Busch Lab

ZMP

si:dkey-21p1.3

Ensembl ID:
ENSDARG00000002295
ZFIN ID:
ZDB-GENE-081105-162
Description:
Novel collagen protein [Source:UniProtKB/TrEMBL;Acc:B0UYF9]
Human Orthologues:
COL24A1, COL27A1
Human Descriptions:
collagen, type XXIV, alpha 1 [Source:HGNC Symbol;Acc:20821]
collagen, type XXVII, alpha 1 [Source:HGNC Symbol;Acc:22986]
Mouse Orthologues:
Col24a1, Col27a1
Mouse Descriptions:
collagen, type XXIV, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:1918605]
collagen, type XXVII, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:2672118]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa15248 Nonsense Available for shipment Available now
sa21230 Nonsense Available for shipment Available now
sa41153 Nonsense Mutation detected in F1 DNA Not yet available
sa9363 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21231 Essential Splice Site Available for shipment Available now
sa45314 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45315 Nonsense Mutation detected in F1 DNA Not yet available
sa640 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa15248
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098151 None None 190 None 7
ENSDART00000125681 None None 185 None 8
ENSDART00000128489 Nonsense 13 103 1 5
ENSDART00000129712 None None 114 None 6
ENSDART00000134775 Nonsense 145 1125 9 52
Genomic Location (Zv9):
Chromosome 8 (position 15383158)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14828502
GRCz11 8 14866207
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATTAAATCTCTWCAGGGAAAACCAGGAGGTGATGGACCACCAGGTCAA[A/T]AAGGAGAGYGTGTATGTGCATCCAATATTATWTTCYGAAAACTTGTAAAT
Long Flanking Sequence:
CAATTAGTGTGAATGAACATTGTATTTATTCATTCATTCATTTTCCTTCGGCTTAGTCCTTTATTTTTTAAGGGTCGCACACTGTGAAATAAACCGCCAACTATTCTAGCTAATCTTTTACGCAGCAGCTGCCCTTTCTAGCCGCAATCCAGTACTGGGAAACACCCATAAACAGACACACTACGGCCAATTTAGTTTATCCAATTCCTCCATAGCGCATGTCTTTGGACTGGGGAGAACATGCAAACTTCACACAGAAATGCCAACTGTCCCAGCCAGGAATCAAACCAGCAACCTTTTTGCTCTGAGGTGACAGTGCTAACCTCTGCATTGTGATCAATGATGTTGAAAACACTTGAATACAACCTAGTTGTTAAATCAATCTGAAATTCGGTATAGTCACTGAGTGTGTTTTTCTTTCCTTCCTCTCTCAAACTATAACTGCTTATCTTATTAAATCTCTTCAGGGAAAACCAGGAGGTGATGGACCACCAGGTCAA[A/T]AAGGAGAGCGTGTATGTGCATCCAATATTATATTCCGAAAACTTGTAAATTATATACACAGTTGAACTCTAATTATGAAATGTATTTCTTATTGAAACAGGGAGATGTAGGAATTGAGGGAAGCATTGGAGGTCCAGGACCACCGGGTATAAAAGTAAGCCTGCGGTTCACTCTTAATGAAGAGTTATGAATTATTTACAATCTCTTTTAATTTATTCAAAATTTTTTGTTACTCCATTTCATTTGCTTCTATGATAATAAAACAAAGCTCAGAGCCACTTTTTTTTGTTTTAGGGTGCCATTGGAAAACCAGGAAATCTTGGACCCTCAGGTGATCCAGTAAGATTACCTCAAACAGCTCCTTAATATGTTAGACGTCTGATTGTTTCTAAACACTTTTATTATGATTTATTACATTATGTTGTACACATTTAGAATTTTAGTTTAAATATACATTGAGCATTTTCAGTATGTTGTCATTCATCTACATTTCCCTCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21230
