ZMP

LOC100334818

Ensembl ID:

ENSDARG00000001937

Human Orthologues:

SLC2A1, SLC2A14, SLC2A2, SLC2A3, SLC2A4

Human Descriptions:

solute carrier family 2 (facilitated glucose transporter), member 1 [Source:HGNC Symbol;Acc:11005]
solute carrier family 2 (facilitated glucose transporter), member 14 [Source:HGNC Symbol;Acc:18301]
solute carrier family 2 (facilitated glucose transporter), member 2 [Source:HGNC Symbol;Acc:11006]
solute carrier family 2 (facilitated glucose transporter), member 3 [Source:HGNC Symbol;Acc:11007]
solute carrier family 2 (facilitated glucose transporter), member 4 [Source:HGNC Symbol;Acc:11009]

Mouse Orthologues:

Slc2a1, Slc2a2, Slc2a3, Slc2a4

Mouse Descriptions:

solute carrier family 2 (facilitated glucose transporter), member 1 Gene [Source:MGI Symbol;Acc:MGI:
solute carrier family 2 (facilitated glucose transporter), member 2 Gene [Source:MGI Symbol;Acc:MGI:
solute carrier family 2 (facilitated glucose transporter), member 3 Gene [Source:MGI Symbol;Acc:MGI:
solute carrier family 2 (facilitated glucose transporter), member 4 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa43001	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43001

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000019804	Nonsense	48	482	2	9

Genomic Location (Zv9):

Chromosome 17 (position 48597955)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	48360302
GRCz11	17	48444455

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTTGACATTTTAAATTAAGGTGATTGAAGAGTTTTTCAACACGACATGG[A/T]GATCCAGACACAATCAGTCAATTCCAGACCACAGTCTGACGTTCCTGTGG

Long Flanking Sequence:

GCCAGCGTTGGATTTGGAACGCTTCGTGTTTGCGCACAGGTAGCTATGATGTCTAGCTTGTGTTGATTTATCGTCTGTGTGTGGATATAGTCCAGATCCCTCGGGTCGAGTTTTCATTAGGAAAACATTGGGACTCGTCTCAAGATATTAGTCATGTCTTTCAAGCAGGTGAAATGAACTTTCAGAGTCAAGTATTAAAATTACAGGCTGCTCTGAGTTTTTGTCCGCATTAGCATTACGTATGCTGTTTGTTTGTTGATTGGATTAAGTAGCGTCTGGAATGAAAATATTCAGACTGAGACTCATTTAATCATTACTCAGGCTCATTAAAATAGCTAAATTTAGCAGAACGGTTTTGGCGAAACAAGAACCACTCAACGATTTTACTTTTTTCATACATTCATTATCAGGAAACATGTGAATAAGGTATGCTATATATGATTAATATATATTTGACATTTTAAATTAAGGTGATTGAAGAGTTTTTCAACACGACATGG[A/T]GATCCAGACACAATCAGTCAATTCCAGACCACAGTCTGACGTTCCTGTGGTCCCTCTCTGTTAGTATTAAGGATTTTGGAGCACTGCTTGGTTCACTGGGGGTCAAAGGTCTCGCTGATACTTTTGGAAGGTGAGAAATGCATGTTTCACAAATTCCATTATTTAATTTAATTTACCCCTACTGCATGAATTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTCTCTCTCTCTCTCTCTCTCTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATATATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA

Associated Phenotype:

Not determined