ZMP
zgc:77816
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393843 [Source:RefSeq peptide;Acc:NP_957163]
Human Orthologues:
DNASE1L1, DNASE1L3
Human Descriptions:
deoxyribonuclease I-like 1 [Source:HGNC Symbol;Acc:2957]
deoxyribonuclease I-like 3 [Source:HGNC Symbol;Acc:2959]
deoxyribonuclease I-like 3 [Source:HGNC Symbol;Acc:2959]
Mouse Orthologues:
Dnase1l1, Dnase1l3
Mouse Descriptions:
deoxyribonuclease 1-like 1 Gene [Source:MGI Symbol;Acc:MGI:109628]
deoxyribonuclease 1-like 3 Gene [Source:MGI Symbol;Acc:MGI:1314633]
deoxyribonuclease 1-like 3 Gene [Source:MGI Symbol;Acc:MGI:1314633]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa754 | Essential Splice Site | Available for shipment | Available now |
hu7885 | Essential Splice Site | Available for shipment | Available now |
sa607 | Nonsense | F2 line generated | Not yet available |
sa17900 | Nonsense | Available for shipment | Available now |
sa32369 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa754
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:
G > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019854 | Essential Splice Site | None | 282 | 2 | 9 |
ENSDART00000121876 | None | None | 327 | None | 13 |
ENSDART00000131308 | None | None | 216 | 2 | 7 |
ENSDART00000133241 | None | None | 158 | 2 | 6 |
ENSDART00000138102 | None | None | 221 | None | 8 |
ENSDART00000140680 | Essential Splice Site | None | 163 | 2 | 6 |
ENSDART00000019854 | Essential Splice Site | None | 282 | 2 | 9 |
ENSDART00000121876 | None | None | 327 | None | 13 |
ENSDART00000131308 | None | None | 216 | 2 | 7 |
ENSDART00000133241 | None | None | 158 | 2 | 6 |
ENSDART00000138102 | None | None | 221 | None | 8 |
ENSDART00000140680 | Essential Splice Site | None | 163 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 5612282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5658349 |
GRCz11 | 22 | 5688195 |
KASP Assay ID:
554-0661.1 (used for ordering genotyping assays)
KASP Sequence:
CAACAGTTGTTTTTTTCTTTTCACAAAAYGCCGCCTTGTTTGTGGTTTTA[G/C]ATTTTATTTAAGGTCGACAACATGAAGATCGCATCTTTTAACATCCAACG
Long Flanking Sequence:
CCATATCAGATGAAAGACAGGAAGTAGGCTTGGCCTTTATTTTCAAATGAGCGCTCATTCATTATTCAGCATAGTTTTATAACAGACAACACTGGAAAAACAAGACTTGACTTCATTGTAATCACAGCAGCTTTGGTAAGAGCTCTTTTTTGTTTTTGTTTGTTTACATGATGATACATTTGAGTACTGAAAAGTGTTTAAATGCAATCGCTGGGACTTTTGGAGACTTTAATAAACTTATGCAATCAGTTAAACTTGTTTTCCTTTCAATTTCTCAAAGTAAAACTTTTTGGTTTTCCTTTCTGTCTCAATCGGTTTCCTGCATTATCGCACATGTCTGCTCTGTGCAAACATTAAGAGTTTCCTGTCTTCACACAATGCATCCTCAAACACCTCTGAGGGTTTACAACAGGAAAATAGCATAGAAACTCCCAACTGACCATAAAGTGACAACAGTTGTTTTTTTCTTTTCACAAAATGCCGCCTTGTTTGTGGTTTTA[G/C]ATTTTATTTAAGGTCGACAACATGAAGATCGCATCTTTTAACATCCAACGTATGGGTCCAAGCAAACTGTCGGACAAAAAAGTAGTCAAAACTCTCATCAAGGTCAGTTTGTCGTCTTATTGTTCAAAGGAATCACTTAAAATGACAACAAAATACTAAAAAAAGGCAACACTTTTCCCCTAGATCTTCTCCCGGTATAGTATAGTCATTGTCCTGGAGGTGGTGGATAAACAGGGGAAAGCCATCAACCAGTTCTTGAACGAGCTCAACAAAACTGGGTCTGTATGATTTCTGAGGCTTCATAGTTCAAAAAGCATGTAGTTCATCCCTCAAACCAAATGTAACTCGCTGTGTTTCCCACAGAGCTAATAAGAACAGTCCGTTCAAGATGGTGGGAAGCTCTAGACTGGGGCGGACGCTCTACAAGGAGCAGTTTGTCTGCTTCTACAGGTACTGCGTATGGTGACTATTGCAAATCTGAAGGATAAAACGAAGCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu7885
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:
G > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019854 | Essential Splice Site | None | 282 | 2 | 9 |
ENSDART00000121876 | None | None | 327 | None | 13 |
ENSDART00000131308 | None | None | 216 | 2 | 7 |
ENSDART00000133241 | None | None | 158 | 2 | 6 |
ENSDART00000138102 | None | None | 221 | None | 8 |
ENSDART00000140680 | Essential Splice Site | None | 163 | 2 | 6 |
ENSDART00000019854 | Essential Splice Site | None | 282 | 2 | 9 |
ENSDART00000121876 | None | None | 327 | None | 13 |
ENSDART00000131308 | None | None | 216 | 2 | 7 |
ENSDART00000133241 | None | None | 158 | 2 | 6 |
ENSDART00000138102 | None | None | 221 | None | 8 |
ENSDART00000140680 | Essential Splice Site | None | 163 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 5612282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5658349 |
GRCz11 | 22 | 5688195 |
KASP Assay ID:
554-0661.1 (used for ordering genotyping assays)
KASP Sequence:
CAACAGTTGNTTTTTTYTTTTCASAAAAYGCYGCCTTGTTTGTGGTTTTA[G/C]ATTTTATTTAAGGTCGACAACATGAAGATCGCATCTTTTAACATCCAACG
Long Flanking Sequence:
CCATATCAGATGAAAGACAGGAAGTAGGCTTGGCCTTTATTTTCAAATGAGCGCTCATTCATTATTCAGCATAGTTTTATAACAGACAACACTGGAAAAACAAGACTTGACTTCATTGTAATCACAGCAGCTTTGGTAAGAGCTCTTTTTTGTTTTTGTTTGTTTACATGATGATACATTTGAGTACTGAAAAGTGTTTAAATGCAATCGCTGGGACTTTTGGAGACTTTAATAAACTTATGCAATCAGTTAAACTTGTTTTCCTTTCAATTTCTCAAAGTAAAACTTTTTGGTTTTCCTTTCTGTCTCAATCGGTTTCCTGCATTATCGCACATGTCTGCTCTGTGCAAACATTAAGAGTTTCCTGTCTTCACACAATGCATCCTCAAACACCTCTGAGGGTTTACAACAGGAAAATAGCATAGAAACTCCCAACTGACCATAAAGTGACAACAGTTGTTTTTTTCTTTTCACAAAATGCCGCCTTGTTTGTGGTTTTA[G/C]ATTTTATTTAAGGTCGACAACATGAAGATCGCATCTTTTAACATCCAACGTATGGGTCCAAGCAAACTGTCGGACAAAAAAGTAGTCAAAACTCTCATCAAGGTCAGTTTGTCGTCTTATTGTTCAAAGGAATCACTTAAAATGACAACAAAATACTAAAAAAAGGCAACACTTTTCCCCTAGATCTTCTCCCGGTATAGTATAGTCATTGTCCTGGAGGTGGTGGATAAACAGGGGAAAGCCATCAACCAGTTCTTGAACGAGCTCAACAAAACTGGGTCTGTATGATTTCTGAGGCTTCATAGTTCAAAAAGCATGTAGTTCATCCCTCAAACCAAATGTAACTCGCTGTGTTTCCCACAGAGCTAATAAGAACAGTCCGTTCAAGATGGTGGGAAGCTCTAGACTGGGGCGGACGCTCTACAAGGAGCAGTTTGTCTGCTTCTACAGGTACTGCGTATGGTGACTATTGCAAATCTGAAGGATAAAACGAAGCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa607
