ZMP
si:dkey-19j7.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate AF4/FMR2 family [Source:UniProtKB/TrEMBL;Acc:B0S769]
Human Orthologue:
AFF3
Human Description:
AF4/FMR2 family, member 3 [Source:HGNC Symbol;Acc:6473]
Mouse Orthologue:
Aff3
Mouse Description:
AF4/FMR2 family, member 3 Gene [Source:MGI Symbol;Acc:MGI:106927]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13564 | Nonsense | Available for shipment | Available now |
sa9758 | Nonsense | Available for shipment | Available now |
sa21467 | Essential Splice Site | Available for shipment | Available now |
sa34615 | Essential Splice Site | Available for shipment | Available now |
sa21466 | Essential Splice Site | Available for shipment | Available now |
sa21465 | Essential Splice Site | Available for shipment | Available now |
sa21464 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13564
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108750 | Nonsense | 786 | 1176 | 5 | 15 |
ENSDART00000131634 | None | None | 181 | None | 2 |
ENSDART00000137922 | Nonsense | 803 | 1196 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 22529376)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 21685162 |
GRCz11 | 9 | 21496031 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CRGGAAAGGCAAAAGAAAAGTCATCAATGAAGCATCTGAACCACTCTGAC[C/T]AACCACCTGGAGATGGCAGAAGTAAAAGAAARGTGAGGGGGGNAAAGAMAT
Long Flanking Sequence:
GCCCTTCTCCTCCACTCTCTCCACCTACCCCTACTCCTGTCGTCAAGCCCACCCATCCATTATCTTCTTCATCCTCATCTTCCTTTTCATCCTCATCATCTTCCTCTGAATCAGACTCTGAGTCTAGTCCACCCAGGAACATTGCGAAAGTCCCTGCAGATTCAACATCAAACAAAAAAACTGTATCAAAGAGCAGGCATGAGAAACAAAATTCAGGCTCAAGTAGTCACCCCGAGAGGTCCTGCTTAAGTACCCCTGAAACAGAAAAACACAGTCGGGGGAGACACAAACTCTATACACTCGTTCCTTTTGGCCGGACTGAAAAGTCCCCCACCATCCCTCATCGAGGCCTGAAAAAACTAGTTGTGAGGATAGACCTCTGTCTTCTGGGTAGGGTCCCGAGTGCAGATGAGCTTACAGAGAGACAGTCTTCGTCTTCATCTGTGTCATCGGGAAAGGCAAAAGAAAAGTCATCAATGAAGCATCTGAACCACTCTGAC[C/T]AACCACCTGGAGATGGCAGAAGTAAAAGAAAGGTGAGGGGGGAAAGACATTTTTTTTTGCTTACAATTCAACAACTTTTACATTTGTGTTCTGTAAAAATGAGATGTTGTTGCACACCTGTATTCTTTGTGTGTGTTTGTCATAGGCTGAGAATGGAGACCTTCAAAGAGAGAATAAGAGAAATCACTCGTGTACAGATAAACAACCATCATCAGTCCATCATGAGACAGAGGAAACCTGTGTGGACAATCAACAAAACGGGTATGTTTGTTTGAGATAAAGACTCTTATCTTGCATTATCTTTGTTATAACTTGCACTGCAAATTGATTTTTTTTTGGTGTTTTATTAATCTAAATACAGAATATATTATATTGTAAATTGATAGTATAAGAGGAAGTCCACAAGCAATTAGCACCGTAAAAGTATTGTTCTACCAAATTGCTTGGGCACATTGAAGGGCATCATGGAAGGCCTCTGTGACAAAACAAAAACACAGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9758
