ZMP
nom1
Ensembl ID:
ZFIN ID:
Description:
nucleolar MIF4G domain-containing protein 1 [Source:RefSeq peptide;Acc:NP_001038297]
Human Orthologue:
NOM1
Human Description:
nucleolar protein with MIF4G domain 1 [Source:HGNC Symbol;Acc:13244]
Mouse Orthologue:
Nom1
Mouse Description:
nucleolar protein with MIF4G domain 1 Gene [Source:MGI Symbol;Acc:MGI:1861749]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa8417 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31587 | Nonsense | Available for shipment | Available now |
| sa40973 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8417
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 |
|---|---|---|---|---|---|
| ENSDART00000084153 | Essential Splice Site | None | 487 | None | 12 |
| ENSDART00000115152 | Essential Splice Site | 343 | 835 | None | 12 |
| ENSDART00000142315 | Essential Splice Site | 106 | 598 | None | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 42045958)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40382268 |
| GRCz11 | 7 | 40653285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTGAGCTGGAGAAGCTGAAGCGCAGTGTGAAAGGTCTGATTAACAGG[T/C]AAGGTGTCACAGAGATNNTAACTTGATTAATGCATTTTAAAGAGGCTTTGTT
Long Flanking Sequence:
CAAATTACAAAAAATGAATTACTGCTCGTGCGAGGCGTTTTTAATGCGGCGTCTGTTGGGCTGAGAGTAAATTTGACCTTATTCTCTCCTCTGGCCGTCATCAGTCTCACACTATTTTTTTACTTTTTCTAAAGGTCTTGATTACACCATCGTGGAGTTTTTCTTTTTTTAGCAAATAGGCTTGTAAAAAATTATTAGTTGTACTCTCCCATTCGCTGCACTTTTCAGTTCACCCAACTATGACGCTTTCCGCTACTGAGAAAACTGAATACTGAAAAGGGTCTATAAGTGCATTATCTGCTCATAATGGTGCATAAGGACACAAACCAGGATACACCTTATACTTTGAAGCTAATATCAGTTATTTGGTCTTCTATTTGCTGTAGAATCCTGCCACAACTGGCAAGTATGTTCCACCTCACCTGCGAGAGGCTGCAGACAGCAAACGCAAAGCTGAGCTGGAGAAGCTGAAGCGCAGTGTGAAAGGTCTGATTAACAGG[T/C]AAGGTGTCACAGAGATTAACTTGATTAATGCATTTTAAAGAGGCTTTGTTTTTAAAAGCATTTAGTGTCGTTGACTTCACCAGTTTGTTGTTATTTGATGGCTCTGCCCTCTGCTTGGCAGGTTGAGTCAGCCCAACATGGCGTCCATCAGCAGTCAGTTGGAAGAGCTGTACATGAACACCAGCAGGAAGGACATGAACGATACACTCACTGACATTCTGCTGGCTGCCTGCGTCACGCCTGCTCTCATGCCAGAAAGGTCTACACTTCTCATAGTGATTTTATTATATAACTCAATTTATTTATGTTGACCTGTTCACTCACTGATGTTCTATTTTAACTATTTGAGTAAAGAGCTTTCAAGCTGCATCCACCACATTTGAGACAGATCTTCAGACTGTTCTGACCTGAGCATGGGGACCTTTAAATGACTTTCCAAATGTTAGCTTTTATCAACAGTCTGGGTGCATCAGTTATAAAACTCAAATTCAGAGTAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31587
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 |
|---|---|---|---|---|---|
| ENSDART00000084153 | Nonsense | 311 | 487 | 9 | 12 |
| ENSDART00000115152 | Nonsense | 659 | 835 | 9 | 12 |
| ENSDART00000142315 | Nonsense | 422 | 598 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 42041546)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40377856 |
| GRCz11 | 7 | 40648873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGACAGTGGATTCTTAATTCTTTCTCAGGTTAGGATTGAAAGACCAG[C/T]AAGAGCGGGAGATTGTTCATGTTTTGATGGACTGCTGCCTGCAGGAGAAG
