ZMP
zgc:101116
Ensembl ID:
ZFIN ID:
Description:
fucosidase, alpha-L-1, tissue [Source:RefSeq peptide;Acc:NP_001003559]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18216 | Nonsense | Available for shipment | Available now |
sa23558 | Essential Splice Site | Available for shipment | Available now |
sa29230 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15377 | Nonsense | Available for shipment | Available now |
sa43309 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18216
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052090 | Nonsense | 113 | 451 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 19 (position 33868820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 32906236 |
GRCz11 | 19 | 32493356 |
KASP Assay ID:
2261-3481.1 (used for ordering genotyping assays)
KASP Sequence:
CTGATTTCCACGCGCAGTTTTTTGACCCTGATGCTTGGGCTGAGATCTTY[G/T]AAGCTTCCGGAGCAAAGTATGKAGGCTAYTGCTGCTTTTGCTTTGCCTAG
Long Flanking Sequence:
GGGATGACATTTGATAAACCAGGAAATACAAACTGGCTGCTGGAGTCTGCATTACTTTGAACCATAAAGGTTTGTCAGGATAAAGTTCTCTTGGCATTCGTGCTCATGTTACACTTCAGTTTCACAGATTTACTGACCTCAGTGCATTTGAGCTGTGATCAAACATGCAAGTGACTCGGAGTCAGATGTCGCTGTTTCTTTGTCTGCTATCATGCGCGTCGGTTATCGGAGCTCGATATACTCCTGACTGGACAAGTCTGGACTCCAGACCTCTGCCTGGATGGTACGACGAGGTGAAGTTCGGCATCTTCGTTCACTGGGGGGTGTTTTCGGTGCCCGCTTTCGGCAGCGAGTGGTTCTGGTGGAACTGGAAGGGGGCACACGACTTTAAGTATATCCTGTACATGGTAAAGAACTACCCTCCAGGTTTCAGCTACGCGGATTTTGCGCCTGATTTCCACGCGCAGTTTTTTGACCCTGATGCTTGGGCTGAGATCTTC[G/T]AAGCTTCCGGAGCAAAGTATGTAGGCTACTGCTGCTTTTGCTTTGCCTAGTTATTCTTTTAGTTTTTACATGGGTGTTTATTAATTTATTTGGCATCTTTCATAGATATGTGGTCCTTACATCGAAACATCACGAAGGGTTCACAAACTGGGAATCCCCGACTTCCTGGAACTGGAATTCTGTTGATAATGGACCTCACAGAGATCTGGTTGGAGATTTAGGCAATGCGGTAAGAAAAAGGTAATGTGTAGTCGTGGTTAAATTGTAACAAAGCTTACAGTATCTTAAATAAACTAGTTCCTAAACCAGTTGTTCTCCTTTTAGGGGAAAAACGCATAATGATATAACAGATAGACTACTAGAGCAAAAGTCAGTCGTTACTGTTTCAGATATGTTTGAATTGTGGACTCATTGAATTGTATTGAAGACTATATGTGTCTTTAATTTTACTGTATTAGAAATTAAATAATAATAAATTCTTTAGGGCAATAAAAAGTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23558
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052090 | Essential Splice Site | 311 | 451 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 19 (position 33865265)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 32902681 |
GRCz11 | 19 | 32489801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAAATATGAAGCTGAGTGAGCTGATGGATCTGCCAGCGCTTATAAAG[G/A]TGAGATGTGATGAGAATGTTCAGGCATTATACAATGTATCAAGTGCATTT
Long Flanking Sequence:
AAACTTTGGTTTATGACACCAATCTCACTGTTCTGATCTTAATGTGTAAAAATCAACCTTTATGGTCGTATAGTTTTACATTAATAAAACAGCTGATGTTTTTGCTGTTTCAGGTACAAGCCAGACTTGATTTGGTCTGACGGCGACTGGGAAGCACCGGACACTTACTGGAACTCTACAGAATTCCTTGCCTGGCTCTACAACGACAGTCCAGTCAAAGTGAGATCATCACATCATGTCTTTATTATTGTGAAACTGAACTTTTAGATCATGAAAATGAATTCTTGTGCTCCTTATAGGACATAGTGGTGGTCAATGACAGATGGGGGAACGGATGTTACTGCAAACATGGAGGTTACTACAACTGCGCCGACAAATTCAGTCCTGGCGAGCTGCCCAAACACAAGTGGGAGAAATGCCAATCAGTGGACACTATATCATGGGGGTATCGCAGAAATATGAAGCTGAGTGAGCTGATGGATCTGCCAGCGCTTATAAAG[G/A]TGAGATGTGATGAGAATGTTCAGGCATTATACAATGTATCAAGTGCATTTTTAACCTCTTATATATATGTGGTGAACACAGGACCTGGTCTACACTGTGGCTTTAGGTGGGAATTACCTGTTGAATGTGGGGCCCACAGCAGATGGTGTGATCGCTCCTGTGTTTGAGGAACGTCTCAGAGGAATCGGAGCCTGGCTGCAGATCAACGGTGAAGCCATCTATGCAACGAGCTCTTGGAGAGTTCAAGCTGAGAATGCCACTGTTCCTGTCTGGTGTGTTGATGTTTTTATATTTTTTTAATATATTAAATACATTTAAAAACGGTTCGCTTTCAACTGCAGTTGCAGTCAAAAAGGGATTGTCATTTAGGGATGACGATTTTTAGTATTTTATAAGGCCATGTTCACACTAATACGTTTTTGTTTAAAAAAGGATTTTTTCTTTCCATCTATACCAAGAAGGCATTTTAGGAAATGAAAAGTATCTTTTTGAAAATGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29230
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 |
---|---|---|---|---|---|
ENSDART00000052090 | Essential Splice Site | 408 | 451 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 19 (position 33864498)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 32901914 |
GRCz11 | 19 | 32489034 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGAACACCTTTGAACTTTCTGCACCCAAAACCTCGGACAACACAGTG[G/A]TAAATAAAATATGGAATGTAAAAAGTAAATTTTTCTTTTGTTAAGATATT
Long Flanking Sequence:
TGTCTGGTGTGTTGATGTTTTTATATTTTTTTAATATATTAAATACATTTAAAAACGGTTCGCTTTCAACTGCAGTTGCAGTCAAAAAGGGATTGTCATTTAGGGATGACGATTTTTAGTATTTTATAAGGCCATGTTCACACTAATACGTTTTTGTTTAAAAAAGGATTTTTTCTTTCCATCTATACCAAGAAGGCATTTTAGGAAATGAAAAGTATCTTTTTGAAAATGCTGTCTAAGGTGTCAAGTTCTCGTCTTAAGGAGGGACTGATCGATTCAGACATTCAAATGATTTGTTCAAAACAGACGATTCATATAGAAGCAAACATTTACATTTTTTACCATGTGGTGTAGTTCTAGTGTAGTAAATATGCTTTTTAAAACTTTGATTTAATTTCAGGTATACATCGAAAAACTCCACAGTGTATGCGATCTTTACCTCCAGTCCCAACCAGAACACCTTTGAACTTTCTGCACCCAAAACCTCGGACAACACAGTG[G/A]TAAATAAAATATGGAATGTAAAAAGTAAATTTTTCTTTTGTTAAGATATTAATTAGTGTCTTTGTTTCTCTTGCATCTGTGTTCAGGTGACTTTGTTGGGGAATCCTAAACCTTTGAAATGGGCTCCTCTGCATTCATCGGGACTGATTTTGTTGCTGCCTGATCTGCCTTTCTCACCCGCACAGGCCTGGACGCTCAAGCTGGAAGGGGTCGCCTGAAACCTTTAAGATCTTAATGAGGTTATCAGGATTTTTTTAATGTTTATGTAGATTTCTGTATTTTTCTACTTGAAGTGTGACCTATGTGAATGGCCTTTATTACCAAAGCTGTGAAATGCTGCATTTTCAAATGGATTGTTTTGAATCGTGCGGTTGTGTTCAAAACACTATTTTTACAGGTCTGTCAGGGGCATAAATTTTTGCATAAATAAATTATTCAGAAAATGAAAAAAAGAAAGTAAAATAGACCATGTGACTATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15377
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052090 | Nonsense | 412 | 451 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 19 (position 33864401)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 32901817 |
