ZMP
glb1
Ensembl ID:
ZFIN ID:
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 |
sa11023 | Nonsense | Available for shipment | Available now |
sa18711 | Nonsense | Mutation detected in F1 DNA | Not yet available |
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.
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.
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:
sa11023
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 > 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:
sa18711
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:
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:
sa19602
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:
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