ZMP
si:dkey-250l23.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate complement component 7 (C7) [Source:UniProtKB/TrEMBL;Acc:B0S6X4]
Human Orthologue:
C7
Human Description:
complement component 7 [Source:HGNC Symbol;Acc:1346]
Mouse Orthologue:
C7
Mouse Description:
complement component 7 Gene [Source:MGI Symbol;Acc:MGI:88235]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17248 | Essential Splice Site | Available for shipment | Available now |
sa18181 | Essential Splice Site | Available for shipment | Available now |
sa12725 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17248
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 |
---|---|---|---|---|---|
ENSDART00000061803 | Essential Splice Site | 113 | 858 | 5 | 18 |
ENSDART00000146933 | Essential Splice Site | 123 | 868 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 32728437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31871163 |
GRCz11 | 8 | 31880395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTTTAAAATACGCATTGGATAGTTTANTTTTTTTCTCCTTTTCTTWTA[A/G]GGGAAATGYATCAGCCTSTCTCTGGTGTGCAATAGTGATCAGGATTGTGA
Long Flanking Sequence:
AGTCCGGGGTTGCCACAGTGGAATGAACCGCCAACTTATCCAGCAAGTTTTTACGCAGCAGATACTCTTCCAGCCGCAACCCATCTCTAGGAAACATCCACACACACACTCATACACTACGGACAATTTAGCCTACCCAATTCACCTGTACCACATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCGAAGGCAGGAAGAACATGCAAACTCCACACAGAAACACCAACTGAGCCGAGGTTCGAACAAGCGACCCAGCAACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCCTCGCCTCAATAAGATATAGTGAGTCAAAATATGGTCAACCATTTGGTCGAGCAGGCAGTTAATTGAAGGATGATTAATTTTTTTCTTCTTCTTAAATGTCACAGATTAAGTGCACTTGCAAATGTGTTTTACCTTTAAAATACGCATTGGATAGTTTATTTTTTTTCTCCTTTTCTTTTA[A/G]GGGAAATGTATCAGCCTGTCTCTGGTGTGCAATAGTGATCAGGATTGTGAGGATGGTTCAGATGAGCAGAGATGTGACAGTAAACCGATCTGTAAAATCTCTGAAAATACTAATCTGCAAAAACCTCCACCGAATGTAGAGATCACTGGTCAAGGGTGATGAGACCTAATAAAGTTATTTGTCTCATATTCAATACAAAAATGCATTTGTATACACTCTAAACCCTAGTGCATAAAGCCACTAAGATTGTGTGTATGTTTGCACTACAGGTTTGACGCGGCGAAGAGAGAAGCCAGAGGTACTGTCATCAACACTAAGAGCTTTGGGGGTCTGTGCCAAAAGACCTTCAGTGGAGACCACAAAGACTTTTATAGACTTCCTCAAAGTGTTCTCAGCTATTCTTTTCAAGCAAGTGAAATATTATCATTATCATAAAAAAAGTAATATAATGAAAATATGTTACATTTTAAATAATAAATTGGGCTTCAACTGTATACACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18181
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061803 | Essential Splice Site | 568 | 858 | 13 | 18 |
ENSDART00000146933 | Essential Splice Site | 578 | 868 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 32739730)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31882456 |
GRCz11 | 8 | 31891688 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTGCCACTGTGTGGAAACTCACTGWCTTACTGATTCTGGCCTGTTTTC[A/T]GYTCAATGGAGCCTCACTGCTTTGATGAYTCGATTAARCCCAGGGAAAGC
