Busch Lab

ZMP

dcbld1

Ensembl ID:
ENSDARG00000015907
ZFIN ID:
ZDB-GENE-050913-77
Description:
discoidin, CUB and LCCL domain containing 1 [Source:RefSeq peptide;Acc:NP_001035066]
Human Orthologue:
DCBLD1
Human Description:
discoidin, CUB and LCCL domain containing 1 [Source:HGNC Symbol;Acc:21479]
Mouse Orthologue:
Dcbld1
Mouse Description:
discoidin, CUB and LCCL domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1913936]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa37130 Nonsense Mutation detected in F1 DNA Not yet available
sa23788 Nonsense Available for shipment Available now
sa43512 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9772 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa37130
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
ENSDART00000015801 Nonsense 110 703 3 15
ENSDART00000099305 Nonsense 110 263 3 6
ENSDART00000138640 None None 445 None 8
ENSDART00000139912 Nonsense 110 289 3 5
ENSDART00000143993 Nonsense 85 207 2 5
Genomic Location (Zv9):
Chromosome 20 (position 42391429)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 42462588
GRCz11 20 42359698
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTTCATTTCTCCTAGTGTACTGGGAGTACTGTGGTGATCCAATGCCC[A/T]AGCCCTCACAGCTTCACACAGACTCCAATGAGCTGACCATTCGCTTTCGC
Long Flanking Sequence:
TTTGCCAACAATTTATGTCAAGTTTATTCAAGTTTTATAGTTGATGTTCATTGTTGACTTCCATTGTATTTTTCGTGCACAACTGAGCCTGGTTTCTCTTGAGTTTTTTCCCTTGTCAATTGGTGAAGTTTTTTTCTTTGTCACTGTCACCGCTGACTTGCTTGGTTTGGGACTTGTGGAGCTGCGCATTGATGGATTTGCTCTTCAGTGTTTGGATTTTCAGCAGTGAAAATTGAACCACACTGAACTGAACTAAACTGAACTTTAACTCCGAAAACTGGACTGAAGCACTCTCAATTTTCTAGAACTTCTGTGTTAAGCTGCTTTGATACAATCTACATTGTAAAAGCGCTATTATTCTTGGATCGTTTCATTTATTCACTGCTACTGTAATACCCTAATAATACCTCAATATGATTCTGATTAATCTTTTATTAATTGTCCTTCACTTGCTTTCATTTCTCCTAGTGTACTGGGAGTACTGTGGTGATCCAATGCCC[A/T]AGCCCTCACAGCTTCACACAGACTCCAATGAGCTGACCATTCGCTTTCGCAGCAGCCAACACATCACTGGAAGAGGATTCCTGCTTTCCTACTCCACAGAAAACCACAAAGGTATCCATACTGTAAAAGTTTAAGTGTGTATCACCTTAACATTACGTTGTACATACATTTGTACATTACATACAGTTGAAGTCGGAATTATTAGCCCTCCTGAATTATCAGCCCCTTCTTGTCTCTTGGTTGACCCTCATGTAAACCTCTGCTCTGTGGCTTGTTCCCTTTTCGTTCTTGAGATGCTTTTGGATCCTTTTGGGATGTTTCTTTAAACGACATGTTTGAACTCAACAGAGCAATTGATAAAAATATAATTGATGTAGAAATGAAAAGGCTGTTGGGTTTTATTCACCCTTATGTTGTTCTAAAGCTGGATGACTTTCATTCTCCAATGAAATGCAAAAAAAAGAGGAATGTCAAGGTCTATCTGTGATCTTCTATCTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23788
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015801 Nonsense 113 703 3 15
