Busch Lab

ZMP

paplnb

Ensembl ID:
ENSDARG00000042186
ZFIN ID:
ZDB-GENE-030131-6023
Description:
papilin b, proteoglycan-like sulfated glycoprotein [Source:RefSeq peptide;Acc:NP_001018400]
Human Orthologue:
PAPLN
Human Description:
papilin, proteoglycan-like sulfated glycoprotein [Source:HGNC Symbol;Acc:19262]
Mouse Orthologue:
Papln
Mouse Description:
papilin, proteoglycan-like sulfated glycoprotein Gene [Source:MGI Symbol;Acc:MGI:2386139]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa17921 Essential Splice Site Available for shipment Available now
sa9174 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa13427 Essential Splice Site Available for shipment Available now
sa11086 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa17921
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061836 Essential Splice Site 186 548 7 14
ENSDART00000140287 Essential Splice Site 186 538 6 13
Genomic Location (Zv9):
Chromosome 20 (position 33547868)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 33606108
GRCz11 20 33508987
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCACTTCTAGAYATGGACCTGGTGCTGCTGTCCATCTGGACACTTACAG[G/A]TTATTCATCACTGTTTTGTTTGTTTGTTTTTTTNGCATCTGTAATGAAATT
Long Flanking Sequence:
GTTATGTTTAGAAGTGTGATGAAAAACCTTTTTTCCCATTAAACGGGGGCTAATAATTCAGGAGGTCTAATAATTCTGACTTCAACTGTAGGCTATATACAAGTGAGAGAGTTCTGCTTTTGTATTATGTTTAGAAACGCTCCTCTGGACTAAGATAAAGTGACCTGCGCTGTTATATTTTTTCCAGCTTCAAACCCGTGTGAGCTGGTCTGTGTGCCCAGAGGAGAGAACTTCTACTACCGTCACAGACCCGCTGTGGTGGACGGCACTCTATGCCACGTGGGCCGCAGAGACGTGTGTGTTGAGGGCGTCTGCAGAGTACGTGTCAACAATGCTACAACAACACAAAACCACACACATACACACACTCATTTCAGTCTAACACCATTATTTGTGCTGAAGGCGGTGAGCCATGGAGAGATTGTGGGCTTTGAGGATCGTGATATTCCTGTCACTTCTAGACATGGACCTGGTGCTGCTGTCCATCTGGACACTTACAG[G/A]TTATTCATCACTGTTTTGTTTGTTTGTTTTTTTGCATCTGTAATGAAATTTAAGTATGCATTAATGCATGTAAATGGGTCAGAAAATTAAAGAGGTTTTGTGTCCTGTTTAATATAATAAAAAAGGTATTGATTCATTAATATAATCAAAAAAATATTGATTATAGAGGCATACTTCGAAAAATAACCATCTGAAAGACTTTGAGGATCTTGAATTTGAGGATCACAATGCAGTCCCAATACACTAATTAATTCAAATGTAATTTACTTTCTTTTTCAATCACTTAAAGAGTATATTGAAGGAAGGTTAGAATTAGCATATTGTTTTATTTTTTCATAAATATATGTAAATATAGCAATAAACGGTAATAGTAGATTCCTTACAAAGGAACAGTGGACAAAGAAAAGTTATTTTGAAGCCAAAAACACGCACACTTAGTCTTAGTTAAAGTGTACTGTACTTACAGCAAGGGCATAGATTCGTTGCATGACATGCATCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9174
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061836 Essential Splice Site 253 548 8 14
ENSDART00000140287 Essential Splice Site 253 538 7 13
Genomic Location (Zv9):
Chromosome 20 (position 33546183)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 33604423
GRCz11 20 33507302
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCAAYGAACACGCCTGTGCYGAAYACAGCGCCGGCCCATTTGGTGATG[T/A]ATGGAATTATTTCATTAATATTTTATCAGTCCTTCCAGGATTTTGTGATT
Long Flanking Sequence:
CATGTAGATGCAATGTGACCTAAATTCAACAAATGGACCATCAAAATAAAGTGTGATCAATTAAAGTATTATATTAAAAAAGAACAAATGTATTTTATAAATGTTCTAATAAATTATAAAGTTCATATATTTATATTACTGTATATGTTTTCCTTATATATTAGTGCTATATTATTGTTATTTGTGAAATGTATTTTTTTCTTTTTCTTATTTTTATATCTTAAATTTTCATTACTTGTTTTGTGTCTAGTCCTTTGATAATAAGTACTTTCAAACTCAATATGACTCTGTTTGTAGATACACATACAGTGCCTACTCTGAGTGTTCCCGTTTATGTGGAGGAGGTGTTCAGAGCCGCACTGTTTACTGTGTTCATGAGAGAACATCGGCAATGGTTGATGAGTCCCATTGCATTGCAAAGGGCCTCAGAAAACCAACTGCACAGGTTGCCTGCAATGAACACGCCTGTGCCGAATACAGCGCCGGCCCATTTGGTGATG[T/A]ATGGAATTATTTCATTAATATTTTATCAGTCCTTCCAGGATTTTGTGATTCTGTGATTGCAATAATTATTAGTTAGTGATTTTATTTGTTCAAAATTCACAGGTCACCAGCAGATTTTGGGCGTCCTTAAAAAGATGGTTTACCTAAAACTGAAAATTCCATCATCATTTACTGGTCTTTACTTGTTCAAGTCATATTTGAGATTCTTTATTTCTGATGAACACAAAAGAAAAGGTTTTAGTTTGATTTAAGACAACATGACAGAGAGAAAATGATAAAGTAATTTTCATTTTTAGATGAACTAACCCTTTAAAAATTAACCATGTGATGTTACAAATATTTTTTTAGGAGATTCCAATACTTTTATTCAGACAACACTTCTAAGTTTTTATGTGTTCAAATTGTTGACAAATTATTTGAAAGGTATTATGCATTATAAGCCTTCAATGGTTCAGAACATAAATAGTGTAAAAAATGTACCAAACAATGGAAACTGATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13427
