ZMP
rel
Ensembl ID:
ZFIN ID:
Description:
v-rel reticuloendotheliosis viral oncogene homolog [Source:RefSeq peptide;Acc:NP_001001841]
Human Orthologue:
REL
Human Description:
v-rel reticuloendotheliosis viral oncogene homolog (avian) [Source:HGNC Symbol;Acc:9954]
Mouse Orthologue:
Rel
Mouse Description:
reticuloendotheliosis oncogene Gene [Source:MGI Symbol;Acc:MGI:97897]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16421 | Nonsense | Available for shipment | Available now |
sa16479 | Nonsense | Available for shipment | Available now |
sa22309 | Nonsense | Available for shipment | Available now |
sa6305 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16421
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077612 | Nonsense | 118 | 596 | 5 | 10 |
ENSDART00000077612 | Nonsense | 118 | 596 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 26040331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25685991 |
GRCz11 | 13 | 25816441 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTTTATTTGTTTYTTTTTCTTTAAACAGTTTTCAGAATCTGGGCATC[C/T]AGTGTGTGCGGAGAAGAGAAGTGAAGGATGCCATCATGCAGAGGGTGACA
Long Flanking Sequence:
GTTCAATCTTTTAAAATCTGAACACTGTCACTCACGAGAAGAAGAAAAAATCTTCATTATCTTTAAATTTTGCTGTAATCCTGTTTGGTCCTGTTACCATTTTCCTCTTAATGAAACGAAACGTTGCTGTGCCCCACATCCAAGTCATTCCTGTGTGCTTTTCCCTTTACTCAGCCCACACACGACCACATTTCTCTTCCGAAGGGCTGTCCATTCTTCTACTTTTTTTTTTATGTTAAAGAAGCATGTTGTTTTAGAATAGGGAGCCATGCAGGGGATTCCCCGGTATGCAAAATGAGAGCTCCAGCTTGCCCTTGATTTGTCTGTATGGTTAATTCTAACCTCACTCTCCCTGTTAGCTTTAGTTTTTGGGATTAGTCATTCAAGTCGGACAGTATAAAGTACTAAACAAAGCTGGAGGTGCAAAATCAGAATGCATACGTTAACAGATTCTTTTATTTGTTTCTTTTTCTTTAAACAGTTTTCAGAATCTGGGCATC[C/T]AGTGTGTGCGGAGAAGAGAAGTGAAGGATGCCATCATGCAGAGGGTGACACGAGGAATCAACCCCTTCAATGGTGAGATTCAACACTGCTTTTTCCTTTCCTGGCCTAAACAGAATCTGCCCGAAAAAGTAGTACATACAAAGTTGATCTGATTTAGAGGGAAATTATTGAAAACCTACTATTTATGCTTTAAATAAATGCAAATGATTTCATCTGGAGTTCCTTATAAATAAGGAAATTTATATTTTCAAAAGGTACTTTTTTGTACCGAAAAGGGTCCGTAATTGTTGTACAAAAGTAAATATTAGTACCTAAAATGTTGACAAGGTACAATACTATACTTTGCAGTAGAGCTGTGCGATTAGGGGAAAATATCTAATAGCAATTTATTGTTTATTTATTTTTTGACAGATAATGTTTTTGCGAGTTGATTTATGATTAAATTTAATCTTAAGCTGATTTGAATTTAATTCATGCTTCAGCTCAATAGTCTGTAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16479
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077612 | Nonsense | 118 | 596 | 5 | 10 |
ENSDART00000077612 | Nonsense | 118 | 596 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 26040331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25685991 |
GRCz11 | 13 | 25816441 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTTTATTTGTTTYTTTTTCTTTAAACAGTTTTCAGAATCTGGGCATC[C/T]AGTGTGTGCGGAGAAGAGAAGTGAAGGATGCCATCATGCAGAGGGTGACA
Long Flanking Sequence:
GTTCAATCTTTTAAAATCTGAACACTGTCACTCACGAGAAGAAGAAAAAATCTTCATTATCTTTAAATTTTGCTGTAATCCTGTTTGGTCCTGTTACCATTTTCCTCTTAATGAAACGAAACGTTGCTGTGCCCCACATCCAAGTCATTCCTGTGTGCTTTTCCCTTTACTCAGCCCACACACGACCACATTTCTCTTCCGAAGGGCTGTCCATTCTTCTACTTTTTTTTTTATGTTAAAGAAGCATGTTGTTTTAGAATAGGGAGCCATGCAGGGGATTCCCCGGTATGCAAAATGAGAGCTCCAGCTTGCCCTTGATTTGTCTGTATGGTTAATTCTAACCTCACTCTCCCTGTTAGCTTTAGTTTTTGGGATTAGTCATTCAAGTCGGACAGTATAAAGTACTAAACAAAGCTGGAGGTGCAAAATCAGAATGCATACGTTAACAGATTCTTTTATTTGTTTCTTTTTCTTTAAACAGTTTTCAGAATCTGGGCATC[C/T]AGTGTGTGCGGAGAAGAGAAGTGAAGGATGCCATCATGCAGAGGGTGACACGAGGAATCAACCCCTTCAATGGTGAGATTCAACACTGCTTTTTCCTTTCCTGGCCTAAACAGAATCTGCCCGAAAAAGTAGTACATACAAAGTTGATCTGATTTAGAGGGAAATTATTGAAAACCTACTATTTATGCTTTAAATAAATGCAAATGATTTCATCTGGAGTTCCTTATAAATAAGGAAATTTATATTTTCAAAAGGTACTTTTTTGTACCGAAAAGGGTCCGTAATTGTTGTACAAAAGTAAATATTAGTACCTAAAATGTTGACAAGGTACAATACTATACTTTGCAGTAGAGCTGTGCGATTAGGGGAAAATATCTAATAGCAATTTATTGTTTATTTATTTTTTGACAGATAATGTTTTTGCGAGTTGATTTATGATTAAATTTAATCTTAAGCTGATTTGAATTTAATTCATGCTTCAGCTCAATAGTCTGTAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22309