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098151 None None 190 None 7
ENSDART00000125681 None None 185 None 8
ENSDART00000128489 Nonsense 44 103 3 5
ENSDART00000129712 None None 114 None 6
ENSDART00000134775 Nonsense 176 1125 11 52
Genomic Location (Zv9):
Chromosome 8 (position 15383480)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14828824
GRCz11 8 14866529
KASP Assay ID:
2260-0307.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCCACTTTTTTTTGTTTTAGGGTGCCATTGGAAAACCAGGAAATCTT[G/T]GACCCTCAGGTGATCCAGTAAGATTACCTCAAACAGCTCCTTAATATGTT
Long Flanking Sequence:
CCTCTGCATTGTGATCAATGATGTTGAAAACACTTGAATACAACCTAGTTGTTAAATCAATCTGAAATTCGGTATAGTCACTGAGTGTGTTTTTCTTTCCTTCCTCTCTCAAACTATAACTGCTTATCTTATTAAATCTCTTCAGGGAAAACCAGGAGGTGATGGACCACCAGGTCAAAAAGGAGAGCGTGTATGTGCATCCAATATTATATTCCGAAAACTTGTAAATTATATACACAGTTGAACTCTAATTATGAAATGTATTTCTTATTGAAACAGGGAGATGTAGGAATTGAGGGAAGCATTGGAGGTCCAGGACCACCGGGTATAAAAGTAAGCCTGCGGTTCACTCTTAATGAAGAGTTATGAATTATTTACAATCTCTTTTAATTTATTCAAAATTTTTTGTTACTCCATTTCATTTGCTTCTATGATAATAAAACAAAGCTCAGAGCCACTTTTTTTTGTTTTAGGGTGCCATTGGAAAACCAGGAAATCTT[G/T]GACCCTCAGGTGATCCAGTAAGATTACCTCAAACAGCTCCTTAATATGTTAGACGTCTGATTGTTTCTAAACACTTTTATTATGATTTATTACATTATGTTGTACACATTTAGAATTTTAGTTTAAATATACATTGAGCATTTTCAGTATGTTGTCATTCATCTACATTTCCCTCTGTTTGTATAAATATGTAATGCTTGATAAGTTGTTGATTGATTTCTAACAACAGAATTATGAGGTATTAAATATTTATTATGTAACAGTTTAATAAAATCACAGCAGGCTACAGCACTTGTCACAATAATCCCAAACGGAATTTTTAATCACATTGTGCTGCCCAAACTAAGAGAAGCTACCTTTTGTGAAATTTTTTCTTGTTGTCTTTGCTTGAAACCTTCAGGGTTTAAAAGCACGTCGTGGAATGAAAGGAGAATCTGGCCAAAAGGGAGATCAAGTGAGTTCACTGAACTATTTACAACAATTCTGGCCAAGTAAACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41153
Status:
Mutation detected in F1 DNA
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
ENSDART00000098151 Nonsense 60 190 2 7
ENSDART00000125681 None None 185 None 8
ENSDART00000128489 None None 103 None 5
ENSDART00000129712 None None 114 None 6
ENSDART00000134775 Nonsense 475 1125 26 52
Genomic Location (Zv9):
Chromosome 8 (position 15389051)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14834395
GRCz11 8 14872100
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTCAGGGTAAAGATGGACCTCTTGGACCCATCGGGCCTGAAGGAGAC[A/T]AAGGCAATAAAGTAGGCTGTATTTTTTTCTTTTCTTATCTTCATTTTTGA
Long Flanking Sequence:
ATTGTTCTGCCATTACAAAGCTGAGAAAAGTCAGGATTTTAATATTAATATAACAAAACTCCAATTGTCTTTGTCTAAAAGAAGAAAGACATACTTTTGCTTTACAAAAAAAAAATATATATATATATATATATATATATATATATATATATTTTGGAAGCAGCACTAATGGAAAAGTATAACAATAATACTACATGTAAGACCTGTCTAGAAATCATGAAATATCTGTGAATGCTATCTTCTGAAGGGGCTACAGGGAAACATAGGCCAGTGGGGTGAGACAGGTGTGCGGGGACTAGAAGGACATCAAGGGCCACCAGGCCTGCCCGGGCCCCATGGAGTAGCAGGGTATCCAGTATGTGATGTTACTCTATTCAACTCATTGTTATGAGAGTGTGTAACCTCTCACATTTGGAAACTAATGGAGTATTGATTGACTCTCTCTCTCTCTCTTTCAGGGTAAAGATGGACCTCTTGGACCCATCGGGCCTGAAGGAGAC[A/T]AAGGCAATAAAGTAGGCTGTATTTTTTTCTTTTCTTATCTTCATTTTTGATGACGAGTTCTCTCACACTGTACTTACTAGTTTTAAAAATATTTTCCAAAGGGACTGAGAGGAGACAGTGGATTGAAGGGAGTTGCTGGTATCGATGGTGAGGAGGTATATTGCTTATAAATCTTATTTATGGTCATGCCTTAATCAGTTAATATCTGATTTTACCAAAGTTTATGTATTGTGTTTAAAGACAGTTTGCTTAGATTCTCCTAAATATCTGGTTTAACCTCAACAAAAAAAAAAAAAATAACTGAATGATGATGGGTGATGTGCAACGGCTGGAAAAAGAGAAAACTCTCATCTTCTCAAACAGAATGGCTGGAGACTTAACAACAAGGTCAAATAAAAAAAAAGTTTTAACATAAAATCAAATATAACAAAGAAAACAGGGTATTAACTCAGAAGGGGGCAAAAATTAAGCTAGCTCCTAAGATGATCTCTTGCTAATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9363
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098151 Essential Splice Site 154 190 None 7
ENSDART00000125681 None None 185 None 8
ENSDART00000128489 None None 103 None 5
ENSDART00000129712 None None 114 None 6
ENSDART00000134775 Essential Splice Site 551 1125 None 52
Genomic Location (Zv9):
Chromosome 8 (position 15392453)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14837797
GRCz11 8 14875502
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTTGCAYATTCTTGTTGNTTTTATGTTTTYTGTGGGTTTGTGAATATTT[A/C]GGGTCATCCAGGTGTAAGAGGTCAATCCGGATTAGTAGGACAGTACGGTC
Long Flanking Sequence:
AGTTATCATGAGCTGATGCTGGAACAGCTGAGAACAATCATAAGCACGTGATCCTCTCGAAATTAGTTTTTAAATAAACTTCACAAAGTATGAAGCTGATTGGTCAGTTCTTCTCACGTGACTCTTGGTACGCTTGTGGTATTCTGAAAGGTTGAGATGTTTTCAACTAAGTGCACCTGAAAAACATGTCGCGCCCTTCAGGTTTCAGATGGAAAAGTGCAAATTCCATCAGGCTGTAGCACTTCAAATACACATCCTGGTTCAAAAACACTTTGGGCATTTATAAGAATATTTACACATGGTGTAAACTTGTGAAAAAGATGTTGTGTGTTTGTTTTTGTCAGGGAATGAGCGGTGCTCCAGGGCAGAAGGGAGATCCTGGATCCTCTGGTGAAAAAGTGAGGATTTTTTTGATGAGGATTGCATATGTGTTTTGGTGCAAGAGATAATGTGTTGCACATTCTTGTTGTTTTATGTTTTCTGTGGGTTTGTGAATATTT[A/C]GGGTCATCCAGGTGTAAGAGGTCAATCCGGATTAGTAGGACAGTACGGTCCTGGTGGAAACATGGGAGAAGGTGGAGATAAAGGTGACAAAGGTCTACCTGGACTTGCTGTGAGTGCCTCGCCCTTCTTTATGCACGATGAAGCTATTGAAGAAATACATGGTCATATTTACAGTTTTTTTTACATATAGGGTGAGACAGGGACAACAGGGCCAATAGGTCCAAGTGGTGTTATAGGATTGCCAGTAAGTTTGGACTACTATATTTGAGGTATTGTATTTTTTGAGATACCCATTACAGATTTATGTTTCATCTAAATGTAGGGTTTGACTGGAAAAGAAGGATTTGGTGGACAAAGTGGAAAACATGGGCCAAAAGTATGTTTTTTTGCTTGTTATTTATTATTTTGGTACCATATTTATAGAAATAATATGCAATGACATACATCACACTAACTTACATCTTTAATCGAGTAATTAAATTAACTTTTTTGTGCACTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21231
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098151 Essential Splice Site 154 190 7 7
ENSDART00000125681 None None 185 None 8
ENSDART00000128489 None None 103 None 5
ENSDART00000129712 None None 114 None 6
ENSDART00000134775 Essential Splice Site 551 1125 30 52
Genomic Location (Zv9):
Chromosome 8 (position 15392454)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14837798
GRCz11 8 14875503
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGCACATTCTTGTTGTTTTATGTTTTCTGTGGGTTTGTGAATATTTA[G/T]GGTCATCCAGGTGTAAGAGGTCAATCCGGATTAGTAGGACAGTACGGTCC
Long Flanking Sequence:
GTTATCATGAGCTGATGCTGGAACAGCTGAGAACAATCATAAGCACGTGATCCTCTCGAAATTAGTTTTTAAATAAACTTCACAAAGTATGAAGCTGATTGGTCAGTTCTTCTCACGTGACTCTTGGTACGCTTGTGGTATTCTGAAAGGTTGAGATGTTTTCAACTAAGTGCACCTGAAAAACATGTCGCGCCCTTCAGGTTTCAGATGGAAAAGTGCAAATTCCATCAGGCTGTAGCACTTCAAATACACATCCTGGTTCAAAAACACTTTGGGCATTTATAAGAATATTTACACATGGTGTAAACTTGTGAAAAAGATGTTGTGTGTTTGTTTTTGTCAGGGAATGAGCGGTGCTCCAGGGCAGAAGGGAGATCCTGGATCCTCTGGTGAAAAAGTGAGGATTTTTTTGATGAGGATTGCATATGTGTTTTGGTGCAAGAGATAATGTGTTGCACATTCTTGTTGTTTTATGTTTTCTGTGGGTTTGTGAATATTTA[G/T]GGTCATCCAGGTGTAAGAGGTCAATCCGGATTAGTAGGACAGTACGGTCCTGGTGGAAACATGGGAGAAGGTGGAGATAAAGGTGACAAAGGTCTACCTGGACTTGCTGTGAGTGCCTCGCCCTTCTTTATGCACGATGAAGCTATTGAAGAAATACATGGTCATATTTACAGTTTTTTTTACATATAGGGTGAGACAGGGACAACAGGGCCAATAGGTCCAAGTGGTGTTATAGGATTGCCAGTAAGTTTGGACTACTATATTTGAGGTATTGTATTTTTTGAGATACCCATTACAGATTTATGTTTCATCTAAATGTAGGGTTTGACTGGAAAAGAAGGATTTGGTGGACAAAGTGGAAAACATGGGCCAAAAGTATGTTTTTTTGCTTGTTATTTATTATTTTGGTACCATATTTATAGAAATAATATGCAATGACATACATCACACTAACTTACATCTTTAATCGAGTAATTAAATTAACTTTTTTGTGCACTGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45314
Status:
Mutation detected in F1 DNA
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
ENSDART00000098151 None None 190 None 7
ENSDART00000125681 Essential Splice Site 54 185 3 8
ENSDART00000128489 None None 103 None 5
ENSDART00000129712 None None 114 None 6
ENSDART00000134775 Essential Splice Site 658 1125 34 52
Genomic Location (Zv9):
Chromosome 8 (position 15393146)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14838490
GRCz11 8 14876195
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATAGGTCTAATTGGGAAGAAAGGAGAGCCTGGAAAACAAGGCAGAGTG[G/A]TGAGATACACTTTACATCCTCATTTATTTCCAATACAAACAACAAAACAT
Long Flanking Sequence:
TGAGACAGGGACAACAGGGCCAATAGGTCCAAGTGGTGTTATAGGATTGCCAGTAAGTTTGGACTACTATATTTGAGGTATTGTATTTTTTGAGATACCCATTACAGATTTATGTTTCATCTAAATGTAGGGTTTGACTGGAAAAGAAGGATTTGGTGGACAAAGTGGAAAACATGGGCCAAAAGTATGTTTTTTTGCTTGTTATTTATTATTTTGGTACCATATTTATAGAAATAATATGCAATGACATACATCACACTAACTTACATCTTTAATCGAGTAATTAAATTAACTTTTTTGTGCACTGTAGGGAGAGCCTGGACTTAAAGGGAGTTCAGGGGGCCCTGGGAAGATCGGATCAGTTGTATGTACTTACCTTTGGTGGTGCATGCATTATAAAATAAAATATCTGGCAAAACTGACCTGAATTGTATATGTTGTTACAGGGTGCAATAGGTCTAATTGGGAAGAAAGGAGAGCCTGGAAAACAAGGCAGAGTG[G/A]TGAGATACACTTTACATCCTCATTTATTTCCAATACAAACAACAAAACATAAGGCTTTTGCTATTGAAAGTTCTGTGAAGTGCTTTGAAATGTGATTTTTTTTATTCTACGTTTGACGTAATCTTAAGTGAAAAAATTAAGAGAGGGTGGTACATCGAGTAGCTCTCCCCTTGAAAAAAAAACAGCTAATAGCATTTGGTTTTATCACAGCTCTGCCAGTGAGAATGGTTGAACTCAAGCACATCAAATGAAAAATGAGTTGCATCTTAAAGGGGGCAGGGCATTTCAAAAATATCAATTAATGAGAAACCTGAAGCATGAGGAAGCAAAAGTTGAAAAACTGCAAACTTTAGATGTTTATATCAGTTTTATATTTTCTGAACACAAATTAACATGAACACACTAGCTAATAGATATTCTTAAAAAGACCTCATTTTAATTTCATAAACCTTTAAAACAAAGACAAAGACATTTCACTTTGGCATGTAGTAAAGTGTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45315
Status:
Mutation detected in F1 DNA
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
ENSDART00000098151 None None 190 None 7
ENSDART00000125681 Nonsense 177 185 8 8
ENSDART00000128489 None None 103 None 5
ENSDART00000129712 None None 114 None 6
ENSDART00000134775 None None 1125 None 52
Genomic Location (Zv9):
Chromosome 8 (position 15394746)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14840090
GRCz11 8 14877795
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGCTGTAAGTAAGCTTGTTTTGTACAGGCATGAAAAATGTGTCAGTTA[T/A]AAAATATTGTTATTATTTTTGGCATAGTTTCAATACTCATTCACAGGGAG
Long Flanking Sequence:
ATTCGCGGTTTTCCTGGGAAGCCAGCAAGTATCCCCAATACAGATCCTAAAACTTTTTGAGTTTTTAATGATTGTGTCAAAGTTTTCTCTTAATCTAACTTCATTTTAGGGACGCAGTGGAACAGATGGACTGCTGGGAGTTATAGGAACCGAAGGGGACCCAGTGAGTAGCTTGATCTTATTTTATAATGAATAAAATGTCAAATTTATCATTGCTATGTTTATTAGGGCCTTTTGCGTTATTTATGTGAGATTTAGCCCATGTAAAATCAGTCAGATTGCTTATAAATCTTATATTCCTTCATTAGAATGACATCCTGGATGACAGATTTAGCACAGAAGTGAGTACCCACTAGCCTATTGTACAGGTACTGTTAAGTGAATGTTTACATAAACTTGCAGGGTGATATTGGATTCAGAGGACGTCCAGGGAGACCAGGTCTGCAAGGTAGTGCTGTAAGTAAGCTTGTTTTGTACAGGCATGAAAAATGTGTCAGTTA[T/A]AAAATATTGTTATTATTTTTGGCATAGTTTCAATACTCATTCACAGGGAGCCACAGGAATACCAGGTTTGCAAGGGAGTCGAGGTCCTGCTGGACCAAAGGTAATTGCCATTCTGACTTTAAAAAAAAAGAAAAGTTTCCTACTGCAGTTTAATGACATTCACCACAGGGCTCTATTGGACTGAAAGGGAAAACAGGGCCTTCTGGACCAATAGGACCAAAGGTAATAAACTAAAGTTTTTTGTTTTGCCTTCAACAGTCCACGAGGATTTAATTGTCTACTGTTTGTTCACTTAAAGGGTATTCCAGGACTTCAAGGTAAAAAGGGAGATGACGGACAGAAGGGAACAATGGTATTATTGTATCTCTTTCTATATTTACTATACACTATGGGCTCTATTTTAACAATCTAGACGCAAAGTCTAAAGCGCATGGAGCAAAAGCATTAAGGGCATATCCGAATCCCCTTTTGCTATTTTAAGCAAAATACGGTTTGCGCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa640
Status:
F2 line generated
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
ENSDART00000098151 None None 190 None 7
ENSDART00000125681 None None 185 None 8
ENSDART00000128489 None None 103 None 5
ENSDART00000129712 None None 114 None 6
ENSDART00000134775 Nonsense 1087 1125 52 52
Genomic Location (Zv9):
Chromosome 8 (position 15400525)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14845869
GRCz11 8 14883574
KASP Assay ID:
554-0549.1 (used for ordering genotyping assays)
KASP Sequence:
CACTTGCATTATATTGCAGGTAACTGCACAGGTGAGGGTTCATGGGAGTT[C/A]AGAGCTCCACAGGGGAGACATGCAGCTACTTCCTATCAGAGATGTTTTTG
Long Flanking Sequence:
GATCCAAAATGTGGTTTAGTGAGCTTCACAAAGGCTTCAAGGTAAATTACTAATTTCGTTTTTCATTATTAAGAGTGGCAGTTATCTCAATAAGTGTATTTCTCTGATTATTGTGCTCCATAGTTGAAGTACAAAGATCTCGATGTTGTCCAACTGCGATTCCTTCGGTTACACAGCAACTCTGCCACACAAAGCATCAGCTTGAAGTGTCCCAAAAAACACAGTCCCACTGTTAATCATTGGAAGACGATGCTGCATTTACGAGGAGACTCCTATGAAGAAATCAATCCGCCCCATGTCATCATAACCCGGCATGGTTGTGAGGTTAGAATTAATCAATGGCTGTGGAAATGGTGTAATACTGTTGACAAAAAACATGAGAAATTTCCACACAGTCAAAGCATGTCAAGTAAATTATTGCACTTTGCACTATTGCATAACAAGAGGTTTCACTTGCATTATATTGCAGGTAACTGCACAGGTGAGGGTTCATGGGAGTT[C/A]AGAGCTCCACAGGGGAGACATGCAGCTACTTCCTATCAGAGATGTTTTTGTGGAGGGCGGAGAAGAGACCTGGAAAGGACATGCAAACATTATCCTGGGACATTTGTGCTTTTTATAGTCTCTTTCCAAAGATAGATGTCATGCGTAGAGCTTCTGCGGGGATTGCATTGCTGCTGGATGATATTAGGGGATTTTATTGTTTATATACATAAGGATCAGTGAATTCCTGCATTGTTCTATAGGTTTAGATTTCTGACTGACTAAGTGTGTATGTGTGCGTGTGTGGATAGATATGTGGTTTACAGAGACACAAAGTTTTATAAGGACATGACTTAGGCCTAATCCCAATTCTACCTCTTTGCCCTTTCCCTTACCCCTACCCCTCATTTTGCGCGTTCCCGTGAATGGGTATGGGTGTCCCAATTCTCTTTAGCTTGAAGGCGTAGGGCTAAGGGGAAGGGGTGAATAGCTCTTCGAACAAAGATTTTTTAGGACCACAC
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461