Busch Lab

ZMP

c9

Ensembl ID:
ENSDARG00000016319
ZFIN ID:
ZDB-GENE-050522-442
Description:
complement component 9 [Source:RefSeq peptide;Acc:NP_001019606]
Human Orthologue:
C9
Human Description:
complement component 9 [Source:HGNC Symbol;Acc:1358]
Mouse Orthologue:
C9
Mouse Description:
complement component 9 Gene [Source:MGI Symbol;Acc:MGI:1098282]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa15909 Essential Splice Site Available for shipment Available now
sa598 Splice Site, Nonsense F2 line generated Not yet available
sa33641 Nonsense Mutation detected in F1 DNA Not yet available
sa15017 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa15909
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051374 Essential Splice Site 26 280 None 7
ENSDART00000115273 Essential Splice Site 26 658 None 12
ENSDART00000147132 Essential Splice Site 26 673 None 11

The following transcripts of ENSDARG00000016319 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 33983014)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31745246
GRCz11 5 32345399
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTGAGAATTGCAAAGATRMTAAATCTGATCACTRTGTATCTTTCTWAA[A/G]GTCAAGGGTCCAGACGGGAGGTGCGGCAAATAAACGATCCACCACCAGTT
Long Flanking Sequence:
ATGGTAAAATCTGTGAAAAATAAAATAAATATAAAAAGAAATCAAAAAAAGAAAAACATAAGAAATGATACGGTAAACGAAAATCTGCAGTTAAAACGAGGCAAAAAAACAGCTCTAAATATGTTAATGTAACAGTTTAGCATTAGACGGTTATGGTAAATGGTGTGTGATCATGTGATATTTGGGAAAGCACAGAGATGTACACAAACCTCTTGTCAACTCTGAAAGGTTCATGTTAATTATTAACAGTGAACCAATGCTTAAATACAAGTGTACACATTTCTACATTCAGTGACCTGTCCAGAGCTTCACCATGAAGGCTTTAGCTGCTTTATGTGTGACAATATGTCTTCTTTATCAGGCTAATGGAAAGAGCATAACAGACCCGGTGTATGTATGCGCAAATTTGACAACAAAACAATGGAGTGTATTCCTTTCTGTTTACTTTTAGTTTGAGAATTGCAAAGATGCTAAATCTGATCACTATGTATCTTTCTTAA[A/G]GTCAAGGGTCCAGACGGGAGGTGCGGCAAATAAACGATCCACCACCAGTTGACTGCAAAATGAGTGCCTGGTCCCAGTGGTCACCCTGCGACCCCTGCACTAACACCACGGTACTGGAGTTCCTCTTCTCCTCTCTATCTCTCTACCTCTCCTGAATGTATATTGTCATCTGAAATCATTCTGCATTTAATAATAATTCACCAAATTGAAGAAATATCTGGCATTCCCCTGTGTCTGTGTAACCCAGTATCGCTCTAGGAGTATTGAAGTCTTTGGCCAGTTTAAGGGCACTGTCTGCTCAAATCCAATTGGAGACCGGAGACTTTGTGTACCCAAAACCAAATGCCAGATGGACGATCCTCCTGTCTGCAAAAGCTCTCAGTGGCAGTGCACCTTTACAAGTCAGTATTATTATTTTTTGACTGTGGCAAGATGGCCAACAGCTGTTTAGCTGTAGGGAGAATTGCTTCACAATATTAAGTATTAAGATTGTCACTCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa598
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051374 None None 280 None 7
ENSDART00000115273 Splice Site, Nonsense 349 658 8 12
ENSDART00000147132 Splice Site, Nonsense 364 673 7 11

