ZMP
LOC100333987
Ensembl ID:
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 |
---|---|---|---|
sa7259 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44244 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13130 | Essential Splice Site | Available for shipment | Available now |
sa3293 | Nonsense | F2 line generated | Not yet available |
sa39473 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24615 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7259
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091894 | Essential Splice Site | 44 | 1151 | 1 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 8901041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8596106 |
GRCz11 | 25 | 8673174 |
KASP Assay ID:
554-4441.1 (used for ordering genotyping assays)
KASP Sequence:
CGTCCAGCACGATCCRGCCAGGAGACAGAAYGGYGGGAACTTTCCGAGGG[T/G]ACGTCGCCGATCSCCTTATRAAGTCTTTTTGTCCCMGATTACATTTTTTG
Long Flanking Sequence:
AAGAAATATTTTTTATTGATTTATTTTATTGATTTATTATTTTTATTGATTTATTTATTTTATTATTTTTTATTTATTGTTATTGATTTAATTTGTTTTCATTAATATATTTTGTTAAAAGATTATGTCAATGGGGCGCAGAATCTGAACTGCAATTTTTTTCTTATGCTTAAAGGAAAAGGATTAACAAAAGAAAGTTCCTGGGTTGCCCGTTTTGACATTTTCTGTGTTGATAAATGCACCAGATGCAAAATTATAGCACTTAAAGTTGGCAAAAGTCTGATTTTCACATTATGTCCCGCCTTGATGCTAAAGGTGTGGTGTTTTGTGTCCTCCACTTTAGCATCTGTCAGATAAGCAGAGGAAGATGAAGCTGAAGAAGCAGGTGACAGTCTGCGGAGGGGCCATCTTCTGTGTGGCCGTCTTCTCCCTCTATCTGATGTTGGACCGCGTCCAGCACGATCCGGCCAGGAGACAGAACGGCGGGAACTTTCCGAGGG[T/G]ACGTCGCCGATCGCCTTATGAAGTCTTTTTGTCCCCGATTACATTTTTTGCTGTGTGGGTCTGTTTGAATGGCTCCATTTATCAAAGCCTTCTGTGTGTGCATGTATGTGTGTGTGTGTGTTTTATGGCTAGCAAGTGTAAAGCAAGTGATGTGAGCATTTCTGGCTCAGGCTGGAGATAATTAACTACTAAATTAGCTGGTAAATGACTCTGTGTGAGTGCTGTTTTTTTCACCACCACAAACCGAAGGCTTTTTAAATGCAAAACCTAATTATTAGAAAAAAGTGCTGGTGTCCTTTTGAGAAATGGTGTGCAGGCTGACGCAGTCGATGGAGCGTGAATTAGCACATTTTATGCACCTAAAATGTAGGCCTCAAGAGAAATAATGCACATTATGGAAATGCAGATGTTGTTTATATTCAAAGCTTGTACTGAATCTGAATTTTTCAATTTGATTGTCAGGGAGTTTGGCACCAGCAAACATTAATGACATTTGATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44244
Status:
Mutation detected in F1 DNA
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:
Not yet available
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 | 130 | 1151 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 8903586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8598651 |
GRCz11 | 25 | 8675719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGACTGCCAGTTTGCTCTGGGCCGCAGGAGCCAAACTGACCTGCAGG[T/C]AAGAATGGACAGTTTGAGGAATGACTTGATTTGAAGGTGCTGTTTGTATG
Long Flanking Sequence:
TAATTGTAGTTTTGTGTTCCCAGTTTAGTCATGTGTGAGTTTGAGGTCAGGAGGTATTTCTTAATTTATTACAAAATGTCTAGTTCTGCTGGTGAGTTCTGTGACTTGTATTGTGTTGAGTGTGTTAGTGTTCCAGTAGATGTGTTACCCGGTCAGCTGTACCTCCTCCTGGTCAGTCGTGCGATGCTGTAGACTGTGGTTGGTAGATAGATCACACCTCCATCCCGCTCCTTGTTTTCAGAGCCAGATTTCGGTGTTGCAGAACCGCATCGAGCAGCTGGAACAGCTCCTGGAGGAGAACCATCAGATCATCAGCCACATTAAAGACTCAGTGCTAGAGCTCACTGATACGGGCGCCATCTCTCCCAGTGGACACCTGCCCTTCCGGAGCGCCAACGGCTCCTGGGTGCTGCCGTTTGATGGACGGCCCACGTTTCTCTCAGTCAAGCCATTGGACTGCCAGTTTGCTCTGGGCCGCAGGAGCCAAACTGACCTGCAGG[T/C]AAGAATGGACAGTTTGAGGAATGACTTGATTTGAAGGTGCTGTTTGTATGGGAGAAGAAGTGAGTTTTGGGATTCACTTGTTGCGGTTTTAGAGTTTGGGATTTCTGGATAAAGTTGAAAAGAATCCGTAACCACAGTTCTGTAATCACTAGGGGTCTGGGAATTCTGTGTATAATTTACTATTTAAATCAACAAATATTTTCTTGTTTTTTAAATTATGATTGTGACATTTATTATATGAAAAATAAATAAATAAATAAATAAATAAAAAAAGCTTTTTTTTGTATGCTTATAATATAGAAATATTGCAAAAAATATATATTTTAAATTATATAAAAATTTGATTTATTTTATTGATTTATTGTTTTTATTTCTGTTTATGTTTTTGGTGATTTATTTTATTTAGTGATAAATTTTTATTAGTTTTATAATCATTAATTTTTTTATTTGTATTGATTATTTTTTTATTTATTATTTATTTATTTATTTTTATTTGATTA