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061836 Essential Splice Site 462 548 13 14
ENSDART00000140287 Essential Splice Site 452 538 12 13
Genomic Location (Zv9):
Chromosome 20 (position 33538865)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 33597105
GRCz11 20 33499984
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCTGCTCTGGGTTACAGAAGAGCGGGATGTCCTGACTCCTCCTATGGG[G/A]TAAAACAGCTCATTTAATTTTCYCTGTCAGTTTTCCTCTCATCATATAAT
Long Flanking Sequence:
TCCCAGCGTTATACTCACTACTTACTACTCTTGAGTACTTTCGAAAGGGCTACTGTTTACTCATACTTTAATACTTAAAACAGGTACTTTAACTCTACTTGCATTACATTTTTGGGTAAGTAGTTGTACTTTTACTTTAGAATGATTATTCAGAACGGTTTCCATCACTAAAGAAAAGGTTTAAGCAAAAAACGGAAACCAAAACTGAAAAATATCCTTTAAAATAGTTTGCATTATGTTCCACAGAAGAAAGAAAGTCATACAGTTATAGGGAGTATATAGATGACATATGGGTGACTAAGTGATATAATTAAATAAAACAGTAGTGAACAGCAATGAACTGGATTTTTATTAAGGCCAGATTTGGATATATTCAGGATCAAACCAGTGAACTGAACGTGTGTGTGTGTGTGTGTGATGAAAGATACGGCTGCTGTCTGGATGGAATAACAGCTGCTCTGGGTTACAGAAGAGCGGGATGTCCTGACTCCTCCTATGGG[G/A]TAAAACAGCTCATTTAATTTTCCCTGTCAGTTTTCCTCTCATCATATAATTTCATCTAATTATATAAACACGTCTTTGCTTTTGTTTTCAGGATCACAGTCCCTCTGCTAGTGTGTGCTCCTTGGCACGAGATGTCGGGCCCTGTTATGAATATAAATCTCGCTTCTACTTTGATCATTCCTCTGGCTCTTGCTCCCAGTTCTGGTTTGGTGGATGCCAAGGAAATGGCAATAACTTTGTCTCCAAGGTGGCGTGCGAGCGGACGTGTAAGGCTTCTGTCAGAGGAAGAGAACCAACGTCCAGGAGAGTGATCTACGATGTCAGAGGTTATAGAGTGAGATCCCGTGCATAATAAATGTCCAGACAAATCCAACTCATAAACATGTAGATAAAACTTCAATTGTGCTGATTTGAAAGCAGTCTTGGGTTTATACTGACATCTACTGGCATTGATTTGTTTAAACTAAGCTTTTTTAAGGGATGAGAGAGAAACACTTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11086
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
ENSDART00000061836 Nonsense 475 548 14 14
ENSDART00000140287 Nonsense 465 538 13 13
Genomic Location (Zv9):
Chromosome 20 (position 33538737)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 33596977
GRCz11 20 33499856
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTTTGTTTTCAGGATCACAGTCCCTCTGCTAGTGTGTGCTCCTTGGCA[C/T]GAGATGTCGGGCCCTGTTATGAATATAAATCTCRCTTCTACTTTGATCAT
Long Flanking Sequence:
CTTTTACTTTAGAATGATTATTCAGAACGGTTTCCATCACTAAAGAAAAGGTTTAAGCAAAAAACGGAAACCAAAACTGAAAAATATCCTTTAAAATAGTTTGCATTATGTTCCACAGAAGAAAGAAAGTCATACAGTTATAGGGAGTATATAGATGACATATGGGTGACTAAGTGATATAATTAAATAAAACAGTAGTGAACAGCAATGAACTGGATTTTTATTAAGGCCAGATTTGGATATATTCAGGATCAAACCAGTGAACTGAACGTGTGTGTGTGTGTGTGTGATGAAAGATACGGCTGCTGTCTGGATGGAATAACAGCTGCTCTGGGTTACAGAAGAGCGGGATGTCCTGACTCCTCCTATGGGGTAAAACAGCTCATTTAATTTTCCCTGTCAGTTTTCCTCTCATCATATAATTTCATCTAATTATATAAACACGTCTTTGCTTTTGTTTTCAGGATCACAGTCCCTCTGCTAGTGTGTGCTCCTTGGCA[C/T]GAGATGTCGGGCCCTGTTATGAATATAAATCTCGCTTCTACTTTGATCATTCCTCTGGCTCTTGCTCCCAGTTCTGGTTTGGTGGATGCCAAGGAAATGGCAATAACTTTGTCTCCAAGGTGGCGTGCGAGCGGACGTGTAAGGCTTCTGTCAGAGGAAGAGAACCAACGTCCAGGAGAGTGATCTACGATGTCAGAGGTTATAGAGTGAGATCCCGTGCATAATAAATGTCCAGACAAATCCAACTCATAAACATGTAGATAAAACTTCAATTGTGCTGATTTGAAAGCAGTCTTGGGTTTATACTGACATCTACTGGCATTGATTTGTTTAAACTAAGCTTTTTTAAGGGATGAGAGAGAAACACTTTATCAAACATGACTGCATCAAAGCTAAAGATAATTTCCTTTCTTTTTATGTTTCGGTGTAAGTACTTTGGTTGTATACTCTTCCTAAGCCATTAAAGTGTTAACACAAACCAACTGCACTGAAGAATTAAC
Associated Phenotype:
Not determined