The following transcripts of ENSDARG00000016319 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 33988949)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31751181
GRCz11 5 32351334
KASP Assay ID:
554-0508.1 (used for ordering genotyping assays)
KASP Sequence:
ATATATATATATTTCATGCTTTTATGACCAGCACATCTTCTCTATTTCAG[A/T]GAAAGACCTTCATGAGAGTAAAAGGCAGAGTGGAGYTGGCCWCATACCGC
Long Flanking Sequence:
CTTTGATGATTCGCCCCGAAACAGGAATTTGTTATAACTCAGACATGCATTGTCCTATCTGCCTCAAAATCCACATGTTTGATAACAGTCCTGACCTGAACACGTTTACATGCCAATATCAGTTACAGTTATAGCGCCACTTGTTGGCAACAGGAAATGACATGTTTTACACTGTAACAAACTCTTCCCACAAATTTGATCAGATTAAATTCAAGTTTTGTCAGTATAATGCAAGAGCATGTCCGTGCCAGACTGACAAAGTTCAGTGTATTCGTCATGAATGGCGAACAACTTTTAACTCGGCCAAACAATATCCGATCTGCCTGAAAATTTACAAGTTCGATGAGATTTCTCTCCTAAAAAAACATAAACATGACAATATTGAGTCACAGTCATAACGCCACCTGCTGGCATAAAACTTTGGCATAAATCTGTAATTTTCTCAGGTTTATATATATATATTTCATGCTTTTATGACCAGCACATCTTCTCTATTTCAG[A/T]GAAAGACCTTCATGAGAGTAAAAGGCAGAGTGGAGCTGGCCACATACCGCATGAGACAGCGCGGGCTAGAAGTGTCCTCAACGTTCCTGGATGATGTTGATGCTCTGCCACTACAGTATGAGAAGGGGCAGTATTTTAGTTTCTTGGAGGAATATGGAACACATTTTACTAAGAACGGAAAGTCTGGTGGAGAATATCAACTTGTTTACGTAATGAATGAGGATATACGCAAACAAAAGCGTAAGTTATCAAATATTTCAATACTTCTTTTTCTGTGAAAACTGGAAGTTTTGTGCAACATCAGAACATTCTATTATAACTTCAAAATAAGATCAAAATACTGAAATGTGAAAATACTGTACATGGTATTTAAATGACAATGTTAATGTGAGGTATATGTCTTCAGCCTGAAAGTGTTTTTAAATTATAATGGCTTCTTTTGATTCAACTTTAACCACAGATGTCACTGAAGCCACGGTCAAAAAGTGTTTTGAGCTTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33641
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051374 None None 280 None 7
ENSDART00000115273 Nonsense 397 658 8 12
ENSDART00000147132 Nonsense 412 673 7 11

The following transcripts of ENSDARG00000016319 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 33989094)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31751326
GRCz11 5 32351479
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGATGCTCTGCCACTACAGTATGAGAAGGGGCAGTATTTTAGTTTCT[T/A]GGAGGAATATGGAACACATTTTACTAAGAACGGAAAGTCTGGTGGAGAAT
Long Flanking Sequence:
GGCAACAGGAAATGACATGTTTTACACTGTAACAAACTCTTCCCACAAATTTGATCAGATTAAATTCAAGTTTTGTCAGTATAATGCAAGAGCATGTCCGTGCCAGACTGACAAAGTTCAGTGTATTCGTCATGAATGGCGAACAACTTTTAACTCGGCCAAACAATATCCGATCTGCCTGAAAATTTACAAGTTCGATGAGATTTCTCTCCTAAAAAAACATAAACATGACAATATTGAGTCACAGTCATAACGCCACCTGCTGGCATAAAACTTTGGCATAAATCTGTAATTTTCTCAGGTTTATATATATATATTTCATGCTTTTATGACCAGCACATCTTCTCTATTTCAGAGAAAGACCTTCATGAGAGTAAAAGGCAGAGTGGAGCTGGCCACATACCGCATGAGACAGCGCGGGCTAGAAGTGTCCTCAACGTTCCTGGATGATGTTGATGCTCTGCCACTACAGTATGAGAAGGGGCAGTATTTTAGTTTCT[T/A]GGAGGAATATGGAACACATTTTACTAAGAACGGAAAGTCTGGTGGAGAATATCAACTTGTTTACGTAATGAATGAGGATATACGCAAACAAAAGCGTAAGTTATCAAATATTTCAATACTTCTTTTTCTGTGAAAACTGGAAGTTTTGTGCAACATCAGAACATTCTATTATAACTTCAAAATAAGATCAAAATACTGAAATGTGAAAATACTGTACATGGTATTTAAATGACAATGTTAATGTGAGGTATATGTCTTCAGCCTGAAAGTGTTTTTAAATTATAATGGCTTCTTTTGATTCAACTTTAACCACAGATGTCACTGAAGCCACGGTCAAAAAGTGTTTTGAGCTTGGACTTAAAGCAGACTTCCAATTAACCCCAGCAGCAGAAGGAGGAGGAGAAGTTAAACCATTAAACGACTGCAATAGTTTAACAAACACAGACACAGGTGTGTATGAGTCTGACTTAAATAACTTAAAGCGATATACATCAGTAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15017
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051374 None None 280 None 7
ENSDART00000115273 Nonsense 479 658 10 12
ENSDART00000147132 Nonsense 494 673 9 11

