ZMP
net1
Ensembl ID:
ZFIN ID:
Description:
neuroepithelial cell-transforming gene 1 protein [Source:RefSeq peptide;Acc:NP_001007768]
Human Orthologue:
NET1
Human Description:
neuroepithelial cell transforming 1 [Source:HGNC Symbol;Acc:14592]
Mouse Orthologue:
Net1
Mouse Description:
neuroepithelial cell transforming gene 1 Gene [Source:MGI Symbol;Acc:MGI:1927138]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33416 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40244 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33415 | Nonsense | Available for shipment | Available now |
| hu2165 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa40243 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33416
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 |
|---|---|---|---|---|---|
| ENSDART00000002682 | Nonsense | 8 | 580 | 1 | 11 |
| ENSDART00000049066 | None | None | 551 | None | 9 |
The following transcripts of ENSDARG00000032765 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 10658649)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 11595276 |
| GRCz11 | 4 | 11594125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCTTTCTCTGTATCGGTTCTGCAGACCATGATGCAGTGTCACAGGAGA[C/T]AGAGCTACACCAGGCTTGGTGTGTGGTACGTACAGGATGTGTCTTTACCG
Long Flanking Sequence:
ATAATCTAATCTAATTGTTAAAGCTTTAAAGCTTTAAAGTTAAAACTTTATAATGCCTTTTGTTCAAATGGTTTAAATTTACTTAAAATCTTTTGAGATGCTCGACTAATGCAGATTCTCCCAATGAGATATCAATGCTCAAATTATATATTGGGCAACCCTAGTTGTAAGCACCCCAAAAGTGTTATCTCAACGTTTTTAATGAAAAGATTTGGTAATAAGGATGTCACATTATTGGGGATTGAAAAAAGCAGCAGGTCTTCTGAAAAAAGACCCCTGGGTATCTTTGTGAACACGACCTCGTTGAGACAGTTGTCACCAGTCCCCAAATAAGGGCCCAGTCAACAATGAGGAGGCAGTGCATTCGTGAGTACATGATGGATAAAGACTGAAGGAGACTGAGAAGACTACAGAAAGCAGTGTGTTTGTTGGAGAGATCAGGGCTGAGTGACGCTTTCTCTGTATCGGTTCTGCAGACCATGATGCAGTGTCACAGGAGA[C/T]AGAGCTACACCAGGCTTGGTGTGTGGTACGTACAGGATGTGTCTTTACCGTAATGGGCTTTTCTTGTGTGGCACATGGATGGACATACTAATGGATCTACATGGTTTGACTGCACGGTATACGTCATTAGTGCACAGCCTCCGCGTCTGGTTGGATGCTTTGTGTTTGTATGGCTGAAGTGGGACTTTTTTATAGGCCTGTGAAACTTATTTGTCTTGTGCTTTTCTCTTTGTAGGCCATCTTTGAGACGAGGAAGCTCTTTTACCTTTCTGACACCTGGACCTCAGTGGGACTTCACACTGGTGAGTGGGATAATGACATCCCTTATGGCTCAACTCTTCCTCAAGTGTACCAATCCCTCTAATCCCTCCATTATCAGTAGTAGAGTCTGACATTATTTTGTTGCTATAATAACACTTTGCTTTGGGCTGGGTATAATTTAATCCCATTTTTCACATTGTATAACATACCCTATCTAGGGTTGCGCACTGTTTAGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40244
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 |
|---|---|---|---|---|---|
| ENSDART00000002682 | Nonsense | 21 | 580 | 2 | 11 |
| ENSDART00000049066 | None | None | 551 | None | 9 |
The following transcripts of ENSDARG00000032765 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 10658400)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 11595027 |
| GRCz11 | 4 | 11593876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAAACTTATTTGTCTTGTGCTTTTCTCTTTGTAGGCCATCTTTGAGA[C/T]GAGGAAGCTCTTTTACCTTTCTGACACCTGGACCTCAGTGGGACTTCACA
Long Flanking Sequence:
AGCAGCAGGTCTTCTGAAAAAAGACCCCTGGGTATCTTTGTGAACACGACCTCGTTGAGACAGTTGTCACCAGTCCCCAAATAAGGGCCCAGTCAACAATGAGGAGGCAGTGCATTCGTGAGTACATGATGGATAAAGACTGAAGGAGACTGAGAAGACTACAGAAAGCAGTGTGTTTGTTGGAGAGATCAGGGCTGAGTGACGCTTTCTCTGTATCGGTTCTGCAGACCATGATGCAGTGTCACAGGAGACAGAGCTACACCAGGCTTGGTGTGTGGTACGTACAGGATGTGTCTTTACCGTAATGGGCTTTTCTTGTGTGGCACATGGATGGACATACTAATGGATCTACATGGTTTGACTGCACGGTATACGTCATTAGTGCACAGCCTCCGCGTCTGGTTGGATGCTTTGTGTTTGTATGGCTGAAGTGGGACTTTTTTATAGGCCTGTGAAACTTATTTGTCTTGTGCTTTTCTCTTTGTAGGCCATCTTTGAGA[C/T]GAGGAAGCTCTTTTACCTTTCTGACACCTGGACCTCAGTGGGACTTCACACTGGTGAGTGGGATAATGACATCCCTTATGGCTCAACTCTTCCTCAAGTGTACCAATCCCTCTAATCCCTCCATTATCAGTAGTAGAGTCTGACATTATTTTGTTGCTATAATAACACTTTGCTTTGGGCTGGGTATAATTTAATCCCATTTTTCACATTGTATAACATACCCTATCTAGGGTTGCGCACTGTTTAGAGGACAACAATTGGCACGATTGAATCAATAAAATAAAAAAAAATTAATGAACTATATAATCAATAGGTTAGGACAGAGGTGGGCAAACTTTTTAGATTAGAGGGCCACGGCAAGTTTTGGAAAGCAAGTGAAGGGCTACATGCTAAATCCTTCATAAGATAACTTATTTATAGTGGCAGTATGCATAGAACATGTATTATCTGACAGGAACATGCATCACATTAACACATATCAGATTTTTTTTAGTTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33415
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 |
|---|---|---|---|---|---|
| ENSDART00000002682 | Nonsense | 261 | 580 | 8 | 11 |
| ENSDART00000049066 | Nonsense | 232 | 551 | 6 | 9 |
The following transcripts of ENSDARG00000032765 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 10641101)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 11577728 |
| GRCz11 | 4 | 11576577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTAGCTGCCAAAGCCCTCCTCGATCAGAAGAAACAGGACCCAAGAGTT[C/T]AAGACTTCCTGCAGCGCTGCCTTGAGTCACCTTTCAGCAGGAAACTAGAC
Long Flanking Sequence:
AAAAGTTTCTGGCTGTAAAATTAGAAGCTGTGCTTATTATTTTTATCATTTTGTGTGTCCAGGCATACCATGACCCAATGCTGAAACTTTCTATTATGTCTGAAGAGGAGTTAACAGCCATCTTTGGAGATTTGGATGCTTACATTCCCCTTCATGAAGGTAAATAACCTACCATATTTACATGACACACCTAATTACTGCGTGAGATAACAAGTAGTGTTAACGTACTTTTTTTTTTACCCTATCAGATCTTCTTGATCAATTGGCAAAGGCCACAGGTACGGATGGCACAGTGAGACAGATCGGCAAGATTGTTGTTGACTGGGTAAGCATCTTTTCGTTGTTCATTATTATGAGGCAAATTAATTGTGGTTCATTCGGAATGTTAAAACTCTCACTTTCCACCACAGCTGCCAAGGTTAAATGCATACAGAGCATACTGTAGCAACCAACTAGCTGCCAAAGCCCTCCTCGATCAGAAGAAACAGGACCCAAGAGTT[C/T]AAGACTTCCTGCAGCGCTGCCTTGAGTCACCTTTCAGCAGGAAACTAGACTTATGGAGCTTCCTGGACATCCCTCGCTCACGTTTGGTCAAATACCCTCTTCTTCTGAAAGAGATTTTAAGACACACACCACCAGATCACCCAGACAAAGGAAGTCTTGAGCAAGCGGTAAGAGCAAGCACCGATCTAACAACTGCAGGCCTTCAGATACACTTGTTTTGGGGACATTCGGTTTTAATATTGCCTTCGTTCTTTGTCTCCAGATAAGTGTCATTCAAGCAGTGCTGGCTGACATAAACATGAAGAAAGGGGAGTCAGAATGTCAATACTATATCGATAAGCTGGAATATTTGGAAGACAAGCAGAAAGACCCACGCATTGAGCAGTGCAAGAGCTTGCTTTGCCATGGGGAACTTCGCAACAAAAGTGGCACGGTGAGTTTAACATCCATCACAGTCTAAACCGCTGGAGGCAAATCAGGCTTTTATTCTTGGGAATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu2165
Status:
Confirmed mutation in F2 line
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002682 | Nonsense | 287 | 580 | 8 | 11 |
| ENSDART00000049066 | Nonsense | 258 | 551 | 6 | 9 |
The following transcripts of ENSDARG00000032765 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 10641022)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 11577649 |
