ZMP
man2a1
Ensembl ID:
ZFIN ID:
Description:
mannosidase, alpha, class 2A, member 1 [Source:RefSeq peptide;Acc:NP_001103497]
Human Orthologue:
MAN2A1
Human Description:
mannosidase, alpha, class 2A, member 1 [Source:HGNC Symbol;Acc:6824]
Mouse Orthologue:
Man2a1
Mouse Description:
mannosidase 2, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:104669]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33726 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9369 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9630 | Nonsense | Available for shipment | Available now |
sa44621 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31479 | Nonsense | Available for shipment | Available now |
sa10617 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33726
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083160 | Nonsense | 381 | 444 | 7 | 8 |
ENSDART00000121500 | None | None | 366 | None | 6 |
ENSDART00000123640 | None | None | 292 | None | 6 |
ENSDART00000143309 | Nonsense | 380 | 1100 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 58517416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 56438015 |
GRCz11 | 5 | 57108232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTGCTGCCAGTTTGATTTTAAAAGGCTGCCAGGAGGAAGAATTAGCTG[T/A]CCATGGAGAATTCCTCCTCAGGCCATCACAGACAACAACGTACAGGAGAG
Long Flanking Sequence:
GCTTCTATGTTATCTGTCACTGCGCTGCTTATGAGTGAGAGGCAGCAGGAGAAGCTACACCCATCAGAGCAACAGAGAGCAATCTTTCTGGCTCTGATACACGTGTGATTGGGGGCGGGGAGAACCAGCTTATTTGCATTAAAAGCACAGGTAACAAAACGGCTACAATGTCTTAACAGCGCAATTTACCAATATACAAAAAGGTATAATAAATAATCTGATGGGTATTTTGAGCTGAAACTTTACAGACAGGTTCTGGAGAAACAAAAGACTTTTATTAAATCTTAAAAAGGGGTTAGATAGGTGCCCTTAAACGGGAATCATAAGGAGAAATATGATTTGCTTTTGTTTTTGATTCCAACAGATCAAGACTCGAGTACAGACATTCTGTGCCACATGATGCCATTCTACAGCTATGATGTTCCCCATACGTGTGGTCCTGACCCCAAGATTTGCTGCCAGTTTGATTTTAAAAGGCTGCCAGGAGGAAGAATTAGCTG[T/A]CCATGGAGAATTCCTCCTCAGGCCATCACAGACAACAACGTACAGGAGAGGTACAACTATACACAGCAGTCAAACACAGTAGGAGCTACTCTATTTACTCATAGAAACCTTAAAAAAAACAGGTATTGTGTCAAACTAGAAATCTGTTCTGATGAGTAACCCTTTCTTTAATCCCTTTTTCATTGTTTGTGGATTAGTGTTCCCTTAAATCTGATCAGATTTAGATTCCCCTCCACTTAGTTTAGTCTCTCCATGTGTAGAGCTCAGACGCTGCTGGACCAGTACAGGAAGAAATCCAAGCTTTTCCGCACCAAGGTGCTGTTGGCACCACTCGGAGATGATTTCCGTTACACTGAAGCTGTCGAATGGGACCAACAGTTTGAAAACTACCAGAAACTCTTTGACTACATGAATTCTCACCCTGAGCTCCATGTCAAGGTCATTCTTCATTGTTTGTCACACGCTGAACTACAGGGCTGTGCAGTATGACAATATATATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9369
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083160 | None | None | 444 | None | 8 |
ENSDART00000121500 | None | None | 366 | None | 6 |
ENSDART00000123640 | None | None | 292 | None | 6 |
