Busch Lab

ZMP

ncf4

Ensembl ID:
ENSDARG00000040812
ZFIN ID:
ZDB-GENE-041124-1
Description:
neutrophil cytosol factor 4 [Source:RefSeq peptide;Acc:NP_991274]
Human Orthologue:
NCF4
Human Description:
neutrophil cytosolic factor 4, 40kDa [Source:HGNC Symbol;Acc:7662]
Mouse Orthologue:
Ncf4
Mouse Description:
neutrophil cytosolic factor 4 Gene [Source:MGI Symbol;Acc:MGI:109186]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa39377 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32408 Nonsense Available for shipment Available now
sa43872 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39377
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032757 Essential Splice Site 39 156 2 11
ENSDART00000059820 Essential Splice Site 39 355 2 10
ENSDART00000133409 None None 259 None 8
Genomic Location (Zv9):
Chromosome 22 (position 31779224)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 29258302
GRCz11 22 29207497
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCAACTATTGCTGATATCGAGGAGAAGAAAGGTTTCATTGTTTACTTT[G/A]TGAGTTTCCCTAGACCTGAACCCCCGGCACTTCAGCTTTCCTCCAGTCTT
Long Flanking Sequence:
GTTTCCCAGTAATGGGTTGCAGTTGGAAGAGCGTCCGCTATGTAAAACATATGCTGGATAAGCTTGCAGTTTATTCCGCTGTGATGACCCCTGATGAATAAAGGGACTAAGCTGAAGGAAAATTAATGAATGGGTCCAAATTGACTCGGAATATGAAAATAGTACATATTTTAAAGGTTAACAAAATTGCCATACAGATATTTACAATAACAACAATTATATAAAAAGTAGAAATTATAATAATTCTTCAACAAAAATGTAAACTATGTTACACACACAAACACACACATTTAATTTTAGTCCTGTTTGTAAGTATAACTCAAATCTCTTACTCAAAATTGTATTGAATAAAAGCATACTTGGAAAACATTTATTCTGTGGTAATAAAATTGTGTAATATTTGTTCATGCTACAGTGATTTTGACCAGCTTCCAGACAACATCCCAGTCACCGCAACTATTGCTGATATCGAGGAGAAGAAAGGTTTCATTGTTTACTTT[G/A]TGAGTTTCCCTAGACCTGAACCCCCGGCACTTCAGCTTTCCTCCAGTCTTTTCTTTAATAATCTTTTGGCCTTATAGTCTGACAGTTACCTGTGGCTTATGTTTAACCAAAAGCATACACCTAAAACAAGATGTTCAAAGATAATCATAAAATACTTAAGTTAAGAACACACATTCTTGCATCATTTTTGTTATTTATTTATATTTGTGCCAGATTAATATCTTAAGCTGTTTTGTCAGTGAGTTTTTAACCTTCACGGCAAAATGTAAGTAAAAATTGTAAAAATCGAGAGTTTTTGTCTTGTTTCTTAAAACACAGGAAAAAAAATGTTTTGTTTTCAGAATGAAAATGTATAATTAAACGTGTTTAACCTAAAAAAAGCCTGAAAAATAAGTGTAATAATCTCATTTCAAACTAAAAACAATATTATTTTACTTAGGCCCTGTTTAAACTGCCAGATAAATGTGACCCAATTTAGATTTTTTGCTCATATGTGACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32408
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032757 Nonsense 54 156 3 11
ENSDART00000059820 Nonsense 54 355 3 10
ENSDART00000133409 None None 259 None 8
Genomic Location (Zv9):
Chromosome 22 (position 31781531)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 29260609
GRCz11 22 29209804
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGCAGAGTTTCGTGATTGAGGTGAAGACCAAAGGCAACAGTAAATACT[T/A]AATCTACAGAAGGTATCGAGAGTTCTTTGCTCTGCACCAGAGTTTGGAGC
