ZMP
neo1
Ensembl ID:
ZFIN ID:
Description:
neogenin [Source:RefSeq peptide;Acc:NP_775325]
Human Orthologue:
NEO1
Human Description:
neogenin 1 [Source:HGNC Symbol;Acc:7754]
Mouse Orthologue:
Neo1
Mouse Description:
neogenin Gene [Source:MGI Symbol;Acc:MGI:1097159]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17579 | Essential Splice Site | Available for shipment | Available now |
sa11491 | Nonsense | Available for shipment | Available now |
sa21085 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17579
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060405 | Essential Splice Site | 25 | 1428 | 1 | 29 |
ENSDART00000073514 | None | None | 1427 | None | 29 |
ENSDART00000131011 | None | None | 294 | None | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 55569034)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 53485476 |
GRCz11 | 7 | 53755128 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCTCTCTCWKTTCTGCCTCACGATCACAGTTTCACATGCTGAAAAAGG[T/A]AAGAATGGGATTGAAGAGCATTCAAACTTTCTGCGGCGCAGCCCGCTCCC
Long Flanking Sequence:
AAATCCACTTCCGGCTTTCCCAGGTTCCGATCTGAATTCCTACTGCTCTCTTTCTCTCTCAGTGAGATCAGTGAAAAATATCTCCAACCGTCCGGACTGACTCTCTCTCTCTCTCTTCACCTTTACACATTATGTCTGCGCTGACGCCTCGCATTTCGCTACACTCCAGCTCGGCGTTGGTCTAATCTCGGAAATATGGATTGACTTTGATTTTTCTCGGTCGCCTGTTGAAGTTTCAAAGCGCATTTCTGCGACTGGTCGTGTGTCTCTGCTCAACGAGCTTCATGTTTCCTTCGGCAACTTTCGGAAGTAACTCGTTCCGGATGTGTTCACACTGTTGAACTGCTCCGTGCGCACGATCAGAGGGATTTTAAATAAGGATTGATTCCGTGGCTTTTCACACTTCTTTTATTCGTGTTTAAAGTGATGGCGGAGCGGGGAGCCCGGCTGCTCCTCTCTCTTTTCTGCCTCACGATCACAGTTTCACATGCTGAAAAAGG[T/A]AAGAATGGGATTGAAGAGCATTCAAACTTTCTGCGGCGCAGCCCGCTCCCTGTTGTTCCCAAGAGTGTGAAATATGTGTAAATATGTGCAGGAACGAGTGTGTGTGACTAACATTTTAATCTCAACTAACTTTGAAAATCAATGGTATTTATCCAGTTCATTGAACACGTACTGCTGACAGCCCCATTAATCAAAACATTACGTCTAATCCAGCCGTGGTCTTCATATTTGCTCTGAAAATCTAATTTATGGAAAATGTATGATCTGCATTAACACCTTAACATGTCCACCTGAATAGAAAATCTCATTATTATTAACAAATGAGTCACCAAACTGGCTTGATGGAAAACAGCGTAAATGATTGTTCATTTTAGGCTAATAACCTAATTTCTATTGGGCTTAAAGAGTGTTTCTTTTGCATCATACTACACATAAGAAGTTTATATTAGGATTTTAAACATTGTTGTACAGTGCAGATATGCTAGAAGTTGAATTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11491
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060405 | Nonsense | 260 | 1428 | 4 | 29 |
ENSDART00000073514 | Nonsense | 259 | 1427 | 4 | 29 |
ENSDART00000131011 | Nonsense | 236 | 294 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 55370250)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 53684260 |
GRCz11 | 7 | 53953912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGGCGAAAGTGTCCTGCTCCCCTGTGTGGTGACGGGATATCCCACTCCT[G/T]AAATCACATGGATGTACAAAGACCAGCTCATTGAGGACAGGTAGGCAATR
Long Flanking Sequence:
