ZMP
dennd3b
Ensembl ID:
ZFIN ID:
Human Orthologue:
DENND3
Human Description:
DENN/MADD domain containing 3 [Source:HGNC Symbol;Acc:29134]
Mouse Orthologue:
Dennd3
Mouse Description:
DENN/MADD domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:2146009]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11410 | Nonsense | Available for shipment | Available now |
sa18385 | Nonsense | Available for shipment | Available now |
sa2847 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11410
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035583 | Nonsense | 30 | 1262 | 2 | 25 |
ENSDART00000124555 | None | None | 256 | None | 5 |
ENSDART00000131356 | None | None | 306 | None | 6 |
ENSDART00000141403 | None | None | 113 | None | 2 |
ENSDART00000143996 | Nonsense | 30 | 452 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 33204667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 30943182 |
GRCz11 | 16 | 30901109 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGCATGCACCCTKTGATTTSTATGTTTTCTTTATTTTSTTCAGTCTT[T/A]GTCACAACTGAATGGAAGTCCTCTTCCTCTGYTCGATCCTGAGGTTCTGC
Long Flanking Sequence:
CAGATATATTGTGCCTTAAAATGACACAATTTTTTACGTCAACTTTTTTAAAGATTTGCAGCAATATTTGTGGCATTTCTGTAATAATAAACACAAATTGACATAAATTAATTCTTCATTAGTTGTTTGACCTCTTGAACCACCTATATGAATGAAACACTGGAAAACTTTTATCTAAAGGAAATATAGTTCATTTGCTTTAATTCACTAAACTTTCTACATAAGTGTAACTGTACTTTTTTGTTCTGTATTCTCACTATAAATCAAATGGGCAATTAATATTATAGTAACCTAAAATAATAATTTCTGTAAATGATTGAAGATTATTGGAAATTATTTGGTTATGCAACAAACAAGCACGTTTGAAAAACGGGTGTCAAAATCTTAAGATCACTTTCATATGCTCAAACAGAAACATTGCTTAGTGCACTTTTTTTAGACTAATCACTATGCAGCATGCACCCTTTGATTTGTATGTTTTCTTTATTTTCTTCAGTCTT[T/A]GTCACAACTGAATGGAAGTCCTCTTCCTCTGCTCGATCCTGAGGTTCTGCAGGTCCACAGGCCTCTGTTTTGCCTTAAACAGAATGTCACGGAACCGGCTGTGGAAACCTTAAGTCCGACTCAGCAATGGTGTTCTCCGATTCAGAAAAACAACGATAAGCCCACTTTTAACACCGTAAACCCCAAGGAGGAAGCCACAGAGAATGCCAGCACTCTTAAAGAACTGGATCTGGCAGCTTTACCACAACTGTGCTTTCCAGGTGAAACAAAATTGAATGGAAATGCTTGACTTTTTTTTACTGCGGTTCAAGTCCACAAAGATATTCATACATCACACAGATTAATATTTAAAAAGTAGGGCTGCATGATATAGAAAAAAATCTGACATTTTGATTTGGCGCAATATATATTTTACTTTGACCAAATGATTTGAATGGCTCTATCTGAAAATAATTCATTAGTCTTATTATTCTATGCGCTGTGTTTGCATATGATATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18385
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 |
---|---|---|---|---|---|
ENSDART00000035583 | Nonsense | 231 | 1262 | 5 | 25 |
ENSDART00000124555 | None | None | 256 | None | 5 |
ENSDART00000131356 | None | None | 306 | None | 6 |
ENSDART00000141403 | None | None | 113 | None | 2 |
ENSDART00000143996 | Nonsense | 231 | 452 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 33201137)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 30939652 |
GRCz11 | 16 | 30897579 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAAGGAGTTTTCTGCTAAACTATCTGTGGTCCCAGTTCCCCCTCCTGGT[C/T]AGCTGCATGTGGTGGGTTCAGAAGATCAGGAGGCWGATTAAAACTGTAAA
