ZMP
c3b
Ensembl ID:
ZFIN ID:
Description:
complement component c3b [Source:RefSeq peptide;Acc:NP_571318]
Human Orthologue:
C3
Human Description:
complement component 3 [Source:HGNC Symbol;Acc:1318]
Mouse Orthologue:
C3
Mouse Description:
complement component 3 Gene [Source:MGI Symbol;Acc:MGI:88227]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32792 | Nonsense | Available for shipment | Available now |
| sa16773 | Nonsense | Available for shipment | Available now |
| sa12266 | Essential Splice Site | Available for shipment | Available now |
| sa25701 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa15993 | Nonsense | Available for shipment | Available now |
| sa18244 | Essential Splice Site | Available for shipment | Available now |
| sa13120 | Nonsense | Available for shipment | Available now |
| sa39716 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32792
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 |
|---|---|---|---|---|---|
| ENSDART00000019644 | Nonsense | 191 | 1654 | 5 | 41 |
| ENSDART00000127714 | Nonsense | 168 | 1628 | 4 | 40 |
Genomic Location (Zv9):
Chromosome 1 (position 56782599)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55566532 |
| GRCz11 | 1 | 56235828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAGCATCAGATGCAATAAAGGCAGAGAAAGGTGTGAAGTCTTCAATCTA[C/A]AACATCCCTGATGTTACTAGGTGTGTACAGTAAATCACTGTTGAGACAAA
Long Flanking Sequence:
ACAGGATTTTTTCTATGACACCCAACTTGAAACCACTCAGTCAGCCTGGAATCACAGTGGATATCATGGTACATTCCTTTGTTCTTACCACTTCTATAACTATAACACTGGCAATAAACTTTTACCCCAAAATGTGTAGTAACTATAACAGTAACAGCACTCGCTAAAGAACTATAACAGTAAAAATATGCACAGTGTTAAAATGAAACATAGTTTAAAGTCTAAATTTCCAATACTTGCTTTGTGGCCTGATACCTGTACTTTTCACAATCCTCGTAGATAGAATTGTTTACTAAATATTTTTGTTAACTATAAAACCCTGACAGCCAATCAAATTCCTGCTAAAGACTACAAATATTTAATATAGCAAATGGCAAAACTTTGATGAATTGATGAAAAATGAGTTGAATGATGATTTCTGTGTTTCCTAAGAATCCACAAGGCATCACGGTAGCATCAGATGCAATAAAGGCAGAGAAAGGTGTGAAGTCTTCAATCTA[C/A]AACATCCCTGATGTTACTAGGTGTGTACAGTAAATCACTGTTGAGACAAAAATTTTTCAAGTAGAGTTAACTGGTCAAACTTAATTTCTAGTTGCCTTTTATATTTAATTCCGGAAAGTATAACGTTAATGTAATATATTGACATTTTGATGCGCAACAGGAGCCTCAACTGCTCTACTATCATCCGCTCATGGTGACATCTTATGATTTTAAAATATTTCCACATAATTAAGAAGTTTATTTACAAGCTAATTTCGAGAAGATCATGTGCTTATGATTGATCACAGCCGGTCCTGCACTAGCTAACACAGGATTCACCAATCAGATGATTCCTAAGTCACTATAAATAACCAGAATTTCATACCTCAGTTATCTTCATCTTACCCATCCACCCATACTCCTCCCCCTTTTCCTAGATAGGGCAGCACGGCAGCTCAGTGGTTAGCACTGTTGCCTCACGGTAAGAATGTCACTGGTTTAAGTCCTTACCAGTCCAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16773
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 |
|---|---|---|---|---|---|
| ENSDART00000019644 | Nonsense | 787 | 1654 | 19 | 41 |
| ENSDART00000127714 | Nonsense | 764 | 1628 | 18 | 40 |
Genomic Location (Zv9):
