ZMP
wu:fi14a03
Ensembl ID:
ZFIN IDs:
Description:
Wu:fi14a03 protein [Source:UniProtKB/TrEMBL;Acc:A6H8S2]
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 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22687 | Nonsense | Available for shipment | Available now |
sa22686 | Nonsense | Available for shipment | Available now |
sa45548 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35937 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45547 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35936 | Essential Splice Site | Available for shipment | Available now |
sa35935 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42584 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22685 | Nonsense | Available for shipment | Available now |
sa12226 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22687
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 |
---|---|---|---|---|---|
ENSDART00000028349 | Nonsense | 267 | 1700 | 8 | 41 |
ENSDART00000125214 | Nonsense | 267 | 942 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31627454)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32523106 |
GRCz11 | 15 | 32381085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTTTCAGATATACTTATGGAAAGGGGGTCAATGGGATTGCATATGTT[C/T]GATTTGGACTTGTTGATGAAAAGCACAATAAGATATATCTTCCAGGCACT
Long Flanking Sequence:
CAAATATGCAATATAATATGCATCATAAAATAATTTCACGATAGGAAGCATTGTATTCTAAGAAAGGGTTGGCCTTTTAATGAATCTCAGTGATATTTCATGCAATTTTTATTAATCCTTCAGAACAGGCAAATGGAAAATCATTACGTCATTTCATAAATTCCCAGAATCGACCACAACAGTGGAGTTTGAGGTCAAAGAATATGGTAGGTGTCATCCGACTATTCAAAGAGTTCTTAATTATTTAATCTGTCAGAATAACCCCCTGAAATGCTGTTTCACAGTTTTGCCCACATTTGAGGTGAAGATTGAGGCTTCACAGCCTTATCATATTTTGATGAGCGAGTCCTTTCCCTTCAACATTTCTGCTAGGTTTGTTCAGTATACTGTCACGTTTAGATTGGGTTGGTTGTTGAATTAAGGTTTTGTGATCTAACCCATCAGTCTTTGGTGTTTTCAGATATACTTATGGAAAGGGGGTCAATGGGATTGCATATGTT[C/T]GATTTGGACTTGTTGATGAAAAGCACAATAAGATATATCTTCCAGGCACTGAAAAGCAGATAACTGTGAGTAAAAAATTGCAGTAAAATGTTTGTGATAACAAAAAAAAAAAAAGAAATGTACTTGTCAGAATCTGATGTGTTTTATTTGACATTCTGCTGTTTTGTAGGTAGAGGACGGCACTGCAGGAACAGCAGTACTTACTAAAGACTTAAAAACAGCATCACAAAATATCACTCAAGGCTATATAGAAGGATATTATATTTATATTGCGGTCTCAGTTTTGGACAAAGCAAGTAAGTCATAATTGAATTTTTTTTGTAGATCAAAAAGTGCATGCAGCTAATCAGAAATTTACAATTAACAATTACAATTAGCATAAACATTTTATTTTTATTTTTGTTTTATTTTTGCTTATTTTATTTAAATTTTGACTTTTTTTTAGGTTTAGCTGTGTGGCAAATATCTGTTTTTTAATCAATGTATTAAATAATTATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22686
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 |
---|---|---|---|---|---|
ENSDART00000028349 | Nonsense | 286 | 1700 | 8 | 41 |
ENSDART00000125214 | Nonsense | 286 | 942 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31627397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32523049 |
