Busch Lab

ZMP

col28a1

Ensembl ID:
ENSDARG00000077084
ZFIN ID:
ZDB-GENE-070705-84
Description:
Novel protein containing collagen triple helix repeat domain [Source:UniProtKB/TrEMBL;Acc:A5WUJ9]
Human Orthologue:
COL28A1
Human Description:
collagen, type XXVIII, alpha 1 [Source:HGNC Symbol;Acc:22442]
Mouse Orthologue:
Col28a1
Mouse Description:
collagen, type XXVIII, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:2685312]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa5797 Nonsense F2 line generated Not yet available
sa17603 Nonsense Available for shipment Available now
sa29212 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa5797
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
ENSDART00000112808 None None 1170 None 34
ENSDART00000132934 None None 312 None 7
ENSDART00000143292 Nonsense 89 133 4 6
ENSDART00000144300 None None 313 None 14
Genomic Location (Zv9):
Chromosome 19 (position 25991040)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 25921152
GRCz11 19 25505375
KASP Assay ID:
554-3577.1 (used for ordering genotyping assays)
KASP Sequence:
GGAGAACATGGAATGCCTGGACAAACAGGATCCAAGGTAAAAGCTTGTTA[C/A]CAGTTAACCAAWGTTGACATTACAGTTCTAGATCATCTCTGTAGGGTTGT
Long Flanking Sequence:
AATTATTTGCTCAACATAAAGCATGTTCTCAATACACATATATAGGGTGCCGTTGGGCAGCCTGGTGCTCCTGGTCTTTCAGGCCCACCAGGAGAGGGAATTCAGGGTCCCAAGGTAAGACATTGAGACCTGCAGGCCTTACTAATGGTTTAGCAGCTTAAACAACAAGAAAGTCATTAATATACAAAAAATTTATATACTAAAGCTTTAGCATACAGATCACTAAATTAGCTTTTGTCTTCACAGGGTGACCCTGGATTTCAAGGGCTTCCTGGCCCAAGAGGCCCTCCAGGTGATGGTCTGCCAGGGGAGAAGGTACTATAAAACACTGACTGGATTATACGTAATTGTTAATTTGTCGTTGCATTTCAAATGTAACATAACTACAAATCACAAATGTTTTAGGGGGACAGAGGCCTATCAGGAGAGCGTGGGAGAAAAGGAGAAAGAGGAGAACATGGAATGCCTGGACAAACAGGATCCAAGGTAAAAGCTTGTTA[C/A]CAGTTAACCAATGTTGACATTACAGTTCTAGATCATCTCTGTAGGGTTGTCCAGACCTTTAAGAGCAATTTTTAATTGAGATTTGCAGAGGGTCTGAAGAGAGCACATACATTGTTGTATAACTCTAGATCAGGTATGATCTTTAATCCAACTCAAGACAGTCTCCAAATGCTCTCAAGTCAATAGTAAGAAAATGAAAATCAAGACTTAAAACTTGCATGTTTTGGTCGAAAACACACTAAAATAAAGCATCCTGAAATTTACTAATAAAATTCTACTTAAATTTTAGGGAAAGCCTGGAGAGAAGGGAGATCCTGGCCTATCTGTGAGTTAAAACATTTTCCTCAGTTGTTTTTTTTCATCAGAACACTCACTAATATTGTACAAATAACACTGAACTATACCTCGCAGAGAGAAGAGGTGATCAAAATAATCCGGGAAATATGTGGTATGTTTTGGTACTCTAACACAAACTAAATGGGCATCCTGTGTTAGGTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17603
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112808 None 807 1170 31 34
ENSDART00000132934 None None 312 None 7
ENSDART00000143292 Nonsense 125 133 6 6
ENSDART00000144300 None None 313 None 14
Genomic Location (Zv9):
Chromosome 19 (position 25991620)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 25921732
GRCz11 19 25505955
KASP Assay ID:
2261-3337.1 (used for ordering genotyping assays)
KASP Sequence:
GGRTGTGGTGTGAAATGCCGGACGAGTCCACTGGAGCTGGTKTTTGTTAT[C/T]GACAGCTCAGAAAGTRTGGGTCCAGATAACTATGAAGTGGTGAAGGATTT
Long Flanking Sequence:
GATTTGCAGAGGGTCTGAAGAGAGCACATACATTGTTGTATAACTCTAGATCAGGTATGATCTTTAATCCAACTCAAGACAGTCTCCAAATGCTCTCAAGTCAATAGTAAGAAAATGAAAATCAAGACTTAAAACTTGCATGTTTTGGTCGAAAACACACTAAAATAAAGCATCCTGAAATTTACTAATAAAATTCTACTTAAATTTTAGGGAAAGCCTGGAGAGAAGGGAGATCCTGGCCTATCTGTGAGTTAAAACATTTTCCTCAGTTGTTTTTTTTCATCAGAACACTCACTAATATTGTACAAATAACACTGAACTATACCTCGCAGAGAGAAGAGGTGATCAAAATAATCCGGGAAATATGTGGTATGTTTTGGTACTCTAACACAAACTAAATGGGCATCCTGTGTTAGGTGGAAACACTTCATTTTTGTGTGTTTTCTCCCAGGGTGTGGTGTGAAATGCCGGACGAGTCCACTGGAGCTGGTGTTTGTTAT[C/T]GACAGCTCAGAAAGTGTGGGTCCAGATAACTATGAAGTGGTGAAGGATTTCGTAAACTCTCTGATTGATCATGTGTCTGTAAGCCGTGAGGCCACACGTGTTGGGGTGGTGCTCTACAGTCACGTGGAGGTGGTGGTGGCCAGTCTGCAACAGCTGTATGACCAGGCTGCTGTCAAGACTGCTGTGCGCAGGATGCCATACCTGGGTGAGGGCACCTTTACAGGGAGTGCCATCCGACGGGCAACTCAGCTGTTCCAAGCAGCACGACCAGGAGTTAGAAAGGTTGCGGTTGTGCTGACGGATGGCCTGGCAGACAACCGGGATGCAGTGAGTTTAAAAGATGCTGCAGAAGGTGCACACAGTGCTGGGATTGAAATCTTTGTAGTTGGTATTGTGAACAACAGTGACTCTCAGTATGCAGAGTTTAAGAATGAGATGAACATTCTGGCATCTGATCCAGATGAAAATTATGTCTACTTGACTGATGACTTCTTGAAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29212
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112808 Nonsense 858 1170 31 34
ENSDART00000132934 None None 312 None 7
ENSDART00000143292 None None 133 6 6
ENSDART00000144300 None None 313 None 14
Genomic Location (Zv9):
Chromosome 19 (position 25991771)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 25921883
GRCz11 19 25506106
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGGGTGGTGCTCTACAGTCACGTGGAGGTGGTGGTGGCCAGTCTGCAA[C/T]AGCTGTATGACCAGGCTGCTGTCAAGACTGCTGTGCGCAGGATGCCATAC
Long Flanking Sequence:
AAAACACACTAAAATAAAGCATCCTGAAATTTACTAATAAAATTCTACTTAAATTTTAGGGAAAGCCTGGAGAGAAGGGAGATCCTGGCCTATCTGTGAGTTAAAACATTTTCCTCAGTTGTTTTTTTTCATCAGAACACTCACTAATATTGTACAAATAACACTGAACTATACCTCGCAGAGAGAAGAGGTGATCAAAATAATCCGGGAAATATGTGGTATGTTTTGGTACTCTAACACAAACTAAATGGGCATCCTGTGTTAGGTGGAAACACTTCATTTTTGTGTGTTTTCTCCCAGGGTGTGGTGTGAAATGCCGGACGAGTCCACTGGAGCTGGTGTTTGTTATCGACAGCTCAGAAAGTGTGGGTCCAGATAACTATGAAGTGGTGAAGGATTTCGTAAACTCTCTGATTGATCATGTGTCTGTAAGCCGTGAGGCCACACGTGTTGGGGTGGTGCTCTACAGTCACGTGGAGGTGGTGGTGGCCAGTCTGCAA[C/T]AGCTGTATGACCAGGCTGCTGTCAAGACTGCTGTGCGCAGGATGCCATACCTGGGTGAGGGCACCTTTACAGGGAGTGCCATCCGACGGGCAACTCAGCTGTTCCAAGCAGCACGACCAGGAGTTAGAAAGGTTGCGGTTGTGCTGACGGATGGCCTGGCAGACAACCGGGATGCAGTGAGTTTAAAAGATGCTGCAGAAGGTGCACACAGTGCTGGGATTGAAATCTTTGTAGTTGGTATTGTGAACAACAGTGACTCTCAGTATGCAGAGTTTAAGAATGAGATGAACATTCTGGCATCTGATCCAGATGAAAATTATGTCTACTTGACTGATGACTTCTTGAAACTGCACGGTATGTATTTCTGTATTTCTTTTAAAAGGGGTGGTCCAGAGTTTATTTTTTAAGGCTTGGTTGGTTTTATAAGATGCACAGCGATGTGTGCTCATGCTTCATTTACAGAAAATCACGTTATTTTTCATATACCTTACTTTGATTAT
Associated Phenotype:
Not determined