ZMP
zgc:66313
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393400 [Source:RefSeq peptide;Acc:NP_956722]
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]
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]
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10462 | Nonsense | Available for shipment | Available now |
sa28917 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10462
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042681 | Nonsense | 22 | 512 | 1 | 10 |
ENSDART00000132673 | Nonsense | 22 | 259 | 2 | 6 |
ENSDART00000133317 | Nonsense | 27 | 253 | 4 | 8 |
ENSDART00000133874 | Nonsense | 22 | 278 | 2 | 6 |
ENSDART00000134272 | Nonsense | 27 | 517 | 1 | 10 |
ENSDART00000140316 | Nonsense | 27 | 259 | 3 | 7 |
ENSDART00000142929 | Nonsense | 22 | 37 | 4 | 4 |
ENSDART00000148090 | Nonsense | 27 | 87 | 3 | 4 |
The following transcripts of ENSDARG00000030357 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 43915076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43754754 |
GRCz11 | 17 | 43868519 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGGCTGCTCTYGTAGGACTGTGTCTTTCCCAGCACAACACTAACTTT[A/T]AACAWAACCGGACSTCCATCGTTCATCTGTTTGARTGGCGTTGGGCAGAT
Long Flanking Sequence:
GCATATGTGACCCTGGACCATAAAATCAGGTAATTTTAAGAAAATAAAAGTTATACACCATCAAAAATCTAAATAAATTTGCTTTCTATTGATGCATGAAACGTATTGGACAATATTTAGCTGCAATCTGAGGGTTAAAAACACAAATGTTAAGAAAATTGACTTTAAAACTGTACAAATTTTATTTTTGGCAATGCACATTACTAATAAAGGTTTTGATATATTTATAGTAGGGAATTTACAATATAATGCTCATATAACATGGTTTTTATTTATAGTTATAATCATTTTAGGCTTAAAAAGGCAATAATTTAAAAGCATACAATTGATTTTTGACTTTTCCCTCAAGGATATCTAGGGTAATATGACCTCATTCATTGGCTAGTGTTTATATTAGATAACTCTCTCTCAGCTGTTTTTTTATGCGCAAAGGGACAATGAAGCTCCTGGTTGTGGCTGCTCTTGTAGGACTGTGTCTTTCCCAGCACAACACTAACTTT[A/T]AACATAACCGGACGTCCATCGTTCATCTGTTTGAATGGCGTTGGGCAGATATAGCTAAAGAATGCGAGAGATACCTGGCACCAAACGGCTATGGAGGAGTACAGGTAAGGTGCATTTACTGCACTCAACAAAAGTATAAACGTAACACTTTTGTTTGTGCTCCCATTTTCACAACCAAAGCTCTTTCTATGCTTACAAAAGACCTATTTCTCTCAGACATTGTTTAAACATTTGTCTAAATCTGTTAGTGAGTACTTCTCCACTGAGATAATCCATAAGTGTTGCATTTTTATTTTTGTTGGGTCTAGTGAAAGAATGATGTGTGATCTTTTGGATCTTTCTGAGCTTTTAAATGTGCTGTGTTTAAGTTTTTGACTGTTCTAAAAGATAAAAACAGCATAATATGTTTGCAGATATTTAAGAAACGTGCTAAGTGAACATTCTTGTTTATCTGAAGAACAATGCTGAAGTCAGATATTCTGCTTTGAAAATGTAAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28917
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 |
---|---|---|---|---|---|
ENSDART00000042681 | Nonsense | 348 | 512 | 7 | 10 |
ENSDART00000132673 | None | None | 259 | None | 6 |
ENSDART00000133317 | None | None | 253 | None | 8 |
ENSDART00000133874 | None | None | 278 | None | 6 |
ENSDART00000134272 | Nonsense | 353 | 517 | 7 | 10 |
ENSDART00000140316 | None | None | 259 | None | 7 |
ENSDART00000142929 | None | None | 37 | None | 4 |
ENSDART00000148090 | None | None | 87 | None | 4 |
The following transcripts of ENSDARG00000030357 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 43925897)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43765575 |
GRCz11 | 17 | 43879340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTAGGCTTTATAAGATCGCGACAGGACTTATGTTGGCTCATCCATA[C/A]GGTGTAACAGCAGTCATGTCCAGCTACCGATGGGATCGACATTTTGTGAA
Long Flanking Sequence:
ATGCCGTATATACAGATTATTGAAAGTTTAAAGCAATGTGTTTGCTACTTTTAAAATAATGAACTCATTCTCTCATTGACTGTGTGATTCATAGTGACTACTTTAATTTAAAGCAGCAGTTTATTTTTAAAAGCTCAAATATTATTTCTTATTTTTTTTAAGTAATGCGTTACTTTACTTGAAAAGTAATATTATAAAATAAATTTCACTTCATGTTTCAGCTTTAATGGTTTTTAAATGGTGTTTTGGTTTAGGAACTGGGGAGAGGGCTGGGGGTTCATGCCCTCTCATAAAGCCTTGGTTTTCGTGGACAATCATGATAATCAGAGAGGCCACGGTGCTGGTGGAGCTTCTGTTCTGACATTTTGGGACTCTAGGTAAAATCAAATGTTTTAATTTGTATGACAGCTTATGCGTATTCCTGCTGCAAGTGGTTTGTTTTATGCTGTGTATTTTAGGCTTTATAAGATCGCGACAGGACTTATGTTGGCTCATCCATA[C/A]GGTGTAACAGCAGTCATGTCCAGCTACCGATGGGATCGACATTTTGTGAATGGGAAGGTAAATACTTGCACTTAAAGTTATGACTATACTGTCCTGTTTATGACTATGACATAAATGAAGAGAAGGAAAAAAGATAGATGCTGTGTGTGTTGGTACCTGGATGGTTTTGTGATTAAATATATTAGCAAAAAAAAGGATGGCATGATTTTCCTGATTTATTATTTATGCTTAAAATTGTGGAGTTCATGCTGAATACTGAAACTTGCTGTCTTTATTTTAAAGTGACATATTTAAGTATATCACCATATTTGGATTGAAACGTTTATATAAAAAAAAAACATATTTTATTTAATTCTATATTAAACAATAAATTGTCATTATGGGGTCCTTTAAACATTATTATTAAGATCTTGGAATTTGTAAAATTTTTATGTATTTCCAAAAGAGCATTATTTGTTTATTTTTTTTTTACATTTTATTGACCAATATTGACTATGAAT
Associated Phenotype:
Not determined