GRCz11 | 15 | 32381028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTGTTGATGAAAAGCACAATAAGATATATCTTCCAGGCACTGAAAAG[C/T]AGATAACTGTGAGTAAAAAATTGCAGTAAAATGTTTGTGATAACAAAAAA
Long Flanking Sequence:
CTAAGAAAGGGTTGGCCTTTTAATGAATCTCAGTGATATTTCATGCAATTTTTATTAATCCTTCAGAACAGGCAAATGGAAAATCATTACGTCATTTCATAAATTCCCAGAATCGACCACAACAGTGGAGTTTGAGGTCAAAGAATATGGTAGGTGTCATCCGACTATTCAAAGAGTTCTTAATTATTTAATCTGTCAGAATAACCCCCTGAAATGCTGTTTCACAGTTTTGCCCACATTTGAGGTGAAGATTGAGGCTTCACAGCCTTATCATATTTTGATGAGCGAGTCCTTTCCCTTCAACATTTCTGCTAGGTTTGTTCAGTATACTGTCACGTTTAGATTGGGTTGGTTGTTGAATTAAGGTTTTGTGATCTAACCCATCAGTCTTTGGTGTTTTCAGATATACTTATGGAAAGGGGGTCAATGGGATTGCATATGTTCGATTTGGACTTGTTGATGAAAAGCACAATAAGATATATCTTCCAGGCACTGAAAAG[C/T]AGATAACTGTGAGTAAAAAATTGCAGTAAAATGTTTGTGATAACAAAAAAAAAAAAAGAAATGTACTTGTCAGAATCTGATGTGTTTTATTTGACATTCTGCTGTTTTGTAGGTAGAGGACGGCACTGCAGGAACAGCAGTACTTACTAAAGACTTAAAAACAGCATCACAAAATATCACTCAAGGCTATATAGAAGGATATTATATTTATATTGCGGTCTCAGTTTTGGACAAAGCAAGTAAGTCATAATTGAATTTTTTTTGTAGATCAAAAAGTGCATGCAGCTAATCAGAAATTTACAATTAACAATTACAATTAGCATAAACATTTTATTTTTATTTTTGTTTTATTTTTGCTTATTTTATTTAAATTTTGACTTTTTTTTAGGTTTAGCTGTGTGGCAAATATCTGTTTTTTAATCAATGTATTAAATAATTATTTTATTTAATTTTTCGGCTTTAGAGCTTTACTTTTTTCTTTTTATTAATCACTAAATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45548
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028349 | Nonsense | 400 | 1700 | 11 | 41 |
ENSDART00000125214 | Nonsense | 400 | 942 | 11 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31625153)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32520805 |
GRCz11 | 15 | 32378784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAATTTACAGCCACCATAACAATTGATGGATCATCAGAGCAGATTCTG[C/T]AAAACGAAAGCTGGGGAAATGAAATGGGAGATGTTGCCATGTCTTTTCAA
Long Flanking Sequence:
TGTGGCGAAGCAGTGGCGCAGTAGGTAGTTCTGTTGCCTCACAGCAAGAAGGTCGCTGGTTCGAACCACGGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGTGTGGGTTTCCTCTAGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGAAGGCTAAATCCGTAGTGTATGCGTGTATGTGTGTGTATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCTGCTGCGTAAAAACCTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGTGACCCCGGATTAATAGAGTGATTAAGCCGACAAGAAAATGAATGAATGAATGTTTAAATGTATGCTAGTACCACATCTGCACTTTTGCATCATTTTTTGCAGGCTACTGCAACTTATCCAGATGGAAACAGAGCCCCGAACTTGAAATTTACAGCCACCATAACAATTGATGGATCATCAGAGCAGATTCTG[C/T]AAAACGAAAGCTGGGGAAATGAAATGGGAGATGTTGCCATGTCTTTTCAAATTCCACCACAGGCTAAGAACTTAGCTATAACAGTAAGCTTTATGTGTCTCTTGTATTGACCAATCGGTATTAAAGATCGAAGCTGTCAGCTTTTCTAACTAATATTTTCGCAGGTATTTGCTGAAGGTGGAGACCAAGTCGTAATTCGTAGTGATAATAAGATGACTGCCAGTGCAATAACAGCTGAAGAACAGAGCTATCTGAGTTTGGAAGTAGAGAAACAGTTCTTACAAGCTGGTGAGGACTTGAAAGCCAGATTGCGGGACATCACCCCTGAGGGTGCAGCCAAACCGACTTTCTTTTATTTTATGGTATGTACCATAGAATGATTGTTTGTTTGTTTTTTTAACAATGAGGAATGTGTCGCTATAGTTTTTAGTCTAATGTCTTTCATTGTTTTAAAATAAACAGGTTTGGAGTAAGGGGCAAATTGTGCAGATGGGGCGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35937
