ZMP
acp5a
Ensembl ID:
ZFIN ID:
Description:
tartrate-resistant acid phosphatase type 5 [Source:RefSeq peptide;Acc:NP_999938]
Human Orthologue:
ACP5
Human Description:
acid phosphatase 5, tartrate resistant [Source:HGNC Symbol;Acc:124]
Mouse Orthologue:
Acp5
Mouse Description:
acid phosphatase 5, tartrate resistant Gene [Source:MGI Symbol;Acc:MGI:87883]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17411 | Nonsense | Available for shipment | Available now |
sa40635 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16094 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17411
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 |
---|---|---|---|---|---|
ENSDART00000004716 | Nonsense | 20 | 339 | 2 | 6 |
ENSDART00000135810 | Nonsense | 20 | 192 | 2 | 5 |
ENSDART00000142752 | Nonsense | 37 | 219 | 2 | 5 |
The following transcripts of ENSDARG00000019763 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 9435482)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8125180 |
GRCz11 | 6 | 8360719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACTAATGCTGGTRTTTTTAAGTGCTCTCCCTGGGGTCCTTTGCTACTA[T/A]TCCTCATTCGTTGACCTGGAAGCTCAAGGAAGTGAGTTGCTATTGATTTC
Long Flanking Sequence:
ATTTCTGAAAAAGAATTCTGAAAGAAGCACATACATTTATTTAAAGGCATAGTTCACCCAAAAATTTAAATTCTATCATCGTTTACTATACAACTACAAAATTTTATAAGCACAAAATGTAAAACTACAGTAGGCAGAATAAATGATTTTCGTTTTTTGAGTGAGCTGCTTCTTTAAGAGAGTATTGCCGATTTCCCGCAATCACGCTGATCAGGCTGATTAGTTTACTAAGAGAAAACAGCTGTAGCTGAAATGAGGGCGTGGCTTATTGGTGATTAGAATGATATAAATGTGAAAGTTAGGCGTTAGTTTGGTATGAGGTGTGGAGAGAGGACTCTCAAAGAGCAGAAGCTGCTGGTGTAGGTGCTTTCTGGCAAGTTTCACTTCTTGGTGTGGTTTTATGAGAATTGAGTGGTTTACTGTTTGTATGTTGTTTTGTAGATGGCGTCACCACTAATGCTGGTGTTTTTAAGTGCTCTCCCTGGGGTCCTTTGCTACTA[T/A]TCCTCATTCGTTGACCTGGAAGCTCAAGGAAGTGAGTTGCTATTGATTTCATGTAGTATGTTTAAAGTTTGTGTGAGCCAGAAGGTGGGACTAATTTTATTATGTTGATGCACTTCCAACTAAAATGTAATGTTGAGTAGAGGCAGGGCTTAATTTCGTGCATATTAACTCATCCCAATCTAATGCAAGAGGGTAGTGGTCAAAGATTAATATACAGCTGAAATGGAAGTCGTCAAAATGACCACTCATAAAGTGGAAGCAAATGGTCAGACGTTGTTGTTTTTATTGAAGACCTTTTTTTTTTTTTTTTTTTTTTTTGTGGACTTGCTGTAAGAACAAGCGTGAGCTGGCAAAATAAACATTGTAAATTTTGGTTTCATGTGGAATTTAAGAATCTCTAAGTTTTGTCAAACTTGACGACTGAGTTTTTAATATAATATTGTCTCCCATCTCAATCAGGTAACCAGTCATCCATCAGGTTCCTGGTGTTGGGGGACTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40635
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 |
---|---|---|---|---|---|
ENSDART00000004716 | Nonsense | 240 | 339 | 5 | 6 |
ENSDART00000135810 | None | None | 192 | None | 5 |
ENSDART00000142752 | None | None | 219 | None | 5 |
The following transcripts of ENSDARG00000019763 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 9438869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8121793 |
GRCz11 | 6 | 8357332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGCCAACTGACTGCCTGCTGAAGAATTTGAGGCCATTACTAAAGAAGTA[C/A]AAGGCCACGGCTTACCTTTGTGGCCATGATCACAACCTACAAGTACGTCT
