ZMP

slc2a15b

Ensembl ID:

ENSDARG00000053269

ZFIN ID:

ZDB-GENE-050508-1

Description:

solute carrier family 2 (facilitated glucose transporter), member 15b [Source:RefSeq peptide;Acc:NP

Human Orthologue:

SLC2A9

Human Description:

solute carrier family 2 (facilitated glucose transporter), member 9 [Source:HGNC Symbol;Acc:13446]

Mouse Orthologue:

Slc2a9

Mouse Description:

solute carrier family 2 (facilitated glucose transporter), member 9 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa19521	Essential Splice Site	Available for shipment	Available now
sa38272	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa19521

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075286	Essential Splice Site	143	522	5	12

Genomic Location (Zv9):

Chromosome 1 (position 31037348)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	30850808
GRCz11	1	31583376

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATTTTGTGAATTAAGTCCCTGTACTGACACTCATGTGCTGTGCTAATGT[A/G]GGAATAGCTCTCAGTGTGGTGCCCATGTATCTGGGAGAAATTGCCCCAAA

Long Flanking Sequence:

CCCAGTAGATCAGCAGTTTCTGAAATACTCAGACCAGCCTGTCTGGTACCATCAACCATGTCACATTCAAAGTCACTTAAATCACCTTTCTTGCACATTATGATGATGCTCAGTTTGAACTGCAGCAGATCGTCTTGACCATGTCTACATGCCTAATGCATTGAGTTGCTGCCATGTGATTGGCTGATTAGAAATTTGTGTTAAAAAGCAGTTGGACTGATGTACCTAATAAAGTGGCAGATGAGTGTACATACAGTGCTTAGAATAAATAATTTAATTATCCTCCACTTGTTGCAAACCGGCAATGTATTTTTATTTTTAATAGAGACCATTTTAGTGTATTGACTTTAGTTTTGGTCCTTCCTTCATCCCTTCCTTTAAAAACTGCCTAGGTGTACTAATACTGAATTGAAATGTTCACCTTAGAATTATTATGTCACTGGTAATGTTCATTTTGTGAATTAAGTCCCTGTACTGACACTCATGTGCTGTGCTAATGT[A/G]GGAATAGCTCTCAGTGTGGTGCCCATGTATCTGGGAGAAATTGCCCCAAAGAATCTTCGGGGTTTTCTGGGACTCGTACCCAGCATCTTCATTTGTATCGGAGTGTTTATTGCACAGATTCTGGGACTTCATGAGCTGTTGGGCAAGGTTAGTTACATTTGGTTTCATTTTCTAATGCTATGTTTTGTCTTTATAGTACAGAGACATTTAATGAAATATTTTGAACTTTTGTTGTAGTATCATCATTTGTCTTGTTAAAGGTGTAGTAGGTGATTGTCTTCAGAAGCATTTTTTGTTGTGCTGGTTGAAAGTCACTTCACAGTCTAATAGTGCGCGCGATCGGTAAAAACATGCTGAATAAAAACTTTTTAAAAAGCTGAATCAATATTGGTGTTACCTTTGCACGCTGGAGAAAGGATGACACTATGGGCTCTATTTTGACGGTCCATGCGCAGAGAGCAAAACGCAGGGCGCAAACGCTTTCAGGGCGTGTCAGGACG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38272

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075286	Nonsense	368	522	9	12

Genomic Location (Zv9):

Chromosome 1 (position 31048714)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	30862174
GRCz11	1	31594742

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTCACTTTCATGGGTCTGTGCTGTGCTGGAATCACCTTCTCTCTCTTAT[T/A]AGAGGTAATTAAACCACAGACACTCATACTAATGCTGAATGTACAATAGC

Long Flanking Sequence:

TGTTAGAATATTTTTATAATTATAGAAAATTGGTGTTTATTAAAAGTGATAAACTTTTTTAAAAGTGATAAACTATTTTCCTTTTGCTATGACATAGCCATAGAAGTTGAAATGGCAATAAAATTAAAACTCTCTCTCTTCTTTTTTGAACCCTTAGATTTCAGATTTTCAAATAGCTTAATCTCTGAAAAACATTGTCCTATCATAACAAACCATACATCAATGGAAAGCTCATTATTTAGCTTTTATATTGCGTATAAATCTCAATTTGTGAAAATGGATGTTTATGGCTTGTAATGGTCAGGTGCTGAGTAAAATGATCTATTCTGGAATGGCAAACTTATAACTGGCTTCTAATTAACACTGAATTATTTATAATCTCAATTCTCTAAATGTTTTCCAGTGTTTTGCTATCGAGCGAGTGGGTAGAAGGCCCTTGATGATTGGTGGTTTCACTTTCATGGGTCTGTGCTGTGCTGGAATCACCTTCTCTCTCTTAT[T/A]AGAGGTAATTAAACCACAGACACTCATACTAATGCTGAATGTACAATAGCCCATACTGTGCGTGCGTGTGTGCATGCGTGCGTGCGTTATACACATACAAATATACACACATATAAATATACACACATATACAGTTGAAATCAGAATTATTAGCCCCCCTGAATTAGTGCCCCTGTTTATTTTTTTCCCCAATTTCTGTTTCTGTTTCATATGTATATGTGTGTATACATGTATGTTTCTTTGTTTGTGATTATGTATAAACAGTTGAAGTCAGAATAGTTCACTTTAAATAATCTAGTTAAACTTTTAATCATCACTTTAAGCTGTATAGAAGTGTCTTGAAAATATCTAGTCAAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTATAAGAAACGAATTTTTGAAACTTATGTTTAGAAATGTGTTGAAAACGTTTTCCCAATAGAAATTGGGAGAAAAAATTAACAGGGGGGCTAATAATTCTGA

Associated Phenotype:

Not determined