ZMP
hspg2
Ensembl ID:
ZFIN ID:
Description:
Heparan sulfate proteoglycan 2 [Source:UniProtKB/TrEMBL;Acc:B2RZI0]
Human Orthologue:
HSPG2
Human Description:
heparan sulfate proteoglycan 2 [Source:HGNC Symbol;Acc:5273]
Mouse Orthologue:
Hspg2
Mouse Description:
perlecan (heparan sulfate proteoglycan 2) Gene [Source:MGI Symbol;Acc:MGI:96257]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24350 | Essential Splice Site | Available for shipment | Available now |
sa24349 | Essential Splice Site | Available for shipment | Available now |
sa29941 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39410 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15637 | Essential Splice Site | Available for shipment | Available now |
sa13580 | Essential Splice Site | Available for shipment | Available now |
sa417 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24350
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 |
---|---|---|---|---|---|
ENSDART00000111029 | Essential Splice Site | 866 | 3422 | 20 | 81 |
ENSDART00000112124 | Essential Splice Site | 866 | 3397 | 20 | 77 |
Genomic Location (Zv9):
Chromosome 23 (position 26870634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26703456 |
GRCz11 | 23 | 26629997 |
KASP Assay ID:
2261-7852.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATGGGAGTGACTAAACAGTGTGCCAGTTCAACCTGGAGCAGAGATCAG[G/A]TAACAGAAAAACGTCCAAATCACTTACATTTTCAGTTATGTCAATTTAAT
Long Flanking Sequence:
AAAAGTACTTTTAGTTCACCTTACTTTGTTATAATGACCTTGTTTGGTGAAGATGCTTAATCTATTTCTTCTCATTAAAGTAAAATACTATTGTCCTGCTTAAGTTGATGAAAAGAAAGTCATTAAAAAATTATATTATTATTATAATTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTAATTAAGTAAAACCAGTATTACATCATTAGCGCACTATATGTTTACTAAGTGTTTTTATTATAGTATTAAATGACCATGTTGTTTTTAGCAGCTTGTAAAAGTATTGTTAAAGCCCTGCTTGATTTTTTCTGTTCCAGTCCAATGTAGCTGGTGCGCTGTGTGACGAGTGTAAGACTGGTGCTTTTCATCTGACGGCTGATAATCCTGAAGGCTGCTTGCAGTGTTTCTGTATGGGAGTGACTAAACAGTGTGCCAGTTCAACCTGGAGCAGAGATCAG[G/A]TAACAGAAAAACGTCCAAATCACTTACATTTTCAGTTATGTCAATTTAATTTAAGGAATTGTTATGACTTTGCTTTTAACTCTTTAAAGTTACAAAAACATGAACTCACAGCATAAATGGTCTCATACATTTACTGTTAAAATGAATCTGTAAAATTTACGAAAAATAAGCAGCATTTGTGGTTGCCATAAAATAACGTAAAAATGCTGTTACCGTTAAAAATACGGTAGACATCATTTTTTGTTATTTATACTGTATGCATGTAACCATAAAATACATACGCCATTGTTTTGAAGTACGAACATCTACACGTACGTTTTGTTACACAGACAAAAATACAATTAATGATATGTTAATGACAAGTTTCACAAACTAATTTTAAGAGGAGCGTGTGATATGATTGACTGCAGCTAGTCACCCATCTATAATCATTAGTTATCCAATTAGATTAATTCAAACTCACTATAAATAGCCTAGCTAGAACTAATCCCTTACCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24349
