ZMP

slc2a1a

Ensembl ID:

ENSDARG00000001437

ZFIN ID:

ZDB-GENE-030131-3158

Description:

solute carrier family 2, facilitated glucose transporter member 1 [Source:RefSeq peptide;Acc:NP_001

Human Orthologue:

SLC2A1

Human Description:

solute carrier family 2 (facilitated glucose transporter), member 1 [Source:HGNC Symbol;Acc:11005]

Mouse Orthologue:

Slc2a1

Mouse Description:

solute carrier family 2 (facilitated glucose transporter), member 1 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43972	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43973	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43972

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025414	Nonsense	41	488	3	10

Genomic Location (Zv9):

Chromosome 23 (position 22501276)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	22280583
GRCz11	23	22207134

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAATCTCATACCCACTTGATAATGTTGTTTTTTTTCTCTCATAGATCATC[G/T]AGGGCTTCTACAATGAGACGTGGCATAACAGGTATTCAGAGTACATTCCG

Long Flanking Sequence:

CAGAACTTGCCAAGATGGTTCAGTTGGTTTAGTTGGTCAGATGGTTTATAGTTTTGGAAAATGCATTCTGTTTTGACACTACATTTCTGCTCCCTCTGCTGTCTCTAATGTGGTACTGCTGGATGACTGTTGACTGAAGTTAGAGAAGTGTAATGATATTTAGGTCACAATTCACAGTATTAACAAACTATTAACAAACACTACTAGCTTAATGAACTACTAATTAGCTGTTTATTAATAGTTAGTTAGTTAGAAGTTGGGTTTTGGTTTTGGGTAGGATTAGGGATGCAGAATAAGATCATGCTTTAGAACTGTTAATGAAAAGTTAATATCTTATTAATAGGCAGGTAATATGCTAGTAGTTAATAACATGAACTGTGACAGAAACTAAAGCGTATAAATACGTTTTTAAGAAAATGAAATTACATAAAAAATGTTGAAATTCCTTATGAATCTCATACCCACTTGATAATGTTGTTTTTTTTCTCTCATAGATCATC[G/T]AGGGCTTCTACAATGAGACGTGGCATAACAGGTATTCAGAGTACATTCCGCCGACCACTCTAACCACACTCTGGTCTGTATCAGTGGCCATTTTCTCTGTGGGCGGCATTCTCGGCTCCTTCTCAGTGGGACTCTTTGTAAACCGCTTTGGCAGGTAACTTCAAAATCTACAGCAGTCAGAACCTTACCGATACTTTGCTCCTCTTCTGGATCTGAAACTCTTTGTGATCTTCCAACAGGAGGAACTCAATGCTCATAGCTAACATTCTGGCCTTCATAGCTGCTGCTTTTATGGGCTTTTCGAAGCTGGCTGAATCCTGGGAGATGCTTATTATTGGACGGTTCATTGTGGGTCTTTACTCGGGCCTGTCTACAGGCTTTGTGCCAATGTATGTTGGAGAAATTGCCCCGACTTCATTACGTGGGGCGCTGGGAACTCTTCATCAACTTGGCATTGTCATTGGCATCCTCATGGCACAGGTGTTTAAGTATTTAAGCAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43973

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025414	Essential Splice Site	227	488	6	10

Genomic Location (Zv9):

Chromosome 23 (position 22503185)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	22282492
GRCz11	23	22209043

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCACTTAAGATGTTGCCTGTGCCCTCAGCCTAACTAACTGATTTCCACA[G/T]TGCTAAAGAAGCTGCGTGGCACTGATGATGTGGGCGCAGACATGCAGGAG

Long Flanking Sequence:

GAACAGCAGGCACGGATGGCAATTTGAGATGTCAAAAAGTGTACACGGTGGCCTCTGTGGATTTGCAAAAACCAAAAACTGCACAAAAACCTACCTCCTGGGACATATTTGGCACACCCCAGAAATGTATATAGTAGTTACATTTTCAAAATGAGTCTGGGTCGGCTTTTTTTAATAGACATGGCCCGCATATCGTCATCTTCATCATCTTGTCATTTAACCCCAACTGTTTAGACATAAATGATCTTTGTGATCTTTTTCCTGTAGATCTTTGGTATTAAAGAAATCATGGGTTCTCCCACATTGTGGCCCTTCATGCTTGGCTTCACCTTTATCCCAGCTGTGCTCCAGTGTGCCCTGTTGCCCTTCTGTCCTGAAAGCCCACGATACCTCCTCATCAACCAGAACGAAGAGGCCAAAGCCAAGAGCGGTAAGTACTGTGTCTAAAGCTCCACTTAAGATGTTGCCTGTGCCCTCAGCCTAACTAACTGATTTCCACA[G/T]TGCTAAAGAAGCTGCGTGGCACTGATGATGTGGGCGCAGACATGCAGGAGATGCGGGACGAGAGCAGACAGATGATGAGGGAGAAGACAGTCACCATCCCCGAGCTTTTCCGCTCATCACTGTACCGTCAGCCCATCTTCATCGCCATCATGCTGCAGCTCTCACAGCAGTTCTCCGGCATCAATGCTGTACGCTTTCCTGCTTATTTCTTTTCTGGCAATACATCTATTCACTTTCCTATCTACTTCTACTGTACTAGCGAAATATAAATTGATGTTTGCCAACTAATACAAATTTTTTTTAGTATAATTTATTTTATAAATCATTATTATTAAAATAAAACCAAAACAAAGTAAAACATTTTCTATTACTATAACTTAAAGCACCAAATCATCAAAATAGAATCATTGATGGATTATAACACTGCATTCAGCTTTTACAGCTGAAAATAAAATATATTATTTTGTTAACTGAAATAAAAGACATTTACTTTAAATTTT

Associated Phenotype:

Not determined