Busch Lab

ZMP

si:ch73-90n13.2

Ensembl ID:
ENSDARG00000077011
ZFIN ID:
ZDB-GENE-090312-82
Human Orthologue:
UHRF1BP1
Human Description:
UHRF1 binding protein 1 [Source:HGNC Symbol;Acc:21216]
Mouse Orthologue:
Uhrf1bp1
Mouse Description:
UHRF1 (ICBP90) binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:3041238]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa43897 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43896 Nonsense Mutation detected in F1 DNA Not yet available
sa37579 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa43897
Status:
Mutation detected in F1 DNA
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
ENSDART00000114486 Essential Splice Site 590 1353 12 20
ENSDART00000132671 None None 149 None 3
ENSDART00000134183 Essential Splice Site 81 160 2 3
ENSDART00000140986 None None 414 None 10
ENSDART00000146416 None None 144 None 4
Genomic Location (Zv9):
Chromosome 23 (position 346963)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 317954
GRCz11 23 330747
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGACTGACGAACACATCGATATACGCCTGGATGCAACACAGCTGAAG[G/A]TAAACCAAGATCTGTCTGTCTATCTATCTATCTATCTATCTATCTATCTG
Long Flanking Sequence:
TTAGCTATGATGTTTTGCAGTCATTGATCACCAGGCATGTCGATGAGTACATTTACATGCACACAAATGCCACTCACACAGAAATACTCCACGTCTTATTCATGTCTGTTCAGTTTGATTATGACTTTAGTCAGATTAAGGTCATCAAAATTCTCTGTTTACATGGTAGATTCTCCATCAGAGTATTCTCTCAATCGTATGAAAAATGGAGGATTGGTGTCCACGTAAACATAGCCACTGATAATAACTTGCACGATTATTGCATGAAGTTGTTTGTAGTGATTGTAATGCTCTTTGTCTTTGTAGTGCCCTCCTCTAACCTGTATGCGCAGCTCAATGGTCTACAGCTGTGTGTGGACGCTCCGAGCGTCTTATGGATGACTCTGTTTTCACGAGGTTTACACAGGACTTTAGATCAGGTCAAAGCTTTTTACCACCTGCAGGACAGCAGCAAGACTGACGAACACATCGATATACGCCTGGATGCAACACAGCTGAAG[G/A]TAAACCAAGATCTGTCTGTCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCGGTCGGTCGGTCGGTCGGTCGGTCGGTCGGTCGGTCGGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTGTCTGTCCGTCTGTCTGTAATATCTATCCATCCATCCATCCATCAATAGTATCCATCCATCCATCCATCCATCAATAGTATTCATCCATCCATCCATCCATCCATCCATCCATCCATCAATAGTATCCATCCATCCATCCATCCATCCATCAATAGTATCCATCCATCCATCCATCCATCCATCTATCTATAGTATCCATCCATCCATCCATCCATCAATAGTATCCATCCATCCATCTATTTATAGTATCCGTCCATCCACCCATCTATCTATAGTATCCATCCATCCATCCATCAATAGTATCCATCCATCCATCCATCCATCCATCAATAGTATCCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43896
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114486 Nonsense 934 1353 13 20
ENSDART00000132671 None None 149 None 3
ENSDART00000134183 None None 160 None 3
ENSDART00000140986 None None 414 None 10
ENSDART00000146416 None None 144 None 4
Genomic Location (Zv9):
Chromosome 23 (position 344122)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 315113
GRCz11 23 327906
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAAGTGTTGCTCCTACAACTCCTCCGGTTTCCCCTGGGAACTCTGCGT[T/A]ATTGTCCCGGCACAGCTCTACTTTCAGCATTGAGGGGGATTTTTCCAGTG
