Busch Lab

ZMP

egfl6

Ensembl ID:
ENSDARG00000045958
ZFIN ID:
ZDB-GENE-040718-157
Description:
epidermal growth factor-like protein 6 [Source:RefSeq peptide;Acc:NP_001002457]
Human Orthologue:
EGFL6
Human Description:
EGF-like-domain, multiple 6 [Source:HGNC Symbol;Acc:3235]
Mouse Orthologue:
Egfl6
Mouse Description:
EGF-like-domain, multiple 6 Gene [Source:MGI Symbol;Acc:MGI:1858599]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa21615 Essential Splice Site Available for shipment Available now
sa6120 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21615
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
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000067544 Essential Splice Site 277 506 8 12
Genomic Location (Zv9):
Chromosome 9 (position 56297209)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 54710599
GRCz11 9 54658396
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACAGATCCTGGGACAGCAGTAAAGGAAACACAGATGTGCTTGTGAACG[G/A]TGAGAAAGACGCAGTTTAACGGCTGAATGAGCTGATGGAAATACATCTGA
Long Flanking Sequence:
GCACGTCGAACACACACAAGTGCAGTCATCACGCTGAATGCATCAACACTCTTGGGTCCTACAAGTGTAAATGCAAGCAGGGCTTCCGTGGCAGCGGATTCGATTGTTCAGGTGAGAAATGACAGCATTAATGAAACAGCGAAAATTAAACTACACTTTTAAAATATCCATAAATGAGCAGTTTTCCATATTTTGTGATTTATGTTTTAATTTTTAATTTTTTCCTCCTTTATTTATGCTTTTGAATTGCATCATGGGACCCAACACTGGGTTACAACAACCCAGCATTTCGTGTGTGTTTAATTAAATAAATACAGCATCGCTGAGCATTTTTTAAACATGCTGAAACAAACAGTACAATTTCCAAACTTGTGTGGATGTTTTAGGAGAAATGTTGTAGATATAATTTGTGAACCGAATGCTTTGTGTTTGTGTAGTCAAGCCATTTTATCACAGATCCTGGGACAGCAGTAAAGGAAACACAGATGTGCTTGTGAACG[G/A]TGAGAAAGACGCAGTTTAACGGCTGAATGAGCTGATGGAAATACATCTGATATTGTAAAACATCAGCATTAGATGAACATCAGCTCCTGCGAGAGGGGTCTGGCTGCAGACCTAGTGCAGTGCAATCTGAGCTGCATCCAATGCTTTTTAATGCGCTCACCTAACCCCGCCCCTAACCCTACCCGTCACAGTGACGTCACTCACTCCATTGAGTGCATTGTGTCTGACATTGCATCGCTAAGTGATGCAATCTCAGCTTGCACCATAAAGGCTGCATCCAGATACTATTGGCTCCTGCGCTCTGCTGGATGCTTTGCAGATACATTTAGAAACACTCTAATAAGCTTTGCAGATGTTAATGCATTATCTGGACCATGCCGCTGGGAAAACAAATGAAAGATGAAAGTTGTCATGCAGCTTGGTTATAATGATTGTGAATGGCTTGTCATGCAGTGCACATGCAGTCATGGCAGATGTAAAGCATGCCTGATTAATGCAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6120
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
ENSDART00000067544 Nonsense 310 506 9 12
Genomic Location (Zv9):
Chromosome 9 (position 56299947)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 54713337
GRCz11 9 54661134
KASP Assay ID:
554-3819.1 (used for ordering genotyping assays)
KASP Sequence:
AGAACAGCATCCCAGAGCCTGYGCTGACTGAATCTCCTCGACAGCATCTG[C/T]AACCCTTCGATTATGATGGAGAGGTTTACATCGGCGCTCCACAGGAAACA
Long Flanking Sequence:
TGAGGCGACAGCACTACCTAGAGCTCATTGCGTCGCCTAATATTACATTTAAATATGTTAGTATTATTATTATATTAGTAGTAGTAGTAGTAATAGTAGTAGTAAGCAGTTAGTTTATTGTGTGCAATAAATAGCTATTATTAAATTTAAATATGTTATTATTATACATTTGGTTTATTCTGTATATAAAATTACTATCTACAGTTATATTTAACTATATATTATTTTACACTCCATTTTAATTTTAGTTATATTTTTACTATTTATATTTTTAAATATCATTAAATATTTTTTTACTATATAAATGCTATTCAAATAAGCATTTTTGTCTTTTTGTATATTGAATGCATGACTCAGCATTAACAAACAAGATTTCCACTGACAGATTTCTGTTTGATTCTGCAGCGATTCCCGATTTTCCGTCCAAAACCCGGATTTTGGGTAAATTTGAGAACAGCATCCCAGAGCCTGTGCTGACTGAATCTCCTCGACAGCATCTG[C/T]AACCCTTCGATTATGATGGAGAGGTTTACATCGGCGCTCCACAGGAAACACCAGTGTTTCCTGAGGAAGAAGAAGTGGAAGAGGAAGAGGAAGAGGACACAGAGAACCAGCTGGAGGATGAAGAGCTGACCAGCAGAGGAGACGTGTTTTGTGAGTGACTTCAAAAATACTCTTTACATTCATAAACAGCTGAAGTGAGATTTCCTATGTGCTGTTTAAGAGAGCAGGGATTACAGTAATTCCTATTATATTTTTCCCCTGAAGAAAGTCTTATTTCATTAAGTTTGGCTATTTTTTAATTATTTAAATATTAATTTAGTGGTTATCATTTGCCACCTTAAGATAAAATTATAATTCAAATATTTCCAACATTATGCTTCAGAGAGCAAGAAATCTTTCACAGTAATTCCTATAATATTTATTTCATCTGGAGAAAGTATTATGTTCTCAGTTTGTTTGTTTTTTTTTGTTTTTTTAATAATGTTGTGGTCAATATTTTT
Associated Phenotype:
Not determined