Busch Lab

ZMP

glb1

Ensembl ID:
ENSDARG00000036415
ZFIN ID:
ZDB-GENE-050410-9
Description:
beta-galactosidase [Source:RefSeq peptide;Acc:NP_001017547]
Human Orthologue:
GLB1
Human Description:
galactosidase, beta 1 [Source:HGNC Symbol;Acc:4298]
Mouse Orthologue:
Glb1
Mouse Description:
galactosidase, beta 1 Gene [Source:MGI Symbol;Acc:MGI:88151]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa8423 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24857 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18711 Nonsense Mutation detected in F1 DNA Not yet available
sa11023 Nonsense Available for shipment Available now
sa19602 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa8423
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
ENSDART00000033761 Essential Splice Site 126 651 3 17
ENSDART00000124682 Essential Splice Site 151 676 3 16
ENSDART00000136942 Essential Splice Site 126 651 3 16
Genomic Location (Zv9):
Chromosome 1 (position 52960118)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51830717
GRCz11 1 52465455
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTGGTYATCATGAGACCAGGACCCTACATATGTGCCGAGTGGGATATG[G/A]TGAGAAAACACTGTACTTTCTATAGGCAGRGAATRTATGTTAGGATAGGG
Long Flanking Sequence:
GGTGTAATATTGACTTAATATTAAATTTTGGGTGAGCTGTTCATTTAAAGCACTTTGTTTTGCCTGTTGTTTCAGTACGCCACAACTCCCACTTTTTCTGTGGATTACCATCGAAACTGCTTTCTTAAAGATGGAGAGCCATTCCGCTACATATCTGGCAGTATCCACTACAGCCGGATCCCTAGAGTCTATTGGAAAGACCGGCTACTCAAGATGTACATGGCTGGATTGAACGCCATCCAGACGTAAGCACAACCATCAATGATTTAGCTCCAGTCTTGTAGAATATTTAGGATTTCCAACAGTCTTTCCAACTCATTCCAGCTCGGATTTTGCAAATGATCCACAGATATGTGCCGTGGAACTTCCACGAAGCAGTTCCTGGTCAGTACGACTTCAGTGGAGATCGAGATCTGGAGCAATTCCTCCAGCTCTGCCAAGACATCGGCCTGCTGGTCATCATGAGACCAGGACCCTACATATGTGCCGAGTGGGATATG[G/A]TGAGAAAACACTGTACTTTCTATAGGCAGAGAATATATGTTAGGATAGGGCAATATTTCACAGAGAAACTTAAATTCCAGAACTGAATAATTGTGTGCAAACAATAAAATAAAAATATTGAGAACTTTCCCTTTAAAGGTGTCTAAAATAAGTGCTTAGCAATGCACATTACTAATCAAAAAAGTTCTGATATATCCATAGTATGTTATTTATAAAATATCTTCATGTAACATGTTTTTAGGCATTAAAAAAGTCAGTCATTTTGACTAATACAATGGGCCCTATCAAACACTCGGCGCAATGTGGCACAGGGCGCAACGCAATTGTTGTTTGCTAGTTTCAGCTCGGCGTAAGAGTCGTTTTGGCGTTTTGCACCACGCTTTTTAAATAGCAAATGTATTTGCACTCCACAAGAGTGAAAGTGAAAGTAAATATTGAGGAGGCTTATCTCTCATTCTCGCGCTGTAGATGCTCTGTTTAACTGTTTTCTCTCTAGTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24857
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033761 Essential Splice Site 126 651 3 17
ENSDART00000124682 Essential Splice Site 151 676 3 16
ENSDART00000136942 Essential Splice Site 126 651 3 16
Genomic Location (Zv9):
Chromosome 1 (position 52960119)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51830718
GRCz11 1 52465456
KASP Assay ID:
554-7376.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGTCATCATGAGACCAGGACCCTACATATGTGCCGAGTGGGATATGG[T/G]GAGAAAACACTGTACTTTCTATAGGCAGAGAATATATGTTAGGATAGGGC
Long Flanking Sequence:
GTGTAATATTGACTTAATATTAAATTTTGGGTGAGCTGTTCATTTAAAGCACTTTGTTTTGCCTGTTGTTTCAGTACGCCACAACTCCCACTTTTTCTGTGGATTACCATCGAAACTGCTTTCTTAAAGATGGAGAGCCATTCCGCTACATATCTGGCAGTATCCACTACAGCCGGATCCCTAGAGTCTATTGGAAAGACCGGCTACTCAAGATGTACATGGCTGGATTGAACGCCATCCAGACGTAAGCACAACCATCAATGATTTAGCTCCAGTCTTGTAGAATATTTAGGATTTCCAACAGTCTTTCCAACTCATTCCAGCTCGGATTTTGCAAATGATCCACAGATATGTGCCGTGGAACTTCCACGAAGCAGTTCCTGGTCAGTACGACTTCAGTGGAGATCGAGATCTGGAGCAATTCCTCCAGCTCTGCCAAGACATCGGCCTGCTGGTCATCATGAGACCAGGACCCTACATATGTGCCGAGTGGGATATGG[T/G]GAGAAAACACTGTACTTTCTATAGGCAGAGAATATATGTTAGGATAGGGCAATATTTCACAGAGAAACTTAAATTCCAGAACTGAATAATTGTGTGCAAACAATAAAATAAAAATATTGAGAACTTTCCCTTTAAAGGTGTCTAAAATAAGTGCTTAGCAATGCACATTACTAATCAAAAAAGTTCTGATATATCCATAGTATGTTATTTATAAAATATCTTCATGTAACATGTTTTTAGGCATTAAAAAAGTCAGTCATTTTGACTAATACAATGGGCCCTATCAAACACTCGGCGCAATGTGGCACAGGGCGCAACGCAATTGTTGTTTGCTAGTTTCAGCTCGGCGTAAGAGTCGTTTTGGCGTTTTGCACCACGCTTTTTAAATAGCAAATGTATTTGCACTCCACAAGAGTGAAAGTGAAAGTAAATATTGAGGAGGCTTATCTCTCATTCTCGCGCTGTAGATGCTCTGTTTAACTGTTTTCTCTCTAGTGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18711
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033761 Nonsense 325 651 10 17
ENSDART00000124682 Nonsense 350 676 10 16
ENSDART00000136942 Nonsense 325 651 10 16
ENSDART00000033761 Nonsense 325 651 10 17
ENSDART00000124682 Nonsense 350 676 10 16
ENSDART00000136942 Nonsense 325 651 10 16
Genomic Location (Zv9):
Chromosome 1 (position 52964743)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51835342
GRCz11 1 52470080
KASP Assay ID:
2259-1156.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCACATTATAGGTGCCAACACTCCTTATGGTCCTCAACCCACCAGCTA[T/G]GACTATGACTCTCCTCTTACAGAGGCTGGAGATCTCACTGAGAAATATTT
Long Flanking Sequence:
CATAATTTACTTTACTGATTATAAAATATATTATAATATTGGCTGGCTAACTTAATTGAACTACATTGTGTCAGAATTCAAGCATGATGTGTGTTCTGTACTAATAAAACTAAAGGAAGGGTTTTGCAGGTGAACTCTGAGTTTTACCCCGGCTGGTTGGATCATTGGGGCGAAAAACACTCGGTGGTTCCTACATCTGCTGTAGTCAAGACTCTCAATGAAATTCTGGAAATTGGAGCCAATGTCAACCTGTGAGTTTTCATCTATAACAACTAACAACAGAAATGTATTGCATCATTGCATTTGAGTTCATTATGTAATTCATTTGTCAGGTATATGTTCATCGGTGGAACTAACTTTGGCTATTGGAATGGTAAGTTGGAGATTTATACATAAACAAGACTAAAAATAAATTAAAACGTGTCCATATTCATGTCTGTTTTCTATTTTTACCACATTATAGGTGCCAACACTCCTTATGGTCCTCAACCCACCAGCTA[T/G]GACTATGACTCTCCTCTTACAGAGGCTGGAGATCTCACTGAGAAATATTTCGCCATAAGGGAAGTCATCAAAATGGTAAATTGAGAGGGGGGGATTTAGATTTTTTTTCGGGTCATGCTTTATTTTAAGGGACAATTATTGCTAATAACAAGCCAATAACTGTGACTTTTGCCTCAATAAACTCATATTTGCTGCTAAATAATAGTTATTAAGGTAAAAGTTGGGTTTAGATATTGGCTATTAAGGATTCAGAATAAGATCATGCAGAATATGTACTGTGTTTGACCCATAAACATTTCCTGCATGTTATTAAACTGTTTTATAGCTGTAACAAGAGGCAATTCACTCATAACCTAAAGTTAAACGGTTGTCATAACATTATTTATCAATATGGGACTCTTATTGGATTCTCAGATGCTATCGAAGTTAAAAATGTGGAACAGGAAATACGTTGGGACCATTGTTTTTTGTTTACATCCCTCAAAATGGTCTATATGTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11023
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033761 Nonsense 325 651 10 17
ENSDART00000124682 Nonsense 350 676 10 16
ENSDART00000136942 Nonsense 325 651 10 16
ENSDART00000033761 Nonsense 325 651 10 17
ENSDART00000124682 Nonsense 350 676 10 16
ENSDART00000136942 Nonsense 325 651 10 16
