ZMP
c9
Ensembl ID:
ZFIN ID:
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 |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa15017
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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