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108750 | Nonsense | 815 | 1176 | 6 | 15 |
ENSDART00000131634 | None | None | 181 | None | 2 |
ENSDART00000137922 | Nonsense | 832 | 1196 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 22529176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 21684962 |
GRCz11 | 9 | 21495831 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAATGGAGACCTTCMAAGAGAGAATAAGAGAAATCACTCGTGTACAGAT[A/T]AACAACCATCATCAGTCCATCATGAGACAGAGGAAACCTGTGTGGACAAT
Long Flanking Sequence:
GAGAAACAAAATTCAGGCTCAAGTAGTCACCCCGAGAGGTCCTGCTTAAGTACCCCTGAAACAGAAAAACACAGTCGGGGGAGACACAAACTCTATACACTCGTTCCTTTTGGCCGGACTGAAAAGTCCCCCACCATCCCTCATCGAGGCCTGAAAAAACTAGTTGTGAGGATAGACCTCTGTCTTCTGGGTAGGGTCCCGAGTGCAGATGAGCTTACAGAGAGACAGTCTTCGTCTTCATCTGTGTCATCGGGAAAGGCAAAAGAAAAGTCATCAATGAAGCATCTGAACCACTCTGACCAACCACCTGGAGATGGCAGAAGTAAAAGAAAGGTGAGGGGGGAAAGACATTTTTTTTTGCTTACAATTCAACAACTTTTACATTTGTGTTCTGTAAAAATGAGATGTTGTTGCACACCTGTATTCTTTGTGTGTGTTTGTCATAGGCTGAGAATGGAGACCTTCAAAGAGAGAATAAGAGAAATCACTCGTGTACAGAT[A/T]AACAACCATCATCAGTCCATCATGAGACAGAGGAAACCTGTGTGGACAATCAACAAAACGGGTATGTTTGTTTGAGATAAAGACTCTTATCTTGCATTATCTTTGTTATAACTTGCACTGCAAATTGATTTTTTTTTGGTGTTTTATTAATCTAAATACAGAATATATTATATTGTAAATTGATAGTATAAGAGGAAGTCCACAAGCAATTAGCACCGTAAAAGTATTGTTCTACCAAATTGCTTGGGCACATTGAAGGGCATCATGGAAGGCCTCTGTGACAAAACAAAAACACAGAGGAGGTCAATTTGTTGCTGTTATTCTTGCCCACTGGGACATGTTAGTGTAATCTGATGTTTTCTGTATGGCTCATGCTCTTTGGGTGACATCTCTTCTTAAATGCCGTTTATGCAGATGTCAGGATGATTACTTTTACTCCAAGAGGCCAGTGTCCCCATTATCTCCTCCGTCTAACATACTGGAGCTCTCAAAGCACTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21467
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108750 | Essential Splice Site | 835 | 1176 | 7 | 15 |
ENSDART00000131634 | None | None | 181 | None | 2 |
ENSDART00000137922 | Essential Splice Site | 852 | 1196 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 22528763)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 21684549 |
GRCz11 | 9 | 21495418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATGGCTCATGCTCTTTGGGTGACATCTCTTCTTAAATGCCGTTTATGC[A/C]GATGTCAGGATGATTACTTTTACTCCAAGAGGCCAGTGTCCCCATTATCT
Long Flanking Sequence:
CACACCTGTATTCTTTGTGTGTGTTTGTCATAGGCTGAGAATGGAGACCTTCAAAGAGAGAATAAGAGAAATCACTCGTGTACAGATAAACAACCATCATCAGTCCATCATGAGACAGAGGAAACCTGTGTGGACAATCAACAAAACGGGTATGTTTGTTTGAGATAAAGACTCTTATCTTGCATTATCTTTGTTATAACTTGCACTGCAAATTGATTTTTTTTTGGTGTTTTATTAATCTAAATACAGAATATATTATATTGTAAATTGATAGTATAAGAGGAAGTCCACAAGCAATTAGCACCGTAAAAGTATTGTTCTACCAAATTGCTTGGGCACATTGAAGGGCATCATGGAAGGCCTCTGTGACAAAACAAAAACACAGAGGAGGTCAATTTGTTGCTGTTATTCTTGCCCACTGGGACATGTTAGTGTAATCTGATGTTTTCTGTATGGCTCATGCTCTTTGGGTGACATCTCTTCTTAAATGCCGTTTATGC[A/C]GATGTCAGGATGATTACTTTTACTCCAAGAGGCCAGTGTCCCCATTATCTCCTCCGTCTAACATACTGGAGCTCTCAAAGCACTCTGTGAAAGCTCAGCATGCAGAGAAGTACTACACACCTCCAGAAAAAGACAATGATTCAACAGCACAGAAAACCCAGGTCCTTAAAATACCACTCAAACACCATCTGTTAGCTTTCTTATTGTTCTTTTCTTCTACATTTATTCATCTCACTTTTCAGTCATAGGCTCAATTATAATTTCTTAGATTGTCCAAACGCTCTACATTACATTTTTCTACAGACTTTTTATTTCTATAAAGAATGTTTTAAGTTCCACAGAGAATGTTTTTATACTTTAGTTCTTTACAAGAACTGAAGCATTTTCTATACTGGAATTTAGAGCTATTAAAACAAGTCTGTCTCAATAGATCCAAAAGACGCAGCCCAAGGTAGAGGTGGAATGTATTGGGGTGTCAGGACATCTACAACCTCTCTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34615
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 |
---|---|---|---|---|---|
ENSDART00000108750 | Essential Splice Site | 933 | 1176 | 8 | 15 |
ENSDART00000131634 | None | None | 181 | None | 2 |
ENSDART00000137922 | Essential Splice Site | 950 | 1196 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 22528198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 21683984 |
GRCz11 | 9 | 21494853 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCCAAACCTTCCTCTTCACTACAGAGGAACAGTACCTATTAGTGATGT[G/A]TAAGTTAATGTCTTCTTCAGTGAACAACACTAGAGCATAGTTTGGCATTC
Long Flanking Sequence:
ACTGGAGCTCTCAAAGCACTCTGTGAAAGCTCAGCATGCAGAGAAGTACTACACACCTCCAGAAAAAGACAATGATTCAACAGCACAGAAAACCCAGGTCCTTAAAATACCACTCAAACACCATCTGTTAGCTTTCTTATTGTTCTTTTCTTCTACATTTATTCATCTCACTTTTCAGTCATAGGCTCAATTATAATTTCTTAGATTGTCCAAACGCTCTACATTACATTTTTCTACAGACTTTTTATTTCTATAAAGAATGTTTTAAGTTCCACAGAGAATGTTTTTATACTTTAGTTCTTTACAAGAACTGAAGCATTTTCTATACTGGAATTTAGAGCTATTAAAACAAGTCTGTCTCAATAGATCCAAAAGACGCAGCCCAAGGTAGAGGTGGAATGTATTGGGGTGTCAGGACATCTACAACCTCTCTCTGGATCGAGGGTTCCTCCCCCAAACCTTCCTCTTCACTACAGAGGAACAGTACCTATTAGTGATGT[G/A]TAAGTTAATGTCTTCTTCAGTGAACAACACTAGAGCATAGTTTGGCATTCAAACTCTTCACATGGTACTCACTAATATTTCCTTTTTTTCCCTCATGCTAGCTCTCATCATGCTGAGTATTATATGCATGAAGCCAAGAGATTGAAGCATCGAGCAGACGCTATGGTAGGACAACATTGTGAATATACTATTACACAAATTACTCTTATAACATATATCACCCCTTTGGTTCTGCTTTCACACCTCTGAATGTTATTCGAACCAATGTCCAGGCATGGGAGGCAGCATTCTAACAAGGATTGTTATCAGTTGCAAGTGTGCCTTTTGGGGATGGGGAGCAAGATTTACAGCACTTACTAACTGGCCACCATCAATCAAACCTAGACACAATGTACAATTGTAACCTCTTGGGTTCTACTTCCACAGCTTTAAACATGTTTTATCCTGCGTTTCTAGCATGGGAGCTAACAAGGATGCAATAGAACTCAATCTCTAGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21466
