ZMP
NP_001139777.1
Ensembl ID:
Description:
plexin domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_001139777]
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 |
|---|---|---|---|
| sa14294 | Essential Splice Site | Available for shipment | Available now |
| sa40979 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14294
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083929 | Essential Splice Site | 102 | 525 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 44304205)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 41294505 |
| GRCz11 | 7 | 41574578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAACAYTGGCTGATGACGACGGAGGAGACAACAGCTCACAAATTATGG[T/A]AACCATGAATATGTTGNNNNNNNNNNNNNNNNNCACAYYAWAAATTTTCCMTAAAAAAAAAAAAAAA
Long Flanking Sequence:
ATACCATCTGCTCTTAAACAGGCTCATATAAAACAAAATCAGCCTTTCTCATGGCTGAGCGGGAGAGGGAGTATAAAGCATGTACATGTGTCTACGTAACCGTAAAAAAATACATAGACGTGTGGGTGATGTTTCAGTCTGGATTGAATTTGATGTAATCGAGCAATCAAACTGATTCTCAAGACCTCTGGAGATCTTTTGATGAGGAAAACTGTGTATGTTTAAAAGAAATAGGAAGCATTTCATAGCATTGTGCAATTTTAAAATGTGCCCATGTTGCTTTGTGTCATTTCCAGGAGCTGCTTATTCAATTCTTCACGGATGGTCACATGACGCTGATGTCACAGTGGAGCTGCTCAGGAGGAGACGCTGGCTTCTGATGGAGCCTCTACCAATGGAGACTAAGAAAGCCAGTCAGGATGGTTTGAAGCTCGAGTCTCAGGATTCACCCAGAACACTGGCTGATGACGACGGAGGAGACAACAGCTCACAAATTATGG[T/A]AACCATGAATATGTTGCACACTATAAATTTTCCCTAAAAAAAAAAAAAAAAAAAAAGATAAACACTAAATTGATTTTTTTTTAAACAAAAAATATTTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATAAAAGCACTCTGAATAAGAAATGTTGCAAGAGCTGCAAATCAGCATATTTGAAGGATCATGTGACACTAAAGACTGGAGTAATGGAGCTGAAAATTCAGTTTTGCCATCACAGGGGTAAATTGCATTTTTAAATTATTATAAGTGAATTAGACAGTTTTTCTCTCACTCACTCACACACACACATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAATCTCTAAGCTAGAACACAGCAGAGTGAAAAAAGGTGAAGTTAATTTACTGTGAAAGGGAATAAGGAAAAGAGTCAGAGATTTCAGCTCAGGTTTGTTTTTTAGGGAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40979
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083929 | Nonsense | 410 | 525 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 44268615)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 41258915 |
| GRCz11 | 7 | 41538988 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCACAAGGAACAGAGGAACTACTGAGGGTCACTCGAGCCGAGCCCCAT[C/A]ACACATGCCCACCAGCATACCGACAGAAGGTACAGACACCACAGAACATT
Long Flanking Sequence:
CTATCAGGTCATTTTGGACCAAAATCTTGGAGGAATATTTCCATTACCTTGCTGATTCTATGCCATGAAGCATTAAGGCAGTTCTGAAGGCAAAAGTAGGTCCAACCCAGTACTAGTAAGGTGTACCTAATATAGTGGCCACTAAGTGTATTTACAAAATATATGGAACATGGCCCTCACTTCATATACTTATGATTTTTGGCATAAAAGAAAAATCTATAATTAATGCATTGTCGGCTATTTTTTTATATTATAGCTATGCAACATAAGACATGTCATTGAGGTTGACCTATTGGCACTGATAAGCAATGTCATTTTTGCTTATGTCACATATGTTTTGGTTCAACTGCTAATATCACTTGTCTTTCACTGGCAGACTAAGGATAACTCGTGTGACATTATCAGCACCACTAATATGGATCTGCTGACCACTGCATCAGTGGTGAAGATGAGCACAAGGAACAGAGGAACTACTGAGGGTCACTCGAGCCGAGCCCCAT[C/A]ACACATGCCCACCAGCATACCGACAGAAGGTACAGACACCACAGAACATTAAACTGATCTTACAATCCTCTGAGAGAAAGGAAACAAACGGGTCAGTGATCTGAACCATTAGTTACAAGTGACTGCTCGTGGTAAGAATGCGGCAGGATAATGTTAAGAGGGCACCAATGGATTCTACATAAATCAATAGACACGGAAAAAGAAAGGCTTATTTGTGCTTTATGCGCTTGAGGAAAATCAATTCCTGGAGAAGAAATGTTCAGTGTGTAAGAACATTCAGAACATGGTTAAAGGGCTTTGCTCATAAATGGCTTCAATAGATAATCATGCTCGTCTTTCTGCTTAAATAAACACTGGCACTTATGAAGACACACACTCTCATCCATTCACCGCTTAAAGGGACAGTTCACAACCTCTTTGAGTTTCTTTCTTCTGTTGAACACAAAAGAGGATACAGAAAGATGTCGGAAAATGTTTGCATAAGAATGAGTGCATTCTTC
Associated Phenotype:
Not determined