ZMP
NTN5
Ensembl ID:
Description:
netrin 5 [Source:HGNC Symbol;Acc:25208]
Human Orthologue:
NTN5
Human Description:
netrin 5 [Source:HGNC Symbol;Acc:25208]
Mouse Orthologue:
Ntn5
Mouse Description:
netrin 5 Gene [Source:MGI Symbol;Acc:MGI:2685330]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45274 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9122 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14934 | Nonsense | Available for shipment | Available now |
sa34041 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45274
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 |
---|---|---|---|---|---|
ENSDART00000052909 | Nonsense | 85 | 839 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 21603725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20194161 |
GRCz11 | 7 | 20446129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGACAATGGAGGACCTCCAGCAAGGACCCAAGACAAATATTAGCACTT[T/A]AACAGATCTTCATAACCCCCACAATCTGACATGCTGGACAGCTTCAGAGG
Long Flanking Sequence:
GGCTGGACTGTGTGTGTGAAATGGTCGACTTAGAACCTAGAATGAATTTCTACAGAGCTGGGATGTTTTTAATTGTGGCACAGTTGGTGCGGTCTGAGAAAATTCATATTGCAATGCTCTCGTCCGTTTGAGCTTCCCTCAAATGTCATGTAAACCCATCAGTTCCCTGACCTTTTATTTAATGGCCTCCTATAATTTTTAAAATCCTTTTTTTCTTCTTCCCTACTGTTACAGGCTTGACGACACCATGTCCAGATATCACTCCCCTCCTTTCCAGACCCTCTCCTTCCTTCTTCTTTTCCTCTTTACCCTCTTCCCTCTCTCACTTCTGTCTCCAATACTTTCTCAATCTCCTCTCAGTTGGACCTCTCCCCATGACCCCTGTTACCACCTGGATGGGCGTCCACGCCACTGCCTGTCTGAATTCATCAATACAGCTTATGGGGTGCCCGTGACAATGGAGGACCTCCAGCAAGGACCCAAGACAAATATTAGCACTT[T/A]AACAGATCTTCATAACCCCCACAATCTGACATGCTGGACAGCTTCAGAGGGCTCCAGTGGTGGGGATTGGACTTTGATAGTTCCCCTAGGAAGACGTTTTGAAATCACATACATTAGTCTTCAGTTTTGTCAACAGGTGGATTCGGTTGAGTCCTACTCCATTACTATCTTAAAGTCAATGGACTTTGGCCAGAGTTGGCGCCCCTTACAGTTTTATTCAAATGACTGCATGGGCTCATTTGGGCGACCTGCACAGTCAATTGCTTTGACAAAACACCAGGAGACGGAGCCACTTTGTTCAGATCCCAGACCACTGCAGAAACATCGAGGAAATATTGTGCTGGCTTTCTCGACTTTGGACGGACGTCCTTCCTCGCCAGACTTTGACTACAGTCCTGGACTACAAGATTGGGTAACTGCAACAGACATAAAGATAGTATTTCATCAATCAATGGACAAAATGAAAAAGCAAGAGGAGAAAATGAATGAAGTGGGAGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9122
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 |
---|---|---|---|---|---|
ENSDART00000052909 | Nonsense | 312 | 839 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 21603045)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20193481 |
GRCz11 | 7 | 20445449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAYAGTGCTGCAAAGCGGCCACAATGTTACCCGAAAGGAGATGGGATCT[C/T]AAGGTAGAGYGGGAAGAGGCCATAGAAAGGACAATAGCAGGCCATGCCAG
Long Flanking Sequence:
TGGACTTTGGCCAGAGTTGGCGCCCCTTACAGTTTTATTCAAATGACTGCATGGGCTCATTTGGGCGACCTGCACAGTCAATTGCTTTGACAAAACACCAGGAGACGGAGCCACTTTGTTCAGATCCCAGACCACTGCAGAAACATCGAGGAAATATTGTGCTGGCTTTCTCGACTTTGGACGGACGTCCTTCCTCGCCAGACTTTGACTACAGTCCTGGACTACAAGATTGGGTAACTGCAACAGACATAAAGATAGTATTTCATCAATCAATGGACAAAATGAAAAAGCAAGAGGAGAAAATGAATGAAGTGGGAGGTGCATACAGATGGAGAGAAAGAGGAGACAAAGCTTTGAGGTTTGGCGAGAAAAACACTGGCACCAAAGCAACCGATGTTTGGGGAAATAGTCGAGAAAAACAGACTTCAACACAGAGATTTAAGAATAAAAGCACAGTGCTGCAAAGCGGCCACAATGTTACCCGAAAGGAGATGGGATCT[C/T]AAGGTAGAGTGGGAAGAGGCCATAGAAAGGACAATAGCAGGCCATGCCAGGATGGCACATGTGATCGATCCCTAAATATCCAACAGCAGAGCTCCAAGGGGAGAGAGTTGAGGAGAAGAAGAAACAACGGCGGAAGGGGGAAGTCCCATTTTAAACAAAGAAAAAATGGCTCACGCCAGCTTGTCCCTTCGTCTCTTTATGCCCCAACGAAACCCACACTTGCACTTTCGGACCTGCAGGTTGGAGGCAGGTGCAAGTGCAATGGCCATGCCTCTCGCTGTCGTCGTGACAACCAGGGGCATGCCGTGTGTCAGTGTGAACATCACACATCTGGGCCAGACTGTGACATGTGTGAGCAATTCTTTTATGATCGTCCATGGCAACGGGCCACACCCAGCCAACCACACCCGTGCGTCCGTGAGTTTAAGCCTCTGTGTGTCTGGTGCTCTGTCTGTCTTAAATGTATCTTTAATAATACACTGATGTTGCCTTGGGAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14934