The following transcripts of ENSDARG00000016319 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 33991971)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31754203
GRCz11 5 32354356
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTAAAAACTATTRTGCACAAACTTGCTCACCAGATGAGAAAAACAAC[A/T]AGGGGGTTATTGATAAGGTCCTGATTGAAGTGAAAGGGGGYAGTGCAGCC
Long Flanking Sequence:
CAACCCGTCTCTGGGAAATATTATTATTATTATTATTATTGTTATTATTATCATCACCTTTTTATAAACATTTTGAAGCCTGACAATCAGAGAATTTCATCTGAAAGTAAACCAGCCTTTGTAAAAGTATGGCTCGCTTAGAAATTACATCTTAAAAATGCATTTATTTGTTTTCTTTTTGGCTTAGTCCCCTTATTATTCTAGCCACAGCAGAATGAACCGCCAATTTATCAAACATATGCTATATGCTGCGGATGCCCTTCCAGATGCAACCCATCACTGGGAAACATCTATACACACATCTAAAAATCTGTTTTCTTATTTGTTATCTTAAAGGCTTACGTTTTTTTCCTCAAGTTCTCATTTGTGTTACATGAAGGACATGTTAAAAGGAACCTTTAGGTTTTTGAGATGCATGCTTTCTCATTATAAAAAGGTTCATTTACAATATTTCTAAAAACTATTGTGCACAAACTTGCTCACCAGATGAGAAAAACAAC[A/T]AGGGGGTTATTGATAAGGTCCTGATTGAAGTGAAAGGGGGCAGTGCAGCCTCAGCAGTAGCCATGAAGTCTCAGCTCACTAAAGATGGCATTCTAGACTACAACCAATATGTGGAATGGGCAAAGACCATCACCATTCTGCCAGCACTCATTCAGAGTGAGGTGAGACTCTTCTCAAATTTGCTTTACATGACATGTCGTGTAATTAAAAAAATTTGTTTTCATTTTTATATGGCAGCCTGAACCCATCTACAATGCCATCCCTTTGAGCTTTCCTGATGCTCAGCCGAGGCGGGACAATCTTAAAAGAGCTCTGGATGAATATGTGGCAGAGTACAGTGTGTGCAAGTGCCAGCCTTGCCAGAACGGTGGCACTGTGATCCAGATAGATGGACAGTGTAAATGCATGTGTTTACCAGGTTCTGAAGGTGTTGCGTGTCAGATCATTGACATGGAAATGATGAAAGGTGTGTGTTTCATGAAACAGGCGGTGAAACCTTC
Associated Phenotype:
Not determined