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 |
---|---|---|---|---|---|
ENSDART00000111029 | Essential Splice Site | 1140 | 3422 | 26 | 81 |
ENSDART00000112124 | Essential Splice Site | 1140 | 3397 | 26 | 77 |
Genomic Location (Zv9):
Chromosome 23 (position 26862309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26695131 |
GRCz11 | 23 | 26621672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCCACAGGCTTGTCGACCCTGTCCATGTCTGGGACAAACCAGTAACCA[G/A]TGAGTTATCCTTATTCTTAATCAAAAGTATTATGAAGAGTTTACCTTTTG
Long Flanking Sequence:
CCACATAAACCAATTAGCCATTTAATAATGATTGATGGACTTGCTGAGCATTGTGAAAATCATTCATTATAATAAGTCCACTGTTGCATGCCTGATTGACTAGTTGTCTACCATGAACAAAATGATAATAATAAAATCAATTCAAGTCAACCCTAATCTATTAATCTCTTATTGGATAAGAAGTTGACATGAAATAGTAAATTGATGCCTTAATAACAAATCAACCTTTTTTAATCAAGTAATCCTTTTTTTTTGTATCTAGTGAACTAGTCAAGAATCTAAAAAAAAAATTCATAATCTTGTCTAATGTCAAGTAATTAGTAAGTCGACCCATGTCTAGTCTGGAGTTCTTCATCATCTTTTCTTTTGTTTTAGAATTGCCTGCACAACACAATCGGACGCCGTTGCGAAAATTGTATCTCTGGATACTATGGAAATCCAAAGACTGGCGACCCACAGGCTTGTCGACCCTGTCCATGTCTGGGACAAACCAGTAACCA[G/A]TGAGTTATCCTTATTCTTAATCAAAAGTATTATGAAGAGTTTACCTTTTGGACATAACAAATAATTCATCTGATCTAATACTCTTTGTCTGTCAAAGGCCTTCATCTTGTTACTTGGGCTCTGATGGACAGCCTGTATGTGAATGTCCTGCTGGTTATACTGGAAGGCGCTGTGAAAGGTATGTTTCTATTGTCTTATTAGAGGGTAAATCTCTCATTTAGTTTGCTTGTAATGCTGGGCTCTTCAAACTGGTGATGGAGGTGATCAGGATCTCTTTATTTACTGCCAGAAAGCATGTTGCTTTGCAGCATCTCTTCAGCCATTTGTGATTGAATGGCGTTTTTCTGGTGGTATGGGAGAAGCGAGTCTTGAATCAGTGCCACCCATATCAAAGTGTCAATGTCTGTCTGAAGTGCCTTTTTGGAGGAGTTTGTAAGTGGAAGCTGTAGCGCTTGAAGTATTCATGTACGTTATGTCTGAAATCTGTACCGATTTCATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29941
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 |
---|---|---|---|---|---|
ENSDART00000111029 | Essential Splice Site | 1322 | 3422 | 31 | 81 |
ENSDART00000112124 | Essential Splice Site | 1322 | 3397 | 31 | 77 |
Genomic Location (Zv9):
Chromosome 23 (position 26855228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26688050 |
GRCz11 | 23 | 26614591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGGAGCCTCATTATTGGCAGTTACCCAAGGCCTATCAAGGAGACAAG[G/A]TTGAGATTGACAATTTTTTGCATTTTATTGTTCCTACACTTTGCAAAACA
Long Flanking Sequence:
GAGTCTGTCGTTGCAAGGTAAAAAAAAAATCATGTTGTGTACATCTCAATTATAGAAACCATTTTAAAGCAAACTTTTTTTGTACTTAGATGAACGTTGAGGGTCCAACATGTTCCTCCTGCAAGCAAGGAACCTTCCACCTTAGTCCAGCTAACAAAGATGGCTGTCTGTCCTGCTTTTGCATGGGCGTCACTCAACAGTGCACCAGCTCCCGTCACTACAGGGATGTGGTAAGGCCTGATCAACTACACCAGGGTTTTTCATCAGGCGTATTTGCATGTGTTCATTTCCTGTCCCTTTTCCTTCAGGTTTCCACCATGTTTTCCCCTGGAAACTACCAAGGTTTTGCTCTTGTAAACCGCCAGCGCACAAACCGCATTGACAATGGCTTTTCTGTAGAGCTGTCCACTGAGGGGACACAACTCTCCTACACCAACTTCAACTATCTCGGACAGGAGCCTCATTATTGGCAGTTACCCAAGGCCTATCAAGGAGACAAG[G/A]TTGAGATTGACAATTTTTTGCATTTTATTGTTCCTACACTTTGCAAAACATACTTTCATACTTAGAATTTTTGTATAAATTCAAGTCTAAATATCTAAAAATTAAAAAAAATTACAAGCATTTTCTAGATGGGTAATATATAATGTTTTTTTCCTTCAGAAATTATAAATCAAAATGATAAAAATAATCTTGTTTTTGGTTTGAAATAAGATTATTTCACAACCCATTGCCATCTTATTTTTATTTATTAATTCATTTTCCTTCGGCTTAGTCCCTTTGTTCATCAGGAGTCGCCACAGCAGAATGAACCACCAACTATTCCAGCATATGATTTACATAGCAGATGCTCTTCCAGCCTCAACCCAGTACTCAGAAACAACTGTACACTCTCGCAAGCACACGTTCACTCATACACTAAGGCCACTTTACTCATAGCTTTACCTTTGTTCACGTGGGCTTTCTCTGGGTGGTCCGGTTTACCCCCACAGTCCACAGGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39410
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111029 | Essential Splice Site | 2149 | 3422 | 54 | 81 |
ENSDART00000112124 | Essential Splice Site | 2140 | 3397 | 50 | 77 |
Genomic Location (Zv9):
Chromosome 23 (position 26814178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26647000 |
GRCz11 | 23 | 26573541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAACTTGTACGGAATGACTCATAGCATCGTGTCACTCATTGTGAGAGG[T/C]AGAGCAACATTAAATGCGACATTTTTTGAAAAACTGGTTTTGTGAATTGT
Long Flanking Sequence:
TTTAGAAGGGCTCGAGTGTCCACTTACGTGGAAAGCACATTTTAGCTCTTTAGTGCAAGCCTCGCGTTTTAACCGGCTGCTGCACCTCGCATTTTTAATATATAATATATAATATATAAAAAAATCATAATATATAAAAAAATCTGCTTTTTGTTAATGTGACATGTTTCTGTCCGATATTACAAGATCCATGCATACTGCCACTATAAATAAAAGTTGTGTTTTGAAGGATTTGACATGTGGCCCTTTACTTGGTTTGCAAAACTTGATGCGGCCCTCGGGTCTGAAAGGTTTGCCCACCACTGTGTTAGAACATGTCAAAATCTCCATATGTGATATGTCCTTATGAACTTCTCTTCTTTAGATAATGTAAAGGTGGGTCCTGACAGTTCAATCATGACTGTTACAAATGCCCAGGCGAAAAACCAAGGCACCTACCGCTGTGTGGCCAGCAACTTGTACGGAATGACTCATAGCATCGTGTCACTCATTGTGAGAGG[T/C]AGAGCAACATTAAATGCGACATTTTTTGAAAAACTGGTTTTGTGAATTGTATTATTGCCTTCACACTTAGCACATACTATTTCTGCTTGAGATTTTCCTTACATTTATTATCATTGTTCAGGCATAATGCTCATTTCTCTCTCTTTTTTTTTCTTATTTCATTGGTAGAATCTCCTAAGGCTGTGGTGACCCCTGCAGGACCAGTGCGAGTCAGGGTCGGTGATCCCATTAATCTTGAATGCCAGGCCGCTGGAGAGCCAAGACCCTCAGTCAGATGGCACAGACTGGACAACAATCGCAAGACAATGCTGAGCAGCACCGTGCCTGTTGACTCCAGTGCTATCATACAGGTTATGAATCATTTGTTGTATTGATGATGTTGATTTCCTGATTGTTTGGCCTTTATGTTCATCAGAAAGGTTTTATACTTTGTTTACAGTGAAGAGAAAAATTAGAGAGCAGTTCAAAACACCTTTTTTGTTTGTTTTTTTATTATGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15637
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 |
---|---|---|---|---|---|
ENSDART00000111029 | Essential Splice Site | 3228 | 3422 | 75 | 81 |
