ZMP
nomo
Ensembl ID:
ZFIN ID:
Human Orthologues:
NOMO1, NOMO2, NOMO3
Human Descriptions:
NODAL modulator 1 [Source:HGNC Symbol;Acc:30060]
NODAL modulator 2 [Source:HGNC Symbol;Acc:22652]
NODAL modulator 3 [Source:HGNC Symbol;Acc:25242]
NODAL modulator 2 [Source:HGNC Symbol;Acc:22652]
NODAL modulator 3 [Source:HGNC Symbol;Acc:25242]
Mouse Orthologue:
Nomo1
Mouse Description:
nodal modulator 1 Gene [Source:MGI Symbol;Acc:MGI:2385850]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26716 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33836 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7035 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10937 | Nonsense | Available for shipment | Available now |
sa15655 | Essential Splice Site | Available for shipment | Available now |
sa26715 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26716
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112867 | Essential Splice Site | 85 | 1217 | 4 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 16699170)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 16590233 |
GRCz11 | 6 | 16717173 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTGTGCACCAATCAATGGTTACTTCATGATCCCACTGTATGACAAGG[T/C]ACAGTAACTCACGTACTGGAATGAATGGATTGACTGGGTGGATTATCAGG
Long Flanking Sequence:
CTGTTTAAAAATGATTAGTGGCTAGCTACGTTAGCGCTTGGCGTTCCGGAAGTGAATTGATAGACCGATCTGTATGTCATCTGCTGCCCTAAACAGTGATGCATTTAGGTTGTAGATCGCATAATCTGGTGATCCGTCTGTAGCAGGTTGCGTGACGGCTACCTAACCAAACTGTCAAGCATTGTCAGCAAAACACATGATTTGTCCAAGCTTGTGTAATTAGCTTTGGCTAACGTTAATCACTTTAAGATTCCATACAGTCTGACGACCAGTACAAGAAGCTCGTTGTAGTAATAGTGATGTTGTTGTTTCATTTCGTTATGTATGTGTTACTAAATAAGTATGATTTTAAAGGTAACACCGTTACATTGTCAAAAAATAAAATGTATTACTTATGTGTTCATTACAGATAAAGTTGTACACCAAGCAGGGTTCTCTGAAATATCAGACTGACTGTGCACCAATCAATGGTTACTTCATGATCCCACTGTATGACAAGG[T/C]ACAGTAACTCACGTACTGGAATGAATGGATTGACTGGGTGGATTATCAGGCTTTCAAGGTCATTTAAGAATGTCCTGCAACATGTAGTTTATACAGAATTATAAGCAATTGTTTTCTTATAGATCAAATAGATTTTACACAAAATAAAGAAGACTTTTCAGATTGTTTTTTAAAGACATAAGGTAATGTAGTCCAATCTGCATGTTTCCTGTTTTGTCTGGTTAAAGGAATTAGTAAACAAAGGCAAACTATCTTCTGTAAAAATATTATAGTTGGTTTTACATTCGACTGTCTTCTTAATATTGTATTTTCAGTAAAGTATTACTTGCATATTCTTTATAGGGAAATGATATTAGCAGCCAAAGACTAACAAAGTGCAACATTGTTCAGTCAATGAAATAGTGCTAATGTTGTTTTGAAGACATACTTGCATGCTTTTTCTGACCGAATATTCAGTTGCATGGTAAACAATATAGTGACAAGTTGTCACTGAACAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33836
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 |
---|---|---|---|---|---|