ENSDART00000143309 | Nonsense | 549 | 1100 | 10 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 58503625)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 56424224 |
GRCz11 | 5 | 57094441 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTCTCTGACCTTGGCCAACATTCAGAAGTACGGGCAGCCCAGTGATYA[C/A]CCTGCCGGGGAGAATTACAAACTACTGACTGAAGCCAGRCGCAATCTAGG
Long Flanking Sequence:
TGCTGTAATGAAACGAAGAGACAATTCTTTTATTGGAGTAATAACATTTGTACAGTCTAAATGGGCCGCCATAATAATGCTGAAGTAAAAAACCTACTAACATATGACTCTTGTTGGACGGGGTTAGTGGGATTCACCCAACTATATATTTCCATCTCCTTTAGAACATTCGAGAAGGTCAATCTTTGAAGATTATATTGTTAGCATAATGTGGAGAGATTTGGCTTTTATTGTCCTCGCACTGACACTCCCAACACAGCAGGAACTAAACCCACACTGTTGTCTTGCTTTTCCCGGAATGTGAACTGACACAGGATGTGTTTTGATGCCAGGTGGATTCTGATAGCGCTGTAGATTTATTCAGTGTGGATTTGAGGGGACTTTAGATCTTGCGAATGAGGGAGTTTCACTTGTCACTTCATGTTTGTCCGCAGGGCAGCTGAAGTCCTCTACTCTCTGACCTTGGCCAACATTCAGAAGTACGGGCAGCCCAGTGATTA[C/A]CCTGCCGGGGAGAATTACAAACTACTGACTGAAGCCAGGCGCAATCTAGGCCTCTTCCAGCATCATGATGCCATCGCGGGTACAGGCAAAGATTGGGTGGTTGTGGACTATGGAACCAGGTAGTTTTATTTTATTTATTTATTTATTTTAGATTTATTTCAAGTGAAAGCTTTAGAAGACATTCTCTTATCCAGTTCAATTACTCCACTTCCCCTGGAACAAACTCGGCCTAAGTCAATATTTATTATCTCTGAAAGTATTTGAAGGTGACCAAAGCTCAAATTGTTCCTAACAGCTTATATGTTACTGTAATATAGAGCACTGTGTCCAATATATGGGATATCAAAATATGATACTGTTAAAAAGTTTGAACATTTTTGAAAGTGCCTTTGTCTATTCGATTGAATGCAGTAATGCAATACATTCATTCATTCATTTTCCTACGATTTAGTTTCTTATTTATCAGGGGTCGCCACAGTGAAATGACCCGCCAAGTATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9630
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083160 | None | None | 444 | None | 8 |
ENSDART00000121500 | None | None | 366 | None | 6 |
ENSDART00000123640 | None | None | 292 | None | 6 |
ENSDART00000143309 | Nonsense | 720 | 1100 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 58498264)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 56418863 |
GRCz11 | 5 | 57089080 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACAGTTGTCATTTGTGGCTCATGCTGCTCCTCTGGGTCTGAGCGTGTA[C/A]CAGCTGATTGAGGTAATGGAGCCCAGGACAGATGCTTCGAAGTACATGTT
Long Flanking Sequence:
AGTCAAGGGCAGATTCTGCTTGACCTGTGTGTATTAAATATTGAACTCCACGGTATTATAAATGTGATTTTTTGTGATTGTTTGTTTTATTGCAATATTTTATGTATATCCAATTTACCAAAAAGTTGCATTTTATTTATTTTATTGGAGTGAGTTTATAGTGAGTAACGCTTTATAGTCATATTTTCTATTTATTTTTAAATATTAGTAAATTAAATTAAGAATTTTCCCCTGGCAACTTTAATGTATTATAGTTTTGCTATATTTACTTTCGGCCCACAGCTCTCTATGATATTTGGTTTTTGGCCCTTTATACTAAAAGGTTTGTGCACCCCTCATGCAGACTTTCCAAAAAGTCATAGAATACTTTGCAAATAGACCAAAATATATGAAAGTCCATGTTTGTTAGTTTAAGGTCATGTAAAAGCTCTTTGAATGTGTTTGTTCACTCCACAGTTGTCATTTGTGGCTCATGCTGCTCCTCTGGGTCTGAGCGTGTA[C/A]CAGCTGATTGAGGTAATGGAGCCCAGGACAGATGCTTCGAAGTACATGTTTCTCCAGGAAGGCAGACAGCTCTCAGACAGTAAACTGGAGCATTTCCGTCAGTTCTATCAAGACGATGGAGCTCCTGTGGTCATTGAAAATCCTCACCTCAGACTTTCCATCTCTGGAGCTACAGGCCTTTTAGAGGTTTGAGCGTGTACTTCTGCTCTTTGGGGTTTGCCGTAAAGTGATACATTTAGGAATACCTCTGTGTAATGTTCAGAAATCATCTCTTTGTTTATAGAAAATGATGTTGAAGGAAGATGAATCTGAGCACCAAATGAAGGTGGAGTTTGTTTGGTATGGAACCACCAGCAGTAAAGACAAGAGTGGCGCCTACCTATTCCTGCCCGACAAAGAAGCAACAGTAAGGATTTTGTTTGAGTAATTTGTTGAACGATCATTTATTCTATATCTTGCCCAGCAGTATTTTTTGAAAAATAAAAGAAACTACATTGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44621
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083160 | None | None | 444 | None | 8 |
ENSDART00000121500 | None | None | 366 | None | 6 |
ENSDART00000123640 | Essential Splice Site | 96 | 292 | 2 | 6 |
ENSDART00000143309 | Essential Splice Site | 954 | 1100 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 58434546)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 56355145 |
GRCz11 | 5 | 57025362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCGCTGCTCACTGCACAGTCGCTTGGAGCGGCCAGCCTTAAAAGCGG[T/A]CAGTCTTCACTCACTCACAAGTGCTTCAAGCTTTCCTTTTGTTTAAAAAC
Long Flanking Sequence:
CTGTCATGTTTTCTTGACATGCTGGAGTATTAGCGTGGCATTTAATTAGCTGATAATGTTTCCCTGGTCTTGGCCGGGATTAAGAGCTTCTCTTCGGTCCAAACTAATTAACTGGCTTCACAAAACAAATGCCTCATGAATAAAAACAGTGGAATATCCCATCCATTTTTTCCTCCAAGTCACATCAACACACACACACACACACACACACACATTGGAGCTCATCAATTTACAGTGTTTTTCTTTCAGAGAAGTGTCTCCACATGCCCACACTCCATGTTTGCAATTCTCTGAACAAGGAGAATTTAGAATCTTTCCTCTCTGCAGTGTTCAAATTGCCTTGGGCTGTTTTTCCAGGTGCAGCCGAGGAAAACCATGGCTAAACTCCCCCTGCAGGCAAACTTCTACCCCATGACCAGCATGCTTTACCTGCAGGACTCCAGCGCCAGACTCTCGCTGCTCACTGCACAGTCGCTTGGAGCGGCCAGCCTTAAAAGCGG[T/A]CAGTCTTCACTCACTCACAAGTGCTTCAAGCTTTCCTTTTGTTTAAAAACCTCAAGTATACACTAATGGAGGGTTTACCCCATGTTTGTTAGAGGCCATCGAAGATCCAGAAATTTAGAAAAAAAAGTATTATTTTAATGAATAATGGCCTCACAAATGCTTGAGTTGAAAAGCTTAGATATTGGAATTTTTTCTTATTTAAATATACCTATTCAAATGGTAATTGATACGTTAATAATGTATTTTACCAATTAGAAATGTTGGTATAAGTGAGATTTATTCATTTACATCTTACCAAAGTACAATTGCTGACAAAATATTAAGCAGACCGGGTGTTTTCAGCATTGATTATAATAAGAATTTGTCATATTTTATTTTAATGTTTAATTTAATAATGGTCATATTTTATTTTAATAATTAACTTTAAAAATAGTACCATATATAGCAATATCGCACCCGTAGCAGTGCGATATGGCTGGTTGTGTGTCCCGCCAGTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31479
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083160 | None | None | 444 | None | 8 |
ENSDART00000121500 | None | None | 366 | None | 6 |
ENSDART00000123640 | Nonsense | 116 | 292 | 3 | 6 |
ENSDART00000143309 | Nonsense | 974 | 1100 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 58430838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 56351437 |
GRCz11 | 5 | 57021654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGATAATGGACCGCAGGCTCAATCAGGATGACAATCGAGGGTTGGGA[C/T]AGGGAGTGCTGGACAACAAGATCACAGCCAACTCCTTCCGCCTGCTGCTG
Long Flanking Sequence:
GAGCTAGAATCGTATTCTCAAGGACGTATACATTTGATATTTATTCAGTAAAAAGCTCTTTATAATGATGATATCCCTCTCAGATAAATAAATACCACGTGCCAGCCTAATGCTGCAGCAAAATGATTTGGCAGCCTATCAATCAAACACACTAACAACTATCCTTCGAGGTATGCTTCAATATACACGGCCTTACATAAATAAATAAATAATAAATAAAGCACTGCTTTAGGTGTATGTGAATTAGAGGTTAAAAAACACTCCATTGTTGACTGTGAAGTGCTTTTGTCTATAAAATACAATCTGTCAAGTGTCAAGTTTATATAAACATAGATGGTGCTCAAACGTGAGACTCACACATGATTTCTACATGTCATCAATCAGTGTTCGGATGAAGTACATGTGATGTCCTGCTGAAGCTCATTAGTGTGGTTTCCACAGGTCAGCTGGAGGTGATAATGGACCGCAGGCTCAATCAGGATGACAATCGAGGGTTGGGA[C/T]AGGGAGTGCTGGACAACAAGATCACAGCCAACTCCTTCCGCCTGCTGCTGGAGAAGAGGATCTCTGTGGAGGAGGTAATCAGGACGGACAGATGATTGAATTAAAACAGAACTAATGTGCATTTATTCTTTGGTGCATATGATCACATCAATCTGATCAGTCTTGGCTGGTTCCTACAATGTACACTCACACCGGTGTGATTTCAATGTTCAGTGTGTAGCCTGATCAGCTGCTAAATTCAAATCTTGTTTCCTGTCAGAAAATTTTGAAAATGGGGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAACAATTTTGGCTTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATACTTTTTTTCCAAGACGAGAATTTTTTGCTCGTCTAGAAAATGCTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10617
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083160 | None | None | 444 | None | 8 |
ENSDART00000121500 | None | None | 366 | None | 6 |
ENSDART00000123640 | Nonsense | 149 | 292 | 4 | 6 |
ENSDART00000143309 | Nonsense | 1007 | 1100 | 20 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 58428468)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 56349067 |
GRCz11 | 5 | 57019284 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCACTTTCCTGTATTTKACCCAGAATGAAGCGACKGCACCATACAGCTA[T/G]CCATCTATCCTGAGCCACATGTCRTACATGTACCTGAACCATCCTCTCAT
Long Flanking Sequence:
CAGATTTTGTAGGAGGTTCGAGCTGTAGCCACTTTCGAGGCTTGAGGTTGCTAAAAGTATTTTTATTAAATTCTGGTCTTTTACCATTAAGTTGGCTGCAGTATTTTCCAGGTTAATTGTTGTAAAAGAAAGATTTATTCCATCATCAAAAATACTATACTAATACTATTATTTACATTACATCCTGCCAGTATGACTAAATGCAAACTTTATATATTATTTACATTTTTAATAACATATTAGAAACTGGCTTTGATATGACAAATCACAATACTTAATCAGGTGATTAAAGTTAAGTGTTATTTTGCATAAATTTCTGAGTTTAATTTAGACTAACTTGCTTTCCTAGAAGGCCATGCCAGTCATATATAAAAGAATATTTGTGCTAATGCAGAATCACATCCTTGCGTAGTTTCCAGGTTTATAAGACAAATAAGTCTGTGCTGATGCTTCACTTTCCTGTATTTGACCCAGAATGAAGCGACGGCACCATACAGCTA[T/G]CCATCTATCCTGAGCCACATGTCGTACATGTACCTGAACCATCCTCTCATCTCAATGGCAGTTAGTCAGCACTTGGAAGCTCCATCTGTGGTCCCCTACAGCCCTCTGAAAGCCTCCTTCCCCTGCGACATGCATCTGGTCAACCTGCGCGCTATCCAGTCTAAGGTACGTCTCTATCTTCTAGAGCAGAGTTTTTTTCCAGGAGACCTCTACTTTAACATTCAAAATCTTTAATGACCCCTGAGGCCTTAGAAAGACTTAGGCAGACAAGATTTAAAGGTCAGTTGTTTTTTAACACATGCAACTGGTGTTAGATCACACTCTTCACGCCAGATAAATAAGAGCCCTGGACGCCAGTTCCAGTCAGGAAATGTCTGTTTTTCTGAGTATCCAGACAACAAGCTAGCACAGCCACCCAATACCCAAACCTGTTAACCCGTATTCAACTAAATCAACAGTTTCCTATCAATATAGGAGTTGACTGAGAAAACCAGAGAGAA
Associated Phenotype:
Not determined