ZMP
nrp2b
Ensembl ID:
ZFIN ID:
Description:
neuropilin 2b [Source:RefSeq peptide;Acc:NP_998131]
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41380 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34591 | Essential Splice Site | Available for shipment | Available now |
sa34590 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7177 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41380
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056103 | Nonsense | 140 | 920 | 3 | 17 |
ENSDART00000056103 | Nonsense | 140 | 920 | 3 | 17 |
ENSDART00000056103 | Nonsense | 140 | 920 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 14746080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 14498645 |
GRCz11 | 9 | 14469848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGACTACGCCCACCAGGGGGCAGGGTTTTCGCTGCGCTATGAAATCTA[T/G]AAGACAGGTAAGCACGCGTTACTCAGCATGATGTACTGCATCATTAACAA
Long Flanking Sequence:
GGTGGGTGTATATATAGATTTTTTCATGTTCATGTTCAGCATTGTTCTGCTGCTTAGTGAGGGGAAGAGAGTGTTTTTTTATTGTGTGCCCTTAGCTGTGACATAGATGAACTTGAATTGGTTCTACTGCACCTTTACTGTCAGTAAAGGAAATGTGTCCAGAGTTAGTCATTTTTAATTACCGCCGTATCGCCGTAGTATACTACTCACCTCTATCACCATAGTATGCTACCGTGACCAATAACAAATTGTTATTCTCAATGCACTGTTGAAACTATTAACTTTGACACTCCTAATAAACATGCCTTGTTTGTTCTGTTCTAAAGATATGACTTCATCGAGATCCGGGATGGAAACTCGGATGGCGCCGACCTTTTGGGAAGACACTGCAGTAACATCGCGCCCCCTGCGATCATATCCTCAGGCCCAGTTTTGCACATCAAGTTCGTCTCAGACTACGCCCACCAGGGGGCAGGGTTTTCGCTGCGCTATGAAATCTA[T/G]AAGACAGGTAAGCACGCGTTACTCAGCATGATGTACTGCATCATTAACAATGTGGTGCCAAAGCTTCGCCTGCTGTTTACACATCTCTCCTGTGTGCTTTAAGCAAGAGCCCTGTGTTCTTGCTCTTGTACTAACACAGCGTTTACAGCGTGGGGAGAGTTCATGTGGGTCCAGCGAGCCTGTTAGGAAAGCTTGATTTCTCTTAACACAGATCACAAATTCACCTCTTCGCACAGGAAACACGTACTTCACCTTTTCCTTTGTTTACCCACTCATTCTTGAATCATAGACTGCGATGTGTTAAATCCCACCTGCCTGAGAAGTGTTGATTGGCTTTTGTCAATCGGAGGGAAAAGTCCCTATTGGTCAGTGTGGTGTCACTGGCAAACCACCGCTTTTATTACTTGCTGGAAAGGTGTAGATTTGCTTTTGGAAACTGGAGAGAAAGGCTCTCATTGGTGAGTGCAGGGGCTGGAAGACAGGGGTTGCCATTTATGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34591
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056103 | Essential Splice Site | 593 | 920 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 14685196)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 14437761 |
GRCz11 | 9 | 14408964 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGCTGGCATTGGGATGAGAATGGAGATACTGGCTTGTGACTTGCCAGG[T/G]AAGACCCATTTTATTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGT
Long Flanking Sequence:
TGAATTAGGTTAATTAGTTAATCGTGCAAATTTAAATATCTCGGGTCGTTGAAAAGGCTACAGTAATGAACAGTTTGCCAGAATCAGATTATTAACAGACTCATTTCATTCTTTCCTGCTCGTCTCAGCGACTCAGCATTTCACTTCTAGATTCCCAATCTCCCACTCTGAGAGCAGAATTCAATTATGCTGCGAGCTTTGATAACATTCCAGTGAAATCATCCACAGTTGTGTTAATTAAAACCTGAGCTGCAGAGATGCGTCAGAGACTCGGAAATATAGAGCATATCCAGTAGCTTTGCTCTTTCAATCACACAGCTGTGCTAAAGTGTTTTTGCGATTTTGTTCCTCCAGATTTTTGAGGGTAACACACACTACGACACCCCAGAGATCCGTCGATTTGATGAGATTGTGGCCCAGTTTATCAGGGTGTATCCGGAGAGGTGGTCGCCCGCTGGCATTGGGATGAGAATGGAGATACTGGCTTGTGACTTGCCAGG[T/G]AAGACCCATTTTATTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTAAATTGAACTTTATTTTAATTACATTTTTTATTTTTAGTATTTTTATTATTTTATTGTATTGTATTTTTTATTTATTTTTTATTTTGATTTATTTTATTTTATTTACTTTTAATTTTATTTTATTTTACTTTATTTTATTTATTTATTTTTTAGAGTATTACATTAGCTTTATTGGACTTCGATTCTATGGATTTGCTTTTTTTTCTCTATTCTTAGATTTTTAACAGTATGCCGTTTCACATGACACATCAGATTCATAATAATCATGATAAACAATTAATTTGCTGAGTAATAAAGTTCATTAACCTAGCCAAAGGCTGTTTACATTGCCTGTAGCAATATATAATGCAAATGATGTACGATCACACCAATATGTGAATCCATTGGCTGTTGGCAGCAAACTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34590
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056103 | Nonsense | 649 | 920 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 14663139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 14415704 |
GRCz11 | 9 | 14386907 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGAGTATGTGTGGATGGACCCACGACCCCATGTCTGATCTGAAGTG[G/A]TCTATGTATAGTTCCTCCAGTCCGAGTTTGGACCTGACACACGGACCTGA
Long Flanking Sequence:
TTGTTCTATGTGTTTATCTTGTAACACTTAAAAAACTGTGTATTTTGTGTGCCATTTATTTTCTAAAATCAGCATTTTAGTGCCTATTGCTTGTATTACACTCTGCACTAGGAATCTGAGTTCCTGCAAATGCAAACTTCCCAATAGTTTGTACTTCCACTAGTAGTTCTAAAAACAATGAAAATGTTCCTTGTGTATGAAAGCCCCTGATATTCACATGATAGCTCAGCGGGCATATGGTAGAGTAGTGGTTTTGTGACTATTTTTTTTTTCAGTTACTGTATAAAAGCAATCCAATTGAATAGATTTGGATATAGATGTCATGAGACAGTAACATGGGAGAACCTACACCAGGGTCTGCGGTCATGGAAAATTAGTATAATCTGTTTCTCTCTCGTTTTCTCCTCAGCTCCCACTACTCTTTCGTCTCTGGGTGGTCTGTGTGACTTTGAGCAGAGTATGTGTGGATGGACCCACGACCCCATGTCTGATCTGAAGTG[G/A]TCTATGTATAGTTCCTCCAGTCCGAGTTTGGACCTGACACACGGACCTGATAGTAAGTCCATCTTAATAAAAGATATCGCATAACCTAAAACAAACTAACAAATGTTTGCACGGATCTCTGCAAGTATAAACAAAATGATTCATTTGGGTTTGCATTGGGAATATAGGGAACTCTGAGAAGACCTCTGTTGAGAAAATAAACTGTGTGACTTCCCTTGATCGCACCAAACAAAAGACTTTTTAGACCTTCCTTTGTCCTTGTCAGCTTTACCAGTCCAGACCCTCACACACACGGTCACCTCTCATTTTCCATCCATCCATCTCATTACTGATGTGTAATTAATGTGATAGTTGAAATCTGGGAATAATATCTGTCACTCTCTCAGCCTGTCCTCACTCTTCCTCTGGGAGTTTGTACATCTCCTCATATCCCTGAGCTTCGGTGACCTTTATTAACCCTGCATGAAAAAAAAACAAAATGATTTTGCGCACAACACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7177
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 |
---|---|---|---|---|---|
ENSDART00000056103 | Nonsense | 681 | 920 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 14657489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 14410054 |
GRCz11 | 9 | 14381257 |
KASP Assay ID:
554-4893.1 (used for ordering genotyping assays)
KASP Sequence:
TNGCTGCAGATTTTGGGAATTTCCTGTATGTGGAAGCGAGTCCCATGTCA[G/T]AGYCTCAGCGGGCACGKTTATTGAGCCCATCGGTGGGACCYGAACGGCGT
Long Flanking Sequence:
CAGGAGAGTTTTCTTCCTGGTTTGGTCCATCTTTAATCTGACATTATGACGGTTGAGATCATACAGTGTGACATAAGAACTATGTTTGTGCAGTCTGACATGTGACAATCGTTCAGGATTATAAAAATTCTCACAGTATGAGCTGGCCTTTAGACAACCAAATTGTGGAGCAGTTTTAAACAGGGTCATTCTTGTGGGTCAAAGATGACAGAATAATGTGGACAACAGGTGTGAACATATGCGTTTAAAAAAAAAAAAAAAAAAAAGCATTAGTGTAAGTGCCACCTTGGAGGGACAATGTCCTGTAGAGTTTATCTCCAAACAACTCCAACACATAGGGTAATTTCTAGTTAGTCTAAAGACTTTTGTCAACTTGTTTAGGTGTATTCAGGTTTGAGTTATGAATCTCTGATGAACTAAAGATGTTTAACTTTGTGACTTGTTTCATTTTTGCTGCAGATTTTGGGAATTTCCTGTATGTGGAAGCGAGTCCCATGTCA[G/T]AGCCTCAGCGGGCACGTTTATTGAGCCCATCGGTGGGACCCGAACGGCGTCTCGTCTGTCTGCTCTTCTACTACCAGCTTCGGGGTGCAGGTCAGGAAAGTCTTCGTGTGCTGCTGCGGGACGACGACCAAGAGGAAACTCTGCTTTGGACACTGAAAGGAGACCAGGGGTCCATGTGGAGGGAAGGTCGCACCATCCTGCCTCAGTCCCCTAAAGAATATCAGGTACATTCACATTAATAAGCTATGAGAGTTTATACCATGCTAAAGATTGACTTGAGAAGAATACAAGTTTAATTTCCTTTTTTTGTTTGTTTTTAAATTGAAGGTTGTGATCGAAGGATTTTTTGAGCGTGGCAGTCGAGGACACATCCGGATTGACAACATCCATATGAGCTCCAGCATTGATCTTGAGCAGTGCACACGTAAGTATCAACAACTGGAACTCTCTCTGTTTCTCTCTTTCAGCCGTTACCCACCAAATTTGGCACTGGGGACCAA
Associated Phenotype:
Not determined