Busch Lab

ZMP

ddb2

Ensembl ID:
ENSDARG00000041140
ZFIN ID:
ZDB-GENE-050419-169
Description:
DNA damage-binding protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q2YDS1]
Human Orthologue:
DDB2
Human Description:
damage-specific DNA binding protein 2, 48kDa [Source:HGNC Symbol;Acc:2718]
Mouse Orthologue:
Ddb2
Mouse Description:
damage specific DNA binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:1355314]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa18412 Nonsense Available for shipment Available now
sa2975 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa18412
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
ENSDART00000060302 Nonsense 82 496 3 11
ENSDART00000100665 Nonsense 82 497 3 11
ENSDART00000147867 Nonsense 82 490 3 11
Genomic Location (Zv9):
Chromosome 18 (position 20249491)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20479714
GRCz11 18 20468780
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTGGGCCAAAYAAGCATTCTTCATTACATTTACAAAAGTTCATTGGGA[C/T]AGAGTATCCATGCTCAACTGCGCCAGGTAATGACAATTGAAGTTTGGGGW
Long Flanking Sequence:
CCTTAAACACTTGAAAGAAAGACAAGGTAACGTTGTGCATGATTGTAGTCGAACGGGTCATTATCTATATTTTGTTCTCACGAGTAATGCAATTGCTATATGACATGTCTTTGTTGACCCTTTCCAATCAGAAAGTAGCTTTGCAATGGCGCGAGGAAGAGCTCAGACAGACTCTGCTGCATCGAAGCAGACGAAGACTGTCAATTCAAAGAAAAGACCGAATGAAGAAACTCCGCAACCTTCCACCAAAAAGCTGAAAGCTAAACAACAACATAAGAGCAAACAAAAAGAAGGTAAGCGAAACTGCGAGTTAAGTTATATAATTGATTGGGTTTAAATGTGCAAAGAAAAAGTTGAACCACTCATTAATGTAATCTTATGAGGTAAACTGTGTTTGTGTACCAGAAACCTATATACAAGCAAGTGTGAAATGGACAGGAGGTCAAAAGAAAGTGGGCCAAACAAGCATTCTTCATTACATTTACAAAAGTTCATTGGGA[C/T]AGAGTATCCATGCTCAACTGCGCCAGGTAATGACAATTGAAGTTTGGGGAAAGAAGATTAAAGTACACCAGTTACTCGCTAGAATGTTAGATATCGCCACCCATATTAAATAATGATTTAATGTTGTATGAAAATCATACATTTTTAAAGAAGCTTAGTACATGACTGCAGAATTATGCAGCATATGTATTTCAACTATACAGTAAAAAACATAATTTCCCCCTTCTTGTCTTAACTTTGGCATTTGTTCATTTTGGTGACATATTTGCCACAAACTCCTATTTATATCTGAACCTGGTCGTATAAAACATTGTTTCTTGTGTTACAGTGTCTGCAAGAGCCTTTCATACGCTCACTTAAATCTTACAAGCTGCACCGAACTGCCAGTCCCTTTGACAGGAGGGTCACTAGTCTGGAATGGCATCCCACACATCCCACCACCGTTGCAGTGGGATCAAAGGGTGGAGACATCATCCTGTGGGATTATGATGTGCTGAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2975
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060302 Nonsense 280 496 7 11
ENSDART00000100665 Nonsense 287 497 7 11
ENSDART00000147867 Nonsense 280 490 7 11
Genomic Location (Zv9):
Chromosome 18 (position 20256344)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20486567
GRCz11 18 20475633
KASP Assay ID:
554-3173.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCTGTTGATGCTACAGTCAAGCTGTGGGACCTCCGGAATATTAAAGAC[A/T]AAAACAGTTACATCGCTGAGATGCCTCATGAAAAACCAGTCAATGCTGGT
Long Flanking Sequence:
TGCACGTTATTTATTAAGATAATTCTTTGTGCTCTTATTTATTTGATTATTTATATTGTTTCATGTTTATGGGGGGACAGGGACATTTTAAGGTTTTTATTACTATTGTGTAGAGCAGTGTTTCCCTACCCTGTTCCTGGAGGCCCACCAACAGTACATATTTTGGATGTCTCCCTTATCTGACCCATTAACCTCAGGTTTTGGAGTCTCTTCTAATGTTCTGATGAGTTGATTCAGGTGTGTTTGATTAGAAAGAGGTTAAAATGGGTACTTTTGGTGTGCCTTAAGGAACAGGGTTGGGAAACACAGCTGTTGAGAGTTGATTTATATTTTTCAATTATTTTAATTTTTTTGCCCAAAAATATATTTAGATTTTCAAAGAGAAGCTGCACAAAGCCAAAGTGACCCATGCCGAATTCAACCCTCGCTGTGATTGGCTGATGGCAACATCCTCTGTTGATGCTACAGTCAAGCTGTGGGACCTCCGGAATATTAAAGAC[A/T]AAAACAGTTACATCGCTGAGATGCCTCATGAAAAACCAGTCAATGCTGGTAAGGGACCATATTATCAGAAAAGTGAGGAAAGGAGAAAGTCACCTGTACAGTAGCTTTAAATACTAATACATTCAAATGAACTATTTTTGTCAGCATACTTCAACCCGACAGACAGCACCAAGTTGCTTACTACTGATCAGAGGAATGAGATCAGGGTGTACAGTTCATACGACTGGTCTAAACCGGATCAAATAATTATTCATCCTCATCGGCAGTTTCAGCACTTGACTCCCATCAAGGTTAGAAATTTAATGCATTTCTTTCTTTACAGGACTGCTGACATCATGGTTATACTTTGCTCCATTTTTCTATTTTTTCAGGCAACCTGGCATCCCATGTATGACCTCATTGTGGCTGGCCGTTACCCAGATGATCAACTATTACTCAATGATAAAAGAACTATTGACATTTATGATGCCAACAGTGGTGGACTTGTGCACCAGCTGAGA
Associated Phenotype:
Not determined