ZMP
si:ch211-208m13.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ring finger protein 123 (RNF123) [Source:UniProtKB/TrEMBL;Acc:A5
Human Orthologue:
RNF123
Human Description:
ring finger protein 123 [Source:HGNC Symbol;Acc:21148]
Mouse Orthologue:
Rnf123
Mouse Description:
ring finger protein 123 Gene [Source:MGI Symbol;Acc:MGI:2148796]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39382 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39381 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa45777 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39382
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044429 | Nonsense | 316 | 789 | 9 | 22 |
| ENSDART00000148147 | Nonsense | 209 | 681 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 22 (position 37385244)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 34554744 |
| GRCz11 | 22 | 34529651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTGAACCACCTGAGTCGTAGGTTGGCCTGGATCAACGCCACCATCTA[C/A]TCCAAGGTATCGCTGACACTCTGGCCAGAAAAACACTGGGAAACAGTGGA
Long Flanking Sequence:
ACCTTTATGTGCATTTTTTTAAATATTAAAATATATATTATTAAAATTTAACATTTTGTATGCATATATATATATATATATATATATATATTAGGTTTTTTTTTAAATAAAATGATGTAGAAAAAAATAATAGAATGCAAAGGAAATGTTTAGCTAATAAATAAAGCTTTAAAACAAGCATTTTCTCTAGAAAATCAGTTTGGCCCATCAAAAACATTTAGAGAGTGAGGTGGGCCTCGAATTGAAAAACCCCTGTGTTAAGGCATACATGTATTGAAACTCAAGGTTTCCTTTAAGAAGCTTTGCAGTATTTTTATTGTTGCTTTTTTATTCTATTATTTTTTGTTTAGTCTCTTTATTTGATCAATGTTTATGTGAGTGTGTTATTTCGTTTGGCAGAGGCCGGATATTCTCGAAGAGCTGCAAAAGAGCCAAAAGGTGTTTGCAGAAAAGCTGAACCACCTGAGTCGTAGGTTGGCCTGGATCAACGCCACCATCTA[C/A]TCCAAGGTATCGCTGACACTCTGGCCAGAAAAACACTGGGAAACAGTGGAAGGCAGCTGTCATTTTTGTGTGTGTCCTGCATGATTTACTTTAATTTTACAAGGTAACACTCAGTGTGAGGTGCTGTAATGAGTTTTGACGATGTGCCCCATAAAAAGCCGACATTTAAGTTAAAGTTGGAATGGCTATTTCATTTTTATTTTATTTTATTTTATTAATTTTTTTATTAACTGTGTTTTTATTAAAGTTTTTATAAATATAGTATACAAATAACATTTACTTAGATTTTACAATCACCAAAAAAGGAAACAATTAGAAAGAAAATAATAATAGATATAAATTATAATAATAGATAAATAATAGTGACAGCTTGAACACAGTGTGAGGTGCTGTAATGAGTTTTGATGATGTCCCCCATAAAAAGCCGACATTTAAGTTAAAGTTAGAATGGCTATTTATTTTTTATTTAATTTAATTTAATTTAATTTAATTTAATTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39381
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 |
|---|---|---|---|---|---|
| ENSDART00000044429 | Essential Splice Site | 536 | 789 | 15 | 22 |
| ENSDART00000148147 | Essential Splice Site | 428 | 681 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 22 (position 37359950)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 34529450 |
| GRCz11 | 22 | 34504357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCAGCTCAACTGGGCCTTCTCTGAATTCATCGGCATGATACAGGAGG[T/C]AAGAAGCTTTCGAATCTTTCAACGTGTTAGACAAATAGCCTCACCTCAAA
Long Flanking Sequence:
CCATTACCCCCCCACCACCCCCCCCCCCCCCCCCAACACACACACACACACACACACACTTTTCATAAACATTGCGCTTCCTGCCCTTGCCTACAAGTACGGGAACTGTGACAGTGAAAACGCAAGCCTGATCTGGGTGGCCCATACCAAATAGGTTCTGTTCTAAACTGTACCATACTGCTCAGTGAAAATGAGGCATAAGGTCACTGTACAAACTCCACTTGAGGACAAAATTTACAGAAATTTGTGACCTTTTTTATTGGCAATATGACCATTGATAGCTATGCATTAAAAGTATTGTCATGGTGAAGATGTCCTTGCTAAATACATGTCTTGTTGTTTTCTCTGATTGGCTGTAGAGCCCTGTCCATCCCTTCTGCTGCAGAGGCACATGGCTGAACTCCTCATTCAAGACAGAGACATGGCTGCCAGTTTCCTCAATAGCGTCTTAAACCAGCTCAACTGGGCCTTCTCTGAATTCATCGGCATGATACAGGAGG[T/C]AAGAAGCTTTCGAATCTTTCAACGTGTTAGACAAATAGCCTCACCTCAAACTCAACAAGACAATGTTGATGTACTGATACGCTGAAGTTTTTTGAGAGCACTTTACGCTAAGATTTCTTTAGCCAAATTGCACACTAATTCCAAATGATCTATATTGAGTTGCAGAGCTAAATCAAACTCCGCTTGTTTAAAACTACGGGTTCGTTTTCTTCGCTCTGCTGATTAGCCCTGTAATATTACTTCGCACTAACTCTATCAGACTCTGTAAATTATTCATAATGACAATGCAATCATGATTTCCCTTGATGTTTAACTGAATTGCCACCGTCGTGTGTTTAAAATGAATCTTTGCATATTGCAAGTTACTTACTCTCTAAAATATTTATTAGCCATTGATTGTGTCGAGAAGACGTGCCTCATAACTAGACTTATGGAACTTTTTGAGGCCAACACGAATGCAGAAATTGACACCATGATGGAGGGGTGTTTTTAATACATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45777
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 |
|---|---|---|---|---|---|
| ENSDART00000044429 | Nonsense | 553 | 789 | 16 | 22 |
| ENSDART00000148147 | Nonsense | 445 | 681 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 22 (position 37352417)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 34521917 |
| GRCz11 | 22 | 34496824 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCCAACAGGCAGCCGAGCGACCAGAGAGGAATTTCGTGGACACCCGG[C/T]AGCTAAAGGTGTGCTCGACCTGTTTTGACCTCTCAGTCAGTCTGCTGCGG
Long Flanking Sequence:
TGATTAAAGTAAATATGCAGTAAATATTTTCCGAACATTATATTTATTCAAATAAGGATAAAAGCAATATAGTGTTTTTAGAACAAGAAATTAAATTGAAATTATAATATTTTAGGGCCTATGGCATGAAGATTACCATTGGCCTAGGTCTTTAAAGCCTACAGTCTTTTCCTCTGCATATGGCTGTTACGTAGGTTTTTTAGTGGTTGTTGGAAGGTTGCTGGGTGATCTAATTCGTAAGAGTACACAGTCTTATTCTCAATGTATTTTTGTTCCTGCATATGGTTGCGCAAAGGTTGTTTGGGTTTTTTTTAGGTGAATGTTTGGTTGTCAGTGTCACAATAGCCCACAGTCTTGTGGTTGATGTAGTGTAAACGTTCTCATACTTTTCTTTTCTGACCTTCTGTTCCTTTCTATTGTGTCTGTTCATGTTTTTATTTATTTCTCATCAGATCCAACAGGCAGCCGAGCGACCAGAGAGGAATTTCGTGGACACCCGG[C/T]AGCTAAAGGTGTGCTCGACCTGTTTTGACCTCTCAGTCAGTCTGCTGCGGGTCCTGGAAATGACCATCACGTTAGTGCCAGAAATTTTCCTGGACTGGACCCGCCCCTCTGCTGAGCTGCTGCTGCGGCGATTGGCTCAGGTAAGCCTGATTGACAGCTGAAAGGTGAACTAAATATAAAAATAAATATAAATATGCAGTTCTCAAGTTCAGAAAGTTCAAAGTGAATGAAGCTCGTTTTAAGCACACCATTAAGATTCTTCTTATAGAGCAGCTTCATGCAGAAACTCTTGAGTTAATGATCCTGTTTGATGCAATTGCTATTAAACATGAGGTTTCTGTTTATTTTCTCAATGTCTTGCAGTGCACAGCTCTCTAAATGTAAATTATTAACAACACAAAGAAAACTTTTAGGCCTCAATCAAATGTTCTGCTTCAAAGGGGTCATATTTTTCTATAAAAAAACATCTTTGGTTATCTAAGTAGACTAGCCTGTAAACA
Associated Phenotype:
Not determined