Long Flanking Sequence:
ACACACTTACTATAGGTGGAGTGGAGAGATAGTGATAGAGCCAATTAGGTGGATCGGGATGATTGGGAGGCCATGATGGTAAGGGCAAATGGAGGGAATTTGGCCGAGACACTGGGGTTACACCTTAACTCTCTAAGCAGCGCCATAGAATTTATAATGACCACAGAAAGTCAGGACTCCCATCCTGGTACTGACCAGGCTCAGCCCTGCATGCTTCAGTAACCGGTCTTAAGCTGCTTGGTGATATGTTTTGATGAAAAAAATTACTCGATTTTGACAACTTATTTCTGAAAACAAAACAATATTTTTTACTTTTGAAATGCTACTTGATTAAATTTTTACAAGATATCAGGACTAGAAACATGACAAAAACTCTTAAGTACATTTTTTTGCAGTTTTCTCTCTCTACTACAAACCAAAAAAATTGACTTGGTTATTGTTTATCACCTTCTTGCAGAGTTTCGTGATTGAGGTGAAGACCAAAGGCAACAGTAAATACT[T/A]AATCTACAGAAGGTATCGAGAGTTCTTTGCTCTGCACCAGAGTTTGGAGCTCAAGTACACAGCTGAAGCCCAGTCGGGATACTACAACTGCCAGCTACCAACCCTGCCAGGTCAGCTAATGCACAAACTTAAATAAATCACAGTGTTGTAGAAAAATCTAGATTCAGAAGCACAAGAAACATACAAACAGCAGCTAAATATGGCTGTCACAATTACCATAATGCATAATCCCATTCAGAGGAAGAGCCATAGACCAAATCTGAATTTAACTATTTATAAACTCAGGTACGGAAAATGAAAGATTCATTAAACATAAAAGTGTGCATAAAACGCACATTGCTGAGACTTTTGTTAATTTGACTATTTTCAATTTCATTTATTTCCTTTTACAACATCGATGTTCTAATGTAATTCAAATATAGTCTGTTAAATAGACTTTAGTGCTCATTTAAAATGCTGGTGTAAAATTAATTTTCAGATTTTAAAGCCTTGGTGGGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43872
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
ENSDART00000032757 None None 156 11 11
ENSDART00000059820 Nonsense 331 355 10 10
ENSDART00000133409 Nonsense 237 259 8 8
Genomic Location (Zv9):
Chromosome 22 (position 31822603)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 29301681
GRCz11 22 29250876
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTCGTTCTCATGGTGCAAGAGAGCAAACGCACTGAGTCAAAGGTCAAA[C/T]GACCCGTCAATCAGTTTCCCTGGGAGCTGCTGGTCACGCATGCCAAAGAT
Long Flanking Sequence:
GCCTCAAGGTTGGAAAAGTTGCGCATTTAGAGATGCGATGCTCTTCTGCAAAGAAAATGAATGATGTTGCAAGAAAAAAAAAATTGAAATTGTAAAGTTAAAATTGGAAGATCAACATTTACTGAGATGTAACATCAGAATTACAAGAAAAAAAGTCCAAAATGTTGGAACATTAGAAGGTAGTGCCTCTGAATTACAAGAAAAATTAAAACATGTAGCTAAATTTAAAAAAAGTCAATTGTGTTAAATACACATCTGTTGTTTGAGTGGTGAAAAATTTAAACGACTGGTGACAAATGGCAACACACATGTTATATTTGCACTTGTTATGACCTCCAAACTGTGCAAATTGTTTTCCTCTTTCCCTCAGGGACGTCTTTCATGTGGACGATATTGCTTTGAACTACCGAGATGCCGAGGGTGACCTGATACGGATATTAGACGATGAAGACGTCGTTCTCATGGTGCAAGAGAGCAAACGCACTGAGTCAAAGGTCAAA[C/T]GACCCGTCAATCAGTTTCCCTGGGAGCTGCTGGTCACGCATGCCAAAGATCTGACCGTCTACAACACCGAGTATTAACATAGACATGCTTTTATGTGTCTCTCTGTATGGTCCTTGTCATTCCAAAGTCACTAGACATTTGTTTATTTTTTGTGGTTTTCAAATTGAAAACGTGTTTGGTTATTACAACCCCAAATCAGGAAAAGTTGGGACAGTAAGGAAAATGCAAATAAAAAAGAAAGTAGTAATTTCTAAATTTACTTTGATTCGTATTTCATTGCAGACAATAAAGTAAACCATTTTTAATGAGTTCCTTATGATTTTTATTTTATTTTTTAAAATAAACACGTACTCCAGTTTTGTTTTTGAAAGACATTTCAAAAAAGTTGTAACAGTAAAGCATTTGCCACTTTGTACTATTTTTCATTCCTTTTCTCAACACTTAATGAAGTTTAGGGACCGAGGACACCAAGTAATAAAGTGTTTAAGGTGTAATTTTGT
Associated Phenotype:
Not determined