ZMP
elavl4
Ensembl ID:
ZFIN ID:
Description:
ELAV-like protein 4 [Source:RefSeq peptide;Acc:NP_571528]
Human Orthologue:
ELAVL4
Human Description:
ELAV (embryonic lethal, abnormal vision, Drosophila)-like 4 (Hu antigen D) [Source:HGNC Symbol;Acc:3
Mouse Orthologue:
Elavl4
Mouse Description:
ELAV (embryonic lethal, abnormal vision, Drosophila)-like 4 (Hu antigen D) Gene [Source:MGI Symbol;A
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45316 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34358 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16615 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45316
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 |
|---|---|---|---|---|---|
| ENSDART00000028601 | None | None | 367 | None | 8 |
| ENSDART00000110171 | None | None | 403 | None | 8 |
| ENSDART00000134787 | Nonsense | 13 | 408 | 1 | 8 |
| ENSDART00000141173 | Nonsense | 13 | 130 | 1 | 4 |
The following transcripts of ENSDARG00000045639 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 16524074)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 15968962 |
| GRCz11 | 8 | 16004674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCACCAACAAGATGTTTGAAATCAGCCGAACACTGAACGCTGCTTTGT[T/A]GAGCAATGAGGTAAAGGAATCGGATTTTCTTCTTCTTCTGTCACCTCACT
Long Flanking Sequence:
AGGAGTTTAAACTAAGAGCTATGTTTTGGGACGAACTAATCTGCTAGAGAGCAGTGTGAGGATCGGAACGCATTGTGCGAGCGAGTGTGTGGAGGACAGATAAGGGAAGAAGCCCGGCAGACCGACTGCTTGTTTTAATGTGCTGACTCTGGGGAGCTAAAAAAAAAAAAATATTGACTCTTCAGTCGTGCGGCGTGAGCCAGGGCACAAGCGCCACATTTAACAAGAGGTGCACCAGAAAACACGGGCGCAAGAGAGGAGAGAATACATCCAGCCAGACAGCACATATAGAGGATTTCTCCTTCCTTTTCTTCTTTTTTTTAATCTGTTCATTTTTCTTTCTTTTTTTATTTCTCGGGACTGATTCCCATTTCCAGTAAAGAAAAAGGAGCCGTAGAGCCAGGAGAACGCCAAAAAGAAAGCCCCGCAACAAAGCGACAAGAAACGAAACACCACCAACAAGATGTTTGAAATCAGCCGAACACTGAACGCTGCTTTGT[T/A]GAGCAATGAGGTAAAGGAATCGGATTTTCTTCTTCTTCTGTCACCTCACTTCTCTAAGTGTGTGTTCATTATTCCGTTGTGCGTAACGTTTCTATGTTTGATCATGCTTCTAAATGTGGCAGGTCTAAATGAATGTGCAGGGATTGAGCATTTAGGTCCAGTTAAACGGCTGCTAGCTGAAGGCAGAACCTCTTTGCTCTCCGGGCGTACTGTAATGGATGAGAGACTAGACTCGCTCTCTCTCTCTCCCTCTCCCACGCACAATCATTTCATTTTCTCATTTACTCAAAGCAAGATAGCTGTAACTGCTGAGCTTGCTTGATGACTTGCCCATCTGGGGCTTGCACTGACTGTGTGTGTGTCTGTGTGTGTGTGTGTGTGTGCAGGGTAAATGTGAACGTAAGCACTCGGCTCTTTATCACTGTGGCAGTTCAGTTTTCTCTTTTCCTTTCGCCACTTGCTTTTTCTTTAGCCTGTATATTTGGTTACCACCTTGGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34358
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 |
|---|---|---|---|---|---|
| ENSDART00000028601 | Nonsense | 119 | 367 | 5 | 8 |
| ENSDART00000110171 | Nonsense | 155 | 403 | 5 | 8 |
| ENSDART00000134787 | Nonsense | 163 | 408 | 5 | 8 |
| ENSDART00000141173 | None | None | 130 | None | 4 |
The following transcripts of ENSDARG00000045639 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 16612693)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16057581 |
