ZMP
si:ch211-255l18.3
Ensembl ID:
ZFIN ID:
Human Orthologues:
RNF216, RNF216L
Human Descriptions:
ring finger protein 216 [Source:HGNC Symbol;Acc:21698]
ring finger protein 216-like [Source:HGNC Symbol;Acc:33610]
ring finger protein 216-like [Source:HGNC Symbol;Acc:33610]
Mouse Orthologue:
Rnf216
Mouse Description:
ring finger protein 216 Gene [Source:MGI Symbol;Acc:MGI:1344349]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17630 | Nonsense | Available for shipment | Available now |
sa33273 | Essential Splice Site | Available for shipment | Available now |
sa30838 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40135 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33272 | Nonsense | Available for shipment | Available now |
sa15199 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17630
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 |
---|---|---|---|---|---|
ENSDART00000130058 | Nonsense | 290 | 834 | 4 | 16 |
ENSDART00000138783 | Nonsense | 290 | 834 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 3 (position 40650930)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40514290 |
GRCz11 | 3 | 40656148 |
KASP Assay ID:
2259-3927.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGGATGCATATGTAGCAGAACTGATAGAGAGAGGTGACCTGAAAGATT[T/A]AAATGYGTAAGCACAAACTATTTTCTGCAAATTTTTGGTTTAGAAATACT
Long Flanking Sequence:
GGACTCACTGCCTCTTCAAACGGACCCTTCATCTAGCACACACTCAGTAAATCAGGCCAATTCTGCATTTTCACCTCCTTCCACCACTGAATCAGGTCAGTCAGACTCGGGCCACAAAATCGAAGTCGTCGTTTGGCCGAGAACTGAAAGGACCATAAAAAGACCTCGGACGCCACAGGAGACTGTGTTAGTAGAGGTCAGACGAGATGAGCAGCCATTGGCTCCTGGTATCCCTGCACAATTACCCGCACCGGCTGACAATGAGAGGCCTGGACCGTCAATGCCCAGAGAACCCCTAATACCGCAGGACTCTCACAGGACGTCCCTCGATCTCCTGGTGAAGGGGGTGGTGAGTTTTGTGATTGACACCTAGTGTTCAATCAGTATTGTTTTTATTGTACACTAAGGGTTTGTTTTAATGTTTTTTCAGACGGACCTCTTTCCCGATGTGCAGGATGCATATGTAGCAGAACTGATAGAGAGAGGTGACCTGAAAGATT[T/A]AAATGTGTAAGCACAAACTATTTTCTGCAAATTTTTGGTTTAGAAATACTTAGTTCACATGTAATCTTTATAAGAAATACTTTTTAATTCACAGAATATGCAATATTTTGTTGGAAAATCCTGACTATCCGAAGAAAGCAAACTCAGTTTTGACTCAAAGTAGTGTTCTTCTTGAGACGAACGATTCTGAGACGCAGGTTTGCATGTATTTTGTTGAGGTTTTGATACTGTGGATTCTCAGAAATAAAAGAAATGTAACTGATTTGGCATGTTGTGCTTGCTTTTTCTTTCTCACGCAGGAAAGTGAAAATTATTTTGATTATTTCAAACTTAAGACTGTTGGCCCAGAGGTTGTCGTTCAGGCTGCAGACATGCTGATGGGTGACTTCAGAATGTTGAGCTGTCAGGATATCAAATGGGCACTGAATTGCCTCAAAGGACACTATGCAATCACCCGAAAGGTGAGCGATATTTTCAGTTATCAAATATTATTGAGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33273
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130058 | Essential Splice Site | 419 | 834 | 7 | 16 |