Long Flanking Sequence:
AGAATCTCTAATCAATTCCCCAACAGCATCAGTTCATATTTTAGCCCAATCCATTACTCCTGTGAAAATGTGGCTCAATCATTATCAGTTTATAGCTCTTTTAAGGATGAAGGACTACCTTGGCAGGCTCGCCGAAGATTTGACTAGGGATTCCCAAGCTGAATCCAAAAACAAGTCATCAGATCCGCCATCGGTTTGTGTCTCAATCCTGATGGAGGCCATTGAGCTTTCTTTGCTGCTTCCACCCGCAACGTGCGAGCCAGAACAACAAGCTGATTCTCCAGGAGAAACGGACACTAACAGCCTGACCGAATCTGATTTCTCACCATCCCACCGTGCTGATCCTGGGAATGAGGATCCAGAAGATGAGGAGCAGGAGGGATCAGTAGAGGAGGCCTGTGAAGCCGTGGAGGAAGCCGTAGATCAAACTCCACACGATGATGATGAGGATGGAAGTGTTGCTCCTACAACTCCTCCGGTTTCCCCTGGGAACTCTGCGT[T/A]ATTGTCCCGGCACAGCTCTACTTTCAGCATTGAGGGGGATTTTTCCAGTGCACTGAACGCCACTAAAGGGGTCACCAAAGACGCCCTCAGCGCCTCCCTGGATTTAACCAAAGGAGCATTGTCCATCACTAAAGATGCCTTCAGCATGCTGAGCCGAGGGTCTGGCATGAACAAACTCTTCACGCCTCAAAACAAGTAAGAGCATCTGCTTTCTTGAAGGACGTCTTGAGGTTGAGACAAGATTGTGATTATCTAATGTGATACTCAGATGTTACTCAAATCTACATTTGAAGACGAACTTTAGTGGTGTATAATCGAGGATAATCCGCATAGCAGTGAAACTCAAGGCAGTACATTATATATACAGTACAGTACAGGGTAGTACAGTACAGTACATGGACCCAGAACTGAACCCTGAGGAACTCCCTATTGAAAAATACTGTATTAGACACGATTTTCCACACTAGCAAACTGGGAAACATTGGATTAGTAGACTAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37579
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114486 Nonsense 1264 1353 18 20
ENSDART00000132671 None None 149 None 3
ENSDART00000134183 None None 160 None 3
ENSDART00000140986 None None 414 None 10
ENSDART00000146416 Nonsense 72 144 2 4
Genomic Location (Zv9):
Chromosome 23 (position 337939)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 308930
GRCz11 23 321723
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCGCTCCTCAGCCCGTCCCGGTGCTCTTCTCTCTGGATAATGTAGTGT[T/A]GGAGCGTCTGGATGATGGAGTGCTGCGCTTCAGACGTGAGTGCTTTAGGT
Long Flanking Sequence:
TGCGGGACACCACTGTCACTCTCAAGGTGAGTGCAACACTCCGTTATGCTTCAAATTGTATGAATATTAAATGAGTAAACAGTGGGCGTGGCTTGTTTATCTACTGCAAGCTGATTGGATGTAGTAAAGTAGGCGTGTCATTCAGAAAGATGGGGGGAAAGGGTTATTACAGACTCCTCCCCCTCACCAATTCTGTCTGTTGAGAAAACTGACACTGGAGGGGCGTGGTTAAGTATGATAGCTCCGCCCACTACCTTAACCGATGTGATTCTGCATGATTTGTTGGGCATCTCCATCAGTTTTGATCATCACACTTCTGACTGAGTGTTCAGCCGACTCTCAGTCCATCATTACATCCCGGCTACTGTGTTCTGTTCTGAATGATGGTGCAGTAGTTATCTTGTGTTTATCATTGTGTTTGTGTCAGGATGATGGTCCTCGTGTGTACCCGACCGCTCCTCAGCCCGTCCCGGTGCTCTTCTCTCTGGATAATGTAGTGT[T/A]GGAGCGTCTGGATGATGGAGTGCTGCGCTTCAGACGTGAGTGCTTTAGGTTTGAGTTACAGACTGACCAAAAGGGTCCATATGCTCAGCTAGAACACATATTTGACTAGAATGTGAAAGTTTAATAAGATTATTATAATGAAAACAGGTATAACCCGGACCCATTTGAATTTATTTGTCAAATATTGAATTGTGGAATCATATTTAGCTTTAAATATACACGTTTTTTAATGAATTTAATTGATTTATTTCTATTTCTGTATTTGTGTATTATCCCTGTTCCACTCTTATAAATGCAGCAGCTCAGAGCCAATCAGGAGCTGAGAAAGAAAATGCAGACCAATCCTGCCTTGGAGACCGAGAGAGGAACAAGGTATGATATGATTTATCCATGCGCATGTTTAATCCTGATATTAACATACTCATCACAGTGGTTTTATATTCACACTTACACCTTAATATAACCTCAGAAAACTCTAAACAGGTCAATCAGCCAATGAC
Associated Phenotype:
Not determined