ZMP
uhrf1bp1l
Ensembl ID:
ZFIN ID:
Description:
UHRF1-binding protein 1-like [Source:RefSeq peptide;Acc:NP_001093475]
Human Orthologue:
UHRF1BP1L
Human Description:
UHRF1 binding protein 1-like [Source:HGNC Symbol;Acc:29102]
Mouse Orthologue:
Uhrf1bp1l
Mouse Description:
UHRF1 (ICBP90) binding protein 1-like Gene [Source:MGI Symbol;Acc:MGI:2442888]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16858 | Essential Splice Site | Available for shipment | Available now |
| sa10068 | Essential Splice Site | Available for shipment | Available now |
| sa14650 | Essential Splice Site | Available for shipment | Available now |
| sa33448 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40271 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa20255 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16858
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 |
|---|---|---|---|---|---|
| ENSDART00000046871 | Essential Splice Site | 55 | 1402 | None | 20 |
| ENSDART00000135330 | Essential Splice Site | 69 | 1416 | None | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 17330025)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 18272865 |
| GRCz11 | 4 | 18261841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACCTGGCTCGCCATTAATAAAGTCTTCTGCAATAAAGCYGCCATCCGGG[T/C]AAGAGACACGTCTGCTCGTTCAAGACAKCATCACTTTGAGTCCCTCTCAT
Long Flanking Sequence:
GAATTTTTCCTCCAAAAATGATACTCAGCTGCAATGTTCTCAGTGGCTCAGATGTCAGGAGTCTGCTGAGACTTTCATGTTCATTGCTTCATCCAACTAGAACATTTGGAGTGTTTATCAGGCACCGACATTGTAAATGGGGATTGTGGTAAATAAGTAAAATCTGAATGGCACTTTTTAGTTTAGTAATATAAAATTATCGGGTTTTTCTTGGTTCTGTGCTTTTTGAGGTTGGTAGAATTACACAGCGTTTAAACACTGAAAAGTCACATTTTCATGATGTGTTACTTTTATTTGTACTGACTTTTCCCCCCTTCTTTTTCTCTCTGTCTGCAGGTTTGCTAAGAACCTGTCTCCAGATAAGATTAATCTGAGCACTCTGAAAGGGGAGGGCCAGCTTACCAACCTGGAGCTGGATGAGGAGGTGCTGCAGAACATGCTGGATCTGCCCACCTGGCTCGCCATTAATAAAGTCTTCTGCAATAAAGCCGCCATCCGGG[T/C]AAGAGACACGTCTGCTCGTTCAAGACATCATCACTTTGAGTCCCTCTCATGCTGTAAATGAAGGATATGCTGGGATGATAATTGCACTCTTGGGCTGCAGCCAAATATACTTAATATAACTATCCTGAGATGGGAATTAATGCAGAAGCACAGTGTATGCGTACAATCTTGGTTACTAGACAGTTATTTGTTTGTTATGTCAGACACTGTTGTATATTTGATTAATATTTAAGATTTTCGCACTTGTAATCTAGTAATAATTTGATCTAGTACTTGTCAGTTAGTTTTTAAAATAAATTATTTTTGATAACATCTTTAACAAATGTAAAAAAAGTCCCTAAGGTACATAATGTGGTCTAAATAAAACTAAAGTGTTTTTGTAATGTATTTGTTTTATTCAACATTTGCTTTAATGTACTATATTAGTATTCCTGTAACAGGTAACATAATGTTCCATACACTTACTATAGTTATTACATTGAATTATGCACAACTAATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10068
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 |
|---|---|---|---|---|---|
| ENSDART00000046871 | Essential Splice Site | 266 | 1402 | 6 | 20 |