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108750 | Essential Splice Site | 1055 | 1176 | 12 | 15 |
ENSDART00000131634 | None | None | 181 | None | 2 |
ENSDART00000137922 | Essential Splice Site | 1075 | 1196 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 22525575)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 21681361 |
GRCz11 | 9 | 21492230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAGACCATGCCCTGAAATACTCTAAAGTCCTGCTAGACTACTTCAAG[G/T]TAGGCATTATTCAAGAGAAATGCCTACTAATGCTAAGTACAAACTGTTGC
Long Flanking Sequence:
GTTGAATAGGTGTCATGTCTATAATAGAAAACAGTCATAGCTCCTTGTGACATCAGCTTTAGTGCTGTGACACAATCAACATGCCACAAAAATTCATGTGTGTGTTATCAGTATGTCATATATTTTTTATTGTTAATATATTTTTATGCGTGATGATTGTCATTTGACATATGCTAAAACAGAAAGGTGCTATATTTGTCAGAATCTCTGTGTTGATTTGACATGTTCTGTGTGTTGGTTAGATACGCTATGAGACTAAAGAGCCACGCAGGGCCTGGAGCCAGTCAGGAAGACAAACAGCTAGCTGTACTATGGTAAATATATCACTACAACTGTCTATATTGTCATTTTGAGAACTTGCTAAATTTTGATTTAAAAAAAAAAAAACTTGTTTCCAAACCCACAGTTTCCGCTGTCTTGCTCTTCTTTATTGGCAAATGTTCAGACTTAAAAAAGACCATGCCCTGAAATACTCTAAAGTCCTGCTAGACTACTTCAAG[G/T]TAGGCATTATTCAAGAGAAATGCCTACTAATGCTAAGTACAAACTGTTGCATCTGTTCTGTTCCATGACTTACCCATACATGTTTTATTACCTTTTTTAAATCAGAGTTCTCCAAAAGGACCTCACAACCCCCCTACAAGGAACGATTCTGGAAAGTAAGATACAATTATAGCTCTTAATAATATACGATCAGTATGAAAGAGCTTTATGTTGTGTTTGGAGCTCAGTGTATCTCTATTTGTGTTTCCACAGAGGAACTATTCCTCCAGCCTCTATTTGCTCTGTCAGTATAATGGGATCTCACACAGGCAAATCACCAAGCACAGTCATAAGCATTCCACATCGCATCCACCAGATGGCAGCAAATCACCTCAACATCACCAACAGTGTCCTGTACAGTTACGAGTACTGGGAGGTGGCTGATACGCTGGCCAAGGAGAACAAAGGTGAGCTTTTATGCAGTTGTGTTTGGGAAAGCAGTGTGCTTTTCTAATCCAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21465
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 |
---|---|---|---|---|---|
ENSDART00000108750 | Essential Splice Site | 1055 | 1176 | 12 | 15 |
ENSDART00000131634 | None | None | 181 | None | 2 |
ENSDART00000137922 | Essential Splice Site | 1075 | 1196 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 22525574)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 21681360 |
GRCz11 | 9 | 21492229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGACCATGCCCTGAAATACTCTAAAGTCCTGCTAGACTACTTCAAGG[T/C]AGGCATTATTCAAGAGAAATGCCTACTAATGCTAAGTACAAACTGTTGCA
Long Flanking Sequence:
TTGAATAGGTGTCATGTCTATAATAGAAAACAGTCATAGCTCCTTGTGACATCAGCTTTAGTGCTGTGACACAATCAACATGCCACAAAAATTCATGTGTGTGTTATCAGTATGTCATATATTTTTTATTGTTAATATATTTTTATGCGTGATGATTGTCATTTGACATATGCTAAAACAGAAAGGTGCTATATTTGTCAGAATCTCTGTGTTGATTTGACATGTTCTGTGTGTTGGTTAGATACGCTATGAGACTAAAGAGCCACGCAGGGCCTGGAGCCAGTCAGGAAGACAAACAGCTAGCTGTACTATGGTAAATATATCACTACAACTGTCTATATTGTCATTTTGAGAACTTGCTAAATTTTGATTTAAAAAAAAAAAAACTTGTTTCCAAACCCACAGTTTCCGCTGTCTTGCTCTTCTTTATTGGCAAATGTTCAGACTTAAAAAAGACCATGCCCTGAAATACTCTAAAGTCCTGCTAGACTACTTCAAGG[T/C]AGGCATTATTCAAGAGAAATGCCTACTAATGCTAAGTACAAACTGTTGCATCTGTTCTGTTCCATGACTTACCCATACATGTTTTATTACCTTTTTTAAATCAGAGTTCTCCAAAAGGACCTCACAACCCCCCTACAAGGAACGATTCTGGAAAGTAAGATACAATTATAGCTCTTAATAATATACGATCAGTATGAAAGAGCTTTATGTTGTGTTTGGAGCTCAGTGTATCTCTATTTGTGTTTCCACAGAGGAACTATTCCTCCAGCCTCTATTTGCTCTGTCAGTATAATGGGATCTCACACAGGCAAATCACCAAGCACAGTCATAAGCATTCCACATCGCATCCACCAGATGGCAGCAAATCACCTCAACATCACCAACAGTGTCCTGTACAGTTACGAGTACTGGGAGGTGGCTGATACGCTGGCCAAGGAGAACAAAGGTGAGCTTTTATGCAGTTGTGTTTGGGAAAGCAGTGTGCTTTTCTAATCCAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21464
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108750 | Nonsense | 1059 | 1176 | 13 | 15 |
ENSDART00000131634 | None | None | 181 | None | 2 |
ENSDART00000137922 | Nonsense | 1079 | 1196 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 22525460)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 21681246 |
GRCz11 | 9 | 21492115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACTTACCCATACATGTTTTATTACCTTTTTTAAATCAGAGTTCTCCA[A/T]AAGGACCTCACAACCCCCCTACAAGGAACGATTCTGGAAAGTAAGATACA
Long Flanking Sequence:
TCATATATTTTTTATTGTTAATATATTTTTATGCGTGATGATTGTCATTTGACATATGCTAAAACAGAAAGGTGCTATATTTGTCAGAATCTCTGTGTTGATTTGACATGTTCTGTGTGTTGGTTAGATACGCTATGAGACTAAAGAGCCACGCAGGGCCTGGAGCCAGTCAGGAAGACAAACAGCTAGCTGTACTATGGTAAATATATCACTACAACTGTCTATATTGTCATTTTGAGAACTTGCTAAATTTTGATTTAAAAAAAAAAAAACTTGTTTCCAAACCCACAGTTTCCGCTGTCTTGCTCTTCTTTATTGGCAAATGTTCAGACTTAAAAAAGACCATGCCCTGAAATACTCTAAAGTCCTGCTAGACTACTTCAAGGTAGGCATTATTCAAGAGAAATGCCTACTAATGCTAAGTACAAACTGTTGCATCTGTTCTGTTCCATGACTTACCCATACATGTTTTATTACCTTTTTTAAATCAGAGTTCTCCA[A/T]AAGGACCTCACAACCCCCCTACAAGGAACGATTCTGGAAAGTAAGATACAATTATAGCTCTTAATAATATACGATCAGTATGAAAGAGCTTTATGTTGTGTTTGGAGCTCAGTGTATCTCTATTTGTGTTTCCACAGAGGAACTATTCCTCCAGCCTCTATTTGCTCTGTCAGTATAATGGGATCTCACACAGGCAAATCACCAAGCACAGTCATAAGCATTCCACATCGCATCCACCAGATGGCAGCAAATCACCTCAACATCACCAACAGTGTCCTGTACAGTTACGAGTACTGGGAGGTGGCTGATACGCTGGCCAAGGAGAACAAAGGTGAGCTTTTATGCAGTTGTGTTTGGGAAAGCAGTGTGCTTTTCTAATCCAATAATGTAATTTAAATTATTCTCACCAGAATTTTTCAACTATCTGAACACGCTGACTGGACCGTTGACTCTGCACAGCAGCATGGCTCACATCGTTCAGTACACCAGGCAAGGGCTCC
Associated Phenotype:
Not determined