ZMP
si:dkey-164k14.1
Ensembl ID:
ZFIN ID:
Description:
Plexin A2 [Source:UniProtKB/TrEMBL;Acc:B6E521]
Human Orthologues:
PLXNA2, PLXNC1, PLXND1
Human Descriptions:
plexin A2 [Source:HGNC Symbol;Acc:9100]
plexin C1 [Source:HGNC Symbol;Acc:9106]
plexin D1 [Source:HGNC Symbol;Acc:9107]
plexin C1 [Source:HGNC Symbol;Acc:9106]
plexin D1 [Source:HGNC Symbol;Acc:9107]
Mouse Orthologues:
Plxna2, Plxnc1, Plxnd1
Mouse Descriptions:
plexin A2 Gene [Source:MGI Symbol;Acc:MGI:107684]
plexin C1 Gene [Source:MGI Symbol;Acc:MGI:1890127]
plexin D1 Gene [Source:MGI Symbol;Acc:MGI:2154244]
plexin C1 Gene [Source:MGI Symbol;Acc:MGI:1890127]
plexin D1 Gene [Source:MGI Symbol;Acc:MGI:2154244]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37759 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12731 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37759
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084985 | Nonsense | 293 | 553 | 5 | 11 |
ENSDART00000147998 | Nonsense | 1353 | 1850 | 21 | 31 |
Genomic Location (Zv9):
Chromosome 23 (position 32849942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32709740 |
GRCz11 | 23 | 32636271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGTGATCGCGGTAACGTGGCGTCGCTCATCATGACGGCTCTACAGGGT[C/T]GACTGGAATACGCCACGGACGTCCTCAAACACCTGCTGTCCGACCTCATC
Long Flanking Sequence:
TCACTATACTGGGGCATAAGGACCCACACAGACCGCAGGTTGGGCGCCCCCTGCTGGTACTAACACCACTTCCGGCAACAACCTAGCTTTCCCATGTGGTCTCCCATCCAGGTACTGACCGGGCGCAGCCCTACTTAGCTTCAGTGGGCGACCATGTGAGAGTTGCAGAGAGCTAGCTGCCGGCAAGATCAGCTGAATGTATTTAAAATTGATAAAACTCAACTAGACGAGTTGCACAATTAGCCTGTTTACAAAAGAAGCAGCATTTTGATAGGGTAGACACTGGCTAAAGATGGTGATCTTGACTGTGAAGTTGTTGTGTGTTCCAGGTCTCTGGTAACGGGCAGTTGTGTGTGGAAAAAGCTCTGAAGCTGTTCGCCCAGCTGATAAACAACAAGGTGTTTTTGCTGACGTTCATCCGTACACTGGAAATGCAGCGTTCGTTCTCCATGCGTGATCGCGGTAACGTGGCGTCGCTCATCATGACGGCTCTACAGGGT[C/T]GACTGGAATACGCCACGGACGTCCTCAAACACCTGCTGTCCGACCTCATCGACAAGAACCTAGAGAGCAAAAACCATCCCAAACTACTGCTCAGGAGGTGCGTGCTTTACTTCGTGCATCCAGTTTTTCATCCACTTTATAGTGTCAAATGAATATGCAACAAAGTTTCATTCTGTTATCTTAGCATAATAGCTATATTGATTCACGATCCATAAGAGCATCCCTCCAGTCTCTCGGTACGGCCCCATTGTCAGTGTCACTTATCATTTGTGCACTAGGTACTCATAAAACATTCATGAGCAGCTCAAATCCACTTGTTTTTTTCCTCTCTTTCTCTCTCGCTCTCGGCTATCCTCTATCCCTTTCCTCTAAATTTGTATAGGTTTTTCGAAGTCTTTCCAAAGCAGTGTGTCAACTAGAAGATTTAGACTAATAATGATTAAACAAAGAGTTGCCCGAGGGCTAGCATGCAGCGCGGTCCGCAGCCGCTTTCATTAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12731
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084985 | Nonsense | 423 | 553 | 8 | 11 |
ENSDART00000147998 | Nonsense | 1483 | 1850 | 24 | 31 |
Genomic Location (Zv9):
Chromosome 23 (position 32835411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32695209 |
GRCz11 | 23 | 32621740 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACAGCCCRGAGATCCCGGTCAAGGTTTTGAACTGTGACACCATCACG[C/T]AAGTCAAGGAAAAGATTCTGRATGCTGTGTATAAAAACWTGCCGTATTCW
Long Flanking Sequence:
CTGTACTGTGCCATAAAACAGCAGATGGAAAAAGGCCCAATAGACGCCATCACTGGAGAGGCCCGATACTCCCTCAGCGAAGACAAACTCATCCGACAGCAGATCGACTACAAGACGCTGGTCAGCATCATAATTACACTAACTACTTTAGTATCTCATGAACTCTGATGAATGTCAGAGTATATGCGTATGTGTGTGTGTGTGTGTGTGTGTTTGAAAGAAGACAGTCTGGCAGAGGGAGACTAGTGTTCATTAGTCTCTCATACCCTGCTAAGGCTGAGATTGGGGTCCTGCAGAGGGTGTGAAATTAGATTTCTCGGGCCAGGAAATGGCCTTTTCCAGAGCCCCGCTCCGCACCTACGGCTTCACCCACCACAGCCCAACATCTCATCATGCTCATCCTCTTTTTTTCTGCCCTCCAGATCTTAAACTGCGTCAACCCAGAGAACGAGAACAGCCCGGAGATCCCGGTCAAGGTTTTGAACTGTGACACCATCACG[C/T]AAGTCAAGGAAAAGATTCTGGATGCTGTGTATAAAAACATGCCGTATTCACAGAGACCCAAAGCTGTAGACATGGACCTGGGTGAGTGAAGTGTGCTTAGATTAGTTCTGTGCCAAAAAGATTTGCCTTGCAAGCTGGTAAATGTGGTATTGCTTTTAAACAACAATACCAAGAGGTTATAATAATACTGGTTATATAAAAATAATAATAATAATAATACTGAACATTTATTTTGCAATGTTTTTTTTTTTACTAAAAATAGTAACAGATGCAACATGTAGCAGACAAATGCAACATTAGTGCCATTCCCAAAAGAATAAGTGTTTTGGAATAGTAAATATTTTAGTGTGAAATCCCTGCAGTATTAAAAGGAATTGTTCACACAAAACTGAAAATTACCTCAATGATTTAAATCGATATAAGATTATTTCTTCTGTTGAACACAAAACAAGATATTTTGAAAAACCATTGTTGCTGGGACCATCGACTTCCATAGGGAA
Associated Phenotype:
Not determined