ZMP

LOC100331516

Ensembl ID:

ENSDARG00000074556

Human Orthologue:

GANC

Human Description:

glucosidase, alpha; neutral C [Source:HGNC Symbol;Acc:4139]

Mouse Orthologue:

Ganc

Mouse Description:

glucosidase, alpha; neutral C Gene [Source:MGI Symbol;Acc:MGI:1923301]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36510	Nonsense	Mutation detected in F1 DNA	Not yet available
sa9837	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa36510

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109532	Nonsense	666	898	17	24

Genomic Location (Zv9):

Chromosome 17 (position 45462121)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	45181303
GRCz11	17	45295068

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTGCGATCCGCTCTGCTGTTCAGGACAGATACTGTCTTCTGCCGTACTG[G/A]TACACACTGTTTCACCAGGCACACACAGCTGCACTTCCACCTATCAGGTA

Long Flanking Sequence:

GGAGCTAAAATCTGCTGGACACCGGCCCTCCAGGAACAAGTTTGGTGACCACTGCTTTAAGACACCAAAGACTGTACTAAAGAATGCTGAAAATGAAACTTTGACTTGAAAGGAAGTTAAATTGAAAATGTATTGAAACAAAATAGTTATTTATTATATTAATGTCACATTATTACTTTTTTTAAACTGCATATTTGGTTATAAAATCAATAATAAATCATGTTTTGGTAAACATAAGAGACAGTTTTGGAGTTTGGAGTTTGGTGTAAAGGGATTAAATATCATCATGTGTATGTGTGTGTAGCTGATGTAGGGGGCTTCGTGCAGGATCCAGACCCTGAGCTTCTGGTTCGCTGGTATCAAGCAGGGGCCCTTCAGCCATTTTTCAGGGCACACTCTGCCAAAATGACCAAGCGTCGTGAGCCGTGGCTGTTTGGAGAGGAGGTGACCTCTGCGATCCGCTCTGCTGTTCAGGACAGATACTGTCTTCTGCCGTACTG[G/A]TACACACTGTTTCACCAGGCACACACAGCTGCACTTCCACCTATCAGGTACTGCTTTTTCAGCCCCAGTACAATATTTGGTCCCACTTTATATTAAGTGGCCTTAACTATTATGTACTTACATCAAAAAATAAATACAATGTACTTACTGTGTTTATAATGTATTTGAGAACACTTGTGGTGCTTTTGAGTTGGGATAGAGGTTGGGTTATGGACAGGTTTGGTGGCAAGGGTAGGTGTAAGGGTGGGTTAAGGTGTAAGGGATGGTCAACAGTGTATTTACAAATGTAATTACAAAAGTTAATTACAGATGTAATTACATACATGTACAGTATTTTATCAAGCATAAGTACACAGTAAATACATGTATTTACACAATAAGTACATTGTAACAAACTATTAGTTCCTATGTAAGTACATATTAGTTAAGGCCACTTAATATAAAGTGGGACCCTATATTTTATTTATATGGATTATATTTATGCTCATAACAGTATTCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9837

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
Order Allele From EZRC

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109532	Nonsense	886	898	24	24

Genomic Location (Zv9):

Chromosome 17 (position 45469619)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	45188801
GRCz11	17	45302566

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGTCATGTTTGARTTTGACAAAAAACGAGGCGTATTAACATTAAGTRGTT[T/A]GGAACTTGAAATATGCAAAGACTGGGAAATAATAATATAGCCATGGTGNNNNNNNNNNNNNNNNTT

Long Flanking Sequence:

CAAAGCTGATGGATTTCTTTATTTGGATGATGGCCACTCTTTTAATTACAGAGACCAGATGCAGTTCTGTCTGCGGCGCTTTAGCATGCAGGCCGGCAGGCTTGTCAACAGGTAATAACCCAAGTTACATCACTTTATTTCCTTCCTGTTTTGTTTTAGGTTCCGTACCATTGAGTATTCATAGACCTCAGAACGTCATTCTCCTTTTCAGCTGTGCTAACGATAAAGGCTTGTTTGTCTCTGATGACAAAGTGGAAACGGTGGTCATTCTTGGTCTGAAAAGTGTGAAAAGGAAACCCAAGCTCAAATCAGGTGGGAAGAGGCCTAAAATGTCCTTCCATGTTAAGTATTAGTAGATTACTACATATATAAATGATGTGACGGTAAACAAAAGAGACGCTCGTCACTAAAACTTCTTTTTTTTTTTCTTTAAGGTGCAAAGAGGACATCGGTCATGTTTGAATTTGACAAAAAACGAGGCGTATTAACATTAAGTGGTT[T/A]GGAACTTGAAATATGCAAAGACTGGGAAATAATAATATAGCCATGGTGTTTTTTGGGGTGCTGTTTAAACCTCACGGCAGTTTATCATTGCAATGATATGTTATAGTTGTTCATTGTAATTAAATCAGTGGTTTAATATTTAAGATTCCCTCCAAAATGATTTACTACCTCAAGTTATTTTAATAATAATGTGATGACATTTCAGCTGTTGGGTTCTTTTATCTTTAATTTGATATAAAACTGTAGATTTGACAACATTGGAGGGACAAATGGGTTTTGAAAATATACAAAATTTGCTGTTAAACGTTTTGATTCCTAAATAAAGGATTGTCAAAGAGCAAAGTCATATCTTTTATTCATTAGCGATATACAGCTATTAAAAAAAATTGAAGACCACTTGAACAGTCTTATGAGTATGGTTTTGATTTAATTTTGATTTATTTATTTCGAACAAGAAAAAAATTAATTATTCAAAACAATTCTTCAGACAAAATACATTT

Associated Phenotype:

Not determined