ENSDART00000099305 Nonsense 113 263 3 6
ENSDART00000138640 None None 445 None 8
ENSDART00000139912 Nonsense 113 289 3 5
ENSDART00000143993 Nonsense 88 207 2 5
Genomic Location (Zv9):
Chromosome 20 (position 42391420)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 42462579
GRCz11 20 42359689
KASP Assay ID:
2261-4816.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCCTAGTGTACTGGGAGTACTGTGGTGATCCAATGCCCAAGCCCTCA[C/T]AGCTTCACACAGACTCCAATGAGCTGACCATTCGCTTTCGCAGCAGCCAA
Long Flanking Sequence:
AATTTATGTCAAGTTTATTCAAGTTTTATAGTTGATGTTCATTGTTGACTTCCATTGTATTTTTCGTGCACAACTGAGCCTGGTTTCTCTTGAGTTTTTTCCCTTGTCAATTGGTGAAGTTTTTTTCTTTGTCACTGTCACCGCTGACTTGCTTGGTTTGGGACTTGTGGAGCTGCGCATTGATGGATTTGCTCTTCAGTGTTTGGATTTTCAGCAGTGAAAATTGAACCACACTGAACTGAACTAAACTGAACTTTAACTCCGAAAACTGGACTGAAGCACTCTCAATTTTCTAGAACTTCTGTGTTAAGCTGCTTTGATACAATCTACATTGTAAAAGCGCTATTATTCTTGGATCGTTTCATTTATTCACTGCTACTGTAATACCCTAATAATACCTCAATATGATTCTGATTAATCTTTTATTAATTGTCCTTCACTTGCTTTCATTTCTCCTAGTGTACTGGGAGTACTGTGGTGATCCAATGCCCAAGCCCTCA[C/T]AGCTTCACACAGACTCCAATGAGCTGACCATTCGCTTTCGCAGCAGCCAACACATCACTGGAAGAGGATTCCTGCTTTCCTACTCCACAGAAAACCACAAAGGTATCCATACTGTAAAAGTTTAAGTGTGTATCACCTTAACATTACGTTGTACATACATTTGTACATTACATACAGTTGAAGTCGGAATTATTAGCCCTCCTGAATTATCAGCCCCTTCTTGTCTCTTGGTTGACCCTCATGTAAACCTCTGCTCTGTGGCTTGTTCCCTTTTCGTTCTTGAGATGCTTTTGGATCCTTTTGGGATGTTTCTTTAAACGACATGTTTGAACTCAACAGAGCAATTGATAAAAATATAATTGATGTAGAAATGAAAAGGCTGTTGGGTTTTATTCACCCTTATGTTGTTCTAAAGCTGGATGACTTTCATTCTCCAATGAAATGCAAAAAAAAGAGGAATGTCAAGGTCTATCTGTGATCTTCTATCTTTATTTAGTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43512
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
ENSDART00000015801 Essential Splice Site 349 703 10 15
ENSDART00000099305 None None 263 None 6
ENSDART00000138640 Essential Splice Site 103 445 3 8
ENSDART00000139912 None None 289 None 5
ENSDART00000143993 None None 207 None 5
Genomic Location (Zv9):
Chromosome 20 (position 42340895)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 42412054
GRCz11 20 42309164
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTTGTCATTCATCTGTTTTAATTGTTCATTGTTGTATTTTTCCTCA[G/A]GTTTTTGAAGGAAACACTAACAGCCTCCACCAAACGCGCAACACCTTCCA
Long Flanking Sequence:
TTTTTTTTCAGATTATAGTTCTGTAATTTACAATATCTGAGAGCTTAAAATATAATTTGAAGAAGGAGAAAACAATTTCAAGATAAATAATATAAATTTTGAACAAAAACAGCAGGGTAAAGTACATTGTAAGGGTGGTCTTGCATGTTTACATTCACAATACTGTAATATATCCATATACACATATACATGTGTAAACAGAAGCCATTGCAGAAGCCATTTACAAGTAATAGCCTTCTACGCTGAAAGAAGTATTCTCCATAAATGTGTCTATAGCCTCAAGCAACTCAAAAATTTCAAAATATAACACCTCCGATGTCCTGTGTATGTCCCTAATTACAAGTCTATAGCTGGACATGCCCAGAAAATATGATGGTGATTAGCAAACTCAGAATTGCAATGCCTCCAACACCTTGTTAAACTTTAATTTCTTAATAATATCTGTCTAACTTTGTTTGTCATTCATCTGTTTTAATTGTTCATTGTTGTATTTTTCCTCA[G/A]GTTTTTGAAGGAAACACTAACAGCCTCCACCAAACGCGCAACACCTTCCATCCCTCCATCATATCGCGATACATCCGAGTCGTACCCCAACAGTGGCACCGGACGATTGCCATGAGACTGCAGCTACTGGGCTGCTCTTACGTCAAACCCATTCCAGGTATGTTTCTGAATCTTCACAGCCTAATTTTTCTCATTAAATTGCTTGACTAAAGCTCTTTTTGTCCTATTGTAGTGAATGCATCATCTCAGGTGACGCAGGAGGCTCAGCCTACACAGCCCATTCACAACATGACCAAACCTGTGGCCTCGCAGGCAGATTTTGGTATGATTTTAAGAACACACGTTAATTAACGCTCATTAATTATTATATGTTATGTTAGAGATGTACTAAACGAATGTCAGAGAATATGATATGCCTTTTATTTCTACACTTATTCAAGTTTCAACTGCAAGCTCATAGTGATAAAGACATCTTGCCTGTCTGTCGTTCTGTCATTCGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9772
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015801 Nonsense 613 703 15 15
ENSDART00000099305 None None 263 None 6
ENSDART00000138640 Nonsense 355 445 8 8
ENSDART00000139912 None None 289 None 5
ENSDART00000143993 None None 207 None 5
Genomic Location (Zv9):
Chromosome 20 (position 42331692)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 42402851
GRCz11 20 42299961
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGTGCTAAACAAAARCCCATCGTTTCGGGCAGTCGAAGGCGGGAACTG[T/A]AGGAAAGTGATYGGAGGGCTGGCCGGGGGCTACCAAACACCTCAAGTAAA
Long Flanking Sequence:
AAATGTGTTGAAAAAATTCTAAATATTCAGGGGGGCTATTAATTCTGACTTCAACTGTATATTAATTTTATCCCCAAGAATGTACATAAATATTACAGATATAATTTTAAATAGTACATTAAAAAAAAACGAATCTCCCACTAATCCCAGAGTTCTCTTTAGAACAACAATTCTAATTCCAGTTATTTCCCTTCTCAATTTTCTTCAGCAGAGTACCAACAACCACTGATGCTCGGCACGGACACAGTGTCCCGAAAAGGCTCAACGTTCAGACCGATGGACACCGAAACTAAAGACATGGAAAGTTCTCACTATGACCACCTGCAGACAGGCATCCAGTACGCCTTGCCACTGACCAATCAGGAGCCTGAATATGCCACACCCATAATCGAGCGCCACGCCTTCCGCAAAGACCCCTTCATCCCTGACGCTAGCTATAGTGTGCCAGGAGTGGTGCTAAACAAAAGCCCATCGTTTCGGGCAGTCGAAGGCGGGAACTG[T/A]AGGAAAGTGATTGGAGGGCTGGCCGGGGGCTACCAAACACCTCAAGTAAAGCCGGATCGAGGGAATTCCCCAGAGGACATCTATGATAGCCCTAAAATCCGCAAAGCTGTTGTCCTGAATGGCCCTGAATATCAGAGACCCCAGATTAAATCTCAGGATCAGGAGTGTTACTCAACTCCCAGAGATTGTGTTAGATTGCCTTTCTCCGGATTGAGACCAGATCCCGAAGGAAGCCGGTCTGAGCCTGAAGGCAGCAGCTCTGATGGAAGCTGAGATGAGTTTTACTGCCTTTTAATGTACCTGACTCAACAAAATCACCTCTTCGTAACTTATTTGAGTATTAGCGACATGTTTTTTAGTAAGTTCGCAGGAAAGGACTGTGGAGGCCAAAATTGGTTTGTTGTAATTTAATGGTTTTTATATGAGATTTTCTTTTTTTTTTGTCTTGATGAATCAATATTTTTTAAATTGTGCTGTTTATTTTATTATTAATATGCAGT
Associated Phenotype:
Not determined