ZMP
nrp2a
Ensembl ID:
ZFIN ID:
Description:
neuropilin 2a [Source:RefSeq peptide;Acc:NP_998130]
Human Orthologue:
NRP2
Human Description:
neuropilin 2 [Source:HGNC Symbol;Acc:8005]
Mouse Orthologue:
Nrp2
Mouse Description:
neuropilin 2 Gene [Source:MGI Symbol;Acc:MGI:1100492]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30798 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13721 | Nonsense | Available for shipment | Available now |
sa25512 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13255 | Essential Splice Site | Available for shipment | Available now |
sa32581 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30798
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 |
---|---|---|---|---|---|
ENSDART00000103769 | Nonsense | 2 | 787 | 1 | 14 |
ENSDART00000125437 | None | None | 165 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 4565759)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 4983481 |
GRCz11 | 1 | 5681276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTTCTGTCATTGTTATCTTAATCCGTGTTTCTCCTTTGTGTCTGTTTG[T/A]TCTGCAGGAGCTGAGCATTGTTTCCGTAATTTCAGTTCCCCAACCGGAGT
Long Flanking Sequence:
GCGGAGTAATACACAAGGGTGAAGAGGCTGTTCCACTGCTGATGTTAATTTAAAATCTCATATCTCATCAGCCAATCAGATTCAAAAACCAGACAGAATTGTTGACTGTTATAAAATATACATGAAAATATGATTTAGTAAGTTTAAAAACAACAGAAGTCTATGCAGATTCTCCTCATTTTACTGAAACAATGCTTAATCTTAATATAGCATTGAAAATACATACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGAGGATAGAAAATATTGTTTAGCCACTATAAAATCAAAAGAAAGCTCTGTGGATCATCCCCACAATCCACTGAAACCAAGCATTTGTGTATGTGCTATAAAAACATGTTTTTCCTCACACTGGAATAATGTAAGCACCGCTAATGAATAACGTTCTGTCATTGTTATCTTAATCCGTGTTTCTCCTTTGTGTCTGTTTG[T/A]TCTGCAGGAGCTGAGCATTGTTTCCGTAATTTCAGTTCCCCAACCGGAGTGATCGAGTCTCCGGGTTTCCCTGACAAGTATCCACATAATTTGGAGTGCTCCTTCATCATCATCGCTCCTCCTCAAACCGAGGTCACTCTCACCTTCCAGACCTTCGACCTGGAGAACGACCCTCTGCTGATGGGGGAAGGAGAGTGCAAATACGACTGGCTCGATGTCTGGGACGGCCTGCCGCAAGGTTACTGGCTCTTCTTCATACAGTATATACTGTATCTGTATACGTTTCTACAGAGTTGAAGTAAAAATTATTAGACCTTTTTTCTTTTTTAAATATTTAACAAGTCTCATTGGTTTTATTTTGGCTAAAATAAAAGCAGTTTTAAAAATTTTTAAAACCATTTTAAAAACAATATTAATAGCCTTCTTAAGCATTTTTTCCAATAGTCTACAGAACAAACCATTGTTATGCAATTGATTTGCCTAATTTCCTTAATTTTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13721
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 |
---|---|---|---|---|---|
ENSDART00000103769 | Nonsense | 210 | 787 | 4 | 14 |
ENSDART00000125437 | None | None | 165 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 4556240)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 4973962 |
GRCz11 | 1 | 5671757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGTTCCTCAAGGTTCTGACCGGCATCGCTACTCAAGGAGCCATTTCC[A/T]AAGAGACCCAGAAGTCATACTACGTCACMACCTTCAAGCTGGAAGTYAGC
Long Flanking Sequence:
AATAATAATAATAATTATTATTATTATTATTATTATTATTATTATATCAATTTTGTTAATATAAACACATAAATAAATAAAACTAATGAAAAAAGTAATAATAAAAAATAATAACAACAACAACAATAATAATAATAATAATAATAATAATAATAATAATAATAATCATCATCATCATAATCATCATAATAATAATAAAATCCCTGTTGGAAGGTTTATTGTTTTAAAATAAGCCCTGTATTTCTCTCGCCACTGGGAGGAATGATCTTGTTCTCCATACACATTTTTCAAAATAGATTTATAAACTGCAGAGGAACTCCTCATTACTCATAACAGAAATCCTCATTGATCGGCTGTCGAAAGGGAACTAAATTCGGTGCGATCAGTTGGGCTTTATCGCTCCCTGTTTCCCACTTTCATCAATCATCTTCCTGCTTTCCCAGGTGGATCTTCAGTTCCTCAAGGTTCTGACCGGCATCGCTACTCAAGGAGCCATTTCC[A/T]AAGAGACCCAGAAGTCATACTACGTCACCACCTTCAAGCTGGAAGTTAGCACTAACGGAGAGGACTGGATGTTTTATCGGCATGGCAAAAACCACAAGGTAAGACCCACACAATTTTTCTGTTTACAGCTGGATTAAAAAAAAACAACAACACCAACAATTAAATATTAGTTGACTTGTAGAAACAATGTCTAAGATGTGGGATCCATGGACAGCTTCATGTTATTAGAGAGACATTTGTAGTAAAATGCAACATTTATTTGTTTTGCATAAATAAACTAGGAGTTTTACTGTGTATAATTAAAATGAAATACAACTATTAAAATTAAATTATTTTTAATTTAAATTATTTATTATTACAATAAAATAAAAAAATGTTAATTGTATATTCACTATTGCACTCGTGATTTTTTCTTGTCTTTTGTTTAATTTTTTTGCCATGAATTAATAATAGATTTACATTCATCAGTTTAGTTAATTAGATTCACATTTTCAGAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25512
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 |
---|---|---|---|---|---|
ENSDART00000103769 | Essential Splice Site | 407 | 787 | 6 | 14 |
ENSDART00000125437 | None | None | 165 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 4537357)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 4955079 |
GRCz11 | 1 | 5652874 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGGAAAGACTGGAACTTTGTAATAGATAGCAAGACTAGCATGCCTAAG[G/A]TATAACATCTGTCCAATGCATACTCTTAAAGTGTCCCTATAATGCTTTTT
Long Flanking Sequence:
GATTTAGCTTGAAAATTTAAGGTGACCAGAACTTTTACAGTGATAGGTTTACATTGTAATTAATGTAATTGCAGCACCTATTTAAACACATTTTGCACACTTTGTGAGAGCGTTCATCATTTGAAGGCTCATTGTCTTTTGTTTTGTCAGATGCTCCTTGTTCAGAGCTCCAGGGAATGTTGTCAGGACTCCTCCCGGACTCCCAGATCTCAGCCTCCTCAATGCGGGACCTCCACTGGAGCCCTGGAGCGGCTCGTTTGGTGGCCAGTCGATCAGGATGGTTTCCCAGTCCTGCTCAGCCTATAGCTGGAGAAGAGTGGCTCCAGGTAGACCTCGGGACACCCCGGATGGTGCGTGGAGTGATAACTCAAGGAGCGCGGAGTGGTGATGGAGGAACCAGCTCAGAGAACCGGGCTTTCGTACGGAAGTACCGCCTCGCACACAGCCTGAACGGGAAAGACTGGAACTTTGTAATAGATAGCAAGACTAGCATGCCTAAG[G/A]TATAACATCTGTCCAATGCATACTCTTAAAGTGTCCCTATAATGCTTTTTATTGTTTATTATTATCTATTGAAGCAGCAAAAGAAAAAGAAGTAGAATTATATAAGTAGAACATATATAAATGACACCACTTCATCAAAACACCTGACAGCGGTTGGGATAAAGGATCATCTAAATCTCTATGTGGATCACTGGGGCTTTACTAGTCTCTCACTGAATGTGCTCTTAAGTGTTCTAATGGTATTATTTAGTGGATGTCCTTCATGATCTTTAATTTAGCTCTTGATCTCTTTTTTACAGTCGCCTCAAGTAATTCAGGATTAAACCAATAATAATTGTATCGATCCTGTTTCTTTCAAGGCAATAACAAGGCAATAACATTGTTGTCTCCTAAATTAAAGAAATGATTAATCACTTAACTGACTTAAATCTAATAAATTGATTAATTAGTTATTGAAAAAATTATGGGATATATGGGGTATTGGGGTTGGTGATATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13255
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103769 | Essential Splice Site | 456 | 787 | 7 | 14 |
ENSDART00000125437 | None | None | 165 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 4535660)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 4953382 |