| ENSDART00000135330 | Essential Splice Site | 280 | 1416 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 17317566)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 18260406 |
| GRCz11 | 4 | 18249382 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGAAATCMGCTTCGCARAGGAAGAGCATGGCCCCYGACACTACACAGG[T/C]GCGAGTTTGAGGACTCTTCCCTKCCTCCTACCCCARTCACCACCACCAAC
Long Flanking Sequence:
TTGCCCTAATTAACCTAATTCAGCATTTTAATTGCACTTTAAGCTCAATACTAATATCTTTAAAAATGACTAGTAACATTCTGTACTGTCATCATGACAAAGACAAAATACATTAGTTTTTAAAAATCTTATGTTTAAAAAAATTATAGAAAAAAAAACAACAACTTCTCTTCATTAAACAACACTTGGGAAATATTAGAGAAGAACTCATTTCCCAGGACGGCTAATAATTTTCCCTCCAACTATATACTATTTTAAATATGTGTTTCTCTATTGATTTAAATAACACAATGTTCATCTTGGCTCTATACACGTATGTGTTTTCCAGATGAAGGACTGTAATGTGATTGCATCAAAGCTGACTCTGATCCTGGATGACCTGCTCTGGGTGCTGACGGACTCTCAGCTCAAGGCCATGGTGCAGTACGCTAAGTCTCTTAGTGAATCCATGGAGAAATCCGCTTCGCAAAGGAAGAGCATGGCCCCTGACACTACACAGG[T/C]GCGAGTTTGAGGACTCTTCCCTGCCTCCTACCCCAATCACCACCACCAACTACCTCTTTTTTTTAATATATGCTTTCGATTCTTAAAATACTGCTTTGCTGCTCCCTACTGGTTGTATCTTTTATTGTTCCCTTTCAGATGTCTGTATGTTTAGTATTATCAAACCTTTAGTCACGGCTGATTGATGTTTTCAGGTGACACCGGCACCCCCCACAGCCCAGCAGATGCGCACGCAGCAGGCTTCAGCCGCGGCAGATCAGACCGCTTCCATGGCACGGCTCTTCACCGCCTATGATGTTCGTGAGACGTCACACCACCTCCAGATCACACACTTGGACCTGCATATCTGCGATGACACCAATGCCAAGGATAGAGGTACCACATGTTCACACATAATACAGTTAACATTTACGTTTGGTGTTGTCATTCTAAAATACGTCTTTTCTTTGAAATCTGCAGGAATTAATAAGAGATTGGATGGTGGTGCAATGCAATTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14650
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 |
|---|---|---|---|---|---|
| ENSDART00000046871 | Essential Splice Site | 355 | 1402 | 8 | 20 |
| ENSDART00000135330 | Essential Splice Site | 369 | 1416 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 17317021)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 18259861 |
| GRCz11 | 4 | 18248837 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTCTTTTAGTTCTATCAGYGTAGACTATTACCCTTTCCACAAAGCTGG[T/C]AATAYATTARATACATTATTTGTACTATACTTTTGAAGAGGAAARTRTTR
Long Flanking Sequence:
ACCAACTACCTCTTTTTTTTAATATATGCTTTCGATTCTTAAAATACTGCTTTGCTGCTCCCTACTGGTTGTATCTTTTATTGTTCCCTTTCAGATGTCTGTATGTTTAGTATTATCAAACCTTTAGTCACGGCTGATTGATGTTTTCAGGTGACACCGGCACCCCCCACAGCCCAGCAGATGCGCACGCAGCAGGCTTCAGCCGCGGCAGATCAGACCGCTTCCATGGCACGGCTCTTCACCGCCTATGATGTTCGTGAGACGTCACACCACCTCCAGATCACACACTTGGACCTGCATATCTGCGATGACACCAATGCCAAGGATAGAGGTACCACATGTTCACACATAATACAGTTAACATTTACGTTTGGTGTTGTCATTCTAAAATACGTCTTTTCTTTGAAATCTGCAGGAATTAATAAGAGATTGGATGGTGGTGCAATGCAATTGTCTTTTAGTTCTATCAGCGTAGACTATTACCCTTTCCACAAAGCTGG[T/C]AATACATTAAATACATTATTTGTACTATACTTTTGAAGAGGAAAGTGTTATGATTATTAAAAGATGATCTTTTTGTGTCTCAGGTGAGGGCTGTTTGCATTGGATGCACTATGGCGAAGCAACAAAATCTCGTGAAACCTGGGCGCGTTCTCTCCTGGACGAGTTTAAGTCTAATGTCGATATGCTGAAAAACGCAGTCAGCGGACAGTCCCAGGGCTCTCCTCAGCACGGTGAGAACAGCATGCCTGTTAGCAGACTCCGATTGGCTCACTGTTGCTGAAAAATGGGTGAATGTCATTACTCCTTTCCTAATGTCTGGATTATATTTGACCCAAAAATCCAAGAAATAATTAAGAACCAATTTTGTGCACTCATAAGTCTTATATTTTGCAGTTAGGGAAGTGTTTTTAGAACAATTAAGCTTTTTTTGCTTTTCATTTTCCATATTAATTTAATTATTAGCCTCCCTTTGAATTTATTTTCTTTTTTAAATATTTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33448
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 |
|---|---|---|---|---|---|
| ENSDART00000046871 | Nonsense | 457 | 1402 | 11 | 20 |
| ENSDART00000135330 | Nonsense | 471 | 1416 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 17311135)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 18253975 |
| GRCz11 | 4 | 18242951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCTTCAGCAGACCAGCCACGCTCTAGTCCTCAAACCATGATATCCTG[C/A]AATAAGAAATCCCTCTATCTCCCCCAAGAGATGCCGGCTATTCACGCCGA
Long Flanking Sequence:
CAAAATTAAAGTGCAGCTTTTCGCATATAGTGTCTTATTGCTTATCGTCATAAATTAAAATAAGGACGCATGACAGCTGAGCGGGACTCTGACCAATGTTAGGAGAGTTTACTCGCACGTGACTTGTTTTAGCTGTTTTGGTCTGTTTAGAAACTTTGCCGTGTGAAAGCGAACTACACCAAGAACAAAGTGCAACAATGTAACAATTTAATCCCTGTTTCGGAACAAACCAATTGATCTACAGGTGTAAAAGTGCCCTTAGTCCTCTTAGGTGTACTTGACTCGCATGCAGATACGATGTAATGTGGTGCCAGGCTTGATATAAAATAACAAAGTATGTTAGATCAGTCATCCAGTATTCCAGATCTAGTCATTCTGTTACTAAGTAAATGATGAAATTTGCATTGATGAGAAACCATTTAAAAGTAAAAATATTTGACTATGTTAAAGGTGTCTTCAGCAGACCAGCCACGCTCTAGTCCTCAAACCATGATATCCTG[C/A]AATAAGAAATCCCTCTATCTCCCCCAAGAGATGCCGGCTATTCACGCCGAATTCACAGAGTACTACTTCCCAGATGGCAAGGACTATCCAGGTAAAACAGAAGGGATCCCATCCATCAGAATGTTCAGCTTTTTCTGCTTCTACTCAAGCGTTCTCTGAATTGACAATGAACACACTCTCTCCCTGCAGTCCCTTGTCCCAACCTCTATGTGCAGTTGAACGCACTACAACTGGTGCTTGACTCGAGAAGTCTGGTTTGGCTTAATCTGTTCGCACTGGACCTTCGGCAGAGTTTGGAGCAATTCATGGATCTGTACAAACTCAATGACTCACAGAAGCCTGAAGAACATGTAGATATCAAAGTGGATGGACTCATGCTTAAGGTAGACATTTAATTGAGGTTGTAAACTTTCTGTGAATTTTGGATTGACAGCTGTTTCTCAGATTATGTGCATCTAAGGTACCTCATGTTGACTATGATGCAACCCCTTTCCTAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40271
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046871 | Essential Splice Site | 1033 | 1402 | 14 | 20 |
| ENSDART00000135330 | Essential Splice Site | 1047 | 1416 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 17305628)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 18248468 |
| GRCz11 | 4 | 18237444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACTTGTGCTAGAACTCACCGTTGCTATTTCTTGTGCCTGTACTCTGC[A/C]GTGGTCGTTTGATGCAGGGCAAGTCGCAGTCAAGTTTCTCAGTGTCCTAT
Long Flanking Sequence:
TTTTGAGAGTAAAACACAATGCACAACTGTATTGTTTGACTGAATGTGACCTCTGGGCATATGTGTGTTTGTTCACTCTCTCTCTTCTGAAGGAAAGGCAGTTTTTCAGTGGTCTCTGACCTCTTATCCTCCACGCACAGCAGGTCTACCTCCTTATATTCCATATCCAACATGTAAGACACCCTCTGTAGGACTCTGTGGCCATCTGTGTATGCGTGAATGTTTGTGGACAAAACTGTGGTGTTGTGACTGTAATCATTTCACTCTAGCTTGTCCCTTGTAGTGATGTGTGTAGGACTGTGGACGTCTGCAGGGTTTGCCGATTCGATTGCTGATTGGTGTTTTGATTTTGCAAGAATTGTTTCGTACTTGCACCCAAACTCTCTTTTTGTTGTTGTTGTTGTATTGGTCTCATTCTTTTTTTTATTTATGTTAGCAAAGATAGGTTCATCCACTTGTGCTAGAACTCACCGTTGCTATTTCTTGTGCCTGTACTCTGC[A/C]GTGGTCGTTTGATGCAGGGCAAGTCGCAGTCAAGTTTCTCAGTGTCCTATAAGAATATGAAGAAAAGTCCTTCACTACAGTCTTTGGATGATCTCTCCATGGACAGCTATCTACTAGAGGACTGTGACAGCTACAGCCTGCTGGACAGAGGTACATGCACAAACACATTTCACTCAGGCAGTGGATTCATTTTACGTTTGTCACCACAAGGTGGCAGTATTGCAGCATAAATCTTTTTGTGTCATTTTTGTTCCTTTGCTGGAGCTGTAGGAATTTTTTTTGTTCTTAACCAAAAAAGCGTTAATTTACGTACCTTTGAATTTAAAATAAAGCTTAGTATCAGTATGTTAGTCTTAACGATATCTATAAAATATGTTCTCCAAAACTGTTACTAGATTTTCATTTAGATGAGATAAACATCCAAAACTTACAGTTTGTCACTTCAGCAGCATAAATGAATAATTTATATTTTGATGTCACCACGTACTTACGGAATCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20255
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046871 | Nonsense | 1365 | 1402 | 20 | 20 |
| ENSDART00000135330 | Nonsense | 1379 | 1416 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 17277623)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 18220463 |
| GRCz11 | 4 | 18209439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGATCTTTTTCCATCCACACAGCTGCTCGTGGAGGAGAATGAATGCT[T/A]GAAGCTGGAGCTCTCCAAAGCCAAGATGGCGTTAGCAGAAGCGCAGATGG
Long Flanking Sequence:
TACACTTATGCAAATACATGCATTTATTAGTAAATATGTGTATTTAGTTATATATGTTTATTACATAATATTTATTATTATTTAAAAGTTATAATGAAAGATATGTTAATGCGCAGAAACAGTTAGAGGCCCTCAGTGAAAATGAGTTTGACACCCAAGGCTTAAATGCTGTGCTGGGTTGTAAGTAGCAGCTACAGCTTTGCACGTTCTTCTGAAAACGCCATTGTTAGTTATATATGACTGACATTGTATTTATATCAACATCTTGTCATCTTGAATTGCAGGTGCCACAAAACAATAACCTGAGTACTATTTATAAGTGATCCTTGTATGGGGAAAAACAATTAATAGCTTACAACATGACCCCTTCAATATCAATTATACAATGAGGATTATCACTCAAGGAAAGCGATCCAGGCTGACAAACTACAAGCGGCGTGTGTGCCAAGCTAATGATCTTTTTCCATCCACACAGCTGCTCGTGGAGGAGAATGAATGCT[T/A]GAAGCTGGAGCTCTCCAAAGCCAAGATGGCGTTAGCAGAAGCGCAGATGGAGAAAGACTCTCTCCAGCATCAAATGAAGACGCTTAAACTCACCAGCGGGGGCAGCAATAGCTAGTGTGTGTATGTGTTTGTGAGTGTGTGTTCAAACAGGACAGACACTCGCCACAGGGGAGCAGCAGAGGGCTTGAAGGGGCCCGGAGCCATAGCAAATCCCAAATCTGCAGCAGAGAAGATGATAGTGTGTGTGTGTGTGTGTGTGATGGAGATCCAGAGCAAATCAAAGAATAGTGTTTTTTTTATTGTAATGTACACACAATCAGATCATGTGTTGCAAAAAAAAAAAAAAAAACTCTTCGGAGCCTGTGGAGCTTCACATACTTTTTTTTTTTTGCTTTTATTATTTACTTGCGCTCTTCGTTTGCAGTGTAGAAGCACATTCCACCCTTGACCTTTGACCCCAGGACAGTCTTACACTGATAGTGTTGAATGTCATATCTATG
Associated Phenotype:
Not determined