ZMP
si:ch211-106h4.6
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate plexin domain containing 2 (PLXDC2) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
PLXDC2
Human Description:
plexin domain containing 2 [Source:HGNC Symbol;Acc:21013]
Mouse Orthologue:
Plxdc2
Mouse Description:
plexin domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1914698]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39851 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31284 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39851
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 |
---|---|---|---|---|---|
ENSDART00000111038 | Nonsense | 166 | 558 | 4 | 13 |
ENSDART00000134541 | None | None | 65 | None | 2 |
ENSDART00000140561 | Nonsense | 166 | 368 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 31333121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31634181 |
GRCz11 | 2 | 31617399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTACAGAGAGTCAATATGTCTTTTGATTTTCCTTTCTATGGACATTCAT[T/A]AAGAAAAATCTATGTAGCAACAGGAGGTGAGAGCAATTTTTTATACAGTA
Long Flanking Sequence:
AATCCTGGTGAAAGTTATTTACTGATTTCTGTAAATAAAAAGATGAATTTGTGATGACTTTAGGAGACATATTTACAGTATTTTTAAAAAGGTAAACAACATTAAAAACTGATTGAAGACTATTGAAGAATAGAGGCAAAGTAAATATGTGATAGCAATCATTTTGTATAGAAAAGGTGAAGCTGTTATTGTTTTATTGCGTGAAAATCTTTTTTCTGTTCATCAGAGAGATATGGATCATATCTACTACACATCCAAATTCTATAAGCTTACAGACAGTTCACACAAGGATTTGTGGGTAAATATTGAGAAAATGGACACTGGAAAAGTTCATGAAATCCTCTCCAACACACATCGACAAACTTTGGTAAGATCATACTGTCAGATACACTTCCTAAAAAAGTATTCATTAACTAATTACTTTTAAATACGCCAAAACTGTTGTTTTGCGTTACAGAGAGTCAATATGTCTTTTGATTTTCCTTTCTATGGACATTCAT[T/A]AAGAAAAATCTATGTAGCAACAGGAGGTGAGAGCAATTTTTTATACAGTATATACATTACATACATACAATCAAACCCGAATTTATTCATACACCTGCCAAATTCTGACTTAAAGTTAGGCTACTTTTATTCAACCAGAAAGTTATTTTTTGACAGAAAATGGCGCAGGCTTCTCCCAAACGATAATTAGACAATGTACAAGCGGTGGAAATAATTTTTTTTTACATTTGAACAAAAATTTTAAGTCATAATTTGCCACGGGCATGAATAATTTCAGGCTTGACTGTACATACAGTGCTCATAACTGATTACACCCCAGTTTAAAAATGAATATTTGTTTCTATTTCTCAGTGAATATAGGCAATGTATTTTGGTGCATTTAAACACAACAGATTTATTAAACAGATATATTTATTCAAATAATATTTTACTCAAGCATATTTAGATATTGGAAGATAATACAAATAAATTCAAGCAAAATATTGCAAAAAAAATTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31284
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:
G > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111038 | Essential Splice Site | 289 | 558 | 8 | 13 |
ENSDART00000134541 | None | None | 65 | None | 2 |
ENSDART00000140561 | Essential Splice Site | 289 | 368 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 31335404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31636464 |
GRCz11 | 2 | 31619682 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTCATTTTGTGGTTTTAATAAATCCTCTTTCATCTTTTTCCATGATA[G/C]ATGTTTGGAGGAGAACTATATATGAGTATCATCGTGTAGAGCTCTTAAAA
Long Flanking Sequence:
TTTTGAGAGTCAATAATTTTATACACGATGCACTTTCAGATTTCAAACTCAGCTGAATATTTTATACACTTAGAGAGCTGTGTTACACACTGCATGTAAGGTCATTATGAAAAATAAAATAGGGACCATTTATGCACTGTATATGAAACATTCAGATGCAAAACAAAACTTGACATTTTCTGATCAAATTAGCATTTTCCTATATGTGTACAGTAGGTTCAGTAATTTCACGTTTGTGGTGAATAATATGTTATTTTTTTTAACTTGAAATAACTGAACCTACACAAACTGTAGGAGACTAAGAAAAATTCTCCTTTTAGAAGAAAACTTTAGATTTAATCTGCACTTGAATTAATCTGAACTCCTCTTATCCTATATGAATTTCAGTTAACAGTTTATTTAACATTTATTTTAGTTAACATTTTTAGTTTAGCAGTTTTGCCTATTCTAGTCTTCATTTTGTGGTTTTAATAAATCCTCTTTCATCTTTTTCCATGATA[G/C]ATGTTTGGAGGAGAACTATATATGAGTATCATCGTGTAGAGCTCTTAAAATCTAAGATCACGAATGCGACTGCTGTTGAGATGCTTCCGCTGCCGAGTAAGTCTGAACTGCTCACACATTCATTCATTCAATTTTTTCGGCTTAGCCCCTTTATTAAACTAGGGTCACCACAGCGGAATGAACTGCCAACTTATCCAGCATATATTTTATGCAGCAGATGCCCTTCTAGCTGCAACCCATCACTGGGAAACACCCATACATACTCATTTACACACACACACACACATACACTACGGACATTTTTAGCTTACCCAATTCATCTGTACCACATGTCTTTGGACTGTGGGAGAAAGTGAAGCACCGGAAGGAAACCCACACGAATGCGGAGAGAACATGCAAACTCCACACTGAAATGCCAACTGACTCAGCCGAGGATCGAACCAGCAACCTTCTTGCTGTGAAGCAACAGCACTACCGCGTCAATGCTCACACAACTAGAT
Associated Phenotype:
Not determined