Busch Lab

ZMP

zgc:92137

Ensembl ID:
ENSDARG00000009443
ZFIN ID:
ZDB-GENE-040801-179
Description:
hypothetical protein LOC445049 [Source:RefSeq peptide;Acc:NP_001003729]
Human Orthologues:
AMY1A, AMY1B, AMY1C, AMY2A, AMY2B
Human Descriptions:
amylase, alpha 1A (salivary) [Source:HGNC Symbol;Acc:474]
amylase, alpha 1B (salivary) [Source:HGNC Symbol;Acc:475]
amylase, alpha 1C (salivary) [Source:HGNC Symbol;Acc:476]
amylase, alpha 2A (pancreatic) [Source:HGNC Symbol;Acc:477]
amylase, alpha 2B (pancreatic) [Source:HGNC Symbol;Acc:478]
Mouse Orthologues:
Amy1, Amy2a1, Amy2a2, Amy2a3, Amy2a4, Amy2a5
Mouse Descriptions:
amylase 1, salivary Gene [Source:MGI Symbol;Acc:MGI:88019]
amylase 2a1 Gene [Source:MGI Symbol;Acc:MGI:104548]
amylase 2a2 Gene [Source:MGI Symbol;Acc:MGI:3711220]
amylase 2a3 Gene [Source:MGI Symbol;Acc:MGI:3714985]
amylase 2a4 Gene [Source:MGI Symbol;Acc:MGI:3711258]
amylase 2a5 Gene [Source:MGI Symbol;Acc:MGI:88020]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa9334 Nonsense Mutation detected in F1 DNA Not yet available
sa19184 Nonsense Mutation detected in F1 DNA Not yet available
sa42986 Nonsense Mutation detected in F1 DNA Not yet available
sa19185 Nonsense Mutation detected in F1 DNA Not yet available
sa11021 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9334
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024558 Nonsense 52 512 1 10
ENSDART00000024558 Nonsense 52 512 1 10
Genomic Location (Zv9):
Chromosome 17 (position 42998881)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 42711607
GRCz11 17 42988113
KASP Assay ID:
2261-1450.1 (used for ordering genotyping assays)
KASP Sequence:
TGGGCAGACATAGCTGAAGAATGCGAGAGATATCTGGCACCAAACGGCTA[T/A]GGAGGAGTTCAGGTGCGTTTGAAATGATTTCCATGACCATTGGGATTGTA
Long Flanking Sequence:
TTTTTAAATTAGCATTTTCAATACGGTTTAAAATTTTTCTTGTTTGCTGTTGTACATATAGTGTATAGATGTAAATATTTTTAGAATACGACCTGATATTTAAAATGTTAAACACACATGCATTTATTGGTTACATTTATTTGATGTATGTGCTCTGGGAAGGCCACAAGAGTTTACATCTGTGTTATCTTGAGAAATGATAACACTATATCTGTAGGCCTATTTATTTTCCAGCTTGCTTTTTTTCTGGGGTTTCCCGATGGTGGGTGTCGCTCAGGGTTGCAGTATAAATAACATTTAACAGATCATGCAGCCACACAAATCCTCAAATTGTGGTCTGGCACAATGATGCTCCTGATTCTGGTGGCCATCTTTGGGCTGGGTTTGGCCCAGCACAACCCAAACACGAAAAATGGTAGAACGTCCATTGTTCATCTGTTTGAGTGGCGTTGGGCAGACATAGCTGAAGAATGCGAGAGATATCTGGCACCAAACGGCTA[T/A]GGAGGAGTTCAGGTGCGTTTGAAATGATTTCCATGACCATTGGGATTGTATTAGCATTTGGTGATCATGCACGAATTCTTTTTTTTAAAAGATGTTTTTTAATTTAATAAGGATTATTTCTGAACAGATCTCTCCCCCAAGTGAACACGTCAAGCTGACCAATCCTTGGCATCCTTGGTGGCAGAGATATCAACCAATCAGCTATAACCTGTGCTCCAGATCAGGAACTGAAGCAGAACTTAAAGACATGATCACACGCTGTAACAATGTTGGGGTAATGTAAAACTGAAGCTTAAAGTATTGTACCTACCCAGTGGGCACAGAAAACATGGATTTGATGTCAGTCGACTTTGTTTATGTCAAAATTACATCAAATTGACATCTAACACCTAAAACACAAATCAAAAATTTATTACAAGTCAATTAAATGTTAATCTTTTGAAATCAATTAACTTTGATGGTATACAAGAAAACAGTGTACCTTTAGTCATTTTTAACCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19184
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024558 Nonsense 52 512 1 10
ENSDART00000024558 Nonsense 52 512 1 10
