ZMP
PAPPA (1 of 2)
Ensembl ID:
Description:
pregnancy-associated plasma protein A, pappalysin 1 [Source:HGNC Symbol;Acc:8602]
Human Orthologue:
PAPPA
Human Description:
pregnancy-associated plasma protein A, pappalysin 1 [Source:HGNC Symbol;Acc:8602]
Mouse Orthologue:
Pappa
Mouse Description:
pregnancy-associated plasma protein A Gene [Source:MGI Symbol;Acc:MGI:97479]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17987 | Nonsense | Available for shipment | Available now |
sa33777 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25323 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17783 | Nonsense | Available for shipment | Available now |
sa33778 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17987
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 |
---|---|---|---|---|---|
ENSDART00000082858 | Nonsense | 135 | 1591 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 5 (position 73416542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 69617703 |
GRCz11 | 5 | 70356127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTYAACTGTATTTATTATTGTACTTTCCCACTTAYAGGTCTCTTCGAC[A/T]AATGCTTCTACGCCTCTAGTGATCGTGGATGGCTCTTGGGAATTAAATCY
Long Flanking Sequence:
ATAAAAACAAATCTAAACAGTTACATCTACATGAACACTTTCGGCTGTGGGACTGCATGTTATTGTGTTAAATGATTTTAAATTAAACAATAACAATATTATATTCGTTTAAAATGCAAAATAATGTTTTTTAACAAAACATATTTATTTATTTTTATTATTTGAAACTTTTAATGAGGATAATTTTAAAAATAGTTTTGGCACAACGGCGCCCCCCCATGTGTGGCGCCCCTATGCGCCGCATATACTGCATACCCCCTTGTTACGCCACTGGTCATCGTTGTCAATTTTCTGCAGCCCTAATCTCGAAAAACATCTAGTCGAACATCATGTGCTGTCATCGTGGCGAAGATAAAAGAAATCAGTTATTAGAAATGAGTTATAATGTTTAGAAATGTGTTGAGGAAATGTTCTGTCTGTTAAACAGAAATATGGTGATATATAATTCTGACTTCAACTGTATTTATTATTGTACTTTCCCACTTACAGGTCTCTTCGAC[A/T]AATGCTTCTACGCCTCTAGTGATCGTGGATGGCTCTTGGGAATTAAATCCGTGAGTGAACAGGGAAACCGCGACCCGCGTTTCTTCTTCTCCCTGAAAACGGATCGAGCTCATAAAGTTGCCTCCATTCACTCCAACGCCCGATATCTGCCCAATCATTGGGTTCACGTGGCCGTCACCTACAACGGCCTCTTCATGAAGTTATACATCAACGGCGCTCAGACAGCGGTCAGCAGGGAGCAGTCAGGTGATGTCTTCAGCCCACTCACTAAAAAGTGTAAGGTGAGTTTCATTCTTTTAGCACATTTTACACCGTATCTTTCAAGAAATTGACACACTATCAAATTTATATTGTATTTTTGTTAGTAGTGATGCTTGAGTGTGTACACTACCTGACAAAAGTCTTGTCGTCTATCCAAGATTTAGGAACGACACATAATAACTTGACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTATATTAAAGGCCTCTAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33777
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 |
---|---|---|---|---|---|
ENSDART00000082858 | Essential Splice Site | 490 | 1591 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 5 (position 73434148)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 69600097 |
GRCz11 | 5 | 70373733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATCTAGACATACGCGTATGTTCACTCTCCCTCTCCATCTGTGACTCC[A/T]GGGCCTATCTAGATGTGAAGGAGCTGAAAGAGATCCTCAAGCTGGACGGC
Long Flanking Sequence:
ATTACACTGTGGCAACCCCGGATTAATAAAAGGACTAAGCAGACAAGAAAATGAATGAATGAATGAATGAATGAATGAATAAATGAATGAATGAATGAATGAATGCAGGCAGCATGAACTGGAAGTTGCTGAGACTTTTTAGTATGTTGATGTACTTCCAACTGAAACGGAATATTGAGTAGGGGGCGGGGCTTTCTACTTGCACATCATCTGCTTAAACTAACAGTAAGAGGGGCGTGGCTTATAATACAGTGGCTGGAGCCGTCAAACTAACACATCATGTAGTAGGAGCCAATTCAAGACACAGAAGCAGATGTGCAGACTTTGATTGAAGAAGAACAAAACTAACGTGTATTTCAGTGAATTAGCTACTAGAATAAATATGTGCGCTAGCAAAATAAACATTGTACATTTTGATTTCGCACAAACTTAAATAACTAGTAATTGAGATGAATCTAGACATACGCGTATGTTCACTCTCCCTCTCCATCTGTGACTCC[A/T]GGGCCTATCTAGATGTGAAGGAGCTGAAAGAGATCCTCAAGCTGGACGGCTCCACACACCTCAATATCTTCTTCGCCAATTCCTCCGATGAAGATCTGGCTGGAGTCGCCACCTGGCCGTGGGATAAGGACGCGCTGGCGCATCTCGGTACGGAGAAATTACTGCATACATGTTTGAGTTATATTCCTAAATCATCTGATGCTGAACGCCGCGCTCTGTCACTCTGTGACATTATTTCAGTGGTTCCTCTTCTCAACAAGTGTTTGTTCATGTTAAGGGCGGTATAAATCATTCTGTTGGAGGTTTAGAGTAAATAATCAAAGCAAATTGAAGCGTAATAGCTGCATAAGCAGAAGAAGTGAAGACACATTTACTGTATATGCAAGTGCAATGATCTGACATTTCAAGGATGCCGTTCGCATCGCATTCAGACTTTTGTTTCAGTTATTTGGTATCGAAATGGTAAAAACTATAAAAATTACCAACCCAGGCTCATTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25323
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082858 | Nonsense | 801 | 1591 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 5 (position 73470851)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 69638001 |
GRCz11 | 5 | 70410436 |
KASP Assay ID:
554-7515.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATATGCGGTGGTCCCCGATTCCCTGACAGTTTGGGTCACTTTCTCCTCC[C/T]AAGACGAAACGGTTCTTCCAGCAATCCACAATATCATCCTGTTGACCGTC
Long Flanking Sequence:
TCGAATCACCTTAGTCACATGACCTGGGTGTTTCAAATCACCTTCGCCACGTTACCTGGGAGTTTCTAATCACCGTAATAGCGTTGCCTGGGTGTTTCGAATCACCTTCGCTACGTGACCTGTGTGTTTGAAATAACCTTCGTCATGTGACCTTTGGGTGGTTCCGATCATGCTTCGGTGGCCTTTTGAAAAGCTGCTTTGAAACAATACTTATTGTGAAGAAACGCTAACCCCCATTTTAAAAACATTTTTTAAAAATATTTATAAATTTATTAATATTTAATGACTCTATTTGAATACAATATATATTTTTGCATCTCTCAGGACCCCCAGATGTGGAGCAAGCGTGCGAGCCAAGCGTCCACACTTGGAGTCCTCATAACGGGATGGATCTGGGTTTGGTTCCTCCTCCGTGCCCTCTGCAAGGCTGCATGCTTCAGCTGGAGTTTGCATATGCGGTGGTCCCCGATTCCCTGACAGTTTGGGTCACTTTCTCCTCC[C/T]AAGACGAAACGGTTCTTCCAGCAATCCACAATATCATCCTGTTGACCGTCGGCGGAAACAACCTGTCTCTGGGTCCCGCAATTTATTCTGCGACACCCCGTTAACCATTAAACTGGATGTGCAGGAGAAGGTGTACGGCGTGCAGTTTTACACCATGGAGCAACATTTGGAAATCGACGCTACTTTGTTGACGTCCAAACCCGATGTCCGCTCTGTGGAGATTGTGAGCCATTGCATTTTCGGCTTCTTCGACAGCCACCATTCAGCAACAGTAAACAGGGCATCATGCTGAGCGACTCCACTAGAAGATACACAGACAGGTCAGTCTTTAAGATTCATATATGCGTAAAGAAATTGCTCTCCATGTCATAATGAATGCATAAAGGGGGTAAGGGGGTACATGTAGGAATATTAATCACTACAACAAAAACTAATATATTCATGACAATTCTATATATATATATATATATAGATATAGATATATACCCTGCTGAAAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17783
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 |
---|---|---|---|---|---|
ENSDART00000082858 | Nonsense | 1078 | 1591 | 14 | 24 |
Genomic Location (Zv9):
