ZMP
ubap2l
Ensembl ID:
ZFIN ID:
Description:
ubiquitin-associated protein 2-like [Source:RefSeq peptide;Acc:NP_001076535]
Human Orthologue:
UBAP2L
Human Description:
ubiquitin associated protein 2-like [Source:HGNC Symbol;Acc:29877]
Mouse Orthologue:
Ubap2l
Mouse Description:
ubiquitin associated protein 2-like Gene [Source:MGI Symbol;Acc:MGI:1921633]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32231 | Essential Splice Site | Available for shipment | Available now |
sa43218 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36779 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36780 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43219 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32231
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092112 | Essential Splice Site | 200 | 1144 | 6 | 27 |
ENSDART00000092138 | Essential Splice Site | 200 | 1196 | 6 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 8387974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7846513 |
GRCz11 | 19 | 7765438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGTGGAGCTGGAAGGCGAGGAGGGAGGTTTTCAGCTCAGGGCATGGGG[T/A]AAGTTTGTGTGACTCCACTCAGGTTCTTGCCCTTTTTGCATGTGTTTTTT
Long Flanking Sequence:
AGCAATCTTTAAAAGCTTTTACTGTGGAGGCTGCTTTTAACCTTCATCAAAGATAGGCTGGCATGCCACTTAATGGAATACTTCAGTGCCGTAAAAACAGTTCACAGATAAATTCAAAGTAAAGTGGCTTGATGTGTGCTTTGGCATTTTGGGCACTCAGACTTGACCAGTTTTCATTGTTAGGATCTGTTTTAATAGTAAAACTAATGTCTTAAAGGCCCATTAGGTTCCCTTTTTGTATATTTCACTTCAACTCTTTCCATTCTTTGTTCCCTGTCTTCAGTCCGTGGGCAGGAGAATGGTTTGGATGGGGCCAAGGCAGGTGGAGTCGCGGGCAGGGGAACTGAGCGAGGCCGTCGGGGAAGAGGCAGAGGAAGAGGTGAGTTCTGCATACTCCTCATCTAGATAAAGGATTTGGTGGTTTCTGGTCTGACTTGTCTTCCTGTGCAGCAGGTGGAGCTGGAAGGCGAGGAGGGAGGTTTTCAGCTCAGGGCATGGGG[T/A]AAGTTTGTGTGACTCCACTCAGGTTCTTGCCCTTTTTGCATGTGTTTTTTTGCAGAGAGCCGCCAGAATGGTAGATTCTGGGAAATGCTGGTCTTTAGCTTGCTTGTTAAATTCATCATCTTGTTTTTTTAAAAGTGGCTGAAGGTATGGTGCAATATTTGGTGCTCTTCTGTGGAGTCAAACCTGTCAGGTTTTAAGCCTGTTGGTCTGTTTAACTTGAAACTGTGTGTGCATTTGTAAGGCTTAAGGTTTTTAATCATATTTTGAATGCACTAATGTAAACAGGTAAGTAAGAGAGGATTTTTTTAGTGAATTTTTGTGCTTTTAGGCTGGGTGCTTGTTTATTTACAGAGTTTATTTAATTTATTTGATGGCAACTGTGGGTGGGTGATTAGATGTACTGGTATGAGGGTCAACCTCTAGATATTTGAGCGTGAATGAATAACAGTTATGTAAAATGGCTCCTCAGTAATAAAGAGAAAGTCTGTTGTGGCCACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43218
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092112 | Essential Splice Site | 714 | 1144 | 17 | 27 |
ENSDART00000092138 | Essential Splice Site | 714 | 1196 | 17 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 8402166)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7860705 |
GRCz11 | 19 | 7779630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCCATGAAGACGTCTCGCCCAGCTCATTGGCCACTCAGCACAACAAG[T/G]ATGATGTCTTTCATTAAATTAGTTTAGTATCATCCGATTTAGAGAGATGC
Long Flanking Sequence:
GTTTTGAGTTATAGGAATGATGTCAGAAGTAAATTTGATGTAAAAACCAAAGTAAAACCTTCACATCCAATCACAGTTTATCCCTCAAAGTTGCACACATGACTATTGATGTCCTATGAATTTTTGGATTGCCACTGTAGTTATTGCTACCTTAAAAAAAAAAAAAAAAAAAAAATCTTGTCAATTTTTTGTTTGGAGCGCACTAGCTTATAGAGATCATAAAAGCTAACAAAACTGATACTAACATCTTAAACTCTGTTTATTTTCATCTGACCTTTAACCCTTTCAATTTTGCTACTGTCTCAGCTGCAGCAGGCTCTGCAGTGCCCGTGAAGCCAGTGTCTGAATCAGTCGTCCCGCCATCGGTTTCCAACATGGTGTCATTGGCAGACCCCTCATCAGGCCCTACTTCCCTGTTGACTACGTCCAATCAGACTCCTCTCAGTGCTCTCAGCCATGAAGACGTCTCGCCCAGCTCATTGGCCACTCAGCACAACAAG[T/G]ATGATGTCTTTCATTAAATTAGTTTAGTATCATCCGATTTAGAGAGATGCTAATGATTCTGCTATTTTTTTTCCTTCCCACATCAGCTCCCTTTCTACACAGCAAAACAGTTTGGCACCTTCTTCAGTTCGCACTTCAAACACAAGTCTGCTGGTGAGTTTATTGTAAAATACTCTATATGAATTTAGATATCAAATAAAATCTTGGTCCCTCTTTACATCACTTGTGTACTTGTAATGAAAAACACTAAATTGACATGACTTTTGTAGTTTAAATAGAGTCAAGCAAATGGCTGCTGCCATAGTTTGTTTACATAGATATTTTATGTAAGTTTGATAATGATTGTTTGACGAATGTTTTGAGATGCACAAATTTTTCAGGAAATGGTTAAATAGTCCTTGCCTGCATTATTTCATATCCCTTTGCTAATCATTTCAGTTATTTCAAAGGTTGTTGTAGCCTGTAACAGCAGAAGAACCAAAACTGATAAACACTGGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36779
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 |
---|---|---|---|---|---|
ENSDART00000092112 | Essential Splice Site | 736 | 1144 | 18 | 27 |
ENSDART00000092138 | Essential Splice Site | 736 | 1196 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 8402321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7860860 |
GRCz11 | 19 | 7779785 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAGTTTGGCACCTTCTTCAGTTCGCACTTCAAACACAAGTCTGCTGG[T/C]GAGTTTATTGTAAAATACTCTATATGAATTTAGATATCAAATAAAATCTT
Long Flanking Sequence:
AAAAAAAAAAAAAAAAAAAATCTTGTCAATTTTTTGTTTGGAGCGCACTAGCTTATAGAGATCATAAAAGCTAACAAAACTGATACTAACATCTTAAACTCTGTTTATTTTCATCTGACCTTTAACCCTTTCAATTTTGCTACTGTCTCAGCTGCAGCAGGCTCTGCAGTGCCCGTGAAGCCAGTGTCTGAATCAGTCGTCCCGCCATCGGTTTCCAACATGGTGTCATTGGCAGACCCCTCATCAGGCCCTACTTCCCTGTTGACTACGTCCAATCAGACTCCTCTCAGTGCTCTCAGCCATGAAGACGTCTCGCCCAGCTCATTGGCCACTCAGCACAACAAGTATGATGTCTTTCATTAAATTAGTTTAGTATCATCCGATTTAGAGAGATGCTAATGATTCTGCTATTTTTTTTCCTTCCCACATCAGCTCCCTTTCTACACAGCAAAACAGTTTGGCACCTTCTTCAGTTCGCACTTCAAACACAAGTCTGCTGG[T/C]GAGTTTATTGTAAAATACTCTATATGAATTTAGATATCAAATAAAATCTTGGTCCCTCTTTACATCACTTGTGTACTTGTAATGAAAAACACTAAATTGACATGACTTTTGTAGTTTAAATAGAGTCAAGCAAATGGCTGCTGCCATAGTTTGTTTACATAGATATTTTATGTAAGTTTGATAATGATTGTTTGACGAATGTTTTGAGATGCACAAATTTTTCAGGAAATGGTTAAATAGTCCTTGCCTGCATTATTTCATATCCCTTTGCTAATCATTTCAGTTATTTCAAAGGTTGTTGTAGCCTGTAACAGCAGAAGAACCAAAACTGATAAACACTGGCCTAAAAAACAGGAATTTGATTTGCATATGTTGTCATTTCTGTAGCATGAAATTCAGTGGATGGGCTATTATTATTATTATTATTATTAATTATTATTATTATTTAGATATTTTATGGTTGCACAAAGCTCTTCATTTCTCGCTTTTTCCAAACGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36780
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 |
---|---|---|---|---|---|
ENSDART00000092112 | Essential Splice Site | 871 | 1144 | 20 | 27 |
ENSDART00000092138 | Essential Splice Site | 871 | 1196 | 20 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 8407243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7865782 |
