ZMP
rlf
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human rearranged L-myc fusion sequence (RLF) [Source:UniProtKB/TrEMBL;Acc:Q
Human Orthologue:
RLF
Human Description:
rearranged L-myc fusion [Source:HGNC Symbol;Acc:10025]
Mouse Orthologue:
Rlf
Mouse Description:
rearranged L-myc fusion sequence Gene [Source:MGI Symbol;Acc:MGI:1924705]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23079 | Nonsense | Available for shipment | Available now |
| sa9124 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36408 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36409 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23079
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 |
|---|---|---|---|---|---|
| ENSDART00000092941 | Nonsense | 451 | 2021 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 24425759)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 24579201 |
| GRCz11 | 17 | 24597602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGCTGTGAGCTGCTACTTTCTCTGAAAGCACATTGGCCCATTGACCCT[G/T]AATTCTGGGACTGGAAAACTTTAAAACGCTACTGCATTCAGTTGCTGGGG
Long Flanking Sequence:
TGTGTCCCTTGAGTCATTTATCGAACGCTGTCTCCAGTTTGCAGCCATCGCCAGGACTATCTACCATCTTCTTTTCCTTATTCGTGTAATTCAAACTGAGGTGAATTTATTTTCTCCTCCTTTATATGGTTATATCTTGAATGTACACCAAGTTGTTTTCTGACATTTTTATCCGTTGTATTTTTTAGGCAATGCAGCTTGGCCTTGCAGTATCAGTTGAGCTGTGTGTGAAGGCTCTACGCCTTCCAAGGCAAGATGACATTGAAGCAAAAACAATGGTCTGCAAAGCTGTTGTCTGTCTTCTCCCTGATGATCTTGAGGTGATACGGGCTTGCCAGCTTACAGAATTCCTCTTGAGCCCATCCCAGGAAGCATTTGATATCCTTGAGGAGCTCTATCTGCGTCCTGATGAAAAATATGATGAGGAAAACGCCATAATTCCAAATTTCCTGCGCTGTGAGCTGCTACTTTCTCTGAAAGCACATTGGCCCATTGACCCT[G/T]AATTCTGGGACTGGAAAACTTTAAAACGCTACTGCATTCAGTTGCTGGGGCTGGAACCTGTGGATGAAATTGAAGATGAAGCAGCACCTGGGGAGCTATGTAATCTTGGAGTGGTTTTGAATGAAGAGGCTGGGAAGGAGGAGGAAGACGAATGTGAGCTTGATGCGCTCAGCAGCGCAGGGGAGCAGCAAACTGTGGAAGAATCAGAAAAGGGACAAAAAGATTCAGAAGATGTCTCTAAGTTAGCTGATAAGCATCAGAGGGATAAATTTCTCTGCCAGATATGCCATAAAGAAGTGGCAGAGACCCGGTTCTGTCACCACGCCAGAAAACATATGGAGGATGGCATGTGGACATGCCCTGTGTGTCTACAAAAGTTTAAAACTAAAAAGGAGTTTGAGCCACACTCCAAAAAACACATTCAGATTTCTGCAAAAGATCACTTTAAAAAGAAAAAAGTGAAGAAGAAGGTGGACCAGACTAAAGATTTCTTCAAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9124
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 |
|---|---|---|---|---|---|
| ENSDART00000092941 | Nonsense | 647 | 2021 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 24426348)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 24579790 |
| GRCz11 | 17 | 24598191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACCCTTCACTTGCCATGTACTACCAGTCCACCCATGATCCTGTAGTAT[T/A]GGAACATATATTAGAGAAAGCTGCCAGTGTGCCTGAAAAGCAAGTAGAAA
Long Flanking Sequence:
TGGGGAGCTATGTAATCTTGGAGTGGTTTTGAATGAAGAGGCTGGGAAGGAGGAGGAAGACGAATGTGAGCTTGATGCGCTCAGCAGCGCAGGGGAGCAGCAAACTGTGGAAGAATCAGAAAAGGGACAAAAAGATTCAGAAGATGTCTCTAAGTTAGCTGATAAGCATCAGAGGGATAAATTTCTCTGCCAGATATGCCATAAAGAAGTGGCAGAGACCCGGTTCTGTCACCACGCCAGAAAACATATGGAGGATGGCATGTGGACATGCCCTGTGTGTCTACAAAAGTTTAAAACTAAAAAGGAGTTTGAGCCACACTCCAAAAAACACATTCAGATTTCTGCAAAAGATCACTTTAAAAAGAAAAAAGTGAAGAAGAAGGTGGACCAGACTAAAGATTTCTTCAAGGAGGATAGTTCTGATGAGCTAGAGCCTGGTCAAATTCCTTTAGACCCTTCACTTGCCATGTACTACCAGTCCACCCATGATCCTGTAGTAT[T/A]GGAACATATATTAGAGAAAGCTGCCAGTGTGCCTGAAAAGCAAGTAGAAAGTGACTATGTTACATTTGACTACATCAACACGTACTTTAAGTTACAGGATCGTGATGTTTACCAGTGTCCAGCCACTGACTGCTCAAAGAATTTTAAACTTTTCAAGTACCTGGGTGTGCACATCAAAAATGAGCATGATAGTGAAGACCCCAATTTGAAACATTATCTTAAGATGAAAGACTGTCGGGAGAAATGCACTTTCTGCCGGAAGACATTCATGACCGCCTATCACCATCGACTGCACCGTTGGATTCATTATGGGGATGATCCTTACATGTGTGTGGTCACAGGTTGTGGTGCCCGCTTTGACACCACCAATGAACTTTTAGCACATAAGCATGGCCATGGGTTTCGATTGTCCTACTGTTGTGAGTTAAAAGGCTGCAGTTTCTCCTACTGTGACCTTGGGCAGCTTTACCACCATGAGGCGCAGCACTTTCGTGATGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36408
