Busch Lab

ZMP

fuca1

Ensembl ID:
ENSDARG00000035890
ZFIN ID:
ZDB-GENE-030131-7434
Description:
fucosidase, alpha-L-1, tissue [Source:RefSeq peptide;Acc:NP_997905]
Human Orthologue:
FUCA1
Human Description:
fucosidase, alpha-L- 1, tissue [Source:HGNC Symbol;Acc:4006]
Mouse Orthologue:
Fuca1
Mouse Description:
fucosidase, alpha-L- 1, tissue Gene [Source:MGI Symbol;Acc:MGI:95593]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa18262 Nonsense Available for shipment Available now
sa44919 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18262
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052104 Nonsense 29 451 1 8
Genomic Location (Zv9):
Chromosome 19 (position 33875564)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 32912980
GRCz11 19 32500100
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTSTGCTATCATGCGCGTCRGTTATCGGAGCTCGATATACTCCTGACTG[G/A]ACAAGTCTGGACTCCAGACCTCTGCCTGGATGGTACGACGAGGTGAAGTT
Long Flanking Sequence:
TATTCCTTTTAAAAACTGCAGTATTTTGTAGGGGTTTGGAAGTAGTTTCACGAATAAATAATGATTTTTAAAAAAGTTCCCGACCAAACCACTATTTTTGTAGCGAATCAAAACCATACGGCGAGTCTGATTTCAGAATCAGAACCATAATTATTTGTTTATTTTCTTTTATCCTCGAGTTTATTCCCTTGTGGCGAGTTGTTTTGCAGGTGAAGTCATGTGCAGTAGTCACATGAGTGTTGTCATATGATAAACCAGGAAATACAAACTGGTTGCTCTGGTTTTCTGCAACGGCATTATGTTTGGTCCCAAGGTAAATCGACCGACATCCCTTTGTAGTGCAGAAGTCATACTGACAGTCGTGATAGCGAGTCACTTTAGCTGACCACAGTGAGCGCAATCACGTCTGCAAACATGCAGGTGACTCGCAGTCAGATATCGCTGTTTCTTTGTCTGCTATCATGCGCGTCAGTTATCGGAGCTCGATATACTCCTGACTG[G/A]ACAAGTCTGGACTCCAGACCTCTGCCTGGATGGTACGACGAGGTGAAGTTCGGCATCTTCGTTCACTGGGGGGTGTTTTCGGTGCCCGCTTTCGGTAGCGAGTGGTTCTGGTGGTACTGGAAAGGCGCACAAAATCCCGATTACGTCCAATTCATGATCAAAAACTACCCTCCAGGTTTCAGCTACGCGGATTTTGCGCCTAATTTCCACGCGCAGTTTTTCGACCCTGACGCTTGGGCTGATATCTTCGAAGCTTCCGGAGCGAAGTACGTACTTAAGCGTTTTTCGTTAAATCTTACTGTATTAGATTATGTAGTTATTTCTAGCTTTCTCCCATAGATATGTCGTCCTTACATCGAAACACCACGAAGGCTTCACAAATTGGGGATCCCCGACCTCCTGGAACTGGAATTCGGTTGATGACGGACCTCACAGGGATCTGGTTGGAGATTTGGGCAATGCTATAAGAAAGAAGTAATGTGTGCTGTATTATTACAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44919
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052104 Essential Splice Site 163 451 2 8
Genomic Location (Zv9):
Chromosome 19 (position 33875088)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 32912504
GRCz11 19 32499624
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCTCACAGGGATCTGGTTGGAGATTTGGGCAATGCTATAAGAAAGAAG[T/A]AATGTGTGCTGTATTATTACAAAGCTTTGATATCTAATACTTTTTAGTAA
Long Flanking Sequence:
CGGAGCTCGATATACTCCTGACTGGACAAGTCTGGACTCCAGACCTCTGCCTGGATGGTACGACGAGGTGAAGTTCGGCATCTTCGTTCACTGGGGGGTGTTTTCGGTGCCCGCTTTCGGTAGCGAGTGGTTCTGGTGGTACTGGAAAGGCGCACAAAATCCCGATTACGTCCAATTCATGATCAAAAACTACCCTCCAGGTTTCAGCTACGCGGATTTTGCGCCTAATTTCCACGCGCAGTTTTTCGACCCTGACGCTTGGGCTGATATCTTCGAAGCTTCCGGAGCGAAGTACGTACTTAAGCGTTTTTCGTTAAATCTTACTGTATTAGATTATGTAGTTATTTCTAGCTTTCTCCCATAGATATGTCGTCCTTACATCGAAACACCACGAAGGCTTCACAAATTGGGGATCCCCGACCTCCTGGAACTGGAATTCGGTTGATGACGGACCTCACAGGGATCTGGTTGGAGATTTGGGCAATGCTATAAGAAAGAAG[T/A]AATGTGTGCTGTATTATTACAAAGCTTTGATATCTAATACTTTTTAGTAATGTTCCGTAGATTTATATCTTGTTCAGTGTATTGTCTTTAATTTAACCGTGGATATGATTAATATTTTGAGAAAGTTTTGGTTTATTAAAGTATTTTTGTGCGTTGTGCTAGGGGCTTGCATTATGGACTCTATCACTCTCTGTACGAATGGTTCAACCCCCTCTACCTGAGTGACAAACAATCTGGCTTCAAGACCCAGGAGTATGTTGCAAGAAAAGCAATGCCTGAACTCTACGATCTGGTCAGCAGGTAAATATGAGTGAGTCATATGATGTCAGGCTAGAGAAGAAAAAAAACTAAAAACATTGGTTTATGACACTAGTCTCACAGTTTGCGAAAAGATCAATCCTAATCAGACCCGTAGCTAGTCTGGTGAAAGCGGTGGTTCTTTTTTCTCAATAAGTGGACCTTTTTGCAGTTATTCGCCTCTTTTTCTATTTAATTATAAG
Associated Phenotype:
Not determined