Busch Lab

ZMP

plod1a

Ensembl ID:
ENSDARG00000059746
ZFIN ID:
ZDB-GENE-030131-3165
Description:
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 [Source:RefSeq peptide;Acc:NP_001071210]
Human Orthologue:
PLOD1
Human Description:
procollagen-lysine 1, 2-oxoglutarate 5-dioxygenase 1 [Source:HGNC Symbol;Acc:9081]
Mouse Orthologue:
Plod1
Mouse Description:
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 Gene [Source:MGI Symbol;Acc:MGI:99907]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa21385 Essential Splice Site Available for shipment Available now
sa25408 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa31681 Nonsense Available for shipment Available now
sa13867 Essential Splice Site Available for shipment Available now
sa14077 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa21385
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
ENSDART00000083395 Essential Splice Site 251 730 8 19
ENSDART00000147159 None None 50 None 4

The following transcripts of ENSDARG00000059746 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 50034276)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 47886253
GRCz11 8 47875245
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACTGTCTTCAGTTCAACCTGATTTATTTTGTGCTCTTTTTTTTCTTCA[G/A]CTTCAGATAAACTACCTAGGGAACTACATCCCGAATCTGTGGACATTTGA
Long Flanking Sequence:
GGCTGCGTCCGAAACCGCATACTTCCATACTATATAGTATGCTAAAATCAGTATGCGAGCAGAGTAGTATGTCCGAATTCTTAAAATTCGAAAATCAGTATGCGAGAAGTACCCGGATGACTTACTACTTCCGGCGAGATTCTGGAGTGCGCATCTCGGATTCGGACGGTTTCGGTTTCGGACGCAGCCTATGAATAGTCAACTTTGTCTTCTTCTTTGTTACAAGCGGATGTCAGAAGCTTAAAGTAGTGCAGCACCATGTAACGTCAAGGAGTGGTTTTGCATACTCTTCTGCTCGACGCCAGTGAAAATTGCTTGGGTTTGAATCCTTGAAAAACGCTGACGATTAACGCAAGCGAAAAGCGTCCCGGTGTGTACGAGCCTTAAGAGAGGAGATGATGTTATTTTGTTATGTAAATGACCGTAATATTCAGGCAAGATCTTCTTTAACAACTGTCTTCAGTTCAACCTGATTTATTTTGTGCTCTTTTTTTTCTTCA[G/A]CTTCAGATAAACTACCTAGGGAACTACATCCCGAATCTGTGGACATTTGAGACTGGCTGCACAATGTGTAATCAGGATCGGCGGCTGCTTTCCGGACTGCAGGTCAGCCCTTTACACTCATTCATTGTTTTCATGGTTTCGATTTTACGCTTATCCTTGAGATATGGTTGTGTTTGTATGGCTGTATTAAATAATTGCATTCAAATCCACTTTTAGGGAGTCATGATTTATGTCAATGATGCATGTATACAGAGTACATGTGGTCATTAATTACAAATGTATTATTACAACTTATTAAATATATTTATATTATAGTCATTGTTGGTATAACTTAATCTAATGAGTTCACCTTGGCCACATTTTGGCAAAAATGAGAACAAAATAGTGGAAAATGGTCATGGTTTAATTAAAAAGGTAGCAATTTAATCAAACGTAGCAGCTTATTTTTAAGTTGATGGAAAATTTGTGAATACAATATGTCATTTTTTCTTCTGCATGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25408
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083395 Essential Splice Site 404 730 11 19
ENSDART00000147159 None None 50 None 4

