ZMP
si:dkey-8k3.2
Ensembl ID:
ZFIN ID:
Human Orthologues:
C4A, C4B
Human Descriptions:
complement component 4A (Rodgers blood group) [Source:HGNC Symbol;Acc:1323]
complement component 4B (Chido blood group) [Source:HGNC Symbol;Acc:1324]
complement component 4B (Chido blood group) [Source:HGNC Symbol;Acc:1324]
Mouse Orthologue:
C4b
Mouse Description:
complement component 4B (Childo blood group) Gene [Source:MGI Symbol;Acc:MGI:88228]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22797 | Essential Splice Site | Available for shipment | Available now |
sa12941 | Nonsense | Available for shipment | Available now |
sa44845 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22796 | Nonsense | Available for shipment | Available now |
sa16232 | Nonsense | Available for shipment | Available now |
sa14061 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22797
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079630 | Essential Splice Site | 88 | 1719 | 2 | 41 |
ENSDART00000143550 | Essential Splice Site | 96 | 1725 | 2 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18749808)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCAAAACAATACACCAAAAAGGAAAGTTTGAGACAGTGAATCTTGAGG[T/C]AATGCATATCTTAGTAAAAATGCATTTACAAGTAAATTAAGGCCAAGAGC
Long Flanking Sequence:
TGAATCGTTCAAAGAAATTAAAATGTTAAGTTCAGAGAACTTAAAATATTAATTAAAAGATTTTTGCTGCCTAATGTGTAAGTTAAACACACCTGTTTAACTTGGTATTTTAAGTAATGTCAAGTTATATTAACTTAATATTTTTAATAATTACAACAGTGGGGTTTACAGAATAGATTTTCTGAAATGTGTTGTCAAAGAAGGAAAAGTTGTTGACTTTTTCATAGACTATTTTTGACTAAACAAGATGAGTTAAGCTAAAAAGTTATTGAGGTTTTTTAATCTTTCTTCTTTTTTCCATCTGTGTGCCAGATTCCTCATCACTGCTCCGAGTGTGTTTCATGTTGGTGTGAAAGAACCTATAGTGATTCAGGTCGGGGAGGCACTGGTCGGCAAACCCGTGTCCTGTCAGTTAGAAACAGAGACGCGGGTTCCCATGTCCGCAAAGGAAACCAAAACAATACACCAAAAAGGAAAGTTTGAGACAGTGAATCTTGAGG[T/C]AATGCATATCTTAGTAAAAATGCATTTACAAGTAAATTAAGGCCAAGAGCAGAATTGTATCTTATATGTGTGTGTGTTTTTAGATTACTTAATGAAAGTCTAGCTGTATTATATTCCTGATATAAGCATTCACAGTCCCGTCAGAACAGTCCTGTATATTGTTTATTTTCTCTTCAAGATATTTGCAAATACAGTTTCAAACCTGAAGTCAATCAATGGAGAGCCTCCTTATCTAAATCTGGCATGTGAGGTTGATGGTCAGAGACAGCAGACGCGTGTTCTGGTCTCCAAACACAATGGCTACATCTTTATTCAGACGGACCAACCCATATACAACCCCACACAGAAAGGTACAATGAACACACTTTTAGTTTTCAACCAAAAACTAAAATATTGTTAGCTAAAATGTAAAATATTTATGAATTGTGGATGACAGTTAATATTAGTTTAGGTTCTTCATTGCATGCATCTCACTAGGATTGATTTATTTCATGTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12941
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079630 | Nonsense | 106 | 1719 | 3 | 41 |
