ZMP
wu:fc76b04
Ensembl ID:
ZFIN ID:
Description:
Wu:fc76b04 protein [Source:UniProtKB/TrEMBL;Acc:B3DLG3]
Human Orthologue:
LARP1B
Human Description:
La ribonucleoprotein domain family, member 1B [Source:HGNC Symbol;Acc:24704]
Mouse Orthologues:
Larp1b, Larp1b
Mouse Descriptions:
La ribonucleoprotein domain family, member 1B Gene [Source:MGI Symbol;Acc:MGI:1914604]
La ribonucleoprotein domain family, member 1B Gene [Source:MGI Symbol;Acc:MGI:1914604]
La ribonucleoprotein domain family, member 1B Gene [Source:MGI Symbol;Acc:MGI:1914604]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42944 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42945 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1234 | Nonsense | Available for shipment | Available now |
sa9587 | Nonsense | Available for shipment | Available now |
sa12850 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42944
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 |
---|---|---|---|---|---|
ENSDART00000025096 | Nonsense | 21 | 1076 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 17 (position 26596091)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 26736010 |
GRCz11 | 17 | 26754401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTTGCGAGCGACTTGGACGTGACAATCGGTTGTTTGGGCGAAGGGAAC[C/T]AAAACAAGTCGGACGCGGATCGACCCGAGCAAGCTGACCGAACCACGAGC
Long Flanking Sequence:
GACATGGCAACCCTGCTCTAGCTCTACCACGTTCTGCTGTCCAGCTGTACTGCAGTAAGACCGCAAGGGGCGACAGAGAGGCGCCACACACTCATCCAATGACTCGTGGCCGTTCGTAGTATTTCCTTTTATTTAGGTGAGTTGCAGATCAGCCAAATCGTGGAAGTGTGTTGAAAACATTGGCAAAGTTTCTCTTTCCTTCGCCTGGCTTACTGTAATCGCTTAGTGTGATCCCACAACATGGCTTCTTTAAGGGATCGAGCATTTTGACATTTAAAAACACGACAAAGTCCGATGCAGCTATTCGCCGTGTTTCAAGCTGTTGGCTGTCAACTTGTGCTGTAGCTGCAACAGCTTTCATCGACTCTTTTTCTTCGTTTGGGCTGGAAACAACTATTGCGGGATAGTGAAAATAATAAGAAGGCGTGGGCGTTTGAACCATGACCACTGAAGTTGCGAGCGACTTGGACGTGACAATCGGTTGTTTGGGCGAAGGGAAC[C/T]AAAACAAGTCGGACGCGGATCGACCCGAGCAAGCTGACCGAACCACGAGCCACGAGGAGGGGCAGCAGGATCCTCCTCAGGGCGACACTAAACATCCAAAACAGGGGGTCATGGAGAGCAAAGCGGATGGCTTGAGCACGGACAGCACGAACGACAAGGAGAACGAGCAGAATGCATCAAGCCACGAAGCAGAAACTGCCAAGAAGAAAGTGGTCGAGGCTCCTCCGCCGAAAGTCAACCCCTGGACGAAAAGGAACTCGTGCCCTCCTAATAATACCAACAACAGCTCGCAACAAACAGGTAGGGAGTTTGTGGCCACAACACGCACTTTTATGCCCTCGACAGCATTTATTCTGGTGCACACATGTGCTCTGTTAGCTCGCATGTGCTACTGCAAACAGGAGCGGCCATTGAACTTGTGTCACTTCACTTTTATCGCCCTTTTTGCACGTGCGTGCACTTGTGCTTTGATACGGACCATAACGACGGCTATTCTTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42945
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 |
---|---|---|---|---|---|
ENSDART00000025096 | Nonsense | 509 | 1076 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 17 (position 26623715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 26763634 |
GRCz11 | 17 | 26782025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGCAGTCTCTCTGATCCAGATGCACAGCCGTGGATACAGGTGGAGAAA[C/T]GACACAGAAACACATCTGGGAAAAATAAGGTACTTCTGGATCCACTAAGA