GRCz11 | 19 | 32488937 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTAATTAGTGTCTTTGTTTCTCTTGCATCTGTGTTCAGGTGACTTTGT[T/A]GGGGAATYCTAAACCTTTGAAATGGGCTCCTCTGYATTCATCGGGACTRA
Long Flanking Sequence:
ATTTAGGGATGACGATTTTTAGTATTTTATAAGGCCATGTTCACACTAATACGTTTTTGTTTAAAAAAGGATTTTTTCTTTCCATCTATACCAAGAAGGCATTTTAGGAAATGAAAAGTATCTTTTTGAAAATGCTGTCTAAGGTGTCAAGTTCTCGTCTTAAGGAGGGACTGATCGATTCAGACATTCAAATGATTTGTTCAAAACAGACGATTCATATAGAAGCAAACATTTACATTTTTTACCATGTGGTGTAGTTCTAGTGTAGTAAATATGCTTTTTAAAACTTTGATTTAATTTCAGGTATACATCGAAAAACTCCACAGTGTATGCGATCTTTACCTCCAGTCCCAACCAGAACACCTTTGAACTTTCTGCACCCAAAACCTCGGACAACACAGTGGTAAATAAAATATGGAATGTAAAAAGTAAATTTTTCTTTTGTTAAGATATTAATTAGTGTCTTTGTTTCTCTTGCATCTGTGTTCAGGTGACTTTGT[T/A]GGGGAATCCTAAACCTTTGAAATGGGCTCCTCTGCATTCATCGGGACTGATTTTGTTGCTGCCTGATCTGCCTTTCTCACCCGCACAGGCCTGGACGCTCAAGCTGGAAGGGGTCGCCTGAAACCTTTAAGATCTTAATGAGGTTATCAGGATTTTTTTAATGTTTATGTAGATTTCTGTATTTTTCTACTTGAAGTGTGACCTATGTGAATGGCCTTTATTACCAAAGCTGTGAAATGCTGCATTTTCAAATGGATTGTTTTGAATCGTGCGGTTGTGTTCAAAACACTATTTTTACAGGTCTGTCAGGGGCATAAATTTTTGCATAAATAAATTATTCAGAAAATGAAAAAAAGAAAGTAAAATAGACCATGTGACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATATATATAAATATATATATATATATATATATAAATTAATAAATGGTCTGATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43309
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052090 | Nonsense | 426 | 451 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 19 (position 33864359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 32901775 |
GRCz11 | 19 | 32488895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTTGTTGGGGAATCCTAAACCTTTGAAATGGGCTCCTCTGCATTCAT[C/A]GGGACTGATTTTGTTGCTGCCTGATCTGCCTTTCTCACCCGCACAGGCCT
Long Flanking Sequence:
ACACTAATACGTTTTTGTTTAAAAAAGGATTTTTTCTTTCCATCTATACCAAGAAGGCATTTTAGGAAATGAAAAGTATCTTTTTGAAAATGCTGTCTAAGGTGTCAAGTTCTCGTCTTAAGGAGGGACTGATCGATTCAGACATTCAAATGATTTGTTCAAAACAGACGATTCATATAGAAGCAAACATTTACATTTTTTACCATGTGGTGTAGTTCTAGTGTAGTAAATATGCTTTTTAAAACTTTGATTTAATTTCAGGTATACATCGAAAAACTCCACAGTGTATGCGATCTTTACCTCCAGTCCCAACCAGAACACCTTTGAACTTTCTGCACCCAAAACCTCGGACAACACAGTGGTAAATAAAATATGGAATGTAAAAAGTAAATTTTTCTTTTGTTAAGATATTAATTAGTGTCTTTGTTTCTCTTGCATCTGTGTTCAGGTGACTTTGTTGGGGAATCCTAAACCTTTGAAATGGGCTCCTCTGCATTCAT[C/A]GGGACTGATTTTGTTGCTGCCTGATCTGCCTTTCTCACCCGCACAGGCCTGGACGCTCAAGCTGGAAGGGGTCGCCTGAAACCTTTAAGATCTTAATGAGGTTATCAGGATTTTTTTAATGTTTATGTAGATTTCTGTATTTTTCTACTTGAAGTGTGACCTATGTGAATGGCCTTTATTACCAAAGCTGTGAAATGCTGCATTTTCAAATGGATTGTTTTGAATCGTGCGGTTGTGTTCAAAACACTATTTTTACAGGTCTGTCAGGGGCATAAATTTTTGCATAAATAAATTATTCAGAAAATGAAAAAAAGAAAGTAAAATAGACCATGTGACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATATATATAAATATATATATATATATATATATAAATTAATAAATGGTCTGATGCACTCTATGAATCTCAGATCTATTCAGCTTGTTTTGTAATAAAC
Associated Phenotype:
Not determined