ZMP
larp4a
Ensembl ID:
ZFIN ID:
Human Orthologue:
LARP4
Human Description:
La ribonucleoprotein domain family, member 4 [Source:HGNC Symbol;Acc:24320]
Mouse Orthologue:
Larp4
Mouse Description:
La ribonucleoprotein domain family, member 4 Gene [Source:MGI Symbol;Acc:MGI:2443114]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11471 | Nonsense | Available for shipment | Available now |
sa13614 | Nonsense | Available for shipment | Available now |
sa9281 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11471
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115170 | Nonsense | 279 | 773 | 8 | 16 |
ENSDART00000135023 | None | None | 206 | None | 5 |
ENSDART00000144419 | Nonsense | 279 | 787 | 8 | 17 |
ENSDART00000115170 | Nonsense | 279 | 773 | 8 | 16 |
ENSDART00000135023 | None | None | 206 | None | 5 |
ENSDART00000144419 | Nonsense | 279 | 787 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 27762776)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 27595598 |
GRCz11 | 23 | 27522139 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACCTAAAATTGAATTGAGTTTCTTTGTCTTCACCCAGGCATACAGATA[T/G]TTAAGGGAAGAAGKCAAGACATTTCAGGGAAAACCAATCATGGTAAGACC
Long Flanking Sequence:
ATACGCGAATATGTCTTATGAACCAGTGAATAAAAAGAGTAGCCTCTACAACCAGGGTTTTGGAATCTCCAAGCATCAATCTTTCCATAGGTTTAAAAGTTGTGGATTTAGAAAGCATTTCTGAAATATACATTTTGTAAGGACAAAACTCCTTTAAACATAGAAAAAATTGCTTATTACATTTTGTGGGGTCGCATCGTGTGTTAGGACATTGTGTTACTACTATGAACAGATTTGAATACTTTAGCTCATCCATGAACATGATTTCTGCAGGAGTCCCATAGGATGAAATCAATACATGCCCTCTAGTAGTGTAAAGTACATACTGTAAACATACAGCACATATAGCATCCTCAATCTAAAGCTTTGTTTATTTGTCCATTTTTAAATACTTGTTTTCAATTGTCACAAATTGCATACTGTGCCTTTTGAACAAATAGTTTGCATTTTGCACCTAAAATTGAATTGAGTTTCTTTGTCTTCACCCAGGCATACAGATA[T/G]TTAAGGGAAGAAGTCAAGACATTTCAGGGAAAACCAATCATGGTAAGACCTTTTGCAAAACGTTGCTTTTTAATTTATGAAATCATGTGTGTTTTTATATGTTGTGCGTTCTCTTATTCTTAGGCCAGAATAAAAGCCATCAACACATTCTTTGCGAAGAATGGCTACCGCAGCCTGGACTGCAGTGTGTATCCTCAGCAATCACACACTCCACCCCAGTACAACTCTCCGCTCTTCATGCAGCCTGTTTACAGCCCTCAGCAGCAGTACCCGCTTTACGGCATTGTACCGCCTACTTGGACGCCGTCTCCTACTCCATACTTCGAGACTCCCCTGGTAAGACTTTAATTTTCACCATGGATGCACCTAAAACGATAAGCCCGTCAATTATGTCATTGTAAAACGTGTGTTCCATTATTTGAATTGAAAGTGATATACTGTGTTTTACAGGCACCTTTCCCTAACAGTGGTTTCGTCAATGGATTTAGCTCACCCGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13614
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115170 | Nonsense | 279 | 773 | 8 | 16 |
ENSDART00000135023 | None | None | 206 | None | 5 |
ENSDART00000144419 | Nonsense | 279 | 787 | 8 | 17 |
ENSDART00000115170 | Nonsense | 279 | 773 | 8 | 16 |
ENSDART00000135023 | None | None | 206 | None | 5 |
ENSDART00000144419 | Nonsense | 279 | 787 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 27762776)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 27595598 |
