ZMP
plod2
Ensembl ID:
ZFIN ID:
Description:
procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 isoform 1 [Source:RefSeq peptide;Acc:NP_001007378
Human Orthologue:
PLOD2
Human Description:
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2 [Source:HGNC Symbol;Acc:9082]
Mouse Orthologue:
Plod2
Mouse Description:
procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 Gene [Source:MGI Symbol;Acc:MGI:1347007]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24440 | Nonsense | Available for shipment | Available now |
sa1768 | Nonsense | Available for shipment | Available now |
sa39433 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24440
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 |
---|---|---|---|---|---|
ENSDART00000005901 | Nonsense | 614 | 754 | 18 | 20 |
ENSDART00000106488 | Nonsense | 593 | 733 | 17 | 19 |
The following transcripts of ENSDARG00000011821 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 5387102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 5275595 |
GRCz11 | 24 | 5307382 |
KASP Assay ID:
2261-8378.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCATTAACTGTTGACTGATTATTGTCCTTCTTTTTATCTTCACAGGAT[A/T]AGCGTATCACCGGAGGCTACGAAAGCGTCCCGACAGATGACATTCATATG
Long Flanking Sequence:
TCCTGAATTATTAGCCTCCTGTTTAATTCATGTTTATCGCAAAGAAGATTTTTGTAATACATTTTTAAACATAACAGTTTTAATAACTTATTTCTTCTTTGCCATGATGACAGAACATAGTATTTGACTATTTAGGATACTAGTATTCAGCTTAAAGTGACATTCAAAAGCTTTAAATTAAGTAGGTTAGGATAATTAGGCAAATCATTGTATATATAATGCTTGAGGGGGTAATGATATTGACCTTAAAATGGTTGTCAAAAAATTAAAAACTGCTTTTATCCTAGCCATAATAAAACTATTAAGACTTTCTCCAGACGAAAAAATTATGTAGGAAATACTGTGAAAAGTTCCTTGCTCTATATAACGTAATTTGGGAAATATTTGAAAAAGAAAGGTGGAAATCAATAGATTTTCAGTACACAGCAGCACAACTGCTGATAGGGTTTTTATCATTAACTGTTGACTGATTATTGTCCTTCTTTTTATCTTCACAGGAT[A/T]AGCGTATCACCGGAGGCTACGAAAGCGTCCCGACAGATGACATTCATATGAAACAGATCAATTACGATCAGGAATGGCTGCACTTTATCAGAGAATTTATCTCCCCTGTCACTCTCAAGGTTTTCTCTGGCTATTACACCAAGGTGAGACCGTCTGCCTAGTCTAGACCCAGACATAATCATCTGCTAAAGGGATAGATCACCTCCAAAAAAAAAAAAAAAAGAAGAAAAATGAAGCATCACTTGTTTATTTTCATACCAAAACGTGAAAGAAATGTCCTGCTTATCCATCCAGTATAATAATAGAGAATGCAAACAATGGCATCACATAAAAAAGATGCAAAAGAACGATACTATGCAAGCGTTCTTGATGTACACAAAGCAAAACGTGCTCATCAAAAACACTCACCCTTAAACATATCTCTGCATTTATGATATTATTAGAGAACATAATGATTCCAGATAAACAGAAATGCATCACAAAACCTTCTCTGAGGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1768
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 |
---|---|---|---|---|---|
ENSDART00000005901 | Nonsense | 679 | 754 | 19 | 20 |
ENSDART00000106488 | Nonsense | 658 | 733 | 18 | 19 |
The following transcripts of ENSDARG00000011821 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 5391267)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 5279760 |
GRCz11 | 24 | 5311547 |
KASP Assay ID:
554-1761.1 (used for ordering genotyping assays)
