ZMP

slc27a2

Ensembl ID:

ENSDARG00000036237

ZFIN ID:

ZDB-GENE-050706-104

Description:

solute carrier family 27 (fatty acid transporter), member 2 [Source:RefSeq peptide;Acc:NP_001020470

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 are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa30701	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa23199	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa30701

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
ENSDART00000052638	Essential Splice Site	223	614	2	10

Genomic Location (Zv9):

Chromosome 18 (position 239549)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	66363
GRCz11	18	66363

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATCACCATGAAGAGCCCCGCCCTCTACATCTACACCTCCGGCACCACAG[G/A]TGAGCACAGCGATCCTGTGTGTGTGTGTGTGTGTGTGTTTCAGCTCTGCG

Long Flanking Sequence:

GAAACCGAAGCACCCGGAGGAAACCCACGCGAACGCAGGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCTAGCTTAGACTCGAACCGGTGACCTTCCTGCTGTGAGGCCACAGTGCTGACCACTGAGCCGTGCTGCATGGAGTGATTTGCAGTGGTGTAATATGAGCTGGCCTGAGCTGCAGTGTTGTGGCCCGTTTGTGTCCGCTAATTAACTGAGGAGAATCGCCGTGTGACAGGAGCGTTCTGTACAGCTGACTGCGGTGACTTGACTCTATGTTGCAGAGCTGGTGCCGGCGGTGCTGGAGGTTCTGCAGTCCCTCCGTCAGCAGCAGGTGTCGGTCCTCATGCTGTCAGGAGAGGCGGAGACACAAGACATCATCAATCTGACCAATCAGGTGAGCCGTGCATCTGAAGAGGCTCCGCCCATCAGCCTGAGGCAGCACATCACCATGAAGAGCCCCGCCCTCTACATCTACACCTCCGGCACCACAG[G/A]TGAGCACAGCGATCCTGTGTGTGTGTGTGTGTGTGTGTTTCAGCTCTGCGTGTTCTTCATGTCCGTCTGGTGTCTGCAGGTCTCCCTAAAGCTGCAGTGGTCACCCATGAGAAGGTTTGGATGATGTCGTTCCTGCAGAGGCTGTCCGGCGTTTGCTCCAGCGACATCATCTACATCTGTCTGCCTCTGTACCACAGCGCAGGCTTCCTCGCCGGACTCAGCGGAGCCATCGAGCGCGGTAACACAGTCACACACTGCACTGCATGCATCCAACCTGAGAGTCGTTCACAAGAGACGTACACATGACATTCCTCTATTAACTCCCTCATGTGGTTTTGGTCCAGGGAGAGCTTCATCCATCTGAATCTGATCACTTCTGTGCACCACATTAATCGGCAGTGTGTTATTAACAGTGTGTTCTGCGTCCGCTCAGTGTGTGTGTTCACCACAGGCGATGATAACACACACTAATAAACACTGTTGTTCTGATTGCTGTTCAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23199

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000052638	Nonsense	537	614	9	10

Genomic Location (Zv9):

Chromosome 18 (position 233566)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	72346
GRCz11	18	72346

KASP Assay ID:

2261-1672.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCGGCGCTGCAGCTGACAGACGGGATGGAGTTTGACGGTTCTGCTGCTTA[T/A]GAACACATGAAGAACCTCCTGCCGGCGTACGCCAGACCGCGCTTCATCAG

Long Flanking Sequence:

CTGTAAATGTACTTCAAGCTTTCAGACTGGACTCTCTCACGCCACCATGAGGTCCGTCTGTGAACTGCACTGCTCTAGTTCTAGTTCCAGATCTTCATCTATCAGCTGATCAGTATTCTCCATGGTGTGATCAATAGTCTCCAGGATCGTGCTGATCTGTGATGCTCTTGTGAGTGAGGGCTGCTCTTCATCCGTGGCGTCTGGAGCTCTGATGTTCTCTGGATTCTGATTGGCCGTCAGTGTTCTCTGGGAAACTCCTCTGTGTGTGTGTGTATGGCTGTAGTTGTGCTGTTCTCGAACACCGACACACATCTACAGCTAGATCTTTATCACGGGGATCCTGCTCTGTGTGAACGGCCTTTAGGGTCAGCGTGATCTGGCTCAGGGGTCAGAGGTCAGGCTCAGGTGTTTCTGCTCTTCTTCTCAGGTCATGAGGGTCGTGTGGGGATGGCGGCGCTGCAGCTGACAGACGGGATGGAGTTTGACGGTTCTGCTGCTTA[T/A]GAACACATGAAGAACCTCCTGCCGGCGTACGCCAGACCGCGCTTCATCAGGATACAGGTACAGCTCTGACCCACACGTGCCCAGCGGCTGACCATGACCAGTGTTGGGGGCCGCATTACAGGTGACGCGAGGCGCTGGACACTCTCATACATCTGTACATACGCCATGTAGAGCTCTGCATCACCATCCATTCTCCTTCAGCTCAGCCCCTTTATTCATCAGGGACCGCCACAGCGCCATGAACCACCAACTATTCTAGCATATGATTTACACAGTGGATGCTCTTCCAGCTGAAGACCAGTACTGGGAAACACCCATACACACTCATTCACACACACACACACACACACACACACACACACACACACACACACACTCATACACTACGGCCAGTGTAGTTGATCAGTTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCCAACACGGGGAGAACATGCAAACTCCACACA

Associated Phenotype:

Not determined