ENSDART00000112867 | Nonsense | 425 | 1217 | 14 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 16682787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 16573850 |
GRCz11 | 6 | 16700790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGTGTTTGTGGTCACATCTCCGTCACCCGTCTTCCAGAGACTGTTAAA[C/T]AGCTTGGACGCTACAAAGTTACACTTTCGGCTCAGAGGCAGGATCAGGGA
Long Flanking Sequence:
CTCTGCCAGTGAGACGAAAAGTTTCTTGAAGGGGGCGGGGCATGTCAGATAATAGGGAGTATTTTATTGGTCAAAATTTGATCAGAAACCGTATTAGGAAGTGATGTGAAAAATGTTTTATCTATTTAGATAAGAGTGACAAACTGCAAGCTTTGTATGTTTATATCTTCTACAAGCAAGTTTTGTCACTGTGTTATAGCACTCTAGCTTAAGTATATCTTTAAAACTAACATGCAATTATAAATAACAGAATAAAATGTTCCTATTAAATTAAAGTCTTCTGCATTATTATGCATTAATTATGAATTCAGTTTACTGTAACTTAACCTTTTGTAGTATTAAATCATTAAGGAAAATGAATGGAAACTGCTTTACAGACATACTCTAGTTTAAGTCTTCTGGTTTCATCAGATTGTTCTAAACCTTTTCCCAACTGTTTCATTTTTAGGTTTAGTGTTTGTGGTCACATCTCCGTCACCCGTCTTCCAGAGACTGTTAAA[C/T]AGCTTGGACGCTACAAAGTTACACTTTCGGCTCAGAGGCAGGATCAGGGATTTTTCCGGACTGTGGAAAGTGACAGTCATGGAGCGTTCTGTTTTCAGGTTAAACCAGGAGACTACAGTGTGCAGGTAAAGAGAAGTACAGTGCTCAGCCTAAATGAGTACACTCCATGTTGAAAATAATTATATTGATCCATTTCTCAGTGAATGAAGGTTATGTTTTTTGGGGGGCAAAACAGATGTACTAAATAGATATAAAAAAATAGTCACCAAACACTTTAGAAACAGAAAGAGAATTAATTTACATTAAAAATATAACCAGCCATCAAATATAAACCACTGAATAATTCTTCAAAAATGGCACATATAGCAGTGAAACATCAAATTTTATGAGGGAATAACTGAATCATTTATTAAAAATGAGATTAAAAAAATAAATAAGGGTTGCACAAGTTATAATGTTAGATTTCTACATTCAGCGTCATCAGCAACAATAGTAGTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7035
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 |
---|---|---|---|---|---|
ENSDART00000112867 | Nonsense | 635 | 1217 | 19 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 16677988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 16569051 |
GRCz11 | 6 | 16695991 |
KASP Assay ID:
554-4969.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTAGAGACTAAAGTATGTAACTTACTACTGTKTAATTAAAGGTGTYTA[T/G]AAAGTGACTCCACGCTCCTGTCACCAGTTTGAACAGGATTACTACACCTA
Long Flanking Sequence:
TATTATGATTTTGGACCAAGTCAGGCAACCTTTCAGCAGTACAGACTTTTAGTTTAATAAAGAGATTAACATCCTCTTGTTTTCACTAGTGTCTATCACCCAAGAAGAGTGGTGCTGGAAGCATAAGTCAGTGGAGATCGATGTACTTGACTCGTATGTAGAGGGAGTGGAGTTTCGACAAACTGGATACTTACTGCGCTGCTCACTGTCCCATGCTATTACACTGGTAAAACCTAAAACTTGATGAACATATTTTGCAGAATCACCAGTTACTTGTCTAATATTGTAAAGCAAATAATAATGCATTATTTGTACAAAACTTTAGGAATTTTTCCAAGACGGCAGTTTACCAGAGAATGTTGGCGTTTACAATCTGTCCAAAGGAGTCAATCGTTTCTGTCTGTCAAAGCCTGGTGAGCTCAGTAATTCCTTCAATTTAGTTAAGTTTAAGTTTAGAGACTAAAGTATGTAACTTACTACTGTTTAATTAAAGGTGTTTA[T/G]AAAGTGACTCCACGCTCCTGTCACCAGTTTGAACAGGATTACTACACCTACAACACGTATGTTATTTTAATAACATGAAAGCTTTTGCAGTATGTAGCATTATTAAAGAAATTCTAATCCACATGATTTGACTTTCTTTCTGTTCCATAGGTCTGCCCCAAGCATCTTAACTCTGACTGCTGTCAGACACCACATGACAGGACTTATAACCACTGATAAGATGTTGGATGTCACAGTCACCATCAAGTGAGTGAGAACATTGTTATATTTTTTTCTGTAAAAGAGTGAAGCATATATTTTGTCTTTTGTAGCTTTTATGTTTCTCCTCTAGTTAAACACTCACTTATGGCCCGTTTCCACTGAGTGGTATGGTGTGGTATGGTTCGGTACACTTTTATGGCCGTTTCCACTGTCAAAAGGTACCAAAAAGAGAACCGCACCGTACCACTTTTTGGTACTTTTACAAAAGGGTACCTAGTACAGCTGCACGACTCTGGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10937
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112867 | Nonsense | 746 | 1217 | 21 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 16673823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 16564886 |
GRCz11 | 6 | 16691826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCCCCCTGTGGAAGAGAAACCAGAGGAACTTCGTGAGCCTTTTCACTA[T/G]GAATTCTCCTATTGGGCACGGTAGGATAATAGGAGAAAGCTTGTCATTGT
Long Flanking Sequence:
GGTCAGCTGAAGTATTTAAAACTTTCATGTGAAAGGCTTAAATTAACTGCGGCCGAACAGGGTCAACTTCCCTTTACAATGAAAAGCACTTTGGAACTATTCTCCAGCAAGTCCTATGTTGTGACTTCCTTATCCTGAGTAAAGTGCTTTGATGGATGTAATATCACTCTCACCATTGTGTGTTCATGCTTATGTTTGCATATGAGGAGTTCCGCCCTTTATAACATCAGCTAGTTTTGAATTTAGAAGCAAGTAAGATTTTTAATGAGAATCCTACTCATTAACATTGTAAATAACTTTGCTGGCTGTTATTTTGGCAGATCCTCTATTGAGAGTGAGCCTGCTTTGGTTCTGGGACCTCTACGCTCAAATGAGGAGCAGCGAAGGGAGCAGCAACTTCTGGAAATAGCTGCCCGTAAAAAAGAGAGAGGAGAAGCAGGCGATGAGAAGAGCCCCCCTGTGGAAGAGAAACCAGAGGAACTTCGTGAGCCTTTTCACTA[T/G]GAATTCTCCTATTGGGCACGGTAGGATAATAGGAGAAAGCTTGTCATTGTAGAATTGTACATCCAAAGAATTTGTCTCTTCTGTCAAGTGCAATTATTTTTGTGATCTTAACTTTATATATTGGTGGCATGTGCTGTTTTAGGGCTGGGGAGAAGATCACAGTCACACCTTCATCCAAAGAATTTCTGTTTTACCCTCCTGAAGTAGAGGCTACAATCACTGGTGGTGAGAGTGCAAACTTTGTTTTAAAGGAATGAATGAACTCAGTTGGCTTCAACAGTATAGTACCTTATTAGTTCCAGGTTGGATACTCTTTTGCCTTTAGCTCTGCCTTAATTATTTTTGGCCTAGATTTAAGTGTGCCACAGAATGGATGAGTGTGTATAGCTAGGCATAGTTGAATAATAAGACTTCACTACAATGAAGTTACATACTGTGAGCTTCAAACACACTTGTTCCCTCCTCCCTTATGTAACTCCTGTTTTAAACAAAACACCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15655
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 |
---|---|---|---|---|---|
ENSDART00000112867 | Essential Splice Site | 780 | 1217 | 22 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 16673597)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 16564660 |
GRCz11 | 6 | 16691600 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAGAATTTCTGTTTTACCCTCCTGAAGTAGAGGCTACAATCACTGGTG[G/A]TGAGAGTGCAAACTTTGTTTTAAAGGAATGAATGAACTCAGTTGGCTTCA
Long Flanking Sequence:
TCAGCTAGTTTTGAATTTAGAAGCAAGTAAGATTTTTAATGAGAATCCTACTCATTAACATTGTAAATAACTTTGCTGGCTGTTATTTTGGCAGATCCTCTATTGAGAGTGAGCCTGCTTTGGTTCTGGGACCTCTACGCTCAAATGAGGAGCAGCGAAGGGAGCAGCAACTTCTGGAAATAGCTGCCCGTAAAAAAGAGAGAGGAGAAGCAGGCGATGAGAAGAGCCCCCCTGTGGAAGAGAAACCAGAGGAACTTCGTGAGCCTTTTCACTATGAATTCTCCTATTGGGCACGGTAGGATAATAGGAGAAAGCTTGTCATTGTAGAATTGTACATCCAAAGAATTTGTCTCTTCTGTCAAGTGCAATTATTTTTGTGATCTTAACTTTATATATTGGTGGCATGTGCTGTTTTAGGGCTGGGGAGAAGATCACAGTCACACCTTCATCCAAAGAATTTCTGTTTTACCCTCCTGAAGTAGAGGCTACAATCACTGGTG[G/A]TGAGAGTGCAAACTTTGTTTTAAAGGAATGAATGAACTCAGTTGGCTTCAACAGTATAGTACCTTATTAGTTCCAGGTTGGATACTCTTTTGCCTTTAGCTCTGCCTTAATTATTTTTGGCCTAGATTTAAGTGTGCCACAGAATGGATGAGTGTGTATAGCTAGGCATAGTTGAATAATAAGACTTCACTACAATGAAGTTACATACTGTGAGCTTCAAACACACTTGTTCCCTCCTCCCTTATGTAACTCCTGTTTTAAACAAAACACCACTGAAGAACAGACAAAGCCATTTCTTTTTAAATTGAACATTTCATACTGAGATAACAGCATTAACAATAATTTAGCAATCATTGTTGATTATTGCAATAATGTTAACTGTAGTTGATCCTTGTACTATTCAAATGTACTACCCTTTTGTTATGTTGATGGTTGTTTTCGCTCCATTGACTTCCGTTATAATGACATTGTTTGATTGCAAAGCCATGACACCATATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26715
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 |
---|---|---|---|---|---|
ENSDART00000112867 | Essential Splice Site | 1032 | 1217 | 28 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 16666140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 16557203 |
GRCz11 | 6 | 16684143 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGAAATGATCACATAGAGAGAGCATTGCCACCACACAAGACAATTGAG[G/A]TGAGCGTTCACATTTATACAGTATTCATCTTAGTTTTGGTTTAAACCTCA
Long Flanking Sequence:
ATAAATGCTATTGTTCATTATTAGTTTACGTTTATAAATGTATTTATTGATGCAACCTTATTGTAAAGTGTTACCAAGCAAATAAAGGTAACTTGCACTTTTCAAATAGATATGAAACAGCACAACAATTTTTACCACTGAAAATAATAGTAATAATGTTTCTTTAGCAGCAGGACATAATTTTAGAATGATTTTTGAAGGATCATGCTGCTGAAGAAATGAAAATGATGTCTTTTAAACTGCATTCTTTTTATATTGTAATACTTTTTTACAATTGTACTGCATTTTGATCAATGAAAGTACAGCCTTGGTGAACAGAAAGTCTTCTTTGAAAGGAAAAAGCTACCGATCTAAAGCATTTTTTTGGTAGTCTACATGATTTTGAACAAATTTTGCCGTCTGATGTTTGTTGCCAGCCTGGTTGTAACTACAACATTCAGCTGAGAGGAGAGGGAAATGATCACATAGAGAGAGCATTGCCACCACACAAGACAATTGAG[G/A]TGAGCGTTCACATTTATACAGTATTCATCTTAGTTTTGGTTTAAACCTCATATTTAAAGTTTTTATTTATGTGTAAATATTTTTGGGATTCTTTTAGGTCGGCAACACCGATATTGATGGAATCAACATAATCGCCTTTAGACAGATCAATCAATTTGATCTGAGTGGAAATGTCATCACTTCCCCTGAGCATCTTCCCACTCTATGGGTAAGTGCAATACAACTTGAGGAGTTCAGATGCAAAAACCTCTAAGTGTCATCTAAAATGTTCTTCTAAACTGAGCATTTTTTACAAGCTCCTGTGTATAGGTTCAGTATTTTCACTGTTATGGCAAAGAATAATTTATTTTCATTGCCTTTAAAAGTGAAATAACTGAAAATGATTTAAGTGTAATATCTAAACATAAACATAAAGAGGCTGAGAAAAATGCTTATTCTAGACATGTCTCTCAGTGGAGCAAACTTCCGCTCAAACCTGCTCAGTCAGGACACTGGACCCC
Associated Phenotype:
Not determined