ZMP
zgc:163038
Ensembl ID:
ZFIN ID:
Description:
far upstream element-binding protein 2 [Source:RefSeq peptide;Acc:NP_001082897]
Human Orthologue:
KHSRP
Human Description:
KH-type splicing regulatory protein [Source:HGNC Symbol;Acc:6316]
Mouse Orthologue:
Khsrp
Mouse Description:
KH-type splicing regulatory protein Gene [Source:MGI Symbol;Acc:MGI:1336214]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6606 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39709 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19616 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6606
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 |
|---|---|---|---|---|---|
| ENSDART00000038330 | Nonsense | 278 | 666 | 10 | 18 |
| ENSDART00000140016 | None | None | 136 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 55505382)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54288321 |
| GRCz11 | 1 | 54965972 |
KASP Assay ID:
554-4101.1 (used for ordering genotyping assays)
KASP Sequence:
TTCTGCGAGAGCGGGATCATCCGGGCTTYGAGAGGAATGAGTATGGCTCT[C/T]GAATGGGTGGTGGAGGAGGTGGAGGCGGCGGTGGTGGAGGTGGCGGCGGY
Long Flanking Sequence:
CTGGTGTGAAGATGATTTTGATCCAGGACGCTTCTCAGGGGCCAAACATGGACAAACCACTGCGCATTATTGGAGACCCTTACAAAGTCCAGGTTCGTCTTATATTTATTTTCTTGGCTGCAATTGGCCGTTTCATCTATTATCAGTTGTACTACACTGATTTACCAAGACGTTAGTATTATTGGGTTAGATATTAATACTAGGGCTTTTTTATTGATGGCAAACGTTTTGAAATCCAGCCAGTAGTAGAAAGAAAAGCAAACCCCAATTGTTTTTTTTTGTTTTTTTTTGCTTATGTCTTTGTGTCTGTTGTTTCTTTTTTAAATTATGGAAGAGATGATATGTTGTAAACTTGATCTGGTTTTGCCATAAAATAGCCAGAGAAGCTGATATGACATTTAAATCTCTCTCTTCTCTCCCTCTAGCAAGCCCGTGAGATGGTGCAGGAGATTCTGCGAGAGCGGGATCATCCGGGCTTCGAGAGGAATGAGTATGGCTCT[C/T]GAATGGGTGGTGGAGGAGGTGGAGGCGGCGGTGGTGGAGGTGGCGGCGGTGGAATTGAGGTGTGTATTTAATTGGTCAATCATTATCAATTGGCTAACATGCTGCAGTGTGACATTGTCTTGTTCTGATTGGACAGGTTCCAGTTCCACGTCACTCTGTGGGTGTCGTGATTGGCCGAAGCGGAGAGATGATCAAGAAGATTCAGAATGACGCCGGCGTGAGGATACAGTTCAAACCAGGTCGGTTTAAATGCTTAAATTGATTTAAACTCAATGTGTTAAGTGTCACTTTGATAAGCTTAAGTAGCATGGCCAGAAATGTTGTAGAAATCTAAATTGTGTTTTTATTTATTTTATTTTTTTAATGCCAGAAACCATTAGAATACATTTAATTTCATTTTTATAGATTGTCATATAGTTGTATCTCGACCAAATATTGTTCTATCCAAACAAATCACATATTGATGATAATCTTGTTCAGCTTTCAGCTGTAGTCTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39709
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000038330 | Essential Splice Site | 474 | 666 | 13 | 18 |
| ENSDART00000140016 | None | None | 136 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 55503997)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54286936 |
| GRCz11 | 1 | 54964587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACAGCAGATCGACCACGCCAAACAGCTGATCGAGGACAAGATTGAGG[T/C]GCGCTGAGCATTGCCTTTTTGTTTATTTTATCTTGACATTGGTGTTTGCT