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 |
---|---|---|---|---|---|
ENSDART00000028349 | Nonsense | 614 | 1700 | 15 | 41 |
ENSDART00000125214 | Nonsense | 614 | 942 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31622885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32518537 |
GRCz11 | 15 | 32376516 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGGGGGGATTTGTTTTGCACACAGATGTTTGATTATATGAACTCGTA[T/A]GACCTGGCCTGCTCTGTTGGAGGAGGAGAGGATTCTAGTGCTGTTCTGCA
Long Flanking Sequence:
ATCAATTGAGATTGTGCTCTCACCAATCTTTTCAAAATAAAATGGTCAGCCTATTCTTTTTTTACATATTTTAATAGTTTAGTATAGATCATTTTGAAAATTATATTGCAATCCTGGAGACAGAAAGGTAAAAGATCAATTTATTATCAAAATATTTAATGAAAATATGCGTAGCAGCTCATTGGAAAAAAAAAAAAAAAACAACGGTGTGAAAACTAATGGCATATAGCTGCTTCTAACTCGGGACTGTTTATACTCAAAGTGTTTCTGCAAACTATTGACTGTTTTTATGAAGTGTTTTTATAAAGTGGGATACCAACAGAGGTTAGCTATATTCACATACTGTTGCCACAAAACTGTGTTTATACCCTTTATAAATGTGATTTTTTTCATAATAGGTCCCCTTTAAAAGTACTGCATGTACTGTACCTCTTTAGTATTGGTTCTCATGATGGGGGGGATTTGTTTTGCACACAGATGTTTGATTATATGAACTCGTA[T/A]GACCTGGCCTGCTCTGTTGGAGGAGGAGAGGATTCTAGTGCTGTTCTGCAGAGAGCCGGGCTGACTTTCATTTGTAACTGTGCTCTTAAAACCCCTACAGCACTAGGTAAAATGCCTATGACTACTCTGTAAAAGAAAAATCTTATTCAAAGAACATACATTTTAAGATGAATCCAATTCACTTAGGTCATTAAAACTTAAATTAACTAATTAGTTAATTCAAATTAACTGATCTAAAGGCACAATGTGTCATTTTCACCACTAGAGGTTGCATGTTTGCAAAAAACAAAGGTGTGTGGTATCATGAGCTTTGTGGACTTCATTACATCCTACAATACATCACGAAATCAAGTATTTAGAATTTGTAAATATAGTAGTATGAAGCAGAGTAAGACTAAGTGCTGTTGAAGCGAAAAGAGAACATTGAACCTATGTGTGATGAACAAACAGTTAAGCTTTTATTATTCTACATTTGTTCTCATGACTTTTGATGATAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45547
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028349 | Nonsense | 845 | 1700 | 20 | 41 |
ENSDART00000125214 | Nonsense | 845 | 942 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31619903)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32515555 |
GRCz11 | 15 | 32373534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTGAAGAGAAACGAACAGCTTCAGGTTAAAGCTGTTGTGTACAATTA[C/A]AAGCAGGAGAGTTTAAAGGTAAGCTTCCGGGTGCTTTTCTTGCAAACTGC
Long Flanking Sequence:
GCACCTTTATTCTGTATTATTGATATTTTGATTAAATGTTTATGGATATACACCATCTGAAAGTTGAATAAATTAGTTTACTTAGCAAAGATACAGCAACATGAAAATCTAGAATATAAGAATGAAAAATAGAATTATATAATAAAATTATTATTATTTTTAAATTGAGAAAATCAATTTGAAGTTGCCCAAATGAAGTGCTTAGCTATGCACATTAATTAAAATATGAGTTCTGAATTTGAGTTTTGAAAATGATCTTTTTTTTAATACTCAATCATTTTGATTCATTATACAATACAATGTTTTTCTGGCAGTTGCCTTTCAGTGCAACATAAGACTGGTTTTGTCATCCAGGGTCATAAATGTTGTTGTTTTTCAGGATTTTGCATTGCTGAGCCAAAGCCCTTGACAGTCTTCAAGGATTTCTTTTTGTCCGTCAACCTTCCTTATTCTGTGAAGAGAAACGAACAGCTTCAGGTTAAAGCTGTTGTGTACAATTA[C/A]AAGCAGGAGAGTTTAAAGGTAAGCTTCCGGGTGCTTTTCTTGCAAACTGCCTTTGAAAAATATTGCCTTTGCATGTTAGATAAAAATGAAATGTAGAAATATAGTTTGAGTGTAAGTGCTGAGGATGCTGTATGGTGTGTGTTTGTAGGTAATAGTGAAGCTGAATAAGGTGGAGGGTTTGTGCACTGCTGGAGGTAATGATGTGAAGGAGGAGGTCACAGTTTCTGGTAACTCAGCAGTGACCGTGTATTTCACTGTGGTGCCCCTTATTATTGGGAACCTCCACATTGATGTTCTAGCTTATGCTTCCGAAATCATCCATGATCGAGTCGAAAAGAAACTTCGTGTGGAGGTAAAGTATGTTCATTTTTTAGATATTAATATATTTTACAAATGCTACTGTATGACCATTTCTGTATCTACAGGGGTTTCTGTAGAAATTGCTGCCTTATTCATTTTCGTTTTATGATTGGTTTTGAGACTGAAGTTTAACAGTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35936
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 |
---|---|---|---|---|---|
ENSDART00000028349 | Essential Splice Site | 919 | 1700 | 21 | 41 |
ENSDART00000125214 | Essential Splice Site | 919 | 942 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31619550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32515202 |
GRCz11 | 15 | 32373181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTTCCGAAATCATCCATGATCGAGTCGAAAAGAAACTTCGTGTGGAG[G/A]TAAAGTATGTTCATTTTTTAGATATTAATATATTTTACAAATGCTACTGT
Long Flanking Sequence:
GGGTCATAAATGTTGTTGTTTTTCAGGATTTTGCATTGCTGAGCCAAAGCCCTTGACAGTCTTCAAGGATTTCTTTTTGTCCGTCAACCTTCCTTATTCTGTGAAGAGAAACGAACAGCTTCAGGTTAAAGCTGTTGTGTACAATTACAAGCAGGAGAGTTTAAAGGTAAGCTTCCGGGTGCTTTTCTTGCAAACTGCCTTTGAAAAATATTGCCTTTGCATGTTAGATAAAAATGAAATGTAGAAATATAGTTTGAGTGTAAGTGCTGAGGATGCTGTATGGTGTGTGTTTGTAGGTAATAGTGAAGCTGAATAAGGTGGAGGGTTTGTGCACTGCTGGAGGTAATGATGTGAAGGAGGAGGTCACAGTTTCTGGTAACTCAGCAGTGACCGTGTATTTCACTGTGGTGCCCCTTATTATTGGGAACCTCCACATTGATGTTCTAGCTTATGCTTCCGAAATCATCCATGATCGAGTCGAAAAGAAACTTCGTGTGGAG[G/A]TAAAGTATGTTCATTTTTTAGATATTAATATATTTTACAAATGCTACTGTATGACCATTTCTGTATCTACAGGGGTTTCTGTAGAAATTGCTGCCTTATTCATTTTCGTTTTATGATTGGTTTTGAGACTGAAGTTTAACAGTTATGAAAGTAGTTTAAAGTGCTAGCTGCTATTTTCCTTGTAGGGACAAAGAGTTTTGGTGGATTTTGTTGGTAACTTTGTCATTTGAAATGAGAAATCATTTGTTAAATTTTGTGGCAAGGGAAGGAAAAATAATCTACATTTTATTCCACTTTGTGAAGTTTATTTATAAAATAATTTTGAGAGGGTCACATGCTTATGATTGCTTGCAGCCAGTCCCGCATTATTCAATTTAGGATTTATCAGACGATTCCTAAACCATTATAAATACCTTAAGTTCCATTTAACAGCCATCTTCGTTTTGAAGAATCCTCCTTCCACCCCTACTCCTCGTCCTTTCCTAGATGGGTGGCGTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35935
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028349 | Nonsense | 970 | 1700 | 24 | 41 |
ENSDART00000125214 | None | None | 942 | None | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31617249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32512901 |
GRCz11 | 15 | 32370880 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGTTTAGATACAGTCAGTGCTGTCTCTGTTTCAGGTGGAGTGATGGGC[G/T]AGTCAATAGACAACTGTTTAAACCTGGAGGGTATTGATAAACTGATCCAG
Long Flanking Sequence:
ACCCACTCACTGATTATGTGATAAGTTTTGAAAAACTATTTATTAATGATTTAAAGCAATTCTATAAAAAGAAAACTGTAACACGATTGCACAATGAATCAGTCCACAATAAAGAGAAACAGAAGATATTTCTTTAATGCTTATGATTTCCTTTAATAAATTCACTGTTGAAAAAGCTCTCTTTGTTATCTTCTATATTTAGGGGGAAGGTGAATTAACCTCTATCGACAGGGAGTTCAACATTGACCCAAATTGTAAGAATCAAATATATAAGCAGTATCTGTTATTATGCTTTCCTTCCATTCTAATACACTTTTTTTAATTAACAGTGAAAAAAATAGAGTTTAACATTTCATCCCCTGTTGATGAGGTCCCTGCTGGTTCAGACTCAGAAACCTCTTTAGGTTTTAAAGGTTAGTTGGTACTGTAGATAAATGGATGGATTAGTAGATAGTTTAGATACAGTCAGTGCTGTCTCTGTTTCAGGTGGAGTGATGGGC[G/T]AGTCAATAGACAACTGTTTAAACCTGGAGGGTATTGATAAACTGATCCAGCTGCCCACTGGCTGTGCAGAACAGACTATGGTGAAGATGTCTCCCGCTATTCATGCCATGAGGTATCTGGATGCCACCAACCAGTGGTTATCTCTGAAAGCTGAACGCAGAGATGAGGCCCGATCCATGATCCAAACCGGTGTGTATACATATCTGTAAATTATAAAACATTAATTAAATGGGTGTCCCCTTACAGCAAGAAGGTCGCTGGTTCGAGCCCTGACTGGGTCAGTTGGCATTTCTTTGTGGAGTTTGCATGTTCTCTCTGTGTTTGCGTGGGTTTCCTCCGGGTGCTCCAGTTTCCCCCACAGATCCAAAAAAACATGTGCTATAGATAAGTTGGGTAAGCTAAATTGTCCGTAGTGTATGTGTGTGAATGGGAGTGTATGGGTGTTTCCCATTGAATGGTTGCAGCTGGAAGGGCATTCACTTTGTAAAACATATGCTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42584
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028349 | Nonsense | 1206 | 1700 | 29 | 41 |
ENSDART00000125214 | None | None | 942 | None | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31612717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32508369 |
GRCz11 | 15 | 32366348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTAGCTCAGTTATCATATTTTCTGTTTCATGTAGAAATGTGTTTTTG[G/A]AAAGCCAAGGGTGGCAGAGGTGAACCAAAAGATAAAGCTGATGCTCGATC
Long Flanking Sequence:
TCAATATTATTAGCTCCCTTAAGCAATTTTGTTATTTTGATTGTCTACAGAACAAACTGTTTTGCAATGACTTGCCTAATTAACCTAGTTTAGCCTTCAAATTGCACCTTTCTGCTCAATTTTGGTGTCTTCTAGTAAAAATATTAAATAGTAACACATGTGATGTCATCATGGCAAAGATAAAAGAAATCAGTTATTAGAAATTAGTTATTAAAACTATTATGTTTAAAAATGTGTTGAGAAAAAATAGTTTTCATTAAAAAGAAATTGGAGAAAAAAATATACAGGTGGCTAATAATTCAGGACGGCTAATAATTTTGCTTTCAACATTGTACATTTCCATTGCTAGATCTTCCAAAAAAAAAAAAAAAAAGAAGTGTTCGCTGTGCTTTAGTTGAAATCAGTGACTTTAATTGGTGAAACTTGAATTAAAGAAGACTGCATGTGAGCGATTTAGCTCAGTTATCATATTTTCTGTTTCATGTAGAAATGTGTTTTTG[G/A]AAAGCCAAGGGTGGCAGAGGTGAACCAAAAGATAAAGCTGATGCTCGATCAGTGGAGACCACAGCATATGCTCTGCTCACTACACTCATTGTGGGTGACAAGAGCAAGTCTAAACTCATTGCAAACTGGCTGACAGAGCAGCGCAGACACGGTGGAGGCTTCCGCTCCACACAGGTGGGTTGAGAAGTTATTGTGATCCGGATAAAAAAAATGGGTTAACTGCACTACTTTAAAAAAAAGTTAGATGTTAAATTGTATATTTTTTGTATTTTTTTCTTTTCTTAAAATAGGATACAGTTTTGGCCCTTGAAGCTCTGACAAAATACAGCATACAGAACAATGATGTTGACGATCTGAATCTGAGGGTAGAAATGTGCCTTGAAAATGGCCAAAAAAAAGATTTGCACTTGACCAAAAATAATGCTCTCACTCTCTCAGCTGTGAAGGTAAGAAACTTTGGTCCCACTTTATATTAGATGGCCTTCATTGCTATTGCATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22685
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028349 | Nonsense | 1366 | 1700 | 32 | 41 |
ENSDART00000125214 | None | None | 942 | None | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31608091)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 32503743 |