Long Flanking Sequence:
CACATTGCAGCCGAAAAGTCGGAAAGTTGAAAAAAGTTTTCGTTTCCTAAAAACTCTCTTAGCTTGCCATGGAGAGAAAAATATGCAGCTCATGGCCACTGACATGAGTTGAGCTGCTGGAGAATCAGAGTAGAGCTCATTAATATGCACAACTTTTCAATTATATCATATTAGGGCCCATTCCTAGGATTTACCTAAGCCACATATCTTGTATGGAGATATCGGAGAACAATTTATTATAGTGTATCAATGTGTATGGCACCTTTAATAAATTACATTGCACTCAGTTTGGGGTGTGACCTCAAAGTAATGGCAAACATATTTGTCTCCACACATTGAATGGAAGTTGTAGAAAGTACAGCACCATTTCCTCAATTATTGTTTACTGTCCTATCCACAGCCTCTTACGTGAGCTCAAAATCTGCCAGATGACTGAGATGGAGGAGCGAGCGAAGGAGTTTTCTGCTAAACTATCTGTGGTCCCAGTTCCCCCTCCTGGT[C/T]AGCTGCATGTGGTGGGTTCAGAAGATCAGGAGGCTGATTAAAACTGTAAATCCAATTTTACCCAATTGCATGTAAAATACATTTAAGCAATTTTTCTTTTCAGATGTTCATCATGCAGCCTCTGATGATTGTCCTTCCATCAAGAGAGGATCAACATCATCCTGTGGTTGATTTGGACCTTCATCTTCCATTCCTCTGCTTCAAGTCCAAAGAAGTTCTGCAGGTCTCAAATATAAATGGAAAATCAATAATTGGGGGGTTTCTTGGACAAAAATCTGGAAATCAGTCAGTTAGAGAAGCAAAAATCTCTTTTACCCTATTGTTGACCTCATGTACAAAAATTGGGTCAAAAATCTTTCGCGACTATTTTAGCAGCAGAAAAAAAAAATTATGTTTTTTTTATCTTAAAGTTTGTTGAATTTTTCTAAAATGACCCCAACATCACGACTATTTATCTATTGTCATGAAAGATGTAAACATGTGAGGTAAAATGATTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2847
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 |
---|---|---|---|---|---|
ENSDART00000035583 | Nonsense | 785 | 1262 | 15 | 25 |
ENSDART00000124555 | None | None | 256 | None | 5 |
ENSDART00000131356 | Nonsense | 46 | 306 | 1 | 6 |
ENSDART00000141403 | None | None | 113 | None | 2 |
ENSDART00000143996 | None | None | 452 | None | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 33189261)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 30927776 |
GRCz11 | 16 | 30885703 |
KASP Assay ID:
554-2731.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTGCCTGCTGAGGTCCTGGAGCGCCTGGACAGTAATGAGTGTGTCTAC[A/T]AGCTGTCCAGGTCTGTGAAGACCAGTTATGGTGTTGGGAAAATAGCAATG
Long Flanking Sequence:
AAGTTATTATTTTTTGTTCCTAAAACTTGGATAGGTGTCAAGACTTTCGTCAGGTAGTGTAGATAGGAAGAGTAAAGAGTATGTTTCCGACAGCTGGTTTGTCCAGGTTGGGGTTTGTGGTTCTTGGCTTCTCGCGGGCAAAAGTGCAGAACGGGGGAGTGGGGGTGATTGGGGGGCCTCTAATAGTAACTTTGGGGGCCCCAAAATGGTGTGGGCCCTTAGAATCATCCTAACTCATTTTTAGTGTGTGTGTATTGCATTGTGTTGTTTCAACTCATTTTAAATAAGTAGCTTAAACAAGCAGCAAAGGTAATTTCTTTCAATGTACTGTGTTTTATAATCAAGATTTTTCTTTGGCTTTTGTAGGTGGTCAGAAGCAGATTGTTCCAGAGCTATTCAGGATGTTTTACAAATTCTGGAAGGAGACTGAGGCAGAAGCCCAGGACGTTCTTTTGCCTGCTGAGGTCCTGGAGCGCCTGGACAGTAATGAGTGTGTCTAC[A/T]AGCTGTCCAGGTCTGTGAAGACCAGTTATGGTGTTGGGAAAATAGCAATGACTCAGAAAAGGATTTTTCTGCTGACCACAGGAAGTCCTGGATATGTGGACATCACAAAGTTTAGAGACATTGAGGTTTGTTCATTTTTATGTCTATAGTATACTGTTTAAACTGAGAGGTTTACGCTTGTGGTAACGGTATGAATCCTTTGAATAAAGGAAGTGAAGATCTCTGCCCCTGTACGAATTTTAAGAAATTCATCATTAAAGATCAAGAACAGCCTGAGGGATGAGATATTCGAGGCTAATTTAAAATCTGAGTGTGAACTGTGGAATCTCATGGTCAAGGAGATGTGGGCTGGCAGAATGATGGCAGACAACAATAAGGTAAAGTTAGCTTGTATTGTGATTTTTTTCTTTTTCTTTCTTTCTTACAAATCAAGTCAGTTAATCCTGACATTGTTTACTATGATGTCCAACACAGGCATCTCTGTTGTAATAACCATGATC
Associated Phenotype:
Not determined