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 |
|---|---|---|---|---|---|
| ENSDART00000092941 | Nonsense | 743 | 2021 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 24426635)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 24580077 |
| GRCz11 | 17 | 24598478 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGAAATGCACTTTCTGCCGGAAGACATTCATGACCGCCTATCACCAT[C/T]GACTGCACCGTTGGATTCATTATGGGGATGATCCTTACATGTGTGTGGTC
Long Flanking Sequence:
AGTTTAAAACTAAAAAGGAGTTTGAGCCACACTCCAAAAAACACATTCAGATTTCTGCAAAAGATCACTTTAAAAAGAAAAAAGTGAAGAAGAAGGTGGACCAGACTAAAGATTTCTTCAAGGAGGATAGTTCTGATGAGCTAGAGCCTGGTCAAATTCCTTTAGACCCTTCACTTGCCATGTACTACCAGTCCACCCATGATCCTGTAGTATTGGAACATATATTAGAGAAAGCTGCCAGTGTGCCTGAAAAGCAAGTAGAAAGTGACTATGTTACATTTGACTACATCAACACGTACTTTAAGTTACAGGATCGTGATGTTTACCAGTGTCCAGCCACTGACTGCTCAAAGAATTTTAAACTTTTCAAGTACCTGGGTGTGCACATCAAAAATGAGCATGATAGTGAAGACCCCAATTTGAAACATTATCTTAAGATGAAAGACTGTCGGGAGAAATGCACTTTCTGCCGGAAGACATTCATGACCGCCTATCACCAT[C/T]GACTGCACCGTTGGATTCATTATGGGGATGATCCTTACATGTGTGTGGTCACAGGTTGTGGTGCCCGCTTTGACACCACCAATGAACTTTTAGCACATAAGCATGGCCATGGGTTTCGATTGTCCTACTGTTGTGAGTTAAAAGGCTGCAGTTTCTCCTACTGTGACCTTGGGCAGCTTTACCACCATGAGGCGCAGCACTTTCGTGATGCTGCTTACACTTGTACCAGCCCGGGGTGCAAGAACTTTTACTATTCTCGCAAAGAATTTCTGCAACACTTGGCCACTCATGACATCACTTTCACAGAAAAAGACTTTGAGGCTCAGAGAAAAGCAAAAAGGAAACTCTTGCTCGCAGTTGTAGAAAGTGATTCGGCTTTTGGATCAAAGGTTGAAACAGAGAATTGTGTCCAGAAAAGTGGTTCAAGTTCATCTTCACAGACCTTGGCAAAGGGTCGATCATCAGTCTCGCAAACATGTGTTGCTGTCTGCTTTGATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36409
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092941 | Nonsense | 1092 | 2021 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 24427682)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 24581124 |
| GRCz11 | 17 | 24599525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAAACACATGACAATAATAAAGATGTATCTGATAAGAAGCAAAAAAAA[G/T]AATCTGTCTCAGAGGAGGAACAACCACAAAGCAAGTCCTTAACCAAGCCT
Long Flanking Sequence:
CTGCAAGAGAACTTCAGAAGCACTTGAGAATTGCTCATTCAGACACATTTAATGAGAAGGATCAGTTATGCAAAAAGAAAGTACAAGTAAAGCATTCTACGACTCGAAATGAAGATTTACCTAAAAGTGACCCGGATAACACTGTAAAAACGTCATCTACAGAAAAATCTAGTCCCAAAAAGGCTCTCTCACCTGCGTCTGAGTCTGTAGATTGTGAGACAACCAAATCCAATTTGGACCTTGATGCAGCACTAACCAATATCATGCTTGGATTGGGCCAATTAAACCTTAATTCTTCCAACACCAGACATTCTATGTGTAATTCACAGAGCACTTGTACACCTACCTTGAATACAAGGTCTCCTGCCAAAGCAGCACACAGCAAAAATGAGTCAAGATCTCACGTCACAGGTAGTGAATCAAAAAAGCTGCCAAACAAGTCAGAATCACCAAAAACACATGACAATAATAAAGATGTATCTGATAAGAAGCAAAAAAAA[G/T]AATCTGTCTCAGAGGAGGAACAACCACAAAGCAAGTCCTTAACCAAGCCTTATAACTGCGAAGCCAAAAGCTGCCACTATCAGAGCACTACCAGTTGTGCTTTAATGCAGCACTATATTAAGGTTCATGGTTACTCCGAGAAGATGGTGAAAGAGATGGAGGTGTTTCAATCTGAGACATTGGAGCCTTTCAAAACACCTGACAGCTCTGAAAATTCGGTCTTGGAGGATGATCAATCACAAAGCGAGTTTCTTGTGCAGGCTACAGTCAAGCCTTATGCCTGTGAAGCGAAGAGTTGCAACTACCAGAGTGTTACTAGTCATGCTTTATTGAAGCACTACATCAAGATTCATGGGTACTCCGAAAAGAAGGTGAAAAATATGGAGGTGTTTCAGTCTCAGATATTCAAGCCTTTTAAGTGCCATTTGTGCTCCAAGAGTTACAGAAACAAAAAAGAACTGAGGCGTCATTATATTCAAATGCATCACATAAAAGAAGAC
Associated Phenotype:
Not determined