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 |
---|---|---|---|---|---|
ENSDART00000052909 | Nonsense | 405 | 839 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 21602764)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20193200 |
GRCz11 | 7 | 20445168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACCTGCAGGTTGGAGGCAGGTGCAAGTGCAATGGCCATGCCTCTCGCTG[T/A]CGTCGTGACAACCAGGGGCATGCCGTGTGTCAGTGTGARCATCACACATC
Long Flanking Sequence:
ATGAAAAAGCAAGAGGAGAAAATGAATGAAGTGGGAGGTGCATACAGATGGAGAGAAAGAGGAGACAAAGCTTTGAGGTTTGGCGAGAAAAACACTGGCACCAAAGCAACCGATGTTTGGGGAAATAGTCGAGAAAAACAGACTTCAACACAGAGATTTAAGAATAAAAGCACAGTGCTGCAAAGCGGCCACAATGTTACCCGAAAGGAGATGGGATCTCAAGGTAGAGTGGGAAGAGGCCATAGAAAGGACAATAGCAGGCCATGCCAGGATGGCACATGTGATCGATCCCTAAATATCCAACAGCAGAGCTCCAAGGGGAGAGAGTTGAGGAGAAGAAGAAACAACGGCGGAAGGGGGAAGTCCCATTTTAAACAAAGAAAAAATGGCTCACGCCAGCTTGTCCCTTCGTCTCTTTATGCCCCAACGAAACCCACACTTGCACTTTCGGACCTGCAGGTTGGAGGCAGGTGCAAGTGCAATGGCCATGCCTCTCGCTG[T/A]CGTCGTGACAACCAGGGGCATGCCGTGTGTCAGTGTGAACATCACACATCTGGGCCAGACTGTGACATGTGTGAGCAATTCTTTTATGATCGTCCATGGCAACGGGCCACACCCAGCCAACCACACCCGTGCGTCCGTGAGTTTAAGCCTCTGTGTGTCTGGTGCTCTGTCTGTCTTAAATGTATCTTTAATAATACACTGATGTTGCCTTGGGAAACTATTAATCACATGTTTTTACACAAGATAAAACATGCAAATATTTGCATTATATAATAGTTGAGGGAAATAAAACACACGATGGAGATTTATGTAGAGTTCATAAACCCTTGTAATCGGGACACCATTGGACATTAAGTGAACTGGAGCCAGTACTGTATTGCTCACACTTGCTAACACTGGCAAAACAAAACAAAAAAATTAAAACATAAAAAGTTTTGCAAATAGCTCCTTTATTTATTTGTTTTGCTATTTGAAACAGGTTGAAAATCCTTTAGAGGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34041
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052909 | Nonsense | 727 | 839 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 21591137)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20181573 |
GRCz11 | 7 | 20433541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGGCAGGACACCCGAGGGAAGTGCCTACAGGGAAACACCACTGCACAG[A/T]AACCATCTCACCCAAACTCTTATGAGGAATACACACCTCCACATCTTGAC
Long Flanking Sequence:
TTATGTCAAGAACACAGATTTCTTGTTGGCTGAATTTTGCCACATTACTTGTTCAGAAAATAAATCTGGATAGTGAATTCTTGAGTCGTATTAACATTCTCATCTTCATTGTTTGTGTCCCTTGTCCCTGTCATACTTTCATCCCAGTATTGAAGGTGCAGGTAAAAAGTAAGGAACGCTCTGGTCCCTGGTGGCAGTTTTCCATACTGGTGCAGTCAGTTTTTCGCATGGGCTCTTCACATGTAAAGCGAGGCCTTCAGGCCCTTTGGGTTCCAGATCGGGATGTGAGCTGCGGCTGCCCTGCTCTGCAGATTGGCCGAACCTTTCTCCTGATCGGTGCAGAGGAAAGCAGGCGTAGTTGGGTCCCTGAGGAAAGGAGATTAGTTGCAGACCGCACCACAATGGCCTTGCAATGGAGAGAACACTGGAGCCCCAAATTGAGAGGGTTCCGCGGGCAGGACACCCGAGGGAAGTGCCTACAGGGAAACACCACTGCACAG[A/T]AACCATCTCACCCAAACTCTTATGAGGAATACACACCTCCACATCTTGACAAACTGCAGTCTGTGCCACACAGACTACATAAACATACACACATGGCACATAAGCAGCATCATTTAACACCACAATCAGGATCAGAGCACACACACAATCAAAGGGGGACTCAGGACATACAAGGAAAAAACACAGAAACGCACCTTGAGGAGGACCATGAGGCTGAAAACGTCACACTGAGCTCCTCTCAGGAAACACAAGATCCTCTCTCAGGTACTTCAAAGACGAGTCAGGCCAGTAAACGTGAGCGGTACTACCCAACGGCATGTCCAACCTGGTCACCTGTCTGACAGAATCAGGCATTAAGAACAGAAATACAAATGATACTAAAATGACTGAAGTCAGTCAGTGAGGTAAATTAGCGGTTGTTTCAAATAGGCTGTATCCTGTAAGGGCTTCTCACACTGTGCTACACCCTGCATTTAACCCTGGGTAGAGAACATTTCACA
Associated Phenotype:
Not determined