ZMP
si:ch1073-349o24.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8K0F2]
Human Orthologue:
CCDC108
Human Description:
coiled-coil domain containing 108 [Source:HGNC Symbol;Acc:25325]
Mouse Orthologue:
Ccdc108
Mouse Description:
coiled-coil domain containing 108 Gene [Source:MGI Symbol;Acc:MGI:2444274]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34557 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34558 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41356 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11573 | Nonsense | Available for shipment | Available now |
sa12787 | Essential Splice Site | Available for shipment | Available now |
sa45345 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8772 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13581 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34557
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 |
---|---|---|---|---|---|
ENSDART00000041802 | Essential Splice Site | 25 | 1780 | 1 | 32 |
ENSDART00000145853 | Essential Splice Site | 25 | 1595 | 2 | 30 |
Genomic Location (Zv9):
Chromosome 9 (position 7775033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7755126 |
GRCz11 | 9 | 7733517 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGAGCTCGCGAATCCCCTTTGGAGTCCCAAACAACCCACACAGAAAG[G/A]TAAGGAATGTAAAGTCATTATTATTTACCAGAGTAAACTTTGCCCGGCTT
Long Flanking Sequence:
ATAAACAATAACAGTTCATTTGATGATTCCCCGAGCCAATTAATCACCTTTGCTGTCAGTGATTTTCTTAAGGCAGATCACTCAAGCTAATAGAAAGGTAAAGAAATGAGTGACAGGGTCATAAACTTACACCAGCCTCAGTTAACCTTAGGCAGGCATTATAACATATACTGCTTTTGCAATAAATGTAAATGTATGACTTTCAGCACGCAGCTGTTTAATACATTCAGATTGCCTTATGCAAGACGCTATTTGTTTAATTTATCGGTCAGATGACATTCAGGTTCATCTCTGATAAATGGCCAAATACTGAAAGTACTCCAACCACGTCTAATTTTATATAACAGCTATAGGATATATTTAAAGTTTATAAAAATGAATCATTTGATTTTGACCTACGTTGCTTTTGGTTGGTTTTAGTTGCAATGTTGACAGATCATCCCGTGAATCCTCTGAGCTCGCGAATCCCCTTTGGAGTCCCAAACAACCCACACAGAAAG[G/A]TAAGGAATGTAAAGTCATTATTATTTACCAGAGTAAACTTTGCCCGGCTTACTAATAATTTCAATTTGTTGCTCATTATTATTTATTTATTTTTTTGCAGACTTAATCATGCTTCTGTCGTACTACGACTATTGTTTACAGCAAATTTTATTTTTTATAAGTCTGCTTAAATGGTGTGCTGAAATACAGTGCCCTCTGGTGGTGAAAAATTCAAAAGTCATTGATTTTATTTTCCAGAGGGTCTCAAGCCTCAAGTCAGGATTTATTCAGAAGAGACCCCAGAACTGCTTCTTTGGTGTAGAGACCTGGGCTGAGCTGGTCTGGGAGTACTGGGAGCCGGGGCTAGAGTATACCAAATCTCTGGTCCTTAAAAGCATACATGGAAAACTCCAGAAACTCACATTCAGGCTAGTTTTTTTTTTTTTTTTCTCATCTTCAAAGGCTAAGTGTAATGACAGGTACACCACATTTTCTAATAATGGGGTCTGGAAAATCATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34558
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041802 | Essential Splice Site | 172 | 1780 | 4 | 32 |
ENSDART00000145853 | Essential Splice Site | 172 | 1595 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 9 (position 7777649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7757742 |
