ZMP
si:dkey-27c15.3
Ensembl ID:
ZFIN ID:
Human Orthologues:
GON4L, YY1AP1
Human Descriptions:
YY1 associated protein 1 [Source:HGNC Symbol;Acc:30935]
gon-4-like (C. elegans) [Source:HGNC Symbol;Acc:25973]
gon-4-like (C. elegans) [Source:HGNC Symbol;Acc:25973]
Mouse Orthologue:
Gon4l
Mouse Description:
gon-4-like (C.elegans) Gene [Source:MGI Symbol;Acc:MGI:1917579]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10568 | Essential Splice Site | Available for shipment | Available now |
sa23532 | Essential Splice Site | Available for shipment | Available now |
sa29218 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10568
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079410 | Essential Splice Site | 135 | 712 | 5 | 20 |
ENSDART00000138322 | Essential Splice Site | 129 | 1033 | 4 | 25 |
Genomic Location (Zv9):
Chromosome 19 (position 27174206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27104318 |
GRCz11 | 19 | 26688541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATTYCCACTTGGAATATTTYACCAATTAAGAAGCCAACAGAAGCAAAG[G/A]TGATCAGCAGAGTACATTTGCAAGAAAACATGCATGAGACTGGGAGCAGG
Long Flanking Sequence:
TGCACCATGCGCTTTAGACTTTGTGCCTAGATCGTTAAAATAAAGCTGTTTGTGTCTTTCTTTTTTTTCATTCTTTTAAAACTTGTTTTAAAACTATAATTTAGTCTATTTTAAATAATTTTTATTCTTTATTGTTATTATTTTTTATAGATATATTTCATATCTTTTTAATTTTTGTTTATGTAAAGCAATTTGAATTACTACTGTATATGAAATGTGCTATATAAATAAACCTGCCTTACATTACGTATAACGTAGAAAACTTTTTAATAATGTAAATGTTTAGGTTATGGCTGTTATTTACTTGTATGCATATTTTTAAATCTTCAGGTCCAAATGGATTTAGTATGTTGAAATAATACCGTTTGATTGCATTAAGAGGGTTGTCTCCCTGTAAAATGCTTTAGCAATTAATAAACGCAATGGAGTATTTTTGTTTGCTTTTATAGGTCATTCCCACTTGGAATATTTCACCAATTAAGAAGCCAACAGAAGCAAAG[G/A]TGATCAGCAGAGTACATTTGCAAGAAAACATGCATGAGACTGGGAGCAGGCTGTGAATTAAAGGTAAATAAATAATGGTGTGTGCACTTACAGAAGGGGCCCCAGTTTGTGGATATTCCATTAGAAGAGGAGGACTCTTCTGATGAAGAGTATCGGCCTGATGAAGAGGAGGAGGATGAGACAGCTGAGGAGGTTGGAGAGAATAACTTTTCTTTTATTTGATACTTTCTGCTCTCTGGATTTATAGAGTTTGTTATGTGTGTGTGCTTTATAGACTCTTCTGGAAAGTGACTTGGAAAACTCCTCATCTTCTCCACGGGTGAGTCGAGTACAAAGATCACACTCTGAATCTGAGGATGGAGCCAGTAGATCCAGACTGGTAAGACCTTTGCAGATGGAAATGCTATTGCTAGAAAGTACTGTTGATGTCCATTATCATTCATAGGTTTTGTGTCTGAAATATTTATGAAAAATATCTGTGTAATTAAAGTCTGTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23532
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079410 | Essential Splice Site | 135 | 712 | 5 | 20 |
ENSDART00000138322 | Essential Splice Site | 129 | 1033 | 4 | 25 |
Genomic Location (Zv9):
Chromosome 19 (position 27174207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27104319 |
GRCz11 | 19 | 26688542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCCCACTTGGAATATTTCACCAATTAAGAAGCCAACAGAAGCAAAGG[T/C]GATCAGCAGAGTACATTTGCAAGAAAACATGCATGAGACTGGGAGCAGGC
