ZMP
rnf207
Ensembl ID:
ZFIN ID:
Human Orthologue:
RNF207
Human Description:
ring finger protein 207 [Source:HGNC Symbol;Acc:32947]
Mouse Orthologue:
Rnf207
Mouse Description:
ring finger protein 207 Gene [Source:MGI Symbol;Acc:MGI:2684989]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17871 | Nonsense | Available for shipment | Available now |
sa9730 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17871
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077945 | Nonsense | 280 | 634 | 8 | 17 |
ENSDART00000142000 | Nonsense | 280 | 634 | 9 | 18 |
The following transcripts of ENSDARG00000012409 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 21801061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21580368 |
GRCz11 | 23 | 21506919 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTATTTTTTAGTCAGCATGAAGAGAAGGAGAGAACCTTTAAAGAGCAAT[T/A]ATCTCAWCTTGCTGCACTCCTGCCAACTCTCCAGGTAARTACATTTCCTC
Long Flanking Sequence:
AAGGTATTATCACATATAAGTAGGGGGGATTTATGCAGAATGATTTTGGGGGTATCATAACTAAAAACTTAATATATGAAATAAATTGTATTTAATGTTTACAATGCACATCCAATAAGGTCCACTTATTTGCAGAAATATCTGCATAAATCTGCAGATTTCTGCGTGCTCATATTCCATGTGGGCCTACATAAAAGGTACTGAAAGTACATGTATCTACAGTATATAAAAACATTTCTAAAATGATTTACAAAAATTAAATATATTTTTAAACGTTTGCATAGAGTACATAGTATATTAATATAAAGTGGGTCTGATAATGTAATTTTAACATTTTAATATCTGTCTTTTATTACCTGTCAACCATAATTGTCAGGATTGGACAATTGTCAGAATTATGCTCCAAAAATGTAATAATACAAATATAGCTATTTATTTATACATTTCATAACTATTTTTTAGTCAGCATGAAGAGAAGGAGAGAACCTTTAAAGAGCAAT[T/A]ATCTCATCTTGCTGCACTCCTGCCAACTCTCCAGGTAAATACATTTCCTCCATGTCTCCATAAATATTAGCTTTTCATTTATTCTCGCTTGCTTCCAGACACATTTTTTTTGTTTGTTTGTTTTTTTCTACAGGTTCATCTTGTTACATGCTCTGCCTTCCTAAGCTCAGCAAATAAGTTTGAGTTCTTAGACATGGGATATGTGAGTACAAACTGCAATCCGAATCTATTGCATCGATAGACTCATTAGTTATGCCAAATATGTGAATTAGACTTATATGCACAAACCTGGAATATTGCATAAAACATTTGCGAATAGTTCTCAGTTTTTATCAAAGTCGAAATCGTCACTTTCTGATACACTGGCTAAAGAAAACTTTGGTACCATTGCAGAAAAGCCATAAGTCACTTTCCAAAACCTTTTTATTCAATGTTCGCCACTGTTGGAATAATCTTCCCATTTCAACACAGATTGCAGATTCACTGGAATCCATCAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9730
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077945 | Essential Splice Site | 556 | 634 | 15 | 17 |
ENSDART00000142000 | Essential Splice Site | 556 | 634 | 16 | 18 |
The following transcripts of ENSDARG00000012409 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 21795064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21574371 |
GRCz11 | 23 | 21500922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GKTCCCTACATCCGCTCWATAGCAAAAGTGAAGGAACGTCTGGAGCCAAG[G/A]TACTAGAGAGCTTGATTTATAAGTTTCATGGCTTATAAAGTTTCATGGAT
Long Flanking Sequence:
ATCCAGAAGCTGAAAGACCAGGTGCAGGAGATTCACAGAGACCTGACCAAGCACCACTCCCTCACCAAACCTGACAGCATGAGTGAGATTTTGGAGAAGTCAGTACAGGTGGACAGTCAGATCTCCTCCGAGTATGCTTCAGTGGAGCTCATGCGGGCCATGTTCGAGGAGGTGAGATCCCAGTGCTTTCAATCAACATTAGAAAGAGGTACAATCGGATTCGAAATGTCATCATTTTTGTTCCTAGATCTGGGAGGAGACTTTACAGAGAGTGGCAAATGAACAGGAGATTTATGAAGGTAAACACTATTTTACTCGGTAAGCGCTTCACTCTAGTTGTGTTGTTATATCAAAGTTAACAGTTCAATGATTCTTTTTTTAGCGCAACTTCATGATCTGCTTCAGTTAAAACAGGAGAATTCCTATTTGACAACAATCTCCCGACAAATAGGTCCCTACATCCGCTCTATAGCAAAAGTGAAGGAACGTCTGGAGCCAAG[G/A]TACTAGAGAGCTTGATTTATAAGTTTCATGGCTTATAAAGTTTCATGGATTTATACGTTTTACATTAGAGCAATATAAATCAAGTGAGCCTTTAAAAGTGAAGCTAAACATTATTGCCACCCGGTGGCAGGCTTGAGTATTGTTATGAATTCAACTTGTCATTTTTCGTTCCTATCACGCTGTTGTTTAAGTGTTTTTTTTAAAGAGGTTAATTATTTTATGCATATTTGCAGTTGCGCTTGCAGGATTTTAGGTTCCAGTTGCCACCATCTGTTTCATAATCCAGGGACTTTGGCTTCACATTTCTAGTGTATTGAATGTTTTTTGTGTGTGTGCAAATTTTATCTTCAACAGGCTGAAGGAGCCTAAAGAACTCAAGGATGATCGCACAGAGATCATGTTGAAGCTCTATGAGGACAGCACGTCTACAGCTGACACACAGCCAAGGTGAGTCCACATCAGTATGTTAAAAGCATATCACGCTCTTATGTAGACACATT
Associated Phenotype:
Not determined