ZMP
im:6907121
Ensembl ID:
ZFIN ID:
Human Orthologue:
RNF121
Human Description:
ring finger protein 121 [Source:HGNC Symbol;Acc:21070]
Mouse Orthologue:
Rnf121
Mouse Description:
ring finger protein 121 Gene [Source:MGI Symbol;Acc:MGI:1922462]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14158 | Essential Splice Site | Available for shipment | Available now |
| sa37383 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14158
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084780 | Essential Splice Site | 173 | 331 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 43316716)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 44756374 |
| GRCz11 | 21 | 44780620 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTTTTTACACGTACAARCTCMCGTCACCTCTGTTTCTGYTTKTA[G/T]GATAAAGSCAGACGATTGCATGGACCTTGGCGTTTCACTTCTCTTCTACG
Long Flanking Sequence:
ACAATGTAACATTTGTAATCTCTGTTTCAGAACAACTGAATCGATTCACAGGTGTGAACACAGTCTGAAAGTGTTTTCTCTCTTTCTCTCTACAGGCTGGTTTATAAATGGTTCCTCCTCTTTTATAAGATTAACTACGGCACAGGCATTGTGGGATATGCTATAGTCATGTTAACCCTCTTCGGCATCAATCTCCTATTTGGGTGAGTTGTAAAATTTCATGTTTTAAAGCACTGAGTTATAGGGGTTACCGATTGCAAAAATGTTTGTTATGAATTTCATTGTTATTATTATTATTATTGTGTTACTACAATATTTTACATGGTCATAACAGCTTTTAATGTGATGATTGCAAAATAAATTTATTCTAAAAACATTGTGCATATGTGCAGGGCCGGATTAAGAACACTTGGGCGCTGGGGCTATAGCAAATCCAAGGGCTCCCCTTTTTTTTTTTTTTTTACACGTACAAGCTCACGTCACCTCTGTTTCTGCTTTTA[G/T]GATAAAGCCAGACGATTGCATGGACCTTGGCGTTTCACTTCTCTTCTACGGCCTGTACTTTGGTGTACTCGGCCGGGATTTTGCAGAGATATGTGCCGATGTTATGGCATCTACAATTGGGGTAAATTCTTCAATCAGTTAGCTTTGACCTTTTTTGATGCATTGCCTGATCTATACGGATCTCGATGCTAGTGCTGGTCAAAGATTAAACAGGACTAATCGCATCCAAAAGTTTGTCTTGACTATACTAAGGTATTATTATTATTATTATTATTATTGTTATTATTATTAAACTTGAACTAGCTAAACATGTCAGGCTAAATAATTCAAATTAATCATTGACTTCTGCTGTCTTCATTAGTTTCAAAAACTCAGATTCCTTTACAATTGAAAACGGCATCTTTGGATTTCTTTTCTGCTGGTGATACTGGTGTCCTAAAAAAAAGTCAAATAAAAAGTAAAATAAATAAAAAAATCGTACATATACCTTAGGAACGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37383
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084780 | Nonsense | 309 | 331 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 43320181)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 44759839 |
| GRCz11 | 21 | 44784085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAGCGTCCGCATATGATGTACGGGCAGCTGCTGGACTGGCTGCGGTA[T/A]CTGGTGGCCTGGCAGCCCATTATCATTGGACTGGTACAACTCATCAATTA
Long Flanking Sequence:
GTCACCCTTTCAAAGTGAATGGGAAGCGTTGACGCTGACGCCCCGTGTGAATGGGGCGTAAGTGCTCCTGTTTCCCCCACAGGCCAAAGACAAATGGTACAGGTAAATTGGGTAGGCTAAAACTAGTCAGCAATCGGCTACTGTCTGAACTGGTGTATTTGCATCTGATTACACCAGCGCTTCCGTCAGCGCTTGAAAAGTTGAGAAATTCCCAACTTCTGAAGCAAGCAACGCCAGTGAAGCAGTTCCGACTGATCCGCAATGCAGTTCAGCAACGCTTGACGTCACCCGTTCAAAATGAATGGGAAGCGTTGTGAATGGGACGTAAGCGAGGTGAGTGATGTGACACCATGCATAAACATGTATTAAACACTTATAACGCTTATATTATAAATAAGCCCCTTTTATTCACACATGTTTGAAAGTAATCTCCTTAACTGAGCCGTCAGATGGGAGCGTCCGCATATGATGTACGGGCAGCTGCTGGACTGGCTGCGGTA[T/A]CTGGTGGCCTGGCAGCCCATTATCATTGGACTGGTACAACTCATCAATTACATCCTGGGTTTGGAGTAACAGAAGCAGAGCAGAGGGACTGTCCTGCCGGAGTGGGTCTGCGGCGATGACATCTCTCCGCTTTCACCAACACAGGGATTTATTATTATTATTATTATTATTGCTTTCTTCAAGGACTGTCCTAATGTGTTAATAATACTGTGCTAATGTGTCTTCAAATGAAATTCTACTAGCAGTCGGATGTTGAATGTTTTCGTTGATTACTTTTGTCTGATATTTGTTTAAGGACTACTTGAAGCTTCCGTCATTTCCCACATGCACATCGGGTTTTATAGAAACAAGAGAATAAATCTGTGCTCGCCGTGAGGAGCACAATGGACCATGTGCTGTTTTATTGGGTAATGAAGGCAGTTAAATGCATTTAAAGCTCAGTTTGATGAACATGTCGTGTAGATTGGAGAAGTTTTATCTGGATGATCGGCACACAATTA
Associated Phenotype:
Not determined