Busch Lab

ZMP

zgc:158446

Ensembl ID:
ENSDARG00000090730
ZFIN ID:
ZDB-GENE-030131-2319
Description:
complement factor B [Source:RefSeq peptide;Acc:NP_001077327]
Human Orthologues:
CFB, XXbac-BPG116M5.17
Human Descriptions:
cDNA FLJ55673, highly similar to Complement factor B [Source:UniProtKB/TrEMBL;Acc:B4E1Z4]
complement factor B [Source:HGNC Symbol;Acc:1037]
Mouse Orthologue:
Cfb
Mouse Description:
complement factor B Gene [Source:MGI Symbol;Acc:MGI:105975]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa12079 Essential Splice Site Available for shipment Available now
sa9654 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa12079
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100784 Essential Splice Site 84 751 3 18
ENSDART00000125911 Essential Splice Site 73 440 2 10
Genomic Location (Zv9):
Chromosome 21 (position 26845229)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 27414140
GRCz11 21 27450835
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAAACACAACMATTTTKTMTGCTGCTCTCAAAWCAATTGCTTTTAYCWC[A/T]GAAATCACTTGTCCGGATCCTCGTGCATTTTTAAACGGAGATGTGCATCC
Long Flanking Sequence:
ATTGGATGTTTTTTAGACATTGTGCAAAGAAAAATCAAGTGAATTTTCTTAATAATGTATTTGTCCAGTCACAACATAAAATAATGCAAAATTGGCATTCAAATTTTATTAAAAGTTTCTGCAAAGGTTTTTTATTAAAAATGATTCTTTTAAAATGTTAAAGGTGCAAATTTGCAACACCTTTATTATTTTTCTTATTTGTCCTTCTATAGGTGCACCACCCTCTATTTCATGCCCCGTTAAAGATATCAGAATTAAAGGAGGCAGTTTTTCTATCTCAAAAGATGGGAGCTCCATAATATTCAACTGTCCAGAAAACTATTACCCAACCATTAGAACCCGTCGCTGTACCAAAGGAAGATGGAGCGAGCTGCCCAAAGGAAAACGCCTGGAATGCAAAAGTGAGCAATGTACCATCACCCAAACAAAATCTTAATCTTATTCAGAATTATAAACACAACCATTTTTTATGCTGCTCTCAAAACAATTGCTTTTATCTC[A/T]GAAATCACTTGTCCGGATCCTCGTGCATTTTTAAACGGAGATGTGCATCCATATTCACCAAGGTATTATGTGAACGATACAACCAGATACTTTTGTCAGTCTGGCTATGATTTCCGCGGCTCTGAGTCTCGTGTTTGCCAGGCCAATGGGAAATGGAGTGGAAGCACACCGATCTGTGGAAGAAACTGTAAGTTGGAAATTTCCCTAAAGTGCAACTACAAAAGTTCTGTCCAAAAACCTTTGTTCTTCTTTTTAAACAGCGGATTACTGTCCTGACCCCGGAGTTCCTGCTGGTACTACAAGAACAGGCAACATGTTTCACATTGGTGATAAAGTCACATACCGCTGTGACAATAAATTGAGCTTGATCGGTTCCAAAGAGCGAACATGTCAGGATAATGGACAGTGGTCAGGAACAGAGCCACAATGTTACGGTAAACACCCCTCTCTATGTCTTAAAGGCACAATACGTACGTTTTTTTTTCTATTAAAATGTACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9654
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100784 Essential Splice Site 204 751 4 18
ENSDART00000125911 Essential Splice Site 193 440 3 10
Genomic Location (Zv9):
Chromosome 21 (position 26845665)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 27414576
GRCz11 21 27451271
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATGYCAGGAYAATGGACAGTGGTCAGGAACAGAGCCACAATGTTACGG[T/C]AAACACCCCTCTCTATGTCTTAAAGGCACAATACGNNNNNNTACGNNTTTTTTTTCT
Long Flanking Sequence:
TCTTATTCAGAATTATAAACACAACCATTTTTTATGCTGCTCTCAAAACAATTGCTTTTATCTCAGAAATCACTTGTCCGGATCCTCGTGCATTTTTAAACGGAGATGTGCATCCATATTCACCAAGGTATTATGTGAACGATACAACCAGATACTTTTGTCAGTCTGGCTATGATTTCCGCGGCTCTGAGTCTCGTGTTTGCCAGGCCAATGGGAAATGGAGTGGAAGCACACCGATCTGTGGAAGAAACTGTAAGTTGGAAATTTCCCTAAAGTGCAACTACAAAAGTTCTGTCCAAAAACCTTTGTTCTTCTTTTTAAACAGCGGATTACTGTCCTGACCCCGGAGTTCCTGCTGGTACTACAAGAACAGGCAACATGTTTCACATTGGTGATAAAGTCACATACCGCTGTGACAATAAATTGAGCTTGATCGGTTCCAAAGAGCGAACATGTCAGGATAATGGACAGTGGTCAGGAACAGAGCCACAATGTTACGG[T/C]AAACACCCCTCTCTATGTCTTAAAGGCACAATACGTACGTTTTTTTTTCTATTAAAATGTACAAATGGATAGAAGAATGTTCAAAATGCTCAATTAGCATTTTTAATTAGTTATCACGTCCTCTATGGTCCTATGTTGCAATGCTATTTTCACCACAAAGCCTTGATTTCTGGCTTCCCTGTTTTATAGAAAACAGGGAAAACACCAAAGACGCTTTAATATGTTGTGCATTTTATTTGGGGTATGAGAAGCACCGCTTCTTCTCAACATTGATCCTGCATCTCGCTGGTCTGTAATCAGCAATTGCTTCACCAGTATTGTTTCGCTTTGATGGTCTCACACTGCTTTATATTACCATGATAATGCGATTTAAATACTTTAACTCATGCATGAAGATGATTACTGTAGGGGTCTTGTAGATGTAATGAAGACTACAACTAAACCCCTCAAACTTGTTATACCTAATGAATTACGTTTTTTTCAACTTAAAACCGTTTGAT
Associated Phenotype:
Not determined