Genomic Location (Zv9):
Chromosome 17 (position 42998881)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 42711607
GRCz11 17 42988113
KASP Assay ID:
2261-1450.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGCAGACATAGCTGAAGAATGCGAGAGATATCTGGCACCAAACGGCTA[T/A]GGAGGAGTTCAGGTGCGTTTGAAATGATTTCCATGACCATTGGGATTGTA
Long Flanking Sequence:
TTTTTAAATTAGCATTTTCAATACGGTTTAAAATTTTTCTTGTTTGCTGTTGTACATATAGTGTATAGATGTAAATATTTTTAGAATACGACCTGATATTTAAAATGTTAAACACACATGCATTTATTGGTTACATTTATTTGATGTATGTGCTCTGGGAAGGCCACAAGAGTTTACATCTGTGTTATCTTGAGAAATGATAACACTATATCTGTAGGCCTATTTATTTTCCAGCTTGCTTTTTTTCTGGGGTTTCCCGATGGTGGGTGTCGCTCAGGGTTGCAGTATAAATAACATTTAACAGATCATGCAGCCACACAAATCCTCAAATTGTGGTCTGGCACAATGATGCTCCTGATTCTGGTGGCCATCTTTGGGCTGGGTTTGGCCCAGCACAACCCAAACACGAAAAATGGTAGAACGTCCATTGTTCATCTGTTTGAGTGGCGTTGGGCAGACATAGCTGAAGAATGCGAGAGATATCTGGCACCAAACGGCTA[T/A]GGAGGAGTTCAGGTGCGTTTGAAATGATTTCCATGACCATTGGGATTGTATTAGCATTTGGTGATCATGCACGAATTCTTTTTTTTAAAAGATGTTTTTTAATTTAATAAGGATTATTTCTGAACAGATCTCTCCCCCAAGTGAACACGTCAAGCTGACCAATCCTTGGCATCCTTGGTGGCAGAGATATCAACCAATCAGCTATAACCTGTGCTCCAGATCAGGAACTGAAGCAGAACTTAAAGACATGATCACACGCTGTAACAATGTTGGGGTAATGTAAAACTGAAGCTTAAAGTATTGTACCTACCCAGTGGGCACAGAAAACATGGATTTGATGTCAGTCGACTTTGTTTATGTCAAAATTACATCAAATTGACATCTAACACCTAAAACACAAATCAAAAATTTATTACAAGTCAATTAAATGTTAATCTTTTGAAATCAATTAACTTTGATGGTATACAAGAAAACAGTGTACCTTTAGTCATTTTTAACCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42986
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024558 Nonsense 77 512 2 10
Genomic Location (Zv9):
Chromosome 17 (position 42999071)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 42711417
GRCz11 17 42987923
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGAACACGTCAAGCTGACCAATCCTTGGCATCCTTGGTGGCAGAGATA[T/A]CAACCAATCAGCTATAACCTGTGCTCCAGATCAGGAACTGAAGCAGAACT
Long Flanking Sequence:
TGAGAAATGATAACACTATATCTGTAGGCCTATTTATTTTCCAGCTTGCTTTTTTTCTGGGGTTTCCCGATGGTGGGTGTCGCTCAGGGTTGCAGTATAAATAACATTTAACAGATCATGCAGCCACACAAATCCTCAAATTGTGGTCTGGCACAATGATGCTCCTGATTCTGGTGGCCATCTTTGGGCTGGGTTTGGCCCAGCACAACCCAAACACGAAAAATGGTAGAACGTCCATTGTTCATCTGTTTGAGTGGCGTTGGGCAGACATAGCTGAAGAATGCGAGAGATATCTGGCACCAAACGGCTATGGAGGAGTTCAGGTGCGTTTGAAATGATTTCCATGACCATTGGGATTGTATTAGCATTTGGTGATCATGCACGAATTCTTTTTTTTAAAAGATGTTTTTTAATTTAATAAGGATTATTTCTGAACAGATCTCTCCCCCAAGTGAACACGTCAAGCTGACCAATCCTTGGCATCCTTGGTGGCAGAGATA[T/A]CAACCAATCAGCTATAACCTGTGCTCCAGATCAGGAACTGAAGCAGAACTTAAAGACATGATCACACGCTGTAACAATGTTGGGGTAATGTAAAACTGAAGCTTAAAGTATTGTACCTACCCAGTGGGCACAGAAAACATGGATTTGATGTCAGTCGACTTTGTTTATGTCAAAATTACATCAAATTGACATCTAACACCTAAAACACAAATCAAAAATTTATTACAAGTCAATTAAATGTTAATCTTTTGAAATCAATTAACTTTGATGGTATACAAGAAAACAGTGTACCTTTAGTCATTTTTAACCAATTACACTGTCTTGTCCCAATAGATTTAGACGTTTTTGCAAGAAAGCAAAAATGGAATTATAGCTGGTTTTGATGCTAAATAAAATCTACCTTGTTAAAAGAAAAAGAATTGTCTTAAGTAACATTTATGAAAAACAGCTATGTCATTTACCAGCTAATAACCTTTTCATTACATATAAAATGAAGCTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19185
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024558 Nonsense 482 512 10 10
