ZMP

slc25a26

Ensembl ID:

ENSDARG00000058208

ZFIN ID:

ZDB-GENE-050913-126

Description:

S-adenosylmethionine mitochondrial carrier protein [Source:UniProtKB/Swiss-Prot;Acc:Q4V9P0]

Human Orthologue:

SLC25A26

Human Description:

solute carrier family 25, member 26 [Source:HGNC Symbol;Acc:20661]

Mouse Orthologue:

Slc25a26

Mouse Description:

solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26 Gene [Source:MGI Symb

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31823	Essential Splice Site	Available for shipment	Available now
sa41802	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31823

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

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081035	Essential Splice Site	100	267	3	10
ENSDART00000147190	Essential Splice Site	100	170	3	7

Genomic Location (Zv9):

Chromosome 11 (position 16605897)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	16086597
GRCz11	11	16221232

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAAACCTGGCCCCCATCACTCACATGCTGGCTGCTTCACTAGGAGAAATC[G/A]TAGGTTTCCTGATGTTATTCTTCTTTATTCAGTCCTGTTGTTTTGTCCTT

Long Flanking Sequence:

TTCTTAAACTTTATTTTCTGTATAAAAACTCTATTCCTTTCTGTGCACTAATATTCAAAACGTCTGTAAAATTCAGAAATGTTCTGGGGCTATAAAGAAGTAATTAGTTAATTCTCGTTTATTAAAAGTTAAAAGATGGACAAACTTTGAAAAGAATAATGCCACCCCATTGTACTCAGTTTTTGTGTTAAAGTTTATTTTATAGTCTTATTTTGTACTTTTTAGAATAGTAATTAAATAGTGTAATTAAAATGTCTGATTATGATAAGCAACATATTTAAACCAGACTCACTGAGATCCTCAGGTCTGAGGATACACTTTCAAATGAAATACATGCAAACATCTTCATTTAAATGGCTTGCTTGAAATGAAGTGTTTATTTTCTTTCAGCTGCCGCATTCTTTGTCACCTATGAAAGCACCAAGTCCGTTTTCTCTGGCTACACCACAACAAACCTGGCCCCCATCACTCACATGCTGGCTGCTTCACTAGGAGAAATC[G/A]TAGGTTTCCTGATGTTATTCTTCTTTATTCAGTCCTGTTGTTTTGTCCTTCAGTTTATCATCATTTACCCATTGCAGTCCAACTGAACAGAGTCTGTTTCCCAGACAAATATGCAGAAGGCTTAGAATGGGGTTTTTGTTGGATGTGTTGTTTTTTACTCTGGGTTAAAGCCGGGCCACAGATGACCTTGTATTTTCCCAACAGCTGGCCAAATAGGATCTTATTGTTTTCTGTTGACATAGCTGTTTTCATAGAGAGGAGTCTTGCAGTTTTGTCAAGGGAGATTTAGGTGTTGGAACTGAAAAGAACACCTTCATTTCCTCTGTAAGTGAATCACTGAATGCTCAAAAAAGGGCAGTACTCATGTCATAAAACCAATCAAAGTCAGAAATAAAAAGTGAATCTTTCATTGTTGTATACTACATCTTCAAAAATGTAATTGCGATATAACTTTCTCGAAGATTGTGCAATTTTAAGTGGTCTTTTCCAGAAATTCAAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41802

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081035	Essential Splice Site	151	267	5	10
ENSDART00000147190	Essential Splice Site	151	170	5	7

Genomic Location (Zv9):

Chromosome 11 (position 16622882)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	16103582
GRCz11	11	16238217

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGGATTCAGAGGGCTGTACAGAGGTTATGGCAGTACAGTACTAAGAGAGG[T/C]AAGCTGATTTACTGTATGCACTTTAAGTATTCTTACTGCATCATTTTACA

Long Flanking Sequence:

TGTAACCAAATTGTAATCTACATTTTTAATTGACTTATTATAATTTTATATATTTGCTATTTTATTTGTAATTATTTTTATTTTTAACATGTATTGTATGAAAACGTTTGGTTTGTATGAACAGTACTATTAAATGTTCTGATGAGTTTGTCTTTCTCTTCCTCAGGTTGCCTGTCTGATCCGTGTGCCCACTGAAGTCGTAAAGCAAAGGACACAAGCCAATCCCTCCATCAGTACCTACAGAGTGCTGCTGAACTCACTACAGGAAGAGGTGCGTGTGCATCGTCAGCTAGGCTCGCAGCACACAATGCACTTGAATTCACCTGACAGACAGTTGAATGGTTGGATTGATTGACTGATAAACACGTCATTTTGTAAAACAACCAGTCATGAAAATGCAGTGTTTTTTGTTTGTGCAGAGATGACAGCTCTTTTTGTTTCCCCATTGCAGGGATTCAGAGGGCTGTACAGAGGTTATGGCAGTACAGTACTAAGAGAGG[T/C]AAGCTGATTTACTGTATGCACTTTAAGTATTCTTACTGCATCATTTTACATCATTGTACAAAGGTTTTAGAAATTTAATCTAAGTACCTCTTAAAGGGATAACTCTAAAATACAGTGGGTATGGAAAGCATTCAGACCCCCTTCATGTGTTCACTGTAGTATTACAGCCATTTGTTAAAATCATTTAAGCTATTTTTTCCTCAATAATGTACACGCAGCACCCTATAAAGACAGCAGAATTATTAAATTATTAAAGTTTTGAAGATGCTCCAACCCATTGCTAACACACACACACACACACACACAATCCTTCTTTTTTCAATTATTGAACAAAGAGTGCAACATATAAGGGGGTCTGAATACTTTCTTTACCCACTGTACTGTATATAGTATTAACACAAATAATGCAGGTACTTACTATAAGGTTAAGGTTTAGTTTGGAGTTAGTCATTTATTCTCACTAGTAAAAAGTACATTATGCAAAATTAAGTACATTAAAG

Associated Phenotype:

Not determined