Busch Lab

ZMP

si:dkeyp-35f12.2

Ensembl ID:
ENSDARG00000042071
ZFIN ID:
ZDB-GENE-090313-384
Human Orthologue:
PAM
Human Description:
peptidylglycine alpha-amidating monooxygenase [Source:HGNC Symbol;Acc:8596]
Mouse Orthologue:
Pam
Mouse Description:
peptidylglycine alpha-amidating monooxygenase Gene [Source:MGI Symbol;Acc:MGI:97475]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa16146 Essential Splice Site Available for shipment Available now
sa15072 Essential Splice Site Available for shipment Available now
sa21661 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16146
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061639 Essential Splice Site 120 909 4 24
ENSDART00000136976 Essential Splice Site 120 1017 5 27

The following transcripts of ENSDARG00000042071 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 7706527)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 5715577
GRCz11 10 5716796
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATGATTTTATATGGCTGCAAAACCCCTTATGCTACTCAAGGATACTGG[T/A]GAGTTCCCTCTGATAYTTTTATAAGCATTTTCATTTGCAGACAAAACTAA
Long Flanking Sequence:
AGCTGACTGTAGTATTGGTAACCTGGCAACCAACAGGAAGCAAGGCAAGCATAATGGAGACAGCTATTAGTTAGTGGGTGTGCTGTTCACTAAGTCAAAGTTTATACAGCAAATGAGTTTCCATCTTCCATTTTTCACATTAACCTTATTTAGCATTAAAAAAATTAAGAGATTTTTTATTATTACTTTCACATTTTTGGTGTTTCCATCATTCGTTTGTCATGTGATACATTAAAATAGAATATTTATGGTGAAACCTAGATATTGTTCGTTTGCAGAAAAGCTATGACATTGCAATCATTACAATTTATCAAGAAATTTCAGATCGTCATTAAAGATGTTCATCCTACCATCACCGTATTCTCTATAAGATTACCAAGTTTACCTTAAAATCATCTCTTCTCTTCTCAGTGGACTTTGTTCCCCATGCCAGTATGGACACAGCCCACCACATGATTTTATATGGCTGCAAAACCCCTTATGCTACTCAAGGATACTGG[T/A]GAGTTCCCTCTGATACTTTTATAAGCATTTTCATTTGCAGACAAAACTAAAGTGCCGCTTTACAAGCACTGTCAATTCAAGACAACATTTGTTATGTTGATTTACCTTATTCTAATATTTTAAAGTAATCAAGTTTCAGTGCATCCCACTCCTCTTGCCACTTATTTAAAATGTAAACGTTGATAAAAGGTCTCATTTCTGAAGTAGAAATTTGTTCACCACTTGCTTCAATGCGTCCTTAGCAGCTGCATCAGCCCGCTCATTTACTAAAAGCCTAACATGTCAGGGAACCCAGCAAAAAAATGATGTGATAAAACTGGTTTCGTAGATGGTAAACTTAAGTTAAATATTAACAATCCAAGAATGACACTTGGAGGCATGATTTGGAGTCTGTAAAAATGACAGAGACTGTAAGAAAGATGTTGAAATTCAGCTTCGAATCATGGAAATAATTACATTTTTAAAAATATTTTTAAACAGAAAAGCATTATTTCAAAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15072
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:
G > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061639 Essential Splice Site 370 909 12 24
ENSDART00000136976 Essential Splice Site 370 1017 13 27

