ZMP
slc2a3
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 2, facilitated glucose transporter member 3 [Source:RefSeq peptide;Acc:NP_001
Human Orthologues:
SLC2A14, SLC2A3
Human Descriptions:
solute carrier family 2 (facilitated glucose transporter), member 14 [Source:HGNC Symbol;Acc:18301]
solute carrier family 2 (facilitated glucose transporter), member 3 [Source:HGNC Symbol;Acc:11007]
solute carrier family 2 (facilitated glucose transporter), member 3 [Source:HGNC Symbol;Acc:11007]
Mouse Orthologue:
Slc2a3
Mouse Description:
solute carrier family 2 (facilitated glucose transporter), member 3 Gene [Source:MGI Symbol;Acc:MGI:
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32235 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32235
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016197 | Essential Splice Site | 39 | 541 | 3 | 10 |
ENSDART00000131151 | Essential Splice Site | 38 | 540 | 3 | 10 |
ENSDART00000134816 | Essential Splice Site | 39 | 541 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 10323496)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 9782035 |
GRCz11 | 19 | 9700960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTAAACTAATTAAAAGTATGAGCGTGACCATCAAAAATTAATCTTTC[A/C]GAAACTACGGGCGTTCTTCAATGCCACGTGGATGGAGCGTTACGGGGAGC
Long Flanking Sequence:
ATTTGCAATGCTTTTTTATAGTAGACTGAGCTTAATGAATTTGTTTTGGTGTACATTGCTTAATGTGACCCTCTTATTGGTGGAAGTTTCTGTACGACATTATGGGTAATATAGTTTTCTCTGCACAAATGCCACTACTAAGCATGATCGTTTTAAAAATAGGTTGAATCGATGAAACAAATAAAAACAGCCCTAAGGAAAAAATGAATGGAGTTGTTACTATCAGAACATGATTGTTGTGCTCTTTGATTGGCTGAAAATTCAGCGTTATTACAGAAATACCATTTTAAAATTAAGTAAATTAGAAAATATGAATTTGGATTGGTGTAGGATTTCAGATTATTACTGTAATAACTGCATTTTTTGTTAAATAATTGCACTTACTCTTAGTAACTTACTATAATTATATTAGTATTGCATTTACTTTATTCCTACTTTTTTATATTTGGAAGAGTAAACTAATTAAAAGTATGAGCGTGACCATCAAAAATTAATCTTTC[A/C]GAAACTACGGGCGTTCTTCAATGCCACGTGGATGGAGCGTTACGGGGAGCCCATCAGTCCAGGTGTCTGCACCATTGTGTGGAGTTTTGCCGTGGCCATCTTTAGCGTTGGAGGAATGGCGGGGTCATTCAGCGTCGGCGTCGTAGCCAACAAATTTGGAAGGTGAGTGGGAATTACTCAACAGTATAATGTTTTGAATTGCAAATGCTGACCAATCTGAGCTTTTATAGGTCCCGTGAAATGCTGTCGAGGTTGAAATGTGAATTTTTTTATCAAATGTTTGACTGAAACATGAGGAGAGGGTGGGATCTATAGTAGCTTTGAAAAAACAGCCAATAGCATTTTGCGTCTTGAAGGGGGCAGGGCATGTCAGACACTAGAGAGTATTTGATTGGCCAGAAACTGTAGTATAAGGTGACATGAAAAAAAAATGTTGATCCTTTTAGGAGGGAGAGACAAACGGCAAGCTTTGAATGTTTTTATAAGTTCTATATCTTCTA
Associated Phenotype:
Not determined