| GRCz11 | 4 | 11576498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTTCAGCAGGAAACTAGACTTATGGAGCTTCCTGGACATCCCTCGCT[C/G]ACGTTTGGTCAAATACCCTCTTCTTCTGAAAGAGATTTTAAGACACACAC
Long Flanking Sequence:
GCTGAAACTTTCTATTATGTCTGAAGAGGAGTTAACAGCCATCTTTGGAGATTTGGATGCTTACATTCCCCTTCATGAAGGTAAATAACCTACCATATTTACATGACACACCTAATTACTGCGTGAGATAACAAGTAGTGTTAACGTACTTTTTTTTTTACCCTATCAGATCTTCTTGATCAATTGGCAAAGGCCACAGGTACGGATGGCACAGTGAGACAGATCGGCAAGATTGTTGTTGACTGGGTAAGCATCTTTTCGTTGTTCATTATTATGAGGCAAATTAATTGTGGTTCATTCGGAATGTTAAAACTCTCACTTTCCACCACAGCTGCCAAGGTTAAATGCATACAGAGCATACTGTAGCAACCAACTAGCTGCCAAAGCCCTCCTCGATCAGAAGAAACAGGACCCAAGAGTTCAAGACTTCCTGCAGCGCTGCCTTGAGTCACCTTTCAGCAGGAAACTAGACTTATGGAGCTTCCTGGACATCCCTCGCT[C/G]ACGTTTGGTCAAATACCCTCTTCTTCTGAAAGAGATTTTAAGACACACACCACCAGATCACCCAGACAAAGGAAGTCTTGAGCAAGCGGTAAGAGCAAGCACCGATCTAACAACTGCAGGCCTTCAGATACACTTGTTTTGGGGACATTCGGTTTTAATATTGCCTTCGTTCTTTGTCTCCAGATAAGTGTCATTCAAGCAGTGCTGGCTGACATAAACATGAAGAAAGGGGAGTCAGAATGTCAATACTATATCGATAAGCTGGAATATTTGGAAGACAAGCAGAAAGACCCACGCATTGAGCAGTGCAAGAGCTTGCTTTGCCATGGGGAACTTCGCAACAAAAGTGGCACGGTGAGTTTAACATCCATCACAGTCTAAACCGCTGGAGGCAAATCAGGCTTTTATTCTTGGGAATTAGAAACATAAAGCCACTATATTCCAAATAAGGCTATCAGATGGATTCAATTGGCTTCCTTTGTCTGTCAAGCACATGACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40243
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 |
|---|---|---|---|---|---|
| ENSDART00000002682 | Nonsense | 464 | 580 | 11 | 11 |
| ENSDART00000049066 | Nonsense | 435 | 551 | 9 | 9 |
The following transcripts of ENSDARG00000032765 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 10639708)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 11576335 |
| GRCz11 | 4 | 11575184 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTCAGGGACAGTCGCACACACTGCAGGTCAACGACGTCTTCCACAAG[C/T]AACAGTGGCTCAACTGCCTCCGCAATGCCATGTCCACCCAGAAGGATTTG
Long Flanking Sequence:
ACATTGTAACAAACTATTAGTTCCTGTGTAAGTACATATTAGTTAAGGCCACTTAATATAAAATGGGACCAAACTGTTTAATCAGTCTAATGTTCAAATAACATGTTAATAACCAGTGCTCTCTTCTCCCTCTTTAGAAACTGCACGTATTTCTGTTCACCGAGGTTCTGATTCTGACTCGACCTGTGACGCGGAATGACCGCCATTGCTTCCAGGTGTACCGTCAGCCAATCCCAGTCCAGGATCTTGTATTGGAAGACCTGCAGGATGGAGACGTCCGCATGGGAGGATCATTCAGAGGAGCCTTTAGTAACGCTGATAAAGGTAAGTTGACACCTCTTAGTATTGTGTGAATCACACTCTTTCCTTTTTTGTTGTTTCCTTTGGCTCAACTGAATCCTTTTTTTCTCCCTATAGCCAAAAACATTTTCCGGGTGCGCTTCCAGGACGCATCTCAGGGACAGTCGCACACACTGCAGGTCAACGACGTCTTCCACAAG[C/T]AACAGTGGCTCAACTGCCTCCGCAATGCCATGTCCACCCAGAAGGATTTGACACTCTCTGAGAATGAGCCCTTGACCACCCCAGCCACCGACGTTTGCGCCAAACGGCGCTCTTCTTCTGTCTCCACTGTCATCCAAATGGATGAAATGGATGAGAACTGTCCACGGGCTGCAGCCTCCGCCCCTTCCTCCCCTAGCTCTGAGGAGCCCCCCAGTCCTACACCCTCCGCCACCTCCACCCTCTCCTCATCCTCATCATCGTCTTCAATATCCGCCCCCATCCCCTCCCGCAAATCCAAAAAGGACAAGCGTTCGCTCTGCCCGTTGGGCAAGAGGAAGGAGACCATGGTGTAGATGGAGTGGCACCATGCGGAGGACTTGTATTTATGTGTGTGTGTATGGTTTTTACAGCAGTGTTTCTGTTACTGTCCACAATGGCAGCTATTACTACCAAATCCCTCCCCCCAGCAAACCCTCCTTGGTCCACATGGGCCGCACCAG
Associated Phenotype:
Not determined