ENSDART00000143550 | Nonsense | 114 | 1725 | 3 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18749576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16788987 |
GRCz11 | 16 | 16696964 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGCAAATACAGTTTCAAACCTGAAGTCAATCAAYGGAGAGCCTCCTTA[T/A]CTAAATCTGGCATGTGAGGTTGAWGGTCAGAGACAGCAGACRCGTGWTCT
Long Flanking Sequence:
TTTTGACTAAACAAGATGAGTTAAGCTAAAAAGTTATTGAGGTTTTTTAATCTTTCTTCTTTTTTCCATCTGTGTGCCAGATTCCTCATCACTGCTCCGAGTGTGTTTCATGTTGGTGTGAAAGAACCTATAGTGATTCAGGTCGGGGAGGCACTGGTCGGCAAACCCGTGTCCTGTCAGTTAGAAACAGAGACGCGGGTTCCCATGTCCGCAAAGGAAACCAAAACAATACACCAAAAAGGAAAGTTTGAGACAGTGAATCTTGAGGTAATGCATATCTTAGTAAAAATGCATTTACAAGTAAATTAAGGCCAAGAGCAGAATTGTATCTTATATGTGTGTGTGTTTTTAGATTACTTAATGAAAGTCTAGCTGTATTATATTCCTGATATAAGCATTCACAGTCCCGTCAGAACAGTCCTGTATATTGTTTATTTTCTCTTCAAGATATTTGCAAATACAGTTTCAAACCTGAAGTCAATCAATGGAGAGCCTCCTTA[T/A]CTAAATCTGGCATGTGAGGTTGATGGTCAGAGACAGCAGACGCGTGTTCTGGTCTCCAAACACAATGGCTACATCTTTATTCAGACGGACCAACCCATATACAACCCCACACAGAAAGGTACAATGAACACACTTTTAGTTTTCAACCAAAAACTAAAATATTGTTAGCTAAAATGTAAAATATTTATGAATTGTGGATGACAGTTAATATTAGTTTAGGTTCTTCATTGCATGCATCTCACTAGGATTGATTTATTTCATGTTATATCTCTGCACATGAAATTATCAACAAGAGTATTGCAATGATATATTTTATAACTTTAAATGTAAGCTATTATCTAATGAATGTAGCATGTCTTAACTAAGATTGTATGTGTTTCGTGTTACAGTTCGATTCAGAATCTTCACTCTCGATCACTCCATGCGACCAAAATTAGAGATGTATGTTTATGTCTCTATATATGTAAGTAATATTTATTATTACATTAAAGGAATAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44845
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079630 | Nonsense | 519 | 1719 | 13 | 41 |
ENSDART00000143550 | Nonsense | 527 | 1725 | 13 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18744979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16784492 |
GRCz11 | 16 | 16692469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAGTAAAAAAATCCATCCAAATAAAACCAAACATGACCCCATCCTTC[A/T]GATTGATTGCTTTTTACTATATCAAAGAGGGTGACATCATCGCTGATTCT
Long Flanking Sequence:
ATTCCTATTATTATTTTTATTATTATTATTCTGCTTCTTCTTCTTCTTCTGCCGAATTTGAATGGCAGCCCATATAACCATATGCGGAAGAGTTGTATAATTTGGCACAATGATAGAGGGCAGTTTAAACATGAACCACAGTAAACCTGACATCTCTAACTCGAACTCTGTAGCACCACCACTTGTCCACATTTCACTTACGTTTATCATTATAAGTTTTGAACCGAAAATACTTTGGAAGTCAATGGTTCAAAGTTTTTAACATTTTTAAAAATATATCTTATTTTGCACTTAACAGAAGAAAAACATTTGTAAAGGTTTGAAACAAGCAAAGGATGAGTAAATGATTTTTTGTTTGTATTTGTGAAGTATCCCTTTAAGAAAAGCATGTGTCTCTTCAGATTGTCAGCAGAGGTATGTTGAGATCAACAGGCTCTGTTGCATCAGGTTCTGAAGTAAAAAAATCCATCCAAATAAAACCAAACATGACCCCATCCTTC[A/T]GATTGATTGCTTTTTACTATATCAAAGAGGGTGACATCATCGCTGATTCTGTATGGGTAGACGTAGAGGACACTTGTGATGGAGAGGTAAACAATAAAAAAAGCATTTACATTCATTTTAAATGGTCAAAAGGTTACAGCTATTTGTTTCAATAACAAACACAAACAGGTTTACTGTTCTGCTCTCTTACCTTCCATTTAGTTTGAGGTAAAACTGCATCATAATTATGGCAATCATAATTATGAACCTGAAAGCACAGCTGAGCTTGACATTGATGTAGGACAACAGAAAAATGCAAAAGTAGCCTTACAAGTTGTGGACAAAGCCATTTACGCCTTGGGGGCTCAAAACAAACTCACCCAGAAACAGGTGTGTACTTTTATTTTTACCAGATAGACAATTGATGTTGGATCTTGATGGTTTTTATGTTTCTTATTTACCTGTGCAAAGGTGTTTGCCTCTATGAAGTCTTATGATCTGGGGTGTTCTTATGGCGGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22796
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 |
---|---|---|---|---|---|
ENSDART00000079630 | Nonsense | 856 | 1719 | 21 | 41 |
ENSDART00000143550 | Nonsense | 864 | 1725 | 21 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18733786)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16770669 |
GRCz11 | 16 | 16678646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACCAATACAATCTTCTAAATAATTTTTCAGCTTGTTGTGCGCATGCGA[C/T]AAGTGGATGGTCTTTGTTCACCCGGGTCAGCAACGTCATCATCTTCCGTC
Long Flanking Sequence:
TTATATTATTGTCTATTAAGGCAAATAAATAGATTACTGATGTCCATGTAAACGTATAGTCAGAAGAATCCTTGATATAAGTGAAGGATCCAGAAGGACAACCTGCTGATTTGATTCAGAAGGGCATTTTTTTGTTAGACGGCTCACCGGTCAGGTATACATCCGCACTAAAATATCAAGGTGAAAGTCATCATAGCTTGCATAGAATATACCCAGCTCTGAACCCAACTTTGAGATTAGATTAACGGTAATATTTTTATCACGGGTTAAAAGTCTCGCGCTTACGCAGCATGTTAATGCAGATAACAACCCACCACACACACACAAATATATATATATATATATATATATATATATATATAAATATATAAATTTATAAACATTATAGATATTTAATTAATTTCTATCTATCCTATAAAAATGGCTTGTAGTGCATTAGTAGATTATTGATTACCAATACAATCTTCTAAATAATTTTTCAGCTTGTTGTGCGCATGCGA[C/T]AAGTGGATGGTCTTTGTTCACCCGGGTCAGCAACGTCATCATCTTCCGTCAGATTCAGCCTGAAACCAGCATCTTCTCAAACTGTTACTTTCCCTGCTGTCCCCATGGTAACAGGCGAAATCCCTATCACTATTGCAATCTATGATATTGAAGAAAAAATTGAAGTGGATGCTATTCAAAAGATACTCTTGGTCAAGGTAAGAAGAAGTAGTATGGGGATATACACAACTTTTTCATATACTTTGTTGTTGTTGAAGTTGTAATGGTGTCATTTCAGTTATTATAATATCACTTATTCTTCTTTTCCTTTATGTCACAGAACGAGGGAGTGGAAATGAGAGAAGAGCTGACTTATTTGATTAATCTAGATGGTAAGATTGTTCACTTATTGGTCACGTCATTTCATTTCTCACCACAGATACTGTATAGATTTTTGCTTTTATAAAAATAAATATTTTGGGGGAATTTGTAAAAGCTCTGTCAGTTTTGGACATTGTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16232
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079630 | Nonsense | 1020 | 1719 | 24 | 41 |
ENSDART00000143550 | Nonsense | 1028 | 1725 | 24 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18732901)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16769783 |
GRCz11 | 16 | 16677760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTCTCCCACTGCCTTGTCAATCCGTTACCTGGATAAAAGTCAGCGCTG[G/A]CTKGAACTAGAAGCAGGATCCMGAGACAAAGCACTGGATTTCATTGAGCA
Long Flanking Sequence:
CTTATTGGTCACGTCATTTCATTTCTCACCACAGATACTGTATAGATTTTTGCTTTTATAAAAATAAATATTTTGGGGGAATTTGTAAAAGCTCTGTCAGTTTTGGACATTGTAACTTTACCATGTGTAAAATCTGATTTTTGTTTTATCAGGCAGAAGTGATCACCGCTTATCCATCAATGGATTTTTCCCTAACAACACAGTTCCTGAAACTGATGTTAATCTATTTGTCAAACTAGAAGGTCCAGAGCAACAATTTGTTGAGGATGCTTTCAAATTCTCAATTTTTTAAGTCTAATTTATACTCGATAAAAAAACTAATTGAGCTCAAATTTTGTCCGTGCAGAGGAAATATTTGCCCAGTCCACTGCAGTTCCATTACTTTCATCATCCAAAGTGGAAAATCTGATCCAAGCACCTAAAGGCTGTGGAGAACAGACTATGATCTTTATGTCTCCCACTGCCTTGTCAATCCGTTACCTGGATAAAAGTCAGCGCTG[G/A]CTGGAACTAGAAGCAGGATCCAGAGACAAAGCACTGGATTTCATTGAGCAAGGTTTAGTATATCTGTATGCCATAATTAAAAAAAAAAAAAAACAGACCATGCCATTTTCATTTACTGCAAAAAAACTTCAACAGATTTTTTACTTGTTTCTAGTCTAAGTGTCTAAACATTAAGAATTTTTTCAGAAATAATAAATCATAAGTGAGTTTTACCTTTAAAAAAAAAACAATCTGCCAATGGGATTAGCAAAATCATCTTACGTCAAAAGGAAAAACAAGATTGTTTAGTTTACCCCACTGGCAGATTATTTACATTTTTTAAGGAACAACTCACTTATTTTTGCCATATTATTTCCTAAAACAAGACAAAGTTTTCATCTAGAAAATGCTTCTTGATTTAAGAACATTTCTATATTTTGAACAAAAACAGACAAAAAAAGTAAGAAAAGCATTTTTGCATTGTACAAAACAACAAAAGGTTTTGAGAGACACATGTACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14061
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079630 | Nonsense | 1480 | 1719 | 35 | 41 |
ENSDART00000143550 | Splice Site | None | 1725 | None | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18722772)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16759576 |
GRCz11 | 16 | 16667553 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTTAACTTCCTTTGTTTTTTTNCTCCTTTTCCCTRATTTCCTATGCAA[C/T]AGCTGAAAGGCCTGGTGGACAAATATATTTCTCACTATGAGGTCACACGT
Long Flanking Sequence:
TGTCCAAGACTTAGGGTCTTTTAACCTAAAGATAAAAATACATTCATCTCCAAAACACAAATTACCATAAGATAATTTGAATGACATCTGCGAGCTTCCTCATCCTTAGTAGACAGAAATGGTCCTAAGACACTCAAAGTCCAGAAAGGTACCAAAAACATCCTCAAAACAGTCTATCTGTCTTGAAGTAAGATGACTTTTTCTAAAATGTCCCTGACATTAGATTTTTTTTTCTACTTTTATGAAGCCTGTATATACTACACAACTGTTGTTCTTGGATGACAATTTTGACTAGCCAGTTATAGGTTATAACAAAAATACAGGTATTAATTTTTATCACCAGGCAGCAGATGACAAAACTGAACCATGTGATTATGTTATGTTTGTATATGCTGATATAATTAATATAATTGAACTGTATAATTTTTTTTTTCATTTCTTTGTCCGTTTTGTTTTAACTTCCTTTGTTTTTTTCTCCTTTTCCCTGATTTCCTATGCAA[C/T]AGCTGAAAGGCCTGGTGGACAAATATATTTCTCACTATGAGGTCACACGTGGAAGAGTACTGTTGTATTTCAATGAGGTGAGATGAGCACAAAAAATAGACATATAATTATATCTCTGCATGCTGGATAGACTTTCTTGAACCTGTCTCTCTGTCACTCCTCAGATAGATGGAGGTGAAGCCTGTATTGCATTTGGAGCTGAGCAAAGTGTGCCTATTGGTTTAGTTCAACCTGCTCCAGCTTTGTTTTATGATTACTATGAACCAGGCAAGCTGTTCCTTCATTACAAGTCAGATGTACCATAACAATACTACTTTTTATAAGTTGTAAACTTCCCCTATTGTATACAAAGTTATATACCAATATACACTGCAACTTAAGAAGGTTATGTTGTATAGGGAGCTATATATTCTAATGATATTTATGTTTTTATACTGGAGTACTTCACACTAGCATACTTTTCATTAAATTTTTTTTCTGATTTGTCGTTGCCATGATGT
Associated Phenotype:
Not determined