GRCz11 | 19 | 7784707 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCCCAACCCTTACATTATGGCTCCTGGCCTGCTTCACCCATACCCAG[T/C]GAGTGTTTAGTGATGCATGTTATTTTTTGCTGCTTTCAATCCTGCACTCC
Long Flanking Sequence:
TCAGAAGATATTTTAAATAAAGCTAAAAACTTGTGACATCCATCATAGGAAAAATCTTATGGAAGTCAATAGGTTTCCAGCTCTTCCGGATATCATCTTTTGTGTTCAACAGAGGAAAGAAAAATAAATAAGCTTTGCAACAAGTGGAGGGAGAGTATATGGCTACAGAATTAAACTTGTGTGAACTATCACTTTAAATTAGTTTGTAATTTAACATTGTATTTAGCTAGCAAAACCATTAAAATAATGAATAAAAATATGCACATTATTTGAACATTATTATGTTCAAACAGTTTTTTTTTTTTTGTTTGTTTGTTTGTTTTTTCCATCTTATGAGATGTATTTTTATTTTTGAATATAATTTACACAATTTCTACGTCAATTGATTGAATGCTGCTTGATTAAAACAGGGAAAGCACCTCCAAACCTGCCACCTGGAGTGCCGCCACTGCTGCCCAACCCTTACATTATGGCTCCTGGCCTGCTTCACCCATACCCAG[T/C]GAGTGTTTAGTGATGCATGTTATTTTTTGCTGCTTTCAATCCTGCACTCCCTAATTATGCAAGTATGGTTCATGCGGCATGTTTTGGCTCACCAACCTCTTTGTGTCCTCCAGCCGCAAGTTTATGGCTACGATGATTTGCAGATGCTGCAGACCAGAATACCACTGGTGAGGGATTTTTCTTTTTTTATTAGGGAAATTGACTGACTATATATTTTTTCTGCATATAAAGTTAAAATGCTGTTTCCTTCTTCTCCTGCAGGACTATTACAGCATCCCGTTTGCCACTCCAACCACAGCACTGACAGGCAGGGAAGGCGGTTTGACAAGTAACCCTTATTCTGGTAAGGTTTTTTTTTTTTGGTGAATTTTTGTTCAATCTCTTTATAAGGATGCTGCATCTAAAATGCTCAATCTTTTTAGCTGGGGACCTGTCGAAGTTTGGACGTAATGATGCATCGTCTCCTGCCCCCGCCACAACACTGGCCCAGCCCCAGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43219
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092112 | Essential Splice Site | 1048 | 1144 | 25 | 27 |
ENSDART00000092138 | Essential Splice Site | 1100 | 1196 | 26 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 8417221)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7875760 |
GRCz11 | 19 | 7794685 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACACGGGAGTCCCTGATATTTCAGGCTCTGTTTACACAAAGACGCAG[G/A]TGAGCAGTTGCATTGAACACTGCTTTATTAAGCTGTAGCCAGCGGTTTGG
Long Flanking Sequence:
TTTTAGTGAAATATAGGTGTCCTAATAGTGTTTTTAGCAGTGTGGGACACATATACGACTGTCAACAGCTCAAAAAATGTGTTTTGGTGTTTCGTGACCCTTTAAAACTTGGTAGAGAAGTAGGTTTGAATTGAGTGCCTCATGTGAATTGCCTGGCAGAGGTGATGTCAATATGAATTGTCAATCGGTTGTTGTTGTTGTTGTTATTTATTTATTTTTATTTATTTTTTTAACTATGTTCGTTCAGCTCTTTAAAAAGCAGGCTGTGTTGCCACACACTGTGCGGTTTTCACATGCATCAGTCAATTCACGATGCAGCATTTACAAGTGTACTTCTCAGTACCAGCATTACAGGATCTGTATGTTTTATGAATATGGTTTTGCTAGTTTCAGCATTAACCATTCTGTGTTTTTGACTTTTCTTTACTATAGGAGTCTCTGTGACATCAAGCAACACGGGAGTCCCTGATATTTCAGGCTCTGTTTACACAAAGACGCAG[G/A]TGAGCAGTTGCATTGAACACTGCTTTATTAAGCTGTAGCCAGCGGTTTGGTTGTTGTTAATTCTCCAGTGTTGATCCTCCCTCCGCAGTCTTTTGAGAAGCAGGGTTTCCACACAGGAACCCCCAGCGCTTCCTTCAGTTTGCCGTCGGCTCTCGGCAGCGCAGGCCCCATCAACCCTCCTGCTGCAGCGGGTTACGCTCCCGCTCCATACATGCACATCCTGACGCCGCATCAGCAGCCACACTCACAGATGCTCCACCACCATCTGCAGCAGGACGGACAGGTCAGCTATCTCATTAGTCTAAAAGGTTTTAATTAAACAGTTTTATTTAATACTACTTGTTGTATTAATAGTAGTTTTAAAGGGACAGTTCACCCAATAATTGTTTGTTCTTCCTCATGTGGGTTTAAATGTTTGAGGTTCCTCTGTTGAACAGTAGATATTTTGATGAATGCTGGTTGCTGGCACCCATCAACTTGAAGTCAGTGTGCCCCAGGTA
Associated Phenotype:
Not determined