Chromosome 1 (position 56794186)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55578119 |
| GRCz11 | 1 | 56247415 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAACATTTTGTATCTTTCTCATAACCCAGTTCAAAACCAAGCAAGGAC[A/T]AAGTGATTTACCTARAAGACTCTATTACTACYTGGCAGATCTTGGCTATC
Long Flanking Sequence:
CTGCTGGCCTCACAAACACCACTCCCAGCAGCAACCTAGCTTTCCATGTGGTCTCTAATTCCCTCCAATCCTATTCCAGGCACAGCCCTGCTTAGCTTCAGTGGGCGACCATGTGAGAGTTGCAGAGAGCGAGCTGCCGACTAGCAGCAGATTGTGCCTTTAACTTAACAATGCTTCACAATGTAATGTGCTGTGTGCTCTTAAAAGTATATTCTGATATTTATAATTACAAAAGGTGATGAAGACGAGGAAGGGGATTATAAAGACTATGATGACATTACATCACGCACGCAGTTTCCTGAGAGCTGGCTTTGGGAGGAGTTTGATCTCTGTGACAAGTGGTGGGTAAAAGGAGACTTTTAGACTGTAAACTGAGCCATCAAACATGACCTCTAGCGTATAAAACCAAATAAGTCAGGTGATTTTGCTTTATTTGAACAATAAGCGCAATGAAACATTTTGTATCTTTCTCATAACCCAGTTCAAAACCAAGCAAGGAC[A/T]AAGTGATTTACCTAAAAGACTCTATTACTACCTGGCAGATCTTGGCTATCAGCCTCTCACCAACACACGGTAAGGTGATTCTGCAAACCCAGAATACGCATTCTGAAAAAAGCCACCATAATTAACCTTTTTTGTGTGGGTTTGTTCCTCCTCAAAGGCATCTGTGTGGCAGAACCTGAGGAGATCGTCGTTTTTAAGAGTTTTTTCATTGACCTCAAAGTGCCTTACTCAGCTGTACGAGGTGAACAAGTGGAAATCAAGGCCATTATTCACAACTACACCCCCAAACACCTGAAGAAGGTAGGTTTGACATTCAGAATTTATTAATAAATACCACACGCATCGTAGTAGCCATTTATACCCAAGTCAAATGACAGTAAGTACTGTTTCAGAAAACCAGTGCGAATTTGTGAATCACTCTAAAGAAAGTGTTGTATAATATCAAGCGCAAAAAATAGAAAAGTCTTTCATCATACATTTCATGTACATCTATTTTGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12266
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 |
|---|---|---|---|---|---|
| ENSDART00000019644 | Essential Splice Site | 857 | 1654 | 20 | 41 |
| ENSDART00000127714 | Essential Splice Site | 834 | 1628 | 19 | 40 |
Genomic Location (Zv9):
Chromosome 1 (position 56794487)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55578420 |
| GRCz11 | 1 | 56247716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAATCAAGGCCATTATTCACAACTACACCCCCAAACACCTGAAGAAG[G/A]TAGRTTTGRCATTCAGAATTTATTAATAAATACCACASGCATCGTAGTAG
Long Flanking Sequence:
AGAGCTGGCTTTGGGAGGAGTTTGATCTCTGTGACAAGTGGTGGGTAAAAGGAGACTTTTAGACTGTAAACTGAGCCATCAAACATGACCTCTAGCGTATAAAACCAAATAAGTCAGGTGATTTTGCTTTATTTGAACAATAAGCGCAATGAAACATTTTGTATCTTTCTCATAACCCAGTTCAAAACCAAGCAAGGACAAAGTGATTTACCTAAAAGACTCTATTACTACCTGGCAGATCTTGGCTATCAGCCTCTCACCAACACACGGTAAGGTGATTCTGCAAACCCAGAATACGCATTCTGAAAAAAGCCACCATAATTAACCTTTTTTGTGTGGGTTTGTTCCTCCTCAAAGGCATCTGTGTGGCAGAACCTGAGGAGATCGTCGTTTTTAAGAGTTTTTTCATTGACCTCAAAGTGCCTTACTCAGCTGTACGAGGTGAACAAGTGGAAATCAAGGCCATTATTCACAACTACACCCCCAAACACCTGAAGAAG[G/A]TAGGTTTGACATTCAGAATTTATTAATAAATACCACACGCATCGTAGTAGCCATTTATACCCAAGTCAAATGACAGTAAGTACTGTTTCAGAAAACCAGTGCGAATTTGTGAATCACTCTAAAGAAAGTGTTGTATAATATCAAGCGCAAAAAATAGAAAAGTCTTTCATCATACATTTCATGTACATCTATTTTGGGATGTATATCCTCTAAATCAGGGGTGTTCAAACTTGGTCTTGAGAGGGTTGGTGTCCTGCATAGTTTAGCTCTAACTTCCCCCAACACACCTGTCTGGAAAGTTCTAATATACCTTGGCTGTTTCTCAATTCCAAGAACGCAGAGAACAGACTTGCGTTCTTGTGGAGACTGGTTTTGCCAGGTGTCCTCGGAAGAACTCAGGAGTCTGCAAGGACAGAGGATGCGTCCTGTGAGAAATGAGATGCTGCGTTCTTCCTGATGGTCACATGACCTTCACGTGTTTTAAATGGAATATTAAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25701