ENSDART00000138783 | Essential Splice Site | 419 | 834 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 3 (position 40647805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40511165 |
GRCz11 | 3 | 40653023 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGAGAGCCAAATGAGCGCGCCTACATAGACTTCAAATTTGAGCAGGG[T/C]GACTATGTGTTTTTGTCCTTTCGTTTGCCTCTTAAATCCATCATCAAACC
Long Flanking Sequence:
ACCATGTCCAATCAACTGAATTTACCACAGGTTATCTCCAATTAAGCTGCTGAAACATCACAAGAATAATCAGTTGAAACAGAATTTACCTGAGCTCAATTTAAAGCTTTACAGCAAAGGCTGTTAATACTTATGTACATGTAATTTTTTCAGGTTTTCATTTTTTTAATAAATTTGCAACAATTTCAACAAATCTTTTTTCACATTGTCATTATGGGGTATTGTGTGTAGAGTTCTGAGGAAATGCTGTCACATTAAAAATGTAGAAAACGTGAAGTGGTATAAATACTTTCTGGATGCACTGTATGCATCAACCATCGAAAAACCCATATTGTTTGACCACTAGTTTTTTGTACAATATTAATTTATCTGATTTTTTTGAAGGCCTTATTCGAAGCCCTTAAGAAGTGGCAAGAGAACTCAACCGACCCCTCAGGGAAGAAGAAGAGAAGGAGAGAGCCAAATGAGCGCGCCTACATAGACTTCAAATTTGAGCAGGG[T/C]GACTATGTGTTTTTGTCCTTTCGTTTGCCTCTTAAATCCATCATCAAACCAGACAGAATGTGAAATGCTCATTGCAGCTCATTTACTCCAGGTTCTTTTAAACTGGAGAGAAAGATGTACTTTTTGGAGAAGAATCGCAGGTGGAGCCGAGGTAATGAGACTACACTGGAGGCGTCTCTCGTGAAAGAGCTGCAGTTTTACGAGCAGAAAGCCAAGGAAATGGCTGAGGTATCTCACACGGCTCACTTCTTCAATTTATTTGCCACGCTTCCTCCTGAAATTGCCCTGAGAGATATCTTGCTGTGATCAACTGAGCTTGACAGGATGTTCATTTGTTTAGTGATTATAATAATATTTTCACTTCTGCTGCTTTTAGCATGAAGACTTTCTTTTGGCTTTGCAAGTGAACGAGGAGCAGTATCAAAAGGTGGGTGGGAAAAAACAGCTTTGTTAATGCCATGTCATAAGAAACAAACTGCAGCTTATCTTTTTTAAGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30838
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 |
---|---|---|---|---|---|
ENSDART00000130058 | Nonsense | 479 | 834 | 9 | 16 |
ENSDART00000138783 | Nonsense | 479 | 834 | 10 | 17 |
ENSDART00000130058 | Nonsense | 479 | 834 | 9 | 16 |
ENSDART00000138783 | Nonsense | 479 | 834 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 3 (position 40647384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40510744 |
GRCz11 | 3 | 40652602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAGCATGAAGACTTTCTTTTGGCTTTGCAAGTGAACGAGGAGCAGTA[T/A]CAAAAGGTGGGTGGGAAAAAACAGCTTTGTTAATGCCATGTCATAAGAAA
Long Flanking Sequence:
CAACCGACCCCTCAGGGAAGAAGAAGAGAAGGAGAGAGCCAAATGAGCGCGCCTACATAGACTTCAAATTTGAGCAGGGTGACTATGTGTTTTTGTCCTTTCGTTTGCCTCTTAAATCCATCATCAAACCAGACAGAATGTGAAATGCTCATTGCAGCTCATTTACTCCAGGTTCTTTTAAACTGGAGAGAAAGATGTACTTTTTGGAGAAGAATCGCAGGTGGAGCCGAGGTAATGAGACTACACTGGAGGCGTCTCTCGTGAAAGAGCTGCAGTTTTACGAGCAGAAAGCCAAGGAAATGGCTGAGGTATCTCACACGGCTCACTTCTTCAATTTATTTGCCACGCTTCCTCCTGAAATTGCCCTGAGAGATATCTTGCTGTGATCAACTGAGCTTGACAGGATGTTCATTTGTTTAGTGATTATAATAATATTTTCACTTCTGCTGCTTTTAGCATGAAGACTTTCTTTTGGCTTTGCAAGTGAACGAGGAGCAGTA[T/A]CAAAAGGTGGGTGGGAAAAAACAGCTTTGTTAATGCCATGTCATAAGAAACAAACTGCAGCTTATCTTTTTTAAGTTTGCGAGTTGTGTTGTATTTTGCATTAGTTCATTCAATCATACTACATAAAACTTTTTCCAGGGACAAAATAAAAGTTTGTCATTTTATATTATATGATATCATTTATTTTGTTGCTTCTCACATTATTTAAGGCAGGGGTTCTCAACCTTTTTTACTTCAGGGCCCACTTCTTTCTCCGATCAAATTTTGGAGTCCTACCTGTCTGACTTTAAAATGTTCATAGGAAATGCTCATTTAAACCTTTATATATATATAAATATATATATATATATATAAATATATATATATAAATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACAATTCATTTGTTGTGCCTTCTATTATTTTCTATTATCAGCATATTATAAAAATATAAAGTACTGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40135
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 |
---|---|---|---|---|---|
ENSDART00000130058 | Nonsense | 479 | 834 | 9 | 16 |
ENSDART00000138783 | Nonsense | 479 | 834 | 10 | 17 |
ENSDART00000130058 | Nonsense | 479 | 834 | 9 | 16 |
ENSDART00000138783 | Nonsense | 479 | 834 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 3 (position 40647384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40510744 |
GRCz11 | 3 | 40652602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAGCATGAAGACTTTCTTTTGGCTTTGCAAGTGAACGAGGAGCAGTA[T/A]CAAAAGGTGGGTGGGAAAAAACAGCTTTGTTAATGCCATGTCATAAGAAA
Long Flanking Sequence:
CAACCGACCCCTCAGGGAAGAAGAAGAGAAGGAGAGAGCCAAATGAGCGCGCCTACATAGACTTCAAATTTGAGCAGGGTGACTATGTGTTTTTGTCCTTTCGTTTGCCTCTTAAATCCATCATCAAACCAGACAGAATGTGAAATGCTCATTGCAGCTCATTTACTCCAGGTTCTTTTAAACTGGAGAGAAAGATGTACTTTTTGGAGAAGAATCGCAGGTGGAGCCGAGGTAATGAGACTACACTGGAGGCGTCTCTCGTGAAAGAGCTGCAGTTTTACGAGCAGAAAGCCAAGGAAATGGCTGAGGTATCTCACACGGCTCACTTCTTCAATTTATTTGCCACGCTTCCTCCTGAAATTGCCCTGAGAGATATCTTGCTGTGATCAACTGAGCTTGACAGGATGTTCATTTGTTTAGTGATTATAATAATATTTTCACTTCTGCTGCTTTTAGCATGAAGACTTTCTTTTGGCTTTGCAAGTGAACGAGGAGCAGTA[T/A]CAAAAGGTGGGTGGGAAAAAACAGCTTTGTTAATGCCATGTCATAAGAAACAAACTGCAGCTTATCTTTTTTAAGTTTGCGAGTTGTGTTGTATTTTGCATTAGTTCATTCAATCATACTACATAAAACTTTTTCCAGGGACAAAATAAAAGTTTGTCATTTTATATTATATGATATCATTTATTTTGTTGCTTCTCACATTATTTAAGGCAGGGGTTCTCAACCTTTTTTACTTCAGGGCCCACTTCTTTCTCCGATCAAATTTTGGAGTCCTACCTGTCTGACTTTAAAATGTTCATAGGAAATGCTCATTTAAACCTTTATATATATATAAATATATATATATATATATAAATATATATATATAAATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACAATTCATTTGTTGTGCCTTCTATTATTTTCTATTATCAGCATATTATAAAAATATAAAGTACTGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33272
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130058 | Nonsense | 622 | 834 | 13 | 16 |
ENSDART00000138783 | Nonsense | 622 | 834 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 3 (position 40613180)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40476540 |
GRCz11 | 3 | 40618398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCAGGAAGTGCCATGTGGTGTGGAAGGAGCACGCAGGAAAGACCTGT[G/T]AGCAGGTGCTGGAGAGGGACGAGATCCGCCTGCGGGTGGCCTTGTAAGTG
