Busch Lab

ZMP

cfhl2

Ensembl ID:
ENSDARG00000056778
ZFIN ID:
ZDB-GENE-041114-123
Description:
complement factor H like 2 [Source:RefSeq peptide;Acc:NP_001007419]
Human Orthologues:
CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5
Human Descriptions:
complement factor H [Source:HGNC Symbol;Acc:4883]
complement factor H-related 1 [Source:HGNC Symbol;Acc:4888]
complement factor H-related 2 [Source:HGNC Symbol;Acc:4890]
complement factor H-related 3 [Source:HGNC Symbol;Acc:16980]
complement factor H-related 4 [Source:HGNC Symbol;Acc:16979]
complement factor H-related 5 [Source:HGNC Symbol;Acc:24668]
Mouse Orthologues:
AL837518.1, Cfh, Cfhr1, Cfhr2, Gm4788
Mouse Descriptions:
Putative uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:Q8BMW5]
complement component factor h Gene [Source:MGI Symbol;Acc:MGI:88385]
complement factor H-related 1 Gene [Source:MGI Symbol;Acc:MGI:2138169]
complement factor H-related 2 Gene [Source:MGI Symbol;Acc:MGI:3611575]
predicted gene 4788 Gene [Source:MGI Symbol;Acc:MGI:3646434]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa24167 Nonsense Available for shipment Available now
sa24168 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24167
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079324 Nonsense 180 606 5 12
Genomic Location (Zv9):
Chromosome 22 (position 24152715)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 23720029
GRCz11 22 23746593
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGAGCTGGAGAAAGATTGACAATCACCTGCACTGAAAAAACCTGGTTT[A/T]GATCCAAAGAAACCATCAAAACATTTGCATGTCAAGATGATGGGACGTGG
Long Flanking Sequence:
TCTTGTATTTTTTCTTTGAACCCAGAGGTGACATGCACAACACCTCACATACCAAATGAAGAAGTTGACACATGTGGTTATATTGCTGAAAACTAAAAATTAGTTTGACTTTAGTCTGACTTTTACCTTTATGGCAGAGCTTGATGAATGCAGTCAGCACACCAATATTTGATTAAGTTGACAAAATGTAATAATATTTTATTTTTTTAACATTTCTGGCTGTTTATATAGCAATTGAACAAACACAATAGCTCTTAAAACATTTAAAATGTTTCTGAAATACTTATTTTTTTGTCAACAAATTGAACAGTTTGAACAGTTTAATTGAGGTTTTTTAATTTATTTATTATTTTTTTTCCATATAACTTTGTACTCCTTTTACAGCTGTAACTTGTGAGCTTACTTCAAACTATGAGGTGAAAAGGGTCGTCCCAGAGGGAAAAACTATTTTCAGAGCTGGAGAAAGATTGACAATCACCTGCACTGAAAAAACCTGGTTT[A/T]GATCCAAAGAAACCATCAAAACATTTGCATGTCAAGATGATGGGACGTGGGACTCTAATCCTGGTTGTGAAGGTAAGATTATTTAAGAACACTTCTGGATTTGGTTATGACATTACTGGATGCTATTAAAAGATCTCAAATCATGTTTCAGTGATTACATGTGAACCTCCACATAACCAGCATTTGTCCACCAACTTTTGGAGGACATTGTGGTGGTGGTGGATGTTGTGGTGTTTTCAACATTTTTGTTTCTCATTTGCAAAAATAAATTCAAATTAGTACTGTTTTACAGGAATGTGTGCAAGACCTGATATCCCAAATGCAAAAATTATAGGAGATCTAAGACAAAGTTACAGCACTAATTCAACAATACGATATAAATGTAATCCGGGATTTGAACCTGAAGAAACTGTCCAAATCACTTGTGATCACCAAGCTCAATGGACAGGTTTACAGCAGTGCACTGGTTTGTAAGATTGCTGCCATTAATTCCACTGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24168
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079324 Nonsense 519 606 11 12
Genomic Location (Zv9):
Chromosome 22 (position 24164423)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 23708321
GRCz11 22 23734885
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGTAGGAATCCAGATGATAAAATGCCTACTGAGGTATACTATGAATGC[C/T]AGGCTTACTATGTGCTGAGTGAGAGAAAGCAATATTACAGGTGTGAAAAC
Long Flanking Sequence:
GTCTGCTTCTGTCTGAAATTAGGCATTAGGCAACGTAATTTTTCCAGAAATTATTTACTATTTCCCTGAGGAGTGCACAAGTTTATAGGGGAGCACCACGGCTAATACGGAGAGCTTGTTGGACAGTAAGAAGTGGGGCAGGTTTTACGAAGTGTCACACAGTTCAGATATGAGGGCTTTTTAGTGGTCTGTTTATGCTCAGATCTTTATTTTTGCAACTGAAATAAATGCTGAAACAAACTGAAATGTTAGCTGGGTATGACAAATGGGTGAATTATGTGTAAAACACAATTTTCAAATGTTTTAATAGCATAAAGAATACATGTACACTAAATAGTCACAAAAATAAAGTGGGCTCTAATAAACATAAAATGGATTAAAATGTTTCTGTTGTAAATTGTTTAGGTGACATCTGCCCACCTCCTCCTTATATTGAAAATGGAAGTCATTTTAGTAGGAATCCAGATGATAAAATGCCTACTGAGGTATACTATGAATGC[C/T]AGGCTTACTATGTGCTGAGTGAGAGAAAGCAATATTACAGGTGTGAAAACGGGAGATGGAGAACCCCTCCGAAATGTCTGAGTGAGTCGTGCTTCTCCAGATGATTCTCTTGAAATACTCAAATCATGAAGTGAACTTAATGTTTCATCAGTTTTATTTTGTCTTTGTCACAGAGCCTTGTCAAATTACACAAGATATTCTTGAAGCACACAACATGAGACCCGATCAACAAACAGGCTATATAAAGCATGGTGACTATGTTGACTATTATTGCCAGCATAGATTGATTGTTAGGACAGGACACTACAAGAAAGCAACATGTTCTGATGGAAAGTTGGAAATTGAATCATGTGAATAGATGTGTTTGTGTATTATCAGATGTACAGGAATTAGCTGAGGTCATCAGATGTGCCTATGGCTAATCTACAGTCACATTTACCAACCTGATAATATTGAGGCTCATTTAATAGACCTGTTTTGTTGAGGTTTGATTTGATGAC
Associated Phenotype:
Not determined