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019644 | Essential Splice Site | 947 | 1654 | 23 | 41 |
| ENSDART00000127714 | None | None | 1628 | None | 40 |
Genomic Location (Zv9):
Chromosome 1 (position 56796047)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55579980 |
| GRCz11 | 1 | 56249276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTACAAAATCTGTTCATGCCTCTTCTTTTACATTCTCTGTTTTTATGTC[A/T]AATGGAACAGGGGAAAAACCCTTAGTTCTTCGATCTGGTATACCAGCAGA
Long Flanking Sequence:
TCACCAGGTTCGTGTGGAGTTTTTGGAGACAGCAGGTGTTTGCAGTGCTGCCAGTAAGAAAGGGAAATACAGAACAACAGTAAATGTTGACAAGGACTCCAGCGTAGCAGTTTCCTTTGTGATCGTTCCAATGACACTGGAAAGTCAGCATATTGAGGTGAAAGCTTCAATATCAGATTATGAAGATGGAGTTAGAAAGACCCTGAAGGTGGTGGTACGTCTGATCCAGTTTCAGGACTTAATATGATAGATCTTTCTCATATGTTTCTCATATGTTTGTGGTGTACTAGGATGGTTAATAATATCTCCGTCTTTCAGTCTGAAGGTGTGCTGACTAAATTTCGAACTGAAAAACTGGAGCTTAACCCAGGCAAAAAAGGTTTGATTTACTATGAATCACACATTTTCAGTCATTCTAAGCTCAACACTTGCTTAGTTATAATGCAAAAGTGTACAAAATCTGTTCATGCCTCTTCTTTTACATTCTCTGTTTTTATGTC[A/T]AATGGAACAGGGGAAAAACCCTTAGTTCTTCGATCTGGTATACCAGCAGATCAGGTTCCAGGCACACCAGTTAACTCGTACATCACAGTTACTGGTAAGAAAATGTTTTTATTATTATTATTTTTTTTTTTAAAGAAGCAATACGTGAACAGTCATATTGCACCATGCATTTTAGAATCGTAAACATTGCCACATTTGGTTTTGCGTCTCCCTTTAAGATTCTTTTTCAGAATTCCCTGCAGTTTTGTGGTAGTTAGTCATTTGTTTTTACTATTGCTATTGTTTTGGTCAACTTTTAAGTCCATTTTATATTGTTAAGTGCCTAGGTTCATTTATATGCTGATTGTTGATGTATCTGAGTGTCTAAAGCAGGGGTGCCCAAACTTCGGTGTCCTGCAGATTTTAGCTCCAACTTGCCTCAACACACCTACACGAATGTTTCTTGAAAGCCTTGTAAGAGCTTGATTAGCCCAGGTAGCCCAGGTATGTCTCAGGCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15993
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 |
|---|---|---|---|---|---|
| ENSDART00000019644 | Nonsense | 1100 | 1654 | 26 | 41 |
| ENSDART00000127714 | Nonsense | 1074 | 1628 | 25 | 40 |
Genomic Location (Zv9):
Chromosome 1 (position 56797318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55581251 |
| GRCz11 | 1 | 56250547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTAAGCTTATTGCTATAGAGGAAAMTGTGATCTGCAGCGCCCTCAAGTG[G/A]CTAGTTATGCACAAACAACTACCWGATGGCTCTTTTAAAGAGGATAAACC
Long Flanking Sequence:
TTCATTGCCACTCATTATCTGGACAACACCAATCAGTGGGAATATGTTGGCATTGACCGCCGTAAAGTTGCCATTAACCATATCAAAACAGGTCAGGATACAACATATATATAGAATTTGAACCAAAATTAAAAAGCACTCTTGGATGTTCTCCCGAATCTTGAAATGCACATTCAAATTAATATTTGTTCTACTTTAAGGTTATGAAGGGCAGCTAAAGTTTCGTAAACAAGACGGATCTTACGCTCTCTGGATTGAAACAGAAAGTAGCACATGGTAAAACGTATATATTTTATTTACACTTGTCTGCATGTCCACTTTGTCATCCCATGTGTTATTTAATGTGAAATTCATGCTTGTAACAAATGATCGTTTGTTAATTATTAATTTGGTTGATTTTTGATTTGTTGAAGGCTGACAGCATATGTGGCAAAAGTCTTCGCCATGGCAAGTAAGCTTATTGCTATAGAGGAAAATGTGATCTGCAGCGCCCTCAAGTG[G/A]CTAGTTATGCACAAACAACTACCAGATGGCTCTTTTAAAGAGGATAAACCTGTATATCACCGGGAAATTATGGTAAATTGAATGACATTAAGATGCTATTTATAAACAAATTCCTGAATATATTTTATAAATTTGTACTATTCTGTTCACTTTTGCTTTATTCCAGGGTGGCATAGAAGGCCAAAACACTGATGTCTCTCTGACAGCCTTTGTCTTGATTGCCATGCAAGAAGGCAAAGAGATCTGTGGGGGAGCAGTTGGAGTGAGTATACCTCTTTGCCTTAAATAGTTGCATTTTTCTTCCTCTTGGGTTTAACATCATACACTTTTTTATAGAGTCTGCATGAAAGTATAAGGAAGTCAGTTGCTTTCTTGAAAAATCAGCTCACAAAACTGACCAATCCTTATGCAGCTGCGTTGACGTCCTACGCCCTGGCCAATGCCGACAGTCTTGATAAAGAAATCTTGATGAAGCATTCCACCAAAGGAAACGGTCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18244
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 |
|---|---|---|---|---|---|
| ENSDART00000019644 | Essential Splice Site | 1125 | 1654 | 27 | 41 |
| ENSDART00000127714 | Essential Splice Site | 1099 | 1628 | 26 | 40 |
Genomic Location (Zv9):
Chromosome 1 (position 56797484)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55581417 |
| GRCz11 | 1 | 56250713 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATATATTTTATAAATTTGTACTATTCTGTTCACNYTTTGCTTTATWCCA[G/A]GGTGGCATAGAAGGCCAAAACACTGATGTCTCTCTGACAGCCTTTGTCTT
Long Flanking Sequence:
TGCACATTCAAATTAATATTTGTTCTACTTTAAGGTTATGAAGGGCAGCTAAAGTTTCGTAAACAAGACGGATCTTACGCTCTCTGGATTGAAACAGAAAGTAGCACATGGTAAAACGTATATATTTTATTTACACTTGTCTGCATGTCCACTTTGTCATCCCATGTGTTATTTAATGTGAAATTCATGCTTGTAACAAATGATCGTTTGTTAATTATTAATTTGGTTGATTTTTGATTTGTTGAAGGCTGACAGCATATGTGGCAAAAGTCTTCGCCATGGCAAGTAAGCTTATTGCTATAGAGGAAAATGTGATCTGCAGCGCCCTCAAGTGGCTAGTTATGCACAAACAACTACCAGATGGCTCTTTTAAAGAGGATAAACCTGTATATCACCGGGAAATTATGGTAAATTGAATGACATTAAGATGCTATTTATAAACAAATTCCTGAATATATTTTATAAATTTGTACTATTCTGTTCACTTTTGCTTTATTCCA[G/A]GGTGGCATAGAAGGCCAAAACACTGATGTCTCTCTGACAGCCTTTGTCTTGATTGCCATGCAAGAAGGCAAAGAGATCTGTGGGGGAGCAGTTGGAGTGAGTATACCTCTTTGCCTTAAATAGTTGCATTTTTCTTCCTCTTGGGTTTAACATCATACACTTTTTTATAGAGTCTGCATGAAAGTATAAGGAAGTCAGTTGCTTTCTTGAAAAATCAGCTCACAAAACTGACCAATCCTTATGCAGCTGCGTTGACGTCCTACGCCCTGGCCAATGCCGACAGTCTTGATAAAGAAATCTTGATGAAGCATTCCACCAAAGGAAACGGTCAGTAACACCAACAGGCCAACGATATGTTAAAAAACATGGAACATTCGAATAAACCAGACTTAAATAATAACATAGTACTTTTCTAACACAAGTGCTTTACGCATTTGGGAGGAAGCTCCTCAACTACCATCTGTGTTTATCCCAAATGATTTGACAAACCAAATGATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13120
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 |
|---|---|---|---|---|---|
| ENSDART00000019644 | Nonsense | 1446 | 1654 | 36 | 41 |
| ENSDART00000127714 | Nonsense | 1420 | 1628 | 35 | 40 |
Genomic Location (Zv9):
Chromosome 1 (position 56807782)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55591715 |
| GRCz11 | 1 | 56261011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWTGTATAAAGAATCATCTGCTTTGATTNNTGTCTCATTAGGTTTCTCAT[A/T]AGGAATCAGAAACDCTTGTCTTCAGAATGCACAAGACTTTTAACGTGGGT