Long Flanking Sequence:
TTCTAAAACTGAAATGCGGTTGAAGAGGCTCATATCTATTGTTTGTACATTTTAGATCTGCAGCTGTAATTTTTGCTCATGCAAAATATGCCATTGTATCATTCAACCTTTACCGTACATTTATTTTTAAGTCTGCATGATTACATTTGTTTTCTCACACTACACTGGTTAATCTCTCTCCCCCATCTCTCAGGGTCCGCCTGGTCCTCCTGGCACAGGGATGCCTCCGGGTGGGCGTGGCAGAGGGCGTGGTCCTGGTGGAAACTGGGGTGGTCCGCCTGGCAGTGAGATGACCTTTTCAATTCCTGCCCACAAATGCGGCCTCGTTATTGGCAGAGGTGGTGAAAACGTGAAGGCCATCAATCAGCAAACAGGTGCATTTGTGGAGATCTCACGCCAACCACCGCCCAACGGAGACCCCAACTTCAAACTGTTCACCATCCGGGGGTCTCCACAGCAGATCGACCACGCCAAACAGCTGATCGAGGACAAGATTGAGG[T/C]GCGCTGAGCATTGCCTTTTTGTTTATTTTATCTTGACATTGGTGTTTGCTGGATTTAACTGGTTTGTTTCTCCTCATAGGGTCCCCTCTGCCCTGTTGGTCCCGGACCCGGTGGACCAGGCCCTGCTGGACCCATGGGCCCCTACAACCCAAACCCGTACCAGCCCGGACCCCCTGGTGGACCGCCACAGTCAGTACTGCCTTAATAGCAAATCAGCTTATAGGATAATGTTAATGTTTGGTTTTCCAGGTTTGGTTGGCATGTCTTGAGGATGGTTTTCTGTGTTTCTGCAGTGGTGGTCCTCCTGGTGGTCAGTATCCTCAGGGTTGGGGAAATGCATACCAGCAGTGGCAGCCACATGATCCCAGTGAGTCTTTTGATTTGATTATATCAATGTCAGATTGCTTCCATATGTTGTTCATTATAATTTTCAGTGCAGTAGGGTGAAAACTAATGTAAAGGTGGTTTACTAAAATACTTCTATTGTGAATTATTTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19616
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 |
|---|---|---|---|---|---|
| ENSDART00000038330 | Nonsense | 555 | 666 | 16 | 18 |
| ENSDART00000140016 | None | None | 136 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 55502786)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54285725 |
| GRCz11 | 1 | 54963376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCACAGATCCAAACGCAGCGTGGGCGGCTTATTACGCTCAGTACTAC[C/T]AGCAGCCAGGAGGGGCAGCTATGCCTGGACAGACGCCTGCAGCTCAGCCG
Long Flanking Sequence:
TTGCTCATGGTAAAGTTAAAATATTTGGATAAATGCTCTTCCTTAAGCATAAAATGACTCTGCTTATGTGAATTTTGTGCTACGTGATGCTGTTAACAAGAAACTGCAGAGATTAAAAGCTCTAAGGATTTAACAAAATATTGGTTAAAAATGAAGAGACACAGCTAGAAGTTTTGCCCATGCAGTGGTTAAAAACAACAGGTCTTTTGTTTCACAAGAGGACCAAACTGAAAGACCGATACCCAATATTTTTGGTATGAATAAAACTCTACTAATAGTTTCACTTGTGTCTGAGCTCTTGTGTTCAGATCATATTTAATTGTAAAATTATGGGGATTGTAATTCTATATTTATTCTAGAGCTCATCTTAGCAGGTTGCTTTGGTTTTATTTTATATAATTTAAGTGAATTATTTTTTTTTTTTTTCCCCTCCCACTTTTTTAGGTAAAGCAGCCACAGATCCAAACGCAGCGTGGGCGGCTTATTACGCTCAGTACTAC[C/T]AGCAGCCAGGAGGGGCAGCTATGCCTGGACAGACGCCTGCAGCTCAGCCGGCTGCTCCCGGTCCTGCTGACCAGAGCCAAGCTGCTCCAGGAGCGGCCCAGCCCGACTACACCAAGGCCTGGGAGGAGTATTACAAAAAGATGGGTAAGAGGCATCACTTCCTGCATGTTAGGGATGCTTTCATTGTTCAGTATGATGAAATTGCATGTTTATCAAGATACATTTGTTTTTGTTTACTCAATTAAGACAATAAAAAAATGTTTACTAAACTAAATTGAATTAAATGAAACTATCACTGAAATAATTGCTGAAATAAAATGATTAACAAAAATAATAATTTTTAAAATTAAGCACTCTTTCTGTAGTGGAAAATCTGATCTGTGGTTTGTAGAAACGCCTGTAGATGCTTTTTTACAGCTTAACATGTCAGTCATGATTTAAGTAAGGCATGATTTAACTACAAAAACAAATTTACAGGTAAAATGTGTTTTTCATTTGCC
Associated Phenotype:
Not determined