ZMP

zgc:158482

Ensembl ID:

ENSDARG00000067520

ZFIN ID:

ZDB-GENE-070209-32

Description:

hypothetical protein LOC100009650 [Source:RefSeq peptide;Acc:NP_001076488]

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
sa39185	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39185

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000097163	Nonsense	618	619	10	10

Genomic Location (Zv9):

Chromosome 18 (position 245135)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	60777
GRCz11	18	60777

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACGTCACCCTGACCCCCAACATCTACCAGCAGATCCTAGCGCACAGCATC[A/T]AACTCTGATTACTGCCTCATCAGCGATACTGTTAGAGAAACACAATCACA

Long Flanking Sequence:

AGTGTTTACGGAGTTTGTGTTCCAGGTGGGCTGAGGCTGTGTTTGCTCTGAATCTGCTTCCTCATGATTGATGACATCACTAATGTGTGTGTGTGTGTGTGCGCAGGTCATGAGGGACGCATCGGGATGGCTGCAGTAAAACTGAAGGATGGAGCCGAGTTTGAGCAGAAGCAAGTGTTTGAGCACGTCTCCAGACTCCTGCCTGCGTACGCCAGACCGCGGTTCCTCCGCCTGCAGGTAAACCCCGCCTCCTCCTCCTGAACAGCATGTGAAGCCTGCAGTTCCTCATGAAAGCGTGTGTGTGTGTGTGTGTGTGTGTGTTCTGTGTGCAGAGCTCAATGGAGCTGACCAGCACCTTTAAACAGCTGAAGCTGAAGCTGGTGGAGGCCGGGTTCAATCCCAGCATGACCTCTGACCCCATCTACTTCCTGTGTGAGCGCGAGCAGACGTACGTCACCCTGACCCCCAACATCTACCAGCAGATCCTAGCGCACAGCATC[A/T]AACTCTGATTACTGCCTCATCAGCGATACTGTTAGAGAAACACAATCACATGTGGACAATAGAGCTGACGCAGAGCAGTGAACCGACAAATAAAGTGTTTAAAAGCCGTGTGCTGTTCATCATCTGACCACCAGAGGACGCTGTTTAATCTGATTCTCTGAGCATTGATCAGCACACACAGAACTCTGCTCTGGTCTCTGGGTCATGTGCTGTTATGAGCAGAGCTGAGGGGGAGCGGCTCTCAGGACTCTCAGCTCACAGTAAGCAGACCATGCGTCCCAAAGTGGGGGTGTAAACCCCTCAGAGATAAAGTGGGAGAGTCGCTTGGTGATTTCCAAAAATCCAATTCACTTCATTAAACTAAGAGTTAGCACATTAATCCAGAACATGCAGAAGAACAGGAACAGTCACACTATATCAATATAACAGTGTTTATGGCAGCGGGCTACACTCTCTGACAGCTGTACACACTCACACAGGCCACAACAGGACGGGTCACG

Associated Phenotype:

Not determined