| GRCz11 | 8 | 16093293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAACATGATCACAATTAATACTCGTGTGTTTTGTCTACAGGTGTCATA[T/A]GCACGGCCCAGCTCAGCTTCTATTCGTGATGCTAATCTATATGTGAGTGG
Long Flanking Sequence:
CCATTGTACTTTGTGTGTTTAATTTCTTGGGTGTATCGCTTCTCTTCAGAAACAGGGTTAGAGGTGGTGTACGCTAATATTGAATTTACATTTTCATTCTTCCTGTGAAACAATTTGCAAAGCGCTTTAGATGTCATGTGTATATCCCTTATCTGCGAATGAGCACGGATCACAGAGAATCCCTCGCAGCAACTTGTTCCTATTCAAAATATTATAATAAGTTCTCCTTTGTTCTTAAATGGAGGATTTGGGGGCATTATCTTTCTGAAGTCTCTAGCTGCTCCAGGTCAATTTAGATATACAGACCACCAGCACTGTGTGAGACAAAATAATATGACCTCTGGCATCTCAATGCTACATACTGCCATTATAAAATGCTAAAAAAATATCCTCTGAAACTGGATGGGGAGTTTAAATGAATAATTTGCTTCATTTAAATCCTGCCACTGTAGAAACATGATCACAATTAATACTCGTGTGTTTTGTCTACAGGTGTCATA[T/A]GCACGGCCCAGCTCAGCTTCTATTCGTGATGCTAATCTATATGTGAGTGGACTGCCTAAGACCATGACCCAGAAGGAGCTGGAACAACTCTTCTCTCAGTATGGCCGGATAATCACCTCCCGCATTCTCGTCGACCAGGTCACAGGTATCAGTGGGACCACTTTTCTCTCAACCTAAAGCATGTAAACAAACAAACAAACTGAAATATATTTCGTAATACACAGTAGTCAACATTTGAAGTGGATCAAACCCTTTAATCAAAGTTGTCCTAAAACAATTCAACAATTTTTGAAAAGCCTTTTTGATCCACTTCAAATGTTGACTACTGTATTTTTGGTTTAACCTATATTTGCGTATATATGTCAAACATAAGAAAATACTGGGATACTTTGAGACACTTTGTTGTCTTTATATTAAAGGACATGCTATAAGAAGCAATGTAAACATGGCTGTAGCATTAATATAGCTTTGAACCTATTAGCTATTTCGACCAATAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16615
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 |
|---|---|---|---|---|---|
| ENSDART00000028601 | Nonsense | 302 | 367 | 8 | 8 |
| ENSDART00000110171 | Nonsense | 338 | 403 | 8 | 8 |
| ENSDART00000134787 | Nonsense | 343 | 408 | 8 | 8 |
| ENSDART00000141173 | None | None | 130 | None | 4 |
The following transcripts of ENSDARG00000045639 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 16631493)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16076381 |
| GRCz11 | 8 | 16112093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATCTTCGTCTACAACCTCTCCCCAGACTCGGACGAGAGTGTCCTGTGG[C/T]AGYTCWTCGGACCRTTTGGTGCCGTCAACAATGTCAAGGTGATCCGCGAC
Long Flanking Sequence:
AGGAGAATGAGAGCAGATTTACTCGCTTGCATGCAAAATCTCTGATGAATTTCGAAGGTATTAATGTGCAGAGTTCCTGCAATTTAGTCTCCCAATAGATCCGCGCAGGAAGAGGAGCCTGTGCTTGCGTGCGATGCTTTTGCGTGACCCCATGCCGCCAGCTCTAGAGTGCAGCCTTTTCAGTCGCCTTTCTAAAAGCCCTCCAGTTGCATCCCGCTTAAAAAAACTTAGCAGATATTTAGACTCCGCAGTTATACATTGGAAAGATTGTGTTGCTGAAATTGCTTGTGTGCCCATTCAAGACACAGTTAGTAAGCTTGGCTTGCAGCAGCTCAACTTATTCATCTTCCTCACTCTCTTTCTTGTCCTGCAGGTTCTCTCCCATCACCATCGATAGCATGACCAGTCTAGTAGGGATGAATATCCCCGGTCACACAGGAACAGGCTGGTGCATCTTCGTCTACAACCTCTCCCCAGACTCGGACGAGAGTGTCCTGTGG[C/T]AGCTCTTCGGACCGTTTGGTGCCGTCAACAATGTCAAGGTGATCCGCGACTTCAACACCAACAAGTGCAAGGGGTTCGGTTTCGTCACCATGACAAACTACGACGAAGCAGCCATGGCCATCGCCAGTCTGAATGGGTACCGGTTGGGTGACCGTGTCTTGCAAGTGTCTTTCAAGACCAACAAGACCCACAAGTCCTGAACTCCCTTCCCACCACTTGTGTAGCTCCTTACAGCTCCTCTAATACTAAAAAACCCACCTCAGCCCACTCAGCTACTCTAAACAGGAACACACCCAACCAACAATCCCACAAAAAAAAAAGAACTGGATATGGCTTATAATATAACTTTGGACCTATAAGCCAATGTTGCCTAAGTATTACAAAAACGACAAATTGAGAATATTCATTATTTGGAGACCCTGGAAGTGGTACAGGGATTCTGTTGTATATCTTTTCAAGTTATTGTGGTTGTCTTTACTTTTTTCTTTTTTTTTTCTCTG
Associated Phenotype:
Not determined