ZMP
zgc:123333
Ensembl ID:
ZFIN ID:
Description:
alpha-N-acetylgalactosaminidase [Source:RefSeq peptide;Acc:NP_001032465]
Human Orthologue:
NAGA
Human Description:
N-acetylgalactosaminidase, alpha- [Source:HGNC Symbol;Acc:7631]
Mouse Orthologue:
Naga
Mouse Description:
N-acetyl galactosaminidase, alpha Gene [Source:MGI Symbol;Acc:MGI:1261422]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17862 | Essential Splice Site | Available for shipment | Available now |
sa25269 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14996 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17862
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 |
---|---|---|---|---|---|
ENSDART00000125936 | Essential Splice Site | 146 | 415 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 759719)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 975465 |
GRCz11 | 4 | 988913 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
MATGCTCAAGTTGGACGGATGTTACTCCAACTCGTCCTATCAGGAACAAG[G/A]TACATCGCYAATCTGTGTCAGCTCAGATCTAAAAGSAAGGTCAAGACTTC
Long Flanking Sequence:
TCTGACCTGTGACCTCCTACCTTTAGATCTGACCTCTGACCTTCTACCTCTGAACTCTTAACCTCTGATCTGACCTTTTACCTTCTTGCTGTCTTTTCTGACCTTCTGATCTAAGCTGTGATCTTTTATCTTTTGAACTGACCTTAGATCTAACCTTCTACCTTTGAACTCTTACCTTCTGATCTGACCTCTGACCCTCTGATCTGACATTTTGACCTCTTCAATCCTGACTCTCTGGAGCCATCATGTTCTCCGCACTCTTCTTCATCTTGTGTAATTTTTCTGCAGGTTTCCTCGAGGCATTCCTCATCTGGCGCAGTACGTCCATGACCGTGGGCTGAAGCTGGGCATCTATGGGGACATGGGCACGCTGACCTGCGGAGGGTATCCGGGAACCACACTGGACAAGATTGAGACAGACGCACAGACGTTTGCGGACTGGGGGATCGACATGCTCAAGTTGGACGGATGTTACTCCAACTCGTCCTATCAGGAACAAG[G/A]TACATCGCCAATCTGTGTCAGCTCAGATCTAAAAGGAAGGTCAAGACTTCTTTAAACCAGCACAAATAAAATTAATGCTGTATGTCCCAGAACAAACAATACAGTACAATTAAAGAAGATAAAGCAGTTTCTCAAGCCTTGTAATGGTTTGAAATTGATTCTTTGTTTGTGATTCGGTTAATTCAGGATACCCAATGATGTCGAAGGCCCTCAATGCTACCGGTCGTCCTATTGGCTACTCCTGCAGTTGGCCTGCCTACCAGGGAGGCCTCCCACCTAAAGTGAGTTAGTGTGTGTGTGTCTGAGTGAGCAAAGTTTGAGTGAGTGTGTGAGAATGTGACACACTGACTCTGGTGTGTGTTTTTTTTTAGGTGAACTACACTCTGCTGGGTCAGATCTGTAACCTGTGGAGGAACTATGATGATATCCAGGACTCGTGGGACAGTGTGATGGGCATCGTGGACTGGTTCTTCGACAATCAGGACGCCCTTCAGCCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25269
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125936 | Nonsense | 226 | 415 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 759206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 974952 |
GRCz11 | 4 | 988400 |
KASP Assay ID:
554-7614.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGTTCTTCGACAATCAGGACGCCCTTCAGCCTGCAGCCGCACCAGGA[C/T]AGTGGAACGACCCAGACATGGTGAGCTCCACACCGATGACCCTGAGTTTA
