ZMP
LOC556331
Ensembl ID:
Human Orthologue:
NETO2
Human Description:
neuropilin (NRP) and tolloid (TLL)-like 2 [Source:HGNC Symbol;Acc:14644]
Mouse Orthologue:
Neto2
Mouse Description:
neuropilin (NRP) and tolloid (TLL)-like 2 Gene [Source:MGI Symbol;Acc:MGI:1921763]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14767 | Nonsense | Available for shipment | Available now |
sa43852 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13616 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14767
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090043 | Nonsense | 62 | 534 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 25096047)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz11 | 7 | 41964728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCARTGGACCCGAAATATCAATGGAGGGCTWTTCACATCTCCGAACTA[T/A]CCAAACTCATATCCACCCAAYAAGGAGTGTGTGWACATCCTAGAAGGTAA
Long Flanking Sequence:
TGCACTCCTTTCGAACAGACATTTTTATCTCAATCCCTTTTTTCTAAACTCAGAACATCTTTTTACTTATGTTTTATATGACAAATTTACTGACTTTAAATTCATAATAAAATAAAATCAACGCTGAACATTTTACAGCAGTAATTCCATGTTCTTTTATGAGGACACAAAAGAAATTGAATCACAGGAATGACACCAATATTTGACCTCATTAAAATGCAAAAACAGATCATCAGAATAATGTTGAAGGTATTTTTGTCTCAGTCTCTTTTTTCTAATCTAAAAATACCTTTTTATATGCATGGTCGGTGACATTCGTAAACTGTTAATCTCATCTGTGTTTTAGTTAATATCAGCCAAACCTATTTCATTCATGTTTCCTTTATCCTCCTGTCTTTTCTCACAGAGACCCAAAATGTGGGTGAATCTCCGTCCAGCACTGAACAGTGCGGCCAGTGGACCCGAAATATCAATGGAGGGCTATTCACATCTCCGAACTA[T/A]CCAAACTCATATCCACCCAACAAGGAGTGTGTGTACATCCTAGAAGGTAACCTCGCTAACAGCAAAAGAAAGATGTGTCTCCGGCTATTTATCAGCTGTTAGATGTCAGACTGACAGAAACAGTTAACGAAAGCGTGATTGACGGCTGCCTCAAGTTAATGAGGTTTTCTAATAAAGGAGTGTTGTATTTTTTCCTCCGGGTACTTAAGAACACTTCTCTCTCTCTTTATTATTATGGTATACGCAAAACTAATTTCATTCTCTTAAAAGCATCACTCACAACAGTATTTCAAGCAGTTCAAGAGCTCCCCCTGTGGATGAAGCACAAACAAACAATTGGACATGCTTGAGTCTTGATTTCTTCCAAGCATATTTTTATATGAGATATTAATATGACATTTGTGTAGAATATACACACACACACACATACAGTTGAAGTCAGAATTATCAGCCCCCCCTTTGAAATTTGTTTTCTTTTTTAAATATTTCCCAAATGATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43852
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 |
---|---|---|---|---|---|
ENSDART00000090043 | Essential Splice Site | 77 | 534 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 25096094)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz11 | 7 | 41964681 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATCCAAACTCATATCCACCCAACAAGGAGTGTGTGTACATCCTAGAAG[G/A]TAACCTCGCTAACAGCAAAAGAAAGATGTGTCTCCGGCTATTTATCAGCT
Long Flanking Sequence:
ACTCAGAACATCTTTTTACTTATGTTTTATATGACAAATTTACTGACTTTAAATTCATAATAAAATAAAATCAACGCTGAACATTTTACAGCAGTAATTCCATGTTCTTTTATGAGGACACAAAAGAAATTGAATCACAGGAATGACACCAATATTTGACCTCATTAAAATGCAAAAACAGATCATCAGAATAATGTTGAAGGTATTTTTGTCTCAGTCTCTTTTTTCTAATCTAAAAATACCTTTTTATATGCATGGTCGGTGACATTCGTAAACTGTTAATCTCATCTGTGTTTTAGTTAATATCAGCCAAACCTATTTCATTCATGTTTCCTTTATCCTCCTGTCTTTTCTCACAGAGACCCAAAATGTGGGTGAATCTCCGTCCAGCACTGAACAGTGCGGCCAGTGGACCCGAAATATCAATGGAGGGCTATTCACATCTCCGAACTATCCAAACTCATATCCACCCAACAAGGAGTGTGTGTACATCCTAGAAG[G/A]TAACCTCGCTAACAGCAAAAGAAAGATGTGTCTCCGGCTATTTATCAGCTGTTAGATGTCAGACTGACAGAAACAGTTAACGAAAGCGTGATTGACGGCTGCCTCAAGTTAATGAGGTTTTCTAATAAAGGAGTGTTGTATTTTTTCCTCCGGGTACTTAAGAACACTTCTCTCTCTCTTTATTATTATGGTATACGCAAAACTAATTTCATTCTCTTAAAAGCATCACTCACAACAGTATTTCAAGCAGTTCAAGAGCTCCCCCTGTGGATGAAGCACAAACAAACAATTGGACATGCTTGAGTCTTGATTTCTTCCAAGCATATTTTTATATGAGATATTAATATGACATTTGTGTAGAATATACACACACACACACATACAGTTGAAGTCAGAATTATCAGCCCCCCCTTTGAAATTTGTTTTCTTTTTTAAATATTTCCCAAATGATGTTAAACAGAACAAGGACATTTTCACAGTATGTCTGATAATATTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13616
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090043 | Nonsense | 233 | 534 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 25102984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz11 | 7 | 41957791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTCCCTGCAGATAYACCTCCGTTTYCTTGAGTACCAGATGGAGCACT[C/A]GAACGAGTGCAAGAAGAACTTTGTGGCCGTGTATGAYGGCAGCAGCGCCA
Long Flanking Sequence:
TGGAGGTAGAGCCGAATCAGCAAGTACTAGGAATAAGACTGAGGGATGAAAACAGCATTAAGATGGTCGAGGGATTACACACTCACCTGCGCTAAGCAGACCCGAACACTTAGCAGGCTAAAAAAACATCCCTGAAGAGCTTGCCAGAAGAGTGAGTGATTACAAAGCATAGAGATAAGTCATTAGAGTTATGGGGAGCAACTTTCCTGTGAATTTTTCGGGAGGCTAGTCTCTTTAAGAAAACATTGCCAAGAGCTTTTTTTTTTTGTTGTTTTGTTATTCTCAGTAAGCAGTCCCAATAGATCAGGTCAGTTCACTCTGTCAGACCAAAATGCAGCAGTATTTTTCCTTTCTGCTCAAATATATTTTCTTGCAAGTTGCTGTTTTCTGTCCTGTCCTCTTCCAGTCAGCATTTTGCCAAATGTAGCGGATGCGTTTGTTAAAGGTTGGTTCTTCCCTGCAGATATACCTCCGTTTCCTTGAGTACCAGATGGAGCACT[C/A]GAACGAGTGCAAGAAGAACTTTGTGGCCGTGTATGACGGCAGCAGCGCCATTGAGAATCTGAAAGCCAAGTTCTGCAGCACAGTGGCCAATGACGTGATGCTGGATACTGGCGTGGGGGTTGTGCGCATGTGGGCTGATGAGAGCAGCAGACTGAGCCGTTTCCGAATGCTCTTCACTTCATTTGTGGATCGTGAGTAAAGTTCTTAATCCTAAAATTACAACAGGATGAAAGTACACTCTGTAAAACCCAACAAGTTAAGGCAACTCAAACTGTTTGAGGAAACCAATTGCAACAAACCATTTGAATTAAAAAGCAAGTACTGTGAACTTACTCCATTTAAGTTGAAGTAATGAAGTATTGAACTCTTTACAAATGAGTATAATTAACATAATTATAATTAACATTCAGTAAATTTTGAGTCAACTACACTCATTTTATTTGATAAAGTTGACTGTTTGGTTTTACAGTGCAAGTAATACATTCGGACATAGTCAATAT
Associated Phenotype:
Not determined