ZMP
c6
Ensembl ID:
ZFIN ID:
Human Orthologue:
C6
Human Description:
complement component 6 [Source:HGNC Symbol;Acc:1339]
Mouse Orthologue:
C6
Mouse Description:
complement component 6 Gene [Source:MGI Symbol;Acc:MGI:88233]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23911 | Essential Splice Site | Available for shipment | Available now |
sa37283 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23910 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23911
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000138553 | Essential Splice Site | 29 | 710 | 1 | 14 |
ENSDART00000139430 | Essential Splice Site | 49 | 855 | 2 | 18 |
ENSDART00000144861 | Essential Splice Site | 49 | 243 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 19660211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 20795700 |
GRCz11 | 21 | 20832336 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCCCAATGCACTAAAACCTGTGATTCTGGTACTCAATCACGTTTAAG[G/A]TAACAATTATTGAGCATTTATCTGATGTGTAAAGCTTAATGTTGTGATGT
Long Flanking Sequence:
GCATGCTAGTAACATGCTAAATCAGATCTACTTTTTTTTTTTTACATTTTATATATACTTAAACATCCCATTCCTCAACCCTGATATCTGCTGACTTAAAGATGACAATATTTTTTTATTTTTTTATTATAAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATAAACAATTTGCTTTCGTTAGCTAAAAGATTCATTCTAATGATTTGTGTTTGACTACAGACGCCAGTTGTTTATGTATGTCATTGGAAGTTTAACAAACTCTGTGTTCCCCTATAAGCTATCAATTTCCAACAGGCCGTCTTCTCTATGGATTGTACTTGCATTCTCCTTGCCCTACTCTCCACCCTGGCTTCTTTAAGTCCCACTATGGGGTGTTTCTGTGATCATTACCCATGGAGTTCCTGGTCCCAATGCACTAAAACCTGTGATTCTGGTACTCAATCACGTTTAAG[G/A]TAACAATTATTGAGCATTTATCTGATGTGTAAAGCTTAATGTTGTGATGTAAGTACATGTATTGTTGCAGGGCTGTCCAGTATGATGATCACTGGTTAAAAAACAGCTGTTCCCAGCTGTGTCAGATACATGATAATAGAGTGTGTAATGTTGAGGCCTGCCCTATAAACTGCCAGCTGACTGAGTTTGGACCCTGGTCTGAGTGTTCATCTTGTGCCAAAAAGTCAGTGAGTAAAACACACACACAGTTTAAAATGAGTTGCTCTGGGTGCTCACATAGTTTTCAGTGTTTGAGTTTTTGCATTCTATTGACCTTTTTCTTTCACATTCAAGAGGGTGCAGTCAATGGAACCTTACTGGCTCAAGACTCACATTGCAGATCTCATTCACATTCATTGATTTTTAGCTGTAAAAAAACAGCACAAAATTCAGCTTGATATTACAAACTCGTGTGTTGTTACTATGTGTAGTCATAAAATATGGTCATTTCTGCTATAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37283
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000138553 | Nonsense | 222 | 710 | 5 | 14 |
ENSDART00000139430 | Nonsense | 240 | 855 | 6 | 18 |
ENSDART00000144861 | Nonsense | 240 | 243 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 19652150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 20787639 |
GRCz11 | 21 | 20824275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAACTAAAGAGGAACCTCTACAGAATCTCAGCCAACACTGAGAGATA[T/A]GAACTCAAGGTCAGAAAGAAATCATTTTATGCAAGTATTTGAGTTGTCTT
Long Flanking Sequence:
CTAGCAAGTTTGTACAGTCCTTCAATGCAGTGTTCTAGAAAACTTGGGACAACCAACTTGTTTTTTTTGCCACCAAAGGAAGATGTATACATGCTGATCTGCAATGCAACGATCAGAACGACTGTGGTGACAACTCTGATGAGAGAGACTGTGAGCGCAATAAAAGTGTGTGTTCAAATCAGCAGATGTATGCTTTCGTCCCTGGAGCAGACCAGATTGGTTTTGGGTGAGTTACAGATTGAGATCATTTACTTTCTGAGACCGCAAAACAGCTAAATGGAAAACATTTAGGGTGTTGTCAGCAAAGCATCTCTGGATATCAGAGAATGTGCTTGATTTAAAACTGATAATGATTAAAATTTTAATGATTAAATCAGATTTGATGCTGCAGCGGAGCAGATGAGAGGTGCTGTTCTGGACAACTCGTTCATGGGAAGTAATTGTACTGTAGAAAAACTAAAGAGGAACCTCTACAGAATCTCAGCCAACACTGAGAGATA[T/A]GAACTCAAGGTCAGAAAGAAATCATTTTATGCAAGTATTTGAGTTGTCTTTTATAATTTATTATTATAAAATTATAATTATCATTTTTGCTCTATTTAAACACATATTAACTAATATGGGTTATTTAATAAGAATTGCAAAAAATCTTTATTAATAGTTCTTATAAAGAATTTTAAAAGGAATAATTCATAGTGTTTTGAACAGTACATTCATCATCTTGCAGTGCCAAATTTGTGTAGGGGGAGCTATTTATTTAGCTTTTCACAGCAAAATAGCATAGATAAAAATTCATTTTATGCATTTATGTGAGCAATATCACATGAGTAGCAGTGCGATATGGTTACATATTGACACTGGTGGGAGGTGTGCGTTTATACAAAAATTTGACAGCGTAATCGTGTGTATAAAAAAGAAAATCAAACACGGGACAGTCTCAAAAACGCCTTTGTATGAGGAACTACTTTCTTACTTCACTCATTCAAATCTGCAGCTGATGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23910
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000138553 | None | None | 710 | None | 14 |
ENSDART00000139430 | Essential Splice Site | 839 | 855 | 18 | 18 |
ENSDART00000144861 | None | None | 243 | None | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 19623703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 20759192 |
GRCz11 | 21 | 20795828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTATATTCAACTAAAATAATTCAACAGTCTTATTGTCTTTTCTTCTTA[G/A]TGTCCAAAACGTGTGAGTGTAAGATGCCCAGAGAATGTCCAAAAGACGGG
Long Flanking Sequence:
CCTGCTCTGTTAAACCTAATTTGGGAAATATTTAAAAAAGAAAAAAAATTCAAAAGGGGGCCAATAATTCTGACTTTAACTGTATATTAAAAATATAAGATCGCTGCTTTAATGCAGTGCTATTTGCAGTCATGACCATTTAACACTATGTATTTGTGTATCCTGCAGAGGCTACAGAGAAGACTTGTGCGTTTATGACGCTGGCAAGGAAACTGCCATTATGATGTCCCTCTGTGCTTTTCATGTTGACCGTTGTCATGGAGACAGATTATACTTTATGAATAATGGACCGTGCAAAAGTGACGCACGCAGTCTGGACTGGGCCAAATTCAGGGTCAGTGTATCTGAGCAGAGCTCGGTGCAGGAGCCCTGCGGTTCAGACACCTGTTACGAGTGGGAGACCTGCTCAGGTACAGACCGAATCACAAATCCTTACATAATGCATTCTTTCATTATATTCAACTAAAATAATTCAACAGTCTTATTGTCTTTTCTTCTTA[G/A]TGTCCAAAACGTGTGAGTGTAAGATGCCCAGAGAATGTCCAAAAGACGGGTAGAAAATATACTGCCTGAAAATCGTGGGAACGCAAACCACAAGAAGCATGAATCTGTGTTTTATGGCTGTAATGAAGTGCAGCAGTATAGAGTTTGAGCTTCAGAATGAAGGCCCTTGTGCAGGTTCTTAATTGTGCACCACTTTAGCTGTAAAAATGTTCACAGATTTGCAGCCATTATTGATTCATATTGATAACACATTGTCATTTTAAAATCACTCACAGCATGTTATAGTTATTTGATTGTGCATATGGGCATTCTTGATATTGATCTGGAACAACACAATAAAATATAATCGGACATTCAGATGCCTTCTAGTATTTAAATACTCTTTCATCTGTTAAAGTTGAATGTTAAAATAATTACTTTCTGGCATGTCAGAAATAACGTTTGAGGTTACAGAAGTAACCCTCGGGGAACGGAAGTGCTATAAGTGGATTTGATGTTAA
Associated Phenotype:
Not determined