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077612 | Nonsense | 458 | 596 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 26020089)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25665749 |
GRCz11 | 13 | 25796199 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCAACCGGCAACCAGCCTCGACAGGACCTACTAAACCAGCAGGTTCAG[C/T]AATCCCAACAGCCACCACAAAGACAAGGACAGGAAGGAGCCTGGTATAAC
Long Flanking Sequence:
AAGCCATGAGCTTCATGAACAGAACAAAAGCCGTGTCTTCAACCAACTTGATGAATCAGAGAATCAAAACCGGTGAGACAACACAACAGCCATTACCAAATAACTGCACACACTCTTCATACAAACAATATCACTATATAACATGACAAAATCTTCTTGCAGAGCCACCAAATTTTTATCGCCCACCAAACCAAGGGGTGGCCCGCCAAAATCAGCCAGTCTATTATAACAAAGGCCTTCGGTCCTGCCCTATGATGCCACATCCATCAGAAACCACGACACAAGGAGCTCTAAGCCAGTGGACCAGTCAAGTCACCAACACTTCTGTGCCCAATAATGTTGTAAGTCTACAGCAGGTGAACCCAAGTCCCAACATGCCAAGTGCAGGGGAAAATGGAAACAGCCTTCCTCTGTTGACCTCGATGGATCTGGAGATTCTTCAACCCAACGGACCAACCGGCAACCAGCCTCGACAGGACCTACTAAACCAGCAGGTTCAG[C/T]AATCCCAACAGCCACCACAAAGACAAGGACAGGAAGGAGCCTGGTATAACTACAGCTCCCAACAGCCTCAAAACACACAAAATGGAGCATCAGGCGCTAGTGGGTCACTAGCAACGGGCTACCAGTTTACAAGCGGCTTAGAGGATGATATCTTGCAAAGTCTCATGGGTAATCATCAACCAGGCATCCAGTTGAAACAGGAACCTCAAGGGCTGAGCAACATGGCTCCATTGGTCAACTCGGATTGTGTACAGTCCTTCACAGCCCTCCTAAACTGCAACAATGGAAGTACTCCAGAACACATGAGACAAATAGACCCCAATGGCGCCAATCAGAGGGTCTCGCAGATACAGTATCCTTCTGGAAATATGGGGCAGGAGAGCCATCTTGAGCATTACACCTGGCACTTTCCCGAATAGAGTTGAAGATTTTTCTCGGTCTTTAAGCGTAGGCCACGGTTTATGTTCACTGAATGTATTTTTGATTAAAGATCTGGAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6305
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 |
---|---|---|---|---|---|
ENSDART00000077612 | Nonsense | 538 | 596 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 26019848)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25665508 |
GRCz11 | 13 | 25795958 |
KASP Assay ID:
554-5001.1 (used for ordering genotyping assays)
KASP Sequence:
GTTGAAACAGGAACCTCAAGGGCTGAGCAACATGGCTCCATTGGKCAACT[C/A]GGATTGTGTACAGTCCTTCACAGCCCTCCTAAACTGCAACAATGGAAGTA
Long Flanking Sequence:
GTCCTGCCCTATGATGCCACATCCATCAGAAACCACGACACAAGGAGCTCTAAGCCAGTGGACCAGTCAAGTCACCAACACTTCTGTGCCCAATAATGTTGTAAGTCTACAGCAGGTGAACCCAAGTCCCAACATGCCAAGTGCAGGGGAAAATGGAAACAGCCTTCCTCTGTTGACCTCGATGGATCTGGAGATTCTTCAACCCAACGGACCAACCGGCAACCAGCCTCGACAGGACCTACTAAACCAGCAGGTTCAGCAATCCCAACAGCCACCACAAAGACAAGGACAGGAAGGAGCCTGGTATAACTACAGCTCCCAACAGCCTCAAAACACACAAAATGGAGCATCAGGCGCTAGTGGGTCACTAGCAACGGGCTACCAGTTTACAAGCGGCTTAGAGGATGATATCTTGCAAAGTCTCATGGGTAATCATCAACCAGGCATCCAGTTGAAACAGGAACCTCAAGGGCTGAGCAACATGGCTCCATTGGTCAACT[C/A]GGATTGTGTACAGTCCTTCACAGCCCTCCTAAACTGCAACAATGGAAGTACTCCAGAACACATGAGACAAATAGACCCCAATGGCGCCAATCAGAGGGTCTCGCAGATACAGTATCCTTCTGGAAATATGGGGCAGGAGAGCCATCTTGAGCATTACACCTGGCACTTTCCCGAATAGAGTTGAAGATTTTTCTCGGTCTTTAAGCGTAGGCCACGGTTTATGTTCACTGAATGTATTTTTGATTAAAGATCTGGAGGGTTTGTTGTGTAGGGATTACTGTAAATGCTGATTCACACCGCACTGATAGATGACGATATACAGACAGGACAATCAAAAGAGATTACAGTACATCACTATTTGACCCTATAGATGCCATGAGAAATCATGGAAATGATTGCTGACAAGAGAAAATGTGCTGATCCACAAAAAAAAAAAAAAAAAAAAAACTGTCAATGCGGTAAGAGTTGGCTTTAACATGGTGCCAAAGTTTGCTTAAACT
Associated Phenotype:
Not determined