GRCz11 | 9 | 7736133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTGCTCAACAATGCTCTCAAACCAGCTTCTTCTTTAGGAATTCCAGG[T/C]AAAGATGTATTGGATGGTTGATTATACAGCTGCCATCTAAAGAAATGCAT
Long Flanking Sequence:
GGTACTAACATATACTTTTGAGGTACCAATATGTACCTTTTGAAATGGTACCACCCCAGTGACAGCTACCTTTATTTCTGACAGTGTAGAAACTGACTTATAATGATACACTGACACCTTTAAAAAAAGAGAGAGACAATTAGACTGTGCGTTAGAAGGTTGAATTGACAGCAAAGCTTTATTTTTGCGAAAACTCTCCCTTTAAACAACATTAAAGGCAAATAATGAAAGATGCATGACTTGAAAACCCATAATCAGTTGACTTCAGTGTCAACACCAGTTAATGAAAATGCATAAATGTATCTTGGATTTGCGTAAATACCTCTTTCCAGTGTGAATATGTGGACGCAATAGAGTTTGAGTGTAAGGAAGGCACATTCCAGGTGTGTCTACGAGCTGTGATTCCCCATCATGCTCTGGACGTACCAGAAACAGTGATTCTGCCACCCTGTGCTGCTCAACAATGCTCTCAAACCAGCTTCTTCTTTAGGAATTCCAGG[T/C]AAAGATGTATTGGATGGTTGATTATACAGCTGCCATCTAAAGAAATGCATGTTGAAACATCATACTATATGCATTTTTTTTCCACTAGTAAGCTTCAGACAGTATTCAGGTGGTTTGTGGATCCTCCGTTCCAGCTGTCTCCTGAAACTGGACAGCTAAACCCTGGAGAAGAGTGCAGGGTTACAGTAGAGTTTAGACCTCAGCAGGCTCTAGTGTACCAGGCTGAGGCCAGCTGTGCATTCGGGGATGATGGCGAGAGCAGATGTGCTGTGCTTCTCCGTGGGCTGTGTGAGTACTTACTGTAATGGTTTTCTATGTTTTTGTAATAATAGGAAAATTATTTATTTTCTCCATAGATTGAAAAATGTCAAATTTCTATTAACTTTTAATAGACACTCACAGACATAAAAAGCCACAATGTTATATTTGAATAAACCAAAGGGTTTTTAAAAGCCAAATTCAAGGTCCACTAAGCAGTAAGCATTTTAAATGAGTACGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41356
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 |
---|---|---|---|---|---|
ENSDART00000041802 | Nonsense | 439 | 1780 | 8 | 32 |
ENSDART00000145853 | Nonsense | 437 | 1595 | 9 | 30 |
Genomic Location (Zv9):
Chromosome 9 (position 7783920)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7764013 |
GRCz11 | 9 | 7742404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAATTCAGACCACACTGTTCTGTAGCTTATCATAAGACTGTGACCTG[T/A]TTGCTGATGCACAGGGTAGGTTGGTTTATCAATCAATGTACCATTAATTC
Long Flanking Sequence:
GAGGTGTATGAGGGGACGATCGCACCTTATTCAGTGTTGAAAGTCCCTGTCTGCTTCTCTCCACTCACAGTGGAAAGCATAAGTGTAGACTACATCAGACTTACCTGTCCTGGGGCTGTAAATGAAGAGCTGCTCAAAGTGTCTGGCACATGCATAGGTATAATTCCTAACCCCACGGTAAGACATCTGCTTGGAAACATTTCAGACATGGTCTGATTGTGATCTTCTGTCCAATTTCTAACTTCAGGTCCAATAGTATCTCTAAGCACCTCTGTACTGGACTTTGGCTGTGTAGAAGAAGGCTCAGAGATGTCACACAATGTGCAGATCATCAACTCCTCTGCAGTATTGGCTCATTACCAGTTTGATATGGACACTGGGGGACATAGTGTATTCAGTGTTGATAAGCCTTGTGGCATCCTGGGTGGCAGCAGCAAACTCAACCTGCGTGTGAAATTCAGACCACACTGTTCTGTAGCTTATCATAAGACTGTGACCTG[T/A]TTGCTGATGCACAGGGTAGGTTGGTTTATCAATCAATGTACCATTAATTCATTCATCCATCCTACCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTTTATCTGTTTATTTATCTGTCTGTCTGTCTTTCTGTTCTGTCTTACTGTCCATCCATGCATCCATCCATGCATCCATCCATGCATCCATCCATGCATCCATCCATCCATCCATCCATCCATCCATCCATCCATTCATCAATCCATCCATCATATATTATGTTTCAAATTGTACTGTATGTCTGTCCATTCATCCATCTAATATTCATCCATTCATCTATCCATCCACCCATCCATTCATCCATCCATTCGTCCATTATATATCGAATTGTATATGTGTCCATTTATCCAACATCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11573
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 |
---|---|---|---|---|---|
ENSDART00000041802 | Nonsense | 588 | 1780 | 10 | 32 |
ENSDART00000145853 | Nonsense | 586 | 1595 | 11 | 30 |
Genomic Location (Zv9):
Chromosome 9 (position 7785746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7765839 |
GRCz11 | 9 | 7744230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTCAGTCTCCATCACCAACCACACCARGGGCAAAATCTGTGTGATGTG[G/A]TCACCTGGRGCCAAATCCYCTTTCTCCATYTTTCCTCTCTCCTKTGAGCT
Long Flanking Sequence:
GTGGAGCATTGGTAATACAGGAGGTGTGTGCACAGTATGCCCGTCTTCACTGTGGTGTAACAAGTATTTTGTAACATCTAAGAGTTAAGTCATGTGCTTTAAGTTTCTTTTTACATTTTTAGACCAATATATCCAACATGCAGCCCAGTTTATTGTTCTAATTTCGATTTGCATGATAGCTAATGGGAATAGCTGAATGTAAATTTCCTGGAAATGTAAAGCATTCGTTTCAAATCACAGAACACTAAATATATTAACTGTCTTCAGTTTCCAGCAGATACTGTATATCCCACACGTCTCTTCAACCCACGCAGTCCTATAGAGGAGTATTTCCATGTTAATTTAGCACCTGAAGCAGAAACAGAACTTGGCAACAACTCATCCAAATTCCCCGTTCACCATGTTACCGTTCAACCCTCTCAGCTCCTGTTTTATGATGGCCCAGCGTCAAAGTCAGTCTCCATCACCAACCACACCAAGGGCAAAATCTGTGTGATGTG[G/A]TCACCTGGAGCCAAATCCTCTTTCTCCATCTTTCCTCTCTCCTGTGAGCTGGGCCCTTTAAAGACCACAGCCTTCAGAGTGACGTACAGTCCAAACCAGCAGAACATGTTCCATGCAACACAGCTGGAGTGTTTCACATTTTACAAGGTAATGTGAGATTGAAGGTAATGTGAGATTGAAGGCACTGACAGGACAACAACCTGTATTCACAAATTTTTATTGACTTGATAAAACATTACTATGTAATTGCCTTGTCTTCAGATATTTCATTCATTTATTCATTTTCTATTCGGCTTAGTCCCTTTATTAATCTGGGGTGGCCACAGCGGAATGAACTGCCAACTTATCCAGCATATGTTTTACGCAGCAAGTGCCTTTCCAGCTGCAATCCATCACTGTGAAACATCCATACATTCTCATTCACACACATACACTACGGACAATTTATCTTACCCAATTCACCCATACCACATGTCTTTGGACTTGTGAGGGAAACCGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12787
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041802 | Essential Splice Site | 683 | 1780 | 11 | 32 |
ENSDART00000145853 | Essential Splice Site | 681 | 1595 | 12 | 30 |
Genomic Location (Zv9):
Chromosome 9 (position 7789190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7769283 |
GRCz11 | 9 | 7747674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAAAGAGCCCTTTGTCCCCRAATTCTCTCTTCAACACTCTCAAGTGG[T/A]AAGTTAAATAAGGCACCTTTCATCATAATATGTTGAAAAAAATATAGATG
Long Flanking Sequence:
CACTCGAGAAAAACTAAACACGACCGAACGTACCTCCGGCCACGTAAATCACGGTCTCCAGAAACGTCTGCGGGGCTACATTTCCAGAATGAGCTTGGTTTGATATTGGATATTGGTTACCATTGAAATGTATAGTACTTTTGCTTCTGTTTTGTTTTTGTTTAACTGAATTTTTTATTTATTTTTATAAGTTTTTGGGTAACTATCCGTTTAAATCATTCAGCACTATTCAACAGTACAGTACAGTACACAGAACCCGTGATCCCAGGCAATATATCTCTGAAAAACTGGTTATAATGTGAACATTGGTTCCGAACATGGACATTTCGAGCAACCTATAACTCTGCTTGGAAATTTGCAGGTCTTGAAAAATCATAGAATTGTGGAAGATCAGACTTTATGCCCACCCTGGTGCCTTACAGTCAGAGTAACTGGCCACTCATTTCAGCCTGGAAAAGAGCCCTTTGTCCCCAAATTCTCTCTTCAACACTCTCAAGTGG[T/A]AAGTTAAATAAGGCACCTTTCATCATAATATGTTGAAAAAAATATAGATGGAAAGACAAAGTTTTAACACCATTCATTTCCCTACAGGTATTCCCCGCACTGAAACGGGTGTCATACCGCACTGTCCTATTACAGAATACAGGGGACCTACCTTTGATCTTTAGATTGGATCCCGAGGAGTGCCCATCAGTGTGTGTACTGCCACCCAGTGGTCTGGTGCCACCAGGCAGTCACCAGATCCTCACATTAAGATGCTCTCCATCACCAGACCACCCTTCTAGGATACCTTTGACATTACATCTGAATGCCAGCCCCAATCACACACAGGTTACACTATTTTCTACATAGCCGTAACATGTTTAAATATGTTGACATTTAACTTGCTATTCATAATTGAAGTGGAGGAAGAGTCTGGGGATCTCTTCTAAGACTGCTGCCCCTGTGACCAGCCCCAGAAAAGCAGTTGAAAATGAATGAATGTATGAATGAATTCACCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45345
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 |
---|---|---|---|---|---|
ENSDART00000041802 | Nonsense | 1255 | 1780 | 22 | 32 |
ENSDART00000145853 | Nonsense | 1253 | 1595 | 23 | 30 |
Genomic Location (Zv9):
Chromosome 9 (position 7801488)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7781581 |
GRCz11 | 9 | 7759972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACTGGAGGAGCTGATGGAGGAGAACTTCAGTCACCCGGTCCTGCAGTG[T/A]CTGAATCCTGCTGCAGAAGTGAAACCAGGCCACAGCGCCATGCTTGAGTG
Long Flanking Sequence:
GCTTACGAATCTTTCCAGTTGAATTTTATAGGAGTTACTGTAGAAAGAGATCGGCGCTACATTCACCTCTCCTCCAATCGGCACATTTTTGCCCCAGTGCCCATTGGATGCTTCAGTCCTCCCAAACAGGTTGGTATTTACCTGGAGAGATGTTTTCTCAGAAAACCCTCGATCCACAGCAAACAAGTCAGTATCTGTAATAATTATTACTAATGGTTCTTTCATGGTATTGCTAAAATAAAAAGGCTTGATTTATTTATTTGTCCATTCATTCATCCAAATGAATTGGCCACCCCTGTTCTATGCTCTTTATTGGCAGATAGTTAAGTCTTCTCCTAGATGTCATTTGTTTATTTTTAAGTCACAGAGATGCTAAATGTTTATTCTGCACAGGTGTTTGAGTTGTATAATGCAGGCACTCTCCCACTGAGGTATCACATGGACACTACTCCACTGGAGGAGCTGATGGAGGAGAACTTCAGTCACCCGGTCCTGCAGTG[T/A]CTGAATCCTGCTGCAGAAGTGAAACCAGGCCACAGCGCCATGCTTGAGTGGATCTTCTCCCCACTGGAGGCTAAAACATACACCGTCAGTTACTACCCTTATAAAATATCACTGATCATCATATAGTAACAGTTGTTTTTATCTAAAAAAAAACATTATAAACAACTTAAGTATGCTTTAAAGTACACATAAAGTTATTTTGAATGTCATATTTCATAAAAAGTATTTCGTCACATTTCAGACAGTACTACCAAATAAGCATTAAAAAGTTGTTAAGTTGTGTAGAATTTTGGTAACACTTTATTTTGATGGTCCATTTGAGTATTAGATTGTCTGCTTAATATTTGTTGATTCTGCTCCTTCAACATACATTTAACTGATTATAAGAAACTTTGCAAGTACGTGTCAACTTGCACTAACCTAAACCCCAACCTGACATTCTACTTATAATCTGATGAGAATTAGTTGCCATGTAGATGCAATGTAACTTAAATTCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8772
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 |
---|---|---|---|---|---|
ENSDART00000041802 | Essential Splice Site | 1556 | 1780 | 28 | 32 |
ENSDART00000145853 | Essential Splice Site | 1554 | 1595 | 29 | 30 |
Genomic Location (Zv9):
Chromosome 9 (position 7806834)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7786927 |
GRCz11 | 9 | 7765318 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTACCAGACACATTTCCCTACTCACTTCAACACTCATTACATTWACAG[G/A]TACAAYAAGATGTCAAAATCAGGKRTGGMATTRAAAATTCTTGATATTTT
Long Flanking Sequence:
AATACACTCAGGTGAGAAACCACATATTTAACACTGACAAATACCATTTACTGAATCCAGACATAAGTGCCAATCATATTAACACAAGTGCCAATCATATTAGTAACAAAATTACCTCTTCAGGAAGATGCAGTGTTTGAAAAGAAAACTGGCACAAGAAAATACAAGGTAAATTTTGAGTTTATTTGGCGTGGTATCCAGCTGAAAGTAGTGTGCAATCAAATAAATAAATAAATAAATAAAATAAATAAATATATTTTGTTCTATATGCGGCAGACCCTTCCACCCATTCGTAGTAGTGATCAAGCTGTTAGTTGTGCCACAGCGAAACCCAGTCGGGCTGAACAGCGAGCCCGGCAGCACACAGGCCAGGAAAGGAGAAGACGTCCTGAGCTACCTCGTCCTGCTTTACTACACTTGGGTGTCACTGCACGCTCTCACAGCCTCTTGGAGTACCAGACACATTTCCCTACTCACTTCAACACTCATTACATTAACAG[G/A]TACAATAAGATGTCAAAATCAGGGATGGCATTAAAAATTCTTGATATTTTTCAGTTAAATTTGGAGATAAATAGTGAACTTTATGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAGCAATATCACATGAGTAGCAGTGCGATATGGCTGTATCTGTATATCGGCACTGGTGGGAGGCGTGCGGTGGCACAAGGCCGCACGTTGGCACGGTGGCACTGCCCCCACCAGTGCCGATATACAGCCATATCGCACTGCTACGAGTGTGATATTGCGTTTATACAACAGTTTGACAACATAATTGTGTATATAAAGACAAAATCAAACATGGAAAGTCTCAAAAACCCTTTTGTATGAGGAACTACTTTCTTCCGGATTCAAATTATAAGCTGACAGTTCAACAGTTGAGCATGCATCTTTTAAACTTTAGATCTGTAGTGTCTGCTTTTTACTGGCTATATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13581
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 |
---|---|---|---|---|---|
ENSDART00000041802 | Essential Splice Site | 1598 | 1780 | None | 32 |
ENSDART00000145853 | None | 1596 | 1595 | None | 30 |
Genomic Location (Zv9):
Chromosome 9 (position 7808674)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7788767 |
GRCz11 | 9 | 7767158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGTCATGAGAGAGACATCGTMACRCATCTGCTCACCTCTTTGCTACAG[T/C]AAGTCTTTGAATTTTMMCCACTAGAGGGTGTGTATTCACAACAAAACAAA
Long Flanking Sequence:
GAAATGATAAATACTTTAAAATAGCCATTATTCTTACAAATGAACTGCATAGTTCCAATCTAAACAACTACATTCTCAACTAAAAAAAGCCTCAAAAGTACATTAAGTTGACCAACAGCAGCAATATTTGTCAAACTGTAGTGTGCCTTCTGCTTGTTGCTGTATGTGGGTGGAGTAAAACACAAAGGTGAAGGGTTAAGAGACTGAACGAGTGCTGTTATTTGCAGAATATTGCCTGGCTATCAGCCAATCAGATTCAAGAACCAGACGGAGCTGTTGTATACATATACATAATATATTAATTTATTTAATTACTTTTTTTTTTCTTATATACATTTACATATCAGATATACATAAGAGATATTTCTTTCAGATCTAGGCAGCCAAAGGATTCTTCGTCTGGCACAGCTGAAAGCTTTTATCATCCCTCAGAACTTACTCCTCTTGGTCCTGGTCATGAGAGAGACATCGTCACGCATCTGCTCACCTCTTTGCTACAG[T/C]AAGTCTTTGAATTTTACCCACTAGAGGGTGTGTATTCACAACAAAACAAAGTTTTATAAGTTTTATAGTAGTTTGATGATACTGTGACTTAGTTTGGATCGTCTTCATCACATCCTACTTGACTCCTGCAGAAATCAAATTTATGGATGAGCTAAAGTATTCAAAATGTTGTATCAAGGTAGTATGAGGCAGAGCAGGGGCGTTGCTAGGGTGGGGGTGTTTTGGGTGGCCCGTGCCCCAGTAGAGCTTTATGTCTAGCAACATCGCCTAAAGCGGAAGAGTAAGGCTGAAAGAAACTGAAGAAATTGCTGATGAGAGACGAGCATGATGTGGCACAAAAGCAGCAGAGCTTTTATTATGCCACCAGGCCCAATTGGCTAATCAGGAGGACCGGGAGAATTTTTTGGCCGTGAAGGTCGGTGTCCCTAGCTGCTTGCACTCTCAGCAGTCGCACTTTTTTCATTTATTTATTCATTTGACCATAGCCTCACTCTTTTTAT
Associated Phenotype:
Not determined