ZMP
celf5
Ensembl ID:
ZFIN ID:
Description:
CUG-BP- and ETR-3-like factor 5 [Source:RefSeq peptide;Acc:NP_001124260]
Human Orthologue:
CELF5
Human Description:
CUGBP, Elav-like family member 5 [Source:HGNC Symbol;Acc:14058]
Mouse Orthologue:
Celf5
Mouse Description:
CUGBP, Elav-like family member 5 Gene [Source:MGI Symbol;Acc:MGI:2442333]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37495 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43814 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37495
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093310 | Nonsense | 177 | 597 | 1 | 11 |
ENSDART00000093312 | Nonsense | 107 | 506 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 20329487)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 19986180 |
GRCz11 | 22 | 20011158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAATCCACGAATTGACAGTATTAAAGGACCGATACACCGGCATGCAC[A/T]AAGGTAAACGCGTGATTCCCTTAATGAGAGTGTGATTTGAGCTTGTAAAC
Long Flanking Sequence:
ACATATACTCTGACTGTGTGCGTATGTGTATCGCCGAGAAAGTAAGTCTGTGTTTCCAGCTGACTGCTCGCTCTCTCTTAGTGTGTGTATGTGTGTGTATATGTGTGTGTTGTCATTATTATTATCCAGTCTGCTCCCAGCTCAGAATGGCCAGATTCACTCAGACTGAGACAAGAAGGGAGCAGCACCCACAGCCGCCCCATCCCGCTTACTCCAGCCTGCTTTTCACTGGACCCGGGGCAGCACCGACCCAACATCCACTCCTCCTAATCCCGCACCAGCACCAGTACGCTCAGATCCCATTTCCTAAACCCATGAACGGGTCAGAATCCATCTCCATTCATCCGGAGAACGGCACCATGAAAGACCAAGATGCCATAAAACTCTTTATCGGGCAAATACCGCGGAACCTTGAGGAAAAAGACCTGAAACCATTATTCGAACAGTTTGGGAAAATCCACGAATTGACAGTATTAAAGGACCGATACACCGGCATGCAC[A/T]AAGGTAAACGCGTGATTCCCTTAATGAGAGTGTGATTTGAGCTTGTAAACACTACCATATATTATTGTTTGTTTTTGGAATGACACAAAAATAATAATTAGACCTGGTGAATGTTTAGTTTTTACAAATATTATTTTGCCTTCTGCACAAAATGTACCCAATTCATTAGTGACGCATGCAATATTCTAATATTTATTATGATTCATGCATACATTTTTTGGTCCACTGTCATGTCAACATAAAACCCTAATATAAATATATAAAGCTTTCTAATATAAGGCCGCTTTAGGTACTATTTTACACTTAATCTACATCGTTTACAGATAACTTATCAGCTTAGCTTTGGGTGTTTGCATGAATATTCATATTTATTCTCAAATAAAGCGCCTTTCTTTATGGCAGTTTAATATTGGATGCTTTGGAACTGGGGCAAAGAGGCTTAGAAAATAATTCATATTTAAAGAGTCATCTGCATCTTCCATTCTTTTTAATAGGGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43814
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 |
---|---|---|---|---|---|
ENSDART00000093310 | Nonsense | 229 | 597 | 4 | 11 |
ENSDART00000093312 | Nonsense | 158 | 506 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 20060957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 19717650 |
GRCz11 | 22 | 19742628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGATTCGTGCTGTTTTTCTTTGCTTCAGAAGACAGGAAGCTGTTCGTC[G/T]GAATGCTGAACAAACAGCAGACGGAGGAGGACGTGTACCGTCTTTTTGAG
Long Flanking Sequence:
CAGCTCGAAGAAAGCATTATCTATAAACACAACCAATTAGCACAGACTAAACACAAAAGCCGATGACAGCATCTCACGTTGCTTTGGTTTTCAGGTCAACCGTAGCTTTAGTCTCAGCCTATCTCCACCCTCCAGAGTTTGGTAGAAACTCTGTCCGCTTCTTCCCATTAAAGCAGGCCTCTAAGCAGGACAGCTTAGCGCTATCACCTCAGGCCTACCCTACCATTTCCAACACGGGGTTGAACCCAATTATCCCCCAAATTAAAATGAACAGACTTGGCACGGGGAACAATTACTGCTGCGACTCCATTCCGCAAGCTAAATGGGCCAAGCAAAAGCAGTCCCTGTTTGCCGGTCCTGGCCGAGGCCCAAAAGTCTGAGTGCTATTTGGGCTGTGCTTACAATAGTAATGTATGCGGGTAATGGCTAGGTTAGGGGTGACGCCAGTCGTTTGATTCGTGCTGTTTTTCTTTGCTTCAGAAGACAGGAAGCTGTTCGTC[G/T]GAATGCTGAACAAACAGCAGACGGAGGAGGACGTGTACCGTCTTTTTGAGCCCTACGGAGTCATCGAGGAGTGCACTGTGCTTAGAGGTCCCGACGGAAATAGCAAAGGTGGGTTACGCCACCTTTTATGGCATGATGATATATTAATAGTCAATATGTCAAAAGGAACACTGTTATGTTGACTGAGGATGTGTTTATTTGATGAAATAATTCGTGCAATCTAAGGAGGGATTCCCTTGACTCCATTTTCAACCAAAAACAAACAAAATAAGTTGTTTATTCACACAACAACAGCGTATTTGGCAGACCTGAAAACAAACTTTTTAATGATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTTACTGTATTTTTATCAAATAAATGTAGCCTTGGGGAGCAGAAGACATTTCTTCCAATTATATTAACAAAAAAATAAATAAACAAACAAATCAACA
Associated Phenotype:
Not determined