Long Flanking Sequence:
ATTGCGCGGATTTCCAATTATTTCCAATGTTTTCTTACAGGAACATACATTAAAAAGAAGTTACTGGCGAGTTACTGATGCGCATTGATGTTATATTTATCTTTAAAAAAGCGGGAATCTCATGCGACAGTACAAAACAGGTTTGCTGCTTCAGGATATTTCAGACATATGGACATATTGGATAATTAATTAGAGCAAAGCCACAGCACACGCAACTTGATCTTCGATTGTTAAATGAATTGGATAAGAAGTGCGCAACATTTTATTTTAAATACGAGATCAATGTAGCGAGTTTTGACGCTCTCGCCGCCGGAGCTGAAGACAGACAGCGTTGTCGCCAGGGCGGCCAGAGTGACATTGGACGCTCTCACCGCTTTCGGTGTGAACGCACAGTAACGTCACAAGCATAATACGAGAGCACTAAATTATGTAAGGGCCATTCAAAACAGTAATGTATAAAGAATCATCTGCTTTGATTTCTGTCTCATTAGGTTTCTCAT[A/T]AGGAATCAGAAACTCTTGTCTTCAGAATGCACAAGACTTTTAACGTGGGTTTGCTTCAACCTGCTTCCGTCACCATATATGAGTATTACTCACCCGGTAAGCTGCTGTCCGCACACCCTGTGTTCACACACGTGCACGCACACATTTCAAGAGTTTACACTTAGCTTATAATCAATAAAGTGTAATTGGCATGATGTCCGAGGAGAGAACCCTGAGCTCGTAATATCCTCGAGCCTGTCATCTGTTATTTCTCTCTATAATTAAGCCTATAATGCACAATTCCAGCCAACGTCATCCCCCCCCCCCCCCACACCCCCAAAAAAATTGTTACATCACAATTGTAGTTTTTTTTTAAATTGTCAGTTGTAGGCTATTAAAAGAAAAGTTGGGTCATTGGGCCAGTAAAAAAAAATCTTAGCGTTGAACTCTGATTGTCATATGGCATTTATTGAGATTCATAAATTTCCTTTGCATATCATTAGTCATTTACAGTGTCATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39716
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019644 | Essential Splice Site | 1608 | 1654 | 41 | 41 |
| ENSDART00000127714 | Essential Splice Site | 1582 | 1628 | 40 | 40 |
Genomic Location (Zv9):
Chromosome 1 (position 56813163)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55597096 |
| GRCz11 | 1 | 56266392 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCCCTAAGTCAGCCACTCATTAATGTATGGTCTTTACTTTTGTGTCTA[G/A]TCTGCAGTACATCATAGGAGAGCAGACCTGGATTGAATACTGGCCTACAA
Long Flanking Sequence:
TAGTTAATTTATTATTAATGACGATGTTTAAAAAATAATAATACTATTAATTTTATTTAGTAATACAATTATAATGTAATAGGCCTACATTAATGCAAAACGAGCTAAATATCGTCTTTAAAATCGTCATAGGTCTCAGCTCTTGCCGATATCTTTCGCTCAACCCTATGACGCGATATTGTGAATGTGATGTGATAACGGCAGCAACTGAACCATTAGAAATAGGAAAACAATAGGTTATGAGAAGCATTTGAAGAGACATCATATAACTCAGGATATCTGGTTGTCCCACCTCCGAACTCTTCTGGTTGTTTGCTGCTTTTGAAGCTGACAATGATGAGCTGCGCTGCTTGTGACTAAGCTAATCACAGACATCTGACCAATGCGTTTACAATGAAAACTAATAGAAAGGAAGCACATCGGAGAGCAAAAAAGGCATTCTCTGTGAGCAGCCCCTAAGTCAGCCACTCATTAATGTATGGTCTTTACTTTTGTGTCTA[G/A]TCTGCAGTACATCATAGGAGAGCAGACCTGGATTGAATACTGGCCTACAAGTGACGAAAGTAAATCTGCTGAACACAGAGATCGCTACATAGGCATGACTGCAGTCGAGAATATGTTTACCACAGGAGGATGTTTGACATAACTGCATTACACCTGTTTGCTGATTAAAGATAAAAATTAAACACCATCCTTTCTATTTCCAAATAAATTGTATGTACTGTTGTTTGAGCCTAATCTCTTGTAATTAATTATTAAAAACAAGACTGTATCAAATGATTGTTTTAGATTCCTGCCTAATAAATCATGGTGTTACTGTACATGTTGTTCTCTGCAAAACTATTCTGATTACTTCATTATTCAACATTTGTGTCATATTTCTTTGACCACAAAGTATGTATCTATACAGTCAGTTTAATCATCATAAGGGAGTATGAAGGTGAATTTCTGAACTGATCGAGTGTGATTTAACAGCTCTATATTATTACAGATAAATATATCAT
Associated Phenotype:
Not determined