ZMP

ENSDARG00000088119

Ensembl ID:

Human Orthologues:

SLC27A2, SLC27A5

Human Descriptions:

solute carrier family 27 (fatty acid transporter), member 2 [Source:HGNC Symbol;Acc:10996]
solute carrier family 27 (fatty acid transporter), member 5 [Source:HGNC Symbol;Acc:10999]

Mouse Orthologues:

Slc27a2, Slc27a5

Mouse Descriptions:

solute carrier family 27 (fatty acid transporter), member 2 Gene [Source:MGI Symbol;Acc:MGI:1347099]
solute carrier family 27 (fatty acid transporter), member 5 Gene [Source:MGI Symbol;Acc:MGI:1347100]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa44340	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44340

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000123999	Essential Splice Site	326	622	10	16

Genomic Location (Zv9):

Chromosome 25 (position 33263850)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	31874353
GRCz11	25	32285310

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGATGCAGTACATCGGAGAAACCTTACGCTACCTCTGCAATACGCCACAG[G/A]TAAATAGGCTTGTCACTGCCTAAACGTACAGATGCTTCTTACATATATGG

Long Flanking Sequence:

TTTTTTTAACCATTTTTGGGTCAATATTATTAGCCCTTTTAGGCTATATATTTTTTGGATAATCTACAGAACAAACAATCGTTATATAATGACTTGCCTAATTACCTTAACCTGCCTAACTAACCTACTTAAGCCTTAAAATGTCACTTTAAGCTGGATACTAATATCTAATCAAATATTATGTACTGTCATCATGGCAAAGATAAAATAAATCAGTCATTATAACTATTGTGTTCAGAAATGTGTTGAAAAAATCTTCTCTACGTTAAACAGAAATTGGGGAAGAAATAAACAGGGGGTCTAATAATTCAGGGTGACTTCAGCGGTATCTAGAAAAGCTTGTAAAGTGTTGACTGAAATGTGATTTTCCTCCAGGCAGCACTTTTGTTCTGCGGAGAAAGTTTTCCGCTTCTCAGTTCTGGGACGACTGCAGGAAGTACAACATTACTGTGATGCAGTACATCGGAGAAACCTTACGCTACCTCTGCAATACGCCACAG[G/A]TAAATAGGCTTGTCACTGCCTAAACGTACAGATGCTTCTTACATATATGGCATATGTGACTTAAAATCAGCGCTTTTCCTGGGAATTGAACCAACAAACCTTAGAATTATGCTTTCTTATTTGAGCGCGAGCGCGCGCACGCACGCACGCACACGCACGCACGCACGCGCACACACACACACACACACACACACACACACACACACACACACACACACACACATATATATATATATATANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAAATGTTCACCATAAATAAAAGGGATCTTATCTATTCAGAGGATTTGGATTAATCCGCTTAATTCATATGGATTTTTTTTTACTTCTTCATTTGGAAGCATGCAAGTTCAACGAAGTGACAATTTAATTAACAAATTTATTTGTGCCTATAAATGAATGAA

Associated Phenotype:

Not determined