Long Flanking Sequence:
AACTAAAGTCATGCTACACCTACCAATGGATGTAATAGTTTTTAATTTAAAAAGCTAAAGTGTTTGTTTGTGGAAAAAAATTAGGTAAACATCATTTTGGGTACTTGCCAGTGATTTTTAACACCAATTTGGTGCTTATCAATTGTTATTTAAGGTCCTGCTTTTGCTGTTTAAGGCTTTTAATTTAACTTTATATTTTGCTCTGTTGTATTATTGAGTTAAACTATTATTTTGCTTAATTTTTAAAATCCAGGACTCATCAACTTATTTCTGTTTCTGCGTGTATCTCAGTGTCGTCCTCTCCAGTTAATCAGCACATGGATGAACCCTCTCTAGTGAATGGCCAAACCAGCGATGAGACAGATACAGCCAAACCTCAGTCCAAAGAATCGTCCCCTTCAGACTCAAAGAGCAGCTCTGGTGAGGATGGGAGTAATCTTAAAGAGCGCTCCAGCAGTCTCTCTGATCCAGATGCACAGCCGTGGATACAGGTGGAGAAA[C/T]GACACAGAAACACATCTGGGAAAAATAAGGTACTTCTGGATCCACTAAGAGTATTCTGACATAAGACGCTGTGTTATGTTGCCTGTCAATTCTTACAAATACCAAAATTTGCTGATTTTAAAATGCAATAGGGTTTTGTGAATAAAAATAAAGTGAAAGTTAATGTAAAATAAAGTTAAGTCTTTTTAAATGCAAGTGAGCTTAGGTATTAAAGTGGACAGGCTTATGTGTTTATTTAGATCCCCATTAGCCCCTGCCAACGTAGTTGCTGTTCTTCCTGGTGTCTGACAAACAAAATGACACATTTACATCAAATCATCATCAAAACCAATACAAATAAAAAACATTTAAAATAACACAACAGAAACAAATACCAAAACCAACAGTAGATACAAATATCACAACCAAAACCATAATCATAGAAACAATACATAGTTTAAAATTTGTTTAATACATTGAAAGTATCAAATAACTACATTTAAGTGTAATCAGTATTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1234
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 |
---|---|---|---|---|---|
ENSDART00000025096 | Nonsense | 710 | 1076 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 17 (position 26632732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 26772651 |
GRCz11 | 17 | 26791042 |
KASP Assay ID:
554-1143.1 (used for ordering genotyping assays)
KASP Sequence:
AATCATCCAGTGTGCCTAGAACCCCACGTACACCTCGTACACCTGGAAGA[C/T]AAGATCCCACCAAAACCCCACGGTTCTACCCTGTCATTAAAGAAGACAGC
Long Flanking Sequence:
TCAATGTGGTTAATATTTTTTAGGAAATGGAAAACTTTAAAAAGCTCAACATGATCAGCCAAGATGAGTTTGAAACTCTGACCCCTAAACTTCCCATTGACCCAAACCAAGAGGTCCCGCCTCCTCCACCATGTCAAACAGGTGATTGGACATTTCATTTCTCTATTAGAAAAGCATTGCATTTATCTTTCTGTGATTTGTTTTAATATGCAAACAATTAATGTAATTATTTTTTTCCATATTTTTACAAGTATTTATTTTACTGTTTTATTCAAATAAAGTGTCACAAAATAAATGCATACACATGCTCAGGAAAAATATTTAATATTTAAGAAGTTCCTTGGTTTTCTTTACATTTGTAAAAAAAAAAAAAAAAAAGTTTAATTTTTTTGTTGCTTTTTTCTGTAGATGATTCTAGCATGGCTCATTCTCTCCCTGCGGATGTCCCAGAATCATCCAGTGTGCCTAGAACCCCACGTACACCTCGTACACCTGGAAGA[C/T]AAGATCCCACCAAAACCCCACGGTTCTACCCTGTCATTAAAGAAGACAGCGGCAACCTTGATGGAAAGGTACGTTTGAACTAAAGCAGAATTCTTTGTGGGATTATCAGAATAATGAATAATAAAAAGAGTAATTAATAGTAAACCTATAGACAATTAAAAATATGGCACGTTATAAAGGGATAGTTCTGTGTTCTACAGTGGTTAGATTTTTATTTTTATCAATTTTTATTTTTTTTAAAAACAAGATATTGTGAACAAGAATGCTGGAAAATTTTTAATCTATACACAAAACAGGAATATCACATAAAAGCTTTGTGAATAATGCAGCGTTTCCACCCATTAGTCAAAGAGAACAAAATTGTCTTGATTAACTGGTGCCAAATATTAAAAGTAAAAATGGAATTTGCTGGGGTAGGAGAAGCTGCGTCGATCTTTTTTTCTTTTAATAAATGACTTGTGCCTCAGAAGACAAATGCTGACGTGCCTTTAACACGTGGT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa9587
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025096 | Nonsense | 948 | 1076 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 17 (position 26642513)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 26782432 |