Long Flanking Sequence:
TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGATCATCTACAGAACAAACTATTATGTTTAGAAATGTGTTGAAAAAATCTCTCTCTGTTAAACAGAAATTGTGGAAAAAATAAACAGGGGGGCTAATAATTCTGACTTCAACTATATTCCACTTGGAACCCACCTTGAATGTGCATGGGATCCTGCATGCACATAATTTCATACATCTGAATTATTTTGCACATACGCATATTTACAGCTTTGTTCGTATGCATGAACTAAATGCAAGTCTTTGTACATGAGGTCCCTGGAGATCGGCTGAATGGATTCAAAAGTGGTAAAACTCAACTGTTTAACTCTAGGGGATTTGTAAAATGAGCCTATTTCCAAAATAAAGTAAAGTGGTCCTTTAAGACTATTTTTAAGAGCATTTCTGAGACATTTCTGGGCTGTGAATGTTACTGTGCATCAACACTGCCACTGTGTGGAAACTCACTGACTTACTGATTCTGGCCTGTTTTC[A/T]GCTCAATGGAGCCTCACTGCTTTGATGATTCGATTAAACCCAGGGAAAGCTGTAAAACGCCGCCCTTCGTTCCTAATGGCTTTGTTTTGGTAATAATGATTATATGAAATGTTCTCTTTTCTGATGTAGTTAAATGTGTTTTTGTGTGTAACGATGTTATTCTCCTGTGCTAATTGCAGTATCCTAAAGATGTGTATCCGGTGGGCAGTAAGATTGAGTATACTTGTATCGAAGGCTATCATTTGATTGGCAATGCTATAGCTAAATGTCAAGAAGATCTGAACTGGCTGCAGTACCCAGTGGAGTGCAAGAGTAAGTGTGGAAATGAGGTTTTTGGATTGACACTTTCAGCGACTCCTGATTTTACTTTATTTGTTTTTTGGTGGTGTGTTTATTCAGTCAGTCAGTATTGAGGATTTTTAATATTTAAATTCTTCATTTATTATAAATCATGTAAATATTAAAATATAAAAATAGACAATATGATAAGTATAGGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12725
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061803 | Essential Splice Site | 705 | 858 | 16 | 18 |
ENSDART00000146933 | Essential Splice Site | 715 | 868 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 32741766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31884492 |
GRCz11 | 8 | 31893724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAAATCATTGATGCATAAYAATAATGTAAAGGAAATTACATTGTTCAC[A/T]GCAGTTTTAAAGCCGACGGTTGYGCCAKTGAAATGCCAGCCATGGRAGAA
Long Flanking Sequence:
TTTTTTAGTTATCTCAACTTAACTTTGCATAACTTAAAAAGTTTAGTTGAAACCCTATTAACTTATTAAGTTAAGGTAACATAAGGTACAAAAAAAATAAGGTAACAGGTAAAATTAAGTTAGCAAATTTGTTGTCATGACTTTTTGGTATATAATTTGTTTGTTTTTTTATAGTATATAAAACATATTGCTTTGCTGTCTGCAGAAACACAATGTGATCCTCCTCAGCTTCCTCCAGATGTCACCGCAAACCCCTGGAAACTGAACTATAACATCGGTGAAGCCATTGCTTTGTCCTGCCCTGAAGGCAAAGTCAAAGAAGGTCTGGATGAGATTCAGTGCAATGCTGGCCTTTCCTGGTCACCACAACCAAAAAACACCAAGTGTCTCACAGGTACAAAACTAACCCTAATCCATTTTTACAGCATTTACTCAACTGTAACATGAATGGGAAAATCATTGATGCATAATAATAATGTAAAGGAAATTACATTGTTCAC[A/T]GCAGTTTTAAAGCCGACGGTTGTGCCAGTGAAATGCCAGCCATGGGAGAACCTGGCTAAGGACAAATGTGTGTGTAAAGTTCCTCACCAGTGCAAGTATGTTCACCAACACTAAACAGAGAAACATCTTTCTCTTAATTTTCTTTCATTTGAAGGGATTGTTCACCGAAAAAAATAAATAAAGGTCCTTTCATTATTTATTTAGATTCATTTGATGAAAACCTACTTGCTTGTCTCTGGTAAGAAGATGAAATGCTGGTAGCTGGGACCCATAGAATTTCATAATATTTTTTTTCGACTATGAAAATCAATAGATGCTGTCAACCAGCATTCTTTTTTAGTGTTAAACAGAAAGAAAGAAACTCAAATAGGTGTAAAAGTACATAAGGGAGAAAAAAAATTATGTGGTCATTTTTATTTTAGGCGACCCCTTTAATCATTTTAAGTTTACATTATCATTTTCTGCCCTAAATGTGACGACTCTGCCAAAACCTAAAAGTC
Associated Phenotype:
Not determined