ZMP
zgc:56457
Ensembl ID:
ZFIN ID:
Description:
Nucleolar protein 12 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZWE7]
Human Orthologue:
NOL12
Human Description:
nucleolar protein 12 [Source:HGNC Symbol;Acc:28585]
Mouse Orthologue:
Nol12
Mouse Description:
nucleolar protein 12 Gene [Source:MGI Symbol;Acc:MGI:2146285]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19923 | Splice Site, Nonsense | Available for shipment | Available now |
sa25239 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19923
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055429 | Splice Site, Nonsense | 131 | 228 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 1927193)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 1385405 |
GRCz11 | 3 | 1154054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGACCATCAGCGACCTCGACCTATCAGCAGACAGATTGCTGGAGCCGGCA[C/T]AGGTGAACAGCCAATCATCAACTAGCGAATTATCCAGCACATGACGAGGA
Long Flanking Sequence:
GACAGGTTTCCACAAGAGGAAGCTGGAGCGGCGCAGAGCAGCTCTGGAGGAGATGAAGAGCAAACTGAAGGAGGAGCAGAAACGCCTCAGAGAGGAGGTGAGGAGGAGGAGGAGTGATGAAGATGAGTGAGCTGTGATGATGATGATGATGATGATGATGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTCCTCCAGAGACACAAAGAGTATCTGAAGATGCTGCAGGAGCGACGCCAGGCTCTAGGTGAGTGTGTGTGTGTGTGAGAGAGGTCAGAGGTCATGGCATCATCATATGTTGTGTTGTCTTGTGTGTGGGGTCATGTCGTCATCATGCGCGCGTGTGTGAAGATGAGGCAGACGAGCTGGAGGAGGCGATCACCGCGACCACAGAGTGTGTTCAGTACGATCATCCAAACCACACCGTCACCGTGACGACCATCAGCGACCTCGACCTATCAGCAGACAGATTGCTGGAGCCGGCA[C/T]AGGTGAACAGCCAATCATCAACTAGCGAATTATCCAGCACATGACGAGGAGTCCAGCCTGATTAACTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCCAGAGAGATGGAGGTGATGGTGAGGAGCGAGAGAGAACTGAAGCTCTTCCCAAGCAGGCTGGAAACCCTCTGCTGTCCAAGAAGTATGACTGATTGATTATTGATCGAGTTGTTCCCTCACTGACTATGGAATAAAATCGCTGCCATAAATATTTTGTGTGTAAATCAAATTCCCGCATCTGTAATTATAAACCGTAAAGGGAAGCGGAGCGCACTGCTCATGTTACGAGCACACAAATCCAGAGTCTTTATACACGTTTAAACATGATATTACTCACCAAATATTTATGGCAGTGCTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25239
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055429 | Essential Splice Site | None | 228 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 1928569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 1386781 |
GRCz11 | 3 | 1155430 |
KASP Assay ID:
554-7434.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATGACTCGCTGAATCAATGACTTGCTAAATCCATACTCAATAAATCG[T/A]TGACTCGCTGAATCAATGACTCGCTGAATCGTTGACTCGCTGAATCAATG
Long Flanking Sequence:
TGTGTGTGTGAGAGAAAGAGGTGTGCGTGTGTGTGTGTGATCAGTGTGTGTGTGTGTGTGTGTGGGATCAGTGTGTGTGTGTGTGATCAGTGTGTGTTGATTGGCTCCTGACTCCCGCTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGGATTCAGAGCCTCACGGCGTCCCTCAACAGTCTGGTTAAACAGAAGAAGAGGAGAAAACAGAAGCGGAGACAGGAAGCCAAGCAGAGGAGTCATCAGAGCGACAGGAAGTCGTCATCATCAGCATTCGTCCACAACAACAAGCAGAAACAGGGCAAGAGCACCAAGAGGCAGCGGCGCAGGCAGACCGGCCGCAACGAGCGCAGTCAGGACTGAACAGTCACTACATCAATGACTCACTGAATCAATGACTCACTGAATCAATGACTCGCTGAATCGTTGACTCGCTGAATGAATGACTCGCTGAATCAATGACTTGCTAAATCCATACTCAATAAATCG[T/A]TGACTCGCTGAATCAATGACTCGCTGAATCGTTGACTCGCTGAATCAATGACTCATTGAATCAATGACTCGCTGAATCGTTGACTCGCTGAATCGTTGACTCGCTGACTCGTTGACTCGCTGAATCGTTGACTTGCTGAATCGTTGACTCGCTGAATCGTTGACTCGCTGAATCGTTGACTCGCTGAATCGTTGACTCGCTGAATCAATGACTCGCTGAATCAATGACTCACTGAATCAATGACTCTCTGAATCCAGACCCACTGAATCGTTGACTCGCTGAATCGCTGACTCGCTGAATAAATGACTCACTGAATCGTTGACTTGCTGAATCAATGACTTGCTTGTTCAGGCTCACTGAATCAGCCCAGTGTTAAACTCTGAGCTCTCAGCGTTCACCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCATGTTGGATATCTTCAGAAAATGAATCAGTTCTTCAGT
Associated Phenotype:
Not determined