ZMP

LOC559645

Ensembl ID:

ENSDARG00000090686

Human Orthologue:

SLC35F2

Human Description:

solute carrier family 35, member F2 [Source:HGNC Symbol;Acc:23615]

Mouse Orthologue:

Slc35f2

Mouse Description:

solute carrier family 35, member F2 Gene [Source:MGI Symbol;Acc:MGI:1919272]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa11796	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa11796

Status:

Available for shipment
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Availability:

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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128267	Nonsense	49	332	1	7

Genomic Location (Zv9):

Chromosome 15 (position 24511798)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	25222985
GRCz11	15	25158250

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACCCCTATGCTGCAGAGCTTTAKTAACTACACACTCCTGGGCATCACTTA[C/A]ACCATGGCACTTATCTTCAGAAGAGGTATTTGATCACGAATCATCAGATT

Long Flanking Sequence:

CTTTTGGTGCTGAATCTAAGTAAGAGGTTCTAAATATTCATGAATTTATTTCTCCTGTTGAACGCAAAACAAGACATTATGAAGAATGTTGGGAAAAAATTTCCATTGACATCCAAAAAAATGCTATGGAAGTCAATGGCTATTTATTCCAACAGTCTTCAGTATATCTTCCTTTGTGCTCAACAGAAAAAAAATCCTCAAACAGGCTCTGAACAATTAGAGAATGAGCAATGGTGACAGAATTTATCCATGTCCGTGTGTGAACTATCCCTTTAAAAATGTCATTAGAAAAGAATCGTCTCAAAACCTTGATAAAAGATTGCAATGATTCCAGTGGATGTTGATTGCAGGCAGCTGTTGAAGATTCTGCTGATGGGACAAGGCCTCTCAGCTCTGATCTGTGGCACTGCTGTAACATCACAGTATCTGGCATCCGTTTACTATCTGAATACCCCTATGCTGCAGAGCTTTATTAACTACACACTCCTGGGCATCACTTA[C/A]ACCATGGCACTTATCTTCAGAAGAGGTATTTGATCACGAATCATCAGATTTTCAATGAATTTCAATCTCTTGTTTCAATCTTGTTCATTATTTAAAGCTCTTCAGATATCTGACACTTTCTGGCATGCGATATTCAGGATGCCTCTCTTTTAATGTAGGTGATGGAAATATTTTGCAGATATTAAAGACAAAATGGTGGAAGTATCTATTGTTGGCGGTGGCAGATGTGGAGGCAAATTATGCAGTGGTGAAAGCATACCAGTACACCACATTAACCAGCATACAGGTCAGATTAGATCATATACAGTATCATTATCATTCTCTCATGCTCACTAGGTGTGCTGATTAAAATACAGTAAAAACAGTAATATTGTGAAATAATAGTAGATTTGATATTAGTATTTTCTGTTTGAATATATTTTAAAATTGTCATTTATTCCTGTGATTTCCATCTGAATTGTCAGCATTTTTAGTCTGGATCAGTCTGGATATTTAAGTAA

Associated Phenotype:

Not determined