ZMP
si:dkey-15j16.4
Ensembl ID:
ZFIN ID:
Description:
Putative E3 ubiquitin-protein ligase SH3RF1 [Source:UniProtKB/Swiss-Prot;Acc:A5D8S5]
Human Orthologue:
SH3RF1
Human Description:
SH3 domain containing ring finger 1 [Source:HGNC Symbol;Acc:17650]
Mouse Orthologue:
Sh3rf1
Mouse Description:
SH3 domain containing ring finger 1 Gene [Source:MGI Symbol;Acc:MGI:1913066]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43432 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43433 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37020 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23692 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43432
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 |
---|---|---|---|---|---|
ENSDART00000050559 | Nonsense | 121 | 880 | 2 | 12 |
ENSDART00000132007 | Nonsense | 121 | 857 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 20 (position 23729237)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23848038 |
GRCz11 | 20 | 23747138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAATGGATCGGCAGTGGCGGGGGTCCGAGCGCAGGGTGCCGGGGGAAGC[C/T]AAAGGGATCCTGGTCCCACAGGGGGACAATCTCAGCGTGTCCAAGCAAAG
Long Flanking Sequence:
CTGCAGTGAATGCTAGAGACTTGATCATGACTACGGCATGGGAGTGACGTGACGTCAGGATTGGACTTTCCCTCCTAACAATCTCATATGCACACACCCACACCATGTGCTTCTCTCTCCGGCGAGACAAAACTGACTGAATGAACGAGTACGCTGAGAAAGATTGTGCGAGTGTGAAAATGGACGAGTCTGCGCTCCTGGACCTGTTGGAGTGTCCGGTCTGCTTGGAGCGTCTAGATGCCACGGCGAAGGTGTTGCCATGCCAGCATACGTTTTGCAGACGCTGCCTGCTTGGAATTGTGGGATCTCGTGGAGAACTGCGCTGCCCCGAGTGCCGCACGCTAGTGGAGAGCGGCGTGGATGAGTTGCCTAGCAATATCCTCCTTGTACGGCTACTAGATGGCATCAAGCAGAGGCCGAGGAGGACTGGAAGTGTGCATGGCACATGTGCTAATGGATCGGCAGTGGCGGGGGTCCGAGCGCAGGGTGCCGGGGGAAGC[C/T]AAAGGGATCCTGGTCCCACAGGGGGACAATCTCAGCGTGTCCAAGCAAAGAGCACTCCAGTTAGGGTGAGTTTAGCTGTTTTTACCAGACTCACACAGTCCCACGCGTCAGTGTTTGGTCAAATACAGTAAACATCTGTTTTGGATGTGTTTTTATTTGCTTGATTGGTAAAGAGCTGGTCATGGGTGGTACCGCTCTATTGGCATAAATCAGGCCTTGGAGACATCCTGCAAAGCCGCGGCCTGATATGAAAGGAAGAATAATCTCTGAATTAATTGGGTGTTGAGGGAATTTGAAATATTTCTTTCTCGTTCACTCTGATCTGTGTCATTACATTGGATAATGAACTCTAAAAAAAGTTTGTTTTGGAAGACTCAAATGCACATTCAGGAGAATAAATACTCAGTCGACTAAGTTTAGAAGAAACCACATTCTCTGATGTAGGAATACACATTTTGTTTGCATGCACTGTGAAAGTTAGACTTCAGCCAGAACGAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43433
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 |