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019854 | Nonsense | 99 | 282 | 5 | 9 |
ENSDART00000121876 | Nonsense | 99 | 327 | 4 | 13 |
ENSDART00000131308 | Nonsense | 99 | 216 | 5 | 7 |
ENSDART00000133241 | Nonsense | 99 | 158 | 5 | 6 |
ENSDART00000138102 | Nonsense | 99 | 221 | 5 | 8 |
ENSDART00000140680 | Nonsense | 99 | 163 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 5614704)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5660771 |
GRCz11 | 22 | 5690617 |
KASP Assay ID:
554-0517.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTGCTCAYATCYAACAGAGAAGCTGATGCTAAACTGCTCAACACATAC[C/T]AATATGAAGACAACCAAGTGGGTGAYGAAGATGCTTTCTCTCGGGAGCCG
Long Flanking Sequence:
ATCTGTAATATGTCGATCGTTAAATAGAGGTTTTGAAAGATATTCAAGATGTTTATGATTTAAAATGTTCGAAAAGCATGTTTTATGATATTTATCAGACCTTTCTAAATGGCTTCAGACCAAATGCTCTTCAAAATGTCTTGTAAACATTTGTATGCTATACGGTTTTATGCTATCAACATGCTAAAACATGTTAACTCATGCTAACAAGGTAGGTTAAACATGCTAGCAACATGTAAAAACCCATTAGCAATGTGTTAAACATGCTAAAACATGTTGGAAGCTTGCTAGCAGCATAGTTATTCATGTTAGCATTATGTTTACATGCTAGGAAAACATTTTCTCTTTTTCACATCATCTTAAATATATATTTATAGCTTACATAGCAGTTTTAAACAAAATATGTATGTTCGACTAAGACCAGTCATTCATGTAGCACTATTTAAGGCCTTTTGCTCATATCCAACAGAGAAGCTGATGCTAAACTGCTCAACACATAC[C/T]AATATGAAGACAACCAAGTGGGTGATGAAGATGCTTTCTCTCGGGAGCCGTTCATTCTGCGTTTCCAATGTAAAAACACAGGTAAGAAATCTGCTTGCTTTTCACAGTAGAAAACAAGAGGAGAAAAATATTAATTAATAAACTCAATTACCTGCTCTCTTTTCCAGTGATGAAAGATTTGGTGCTGATCCCTGTCCACACAAAGCCCAAAGACTCGCAGAAGGAACTGGATGAACTGTATGATGTCTTTGTGGAAGTCAGAGATAAATGGAAGACTGATGTGAGTTTAGCATTATGCAACTATTAAACAATATATAATAATGTGCATATTGATAAAATGGGGACATTCCAAAACACTTGACCAAGGCTTAATTAATCTGGTTGGTCAAAACAGGGTATAAACATGCAAGCAACATGCTAAAATGTGTTAACGTATGCTAAAACATGCTAATCATGTTGACAGTGTTAAAAACATAACTGTAACAGACAAACCATGCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17900
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019854 | Nonsense | 214 | 282 | 7 | 9 |
ENSDART00000121876 | Nonsense | 214 | 327 | 6 | 13 |
ENSDART00000131308 | Nonsense | 214 | 216 | 7 | 7 |
ENSDART00000133241 | None | None | 158 | None | 6 |
ENSDART00000138102 | Nonsense | 214 | 221 | 7 | 8 |
ENSDART00000140680 | None | None | 163 | None | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 5619307)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5665374 |
GRCz11 | 22 | 5695220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGGAGATGAYGTTGACACCACCGTCAAAACGACCAAYGACAACACCTA[C/A]GACAGGTGAGGAGCATCAATAAACWTTTGCTSTGCRGTTCTGTTTAAATA
Long Flanking Sequence:
