ZMP
A5D6S4_DANRE
Ensembl ID:
Description:
LOC565774 protein [Source:UniProtKB/TrEMBL;Acc:A5D6S4]
Human Orthologue:
C5
Human Description:
complement component 5 [Source:HGNC Symbol;Acc:1331]
Mouse Orthologue:
Hc
Mouse Description:
hemolytic complement Gene [Source:MGI Symbol;Acc:MGI:96031]
Alleles
There are 14 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33747 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40586 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17323 | Nonsense | Available for shipment | Available now |
sa20567 | Nonsense | Available for shipment | Available now |
sa20568 | Essential Splice Site | Available for shipment | Available now |
sa33748 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33749 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31483 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33747
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 |
---|---|---|---|---|---|
ENSDART00000002540 | Nonsense | 200 | 1050 | 6 | 25 |
ENSDART00000097325 | Nonsense | 198 | 1702 | 6 | 43 |
Genomic Location (Zv9):
Chromosome 5 (position 66665734)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 62811952 |
GRCz11 | 5 | 63505343 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCACTGCATCTTTTATTCACAATCCAAACCCCACCAGTTATGGAATCT[G/A]GAAAATTGTGGCCACATATGCTGACAATTTTGAAACGACTGCTACTGCTG
Long Flanking Sequence:
CCCCTCTAAAACCAGCCTGGTCGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGCTGGATTTTTCAGCAGGGATGTCTTTGGAAACCGGAGCACTTGAAGAAAACTGACGCTAATGCAGGGAGAACATGCATCTCAATTTTCAAAGTTGTGATATTCTTTTTGAATCACACTGTATTATAAGTAGCTGTAATTAAATTACCTAAAAATAAAAAGTTATCTCTCGCTTTACTTTAAGGGCAAAAAAAGTTATTTAGTTACAGTAGTTACTTTGTTTACTTAGTACTTGGTACTTACTGATCACTTAGTGAACTTACTAACATACTTAATTCTTTGTTACCCAAGTAAGGTTGTTGAGAATTAGTTAAGAAGCCTGCCATATGCATATATCCTAAATTTCATCATTTATTTTTATTTTTTTCATGTGTTTTTATCTTTATTTTATGTCACTGCATCTTTTATTCACAATCCAAACCCCACCAGTTATGGAATCT[G/A]GAAAATTGTGGCCACATATGCTGACAATTTTGAAACGACTGCTACTGCTGAGTTTGAGGTCAAAGAATATGGTAAGGCCGCCATTTATGTTTCAACTGGCTGTGCAGACCTTTAGAGTTTGTGAAATCTGAAATCGAGATGTTTTACAGTGTTGCCCAGTATTTCGGTCCAAATTGAGCCGGAAACCAACTACATCAGTGAAGAAAACTTTGACACTTTCAAGCTGAAGATCTCAGCCAAGTAGGTTTTCCTTTTTCTTCAATTTAACACATACAAACTACTTTTCAAAAGTATTTAAGTTAGTCATTTAAAGATTTTTATTGAGCAATGAAATATTAAAGAAACACTCCATTTAAAAAATAAAAAATAATAATTCAGCTGATCTCTGGGTCTGGCGGGAGCACTTTTTGCTTAGCTTAGTTTAACATAGATCACTAAATCAGATTAGACCATTAGCATCTCACTCAAAAATTTCATGAAAGAGCTTTAATAATTGTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40586
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 |
---|---|---|---|---|---|
ENSDART00000002540 | Nonsense | 272 | 1050 | 8 | 25 |
ENSDART00000097325 | Nonsense | 270 | 1702 | 8 | 43 |
Genomic Location (Zv9):
Chromosome 5 (position 66668064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 62809622 |
GRCz11 | 5 | 63503013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCAGGGAATGCCAGTTAAATCAGCGAACATTCTGTTGAAGTTTGGATA[C/A]AGTACTCCAGAAGAAACTGTCATAATACCATCAACATATAGATCATACAT
Long Flanking Sequence:
CACATGTATGTTACTGTTTTACATGACACAAATGCTGACTTTGTAATCCCAAGCCTTTAAACTGAATAGTATGATTATTTTATTCAAAATGTACAATTTCAGCATGTTTATTTCAATACTAAACTGAAATATTAAAATTGCAGGTAACACTTTATTTTGATGGTCCATTTGAGTAATAGCAGACTGTCTTTTTAATATCTGTTGATACAGACATTCAACAGACATTTAACTATAAGACTATAAGACTATAAGAGACTTTGCAAGTACATGTCAACTTGCACTAACCCTTACCTCAATCTAACAGTCTACTTATAATCTAATGAGAATGAGTTGGCATGTAGTTGCAATGTAACTTAAATTCAACAAACATACCATCAAAATTAAGTGTGACTAAATTGCAATTGATGAAAATGACTTATATATACAGTATGTGAATATGCTGACAGGTATGTCCAGGGAATGCCAGTTAAATCAGCGAACATTCTGTTGAAGTTTGGATA[C/A]AGTACTCCAGAAGAAACTGTCATAATACCATCAACATATAGATCATACATGGTAAAGTCAGTATTCTGCTCAAGCAAGATTTAATGTTTGAGTTCAGAGAGTAAACTTTTGTTTTCTTTTTGTCTTAGCTGTATAACGGAAAAATGGAAGTGGACTTGGATATCAGGTCAGCTCTGTCATCCAAGCCTGATGCACCTCAATTCCTGAACGCCATGAAGGAAAACACATTTCTTTATGTGGAAGTTTTGCTGCAGGAGTCCACTGGTAAGGTTTAGTTATTTGTATCAACACAGGATTCAGACATTAGAGTGTCGAGTGAATAAAAGTGATGACCGTAAGCTTACTTTATTTTTTAGGTGGCCTTTCCCAGGAGGCAGTGCTCTCGCATGTGAAATTTGTCGAAACTCCATTTACCCTGAGTATAATTGCAACCCCTCCTTTCATCAAACCGGGTCTACCGTATGCTATGAGAGTAAGAAACCTGCTTTTTTATAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17323
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 |
---|---|---|---|---|---|
ENSDART00000002540 | Nonsense | 509 | 1050 | 13 | 25 |
ENSDART00000097325 | Nonsense | 507 | 1702 | 13 | 43 |
Genomic Location (Zv9):
Chromosome 5 (position 66676688)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 62800998 |
GRCz11 | 5 | 63494389 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTTCCWCTGGATTACTCTTCTCCCCCCCCCGCCCCCCAGATCATCTCC[A/T]AAGGAAAAGTAGTRAAATACRACACAGTCAAGCGTGTCAGTGAAAAGAGT
Long Flanking Sequence:
GGAAATAAAGCTCAGATTTAATAGATGAGGCCCACAGAACCATCAAGATGTTTACACTCTGTTGAAGTCTGAATATATCACACCTGAGCAATGCATGTGACTTCATTCTTCACATAAGAGGCGTCTTTAAGCTGCCATCACCAAAAAAAAGTATTTTATAAAAAGTCTTAAATACATTTAAAGTAGTTTGCTACTTTCTCCTTGTGTCACTTCATTGTTATTACACACAACTCATTTTTCAGATTTGATTTGTTTAATTTTTATGTTCGTATTCTTTGGGTTTTTCCCAAAATTTGGTTTATTTCCACCTCATCAGCTCCTTTAGAAATATTATTCTTAGAAAAAAACATGACGTGTTCAATATTTACTTTCCCCCACTGTAATATAGAAATACAAACCTTTATTTTGGATGTCATTATTCACTACTTTTAGTTGAAGCTCTAAAATAAAAATTTCCACTGGATTACTCTTCTCCCCCCCCCGCCCCCCAGATCATCTCC[A/T]AAGGAAAAGTAGTAAAATACGACACAGTCAAGCGTGTCAGTGAAAAGAGTCAGAGCCTCAACATTAAGATCACCCCTGACATGGTGCCGTCAGCTCGCCTGCTGGTGTATTACGTCCTGTATGGGGAGGAGAAAGCTGAGCTGGTGGCAGACTCTACATGGATCGATGTCAAGGCTAAATGTGTGAAAAACTTAAATGTAATGTCTTTTTCTCTCTCCCCAAAAATGATGCAGGTTTTATGTTGTTCACACGTTGTGAGATCTTATTCTTCTTTGAATATCTTTCAGCTGGAATTATCAACTCTCAAACTACAGGATGACTACAAACCCAAAGATAAACTGGAAATAAAGGTGTCATCTAGAAGCAAAGGAGAGTCACTGGTGGCTTTTTCTGCAGTCGATACAGCTTTATTCAACCTAAGAACTAACAAAAAGGATCCCCTGAAGAAGGTGAAAAGGCATTCATTCATTCATTCATTCATTTTACTTCGGCTTAGTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20567
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 |
---|---|---|---|---|---|
ENSDART00000002540 | Nonsense | 566 | 1050 | 13 | 25 |
ENSDART00000097325 | Nonsense | 564 | 1702 | 13 | 43 |
Genomic Location (Zv9):
Chromosome 5 (position 66676859)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 62800827 |
GRCz11 | 5 | 63494218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGGAGGAGAAAGCTGAGCTGGTGGCAGACTCTACATGGATCGATGTC[A/T]AGGCTAAATGTGTGAAAAACTTAAATGTAATGTCTTTTTCTCTCTCCCCA
Long Flanking Sequence:
ATACATTTAAAGTAGTTTGCTACTTTCTCCTTGTGTCACTTCATTGTTATTACACACAACTCATTTTTCAGATTTGATTTGTTTAATTTTTATGTTCGTATTCTTTGGGTTTTTCCCAAAATTTGGTTTATTTCCACCTCATCAGCTCCTTTAGAAATATTATTCTTAGAAAAAAACATGACGTGTTCAATATTTACTTTCCCCCACTGTAATATAGAAATACAAACCTTTATTTTGGATGTCATTATTCACTACTTTTAGTTGAAGCTCTAAAATAAAAATTTCCACTGGATTACTCTTCTCCCCCCCCCGCCCCCCAGATCATCTCCAAAGGAAAAGTAGTAAAATACGACACAGTCAAGCGTGTCAGTGAAAAGAGTCAGAGCCTCAACATTAAGATCACCCCTGACATGGTGCCGTCAGCTCGCCTGCTGGTGTATTACGTCCTGTATGGGGAGGAGAAAGCTGAGCTGGTGGCAGACTCTACATGGATCGATGTC[A/T]AGGCTAAATGTGTGAAAAACTTAAATGTAATGTCTTTTTCTCTCTCCCCAAAAATGATGCAGGTTTTATGTTGTTCACACGTTGTGAGATCTTATTCTTCTTTGAATATCTTTCAGCTGGAATTATCAACTCTCAAACTACAGGATGACTACAAACCCAAAGATAAACTGGAAATAAAGGTGTCATCTAGAAGCAAAGGAGAGTCACTGGTGGCTTTTTCTGCAGTCGATACAGCTTTATTCAACCTAAGAACTAACAAAAAGGATCCCCTGAAGAAGGTGAAAAGGCATTCATTCATTCATTCATTCATTTTACTTCGGCTTAGTCTCTATTTTAGAGGTCGCCATAGCGCAATAAACCGGCAACTATTCCAGCATATGTTTTTTTAACGCAGCAGATACCCATCCAGCTGTAACCCAGCACTGGGAAACACCCATACACACTCATTCACACACATACACTACGGATAATTACGTTTATTCAGTTCACCTATAGCTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20568
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 |
---|---|---|---|---|---|
ENSDART00000002540 | Essential Splice Site | 768 | 1050 | 18 | 25 |
ENSDART00000097325 | Essential Splice Site | 764 | 1702 | 19 | 43 |
Genomic Location (Zv9):
Chromosome 5 (position 66683664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 62794022 |
GRCz11 | 5 | 63487413 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGGATCTTCGTAAAGAGAATGCAGAAAATATCATTCTAAGCCGGGCAG[G/A]TATGGATGTTTCTCACATGGCATAATATTGACTTGGATTATTAATGTGTT
Long Flanking Sequence:
TCACTCAAAACTGAAAATTGACTCACCGTGCATTTGATGAACACGAAGATAAATATGAAGAAGATATTCTAAAGAAAACTGGAAACCTGCAATCATTGACTTCCATACTATTTGTTTTTCCTACTATGGAAATCAATGGTAATTAGTTTTCAGAATATCTTCTTCATACATATATCTTGTTTTATGTTTAACAGGGAAAAGAAATTCATAAAGGTTTGGAACCACTTGAGGGTGAGTAAATAGTTAGTAAATGTACATTTTTGAGGGAACTATCTCTGAAATATCATCCATGCGAATAAAATATTTACAATATTTTAACATATAGGCCTGTATCTTTAAGTGATGTATTCCAGCAAACTCATGACAATCTTTCTGTAGCAAGAAAACGAGAAGAGATTACGAGAAGGAAAAATATTGTCGACTTGCCTTCGAGCAGTGCTGTGTATTTGCTAAGGATCTTCGTAAAGAGAATGCAGAAAATATCATTCTAAGCCGGGCAG[G/A]TATGGATGTTTCTCACATGGCATAATATTGACTTGGATTATTAATGTGTTCTTTTAAAAAGAAAGATCAAACATTCTCTTTTATGCAATGCAGCTATCGACTTTCTGATGGATGCGCCGCTGTCTCAGGTTAGGAGCTACTTCCCTGAGAGCTGGTTATGGGAGGAACACCTCAGCAAGTAGGAACACTTTCTGAACCATAATCCATTCTGTCTTTTGCAGTTAATTATAAAATTTTTAAAGGAACACTCCTAAAAAACACTTTTTTTTTTTAAATAGAGACTTTTTTTACTATTTTTTGTTTTATTTTTTGTCCATTCTGCTTATTTCTGTGTCTGGCGGGAGCACTATTAGCTTGGCTTAGCATAAATTATTGAAATGTATTAGACCAGTAGCATCTCGCTTTAAAATTTACAAAAATGCCCGATGTTTTTTTTTTTATATTTAAAGCTTGATTATCATAGTCACATCATGTATTAAGACCAACATAGTTGAGAAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33748
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002540 | None | None | 1050 | None | 25 |
ENSDART00000097325 | Nonsense | 1284 | 1702 | 31 | 43 |
Genomic Location (Zv9):
Chromosome 5 (position 66704332)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 62773354 |
GRCz11 | 5 | 63466745 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACAGTTTACGTCCTGCTTAACACTTTAACCAGAGGTGAAACCGAATA[T/G]GCAAAACCCATCTTGAACTGGTTGACACAAGATCAGAGATATGGAGGAGG
Long Flanking Sequence:
TAAAAAAAAATAGGTCTCTAAAAACACAGAAAATGTACTGGCAGTTTATTACAAGGTTTTTGTACCATGCTTTTACATCACCAAATCATACAATACATCCATTTAAACTAATAAAATGTCAATAAAAATTACATTTTCGAACTCTTCAGGGTTACAAGTTGTTGGAAGAAAAATCAAGATTGCATAATGCAATTCAAAAGCATAAATAAACCGGGAAAATAAAAAATTAACACATGAATCACGAAAAAACGGAAAACTGCAAATTTATGGATATGTTTTTACAGTATACTTCTGACCAAAACTCTTGGAAATTTTAGCACCCTTTCATATTTAATACACACCATTTTGTCCTTGTTTACAGGAAACCCACCAAGAGTCTGTTTCTGGCAAGAATCTGATACCAACATTGATCCATTAAAACCCAGCAGTGTGACAGCAAAGTCTGTGGAAACAACAGTTTACGTCCTGCTTAACACTTTAACCAGAGGTGAAACCGAATA[T/G]GCAAAACCCATCTTGAACTGGTTGACACAAGATCAGAGATATGGAGGAGGCGTCTATTCAACACAGGTATGTGTTCTTTTTTTTGTGAAGTTTACTTATTTACTAGTTTCGAGAAGATCACGTGATTATGATTGACCACAGCTGACCCCGCATTACCTAACACTTGATTCACCAATCAGATGAATCCTGTCGCACTATAAATAACCAAAGATTTTTTACTTTAAGTTATCTTCGTCTTGAAGAATTCCCCCTTTCAACACCTACTCCTACTCCCTTTCCTACATAGGGCAGCTCGGCAGCCAAGTGGTTAGCACAGTTGCCTCACAGCAAGAATGTCACCGGAGCAGTTTATATGTTTCCCGTGCTTGCCTGGGTTTCCTTCCACTGTCCAAAGACATGCAACACAAGTAAATTGACTAAATCAAATTGGCACTAAAGATGAGTTCCTAGTCAGTATTTTTTCTTTCCATAAGCAATCCCCATCTGTCGCAAATTAGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33749
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 |
---|---|---|---|---|---|
ENSDART00000002540 | None | None | 1050 | None | 25 |
ENSDART00000097325 | Nonsense | 1291 | 1702 | 31 | 43 |
Genomic Location (Zv9):
Chromosome 5 (position 66704353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 62773333 |
GRCz11 | 5 | 63466724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACTTTAACCAGAGGTGAAACCGAATATGCAAAACCCATCTTGAACTG[G/A]TTGACACAAGATCAGAGATATGGAGGAGGCGTCTATTCAACACAGGTATG
Long Flanking Sequence:
AAACACAGAAAATGTACTGGCAGTTTATTACAAGGTTTTTGTACCATGCTTTTACATCACCAAATCATACAATACATCCATTTAAACTAATAAAATGTCAATAAAAATTACATTTTCGAACTCTTCAGGGTTACAAGTTGTTGGAAGAAAAATCAAGATTGCATAATGCAATTCAAAAGCATAAATAAACCGGGAAAATAAAAAATTAACACATGAATCACGAAAAAACGGAAAACTGCAAATTTATGGATATGTTTTTACAGTATACTTCTGACCAAAACTCTTGGAAATTTTAGCACCCTTTCATATTTAATACACACCATTTTGTCCTTGTTTACAGGAAACCCACCAAGAGTCTGTTTCTGGCAAGAATCTGATACCAACATTGATCCATTAAAACCCAGCAGTGTGACAGCAAAGTCTGTGGAAACAACAGTTTACGTCCTGCTTAACACTTTAACCAGAGGTGAAACCGAATATGCAAAACCCATCTTGAACTG[G/A]TTGACACAAGATCAGAGATATGGAGGAGGCGTCTATTCAACACAGGTATGTGTTCTTTTTTTTGTGAAGTTTACTTATTTACTAGTTTCGAGAAGATCACGTGATTATGATTGACCACAGCTGACCCCGCATTACCTAACACTTGATTCACCAATCAGATGAATCCTGTCGCACTATAAATAACCAAAGATTTTTTACTTTAAGTTATCTTCGTCTTGAAGAATTCCCCCTTTCAACACCTACTCCTACTCCCTTTCCTACATAGGGCAGCTCGGCAGCCAAGTGGTTAGCACAGTTGCCTCACAGCAAGAATGTCACCGGAGCAGTTTATATGTTTCCCGTGCTTGCCTGGGTTTCCTTCCACTGTCCAAAGACATGCAACACAAGTAAATTGACTAAATCAAATTGGCACTAAAGATGAGTTCCTAGTCAGTATTTTTTCTTTCCATAAGCAATCCCCATCTGTCGCAAATTAGGGAAGTTCTCGAGACCTACCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31483
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002540 | None | None | 1050 | None | 25 |
ENSDART00000097325 | Nonsense | 1696 | 1702 | 43 | 43 |
Genomic Location (Zv9):
Chromosome 5 (position 66712780)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 62764906 |
GRCz11 | 5 | 63458297 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACTGCAAACAATATGTCAAAGTTTTGGAAGGATTTGAATTTGAATACT[T/G]ATTAAATGGCTGTGATTTGATGTCATCTCGATAGGACTGGTACTTCATGT
Long Flanking Sequence:
TAAAGTGGCCGGTGAGTGTACATAGTAATTAATTGCATATTATGGTACATTTACCATATTTCCATATGCTATCTTTATTTAGAACAAGTAAGTTATGAAAAGCAAAGCAAAATCCATTGAGGAAACATTGCTGCTTTTTTGGTTATGCACAAATTAAAACTAGAACTAAACAAGCATTAAACACTAAAAAAATCTATAAAGAGCACTATTAGAGATAAACATGGTCATCAAATAGGATAAACGATAAAACAGATGAAATGGGAGTTTGACCTTAATCTGTTGTATTATAACTTGCATTACACTGTATAAACTCAGTATTTCACAAGATTTATTACACTACTATGTACGATGTAGCATGATTTTCTCTAAACCATGTTGCAGGTACAAGTTCCCTTTGGACTCTGAAGCTTGGGTGGACTGGTGGCCGCTTGAATCTGACTGCAGCGATGCTAACTGCAAACAATATGTCAAAGTTTTGGAAGGATTTGAATTTGAATACT[T/G]ATTAAATGGCTGTGATTTGATGTCATCTCGATAGGACTGGTACTTCATGTGTACGTTTTTATTCTTTGAAAAACAAATTCAAAATAAGAATAAAACGAAGCATTTAAATCAGTTCAACTCTTTGTAGAATCATCATTTAACAAACACCAAACATATTTAACAAAAAGTATTAGTTTTCATGTACAATTTAAAGAGAGAGTTTATTCAGAAATAAAAATGACCCACCCTTATCTTGTTCTAAATCTCTTTGACTTTCTTTCTCATGTTGAACACAGAAGAAGATATTTAGAAAAATGTTTATAACTGGAACCCATTGACTTCTATTTGTATCATTTTTTCCCCTACTATGGAAGTCAGTGGGTGCCAGCAACTAGTATTCTTCAAAATATTTTCTTTTGTATTTAACAGAATAAAGAAACAAACTCATAATGGTTTAAAATCACATGAGGTAGAATAAATGATGAGGTAATTTTCATATTTTTGGGTAACTATTCTTTTCC
Associated Phenotype:
Not determined