ZMP
ddb2
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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