ZMP
esf1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC326718 [Source:RefSeq peptide;Acc:NP_956039]
Human Orthologue:
ESF1
Human Description:
ESF1, nucleolar pre-rRNA processing protein, homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:15898]
Mouse Orthologue:
Esf1
Mouse Description:
ESF1, nucleolar pre-rRNA processing protein, homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19593 | Nonsense | Available for shipment | Available now |
| sa38297 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19593
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 |
|---|---|---|---|---|---|
| ENSDART00000033047 | Nonsense | 44 | 517 | 5 | 14 |
| ENSDART00000146612 | Nonsense | 284 | 757 | 5 | 14 |
The following transcripts of ENSDARG00000008740 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 51724987)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 50571484 |
| GRCz11 | 1 | 51215283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTCAGGTCTATCCGTCTGAGTTTGGGAAGGAGAGGATTCACGCTGAA[C/T]AGACTCAGGGTCCACTGGAGCTCAGCAGCCTCCCAGAAAACCCTGACGCA
Long Flanking Sequence:
CTGTGAAAACGTCCTTGCTTTGTTAAACATCGTTTGGAAAATATTTAAAAAAGAAGAAAAAAAAAAATAAAGGGGGCTAATAATTCTGACTTCAACTGTATATTGCATTAGTAATAAAATGCAATATATACTATTGAACATATAAATTTATTACAGAAATTGAGCGATTTATAAAATAATACAAATAAACAAACTTTTGTCTGTGTAAGTTTTTCGATTTTTGCTCAGAATTTGTGTATTTGTAATCTTCTGTGTGTCTGTTTAGACGTCCCGGCGGTTGGCGGTCTGTAACATGGACTGGGACCGACTGAAGGCTAAAGATCTCCTGGCTCTCTTCAACTCATTTAAGCCCAAAGGAGGCGTTGTGCTGTCCGTGACGGTAACTGTTCCTTCACCTTCTCCCACAGCCTCACAATCAGCTCAGTCAGATGTGATTCTCAGTTGTGTTGTTTTGTCAGGTCTATCCGTCTGAGTTTGGGAAGGAGAGGATTCACGCTGAA[C/T]AGACTCAGGGTCCACTGGAGCTCAGCAGCCTCCCAGAAAACCCTGACGCAGACACTGATGAGCAAAGGTAAAGGACACACACTCTATCTTTCTGTCCTCCTAGTGTGTTAAAGGGGTAGTTCACCCAAAAATGTTAAATTTGCTTTTATTATTAATTTCTCACCCTCATGTCATTCCAATCCCCTGAGATCTGCGTTTGTTCTAAAAGATAAGATATTTGACATGAACTCAGAAAGCTCTCGTCCTCTATAGAGAGCAGTGGTTCTGAGAAATCCAGAAAATTAAAGGTTCAAAACTTTCAATGTGACTTCAGTGGTTCGACTGTAATCATGCAAACCAGTTTGTGTACAAAAAAACATATAAAAATCACTCTGTGCACCAATATCTGACTTTTAAAGCAATATGTTGCATTGGCCATAGTAAATGCAAACTCTGACCTAATGAACAAAGATGTTGTTTTTCCGTTTTATTTTGGTAAACCAAATTTTTATTGGAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38297
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033047 | Nonsense | 356 | 517 | 12 | 14 |
| ENSDART00000146612 | Nonsense | 596 | 757 | 12 | 14 |
The following transcripts of ENSDARG00000008740 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 51714196)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 50560693 |
| GRCz11 | 1 | 51204492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACAAAGAGAGCAAGAAGAACAGGAAGAAGGAAGAGGAGCGGACGCCA[G/T]AAGAACAGGAGGAAATGGAAAGGCGGAAGGTGCGTTTCTCTAATCCACAA
Long Flanking Sequence:
CTGCTGATAAAAGCATGAACAAGTTTTTCTAAATCTTCACTAGAAACAAAGCATCTGATTCTTGCTATGTTTTTGAGATGATAGTATGCTGATTTACTGACTGCTTTGACATGACTGTTGAAACTCAGATCTGACTCCAGAGTCACACCAAGATTCTTGACCTTATTTTTTGTCGTTTGACCTTTAGTGCCAAGGTACATCAACATACAGAAATAAAAGTCTACGCAACTTCAATTTCATACAGAGTTTTAAGGGATAGTTTGCCCCAATATTAAAATTGTTACTTTCTCACCCTTCATTTTGAACTCTGGAAACCCCTAACCATTGACTTCCATAGTATTTCTATTTCAATTTAAAAAATGTATTCTGTAAAAAAAACTCAGAACTTTGAACTTGATAATGAAGGATCCCTTTAAATGAGGATGACTCTTGTCTCTGCAGCGTCCCTGAAAAACAAAGAGAGCAAGAAGAACAGGAAGAAGGAAGAGGAGCGGACGCCA[G/T]AAGAACAGGAGGAAATGGAAAGGCGGAAGGTGCGTTTCTCTAATCCACAAGTGTGTTTGTGGGTAATAATGTCATGATTAACTAAATGGAATGGGATGAATGTATAAACAACAAATTTTATGAAGTGAATATGAATTATTACCATTTGGAACATGGACATGACTTGGTTGTACATACAAGATTCCTCAAGATTCATACTTATTGAAAGGTCGAAGAGAAACCTATTTATAAGTTTTGTAAGAATATTTTGATGATAAAACATATTTTAATACAATGTATATTTGTAAATGGTATCAGATATTGTTTTTATTCATGAAATATTTGAAGAGAAATGTTTTAAAAGGTGTCTTCTGCAGGAATTGTACAATATAGGACAAATTGAAAGTCCTTATTTGACCTTTCTGCGTTTTTATTTTTATGTTTTGTTATGATAGCAAATCAAATATTGAATACTGAGTACAAGTGTGGTCATGAATATAGCCAGCGCTGCTGATATGGCA
Associated Phenotype:
Not determined