The following transcripts of ENSDARG00000059746 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 50037472)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 47889449
GRCz11 8 47878441
KASP Assay ID:
554-7428.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTTTAAAGAACGAAGACACACTTAGAATCCTAATTGAGCACAACAAG[T/C]GAGTGAAGCGCCTGTACCTGTTTAATTAGGGCAGATTGTGAATTGTTTAA
Long Flanking Sequence:
AGAGGAGGACATTGATCCTGTGTCCTCACGTAACCTTGGATTGTAAGTGTGCTTTTTATTACTGTTGTTAATTACAAGCATTTAGTGTTGCTCTAAACATAACCCTCCCCCAAAAGGACCCAAACTAAATCCAGGTTTATTCTTTTCTCCATAAAGATAATTGTAAAGAGAGTATCAGATAATGTAAAGATAACTGTAAAGAGAATATTTTTTTACTGAAACTATGGATTTTTAAAAAGATTTTGTTGGTTGCATTATGAAGGTTAACAAAAACTCTATTTTTTCGTAATTTTTAAAACACATATAATGTCCATATGGTTCACCTTAACACTCAACAGTGGTTTCTCTGTGCTCTGAATGGTCCATTGATTTCTTTTGTGTATTTTTGTTGCAGTGATATGTGCCGAGAAGACATCGACTGTGAATACTTCTTCAGCATAGACGTGGATGTGGTTTTAAAGAACGAAGACACACTTAGAATCCTAATTGAGCACAACAAG[T/C]GAGTGAAGCGCCTGTACCTGTTTAATTAGGGCAGATTGTGAATTGTTTAATCTTGTTTAGTTGAAGTTGACGAAGTAAAATAAAATTAAACAACTTAAAAATGTATATAAATATATAGAAATGTTTTTAGGAGATAATTAATTGGTTAATTGTTAATTTAATTTAATTTAATTTTGTTTATAACAAAGTAAAAATATGTAGGAATGTTTTTAGGAAACAGTAAACATGACAAATAGAATTATTTTTCTATTCGATTCGATTTTGATAGTGTGACAGTTTGTCCATCGATTTAGTTGTGCTATTTATTATTTATTTTATTTTATTTACAACCAAGTAAAAATATAAATAAATATTGTTAGAATTCATTAATTGTGACAAATCAAATATTTTTATTTATTTATTTTTATTTAATTTAATATGATAATTTTTTAATAAATTTAATTGTGTTATTTATTAGTTATTTATTTAAAACAAAGTAAAGAAAAGTATATATGTATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31681
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
ENSDART00000083395 Nonsense 536 730 15 19
ENSDART00000147159 None None 50 None 4

The following transcripts of ENSDARG00000059746 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 50043016)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 47894993
GRCz11 8 47883985
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTATTTTTTGTCTTATACTTTTTTTTCTGTGAAACAGGAATGGGAGGAA[C/T]GATACATTCATCCAAATTATTCCAGAGTTTTAAAAGACGAGTTTATAGAA
Long Flanking Sequence:
ATGGAGGATGTGGTGGAACTGGAGATTCCCATCATGGATGTGCAGCCGACAAATTTAAAGCAACTGTGTGATGCTATCATGTCAATATGGAGCAAAAACTCTGAGGAATACTTCCAGTACTTTGTTGAATCTATACCAAGAAGGATTAAGAATTTCTGAAGACAAAAGTGTGTCCAACCTAGTACTTGTAAGGCATACCTAATAAAGTGGCCAGTGAGTGTATAATGCAATTTGACATTTTTGGATAAATATATTGAGATATGTTTTCTCATTCCCAGGGTGTCTTTATGTTTGTGACAAATATGGATACTTTCGGTCGAGTTTTATCGACCGACAATTACCAAACAAACCACTTGCACAATGATCTCTGGCAGATCTTTGAAAATCCTGTGGTAAGATTACATTTACAAATATTATACTGGAAATGCATCATTTATTGTTAGTTTACGGTGTATTTTTTGTCTTATACTTTTTTTTCTGTGAAACAGGAATGGGAGGAA[C/T]GATACATTCATCCAAATTATTCCAGAGTTTTAAAAGACGAGTTTATAGAAACAGTGAGTATTCACCCAAGCAATAAAATTACACAATCTATGAATTGACCCTATAAAAGTCACGTAAAATTGCTTTGAAGTGTGTATTTTGAATTCGATGTTTGACACAATCTCAACCGAAACACGAAAAGAGGGAGGGATATAGTGTAGCTCATCCCCTTTAAAAAACAGCCAATAGCGTTTTGCTTGATCTCCGCTCTGCCAGTGAGAATGGTTTGGTGCATTTGACATGAAGCACAGCTGCAGCCGGTGATCTACCTGATTAGCCGAGCGCAGGCGGGGGCGGAGTTGAAAACGAAGCCACCAGGTTGGACACTTCGGGGCTCAAAGTTGCTGCAGTCATGACTGATCACATGGCGTAATCACTTATTTATTTATGCATTTATTGCAATACCAACAAAAGATTCACAGGACAAATAAAACAGAATAAAGTCTTTACAAACTATAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13867
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083395 Essential Splice Site 553 730 None 19
ENSDART00000147159 None None 50 None 4
ENSDART00000083395 Essential Splice Site 553 730 None 19
ENSDART00000147159 None None 50 None 4

