ZMP
si:ch211-203k16.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate angiopoietin-like protein family [Source:UniProtKB/TrEMBL;Acc:Q5
Human Orthologue:
FGL2
Human Description:
fibrinogen-like 2 [Source:HGNC Symbol;Acc:3696]
Mouse Orthologue:
Fgl2
Mouse Description:
fibrinogen-like protein 2 Gene [Source:MGI Symbol;Acc:MGI:103266]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37135 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37136 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37137 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15152 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37135
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 |
---|---|---|---|---|---|
ENSDART00000100749 | Nonsense | 86 | 425 | 1 | 6 |
ENSDART00000138793 | None | None | 232 | None | 4 |
The following transcripts of ENSDARG00000069305 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 43025960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43097119 |
GRCz11 | 20 | 42994197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTACAGATGAGGTGTCATACTGGCTTCATGAGAACGAAGAGCGCAAA[C/T]AGCAGATCCTAGCACTCAAGGAGACCGTTTCTGAATTGCAGGAGGAGCTG
Long Flanking Sequence:
GTTTAACGGAAAAAAAAAAATTCAACACATTCCTAAACCTTCTCAAAAAGGCAAATCATTTTGACTTCTGTATATATTTATTTTTTAAATATATTTTTTGCCTACATTTGATGTGTTTTTCCCCTCCAGGTGACCTGTCCCGTATTCCTGCGTGTCCTGCTCTTCCCCAGGCCTGAGACTGGAGGTCCGAGAGCTGGTGCCCTGGCCTTCTCCCCCAGGGAAGAGGAGTCAGCCGAGCCGACCACATGGAGGACAGGCCTCAATCTGCACTCTTGCTGACTGTCCTGTTCCTGCTGACCCACGCCAGCGATGACCAGCACTCTCTGCACACGCATCAGGTCAGCACGGCTCAGTGTGGAGAATACAGCAATCAGGTGCTGGAGGACGGCATGTGCCGGCTGATGGCCACTCTGCCGCAGCTGGACGAGCAGCGCTGCCCTGACATGTTTCGCTGTACAGATGAGGTGTCATACTGGCTTCATGAGAACGAAGAGCGCAAA[C/T]AGCAGATCCTAGCACTCAAGGAGACCGTTTCTGAATTGCAGGAGGAGCTGCGCAACCATCGACATCGAGTCAAAGTCTTAGAGCTGCAGGTGAGAAGCACTCAGCACTTTTATACACTATTGACCTTATTCTGCAATGCAGGAGTGCGCTAGTTTTTGTGATTGTTGAGAAATTTTAGTCTCTAAAAAGTCGCTCGCCTAGTAGGCACTCCTTCTGATGTGTTAAACAGACTTGTAGTTCAGCCTCTGAAGACACAAGTTGCTGAAAGTTGAGTTTAAAAGCATCAAAGCGATTGTTCACACCTCTTAAGATTGACTCAGACATCTCCTTGCATAGGTCACGCGGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTCATTAAATGTGGTAAAGTCGAACAAAACAAGGTAATTTAGCAACTTAACTGAGGCCCCGTTTACACTAGTGCGTTTTAGTTTGAAAACGCATAAGTTTTGCTACGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37136
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100749 | Essential Splice Site | 194 | 425 | 3 | 6 |
ENSDART00000138793 | None | 1 | 232 | 1 | 4 |
The following transcripts of ENSDARG00000069305 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 43036048)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43107207 |
GRCz11 | 20 | 43004285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTTTTGGTTTTCTTTATGTTAATATATCTGTATGTGCTTTTGACTTC[A/G]GAGGTGCAGAATGTTAGGAACTGTCCCATCGACTGTGCCTCCATCTACTA
Long Flanking Sequence:
ATTTTAATTGAAATTAAACAACTGGCTTCATTTTCAAATATGATACAACAGGCTTTACGGGTACAGAGTTCAATGGTTCTCAAGGTCAGAAAATTAATAATAAATTAAAATCTGTAAATTTGTGTAACTTTTCACAGCAAAATAATAAAGTAAATGTCTTAAAACTTGCCACAATAATTGCAAAAACTGCCACAAAATCAGTCATTTTAGTTACAAAAATCTTAGTTTTTTTGTGGATCTCAGAAAGACGGCTTTATTGGCTGAAGAACTACATATGATCACTTTTAAAATAATTGAAAACAGTGTATACATAAAAGTCTAGTAGTACTTGTAGTAACAGTACAGGATTTTTTCCCTTTAAAGGGTTAATTGTTAATTACTAGCATTCACCAACAGAGGGTGACAACCCATAGCCTGGTTAATGCCAACAATATTAGAATGATTATCTACTGATTTTTGGTTTTCTTTATGTTAATATATCTGTATGTGCTTTTGACTTC[A/G]GAGGTGCAGAATGTTAGGAACTGTCCCATCGACTGTGCCTCCATCTACTATAATGGCGTTCGTCGCTCTGGCATCTACACCGTGGTGCCCTCACTAGGGGCTATGCCTGTGGAAGTCTACTGTGATATGGACACAGACGGTAAGAAACATACAGTACTGTACAACACCTGCAGTAATGGCTGACAGTAAACAAGAGCATAGTGCTTTGAGGCAGTTGATGTTTTTGTTGGTTGCGGTGATTGAGAGTTTTCTTGATAGTCTCAGCTGATCATCAAAATGTATGTTGTTTAGGATGGAAAGAATTTTCCACAACTATTATAAATAAAATACTGCTTATACACACAAAAAATGATAAAACGCTTAATTAAAAAAAAATTCAAGTTATTTATTAGCCTCTATATCTAATTACATTCATTCGTTTTCCTCCGGCTTAGTCACTTATTTATCAGGGGTCGCCACAGCAGAATGAACCGCCAACTATTCAGCAAATGTTTTATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37137