Long Flanking Sequence:
TAAGTTTATTGATCTGCCGTCACTCTATGTGGACAGAGTAATACAGAAGGGCGAGGAGGCTGTACGAGTGCTGGTATTGCAGAATATACTATGGCTGTCAGCCAATCAAATTCGAGAACAAGACAGAACTGTTGTGTATTTATTTGTTTTATTTTATTTTATAACCTGGTTAATGTATTATTATTTTTACCTGGGGTTAATGTATAAACAATGAAGTCAATTCCAATGGTCATACCAACAATACTAGCGGATTATTCAATGTCCACTCCTGAAACAATGCAGGGAACTCCGGCTTCTGCTTCCGTAAACACAAACAGACGTGAAGGCACAAAACAGAAACACGACTCCCTCGACGGATGAATGAAGTGGTCCAGGTGTTTCTCTTTCCACTCTGTTTGAATGGTGATCAATAACACAGATGCTCATTTGTGTGTCCTCTTCCTCAGGAGAGCTGCAGGAAGTGCCATGTGGTGTGGAAGGAGCACGCAGGAAAGACCTGT[G/T]AGCAGGTGCTGGAGAGGGACGAGATCCGCCTGCGGGTGGCCTTGTAAGTGCTCGACTCGAAACTCTTAGCGTTAGAGCCAGCTTGTTAATAATGCATCCGTGCACTATTGAGGGTACTCGGTAGTTTAGCAAACCACGTGGGAGATCATTAGCAACCCTAATGCTGAGTCAGTGATTTCCCCAGGCCCTTCTCAAAGCGCACTAAAACATTGGGCTGTGTTTGAATGATCCCCTGGAGTGTTTTGTTTGCAAATACACATCATGCCAAGCCCAGCAGCCGGTCATGAGGAAGTGTCTGTTTTAAAGCAGCCTATCACTGTTGTTCAGCCTCTGCACTGGACAGGAAGTGATCGCCTGCTTTCCTTCCTGTCATTGCATGGGGTTTACACGTAGATCAAAAAGCCTTTGTTTCCTGTTTACCCAGAACTTTTTTCTTTTACCTACACAAATAGTGACAGGAAACTGACGCTAACTGAGAGATTGAATGAAATGCACTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15199
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130058 | Nonsense | 665 | 834 | 14 | 16 |
ENSDART00000138783 | Nonsense | 665 | 834 | 15 | 17 |
Genomic Location (Zv9):
Chromosome 3 (position 40610806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40474166 |
GRCz11 | 3 | 40616024 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACAAGTGTGCCACAGGTCTGGTGAAGTCGGAGGGCTGCAACCGAATGT[G/A]GTGCCGCTGCGGCGCCTACATGTGCTACCTCTGCCGAGAGCCAATCAACG
Long Flanking Sequence:
ACCATATTTAAAAAGTTCTGTTATTGCTTTAAAAATTTTTTGTCAAATTGATTTGGAAGATTTTTTAGTGGAATTATTATTATTAATAATAATAATTATTATTATTATTATTTTTTACATTAATTAAATTTTAAATCCTGTAAAAATCCCTTCCAGTATTAATGTTGAAGTCTGTCTTTTTTAGTTCAGTCTGTAGATAGCTAATACAGGAAGAATTAATCCACACTCTTAAGATTATTGTTTTTTTGGCGTTTTATTATACATTTATCAGGGAACAGGCACAAACGTTTAGACTCAAAGCCTGTTCTTCAGACATACTGAAGCCTCATTCACAACAACTGCTGCAAATGCTCTCTAGATAGGCAGCTCACCAGCATGTAAAGTGATCTCAGATTGGGTTTGTTTCCTGATCAGTGAGGAGAAGATGACGGCTGCCCGTGTCAGGAAGTGCCACAAGTGTGCCACAGGTCTGGTGAAGTCGGAGGGCTGCAACCGAATGT[G/A]GTGCCGCTGCGGCGCCTACATGTGCTACCTCTGCCGAGAGCCAATCAACGGCTACAACCACTTTTGCCAGCACGCCCGCTCGCCCGGTGCCCCCTGCAGACACTGCAAGAAGTGCTCGCTGTGGACGGACCCTACGGTAAAACATCACACACTACACTGTTTTTGTGTTAATTAGTGGAGATTATCCTTATAAAAATAGCAAATACCTTCACTTTCTGTACATCTACTAAGTTTACAACAGGTTTACGTCTAGGTTTAAGTCTAGGGCTGGGTATAGTTTTAGATATTGAAACGTCCCATTTTGATATTGATTCACACGCTTTCTATTCTTGATTCTATGAACTTAAATAAATACAAATGATATTTATATTTCTAAAACTGATCAGCAAATATCAGCTTCCAAATGGTGATTAAAAAAAACAAAAAGATTCCTTTTTCTTTTTTTTTCTTCGATACCTTCTGGTAACCCTACAACTCATTTATTTTGGCACTTCAAGCGA
Associated Phenotype:
Not determined