---|---|---|---|---|---|
ENSDART00000050559 | Nonsense | 769 | 880 | 11 | 12 |
ENSDART00000132007 | Nonsense | 746 | 857 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 20 (position 23815133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23933934 |
GRCz11 | 20 | 23833034 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAATGGCTCTGTCTGGGTCAGCAGGGCACAACGGACGCATTGGTGCCTG[T/A]CCTATGGATTCGGAGCTATCGATGTCCTCCTCTTCATCAAACACAGATGC
Long Flanking Sequence:
TGATTTACAATGATCATGTTACCTGGTAGGACAGTATGAGACGCCACTATGACTTTTACTGTGGAACATCTTCAACTTTGTCTCTATTTTTGAATCAGTTGAACCCAAAAGGATGTTTTTTGTTTTTAACAAGTGAAATTTGTGTTACTACAATTATTTGTGTCAAATCCACAGCTTAAATTCATTAATACCCATTGTTGACACTTTTCATTGAGAGCTAATCATCTTCACACATCCTGTGCTAATATTTACATCCTTGGGTAACACCACATTTTCACTGATCTGCATCATTTAACTCATTTCACAAATGTGTGATTTCAGAGAGAGAAGAAAGGCCTGCTGAAACTGCTGTCCAATAAAAAGAAGCTCCGCCCATCTCCTCCATCCTCCCCCACACTGGAGGCAGAGCAATCTGTTAGCATGGAGCTTCCCCAAGGAGCAGTGGGTCCAGAAATGGCTCTGTCTGGGTCAGCAGGGCACAACGGACGCATTGGTGCCTG[T/A]CCTATGGATTCGGAGCTATCGATGTCCTCCTCTTCATCAAACACAGATGCGGTGACACACAGGAGCAGCCCACAGGACAACACTGCCCCCATTGCTCCGCCTCCTCGACAGCCGTGCTCCTCCCTGCTCTCCATGCAGCATGATGGACGGCCAATCGTGTGTGAGAGGTACAAAAATAACCCAAACAGTTACACTAGTGATGGGTAGTTTAGATCATTTTACTGACTCTGACCTTTGAGTCTCGTTGATTGAGATGAACAAATCTTTTATTGAAGTCTAAGCTGGAAACACCCATGGTTAGTTCACCTTTTGAGTCTGTGGGTTTTTGAGTTGTTTGTTCATTACGTGTCAGTACATAAAGAGATGACTCAAAATCGAAGACTTAAGAAATGAACGAACCAAATCTTTTTCCAGCTCTAGATGCATATGATTGGCTTCTGTCTTTCACGTGATGAACAAACAACTCAAACACTATGGAGGACTTGAAAAATGAACTACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37020
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050559 | Nonsense | 826 | 880 | 12 | 12 |
ENSDART00000132007 | Nonsense | 803 | 857 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 20 (position 23817287)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23936088 |
GRCz11 | 20 | 23835188 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTTGTTCATTTTTTTCTAATCATGTTCTGTTCCTCTTCCTCCAGGTA[T/G]CGTGTGGTGGTGTCCTATCCTCCCCAAAGTGAAGCAGAGCTGGAACTCAA
Long Flanking Sequence:
AAGTGATTTAACTAAAATAAAAAGTAACTCGCTTTACTTTTTTTTTAAGTATCTAAATATTATTACTTAGTTTTTATGGAACACATGTTACTTGTAATGCGTTACCCCCAAATCTGCCCATCACAACTTCATCTGCTGTAAAAAATATTTGTACATCCTGATTCCCTAGAAAAGAAGTGCTTTAAGTTAAGTAAGAAGCAGAAGTTGCAGTTGTGTTTTACTCTATAGTGTGACAGGTAAAACTATATGAAAAAAATGTTGGGCTAGATGGCAATTGTTTAAATGGTAGTTTGCATTTGGTGAATGTTAGTAAGTGGTTTCCCTGCCTTTACAAATGCATTATCAGAGATAAGAAGGTTTAAGATTACAAAAGCACATACATAATAATAAAAACACTCACAGATAATTCTGATACAACACAATATTAAATACAAAAGAAGTTCACTTGATTTCTTTGTTCATTTTTTTCTAATCATGTTCTGTTCCTCTTCCTCCAGGTA[T/G]CGTGTGGTGGTGTCCTATCCTCCCCAAAGTGAAGCAGAGCTGGAACTCAAAGAGGGAGACATTGTATTTGTGCACAAAAAACGAGAGGACGGCTGGTTTAAAGGAACACTACAGAGAAACGGCAGAACCGGGCTGTTTCCTGGCAGCTTTGTTGACAGTATCTAACGTACACACAGCAACTAATATTTAGATATCAAATTCTCCATCACTGAAAACCCCACACTGAACTTAAGCCTTCATTCGCTGAGCAGTGGTCTGAAACTCAACTGCTGGAGTTTTGCTTCATCAGCTGCATGGATTTAACCACAGTCTTATGAAAATCTCAGACCAGTCCTAGTCCTTTAGCATTAGATCAAAACCCCCTTTCCCCAAACACTTCAAAGCGGCAGAGTTTTCGTAGTAGGTGCCCTATTTCTAGCTCAGTAGATGAAGTTGTGATAGGATCCGTTAATTTATGCATCTGTAACATTTCAAAGACATTTAATGTGTGCCTTGTACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23692
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 |
---|---|---|---|---|---|
ENSDART00000050559 | Nonsense | 832 | 880 | 12 | 12 |
ENSDART00000132007 | Nonsense | 809 | 857 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 20 (position 23817305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23936106 |
GRCz11 | 20 | 23835206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAATCATGTTCTGTTCCTCTTCCTCCAGGTATCGTGTGGTGGTGTCCTA[T/A]CCTCCCCAAAGTGAAGCAGAGCTGGAACTCAAAGAGGGAGACATTGTATT
Long Flanking Sequence:
AAAAAGTAACTCGCTTTACTTTTTTTTTAAGTATCTAAATATTATTACTTAGTTTTTATGGAACACATGTTACTTGTAATGCGTTACCCCCAAATCTGCCCATCACAACTTCATCTGCTGTAAAAAATATTTGTACATCCTGATTCCCTAGAAAAGAAGTGCTTTAAGTTAAGTAAGAAGCAGAAGTTGCAGTTGTGTTTTACTCTATAGTGTGACAGGTAAAACTATATGAAAAAAATGTTGGGCTAGATGGCAATTGTTTAAATGGTAGTTTGCATTTGGTGAATGTTAGTAAGTGGTTTCCCTGCCTTTACAAATGCATTATCAGAGATAAGAAGGTTTAAGATTACAAAAGCACATACATAATAATAAAAACACTCACAGATAATTCTGATACAACACAATATTAAATACAAAAGAAGTTCACTTGATTTCTTTGTTCATTTTTTTCTAATCATGTTCTGTTCCTCTTCCTCCAGGTATCGTGTGGTGGTGTCCTA[T/A]CCTCCCCAAAGTGAAGCAGAGCTGGAACTCAAAGAGGGAGACATTGTATTTGTGCACAAAAAACGAGAGGACGGCTGGTTTAAAGGAACACTACAGAGAAACGGCAGAACCGGGCTGTTTCCTGGCAGCTTTGTTGACAGTATCTAACGTACACACAGCAACTAATATTTAGATATCAAATTCTCCATCACTGAAAACCCCACACTGAACTTAAGCCTTCATTCGCTGAGCAGTGGTCTGAAACTCAACTGCTGGAGTTTTGCTTCATCAGCTGCATGGATTTAACCACAGTCTTATGAAAATCTCAGACCAGTCCTAGTCCTTTAGCATTAGATCAAAACCCCCTTTCCCCAAACACTTCAAAGCGGCAGAGTTTTCGTAGTAGGTGCCCTATTTCTAGCTCAGTAGATGAAGTTGTGATAGGATCCGTTAATTTATGCATCTGTAACATTTCAAAGACATTTAATGTGTGCCTTGTACTGTCTCACTTTACTGTATAT
Associated Phenotype:
Not determined