ZMP
wu:fd46c06
Ensembl ID:
ZFIN ID:
Description:
complement component 1, s subcomponent-like [Source:RefSeq peptide;Acc:NP_001107921]
Human Orthologue:
C1S
Human Description:
complement component 1, s subcomponent [Source:HGNC Symbol;Acc:1247]
Mouse Orthologues:
C1s, Gm5077
Mouse Descriptions:
complement component 1, s subcomponent Gene [Source:MGI Symbol;Acc:MGI:1355312]
predicted gene 5077 Gene [Source:MGI Symbol;Acc:MGI:3644269]
predicted gene 5077 Gene [Source:MGI Symbol;Acc:MGI:3644269]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17822 | Essential Splice Site | Available for shipment | Available now |
sa28691 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22881 | Nonsense | Available for shipment | Available now |
sa36184 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17822
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114864 | Essential Splice Site | 77 | 458 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 34166028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31703998 |
GRCz11 | 16 | 31661013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACACAATCATTTGAGCWGCAGTAARATGCAGTTTCCATTATTTGCATTC[A/C]GGTTGTRTTTAATAAWAAGGTTCTGTGGAAGTTTTGTGGACAGAATTTCA
Long Flanking Sequence:
GAAGGCATTAGATTGACATCAGCATGTCTGAAAAAATGCTGATATTTTGGTAAGTCCTTTTTTTTATGTTTCACCTGAATTTATAATTATTCTTTTAATAACTATCAGTGAAAAAAAATGTTGTGTTTATTAAATTAATATGAGGATTAACCATTTCGTTCTGTCTACCAAACACACCGATTTAGCCTTCTGTGGGCAAGTGTGGATGTGTGTGAGTGTGATCTGGCCATGTTTGGGGAGGTTTCTTCTCCACAGTACCCTAACCCATATCCAGTGGATTTCATGCAACATTGGAAGCTGGAGGTGCCGGATGGGTATCAGATCCAGCTAACTATCAATCACCTGGACATTAAGCCTTCTCCAAACTGTTGCAACAATTTTCTCATGGTAATTTACTTATAAAAATGTCAAATGTAAATACGGTTGTTTTTTATAATATCTTGTTAAGGCTACACAATCATTTGAGCAGCAGTAAAATGCAGTTTCCATTATTTGCATTC[A/C]GGTTGTGTTTAATAATAAGGTTCTGTGGAAGTTTTGTGGACAGAATTTCACAGACAGGTTTCATCCAGGTGAAAAGCCCATCTTGGTTCCCGGTTCTCATCTGCAGCTCTTTTTTCTGAGTGATGATTCAAACCTTAAATCACACACAGGATTTACTGCATCCTACAAGGCTGTTGGTGAGTTATGATTAAGAAACATTGGTGTTATTGCTGGGAAAATTACATTTTACACAAATAGTATGATCAATTATTATTTTGCATGTATTTTTTTGTTTGCTCTGCCACTAAGAAGTTTTAGCAGTCATGTCTCTCCTTGCAACACTAATTTACACTTATAAAGTGATGCAGGAATAAAATTGTGTGGGAAAAAAGATTTTAAAGTTTAACGATTAGTTCACCCCAAAGAAAAAAATCTGCTCATTGTTATTCTCGTACTGTTCCAAACCTGTGTTAAGTTCAGGAACCAGATAAAGATGTTTTGAATGAAATCTGAGAGATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28691
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114864 | Essential Splice Site | 177 | 458 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 34164433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31702403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATCAGTCTCAAGTGCAAATCTGAATTTTATCAATTAGATAAAAAAGG[T/G]AAGATTTGTGGTTTACATGCATTACGTTAATGTAATTCTCAAAAGTGTAT
Long Flanking Sequence:
GAAACTGGTCTTAAAAATAGTCCTCCTTAATGTTTAATACATAAGGTGCATCCCATTTTGAGTAGGCCTACTTTTTCACAATTCTATGATTTTACAAGTGATTTGTTCTCTTTGATACCTTTTTTTGTTTCCTTGTGATTCTAATATGGCCATAGTCAGTGTTGTTGCTCGAAATTCTGGGCTCTATGTACAGGCTTTAGCTCTAGGCCAGTTTTGATGCTGATTGTAGATCAAATGTCTTTATTCTGTATTCATCACTATCTCTGAGAGAGTGGAATAAACACTGAGGTCAGTTTTGGTGGTGGAGTTGATAATGGAAGGTGTTACTTAAAACAATCAACAATCAACAAAACTCTTTGTGTTTCCTCTTCAGCTGTGGATTGTGGCATTCCAGAACTTTCAGAATTAATGGAGCTCCCAGAAAAAGATCCTCCGACAACTTATCTAAAACAAATCAGTCTCAAGTGCAAATCTGAATTTTATCAATTAGATAAAAAAGG[T/G]AAGATTTGTGGTTTACATGCATTACGTTAATGTAATTCTCAAAAGTGTATTATTTTTCCTTTCATTAGGTAATTTTACCTGCAATGCAAAAGGTAACTGGGTGTCTGAGAATGGTGAAAAGTTAACAAATTTTTTTCCTAAATGTGAACCAGGTACTTATTCATCTTGAATGCACATATCTGAAACACACATATTTGTTTTAACTTACCTTGCCTTCATCTCACACTAGTATGTGGAATAAATATGGAGGACTTGTCTGCTGGAAGAGTCTTTGGTGGGAAGCCAGCAAGATCAGGAGAGATTCCCTGGCAGCTCCTCCATAAGTCCAGCCCTAGAGGTAGTGCAACTCTGATCAGTGATTACTGGGCTCTGACAGCAGCTAGCCTGGTGGATGGAAATGAAAACCGCAACATGAGTTGGCTTGGAGGAATAGTTAATGCTCAGGATACAAATGCAGTTTTTATGGAAACAGAGAAGATCATAATTCACCCAAATTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22881
