Slc25a21

Mouse Description:

solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 Gene [Source:MGI Symbol

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14376	Essential Splice Site	Available for shipment	Available now
sa36477	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14376

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
ENSDART00000085481	Essential Splice Site	89	298	5	11

Genomic Location (Zv9):

Chromosome 17 (position 38372082)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	38256979
GRCz11	17	38204564

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGGAATCCTTCCCCCCATTTTGGCCRAGACCCCAAAAAGAGCAGTGAAGG[T/C]AACAGGAACAGCATTTGAYTCCAAGCTKAAACCCATCACTTAAACTATAC

Long Flanking Sequence:

ATCAAGGGCAGATTCTGCTTGACTAGTGTATTCAGCATTAAGCTTCAATGTGTAATAAATGGGATTGGTTATGGTTTTGGTTAGGGAGTTATAATAAAAAAAAATTGTTAATACAATGTAAAGCAATGTTTTCCATTTATTGAAAATAATATGAAATGAATTAGGAAATGACCCATGGCAACTTTAATGTAAAATAATTTGCTATATTTATCTTTGGGCAACTGCTCTCAGTGATATTTGGTTTTTGGCCTTTCATACAAAAATGTTTGGGCACCCCTGGTTTATAACCTCTTGAGTGTGAGTACATAGTTAGGAAAGTTTTAGGTGATCCTTTAATGGGCTAAATAAATGTTTAAATGTTGCCTGTTCTTAAATCTTTATTAATTTAATAAGCATCTTAAACTCATAGATTGATGTCTATTTTCTCAACAGGGTCTATGGCTTCTACAAGGGAATCCTTCCCCCCATTTTGGCCGAGACCCCAAAAAGAGCAGTGAAGG[T/C]AACAGGAACAGCATTTGACTCCAAGCTTAAACCCATCACTTAAACTATACACACTCTGATCTTTTGCAACCTGGCCTGCAGAGTGTAAACACACACACACACACACACACACACACACAGACCACATATGAATGTCCTCAGCAAAAACACTCATCCCCTCTCTGTGTTTGTCGTCATGCCACATGTGTTTGCTGTTGAAAACTCCCATTATTGACCTACATGGATAGATATTGCTACTGGCCTCACTTCAGTATCATGTATAAACAGTGTGTATATACACGCTTGAGTTTAGATGAGCACTTAGTGTGGCTTTAGGCCATCGGTTATGGGTTCCTCACAATGGCTGTCTGAAAGAAGAGCGAGCCCATTATTTGCTTTCGATTGGTAGACTTAACATGCTTTAACAGTTTAACTGAAAAAAATCTTCACCTGACATGGAAATTCTGTCATCATGTAGTCCTTCTCATGTCATTCAAGTTGTTTGAATGACACTCTTAAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36477

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
ENSDART00000085481	Essential Splice Site	145	298	7	11

Genomic Location (Zv9):

Chromosome 17 (position 38380821)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	38265718
GRCz11	17	38213303

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAAGTAGTGAAAGTGAGCCTACAGGCCAACAGGGATTCATTCAAAGTGG[T/A]AAGAGGCTGCAGCTGCTAATTGTCATCACGCTATTGTTTTTGGCTTTTGC

Long Flanking Sequence:

GTCGAGCAGTTATTGCGCCATCTGAAGTCATTTATCTTTGTCCCAGTCATTTTGTCTGAGCCGCTTCATTCATCTCTGATTCCCGTCTGTGTTTCCTTTCTGAAAATGATTGACGACGGCAGTTTTATTCATTCACTCATTCATTCATTTGTGGGTTAAAGTCAAGTTCTGCGTCTATACAAACACGTTCCTGAAAGGCGAAGTGTCACACTAGCATTGTTCCTGTGAGTTATGCCATTTATGTGTGACATTCCTTCAGTGTCGACTGGTCATCTAAAAAAAAAAAATACAGTCTGTTCTGAATTAAACACAAAGGTACTTTCTTTATAGTCTCCGTGTCTTTCTCGTTCGTCATGTGGCTTCATGTTCTCTTGTAATGTAACTCTGCTAGGCTCTGTCTGTGGCTGGCCTGGGGTCAGGGTTAACCGAGGCACTGGTTGTAAATCCATTTGAAGTAGTGAAAGTGAGCCTACAGGCCAACAGGGATTCATTCAAAGTGG[T/A]AAGAGGCTGCAGCTGCTAATTGTCATCACGCTATTGTTTTTGGCTTTTGCCTTGTCATAGAGGGTCCTGGTGACGTTGTTTCTGTGTTTCTTCCATGCAGCAACCCTCTACTTTTGCACAGGCCAGAAATATTATAAACACAGACGGCTTTGGTCTCCGTGGGCTTAATAAGGGCCTGACCTCCACGCTAGGACGGCACGGCGTCTTCAACATGATCTACTTTGGTTTCTACTTTAATGTTAAGGATGCCATTCCTGCGAGTCAGGTAAGCAAATTTCAAATTCTTTCATTGATTCACCTTCAGTGTTGTTTAAAATATGAATTATTGTCTTAAATATTTAGCAAAAGGTCTTTCTTTTGTTTTTGTTTCTTAAATGTTTGTATAGAAGAGACATCTTTAGTTCCAGAGTGGACCTTTTGGTGAAAAGATTATTTTTGGCGAATATGTATGGAATCTTTTCTGTCCACAAAAAGGTTCTTTATATTTGAAAAGTGTTTCA

Associated Phenotype:

Not determined