Busch Lab

ZMP

hp1bp3

Ensembl ID:
ENSDARG00000044669
ZFIN ID:
ZDB-GENE-060810-79
Human Orthologue:
HP1BP3
Human Description:
heterochromatin protein 1, binding protein 3 [Source:HGNC Symbol;Acc:24973]
Mouse Orthologue:
Hp1bp3
Mouse Description:
heterochromatin protein 1, binding protein 3 Gene [Source:MGI Symbol;Acc:MGI:109369]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa2596 Essential Splice Site F2 line generated Not yet available
sa35145 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa2596
Status:
F2 line generated
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
ENSDART00000077496 Essential Splice Site 247 595 5 12
Genomic Location (Zv9):
Chromosome 11 (position 38782257)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 37349276
GRCz11 11 37616481
KASP Assay ID:
554-2765.1 (used for ordering genotyping assays)
KASP Sequence:
TCTACAAGAGGTCTCTGAAGCGAATGGTTGAGAAGGGTGTTGYCAGACAG[G/A]TGATTTGCATTTTAACACATGAGTATTTTTAGTTTTACATATACAGYAAG
Long Flanking Sequence:
TCTGTATTCCATGCTGAAACCTGCCTGAGAATCAATAAAACTGTTAATCGCTAAAACCTTGACTTTTTCAAACCGCAGTATTCCTTGAAATTGGTTACTGTCCAAATGCCTAGTATGTATAAGAAAAATGCTGTTCTGCTAATTTAGCTTTTTTGTTCCCTTTAAATGTCTATATTTAGAGAATATATTGCCCTATTTGTTTCCTTCAATTAATGCATGTATTATTTAAGTTTTCATTTGTTGGTCTTTAAATGGTTTTATGAAGGTAAAGGTTAAACGTTTAAGAGTTTAGAAGCAAAATCGAAAGTCTGAAAAACTGTGAAAAGTCTCATATGTACATCTTCCTGTAGAGTTGCAAAGAAGACCGCAGTGGTGCTTCTTCAATCATCATTATGAAATACGTCAGGAAGAAGTATCCCGCTGTGGAAATGGACAAAAGGACCAAAAACCTCTACAAGAGGTCTCTGAAGCGAATGGTTGAGAAGGGTGTTGTCAGACAG[G/A]TGATTTGCATTTTAACACATGAGTATTTTTAGTTTTACATATACAGTAAGTCAACTTTGTCCTGTCTTCTTAACCCACAGCTGAAGGGTAAAGGCTTTTCTGGAAGTTTCACCATTGGGAAGGTATCTAAATATAGTGTAACTTTCATTGCTGATAAATACAGTGTAAATGAAGTACTTTTTAAGGATTGATTTATTTTTTTGTCAATGTTGTTGTGTTGTGTAGAAGCCGGCTGCATCTGCTTTACCCAAGGAGACACTGGGAGAGTCTCTACCTCTGATCATCACCCGTCTTTGTGAACCCAAAGAGGCTTCATACATCCTGATCAAGAAGTACCTGGAACAACACTTCCCTCAACTCAATGTGGAAAACAGGTCATTATTGACGTCCTATTAGTAGACGGGGGTGCAATATTGACCCTTAGTTTTTCTTTGAAAATATTTTCATTGGTGAAACAAAAAAAAAGACAATATTATGTCTAAAACTCACATTTACATTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35145
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
ENSDART00000077496 Essential Splice Site 431 595 10 12
Genomic Location (Zv9):
Chromosome 11 (position 38788320)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 37355339
GRCz11 11 37622544
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCATGGACTGAGTGGGTCATACCAGCTTAGTTATCCATTTTACCCAAG[G/A]TAAGTTCAATTGTAAGTTCAATGTAAAGAAGAGACCGTTGTGTAATAAAT
Long Flanking Sequence:
GGAAAATCATTCTTCGGTGAAAATAAAACTGATTTGATGAGAGTGTACATTTGTATTGGACAGTTGAAGAAAGCCGGGAATAAGGTCCTCATGGGTGGCGGTCTGCTGGAAGACGCTGTTGTGGCCGCCATCACTGCTATGAATGAGCCCAAGACCTGCAGCATCACCATACTGCGCAAATTCCTGATGCAGAGAAAGGAGAAGAACGCCTTTCCAGTGGGTAAGGAACACTTCTAGCTTATTGCAGATTCCTAGAGTTAACTTTCTGTCCGAGGCCTGAGGTTTTCAAATGTGTCCTTTTAGTATCAGTAATAACCCTAGTATCTCATTTGGTGTATTTTAATGTGTTATGCAGACTCCTTATGAATGATTTGTGTCTTACTACTAGTGTCTCATCTGAAGAGAACCTTGCAGAAGTGTAAAGTGATGGGATGGATGGAGCAGATTTCTGGTCATGGACTGAGTGGGTCATACCAGCTTAGTTATCCATTTTACCCAAG[G/A]TAAGTTCAATTGTAAGTTCAATGTAAAGAAGAGACCGTTGTGTAATAAATACTGCACTTACTCACCTTATTCTTCGCCGACGAGCGGGCACAGCCATTTGAATCTTTTTGGCTCGAGACTTCCGGTCTCATTACCTTCCATTCATTTTTAGACATTAAAAACTGCTCGTTTCGCTGTTTGATGTTGCAAACTGACATTTTATTATTATATTATTCTATATTATTCTACTTGATCTGTATAGTCATGCAAACATTTGTTTGTAGAGCAAGTAGTTTGACCGTTTTCTGCCGTTTATTATTCCTAGTCATTTCTCCCATAGACGACTAAATCAAAAGTTCTAAAACAATCGCAAAAACAGGCGCACTTCCACATTATAGAATAAGGTCAATAATCAGTGAATATAAGGTGGTTTCACTTTTGAAATGCGGTTTAAATTACTCCCGTTTTTTAATTCTTCTGAACACATTCAGGTGCTGCTTGTCATGCGAGGAACGCCATAG
Associated Phenotype:
Not determined