ZMP
aggf1
Ensembl ID:
ZFIN ID:
Description:
angiogenic factor with G patch and FHA domains 1 [Source:RefSeq peptide;Acc:NP_001073451]
Human Orthologue:
AGGF1
Human Description:
angiogenic factor with G patch and FHA domains 1 [Source:HGNC Symbol;Acc:24684]
Mouse Orthologue:
Aggf1
Mouse Description:
angiogenic factor with G patch and FHA domains 1 Gene [Source:MGI Symbol;Acc:MGI:1913799]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23854 | Nonsense | Available for shipment | Available now |
sa43584 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23854
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 |
---|---|---|---|---|---|
ENSDART00000084380 | Nonsense | 55 | 763 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 7708805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 8031067 |
GRCz11 | 21 | 7768735 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCGCTGCGAGAGGAGCTGAAGACCTGTAAAGATGAGCTCCAGAAGT[T/A]ACAGAAACAGCTCAGCCAAAGCGAACGGCTCCAGAAGACCACAGAAAGCT
Long Flanking Sequence:
TATATATATATATACATACATACATATATACATACATACATACATATATATACATGCACACACACACACACACACACACACATGTATGTAGTTTTTCAGAGAACAATAAATAAAATAAGGATTAAATTGATTTAATTGTTTGAATTTAATGCTTGTTTTGGCACATGCTAAGTTCTGTCTTGAGGCTTCCTAGTTGACAGCCACTTTATTAACAAGTAAAATTTTTTACAGATAAAGACTGACCGTTAAACAGTACTAAATAAACTCAAAACATTTAAATTGTATGCAAAGGTAATACTTCAACTCTTTCTATTGGGGCCGTCTGTACATTGTTGTTTGTAATCTACACTTTAGGTTGAACGTTCTCTCAATGGCTGCAGAAGGAAAAGCCGACCTTGAGGCCGGTGATGATGGTTTAGAGTCAGAGATTGTGTCTTTGCGAACACAAGCAGAAGCGCTGCGAGAGGAGCTGAAGACCTGTAAAGATGAGCTCCAGAAGT[T/A]ACAGAAACAGCTCAGCCAAAGCGAACGGCTCCAGAAGACCACAGAAAGCTACAATGAAGATCTCCGACAGCAGGTGAGCAGGGCCCTCATGGAGAACAGGCACATTTGATGAGTTAAAGAACATAAAAAAAACACGTCTAATTGCTTTTTGGCACTTTGTGGGACTGGTGTGGTTGTAAAAATAGACAAAATAGACACTCTGTGCAGTGTTTTTTTAACAATCTTCTTTTTAATGAGGTATAAGCAAATTTTGACAGTGTAATACAACACAATTTTGTTAGAAAACAATTTAAAAAACAACAACATTGAAGCAAAACTAAAAGATAAAAATAAAGGGAAAAAGGCACAAGTTATTTTAATTAGAAACAGGTTATTCTAGATAATTTAACATGAACAAAAATATTCATCATTACCAGATACCAGATCATTATTTAACAATGGTTTATTTAAATAAATGTCTGGAAATGGGAACACATGTAGATAGAGTAAGTTTCATCTTT
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa29519
Status:
Less stringent filtering
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:
n/a
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084380 | Nonsense | 241 | 763 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 7704931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 8027193 |
GRCz11 | 21 | 7764861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGTCCAGTCAGCTGTACTATGATGCGAACACAGGCATGTACTATTA[C/A]TACGACCCAGAAAGCGGAAAATACCAATTCCACTCTAGGATAGAGGTGCC
Long Flanking Sequence:
ATCTCTATCTCTATTGGAGGTGTCAGTGTTAGTATAGTTAATACTATAGTGTTTATTTTTTTAACCATACATTGCTTTAGTATATTTTCATGTGGGTGTCTGATAACTGAAAATAGATCTGATAATACTAAAATGACAATAATATTGCTTATTGCAGTCCATTTTGTTTCTAAAAATAGGTATTGTGACAGGCCTAAATTTGTTTCTTGCTTTCCTTGTCAGGAGGCCTCAGGAGAAGCCGGCTCTATAGCAGACATGTTAAGAGCGACTGCAGAGGAAGCCATGAACCAGACCAACTTCGTGTTTGACGAAAGCTCCGGCATGTACTATGACCACAGCACTGGATTTTACTACGACTCTGTAAGTCTCGCTCTTCTCTCGGGACCGCTGTTATTTACGTAATGACATGTGTAATCTTAATCGCCCGTGTTAATGTGTTTTTTCCTCTTCCTCCAGTCCAGTCAGCTGTACTATGATGCGAACACAGGCATGTACTATTA[C/A]TACGACCCAGAAAGCGGAAAATACCAATTCCACTCTAGGATAGAGGTGCCTGCAGCCCTACACCCCGAAGTGGAGCAGACGCCACAGAGGAAGACCAAAGATCGGAAAAACAGGAAGTCGGTGAAGAACACAGAAAGAGCTTCCTGTCCCGACGGAGGGGTGAGATGCACACGGACACATTGTCTTTGTAATCGCAGAGATTTGCGTTTGGTGCGTGACGTTAGCTATGTTTCCATCAATCTATTTTTATATACATTTTAGAAAATCTCATGAAAAAAACTAAACAAAAAAAATGATGAATAATATCATCAAGATGTTCAAACATTTTTTTACAAATGTGCAAAAACAATAAATGTATGAGGCAGATACATTTGACGATACTTTCCATCCACAATTTTTTATTTTACTTTAAAACTAGTGCTGTCAATCGATTTAAAAAATTACTAATTAATTACGCTTTTTTTAGCAATTAATCGCGATTAATCACATTTAAAATACTG
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa3148
Status:
Allele not cryopreserved
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:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084380 | Essential Splice Site | 592 | 763 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 7690592)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 8012854 |
GRCz11 | 21 | 7750522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGACAGATCATAGCACACTTGAGCCGCCATAAGAAAGACGAAAGCTCTGG[T/C]ATGCACAACATGACTGCATTAACTTAACCTGATTATGCTTAATAAGCCAA
Long Flanking Sequence:
AAGTGACGTTTAAAGGCTTAACTAGGTTAATTGGGTAAGTCATTGTATACTGATGGTTTGTTCTATAGACAAATGAAAAGGGGCTAATTGCTTAAGGGGCTAATAACATTGACCTTAAAACAGTTTAAAAAAAATTAAAAACTGCTTTTATTCTAGCCGAAATAAAGCAAATAAGACTTTCTCCAGAAGAAACAATATTATAGAAAATACTGTGAAAATTTCCTCCTTGCTCTTTTAAACATAATTTGGGAAATATTTGAAAAAGAAATTCACATAAGCTAGAAATGTTGACTTCAACTGTATATGAAACACATTTCTGCATTCTGTCTGCAGCCCAAAGTTCGCTGTGACCCTTGTCCTCTGACCCACGGGGATGAATTAAAGATGGGAGAAACGGTTTTGTCCTTCCACATCCACGCAGGCACGGCCACTTGTGACGGCTGTGAACCAGGACAGATCATAGCACACTTGAGCCGCCATAAGAAAGACGAAAGCTCTGG[T/C]ATGCACAACATGACTGCATTAACTTAACCTGATTATGCTTAATAAGCCAACACTGCATATGGTCATGTGAATACATTTACTTGTTTTCCATTATTAGAGTTGGGGCATAAACAAGTCTCATTGTATTAGGGGCTGCCTTGAAAGTCAATTCCTTACATACATACAGTTAAAGTCAGAATTATTAGCCCTGCTGAATTGTTGGACCCCTTGTATATATTTCCCCCCAATCTCTGTTTAACTAAGAAGATTTCAACACATTTTTAAACATAATAGTTTTAATAACTCATTTTTAATAAATGTTTTTTTTGCCATGATGACAGTATCATGACAGTTGATACTAGATATTTTTCAAGATTCTAGTATTCAGCTAGAATAGTTAAGTAGAATAATTTTGGTAATTAAGCAAATCATTGTATCAGGGATGTGATTATTCCGTATTAATATGAATTATGAAGTTTTTTTTGAGCGTGGGTGTCTCTACCGTCATCGAAGCAGACGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43584
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 |
---|---|---|---|---|---|
ENSDART00000084380 | Nonsense | 726 | 763 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 7682143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 8004405 |
GRCz11 | 21 | 7742073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGATCCGCCATGTCTGTTGAGGATGCTTCGCTCACCAAATCCAAAACA[C/T]AGAGAAACTGGGAGCGCGCAAGAGAACGGTTCTCTGAAGCCTGCCACACC
Long Flanking Sequence:
TTTTTGTTTGTCTGTATATGTTGTGTTTGTTTGTTGTCTTTGTGTGTGTGTGTTTGTTTGTTTTTTGTCTCTGTGTGTTGTGTCTGTGTGTGTTTGTTTTTTCTTCGTTTTGTGTGTTGTGTCTGTTTGTGTGTGTTGTTGTGTATGTTTGTATATTGTGTCGTGTATGTGTTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTCTGTCTGTCTGTCTGTCTGTCTATTTGTTTGTTTGTTTGTTTGTCTGTGTGTGTTGTATCTGTTTGTGTGTGTGCGCGCGATTGTTGTGTCTGTTGTGTGTGCGCGCCCCCGTGTGTGCTCGTCTGTTTATCTGTCTGTTTGTGTTTGTGCTTGTATGTCGGTGTATGTGTGTGTGTTGTAGATTCAGCTGCACATGCGCAAGGCTCAGTCTGGTCTGGGATCTTCTGGATCCGCCATGTCTGTTGAGGATGCTTCGCTCACCAAATCCAAAACA[C/T]AGAGAAACTGGGAGCGCGCAAGAGAACGGTTCTCTGAAGCCTGCCACACCGACTCCTCCCATCCTGAAAACAGCCAATCACCTAAAGCCTGGGTCAAGAGCCAGGAGACGGAGTGACGCTTCAGATGGACTTTATTTACACTGTTTATCTGAGTCATTTCAGCAGAAGACCTTATTTCCATGAGGTTTGTAAATAGACGCAAGTTCATTTTAATGCCACTCGGAGTGATTTTTGTTTACAGTGAAATTCAATACTGATATAACGAACAAATAAACAAAAGATACAGACAAGCATTCCAGTGTATGCATTTATATTAATGGCACATCTACAAATTCACTCAAAGAAAGACAAAGCAACTGTTTAATAATTATTTTAAGTGTAGAAAATTAGTCCACACCTCAGCTTTAATTATAATGCCACTGAGAAATGATATTTTTATGAACAATTTTTCTTCCAGAATGATAAAAGTGCATTTATTATTAACTTCTCAGTCATGTGTT
Associated Phenotype:
Not determined