Long Flanking Sequence:
GCACCATGCGCTTTAGACTTTGTGCCTAGATCGTTAAAATAAAGCTGTTTGTGTCTTTCTTTTTTTTCATTCTTTTAAAACTTGTTTTAAAACTATAATTTAGTCTATTTTAAATAATTTTTATTCTTTATTGTTATTATTTTTTATAGATATATTTCATATCTTTTTAATTTTTGTTTATGTAAAGCAATTTGAATTACTACTGTATATGAAATGTGCTATATAAATAAACCTGCCTTACATTACGTATAACGTAGAAAACTTTTTAATAATGTAAATGTTTAGGTTATGGCTGTTATTTACTTGTATGCATATTTTTAAATCTTCAGGTCCAAATGGATTTAGTATGTTGAAATAATACCGTTTGATTGCATTAAGAGGGTTGTCTCCCTGTAAAATGCTTTAGCAATTAATAAACGCAATGGAGTATTTTTGTTTGCTTTTATAGGTCATTCCCACTTGGAATATTTCACCAATTAAGAAGCCAACAGAAGCAAAGG[T/C]GATCAGCAGAGTACATTTGCAAGAAAACATGCATGAGACTGGGAGCAGGCTGTGAATTAAAGGTAAATAAATAATGGTGTGTGCACTTACAGAAGGGGCCCCAGTTTGTGGATATTCCATTAGAAGAGGAGGACTCTTCTGATGAAGAGTATCGGCCTGATGAAGAGGAGGAGGATGAGACAGCTGAGGAGGTTGGAGAGAATAACTTTTCTTTTATTTGATACTTTCTGCTCTCTGGATTTATAGAGTTTGTTATGTGTGTGTGCTTTATAGACTCTTCTGGAAAGTGACTTGGAAAACTCCTCATCTTCTCCACGGGTGAGTCGAGTACAAAGATCACACTCTGAATCTGAGGATGGAGCCAGTAGATCCAGACTGGTAAGACCTTTGCAGATGGAAATGCTATTGCTAGAAAGTACTGTTGATGTCCATTATCATTCATAGGTTTTGTGTCTGAAATATTTATGAAAAATATCTGTGTAATTAAAGTCTGTTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29218
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079410 | Nonsense | 676 | 712 | 20 | 20 |
ENSDART00000138322 | None | None | 1033 | None | 25 |
Genomic Location (Zv9):
Chromosome 19 (position 27188913)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27119025 |
GRCz11 | 19 | 26703248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATAAACACAACATACTGTTAAATAATTTCTCCTACATTTTTCAGACGTA[C/A]TTCATGGCAGGAAAATGCCCCTCCATGCCCTTGGCCAGTAAGAGGGTCAG
Long Flanking Sequence:
TATTTAATTTCTTAATGAATAAAATAAAATGAATAAGTGACTCATTGACTCACTCATTCGAAATGTATTGCCATCTATTAGCAGTTTGTTATTTAGAGTATTTTTCACCTTCTTATCAATTAAGACATGTATGATTAATTGTAATTTAAACAATACATATAATTAATAAGCTTAAAAATTTGAATCTTTTGACAGTTTCAGTCTCAAAAAAAAATATTATAAACTGATTATGATTCATTAAAGGGATGTTTAGATACTTTAATCTTACCATGCCTTAAGCTAGTGCTTCCTCTTGTCTGGATGGCTGACATGATGAAGTACTTGAAATACTTTTCACATTATAGTAACTAAACTTTTAAACTCTGCCACAGTATAATAGTAATTTACCTTTGCTTGACATTGCAACCTTTATCACTGTACTATTGTTTCAATTTGTACCTCAAAATCTGTGATAAACACAACATACTGTTAAATAATTTCTCCTACATTTTTCAGACGTA[C/A]TTCATGGCAGGAAAATGCCCCTCCATGCCCTTGGCCAGTAAGAGGGTCAGTCCCTGTGACCAACGCCCCCCAGTAGAAAGAGAACAGAGTCTCATGCCTGATTGGCTCTCAGTAATAACTCTTCTAATTTTATTATAGGTTTTTCATTTAACCCACTGGGTCTCCTCTGTCTTTTTTTGTCAGAATTGTGTGAAACTGTGCCTATTTGAATCTTGCTTTTTTCTCATGTATACATTGCAAAAACAAAGTCACAAAGTGGGCATAAAAAAAACTTTAAAAATCTGTCAAAACTGACCGACCATAGGAAATGAATGAGAAATCTTAAAAAATAAAAATAATTCTTACAATTTTTACACAGACACACACTTATCCACACATATAAAGCTGCATCCCCAATACAGAGCAAAGTTTTGAAAATATGAAAAATCAAATAACTTGTGACAGTCTAAAACATAAAGACTGAAATAAAACACACAAACAAATCTCTAAACTTAAAAGAA
Associated Phenotype:
Not determined