TTGTCTAAGCAAAGTCAGACCTTACTGTCCTAATTAAATAATTAAAAATCAAGACATGATCAAATTTTATTGTGGTTAAAAAAAGCTTAATCTAGAGGCCTTTGCCTTTTTATGTAAGCCACTTTTGATACCAACGATCAACTAGAAGTCGAGTTATTATTTGCTGTTTCTAAAACTTTGATATGCGACAAGACTTTTGTCAGGTAGTGTATACAAAGAATTTAAATAGAAAAGACGGAAAAAATAAAATGAACTTATCTAACAGGTGATTTGTTTATTTAAAATGGAGAAATTCTAATCTTTAGTTTAACCAAATATGAGTAAGACTTTGCTTGCGTTGTCTTACAGAACGTCATGATCCTTGGCGACTTCAACGCAGACGGTGCTTACGTCTCCAAGAAGAAGATGAAGGCCATCAGAATCCGCACCGATACCGATTTCCACTGGCTGATTGGAGATGATGTTGACACCACCGTCAAAACGACCAACGACAACACCTA[C/A]GACAGGTGAGGAGCATCAATAAACTTTTGCTGTGCGGTTCTGTTTAAATATAAAGAATTCAGAGTTACACATTGTGCAAACGGATGCGAAATGTTTGTTGCAACACAATTAAAGTAAATAGTGATGGAAGTAATAAGAAACATAATCAGTTGCACTTCTCTTGAAAGTGAAATGTGTCTTTTGTGGGAATCCAGAGTAGTTCGTAATTACCCCTTATCCAAATTAACTGTGGTTTTATTATGGTCTAGTAAATGTGTGGTAACTTTAAGGTTTGGTGCAATTAGTGTCTTGGCAAAGCCACAGTTTTACCACAAACAGCGTGGTTTAACGGTGATTTATATACTAAAGTTGTAACCCAATTTTGGAACAAATATGCCAAACAAACCCAATGTTTGGTTAATTGTTTCAATTAAATTTAGATAAAAAATGTTTAACCCAATGGTTGGGGTTTTCCATATTTGACCCAACGTTGGGGTCATTTTAAAGCTTAAGAGACGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32369
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019854 | Nonsense | 264 | 282 | 9 | 9 |
ENSDART00000121876 | Nonsense | 264 | 327 | 8 | 13 |
ENSDART00000131308 | None | None | 216 | None | 7 |
ENSDART00000133241 | None | None | 158 | None | 6 |
ENSDART00000138102 | None | None | 221 | None | 8 |
ENSDART00000140680 | None | None | 163 | None | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 5622295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5668362 |
GRCz11 | 22 | 5698208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGGCTCTGGATGTCAGTGACCATTATCCAGTGGAGGTGACTCTAAAG[A/T]AGAAACCTGCAGCAAAGGCCACCGGCAAAACCAAGAAACCACAGAAACGC
Long Flanking Sequence:
ACAATGGGTTTAATCATATTTGACGCAATGCATTTTCTAGAGTGTATTTTCTTTCTGTTGGTCAGTGCTTTAAATTTGTGAAACAAACATCAGCAACATCTGTAAGACAATTTTTTTTCATCAATATTTCAATTTTGCATTAAAATGACAGTTTTCCCCTTCCACATCAAACATCTCCAGGAGTGTGAATGTATAATAAACAGCTGTATTAATAAAATAATGTACAAACCTTTGCAAAATGTTAATGGCAAGTATTTTCTGCAGGATTGTGGTGTATAAAGAGGACATGCTTGAGGCTGTCGTGCCAAGGTCTGCAAAACCGTTCAACTTCCAGGAGGCCTACAAACTCACAGAAGAAGAGGTGCATTTATTATTTACTGTACATGTCTGTTTTATAATGTGTGCTTTGCATGGATATAACATAAATATACACTGAAATGGTTTATCAACGGCAGGCTCTGGATGTCAGTGACCATTATCCAGTGGAGGTGACTCTAAAG[A/T]AGAAACCTGCAGCAAAGGCCACCGGCAAAACCAAGAAACCACAGAAACGCAAAGCATGATGGGATCTTAAAATGTGCTGATACTCAAGTTTAAGAGATGCTACCTCTTTAAAAGGCCAACTTGAGTTTAAAATCATTCATTCTTTAACATACATTTTAATTTACATTTTATATACATTACTTGCATTCAAATGATAGTTCACCTCCATAATTTAAAAGTAAAAATTCTGTCATCATTTACTCCTTCTCTTGTTCCAATCCTGTTTGAGTTTCTTTCTTCTATTGAAAACTAAAAGAAGATATTTTGAAGGATGTTGGAAACTGGTAACCACTGACGTCCATAGTACTTTGTTTCGACTATGAAGAATGTTGGATGTAAAAACACCATTGAATTTAATAGTTGAAACAAAATATACTGTGGAAGTTGGTGGTTACCAGTTTCCAACATTCTTCAAAATATCTTATTTTGTGTTCAACAGTTGAAAAACAAATCATAAAAGT
Associated Phenotype:
Not determined