ZMP

si:dkey-147f23.1

Ensembl ID:

ENSDARG00000013177

ZFIN ID:

ZDB-GENE-081104-49

Description:

LOC100004228 protein [Source:UniProtKB/TrEMBL;Acc:Q1ECW0]

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 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39489	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa38111	Nonsense	Available for shipment	Available now
sa6003	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39489

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
ENSDART00000086334	Essential Splice Site	281	618	3	10
ENSDART00000145015	Essential Splice Site	279	415	3	6

Genomic Location (Zv9):

Chromosome 25 (position 33284478)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	31894880
GRCz11	25	32305837

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATCACAGCTCTGGCTTTGGCCTCGGGTTCGGAGGTTCTGTTGAACGAGG[T/A]ATTTCATTGACTTCTTTTACTGTTAGTTTTGTTTAGTTTTCTGTACATAT

Long Flanking Sequence:

GCGGGGCTTTCCCCCTCTGATGACATGTACAAAGGGAGAATGTAAATCAAAGTGTTTCTGCAGACTGTTTTGATCAAGTGTGATTATGAAAAGTAGAATTAATACAGTTTTACACTTAGAGGCTGGTTGTATTCACAGACTGTTGCCACACAACTGTGTTTAAACCCCTTCTAAAAGTGAAGAAATGGTCCCCTTTAAAGCTACAGGCAGTTCGGAATGCAGACGGAGAGTGTGTGTGAAAAAGGCATCAGACTCTCTACTCTTGACTCCAGAGGGGAATGGATGAAGGTCTCAGTGAAAGGACAGGTGTGTAATTAATGGATGTGTTTGATGGCTGCAGGTCTCCCGAAGGCGGCAGTGATCACTCACCGCAGGCTCTGGGCGATGGCCTTCTTTCAGTCCATCTGTGGAGTGAAGTCTGATGACGTGATTTACGTCTGCCTGCCTTTGTATCACAGCTCTGGCTTTGGCCTCGGGTTCGGAGGTTCTGTTGAACGAGG[T/A]ATTTCATTGACTTCTTTTACTGTTAGTTTTGTTTAGTTTTCTGTACATATCTATTTGCTTTTATCAATGTTTTTCTGGTAACACTTTATTTTTAAGGTGTCGTTATCGCACATATTTAATGTACTTACTGTTGTAATTACAATGAATTATGCACCATTATTCACTCATCAATTTTCCCTCAGCTTAGTCTCTATTACAGAGGTCACCACAGCGGAATGAACCGCCAACTTATCCAGCATACTGTATGTTTTCACAGCAGATGCCCTTCCAGCTGCAACCCAGTACTGGGAAACACCCATAAGCACTCATTCACACACACTCTCATACACTACTGACAATTTAGCTTACCCAATTCACCTAAAGCGCATGTCTTTGAACTGTGGGGGAACTCTGGAGTACCCGGAGGAAACCCACACCAACACGGGGAGAACATGCATACTCCATACAGAAATGCCAACTGACCCAGCCGGGACTTGAACCAGTGATCTTCTTGCTGTGAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38111

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
ENSDART00000086334	Nonsense	412	618	6	10
ENSDART00000145015	Nonsense	410	415	6	6

Genomic Location (Zv9):

Chromosome 25 (position 33279928)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	31890330
GRCz11	25	32301287

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGTTTGATCATGAGAAAGAGGAGCCCGTCAGAAACGCTGATGGATTTTG[T/A]ATTGAAGTTGCAAAGGGCAAGTAATATGGAGCCAATAATGTGACAAAAGG

Long Flanking Sequence:

AAGTATTAAATACATTTCAATAGTTCAGTGTTTTCTCCTTTTCCCACTTTTTTAATGCCCTTTTGGTTTTTCTGCTCCTCCTCTGTGCTCTATCTTTATAATATGCTGTTTTTTCCTCATGTTTGTTCTCTCGCTCTACAAGTGTGTTAGTGACCAAGTGCACAACGTCAGGATGGCCATTGGGAATGGCATCCGGCCGGATATCTGGAGGACGTTCATAAACAGATTCGGTCATGTTGAAATCAAAGAATTTTACGGCTCAACTGAAGGAACTCTGGGCTTCTTGAACTACGCTGGCAAAATTGGGGCCGTCGGTACTGTCAATTCTTTTCATAAGGTAAACTACCCACAATTCAATACTGTTCCCTCATTCATCATGGGAGCTGGACAAAAATGACTTATGTGCGCCAATTTGTGTGGTTTTAGAAACTGTACCCGTATGTCTTCATCAAGTTTGATCATGAGAAAGAGGAGCCCGTCAGAAACGCTGATGGATTTTG[T/A]ATTGAAGTTGCAAAGGGCAAGTAATATGGAGCCAATAATGTGACAAAAGGATTTGAATTTGAATTATTGACACGTGTTGTTTAAAAAAAACTAAATATCAAATGTCATATGTTTTTAGGTTTAAGTCTTTTTCAAAATAGACTATAGCCAAATAGACTAGGGGTACTATTTTAACAATTTAGGTGCAAAATCTAAAGGGCATGGCGCAAAAGCATTAAGGGCGTTCCCGAATCCACTTTTGCTATTTTAAGGACTGAAAAATATGCTCTGCGGCAATGCGCATGGTCTAACAGGGTTGTGCTTATTCTCTTAATGAGTTATTTGTGTGTTTTGAGCATAACGTGCATTAAAACAATCAGAGCATCATCTCCAATTCTTTTTAAGAGTCAGTTGCGTCGCGCCATAGCGCATTTGCTATTTACATGATGTACTTTATAAGTGGAAAAACTGAACAATAGTGAGGAAACAGTTAAACAGAGCATCTGCAGCACAAGGATAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6003

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
ENSDART00000086334	Essential Splice Site	484	618	7	10
ENSDART00000145015	None	None	415	None	6

Genomic Location (Zv9):

Chromosome 25 (position 33276258)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	31886660
GRCz11	25	32297617

KASP Assay ID:

554-3880.1 (used for ordering genotyping assays)

KASP Sequence:

ACCGAGAAAACTTCATCTACTTCCAGGATCGGGTGGGCGACACTTTTAGG[T/A]GAATCAATCACATGAATACAGTGGGTTTACATNNNNNGGCTTCTCCATTC

Long Flanking Sequence:

GTGACCCAACGTGAGGCGACAACACAGTTGGGGTTTTGTTGGTGCTTGTTGTTTTGCGTCAGCTTAGCGTGTCCTGGCCCTTTTAAAAAAAAATCTGTTGTCTCAAATTTCAAATGTTCCATATTCAAGTAAGGAAAATCTGATTCAAAACTGTTTTAAACACCACACCGGATAATTCAAATGTACACAATTCAAGTTTAAATAGTTTTGTCATAGTTTTAGCTCCATAATATTAATAATGTTGATTTGACTGAGAATAGAGTGATAATTCAATCAGGATGGTTATTGCTGATCATGCAGGAGAGACGGGTCTGCTAGTGACACGGCTCACTCAGAAGATTGAGTTTTCTGGATACGCCCGGGATCCCAAACAGACGGAGAAGAAGAAACTCCATGATGTGTTTGAGAAGGGAGACGTTTACTTCAACACTGGAGATCTGTTCAGGACTGACCGAGAAAACTTCATCTACTTCCAGGATCGGGTGGGCGACACTTTTAGG[T/A]GAATCAATCACATGAATACAGTGGGTTTACATAAACTGGCTTCTCCATTCACTTAAAAAAAATTCAGATGTGAGCAAGGTTAAATTTATTTCATACAGTACAGTAAAAAAAACTGTACTATTGTGAAGAATTACATATTAAACTAGCATTTTGTATTGTATTTATTCCTTATTATTTGTTGTTCCTAAATCTTGGAAGACTTTAGTCAGGTTGTGTATTATAATTAGCTAATAAATGCATGATATTCTGTTTTTCAGATGGAAAGGGGAAAACGTCTCCACTAATGAAGTGTCAGACATCATGACTCTGGTGCCTTGTATCGAGGAAGCAAATGTTTACGGCGTCACAGTTCCAGGTATAATGCAGATTTTCTCTTTTCTAGTAAACCCTCCATTACTTTACTGCACTACCTGTTCATATATACAACACACAACTGACGCTTTAATGCATGTGAAGGTTTTGAGGGGAGGATAGGAATGGCCGCCATCATACTGAAGAAA

Associated Phenotype:

Not determined