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100749 | Nonsense | 275 | 425 | 4 | 6 |
ENSDART00000138793 | Nonsense | 82 | 232 | 2 | 4 |
The following transcripts of ENSDARG00000069305 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 43038100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43109259 |
GRCz11 | 20 | 43006337 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGGAAGGAGTATAAAGAGGGATTTGGAGACCTGCACACCGAATACTG[G/A]CTGGGAAATGAGCACATCCACGATCTGACCAGTCAGGGAGATTACATGCT
Long Flanking Sequence:
CAAGGCTCAACAAGGAGTTTTCTATATTGAAATGTCTCATTGGGATGCATCATTGTTTTATTTTTAAACTGTTTATGGGGACATTTGGAGACTTTCAAAAGCATTGCAAAAGAATCTCCAGTAATGAAAATCTGAGTTTCTTCTCTTTTTATGTGCAACGAGTCGTCAGTTTTGTGCTGAAACGGCACCAATGGGGAACATGAGCAGCTTAAAATAGCTTGTGCTGATATCTTTTTGATGACCCGCTAAACATTATGGTATAATTGCAATGGTCATAAGATGAAAACCAAATGACTTGCAGTGTCTATTAAACTCGTATTAAAGAGATTTAATTGTTTTACATTTCCTGCATTATTTAAAAAATGGCTGATTATTCGCTTCATGTATGTCTCAGGTGGAGGCTGGACAGTGATCCAGCGAAGGCAAGACGGCTCTGTGAACTTTGACCGCAGCTGGAAGGAGTATAAAGAGGGATTTGGAGACCTGCACACCGAATACTG[G/A]CTGGGAAATGAGCACATCCACGATCTGACCAGTCAGGGAGATTACATGCTGCGCATCGACCTGGAGGACTGGAGCAACAAACACAAACACGCTCTCTATCAGAGTTTCAGGTGAGGTTTAGCACACACACACTGCTGTTCACAGTGTGATCTTGCAGGATTTGTGAGAATTCTGTCATCATTTACTCAAACTAATGTCTTTCATGTCAATAAGACATGGGTTCATCTGATTTCTATTCCTCCACTGAGAGTGAGTTCATCACAAAATTTTAAAAGTTCATCAAAAGACAATACAAATTGGTAACACTTTACTTGAAGGGGTGTTCATTAGACATTTTTAATCATGACAAGACACATGTTCAGGGCATAATTAACATAAGGGCTAGACAGGGCCTAGCATCTCTTTGTGTTATGCTATCGGATGCCGATAAAGTAAGGTATTCCTTTCGGCTCGCTGCTGTTCGAAAACAATGACACCGCTGAACTGGGAGTGGCTGTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15152
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 |
---|---|---|---|---|---|
ENSDART00000100749 | Essential Splice Site | 312 | 425 | 5 | 6 |
ENSDART00000138793 | Essential Splice Site | 119 | 232 | 3 | 4 |
The following transcripts of ENSDARG00000069305 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 43040988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43112147 |
GRCz11 | 20 | 43009225 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAGGGTGTCTTGRTTATGAGATTGGTGGTAATGRATGGTGTGTGTTTCA[G/T]TGTGGAGGATGAGAACACTCAGTACCGTCTGCATGTGTCGGGCTTCAGCG
Long Flanking Sequence:
TACGATTAAAATACAATTAATGGGAAATTTATTGAAAAATAGAAATAATTCTCGTTAAGAAGAATGTATTCTACAGTTGATTAACCATGTGGATGGATAATAACAGCCTTCTGAGCCAACCCGTAGACGCATAAGGCTTCTACTGGCCCATATCAATCAGTTACTACTGATAACGTCCATTCAGTTGAGTGAAACCATTTGAAACAGCTGCTAAGATCTAAGAATTTTTAGGTATTTTGTTTAGAAACAAGGCAAAGTAAGACGAGCATTATTTTACATTGAGATTATTTCATTTCTGTACCTGAAGACTGTTATAATCTACAGAAAACTGTCAAATAGAGCTATTCAGACTATTGAAACTGTGTACATATCGCAATATTTAATCACAGGCAAATAAAATTTCACAATATACATTTTTCCAATATCGTGCAGCCCTGATTATAAGTATTTTTAGGGTGTCTTGATTATGAGATTGGTGGTAATGAATGGTGTGTGTTTCA[G/T]TGTGGAGGATGAGAACACTCAGTACCGTCTGCATGTGTCGGGCTTCAGCGGGACGGTGGAGGATTCTTTCAGCTGGTATCATGACAAGCAGGGCTTCAGCACACCCGACACAGGCAACATCTGTGCCGAGATCTCCCACGCCGGCTGGTGGTACAACCAGTGCTTCTACACCAATCTCAATGGCATCTACTACAAGGTGGGATCAGACCTGCTGGCTCTTACTGTACACGCACAATAGCACTGCACCCTATCGTGATGAACTTAATCAAGGCTTTTAACCACAAGTTTCTCTTTAACCCTTGTGTGCTGTTATTTCCATCTTAAATGAGTCTTAATTTGGCCATAACTTTTTTTTGTGTTTCAGCCAGCAGAATAACTTTTGGTGACAAATCTTATTTTAATACATATTTTGAGAAAATGCTTTGAATAAAAAAATAAATAAAAAATCAGCAATACACTCTGGTCAAATTGACTACCCTTTCATTATGTTCGAGATGAAA
Associated Phenotype:
Not determined