The following transcripts of ENSDARG00000059746 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 50043071)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 47895048
GRCz11 8 47884040
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTCATCCAAATTATTCCAGAGTTTTAAAAGACGAGTTWATAGAAACAG[T/C]GAGTATTCACCCAAGCAATAAAATTACACAATCTATGAATTGACCCTATA
Long Flanking Sequence:
TAAAGCAACTGTGTGATGCTATCATGTCAATATGGAGCAAAAACTCTGAGGAATACTTCCAGTACTTTGTTGAATCTATACCAAGAAGGATTAAGAATTTCTGAAGACAAAAGTGTGTCCAACCTAGTACTTGTAAGGCATACCTAATAAAGTGGCCAGTGAGTGTATAATGCAATTTGACATTTTTGGATAAATATATTGAGATATGTTTTCTCATTCCCAGGGTGTCTTTATGTTTGTGACAAATATGGATACTTTCGGTCGAGTTTTATCGACCGACAATTACCAAACAAACCACTTGCACAATGATCTCTGGCAGATCTTTGAAAATCCTGTGGTAAGATTACATTTACAAATATTATACTGGAAATGCATCATTTATTGTTAGTTTACGGTGTATTTTTTGTCTTATACTTTTTTTTCTGTGAAACAGGAATGGGAGGAACGATACATTCATCCAAATTATTCCAGAGTTTTAAAAGACGAGTTTATAGAAACAG[T/C]GAGTATTCACCCAAGCAATAAAATTACACAATCTATGAATTGACCCTATAAAAGTCACGTAAAATTGCTTTGAAGTGTGTATTTTGAATTCGATGTTTGACACAATCTCAACCGAAACACGAAAAGAGGGAGGGATATAGTGTAGCTCATCCCCTTTAAAAAACAGCCAATAGCGTTTTGCTTGATCTCCGCTCTGCCAGTGAGAATGGTTTGGTGCATTTGACATGAAGCACAGCTGCAGCCGGTGATCTACCTGATTAGCCGAGCGCAGGCGGGGGCGGAGTTGAAAACGAAGCCACCAGGTTGGACACTTCGGGGCTCAAAGTTGCTGCAGTCATGACTGATCACATGGCGTAATCACTTATTTATTTATGCATTTATTGCAATACCAACAAAAGATTCACAGGACAAATAAAACAGAATAAAGTCTTTACAAACTATAGTTCATTATTAAACAATAAGGGAATTATAAACTAAATTTGAGTTGCCTATTTAACAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14077
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083395 Essential Splice Site 553 730 None 19
ENSDART00000147159 None None 50 None 4
ENSDART00000083395 Essential Splice Site 553 730 None 19
ENSDART00000147159 None None 50 None 4

The following transcripts of ENSDARG00000059746 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 50043071)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 47895048
GRCz11 8 47884040
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTCATCCAAATTATTCCAGAGTTTTAAAAGACGAGTTWATAGAAACAG[T/C]GAGTATTCACCCAAGCAATAAAATTACACAATCTATGAATTGACCCTATA
Long Flanking Sequence:
TAAAGCAACTGTGTGATGCTATCATGTCAATATGGAGCAAAAACTCTGAGGAATACTTCCAGTACTTTGTTGAATCTATACCAAGAAGGATTAAGAATTTCTGAAGACAAAAGTGTGTCCAACCTAGTACTTGTAAGGCATACCTAATAAAGTGGCCAGTGAGTGTATAATGCAATTTGACATTTTTGGATAAATATATTGAGATATGTTTTCTCATTCCCAGGGTGTCTTTATGTTTGTGACAAATATGGATACTTTCGGTCGAGTTTTATCGACCGACAATTACCAAACAAACCACTTGCACAATGATCTCTGGCAGATCTTTGAAAATCCTGTGGTAAGATTACATTTACAAATATTATACTGGAAATGCATCATTTATTGTTAGTTTACGGTGTATTTTTTGTCTTATACTTTTTTTTCTGTGAAACAGGAATGGGAGGAACGATACATTCATCCAAATTATTCCAGAGTTTTAAAAGACGAGTTTATAGAAACAG[T/C]GAGTATTCACCCAAGCAATAAAATTACACAATCTATGAATTGACCCTATAAAAGTCACGTAAAATTGCTTTGAAGTGTGTATTTTGAATTCGATGTTTGACACAATCTCAACCGAAACACGAAAAGAGGGAGGGATATAGTGTAGCTCATCCCCTTTAAAAAACAGCCAATAGCGTTTTGCTTGATCTCCGCTCTGCCAGTGAGAATGGTTTGGTGCATTTGACATGAAGCACAGCTGCAGCCGGTGATCTACCTGATTAGCCGAGCGCAGGCGGGGGCGGAGTTGAAAACGAAGCCACCAGGTTGGACACTTCGGGGCTCAAAGTTGCTGCAGTCATGACTGATCACATGGCGTAATCACTTATTTATTTATGCATTTATTGCAATACCAACAAAAGATTCACAGGACAAATAAAACAGAATAAAGTCTTTACAAACTATAGTTCATTATTAAACAATAAGGGAATTATAAACTAAATTTGAGTTGCCTATTTAACAAA
Associated Phenotype:
Not determined