ENSDART00000112124 | Essential Splice Site | 3203 | 3397 | 71 | 77 |
ENSDART00000111029 | Essential Splice Site | 3228 | 3422 | 75 | 81 |
ENSDART00000112124 | Essential Splice Site | 3203 | 3397 | 71 | 77 |
Genomic Location (Zv9):
Chromosome 23 (position 26794634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26627456 |
GRCz11 | 23 | 26553997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAGCTTCAGCGAGGCCATGTGGAGTTTGGAGGGTAGTGGGGGAAATGG[T/C]ACAGTATGAATTACAGTCTGCCTGACTCGCTCGTCACTAACMAGAGGAGA
Long Flanking Sequence:
TTAAAAGGTCTTAAAAAGTCTTAAATGTGTTACTTTTAGTTAACAATAATGTCCGCTCTATACTTCTGTTTTACATTTAAATAATCTTAAATTACATCATTTCAGAAGTATGGAGACAAACACACAGCTACCTAAACCCAATATTCCTACAAAAATGAATTTTAACTGCCTTATTATCCCTAATACTAATATATTGGTCCCAGTTTGCCTCATTTATCATTTTCCAGAATTCACTCTCTCTCTCTAAGGAAATAAAAGCATTTTTCTGTAGTTCCATTGCATTGTACCGAACCGCAGCTGTAAGTGATTCATCATAAAGCACCATACTGTAGGGAACTAACTATCCGTTCTCTATAACCCGCCATGGCTTCATCGGTAGCGTTTTAGCGGGTGAAAGAGGACACGTGTGACTGAATCTCACCGCTGTATCCCACACACACAGGGCAGGAGTCCAGCTTCAGCGAGGCCATGTGGAGTTTGGAGGGTAGTGGGGGAAATGG[T/C]ACAGTATGAATTACAGTCTGCCTGACTCGCTCGTCACTAACAAGAGGAGAACATCTTCCTCCTCCTCAGGGCCCCGCAGCCCGCCTAACACCCACCGATACAAACTACTGCTGTGCCAAAATGCTGAAGAAGAAAACAGGAAGACGTGCATTTCAGGGGTCTGTTTACTGAGCTTTTATTAGCAAAAGCAAACTAATATTTATTTATCGTTGTTGATTAAATATAATTTGTAAGAGATCTTGATTATGAATGTATCTTAATGAAAGTTACTCAACATCTTTATAGCAAGATTTTGCTTCTGGGAAAAGAACGGACATTATTTTCAGACATTATTGACAAATAGTTTTGTTTGTTTGTTTTAAGCTTTAAATTTCAACGAATTGTGCTTAATTTTATTTTTTTGACAATTATATTTATAACTTTATTAAATAAACCTAAATTTACAATATATTTTTGTTATCTACACTTTAAAAAATGTAACTAGATTTTTTTGACAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13580
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 |
---|---|---|---|---|---|
ENSDART00000111029 | Essential Splice Site | 3228 | 3422 | 75 | 81 |
ENSDART00000112124 | Essential Splice Site | 3203 | 3397 | 71 | 77 |
ENSDART00000111029 | Essential Splice Site | 3228 | 3422 | 75 | 81 |
ENSDART00000112124 | Essential Splice Site | 3203 | 3397 | 71 | 77 |
Genomic Location (Zv9):
Chromosome 23 (position 26794634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26627456 |
GRCz11 | 23 | 26553997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAGCTTCAGCGAGGCCATGTGGAGTTTGGAGGGTAGTGGGGGAAATGG[T/C]ACAGTATGAATTACAGTCTGCCTGACTCGCTCGTCACTAACMAGAGGAGA
Long Flanking Sequence:
TTAAAAGGTCTTAAAAAGTCTTAAATGTGTTACTTTTAGTTAACAATAATGTCCGCTCTATACTTCTGTTTTACATTTAAATAATCTTAAATTACATCATTTCAGAAGTATGGAGACAAACACACAGCTACCTAAACCCAATATTCCTACAAAAATGAATTTTAACTGCCTTATTATCCCTAATACTAATATATTGGTCCCAGTTTGCCTCATTTATCATTTTCCAGAATTCACTCTCTCTCTCTAAGGAAATAAAAGCATTTTTCTGTAGTTCCATTGCATTGTACCGAACCGCAGCTGTAAGTGATTCATCATAAAGCACCATACTGTAGGGAACTAACTATCCGTTCTCTATAACCCGCCATGGCTTCATCGGTAGCGTTTTAGCGGGTGAAAGAGGACACGTGTGACTGAATCTCACCGCTGTATCCCACACACACAGGGCAGGAGTCCAGCTTCAGCGAGGCCATGTGGAGTTTGGAGGGTAGTGGGGGAAATGG[T/C]ACAGTATGAATTACAGTCTGCCTGACTCGCTCGTCACTAACAAGAGGAGAACATCTTCCTCCTCCTCAGGGCCCCGCAGCCCGCCTAACACCCACCGATACAAACTACTGCTGTGCCAAAATGCTGAAGAAGAAAACAGGAAGACGTGCATTTCAGGGGTCTGTTTACTGAGCTTTTATTAGCAAAAGCAAACTAATATTTATTTATCGTTGTTGATTAAATATAATTTGTAAGAGATCTTGATTATGAATGTATCTTAATGAAAGTTACTCAACATCTTTATAGCAAGATTTTGCTTCTGGGAAAAGAACGGACATTATTTTCAGACATTATTGACAAATAGTTTTGTTTGTTTGTTTTAAGCTTTAAATTTCAACGAATTGTGCTTAATTTTATTTTTTTGACAATTATATTTATAACTTTATTAAATAAACCTAAATTTACAATATATTTTTGTTATCTACACTTTAAAAAATGTAACTAGATTTTTTTGACAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa417
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111029 | Nonsense | 3276 | 3422 | 77 | 81 |
ENSDART00000112124 | Nonsense | 3251 | 3397 | 73 | 77 |
Genomic Location (Zv9):
Chromosome 23 (position 26789073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26621895 |
GRCz11 | 23 | 26548436 |
KASP Assay ID:
554-0277.1 (used for ordering genotyping assays)
KASP Sequence:
ACCATTGAGTTAGAGATCAACACTGCCTCAAAGGACGGCCTCATCCTGTG[G/A]CAGGGAGTGGTATGTTTGTACAAATGTGCGCCCTTGTCTTCCCATGACAC
Long Flanking Sequence:
GGTATGTGTAATATCATTATGCCTGCTTCAGCTATATCAGGCTACGAAATGGCAGCTTTTTCAAAATCTGTCAGTCTTAGTACAGGATGTAATTAAAAAAGAGCCAAACTATAAATAGGAACATTATCAAGACTCCTGTTTTGAACATTTTTTTTGGTTTGTTTTTGTTTTTTGAGTGAGACGCTAATGGTCTAATCTGATTCAATTATTAATGTTATGATAAGCTAATCTAAAAATGCTCCCACCAGATCCATAGATGGACTAATTGGATTCAAAAATGGTCAAACTCCAGGGGACTTGTAAAATGAGCCTATTTCCAATAAAGTAGAGTGTTCCTTTAATTGAACTTAAATGGATGCTGTCAAGTTTAACAATAAAATATGTGTTTGGATATTTTCTGGTTGCATTAATGACTGTTTGACTTGTTGCAGTGCTCCTGACTCTCCAGAGACCATTGAGTTAGAGATCAACACTGCCTCAAAGGACGGCCTCATCCTGTG[G/A]CAGGGAGTGGTATGTTTGTACAAATGTGCGCCCTTGTCTTCCCATGACACACACATTTAGAGTCCAAGATATAAATTTTTAGGCACAAATATGTCTGTACAGTATACTGTAAAATGTCCTGTTCAGTGCATATCTTTTAAATCTGCTTATAAATGTTTATTTTGGACACTACATATACTCTCGCATTATGATCATGGGTAACTGATATGGAACTGACATGTTTTACATTTCATATTCAGCCTCAATTTACTAAACTGAGTCAAATGAGTTTGCTTGGAGCTGGATTGTTGATCGATATGCATTTGTTCCTCACACTCACCCTTTTTTTTTGGCTGCACTGCATGTTTGCCTGCCTAACTCACCTTCATCCTCCTCAGGAGTCTGCAGGTGCTCTAAACCTCCATAAGAAGCATGCTAATATAAAGGTATTCACTCTTCACAAGCAGAAAACGATGGAAAACACAAAATTATGTCTGCATTAGCATGATCATATCATTATC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |