Busch Lab

ZMP

si:ch211-203k16.3

Ensembl ID:
ENSDARG00000069305
ZFIN ID:
ZDB-GENE-041014-290
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.
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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