Genomic Location (Zv9):
Chromosome 1 (position 52964743)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51835342
GRCz11 1 52470080
KASP Assay ID:
2259-1156.1 (used for ordering genotyping assays)
KASP Sequence:
TACCACATTATAGGTGCCAACACTCCTTATGGTCCTCAACCCACCAGCTA[T/G]GACTATGACTCTCCTCTTACAGAGGCTGGAGATCTCACWGAGAAATATTT
Long Flanking Sequence:
CATAATTTACTTTACTGATTATAAAATATATTATAATATTGGCTGGCTAACTTAATTGAACTACATTGTGTCAGAATTCAAGCATGATGTGTGTTCTGTACTAATAAAACTAAAGGAAGGGTTTTGCAGGTGAACTCTGAGTTTTACCCCGGCTGGTTGGATCATTGGGGCGAAAAACACTCGGTGGTTCCTACATCTGCTGTAGTCAAGACTCTCAATGAAATTCTGGAAATTGGAGCCAATGTCAACCTGTGAGTTTTCATCTATAACAACTAACAACAGAAATGTATTGCATCATTGCATTTGAGTTCATTATGTAATTCATTTGTCAGGTATATGTTCATCGGTGGAACTAACTTTGGCTATTGGAATGGTAAGTTGGAGATTTATACATAAACAAGACTAAAAATAAATTAAAACGTGTCCATATTCATGTCTGTTTTCTATTTTTACCACATTATAGGTGCCAACACTCCTTATGGTCCTCAACCCACCAGCTA[T/G]GACTATGACTCTCCTCTTACAGAGGCTGGAGATCTCACTGAGAAATATTTCGCCATAAGGGAAGTCATCAAAATGGTAAATTGAGAGGGGGGGATTTAGATTTTTTTTCGGGTCATGCTTTATTTTAAGGGACAATTATTGCTAATAACAAGCCAATAACTGTGACTTTTGCCTCAATAAACTCATATTTGCTGCTAAATAATAGTTATTAAGGTAAAAGTTGGGTTTAGATATTGGCTATTAAGGATTCAGAATAAGATCATGCAGAATATGTACTGTGTTTGACCCATAAACATTTCCTGCATGTTATTAAACTGTTTTATAGCTGTAACAAGAGGCAATTCACTCATAACCTAAAGTTAAACGGTTGTCATAACATTATTTATCAATATGGGACTCTTATTGGATTCTCAGATGCTATCGAAGTTAAAAATGTGGAACAGGAAATACGTTGGGACCATTGTTTTTTGTTTACATCCCTCAAAATGGTCTATATGTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19602
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033761 Nonsense 648 651 16 17
ENSDART00000124682 Nonsense 673 676 16 16
ENSDART00000136942 Nonsense 648 651 16 16
Genomic Location (Zv9):
Chromosome 1 (position 52973106)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51843705
GRCz11 1 52478443
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAAACGGCACCGTGAACGGCCAATACAAGAGACAACTATTCAACAAA[C/T]AAGACCTCTTTTGAGTTTACAGCCGCTTCCAGTTGCAGAAATTGTTTATA
Long Flanking Sequence:
CATCTGCATTAATAAATTAATTAATCAAGTAAAGGTATTTAAATACCAGTTGCAAAGAAGGCTTTTAAATTGGTGGGAAAATAAGTTTTAGTTTTGTATCATTTATTTCAACCTAATTTGGTTTTAAATTGTCACACCAGTTCATTTCATTTTTAAGCTCCCACTGTTGATCATGCTGTAAGCCATTTATAAATGTGAAGCAGTCAATAACAATTCATTAGCACTGGTAAAATAAACAACAAACATAACTTGCATTTTCATTTCAGGGTCAAGTGTGGATAAATGGATTTAACGTTGGCCGCTACTGGCCGTCCCGTGGGCCACAGATCACTCTCTTTGTCCCGGCGCACCTGCTCAGCACCTCCGTCCAAAACAACATAACCGTCCTGGAGCTTGAGGCGTCTCCTTGCTCCTCAGGTTCCTGCATGGTGGAGTTCACTGATACTCCTATTTTAAACGGCACCGTGAACGGCCAATACAAGAGACAACTATTCAACAAA[C/T]AAGACCTCTTTTGAGTTTACAGCCGCTTCCAGTTGCAGAAATTGTTTATATTGTGCAACAAATTTTGTTCGTTTGAAGGAATCTGAGGGATGACGTTGGAGATCATCAGCACTATATGGATTAAATTACAGCTGGATTGTGTGATCACTGTGAAATATAATATCTTGCAAATGATCAGGGGCTGATCAAGGCTGCTCAGGCACTGTATTATTGAAAAATGTGCAGTAGAAGATGTATATTGCTACTCATTATGATGTTAAAGGGATAGTTCACCCAAAAATTAAACCATTTTCTCACATCTCACTCTGATTAAAACCTGTTTGTTGTTTACATTTACATTTAGCAGATGCTTTTGTGCAAAGCGACTTACAATTGAAGAGGTATTCAGGGATTCTACAAGAAAAAGCAATACACACAAATGCTAATATGGCTCAGTGGTTAGCACTGTCATCTCACAGCAAGAAGGTCGCTGGTTTGAGTCCAAGTTGGGCCAGTGGGCA
Associated Phenotype:
Not determined