KASP Sequence:
TATGCGATTATGAACTTTGTGGTGAAGTACACTCCAGACAGACAAGCCTA[T/A]CTTCGACCACATCACGACTCCTCAACGTTCACCATTAACWTCGCTCTCAA
Long Flanking Sequence:
TGTAATAAAAAAGTAAATACAAAACACAAAACAGAATTAAATGCACAATACAATGTAAGCACTAATGAAAATCTTTAAAAAAGCAAGTACAGAACTCATCGCAGCAAAGTAGTGTGTATTCTTGGTATGCTACACTTGAACTTTACATTTTAGCTATTCTTTGCAGAAATATGAGCATTTTTTTTCCTTTGATGGCTTAAAAATCTCAATAGATCAAGGCAAATTTAATTGATCATGTCACGACTCATTTAGTAGCACTTAGGTAGTCCAAACCTTTCCATATCTTCCAAATCCACATGAATAGTTTTATGGGATCGTTTTATACCCATTTAAACTATGATCTGTTTTTTGCATGGAAAAGACTTTGGAACTGTAAAACTTTGAATCACAAGTAAATCAGACACATTTGAGAGGGTTTTATTTGTATCTCTCTTCTTTCCCCCCCAGGGCTATGCGATTATGAACTTTGTGGTGAAGTACACTCCAGACAGACAAGCCTA[T/A]CTTCGACCACATCACGACTCCTCAACGTTCACCATTAACATCGCTCTCAACAACAAAGGCTTAGATTTCCTGGTAAGTTTGAATAATATTAGCCTCGTTATTTTTCTAAAATAGGCTTAAATACATCTTACACCATGTCCTAACTCCACGTGATGCTACAACACACAATAAATGGTATTTTTAGTATTATAAGTATTATTATTATAAAAGTATTACTATTTCTGCAATATTGCAGCAAAACAACAGCATAAACTACTATGACAATGATTACCTCAGGTACTGATTATGTGCTTTATTAAGTGTTTAATGCTACCAATGTGACTTAAAATCCATTTTGCATGACATTTACAGCATTGCCATAAAGCAGCAGCAAATACCAGCAATAACTAGTAACATCCATCACTCATTAGCCTATCAATAATGTTAAAGAGGTTTACTGTGTATTAATTAGATTAAAAAACTTAATTTGGTGTGGACAGTCACTGTCTCTGGAATTTTGT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa39433
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005901 | Nonsense | 712 | 754 | 20 | 20 |
ENSDART00000106488 | Nonsense | 691 | 733 | 19 | 19 |
The following transcripts of ENSDARG00000011821 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 5393384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 5281877 |
GRCz11 | 24 | 5313664 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTTTGTGCTTCTTCTATTTCAGGGCGGAGGTTGTCGATTTCACAGATA[T/A]AACTGCTCCATAGAATCTCCTAGAAAAGGCTGGAGCTTCATGCATCCAGG
Long Flanking Sequence:
ATACATGCACAATAAAACAATCCGCCTGCACGTAAAATCAGTAATTTTACTTAAAATAACGCCCGTTAAATTACTGAAATATACCTTAAAATAACAGATATTAAATTACAGAAATTGCCTTAAGTTTGAATTTCTGTTAAAGTTCTGTAATTTAATTTTCATTATTTTACGATAAATTTGTAAAATAAAATTACAGTTTTTTTTTTTTACAGTGTACTATAACTACAAGCTACAATATTTTAACAATACAGGACTAATCGCAGCAAAGTAGTGTTACAATCCTGCTTTAAATTTAGCTATTCTTTGGAAAAATGCATTTTTTCACCTTGATTTTGTGTCTGTTGTGAAGTGAACTTCACGCATGAACCAACAGCCTAATTACATAAGAATATCACAATTTAAGGCACGTCTGGTGTGAGCGCCCCATTAGAATGCCATGTACTAAAACTAAACTTTGTGCTTCTTCTATTTCAGGGCGGAGGTTGTCGATTTCACAGATA[T/A]AACTGCTCCATAGAATCTCCTAGAAAAGGCTGGAGCTTCATGCATCCAGGTCGACTCACTCACCTTCACGAAGGACTGCCGGTGACCAATGGCACGCGCTACATAGCAGTGTCTTTCGTAGATCCCTAAATTCCCCTCATCCTTCTAGGAATCTTTGAGATGTTTTGTCAATTCTGTTTTGTTGTTGGTGGTTTTTACTGATTTATTCCTGGCTTACATGTCGTGGTGCCTGTTTTATTTGCTGTCTTTTAAAACGTTTACTACTGTCAAGAGAGAAAATGCTGTTCAACACATTCGTAAGACATATCAACACACACACAAACACAGACGAGCATTCACTCCAGCAGATTTTCGCAAATCTTAGTTGTTACTTTAAATTAGAGATTTCCCACAATTTTTATACTTCGACTTTGGCCAAATGTCCTTCCTGAAAGTTTCTATTTGCTAAATTGGAAATTGTGATTTCCCAAATTGTGCTTTTAAATTATTTTCATCACCCC
Associated Phenotype:
Not determined