TAAGCGAGAGAATACTGTCATTTTTCAAAATAAATGACTTTTCCAAATAAAAGATCGTTCAGACTCAGATAATAAATAAAACGGAAATAATTAATGATTTCTTGTGCGGTACCAATTGATCCATGGACCAGTATCGATCTGCGGCCCGGTGGTTGAGGACCACTGCTGGATTTGTGAAAAATAAAACTGCAATTCTTATCCCTGTGCATCTATTTTGTGGTTCCCAAATATGTAGCCCTGGGCACATATCTTCAGTAAGCCTGGGTTGAACAATACACTGCTGACACAGATCAAGCAAACTGAACGTCTTTGAGAGTGTCAGAAATGATTTACGTTTGTGATATTGTGTTTTGTAAGCACTGACTGCATTCATTTCTCGATTTTGTGCAGAAACGGGTGAGGAAAGGACGCTGGAGTTTCTCCAGGAGCCTCAACATGTGTCTAAACTGGTCGGCGAAAGTGTCCTGCTCCCCTGTGTGGTGACGGGATATCCCACTCCT[G/T]AAATCACATGGATGTACAAAGACCAGCTCATTGAGGACAGGTAGGCAATAACGTCTTTTTTTCTTCTTCTTTATCTTCAGGCAGCGTTTTAGTCTTCGCAGATCTCCCGAGTGGATGGAGACACTGTTATTAATAGCTGCCGAGCTCTGAATCAGACAGTGATTTCCACTAACAGGTCATTGATTCCTCGGCGTGACGAACATGAGCTTTGAGTCCCGCTGTGGCAGCAGTGTCCACTTTTAGAGATCACTCTCTGTGTATGTCTGCTGTTGGGCTGGCACACTGCCCCGTCCCAGCTGCCCGAGGAAATAATTAGAGTGACGGCGCCCGCCTGAGAGGTGTAAATGCCAGTCAAGACTGCTGGTGTCTCGAACACACACAATCTCTCTCACACCTCTCCTGGAGAAACACTGGCAGGCTGTTCACAGATTAGACCTGGGAAGCCACTTTTTCATGCTCGATTCTCATTAGCTGTTCGCTGTCCAGAGGGCATGTGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21085
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060405 | Essential Splice Site | 1276 | 1428 | 26 | 29 |
ENSDART00000073514 | Essential Splice Site | 1275 | 1427 | 26 | 29 |
ENSDART00000131011 | None | None | 294 | None | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 55243399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 53811111 |
GRCz11 | 7 | 54080763 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCTCCATCGCCACCCCCATCTCTCATCTAGACAGGGCAGAGTCCACAG[G/A]TGAGAGCGCAAGACCTCCATCAAACCTGGACACAAATGGGTTCGTTCAGA
Long Flanking Sequence:
AGGTTTGTCACCAAAAAAAATCCTTCCATTTGCTGAAACAGAGAAATGTGTGGCTAAATTAAGACTCAAAATCACCCCAGAGTGGAAGAAAACATCTCTACAAGCACACAAGGGTTAAGTACTGAGGTTTCTTGGCACCAGAGCACAGGCACTTGTCTAGAGTATGTTTTTAGTTTTATAAAAATTCTTTAACCTATCAACATATATCATATCTGTCAATCTGTGTTGTTCTTTGTTTTGCATGAGCAGATGTTCTAGCCGCACCATGCTGCTCGCCATAATCCCATAGCTTTTGTGTGTGAGGTCTAAACCATGGCGCTCTTGTTTGTGTCCATTCACAGCTGTGATTAGTGCTCACCCCATCCATTCCCTCGATAACCATCACCATCATTATCACTTGGGCAGCCTGGCCTCGCCGACACGCAGCTATCTCCACCACCAGAGCAGCACGCGCTCCATCGCCACCCCCATCTCTCATCTAGACAGGGCAGAGTCCACAG[G/A]TGAGAGCGCAAGACCTCCATCAAACCTGGACACAAATGGGTTCGTTCAGAGTCCTGGGAAACGCTCTTGTTTTCCTGTCAACGTGAAGGTGAAATTGGTTGGTGACGGTGGGATTTAAGTGAAACTCTCTCTATGAGAATATTGAACCAAAAAACAACTTGAGGTCTTTGTGGATTACTTTTTGTTAGGGCTGCACGATATATCAAATCAGAATCGGTATCGCAATGTGCGCATCTGGAATAGTCACATACACTACCTGACAAAACTCTTGTCGTCTATCCAAGTTTTAATAACAACAAATAATAACTTGACTTCTAGTTGATCATTTGGTATCAAAAGTGGCTTATATGAAAGGCAAAGCTGCCGTGGAAAAAGAATGAATATTGTGGATGACTCCCATGAGCTTGGAGGACTGCATCCATACATCTCTGCAATGACTCAAATCACTGATTAATAAAGTCATCTGGAATGGCAAAGAAAGCGTTCTTGCAGAACTCTCA
Associated Phenotype:
Not determined