GRCz11 | 23 | 27522139 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACCTAAAATTGAATTGAGTTTCTTTGTCTTCACCCAGGCATACAGATA[T/G]TTAAGGGAAGAAGKCAAGACATTTCAGGGAAAACCAATCATGGTAAGACC
Long Flanking Sequence:
ATACGCGAATATGTCTTATGAACCAGTGAATAAAAAGAGTAGCCTCTACAACCAGGGTTTTGGAATCTCCAAGCATCAATCTTTCCATAGGTTTAAAAGTTGTGGATTTAGAAAGCATTTCTGAAATATACATTTTGTAAGGACAAAACTCCTTTAAACATAGAAAAAATTGCTTATTACATTTTGTGGGGTCGCATCGTGTGTTAGGACATTGTGTTACTACTATGAACAGATTTGAATACTTTAGCTCATCCATGAACATGATTTCTGCAGGAGTCCCATAGGATGAAATCAATACATGCCCTCTAGTAGTGTAAAGTACATACTGTAAACATACAGCACATATAGCATCCTCAATCTAAAGCTTTGTTTATTTGTCCATTTTTAAATACTTGTTTTCAATTGTCACAAATTGCATACTGTGCCTTTTGAACAAATAGTTTGCATTTTGCACCTAAAATTGAATTGAGTTTCTTTGTCTTCACCCAGGCATACAGATA[T/G]TTAAGGGAAGAAGTCAAGACATTTCAGGGAAAACCAATCATGGTAAGACCTTTTGCAAAACGTTGCTTTTTAATTTATGAAATCATGTGTGTTTTTATATGTTGTGCGTTCTCTTATTCTTAGGCCAGAATAAAAGCCATCAACACATTCTTTGCGAAGAATGGCTACCGCAGCCTGGACTGCAGTGTGTATCCTCAGCAATCACACACTCCACCCCAGTACAACTCTCCGCTCTTCATGCAGCCTGTTTACAGCCCTCAGCAGCAGTACCCGCTTTACGGCATTGTACCGCCTACTTGGACGCCGTCTCCTACTCCATACTTCGAGACTCCCCTGGTAAGACTTTAATTTTCACCATGGATGCACCTAAAACGATAAGCCCGTCAATTATGTCATTGTAAAACGTGTGTTCCATTATTTGAATTGAAAGTGATATACTGTGTTTTACAGGCACCTTTCCCTAACAGTGGTTTCGTCAATGGATTTAGCTCACCCGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9281
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 |
---|---|---|---|---|---|
ENSDART00000115170 | Nonsense | 740 | 773 | 16 | 16 |
ENSDART00000135023 | None | None | 206 | None | 5 |
ENSDART00000144419 | Nonsense | 754 | 787 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 27752461)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 27585283 |
GRCz11 | 23 | 27511824 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCTCGCAGCAACGGACYCCCCAGAAGCAGTACAGGGGGGTTCAAGCTA[C/T]GAGAGCARCAGAGACGCCCTCCCTTCGGCCATCGCGGTTCCCCCCAGGGA
Long Flanking Sequence:
ATAATTGATGCTTTAATTTATTTTAGTTTATAATATTTATTTTTTATAGTAATCATTTAAGACTTAAGTAATAATAAAATAGAGATAAAACTATAATACATTTATATGCGATTTATCTTTCCAAAATCGTTAAATTCTCCATTAATACACAGATGAAACCATTCACTAAGTATTTAAAAAAGTAACAAACTTTCTCATTTTTCTCCTCTTCTCTTCAGGAACCTCGCAAGCTCAGTTACGCTGAAGTATGTCAGCGACCACCTAAAGATCCCCCTCCTCCAGCATCCTCTTCCAGCCCCAACAATGCAAGCGCACAGCCTCTGAGAGAGCTGCGTGTCAACAAGGTGGAGGAGCAGGCCTCCAGTCCGGCAAGCAAACAGGAGCGGCCTCAGGAATCGGGGGGAAACTGCAAGGCCAGGGAGGGCCGGCCGGCCCGTGACTCCCAGAGCTTCTCTCGCAGCAACGGACCCCCCAGAAGCAGTACAGGGGGGTTCAAGCTA[C/T]GAGAGCAGCAGAGACGCCCTCCCTTCGGCCATCGCGGTTCCCCCCAGGGAGGTTCCAGACACGCTGGAAAAGAGCAAAACATCCCACCCATATCGCCAAAGTAAAGACTCAACAGAAATCCTTAATGTATGAATATTTACACACACACACACATATATATATAAGATATATATGTAAATATATATAAATATATATATATATATATAAAGAGATGAAATATGATATAAAGTCAAAATTTAAAAAGGTATTCACCTCTCCTGCCTGGAGCACTTCCAGAGGAAAAGTCTCATGAAGTGACAATGCACAGACTGGGGTTTCCAGGCAAACGGGCATCAGAAATTGGAAGCATTTGTTGCTTGCTGAAGGACACCATCAAATAGGAAAAATAAGAAAAAAACAAAACATTTCATGCTTCTAACCTGACAATGTCCCTTCAGAATGTAAATCCATGTGAGTTTTATTTTTGTTTGGTTTTTGAGTACGGCCTCTCTTAGCTCTAT
Associated Phenotype:
Not determined