ZMP

LOC100333987

Ensembl ID:

ENSDARG00000063101

Human Orthologue:

MAN2A2

Human Description:

mannosidase, alpha, class 2A, member 2 [Source:HGNC Symbol;Acc:6825]

Mouse Orthologue:

Man2a2

Mouse Description:

mannosidase 2, alpha 2 Gene [Source:MGI Symbol;Acc:MGI:2150656]

Alleles

There are 6 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13130	Essential Splice Site	Available for shipment	Available now
sa24615	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa13130

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
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Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000091894	Essential Splice Site	526	1151	9	22

Genomic Location (Zv9):

Chromosome 25 (position 8928921)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	8623584
GRCz11	25	8700652

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CRCGACCCTTCTACAAAAACCTGGACCGYATTTTAGAATCTCACYTAAGG[T/C]TAGTCAGTCAATACATTAKACATTAGAYGCATCAGGANNNNNTCYAATAAACGTA

Long Flanking Sequence:

TAGTTTATATGTCTACCTTATCTGACCCATTGACTTCAGGTATTTGGAGTCTCTCCTAATGTTCTGAATCTGATGAGTTGATTCAGGTGTGTTTAATTAGGAAGAGGTTGAAAATGTGTAGTTTAGGCGTGCCTTCGACATTTTAATTAAACAAATCATACATGCCTTTTAAAAGTACTAGTGTAGCTAATAGTGATCTCCACCATAGCACTTGTTTGTGAGTAAAGAAAAATTTTTTTTTTAACAAGTGCAGAATCATGTGAAGATTTCCTCCAAGTAACTCTCTATGCTTTCAGGCTCAGTTTGCGACGCTGTCAGACTACTTTGATGCGGTGTACAAGGCTAATGGAGTGACTTCGGGGGCGAGACCACCCGATTACCCTGTGCTGAGCGGAGACTTCTTCGCTTATGCAGACAGAGAGGACCATTACTGGAGTGGATACTACACCTCGCGACCCTTCTACAAAAACCTGGACCGCATTTTAGAATCTCACCTAAGG[T/C]TAGTCAGTCAATACATTATACATTAGATGCATCAGGATCCAATAAACGTACATCTTTCTATCTTATTTGTGCCCTAAATGGTACATATTAGTACTATTAGCCTGTTGCGATATTTATTTTTTGCACGATATATTGCACTAAAATATACACTCAGCGGCTACTTTATTAGGTACACCTGTCTAACTACTCGTTAACGCAAATTTCTAATCAGCCAATCATATGACAGCAACTCAATGCATGTAGGCATGTAGACATGGTCAAGATTATCTGCTGCAGTTCAAACAGAGTATGAGGATGGGGAAGAAAGGTGATTTAAGTGACTTTGAACGTGGCATGTTGGTGCCAGACAGCCTTGTCTGAGTATTTCAGAAACTGCTGATCTATCGGGATTTTCATGAACAACCATCTCAGAGAATGGTCCGATAAAGAGAAGATATCCAGTGAGTGGCAGTTCTGTGGGTGCAAATGCCTTGTAGATGCCAGAGGTCAGAGGAGAATGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24615

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000091894	Nonsense	814	1151	15	22

Genomic Location (Zv9):

Chromosome 25 (position 8943555)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	8638218
GRCz11	25	8715286

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGTTCCTCACCTACGGTACGCGACCCTCCAAGGACAAGAGCGGGGCCTA[T/A]CTGTTCCTGCCGGATGGAAATGCTAAGGTAGCGTCCGCTTGTCTTGCCTG

Long Flanking Sequence:

GTTAAGGAGACGTGGAAAAAGTGCAGAGCTGGTGGTGCTCCAGCAACATGGTTGAGAAACACTGATTCAGACCAAATCATATTGCATTTTGATGTCAGCTGTAATACAAATCATTATCCTTTTCAGCCTTGCAGGATTTGCAAGTAGTAAAGTCAGGGAATAAATACTCCAAACATCAGCTCGACTCATCTAATATTGCATGCTTATAATAAAAAGGAAGTTTCCAAGTTATGACACCAGCAGTCTATTTTTATATCCAGTCATCTGGCTGAGTATTTTTTTATTGGTTGCCAGATGAAATGAAACTCATGTTTTTTTGTAGCACATATGCGTTTATGTCCTCTTTTGCATTCTGAGTCAGCAGATGAGTCTGCAATGATTAATTCTCCCGCTTTTCTCCATCAGAGCATTCGACGGAAAGACGATCCCCAGGAGGTGAGGGTACAGATTCAGTTCCTCACCTACGGTACGCGACCCTCCAAGGACAAGAGCGGGGCCTA[T/A]CTGTTCCTGCCGGATGGAAATGCTAAGGTAGCGTCCGCTTGTCTTGCCTGGCAATTCATCAAACAACCTGAGGCGGATTAAAGCCTGACTTGCATTGTGAGATTTCAGATGTTATTTAGGTATTTGAGACTAATTTAAAAAAATATTTTAAATGATTCATAGAATTGTAGGCTGAAAAAAATCTGTATTTGATCGCAGGTTTGACGTGTTCATCCACAGCCACTTAATGATTACTGAGATCAAATTCTTACTCCAAAAAAATTCTGGCTGTGTCTGAAGATTTAACTAAGATCTAACTACAACCACCGTCAAACCAAGAACCCATAAAAACATCAAAAATTAAGATGCAAAGAGCCTGACAGCTCAAACCAAATTAGGGAAAATTAGAAAAAAATTGATAATTCATTCATTCATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCACCAACTTATCCAGCTAGTTTTT

Associated Phenotype:

Not determined