Long Flanking Sequence:
AAAGCTCAAATTGAGTACAGCCAGAGGTCAAAGAGATGGTACGTGAGCCAAAGTACATAGGCCTCAATGTCTAATTGAGTTTCCTGGCTCTTAAGCCAATTTGCACTGAGACTTGATGTTCATTGCAGCTTTACTTTTTGACTTTGCCCTCTTCTCTTTCCAAATGGGCTGCTTTTAACAATCTTTCCATCTGCCAGGAACTTCCCCTACTACTATTATGAGATGAACTTCCGCATTCCTCGAACAGACAGTACTCTGACAATCATCATGCTGGACACTGTGTTGCTGTGTGGCAACTCTGACGACTTTCTTGACCAGCAGCCTCGAGCTCCACGAAGTGGTGTACTGGCCAACCGGCAGCTGCTGTGGCTTCAGGAACGCTTGGCGAAGTCCAAAGCTGATTATCTCCTGGTGGCCGGCCATTATCCAGTGTGGTCCATATCCGAGCACGGGCCAACTGACTGCCTGCTGAAGAATTTGAGGCCATTACTAAAGAAGTA[C/A]AAGGCCACGGCTTACCTTTGTGGCCATGATCACAACCTACAAGTACGTCTCTAAAGGAATCCTCTCTTTTGAAGCGATCTCCGTTAAATCATTTTACCAATTTTCAATTCTCAGCCAGTCTTTGGGTCTGTCTGGAATGTGCTAAATTGGATTAGACCATTAGCATCTTAAGTTTCAATTTGACTATTTAGAGCTTCTGTAGTTGCATGTACAGTAGTCAACGAAGAGGTTCAAAAGCTTTCATAGTAGTTCTAAACAAGGGTTGTCCGAACTCTGTCCTGAAGGGCTGGTGTCCTGCAGAGTTTAGTTCTAACCCCAATTAAACACCTGAATCATTTAATCAAGCTCTATGTATACTAGAAACTTCCAGCCATGTGCGTTGAGGCAAGTTTGAACTAAACCATGCATAACACCAGCCCTCCTGGACTGCGTTTGGACACCCGTTCTAAACTATTCGGCATTTATTCTTGTCACGATTTGGTCTGCTTCAAAAGTTGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16094
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004716 | Essential Splice Site | 254 | 339 | None | 6 |
ENSDART00000135810 | None | None | 192 | None | 5 |
ENSDART00000142752 | None | None | 219 | None | 5 |
The following transcripts of ENSDARG00000019763 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 9438913)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8121749 |
GRCz11 | 6 | 8357288 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGTACAAGGCCAYGGCTTACCTTTGTGGCCATGATCACAACCTACAAG[T/A]ACGTCTCTAAAGGAANCCKCTCTTTTGAAGCGATCTCCGTTAAATMATTT
Long Flanking Sequence:
GAGCCAAAGTACATAGGCCTCAATGTCTAATTGAGTTTCCTGGCTCTTAAGCCAATTTGCACTGAGACTTGATGTTCATTGCAGCTTTACTTTTTGACTTTGCCCTCTTCTCTTTCCAAATGGGCTGCTTTTAACAATCTTTCCATCTGCCAGGAACTTCCCCTACTACTATTATGAGATGAACTTCCGCATTCCTCGAACAGACAGTACTCTGACAATCATCATGCTGGACACTGTGTTGCTGTGTGGCAACTCTGACGACTTTCTTGACCAGCAGCCTCGAGCTCCACGAAGTGGTGTACTGGCCAACCGGCAGCTGCTGTGGCTTCAGGAACGCTTGGCGAAGTCCAAAGCTGATTATCTCCTGGTGGCCGGCCATTATCCAGTGTGGTCCATATCCGAGCACGGGCCAACTGACTGCCTGCTGAAGAATTTGAGGCCATTACTAAAGAAGTACAAGGCCACGGCTTACCTTTGTGGCCATGATCACAACCTACAAG[T/A]ACGTCTCTAAAGGAATCCTCTCTTTTGAAGCGATCTCCGTTAAATCATTTTACCAATTTTCAATTCTCAGCCAGTCTTTGGGTCTGTCTGGAATGTGCTAAATTGGATTAGACCATTAGCATCTTAAGTTTCAATTTGACTATTTAGAGCTTCTGTAGTTGCATGTACAGTAGTCAACGAAGAGGTTCAAAAGCTTTCATAGTAGTTCTAAACAAGGGTTGTCCGAACTCTGTCCTGAAGGGCTGGTGTCCTGCAGAGTTTAGTTCTAACCCCAATTAAACACCTGAATCATTTAATCAAGCTCTATGTATACTAGAAACTTCCAGCCATGTGCGTTGAGGCAAGTTTGAACTAAACCATGCATAACACCAGCCCTCCTGGACTGCGTTTGGACACCCGTTCTAAACTATTCGGCATTTATTCTTGTCACGATTTGGTCTGCTTCAAAAGTTGACTACTGTGCTGTACTAACAACTGCAGAAAAGTTCTTGGTTGATGTG
Associated Phenotype:
Not determined