ZMP
si:dkey-183c2.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate plexin family [Source:UniProtKB/TrEMBL;Acc:B0S6W7]
Human Orthologue:
PLXNB2
Human Description:
plexin B2 [Source:HGNC Symbol;Acc:9104]
Mouse Orthologue:
Plxnb2
Mouse Description:
plexin B2 Gene [Source:MGI Symbol;Acc:MGI:2154239]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6934 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6934
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000137847 | Essential Splice Site | 481 | 544 | 4 | 6 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 13550424)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 14486277 |
| GRCz11 | 4 | 14485032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGTTTGATTCAACTTTGAATCACCTGTACATCACCACTGGCAAAAAG[G/A]TTTGCTTATGAACACATTMAYAATGTATAGRTAACGTTWKGTCAACAGGA
Long Flanking Sequence:
TCAAACCTATCTACACCAGGAATGACATGCTGACAGCTGTAGCTGTGGCGGTGGAGAACGAACACACTGTGGCATTCTTGGGAACCAGTGGTGCAGACGTCTTGAAGGTGAGTCCCATTGCAAGGTCTGCTTTCTGTTCTTTAAATTTCACTTAAGCCCTTGTGGTTTGACTGGCTGTGGTGGTAGGAACTAGTGGTTAAAGATATGGGCTGGTAACCAAAAGGTTGTCATTTCAAACCCCAGAATTTATGATTTATGAGGTACAGTATAACCACTTTAGCAGTGCGTTCTACTCTAGGACTTGATCTTGCTGTACACAGTATTGGTTTTTACTTGTGTGCGAAATAAATTAACTAACTTTTTCCTTGCAGGTGCATCTTGACCCAAACCACACTGACTTTTACAACAGAATTCCAGGGGATCGTGCAGATGGTGCAGTAAACAAAAACCTTTTGTTTGATTCAACTTTGAATCACCTGTACATCACCACTGGCAAAAAG[G/A]TTTGCTTATGAACACATTCACAATGTATAGATAACGTTAGGTCAACAGGATCACCCATTGGTTAATATTTATTTGAGAAATGTAGACCTGACAAGCTCAATGGATTTCTTTTCTTTTTTTTTTTTTTGCAAAATAGCACAAATGCCTAGATATTTCACACAGCTCTGTAAAATCCTTAGACGCTGTAATCTGCCACATAAATGTGATAGCAGACTGTTGTCATATTCTTTTCACCAACCACAAGACTTTGAGGTGCTCTCGTCCTGTCAATCATTTTACACAATTACACAACGGCTGTATTAGAAGCAGGACTATGATACGGTAGTTAAAGTAGATGCCACAAGCTCCTTCATAAGCAGTGTTAGTTTTCATACACATATTTGATTTTACGAACCAATGTTTCTTAGGCTACATGCACATGACTACAGTGTAGTCAAAAATACTGTCACCTTGTTAGTAGAACAGTACCTGTTTAGGTGTAATGACTAATATGCATTTTA
Associated Phenotype:
Not determined