Busch Lab

ZMP

Q1RLR4_DANRE

Ensembl ID:
ENSDARG00000057004
Description:
LOC563523 protein [Source:UniProtKB/TrEMBL;Acc:Q1RLR4]
Human Orthologue:
FGL1
Human Description:
fibrinogen-like 1 [Source:HGNC Symbol;Acc:3695]
Mouse Orthologue:
Fgl1
Mouse Description:
fibrinogen-like protein 1 Gene [Source:MGI Symbol;Acc:MGI:102795]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa27608 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9778 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa27608
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
ENSDART00000079566 Essential Splice Site 222 345 7 8
Genomic Location (Zv9):
Chromosome 10 (position 25119374)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 24718726
GRCz11 10 24688178
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAGTTCATATGGATGAAGTCTCAATTACATTCCTCTCTGCTCACTAT[A/G]GGATAAATACAGGCTGTACTATGGGATGTACAGTGGTCAAGCAGGAGATG
Long Flanking Sequence:
TTGTATACTGTGACATGGATGATGGGGGGGCCTGGACTGTGATTCAAAAAAGAATCAATGGGAAAGTTGATTTTGACAGGTAAGTACATTGTCTTGTCCTTAGACCGACAAAAATATCAGCATTATTAAATCTGCATTTCTTTTCACAGAAAGTGGGAAGATTATAAAAATGGATTTGGAAATTTTCAGTCAAGTAAAGATGAATTCTGGCTTGGGAACGATCATATTCATGTCCTTCTCAGTGATGGTAAGTTTTGTATATTTATTCGCAAGTTTATTACACTTCTTTTCTGTTCAACAATATTTTATTAACACCCTTTAGGTGACAGTGTGATGAAAATTGATCTGACAGACTGGAAAGGAGGGAAATCATATGCCATGTATGACAACTTCAAAGTGTCAGATGAAAAAGTAATGTTCTTTTAGGTTCTTACCATTATTTATGCATAAAAGAAGTTCATATGGATGAAGTCTCAATTACATTCCTCTCTGCTCACTAT[A/G]GGATAAATACAGGCTGTACTATGGGATGTACAGTGGTCAAGCAGGAGATGCCTTGTCCGGAGGAGCCAATATGGTGGAGCAGTGGTCAGCCTCCCATAATGGCATGCAATTCAGCACCAGGGACCAAGATCATGATCGGTACCTGCAGGGAAGCTGTGCTGCAGAGAACAAGGGGGGCTGGTGGTATAACAGGTGATGCCAAGGGATTTCTGAGTTTTAGGTCTTAAAAGAATACTCCATGTTTTTTGACAATAGACAAATTGGACAATTTTCATAGAGTTAAACAGTTTAGTTTTACCCTTTTGTATCCACTCAGCCAATTTCTGGCTCTGATGGAAGCACTTTTAGCTTAGCATAGATCATTGAACTGGAATAGAGCATTAGCAGCTCGCTCATAAATGACCAAAGAGTTTAAGTCCTTTTCCTATTTAAAGTTAGACTCTTCTGTAGTAAAATCATGTACTAAAATGTTGCTATTTTCAAGGCCTTTATGGCTAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9778
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079566 Nonsense 314 345 8 8
Genomic Location (Zv9):
Chromosome 10 (position 25118468)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 24717820
GRCz11 10 24687272
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTGGAGAGTACAAGGCCAAATATGACAATGGTATTGTTTGGAGCACCT[G/A]GAAAGGACTGTGGTACTCYCTCAGACACACWGTCATGAAGGTCCGGCCCA
Long Flanking Sequence:
AAGAGTTTAAGTCCTTTTCCTATTTAAAGTTAGACTCTTCTGTAGTAAAATCATGTACTAAAATGTTGCTATTTTCAAGGCCTTTATGGCTAGGAACTTCTGACGTAATATTCAAGGAATTTTGCTGCCATACCACATAGGGCATCTATTCCAATTCAATATATATTTCGATAATTGAGTTTTGCAATTATATGAATGCTATTATTTGATTAATTAGAACAGTTTGTCCTTCCAAAATTAGATTAGTAAATTATGCTAAGCTAAAAGTGCTCCCACTCGACCCAATGATGAGCTGAATGGATTCAGAAATGGTAATTGTTGGTTTTATGATTAAATGGTTTATCTCTAGGGTACTTCTTCCCCAATTTTCCAAAAATATTTGTTATTTTATGATACCTATTTTTTTATTTACAGGTGTCATGCTGCCAATCTTAATGGGAGATTTTACAGAGGTGGAGAGTACAAGGCCAAATATGACAATGGTATTGTTTGGAGCACCT[G/A]GAAAGGACTGTGGTACTCCCTCAGACACACAGTCATGAAGGTCCGGCCCAGCTCCCACATGGACAGCGTGGGTAGTGGAGGAGGGCCCACTGAATAGCGAGGTTGCTAAGCATCTTGTTATACACATTTGTGAATTATACTGTGTTAACTATAAGATTTACTGTGGTTTATTAACTTTTCAACCACATGACTGTCGAGCATAGAAAGAATCTTGGAGGGATGAAGGAAGAAAGTAATCTTGGTAGATTTGATGAATCCACCTGTTATTTTTAAAATAATCATAAATAATATAACTTTGCATGCAGCCATATAATAGCACTTGTAGCATACAATATGCATATTACATTAAAACAGCATTTTTACATGTGAAAAGTCTTGACTGATATTGTGTATCACTGTTTCGTAGTATAAAATAATCATTCAGGAAAAAAAAACTTTGTATATATATGTATATTTTGGTTTGTTATGGAAAAAAACCTGAGAATTCACATTTTCCAGTG
Associated Phenotype:
Not determined