Busch Lab

ZMP

elavl4

Ensembl ID:
ENSDARG00000045639
ZFIN ID:
ZDB-GENE-990415-246
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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