ENSDART00000024558 Nonsense 482 512 10 10
Genomic Location (Zv9):
Chromosome 17 (position 43002876)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 42707612
GRCz11 17 42984118
KASP Assay ID:
2261-1451.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTGACATCATCTCTGGAGAAAAGAGTGGGAACAGTTGCACAGGGAAA[C/T]AGGTGTCAGTGGATTCTGATGGAAAAGCCACCTTCAGCATCAGCCACACA
Long Flanking Sequence:
GAGAATGACTGGATGGGACCTCCAAGCTTTTCTGATGGATCCACTAAGCCTGTACCCATCAACCCAGACTCCACCTGTGGCGACGGCTGGGTATGTGAGCACAGATGGCGCCAGATTAGGTTGGTCTCAATTTTAGTCTTAATTTTTTTCAAAAATGCAATTCTCCTAATACTTTATTATTCTCCTAGAAATATGGTGATTTTCCGTAATGTAGTCAACGGTCAGCCCCTCTTCAACTGGTGGGACAACGGTAATAGTCAGATTGCCTTTAGCCGTGGCAGCAAGGGATTTATTGTCATCAATAATGATAATTGGTGAGGAACAATTGGAGAAGAACAAATACATGAGTAATGATTATGTTTACTGTTCAATAATACACATTATATTAACTTGATTTGTCTCTTAGGGAACTGAATGCGACACTGAACACTGGCCTGCAGTCAGGCACGTACTGTGACATCATCTCTGGAGAAAAGAGTGGGAACAGTTGCACAGGGAAA[C/T]AGGTGTCAGTGGATTCTGATGGAAAAGCCACCTTCAGCATCAGCCACACAGAAGAAGATCCATTCATGGCCATCCATGCTGACTCAAAACTGTAGATTCAGTCACAATGAATTATAATAAAGCAACTGAAAATGGTTTCTATGGTCTTGTGTTCTGTCTCCATTTGAGAATTTATAGTGTAAAATAACCCAGCATTTTTAAAGTGTAATTAACAGACCACGTCCAAAACTGGCCATTTATCTTAAAAGTTTAGTTCACCCAAAAAGGAAAATTGTGTTTTTAATTACTCACAATAATTATTCAGTGGTTAGCATTGTTGCCTTAGAGCAAAAAGGTTGCTTGTTCAAGTCCTGACTGGATCAGTTGGCTTTTCAGTGGACTGGATCAGTGTGCATATTCTCCCCATTTTACGTGGGTTTTCTCCAGGTTTCTCCGGTTTACCCCAAAGTCCAAAGACATGCACTATAAGTAAATTGGGTAAACAAACTTGGCCATAGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11021
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024558 Nonsense 482 512 10 10
ENSDART00000024558 Nonsense 482 512 10 10
Genomic Location (Zv9):
Chromosome 17 (position 43002876)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 42707612
GRCz11 17 42984118
KASP Assay ID:
2261-1451.1 (used for ordering genotyping assays)
KASP Sequence:
ACTGTGACATCATCTCTGGAGAAAAGAGTGGGAAYAGTTGCACAGGGAAA[C/T]AGGTGTCAGTGGATTCTGATGGAAAAGCCACCTTCAGCATMAGCCACACA
Long Flanking Sequence:
GAGAATGACTGGATGGGACCTCCAAGCTTTTCTGATGGATCCACTAAGCCTGTACCCATCAACCCAGACTCCACCTGTGGCGACGGCTGGGTATGTGAGCACAGATGGCGCCAGATTAGGTTGGTCTCAATTTTAGTCTTAATTTTTTTCAAAAATGCAATTCTCCTAATACTTTATTATTCTCCTAGAAATATGGTGATTTTCCGTAATGTAGTCAACGGTCAGCCCCTCTTCAACTGGTGGGACAACGGTAATAGTCAGATTGCCTTTAGCCGTGGCAGCAAGGGATTTATTGTCATCAATAATGATAATTGGTGAGGAACAATTGGAGAAGAACAAATACATGAGTAATGATTATGTTTACTGTTCAATAATACACATTATATTAACTTGATTTGTCTCTTAGGGAACTGAATGCGACACTGAACACTGGCCTGCAGTCAGGCACGTACTGTGACATCATCTCTGGAGAAAAGAGTGGGAACAGTTGCACAGGGAAA[C/T]AGGTGTCAGTGGATTCTGATGGAAAAGCCACCTTCAGCATCAGCCACACAGAAGAAGATCCATTCATGGCCATCCATGCTGACTCAAAACTGTAGATTCAGTCACAATGAATTATAATAAAGCAACTGAAAATGGTTTCTATGGTCTTGTGTTCTGTCTCCATTTGAGAATTTATAGTGTAAAATAACCCAGCATTTTTAAAGTGTAATTAACAGACCACGTCCAAAACTGGCCATTTATCTTAAAAGTTTAGTTCACCCAAAAAGGAAAATTGTGTTTTTAATTACTCACAATAATTATTCAGTGGTTAGCATTGTTGCCTTAGAGCAAAAAGGTTGCTTGTTCAAGTCCTGACTGGATCAGTTGGCTTTTCAGTGGACTGGATCAGTGTGCATATTCTCCCCATTTTACGTGGGTTTTCTCCAGGTTTCTCCGGTTTACCCCAAAGTCCAAAGACATGCACTATAAGTAAATTGGGTAAACAAACTTGGCCATAGTGT
Associated Phenotype:
Not determined