Long Flanking Sequence:
GCTGGAGCTTGCTCGTAAACAAAGAATGAACACTGACGTCAGGAGGAACATTTTCTGTGTTCTCATGTCAAGTGAAGACTTTTTGGATGCGTATGAAAAACTATTAAGGTCTGTCAGTGTAGTTTCTGTTTTTTTCTGATTACTTATTAGTGACAGGCTCTGTCTTAATTAAAAGTTTATTTATTTTATTTTCAAAATTTATTTGAATTTTTTGTATTTTTACAGAAAGACAAACACAGTTCGTGATAAAAGGATGCTAAATAAATGTATATTCAGTAATGCATAGTTTATGCAGATGTTTTAAAAGAGGGAATAGAAACAAATTTTTTGTTTTTCAGCCATTCTACTTTAAAATAAAAACAGGATCAGCAGTATGCAAAGTTACAAGCATTTGTTTTTGACCACGAAAATGTGTAGAATTTAATAAGATAAAGACAAATTAAGATAAAATAAAGACAGTGGATTCTTAATTCTTTCTCAGGTTAGGATTGAAAGACCAG[C/T]AAGAGCGGGAGATTGTTCATGTTTTGATGGACTGCTGCCTGCAGGAGAAGATGTTTAATAGATTTTATGCTGTTCTGGCTGAGAAGCTTTGCTCACATGATCGGCGGTTCCAGGTAGAGTAAAAAAGCAGTGTTTCCCTCTTCTCTGTCCGCGTTAGACAGATTTCTGGTTTTAGTTGGTGTCACTGATTTTACTGCATTTAGAGCGGAAGCTTGTGCTTTCTATATTCAACTTGGAATGTCTGCACAAAAACTAATGGTCAAACTATGAATAATTATATATTTTTCAATACTTTGATGCAGCCGTTAAGTTAAAAAAATATATATATATAGCTTTATGAGGCAATGATTATATCAAAAGTAAAACCTGGGAGACTGGTTCCTTCATGGTTCCATCATGATGAAAATTCTGACTTTCGTGTAATTGATAATTAAATATTTTGTTCTACAACAAAAACTAAATAGACTCAAACAAATATTCACATTTTTGATATGTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40973
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 |
|---|---|---|---|---|---|
| ENSDART00000084153 | Nonsense | 325 | 487 | 9 | 12 |
| ENSDART00000115152 | Nonsense | 673 | 835 | 9 | 12 |
| ENSDART00000142315 | Nonsense | 436 | 598 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 42041504)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40377814 |
| GRCz11 | 7 | 40648831 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACCAGCAAGAGCGGGAGATTGTTCATGTTTTGATGGACTGCTGCCTG[C/T]AGGAGAAGATGTTTAATAGATTTTATGCTGTTCTGGCTGAGAAGCTTTGC
Long Flanking Sequence:
GAGGAACATTTTCTGTGTTCTCATGTCAAGTGAAGACTTTTTGGATGCGTATGAAAAACTATTAAGGTCTGTCAGTGTAGTTTCTGTTTTTTTCTGATTACTTATTAGTGACAGGCTCTGTCTTAATTAAAAGTTTATTTATTTTATTTTCAAAATTTATTTGAATTTTTTGTATTTTTACAGAAAGACAAACACAGTTCGTGATAAAAGGATGCTAAATAAATGTATATTCAGTAATGCATAGTTTATGCAGATGTTTTAAAAGAGGGAATAGAAACAAATTTTTTGTTTTTCAGCCATTCTACTTTAAAATAAAAACAGGATCAGCAGTATGCAAAGTTACAAGCATTTGTTTTTGACCACGAAAATGTGTAGAATTTAATAAGATAAAGACAAATTAAGATAAAATAAAGACAGTGGATTCTTAATTCTTTCTCAGGTTAGGATTGAAAGACCAGCAAGAGCGGGAGATTGTTCATGTTTTGATGGACTGCTGCCTG[C/T]AGGAGAAGATGTTTAATAGATTTTATGCTGTTCTGGCTGAGAAGCTTTGCTCACATGATCGGCGGTTCCAGGTAGAGTAAAAAAGCAGTGTTTCCCTCTTCTCTGTCCGCGTTAGACAGATTTCTGGTTTTAGTTGGTGTCACTGATTTTACTGCATTTAGAGCGGAAGCTTGTGCTTTCTATATTCAACTTGGAATGTCTGCACAAAAACTAATGGTCAAACTATGAATAATTATATATTTTTCAATACTTTGATGCAGCCGTTAAGTTAAAAAAATATATATATATAGCTTTATGAGGCAATGATTATATCAAAAGTAAAACCTGGGAGACTGGTTCCTTCATGGTTCCATCATGATGAAAATTCTGACTTTCGTGTAATTGATAATTAAATATTTTGTTCTACAACAAAAACTAAATAGACTCAAACAAATATTCACATTTTTGATATGTGATTTGCTTTATTAATGATAATTTTAATAAATAATTATTTTTTTTAT
Associated Phenotype:
Not determined