GRCz11 | 1 | 5651177 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGGCAGGCATCGGAATGAGAATGGAAGTATTGGGCTGCAACCTGCCAGG[T/C]AAGACACAGTCCTCAGGTACWTCGCTGTTGTCARATCATAAGCAGAATTA
Long Flanking Sequence:
AAATGAGTCATTTTGAATCAATTGATAGATTATGTGAATCATTTATCGGACACCCACTCTAACTGGATCATTTGAATCAGTGAGTCCAGTTATTGCTGTTATTTTCATGTTAACTTCTCTTTAATTCTGACAGCCTTGACAGTTTAGTTTAATTGTGTTTAATTTAATTTTTGAATTCGGGACATTTCAGTCCAACCATGCTTTTCTCATACTATTTTCTTGGATTTTCCAGTTGGGAATCATTCCAAAATGGGACACGAGGCATACTATCTAAACTATTTTACCTTTAGAGGATAGCTATACTTCTTATACATGTTCAGACGTTTAAATTCCCTAACCTCTATTTCACTGCAGCTGTTTGAGGGGAACACGAACTACGACACCCCAGAGCTGCGTCGGTTTGAGGAGCTGCCAGCTCAGTTTATCCGCATCTATCCAGAGCGCTGGTCTCCGGCAGGCATCGGAATGAGAATGGAAGTATTGGGCTGCAACCTGCCAGG[T/C]AAGACACAGTCCTCAGGTACATCGCTGTTGTCAAATCATAAGCAGAATTACTTGTTGATGATTGGGCAGTTCCAGTTGTACGCTGGAAATTTATTCGCAGTCTACACGCCGACACTGAGCTGCACCGTCAGCTGAAATCTATTGCAGCACCAACAAATGTTTTTATTTATTTTTTTGGTCGGGAGAAGTAAAGCGAAAAATATGGATAGACTGATGTAAAGAGAAAATAGAAACATGGAAACAGTAATAGTCTCTAAGAGAAGCGGCTGGGGGAAAACAAGCATTAGATATCGGTGGCTGGCTGAGTGTTGTAAGGAAGAAGCTTTAGTGTGACTTCTCAGTGTTGTGTGCTGTTTAGCACTTCTGCTAAGAAAGCTTTGAGTTTGGTGAGATTATTTTATATAATAAAAAAACTCTAATATTATGGAAAAATTGATTTGTACTGTTAAATGAAATCTATCCCAGCATTTACTGCAGAATTTACAGCATCATTACTCGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32581
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103769 | Nonsense | 767 | 787 | 14 | 14 |
ENSDART00000125437 | None | None | 165 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 4497153)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 4910604 |
GRCz11 | 1 | 5608409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGAGGCTTAACGTCTCGCTCTTCCACCACTTTGGAGAACTACAACTTC[G/T]AGCTATACGATGGGATTAAGCACAAAGTGAAGCTCAACCAACAGCGCTGC
Long Flanking Sequence:
GTCATTATTATGATAAAAAAGGGACAATGTTAATGACACATGATTTAAATATGTGGAATATCACTTTTTTTTTCTCGATAAAGATTGCTGCACTATAGTATCAGCGAACTCTTGTGATCATTTGGAAATGTCTTGAAAGTGCCATGATTGCCCAAATTACAACCATGAATTTCGGTACCATGATATATTTTAACCTATCATCGGATTCTTCATCAAATTCTTAATATCGATAACGTTAAGTTTTGTATTTTGTTTTTCTAGGTTTCCAGTTTCCAGAGTGGGGCACGGCTGAGACCCCATCGGAGCCCCCTGTGACCCATGTTATCGATAAAGACAACTCATGGCTGTACTCTCTGGACCCTATTCTCCTGACCATCATCGTCATGAGCTCTCTAGGAGTTCTTCTAGGTGCTGTTTGTGCTGGCCTACTCCTTTACTGCACCTGCTCATACGGAGGCTTAACGTCTCGCTCTTCCACCACTTTGGAGAACTACAACTTC[G/T]AGCTATACGATGGGATTAAGCACAAAGTGAAGCTCAACCAACAGCGCTGCTGCTCCGAGGCTTGAGGAAAACAGATGGGGTGATATCAAGTATCCTAAAATGACCTCAAAGTTACCCGATTTGACTCTTTGAAGAGAGACGAGCCTCATCTCTTAGTATTCCTGGAATGCATGTCCATCTCAGCTGGAGAGCTCCTAAACTGAACTTCTCCTGGAGCTTATTTTCCAAGCAGTGCTTACTCAGCTCTAACGCTGCTGCCAAGGACTTCCTCGTCTTTCACTGGATTACATCAAAAAAAGGGGAGCGTTTGGTGCCACAAAGACTGAAACACTTTCCAGGGCTCAGCCTCAAAAATAAATGTCGATACATATCAATGTTCTGCTATTCCAAAAAGATAATAGTATATCAGCTTAGATTTCTAAGAGGTCTAGTTTTGAAAATGGGAGATCTGTGGCCGGACCTTCGAGCCATGAACTTCTGTCCACCGTCATTCCCCAAAG
Associated Phenotype:
Not determined