Associated Phenotype:
Not determined
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa3293
Status:
F2 line generated
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091894 | Nonsense | 597 | 1151 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 8936061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8630724 |
GRCz11 | 25 | 8707792 |
KASP Assay ID:
554-2550.1 (used for ordering genotyping assays)
KASP Sequence:
TAATCTCCTCGTCTACCCACAGGCTGTTACGTTCTCTGGTGGGTCTGAAA[C/T]GAGTGATCATTAATGCAGCRCACTTCCTGATAATAAAGAATAAAGACATT
Long Flanking Sequence:
GTACAGCACCCTTAGCATTTGGCTATACTACCTATGCCACGGGCCGGGAGACCACATGGGAAAGCTAGGTTACTGTCGGAAGTGGTGTTATTGAGACCAGCAGGGGGCGCCCAACCTCCGCACTGTGTGGGTCCTAACACCCAGAAATAGTGAAGGGGACTCTATACTGCTCAATGAGTGTCGTCTTTCAGATCCTGGTGTTGTTCCAATGCTAAATGGGCATTTATGTCAAACTTCAAAAGAAGAAATGTAAAAAAGTATGCATGGTGGCTAGTTCCTATTGTGAAACTTCCTTATAATAGCTGAATTTTCAATTTGGGTTGACCTAGCCCTTGGATTAACTAAGTGGAGGATGTTCAGCTAATGAAGGCAGTCTCTCAGGCCGTTATGTATGAAATATCATTTCCAGTAAGTGAGCGTTTTCCGAGTTTGGATTGATGACTTCTTGATTAATCTCCTCGTCTACCCACAGGCTGTTACGTTCTCTGGTGGGTCTGAAA[C/T]GAGTGATCATTAATGCAGCGCACTTCCTGATAATAAAGAATAAAGACATTTATCGCTTCTACCAGACAGAGCCCTTCTTGGAGACGGTGAGGAGCAGCAGGTTTTTTCCTCTAAAGTCAGCCAGTGTGTTTAATGCTCTGACCTGTAACTTCTGTCTCGATGACTGTAGGATGATAGACGCGCCACACAGGACTCTCTCCCGCAGCGTACGCTTATCGAGCTGGAATCTTCACCAAGGTGAGATGCCATCTTTCATGGATGTTGAATGGAGTCATTTTTAGTGTGGAGAATGTAGAGCTGCACAATTCATTCGCTCATTTTCTTTTCGGCTTAGTGTTTTTATTAATCCGGGGTGGCCACAGCGGAATGAACCACCAACTTATCAAGCATATGTTTTATGCAGAGGAGTCCCTTCCAGCAGCAATCCATCACTGGAAAACACCCATACACTTTCATTCACACACATACACTACGGACAATTTAGCTTACCCGATTCACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39473
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091894 | Essential Splice Site | 783 | 1151 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 8943458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8638121 |
GRCz11 | 25 | 8715189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTCAGCAGATGAGTCTGCAATGATTAATTCTCCCGCTTTTCTCCATC[A/T]GAGCATTCGACGGAAAGACGATCCCCAGGAGGTGAGGGTACAGATTCAGT
Long Flanking Sequence:
CAACACTGCTTGTTTTGATTTCTCCTTTGTCTGTCAAACCCATTACAGGTCTTTCCGTTTCTGCTAATGAGCGGATGATCTGAATCAGGTGTGTTTGGTTAAGGAGACGTGGAAAAAGTGCAGAGCTGGTGGTGCTCCAGCAACATGGTTGAGAAACACTGATTCAGACCAAATCATATTGCATTTTGATGTCAGCTGTAATACAAATCATTATCCTTTTCAGCCTTGCAGGATTTGCAAGTAGTAAAGTCAGGGAATAAATACTCCAAACATCAGCTCGACTCATCTAATATTGCATGCTTATAATAAAAAGGAAGTTTCCAAGTTATGACACCAGCAGTCTATTTTTATATCCAGTCATCTGGCTGAGTATTTTTTTATTGGTTGCCAGATGAAATGAAACTCATGTTTTTTTGTAGCACATATGCGTTTATGTCCTCTTTTGCATTCTGAGTCAGCAGATGAGTCTGCAATGATTAATTCTCCCGCTTTTCTCCATC[A/T]GAGCATTCGACGGAAAGACGATCCCCAGGAGGTGAGGGTACAGATTCAGTTCCTCACCTACGGTACGCGACCCTCCAAGGACAAGAGCGGGGCCTATCTGTTCCTGCCGGATGGAAATGCTAAGGTAGCGTCCGCTTGTCTTGCCTGGCAATTCATCAAACAACCTGAGGCGGATTAAAGCCTGACTTGCATTGTGAGATTTCAGATGTTATTTAGGTATTTGAGACTAATTTAAAAAAATATTTTAAATGATTCATAGAATTGTAGGCTGAAAAAAATCTGTATTTGATCGCAGGTTTGACGTGTTCATCCACAGCCACTTAATGATTACTGAGATCAAATTCTTACTCCAAAAAAATTCTGGCTGTGTCTGAAGATTTAACTAAGATCTAACTACAACCACCGTCAAACCAAGAACCCATAAAAACATCAAAAATTAAGATGCAAAGAGCCTGACAGCTCAAACCAAATTAGGGAAAATTAGAAAAAAATTGATAATT
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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