GRCz11 | 15 | 32361722 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGTGATCTTTTTCACCTTACTGTCACAGTGAAGGGAGAGCTGGAGTA[C/A]AGTATGTAACATTAAGGGACACTTTCATCGTAGGACACTCTATTGTTAAA
Long Flanking Sequence:
AGAAGTTGGAGATATGAACTCATATCACATCACATACAGTACTGTATATCTTAACTGCTTACAATTCAGAATTCATCTCAGTTCTGTTTATTTGTTTACGTTTACATATTGCGATGCTGATTTCATTTGGAAATTCTGATTTATACTGTATCTCATAATATCCTGCGTTTTCATTTGAAAATTCTGATTTATGTCTCATAATGTCTTGAGTTTGCAAAACATTACTCTGTTTACACTTTGCAGTTCTTTTTTTTTCTTCTTTGAATTGACTTTTATTTAAATGTTTTGCAATTTTGAGATTATAGGCTCTTGAAATTCTCAGTTTATAATAAAAAGTTGGTGTCATTTTTATTTTGCATAGATCTCCCGCTTAGCTTCATGATAGTTTGACTGACATTTTGCTCGTTGCAGGTTGTGCAGACGTACAGAACTATGAAGAAGGATGAATCATTCTGTGATCTTTTTCACCTTACTGTCACAGTGAAGGGAGAGCTGGAGTA[C/A]AGTATGTAACATTAAGGGACACTTTCATCGTAGGACACTCTATTGTTAAATGAAGCGCATTGCAATGTCTTTAATTTCAATTTTTTAAAGGGGGAGTAGCTACAGACTTTGAGTTCTAAATGCTGTAGCTAAAAAATAAAATAAGTATTCTCTTTTGTAGAAACCGACAATAGTCAAGATCTGCTTGAAGATTATTATGAGAGCTATGACACCAGTGAAGCTCAAAATGATGAGCCCATGAGCAACATGCAGTGGTTTGACCTCCGCAGCCGCAGAAAAAGACAAATCTCGGAGGAGCCGATAAAAGAGAGTTCTCTCATATACACAGTGTGTGTGGGGTGAGTGCAGCAAAACAGCACTGTATGCAGATTTAAAATACATTGATTTGTTCTGTAAATGTTCTGCAGAATTACGATGACTTGAGATCAACTATTCAATTCATCTCTCTTTCAGCCTGAAAAAGAAGAACTCTGAGGGCATGATCATAGTGGACATTTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12226
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 |
---|---|---|---|---|---|
ENSDART00000028349 | Essential Splice Site | 1455 | 1700 | 34 | 41 |
ENSDART00000125214 | None | None | 942 | None | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 31607549)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATTTCTCTTCTGAGTGGACTGATACCAAACAGCAAAGACCTGGAACAT[G/A]TGCATATTATCTATCTATCTATCTATCTATCTRTCTRWCTRTCTRTCTAT
Long Flanking Sequence:
ATTGTTAAATGAAGCGCATTGCAATGTCTTTAATTTCAATTTTTTAAAGGGGGAGTAGCTACAGACTTTGAGTTCTAAATGCTGTAGCTAAAAAATAAAATAAGTATTCTCTTTTGTAGAAACCGACAATAGTCAAGATCTGCTTGAAGATTATTATGAGAGCTATGACACCAGTGAAGCTCAAAATGATGAGCCCATGAGCAACATGCAGTGGTTTGACCTCCGCAGCCGCAGAAAAAGACAAATCTCGGAGGAGCCGATAAAAGAGAGTTCTCTCATATACACAGTGTGTGTGGGGTGAGTGCAGCAAAACAGCACTGTATGCAGATTTAAAATACATTGATTTGTTCTGTAAATGTTCTGCAGAATTACGATGACTTGAGATCAACTATTCAATTCATCTCTCTTTCAGCCTGAAAAAGAAGAACTCTGAGGGCATGATCATAGTGGACATTTCTCTTCTGAGTGGACTGATACCAAACAGCAAAGACCTGGAACAT[G/A]TGCATATTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTATCTGTCTATCTGTCTTTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCATCATCCAAAATTTTATCCATGTTGCTCTCTTTATCTATCCATTCATTCATCCATCCATATTGCACTATCCATCCATCTGTTCATCCGTACCATTCTATCTGTATATCCATCCATCCATCCCCTTTAATTATCTATTCATCCATCCGGCCATCCATTCATCTGTTCATCCGTACCATTCTTTCTATCCTTCCACCCCCTATAATTATACATTAATCTATCCATCGATCAATCTATTAATCCTTCCATCCATTCTATTTTATCTATCTATTTATCCATTCATCCATATAAATATACCCATTCATCCATCTGTACTTTTCTATCCATCCATCTCTGATCTATTAATC
Associated Phenotype:
Not determined