The following transcripts of ENSDARG00000042071 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 7734850)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 5743900
GRCz11 10 5745119
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGCCAGACCATATGATGTCCATGAAGCATGAAKCTTNNNCTCAAAAAG[G/C]TACCGTACAAAATCAAACACTTCAAGATTTTTCATACACAACTCTACATG
Long Flanking Sequence:
ATGCTTGAAATGTACCTGAAATTCTGATTTGAGTCATAAGCTTTAGAGGATTGATTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTCTGTTGGTTATTTTTATACTTGCTGCTTTGTAGCTGTACTTTTTAAAAAAAATTTATTTTGCTAATAGTTTGTTCACATCTCGTTGTTTTCCTCCTCACAGAGGCACCTCCAACGATGAGATGTGTAACTTCTACATCATGTACTACATGGACAACACCCATGCTGTGCCTTACATGAACTGCAGAGATGATGGCAGCAGTGAGCTCTTCAGAAACATCCCTTCTGAGGCCAATATTCCAATCCCGGTCAGGCCAGACCATATGATGTCCATGAAGCATGAATCTTCTCCTCAAAAAG[G/C]TACCGTACAAAATCAAACACTTCAAGATTTTTCATACACAACTCTACATGTAGGCAGTTGAAACAGATAGCTTGTGGAATCACTGAATGTTGCTATGTTTTTGGGTAACTCAAACACTGTTTTTCTTAATATTCTCATTTGCTTATTTGTCATTTAGATGCTGTGGAGCTTCAGGAGCCCAAGAGAGATGAGGAAGTACAGGATCAAGGTAAGCTTTTAAAATAATTCATAAGAGAATTTTGTTCATGAAACATAGTCATTACTGAAATATCATTACAAATCCCCCTCTATAAACAGATGTAGAGGTTAAATTATGCTTTTCAGTAAAACTATGGTATACACCAGGGGTTTTCAAACTTTTAAGTCACCCCGCCCCACTCCCAAGTTTGCCCCAATTTCACTCGCCCCACCAGGCACCCCTCCCTCCAACCAGAAATATAATGTATGTGCAAACATCATTCACATATTACTTCCTGTGTTTAAAGTCTCAATTACATTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21661
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061639 Nonsense 385 909 13 24
ENSDART00000136976 Nonsense 385 1017 14 27

The following transcripts of ENSDARG00000042071 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 7735049)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 5744099
GRCz11 10 5745318
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCATTTAGATGCTGTGGAGCTTCAGGAGCCCAAGAGAGATGAGGAAGTA[C/T]AGGATCAAGGTAAGCTTTTAAAATAATTCATAAGAGAATTTTGTTCATGA
Long Flanking Sequence:
GTTCTGTTGGTTATTTTTATACTTGCTGCTTTGTAGCTGTACTTTTTAAAAAAAATTTATTTTGCTAATAGTTTGTTCACATCTCGTTGTTTTCCTCCTCACAGAGGCACCTCCAACGATGAGATGTGTAACTTCTACATCATGTACTACATGGACAACACCCATGCTGTGCCTTACATGAACTGCAGAGATGATGGCAGCAGTGAGCTCTTCAGAAACATCCCTTCTGAGGCCAATATTCCAATCCCGGTCAGGCCAGACCATATGATGTCCATGAAGCATGAATCTTCTCCTCAAAAAGGTACCGTACAAAATCAAACACTTCAAGATTTTTCATACACAACTCTACATGTAGGCAGTTGAAACAGATAGCTTGTGGAATCACTGAATGTTGCTATGTTTTTGGGTAACTCAAACACTGTTTTTCTTAATATTCTCATTTGCTTATTTGTCATTTAGATGCTGTGGAGCTTCAGGAGCCCAAGAGAGATGAGGAAGTA[C/T]AGGATCAAGGTAAGCTTTTAAAATAATTCATAAGAGAATTTTGTTCATGAAACATAGTCATTACTGAAATATCATTACAAATCCCCCTCTATAAACAGATGTAGAGGTTAAATTATGCTTTTCAGTAAAACTATGGTATACACCAGGGGTTTTCAAACTTTTAAGTCACCCCGCCCCACTCCCAAGTTTGCCCCAATTTCACTCGCCCCACCAGGCACCCCTCCCTCCAACCAGAAATATAATGTATGTGCAAACATCATTCACATATTACTTCCTGTGTTTAAAGTCTCAATTACATTGAAACATAAATGCACATTTTACCTGATTCAGTGTGATGGCTGAGCCTGTTTTTGTGAGGACAACATGCTAATCTGTGGTTGGATTTCTGACAGGACTAACTGTAAATCCTCTTCTACTGTCAATAAGTGTGAGCCATAGCCTTTGATACATATGTACATACAGAAAATGCTGCTTCGCAAAGCCAAGATCGCAGAGCCCTG
Associated Phenotype:
Not determined