GRCz11 | 17 | 26800823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCCAAACTCAAGGAGTACCTCAGCAAATTTAAGAGCATTGATGATTTC[A/T]GAGTAGAAGTRAGTATAAGAATCAGCTGTACGTGAATATCTCTTGCAAAT
Long Flanking Sequence:
TAAAGTGTAGTTGTGCAGAGACTGCAAAATGTTTGACTGCAAGCATTTTTAGCAAATCAATTTAAATAATATCAAAGATTATTTTTTCTCCATCTTGTGTTTTCTTCCATTACCATGCGTTTAGGTCTCAAACTCAATTCCTGGAGGGCCGCAGCTCTGAACAGTTTTGCTCCAACTTTAATCAAACACAGCTTATCCAACTAATCAAGTTTTTCAAGACTACTAGACACTACTAGATCAGCTGTGTTTGATTAGGTTTGGAGCTAAACTGAGCAGAGTTGCGGCCCTCCAGGAATTAGTTTAAGACCCATGGTTTAGACGCTTCATATAATTATTAAAATGGACTAAGCTAATGTTGTGGTTTTTTCATATTATTTGTAGGTCAACTATATGGACTGGAGAAATTCTGGGCTTTCCTGAAATACTCAAAGGTGAAGAATCAGGACATTGATCCCAAACTCAAGGAGTACCTCAGCAAATTTAAGAGCATTGATGATTTC[A/T]GAGTAGAAGTGAGTATAAGAATCAGCTGTACGTGAATATCTCTTGCAAATGGATCATATGGATAAAGTCCACACGAATTTAAAAAATCTTTCTAAATAACATTATTAATTAATTATAATCGAAATCAAATTTTATTTCCTTTGCTCTTAGCCACCAATGGCAGAGGAAGGGATGAGGAGGAAAGCACACTCCTCCGCTGGAGATGAGGTGAAACGTAGACGACACAACTCGACTTCATCATCGAAACAGACCCAAATCACCAAGACCTCCTCAGACAATCAGACGACCGCAAAAACAGCCCATGATCAGGCTGGTGCCTCAGCGGCAACCAAATCCACCAATCAGCCAGCTGCCAAGGCAGCCTCAGCCAATCAGAAACCAGCACCTCTGACCGCCAAGAGCAGCTCAGCCAATGAGCAGCCTGCAAAAGCCCCACCCAAAGAGAATGTGAAGAAGAATACCTCATCAGATGCTCGCAAAGCGGAGGCAGCAACGAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12850
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 |
---|---|---|---|---|---|
ENSDART00000025096 | Nonsense | 983 | 1076 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 17 (position 26642760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 26782679 |
GRCz11 | 17 | 26801070 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGAGATGAGGTGAAACGTAGACGACACAACTCGACTTCRTCATCGAAA[C/T]AGACCCAAATCACCAAGACCTCCTCAGACAATCAGACGACCGCAAAAACA
Long Flanking Sequence:
TTGATTAGGTTTGGAGCTAAACTGAGCAGAGTTGCGGCCCTCCAGGAATTAGTTTAAGACCCATGGTTTAGACGCTTCATATAATTATTAAAATGGACTAAGCTAATGTTGTGGTTTTTTCATATTATTTGTAGGTCAACTATATGGACTGGAGAAATTCTGGGCTTTCCTGAAATACTCAAAGGTGAAGAATCAGGACATTGATCCCAAACTCAAGGAGTACCTCAGCAAATTTAAGAGCATTGATGATTTCAGAGTAGAAGTGAGTATAAGAATCAGCTGTACGTGAATATCTCTTGCAAATGGATCATATGGATAAAGTCCACACGAATTTAAAAAATCTTTCTAAATAACATTATTAATTAATTATAATCGAAATCAAATTTTATTTCCTTTGCTCTTAGCCACCAATGGCAGAGGAAGGGATGAGGAGGAAAGCACACTCCTCCGCTGGAGATGAGGTGAAACGTAGACGACACAACTCGACTTCATCATCGAAA[C/T]AGACCCAAATCACCAAGACCTCCTCAGACAATCAGACGACCGCAAAAACAGCCCATGATCAGGCTGGTGCCTCAGCGGCAACCAAATCCACCAATCAGCCAGCTGCCAAGGCAGCCTCAGCCAATCAGAAACCAGCACCTCTGACCGCCAAGAGCAGCTCAGCCAATGAGCAGCCTGCAAAAGCCCCACCCAAAGAGAATGTGAAGAAGAATACCTCATCAGATGCTCGCAAAGCGGAGGCAGCAACGAGCAAAAACAAAGAAGCCCAACAGCCAAAGAAATGAAGCCCTTACCACACTATATACAGTATTTGAATGCGATACTCTCGAGCTGTGAAAGATTTTTGAATGCTGGTGCAGGCTTACCTTTTACACCCAAAACCTCGGAAGTGAGCCAGTCAAAACCGTTAAAGCAAAGACCAACTGTCAGTCCGTTGCATTCACAAAGCAAAGAGTAAACCAGAAGTGTCTTTGTGTTGTACAAAACGCTAGGTTGACTTC
Associated Phenotype:
Not determined