Chromosome 5 (position 73520404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 69687554 |
GRCz11 | 5 | 70459989 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCTGGTTTCCATGYCGAGAGGCTCACAGTGTTCCCTGGTATCCCCCGTA[T/A]TGGTTGAAGGTGAGCTGTCTTTAWCATTGTAGTTTWATTTTATTTATTGG
Long Flanking Sequence:
CAGACAAAACATGGTGTCCTTGTCTAATGTCATATAGTGTACAGCTTTTTTTTCAGTGAGATTGGATAAAATCATGTTCCCAACACATTACACAACGCAGATCAGCTTAGAGCTGTTATTAGAAATATCCGCCTACTGTATGTATCTAACAAATTAAACAATGACCACATGCTTAATGTCTTCAAATGAATTGCAAAACGAGTTATTATATGTGTATTGAACAGTCAATTTGTCAATATAAGGTTTCATTTACATGGTTGAAGCTTTTAAAATTGATTATATAATAGTAAAATTACATTTACGTCTGTCTGTGTGTGTTTATTGATTGACTCAGGTCTGTAAATTCTCCAGTTGTATTTCTCCCAGTGGTGTAAGTGGATACCGTATGTTGTCTGTCCCCAGACGTGCCAGTCTAAGGTGTTCGACTTGTCTGATGGAGTGTCTCAATATGCCTGGTTTCCATGCCGAGAGGCTCACAGTGTTCCCTGGTATCCCCCGTA[T/A]TGGTTGAAGGTGAGCTGTCTTTATCATTGTAGTTTTATTTTATTTATTGGTCTATCATTATATACTGTAGTTGTCTGTCTAATCTCTATTATTGTTCTACTGAAGGGAAAAGGAAAGCCACTTTAGTTAGACTCATGTGTCAGCTAATGGTATATACATCAAGTGACTCTTCCTGCAGTATATACTTCATCAGCATAAGCGTAAGAGTAAATCTTGTCTCCGACAGGCTTATTTCTCTCATCCTATGGTTGCTGCTGCTGTTATCATCCATTTGGCTGCAGATGGAACCAGCTACATGGACCAAACCCAGTGCAACATCACAGTTCAACTGATCGACACCAAAGAGGCCATTCACAGTTTAGGTGAGAGATCCACATTAGTACTACTACTACTACTACTACTACTACTACTACTACTACTACTACTACTAATAGTAATAATAATAATAATAATAATAATAATANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33778
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 |
---|---|---|---|---|---|
ENSDART00000082858 | Essential Splice Site | 1082 | 1591 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 5 (position 73520629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 69687779 |
GRCz11 | 5 | 70460214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTATATACTTCATCAGCATAAGCGTAAGAGTAAATCTTGTCTCCGAC[A/T]GGCTTATTTCTCTCATCCTATGGTTGCTGCTGCTGTTATCATCCATTTGG
Long Flanking Sequence:
CAATTTGTCAATATAAGGTTTCATTTACATGGTTGAAGCTTTTAAAATTGATTATATAATAGTAAAATTACATTTACGTCTGTCTGTGTGTGTTTATTGATTGACTCAGGTCTGTAAATTCTCCAGTTGTATTTCTCCCAGTGGTGTAAGTGGATACCGTATGTTGTCTGTCCCCAGACGTGCCAGTCTAAGGTGTTCGACTTGTCTGATGGAGTGTCTCAATATGCCTGGTTTCCATGCCGAGAGGCTCACAGTGTTCCCTGGTATCCCCCGTATTGGTTGAAGGTGAGCTGTCTTTATCATTGTAGTTTTATTTTATTTATTGGTCTATCATTATATACTGTAGTTGTCTGTCTAATCTCTATTATTGTTCTACTGAAGGGAAAAGGAAAGCCACTTTAGTTAGACTCATGTGTCAGCTAATGGTATATACATCAAGTGACTCTTCCTGCAGTATATACTTCATCAGCATAAGCGTAAGAGTAAATCTTGTCTCCGAC[A/T]GGCTTATTTCTCTCATCCTATGGTTGCTGCTGCTGTTATCATCCATTTGGCTGCAGATGGAACCAGCTACATGGACCAAACCCAGTGCAACATCACAGTTCAACTGATCGACACCAAAGAGGCCATTCACAGTTTAGGTGAGAGATCCACATTAGTACTACTACTACTACTACTACTACTACTACTACTACTACTACTACTACTAATAGTAATAATAATAATAATAATAATAATAATANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCTACCTTTTTTGCTAAATGTAAAATACGTTTTTTCAGGTACCTTTCGTTGCACGTTTCAGATGACAAATCCACTAGAGGGCGCTGAAATCTGAAAATAAGTTACTAAGGGTACATTTTGTTGTAAATTTCAGATAGACATACTTCTTGTACACATCTAGGAG
Associated Phenotype:
Not determined