Long Flanking Sequence:
CTGTGTCAGCTCAGATCTAAAAGGAAGGTCAAGACTTCTTTAAACCAGCACAAATAAAATTAATGCTGTATGTCCCAGAACAAACAATACAGTACAATTAAAGAAGATAAAGCAGTTTCTCAAGCCTTGTAATGGTTTGAAATTGATTCTTTGTTTGTGATTCGGTTAATTCAGGATACCCAATGATGTCGAAGGCCCTCAATGCTACCGGTCGTCCTATTGGCTACTCCTGCAGTTGGCCTGCCTACCAGGGAGGCCTCCCACCTAAAGTGAGTTAGTGTGTGTGTGTCTGAGTGAGCAAAGTTTGAGTGAGTGTGTGAGAATGTGACACACTGACTCTGGTGTGTGTTTTTTTTTAGGTGAACTACACTCTGCTGGGTCAGATCTGTAACCTGTGGAGGAACTATGATGATATCCAGGACTCGTGGGACAGTGTGATGGGCATCGTGGACTGGTTCTTCGACAATCAGGACGCCCTTCAGCCTGCAGCCGCACCAGGA[C/T]AGTGGAACGACCCAGACATGGTGAGCTCCACACCGATGACCCTGAGTTTACTGTTTATTACGCTGGTGTCCATCATGTTCTTAACTTCTGATCTGACTGGTGACTTTTCGATCTGACCTATGACCTTCTGATCTGACCTTTGTCATTCTTACTGTCTTATCTAAACTCTGACCTGTTTTTGATCAGAACGCTGACCTTCCAATCTTACCTTTGACCTTCTTGTCAGACCTGCAACCTTCAGGTCGGACCTTTTGACCTTCTTACTGTCTTGTCTGACCTATGATCTAAACAGTGACCTTCTGATTTGAACTTTGACCTTTTTGTCTTCTCTGACCTTCTGATCTAACCTTTGACCTTCTTCTGTCTTGTCTGACCTCTTTGTGATCTGAAATCTTGACCTTCTGATCTAACCTTTGACCTTCTTCTGTCTTGTCTGACCTCTTTGTGATCTGAAATCTTGACCTTCTGATCTAACCTTTGACCTTCTTCTGTCTTGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14996
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125936 | Essential Splice Site | 298 | 415 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 758342)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 974087 |
GRCz11 | 4 | 987535 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTYCATCAACCAGGACCCGCTGGGCATCCAGGGCAGACGCCTGCTCAAGG[T/C]GCACACGCCTAAATAATGCTCCTGCTTAATTATTTATTTCAWTATTGTAA
Long Flanking Sequence:
TCTTGTCTGACCTCTTTGTGATCTGAAATCTTGACCTTCTGATCTAACCTTTGACCTTCTTCTGTCTTGTCTGACCTCTTTGTGATCTGAAATCTTGACCTTCTGATCTAACCTTTGACCTTCTTCTGTCTTGTCTGACCTCTTTGTGATCTGACCTTCAGATCTGACCTTTAAATATGTACTGTCTTATCTGATCTGTGATCTTCTAATCTGACCTTTGACCTTTCTTGTTTGACCTTGGCTGACCTTTGACCTTCTGTTTCCTCTTGTTTACCCTACTGTTGATCCTGTGTCGTCCTCAGCTGATCTTGGAGACTTCAGCCTCAGTCTGGATCAATCTCGGGCTCAGATGGCTCTATGGTCCATCATGGCGGCTCCGCTCTTCATGTCCAACGACCTGCGCACCATCAGCAGCGCCGCTCGCTCCGTCCTCCAGAATAAAGCGGTCATCTCCATCAACCAGGACCCGCTGGGCATCCAGGGCAGACGCCTGCTCAAGG[T/C]GCACACGCCTAAATAATGCTCCTGCTTAATTATTTATTTCATTATTGTAAATATTGTCATTAAATGAATTCATTATCATCAGGAGAAGAGCGGGATCCAGGTGTTCCAGCGGCCGCTCTCTAAAGGAGCCAGCGCTCTAGTGTTTTTCAGCCGCAGGTCTGATATGCCATACCGCTACACCACATCTCTGAAGACCCTGGGATACCAGCCTGGAGTATTTGAGGTGAGCCTTCAGGAACACACACATACACACTGTCCATTACACACCTCACACGGGTGAGTAGGCTTGACAAACCACCTGTAGAAAACGCACTCTTTTATCTCTCTGACACTAACATTGCACATTTGCACCATTACTTCAATATTGTGGATAAGCCATGCTGGCCATTTCTCTCTGTCTCGCACTGAACACAGTTGACCAATCGCAAAAGACTGGGACCAATCGGACCAATCAGCACAGATTAGCATCTCGTTAAGTTTAAGAACAAATGAATCACTGT
Associated Phenotype:
Not determined