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 |
---|---|---|---|---|---|
ENSDART00000114864 | Nonsense | 296 | 458 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 34163931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31701901 |
GRCz11 | 16 | 31658887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAGTTTTTATGGAAACAGAGAAGATCATAATTCACCCAAATTATAAG[A/T]AGGTTGATAAAGATGGGCGTCAGTCAGACTTTAATAATGATATTGCTTTG
Long Flanking Sequence:
AGATTTGTGGTTTACATGCATTACGTTAATGTAATTCTCAAAAGTGTATTATTTTTCCTTTCATTAGGTAATTTTACCTGCAATGCAAAAGGTAACTGGGTGTCTGAGAATGGTGAAAAGTTAACAAATTTTTTTCCTAAATGTGAACCAGGTACTTATTCATCTTGAATGCACATATCTGAAACACACATATTTGTTTTAACTTACCTTGCCTTCATCTCACACTAGTATGTGGAATAAATATGGAGGACTTGTCTGCTGGAAGAGTCTTTGGTGGGAAGCCAGCAAGATCAGGAGAGATTCCCTGGCAGCTCCTCCATAAGTCCAGCCCTAGAGGTAGTGCAACTCTGATCAGTGATTACTGGGCTCTGACAGCAGCTAGCCTGGTGGATGGAAATGAAAACCGCAACATGAGTTGGCTTGGAGGAATAGTTAATGCTCAGGATACAAATGCAGTTTTTATGGAAACAGAGAAGATCATAATTCACCCAAATTATAAG[A/T]AGGTTGATAAAGATGGGCGTCAGTCAGACTTTAATAATGATATTGCTTTGATTAAAATGTCTGCTATGGTACCTCTTGGTCCAAACATCAGGCCAGTGTGTTTGCCAAAGAAAACAGATGAAGCTGTTAAAGAGGGCATGATGGGAACAGTTTCAGGTTTTGGAGTTTATGGAAGGACTGTAAGTAATTTATTACGTTATGGTCATGTTCATGTATATAGTCTCAAGAGTTGTGTTTCAGATGGTTTGCCAGTCAGTGATAACATGTTCTGTGCTGGAGATGATGTTCATGGTATTGACAGTTGTAGAGGGGACAGTGGAGGTCCTCTGTTTTTCCCAATGCTGGGCGATGGAACTGAAGAGCATCGCTATGTGGTGAAAGGCATTGTGTCTTGGGGTCCTAAATGTGCTAAAACAATCACTAAAGGTTACTACACTAAAGTGCAAAACTACCTGGACTGGATTGAAGAAACTATGGCAAATAATTCATAATGTGAGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36184
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114864 | Nonsense | 444 | 458 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 34163487)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31701457 |
GRCz11 | 16 | 31658443 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGTCCTAAATGTGCTAAAACAATCACTAAAGGTTACTACACTAAAGTG[C/T]AAAACTACCTGGACTGGATTGAAGAAACTATGGCAAATAATTCATAATGT
Long Flanking Sequence:
ATACAAATGCAGTTTTTATGGAAACAGAGAAGATCATAATTCACCCAAATTATAAGAAGGTTGATAAAGATGGGCGTCAGTCAGACTTTAATAATGATATTGCTTTGATTAAAATGTCTGCTATGGTACCTCTTGGTCCAAACATCAGGCCAGTGTGTTTGCCAAAGAAAACAGATGAAGCTGTTAAAGAGGGCATGATGGGAACAGTTTCAGGTTTTGGAGTTTATGGAAGGACTGTAAGTAATTTATTACGTTATGGTCATGTTCATGTATATAGTCTCAAGAGTTGTGTTTCAGATGGTTTGCCAGTCAGTGATAACATGTTCTGTGCTGGAGATGATGTTCATGGTATTGACAGTTGTAGAGGGGACAGTGGAGGTCCTCTGTTTTTCCCAATGCTGGGCGATGGAACTGAAGAGCATCGCTATGTGGTGAAAGGCATTGTGTCTTGGGGTCCTAAATGTGCTAAAACAATCACTAAAGGTTACTACACTAAAGTG[C/T]AAAACTACCTGGACTGGATTGAAGAAACTATGGCAAATAATTCATAATGTGAGATATTATTAATGTCTAGTTATATATGAGATCACTTAAAATTATGGCCATTATGAAAAAAAAGTCAATTGTAATAATTTGTCTCCTAATGAATGTAAATGTCCCTGTATTTTAAGGCAAAAAAAAGTTAAACAGGACCCTTCACATGTATACATTGTGTAAAAGTTAATTTAAATAAACTAGCTAAAAGTTTTATTAAATTTGATCTTTTTTTTTTTTTTTTTGCTGGGTTAAAATTAAGCAGTTAGTATGAAGTCTGAACTGGTTGAGCAAACTTGTACAATCAGCCTCAAAGTCTGCTTCTCCATTTCTACGTCATGTGTTGTGAGTAAAATATAGGCTAAATTATAAATATACTTGACAAAAAGGGTTCCACAGAGGTGTATTTAGAGTTGTATATTGTGGGTATTGTGTTTGAAACATGATGAGTTTATGTAGTCCTTTCACTC
Associated Phenotype:
Not determined