ZMP
Q08CN5_DANRE
Ensembl ID:
Description:
LOC558626 protein [Source:UniProtKB/TrEMBL;Acc:Q08CN5]
Human Orthologue:
DENND4C
Human Description:
DENN/MADD domain containing 4C [Source:HGNC Symbol;Acc:26079]
Mouse Orthologue:
Dennd4c
Mouse Description:
DENN/MADD domain containing 4C Gene [Source:MGI Symbol;Acc:MGI:1914769]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1910 | Nonsense | Available for shipment | Available now |
sa13987 | Nonsense | Available for shipment | Available now |
sa21119 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16852 | Nonsense | Available for shipment | Available now |
sa38651 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41064 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1910
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 |
---|---|---|---|---|---|
ENSDART00000082930 | Nonsense | 28 | 633 | 2 | 16 |
ENSDART00000114722 | None | 87 | 1942 | 1 | 33 |
Genomic Location (Zv9):
Chromosome 7 (position 65638624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58820364 |
GRCz11 | 7 | 59122794 |
KASP Assay ID:
554-1900.1 (used for ordering genotyping assays)
KASP Sequence:
GCCAATCTCAACCATGGCAGCCTCAAGAGCCCAGAACTCTTCCTRTGTTA[C/T]AAGAGGGGTCGAGGGAAGCCCCCGCTCATTGACATTGGGTGAGTTTGTAT
Long Flanking Sequence:
TTGGGACACCTGTCTTTGGGAATGTTTGCCCTTTCCTCTTTGCAGTACCTCTCAAGCTCTATATATATTTGTTTAATGTTATGAAAATTGTATTATTGACCTAATGTACAACTGCATTGATGGACTGTTTAATACTGTTTACATTTTTATTTTTTTTGTGGTGGTGGTGGTTGCTAAGTCCCAAGACCTACAAGCATGTCAACTTAATAGTATCTTCTCTCCGAACAGGTCTGTCCAGCCATGATTGAGGATAAGGGTCACCGCGTGACGGACTACTTCGTTGTGGCTGGCCTGACAGACAAGTCTACACCACTAGAGCAGGATATATCTGAAGCCAAGTCCAGTGGGCCCAAGGCACCAATCACAGACCTTGCTGTCATCAACAAGTCTTCTGGAGAAACTGTGCCTGAAGGTTTCACATGCATCGAGAGCACCTACAGCGGCCAGCCGGCCAATCTCAACCATGGCAGCCTCAAGAGCCCAGAACTCTTCCTATGTTA[C/T]AAGAGGGGTCGAGGGAAGCCCCCGCTCATTGACATTGGGTGAGTTTGTATGGTGAATGGCTGTTTCACTGTGTAGAGGTACCCTGGAATAGATGCTTTTTAGTTAGTGAAATATGATGTGTGTTTTTTACAGCTCACTTTCCCTGTAGATACAACACTAGATCTCCGTCCCTCTCAAAAACATTGAAGTTGTCTGCATGATCTGTTTCAATTAAGGCCCTCAAAAGTCTTGACTCAAAATTTTCAATCTTTAATGTTGTACTGCAGGATGGTTTAGATTGAAGAGTATTTTCAAAAAGGTAATTATTAACTTGCCATTTACTTGCATAATAAAAACAACACAAAAGTTGGCGTCAATAGCCTATTGGTTAAGTCAGGGTTCATACGGTCATAAAAAATCTGGACCACAGCTGCGTGTTAGTACAATTATAAAAGAAGACGCTTCAATCGCGATTTGTGGACGTTAAATCAGGTTTATTTTCCATTAACATAACAAATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13987
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 |
---|---|---|---|---|---|
ENSDART00000082930 | Nonsense | 384 | 633 | 11 | 16 |
ENSDART00000114722 | Nonsense | 444 | 1942 | 9 | 33 |
Genomic Location (Zv9):
Chromosome 7 (position 65621689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58803429 |
GRCz11 | 7 | 59105859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATCTCATTATTATTTCCTTCTAGATGATCTTCCCCTTCCAGTGGCAATR[T/A]CCATATATTCCTCTTTGCCCTCTGTCTTTGGCGGGGGTTCTCAATGCACC
Long Flanking Sequence:
AAACGGGTCCAACACAAAAGTCTAGAAGTGAAAGCACCCTAAGAGTGACTAAACTTTAAATGTCATGTATCAATATGAACATGTCTTCATACTGCTAAATAAATGACCTTTTTTAAATTCAGCATTTGATATTTTTCTCTCTTCGTATTCTTTACTCAGTGGAGCAGACTACAGTACACTGCTTATGAATCTAGGCCCAGAAAACTGTGCCACACTGCTTCACTTTGTCCTGCTGGAAAGTAAGATCCTGTTGCACTCCCTTCGACCAGCTGTTCTGACTGGAGTGGCTGAGGCTGTTGTGGCAGTAAGTGTTTGTGCTGATTTCACCGCTCTCCTCACTTGACAGTATTTCAGGATCTAATTTTTTGGTAATCAATGAACTTATGTAAATTACAAGTGGGTTACGAATGAAAATATTTCAATTCATTTTTAAACAATTGGATTAAATGTGATCTCATTATTATTTCCTTCTAGATGATCTTCCCCTTCCAGTGGCAATG[T/A]CCATATATTCCTCTTTGCCCTCTGTCTTTGGCGGGGGTTCTCAATGCACCATGTCCTTTCATTGTGGGCGTTGACTCAAGATACTTTGACCTCTACGATCCCCCTCCTGACGTAGTGTGTGTGGACTTGGACACCAACACTATATATTTGTGAGCACTCTTGAACATTTTGAAATTTAATAGTGTTTGTTCTTTATTTACGACTTTGTGTAATTGCTTTTGTCATTTTATTTACACTGCCCAGCCAAAATAAAGTAACCACCTGGATTTGACAAAGCAAATAGATCAGAACCTCCCATTGGTTAATTACTACAGGGATGATTACGTTTCAGCTGGGGGAAGTTGAAGGGGCAAATTATTGGCATGCGTCAAGCAAAGAAACATTTATGCAGAACTACTAAAGCTGGGTTAAGAAATGTCCAACACATAGAAACCGTCATCTTTGAGGAAGACATATGGTAAAAAAAATATCTTGAATGATCAAGGTCGACAATCGATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21119
Status:
Mutation detected in F1 DNA
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082930 | Nonsense | 427 | 633 | 11 | 16 |
ENSDART00000114722 | Nonsense | 487 | 1942 | 9 | 33 |
Genomic Location (Zv9):
Chromosome 7 (position 65621561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58803301 |
GRCz11 | 7 | 59105731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATACTTTGACCTCTACGATCCCCCTCCTGACGTAGTGTGTGTGGACT[T/A]GGACACCAACACTATATATTTGTGAGCACTCTTGAACATTTTGAAATTTA
Long Flanking Sequence:
ATATTTTTCTCTCTTCGTATTCTTTACTCAGTGGAGCAGACTACAGTACACTGCTTATGAATCTAGGCCCAGAAAACTGTGCCACACTGCTTCACTTTGTCCTGCTGGAAAGTAAGATCCTGTTGCACTCCCTTCGACCAGCTGTTCTGACTGGAGTGGCTGAGGCTGTTGTGGCAGTAAGTGTTTGTGCTGATTTCACCGCTCTCCTCACTTGACAGTATTTCAGGATCTAATTTTTTGGTAATCAATGAACTTATGTAAATTACAAGTGGGTTACGAATGAAAATATTTCAATTCATTTTTAAACAATTGGATTAAATGTGATCTCATTATTATTTCCTTCTAGATGATCTTCCCCTTCCAGTGGCAATGTCCATATATTCCTCTTTGCCCTCTGTCTTTGGCGGGGGTTCTCAATGCACCATGTCCTTTCATTGTGGGCGTTGACTCAAGATACTTTGACCTCTACGATCCCCCTCCTGACGTAGTGTGTGTGGACT[T/A]GGACACCAACACTATATATTTGTGAGCACTCTTGAACATTTTGAAATTTAATAGTGTTTGTTCTTTATTTACGACTTTGTGTAATTGCTTTTGTCATTTTATTTACACTGCCCAGCCAAAATAAAGTAACCACCTGGATTTGACAAAGCAAATAGATCAGAACCTCCCATTGGTTAATTACTACAGGGATGATTACGTTTCAGCTGGGGGAAGTTGAAGGGGCAAATTATTGGCATGCGTCAAGCAAAGAAACATTTATGCAGAACTACTAAAGCTGGGTTAAGAAATGTCCAACACATAGAAACCGTCATCTTTGAGGAAGACATATGGTAAAAAAAATATCTTGAATGATCAAGGTCGACAATCGATTAAATGTTAAAAGCAAGCTAGGAAGCATATGAATTGAACTCTGGAACGAATGAAAGAAGTATGGAACAAAATCAATGCCAAAAGTATTGAATTAAAAAGCTTGTTGAACAGCAAAAACTGAAAAAAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16852
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 |
---|---|---|---|---|---|
ENSDART00000082930 | None | None | 633 | None | 16 |
ENSDART00000114722 | Nonsense | 860 | 1942 | 17 | 33 |
Genomic Location (Zv9):
Chromosome 7 (position 65609771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58791511 |
GRCz11 | 7 | 59093941 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGATGAAAAAGGCWGGAGTTGAACCCAATGCTATTACTTATGGATACTA[C/A]AACAAGGTATGGAAATTCTCACTAGTTTAAAGTGGACTACAGCACTAATC
Long Flanking Sequence:
CTGGATAAGTTGGCGGTTCATTCTGCTGTGGTGACCCCAGATTAATAAAGGGACTAAGCTGAAAAGAAAATTAATAAATGAAGGGATTCTGACTTTTTACTGATTGTTTGTTCTGCTTTGTTTGACTTTCACTGGTGGTGTTTAATAACCCATGTCGGCTACTCCTAAATAAAAGCTACACAATATATATAGTTAAAAATGATTTTTTTTAAATAGGAAAATGTTAAGAAAGTAATGAAATAATGTATTTTCATTTTCTATGCATGTATTAAGTGAACTTTTAAGGAAACATTTGGGATGTTTATTTTATTTGTCCTGTGTCGAACTAGATAGGTCAAAGTGGTTTCATTACAGTAAAAAACTGCATGTGTTTGGCAGGTGTGTTACCGTGTGGTGATGCAGTTATGTGGTCTGTGGGAGATGCCCGTCATGGCTGTGCGTGTCTTAATGGAGATGAAAAAGGCTGGAGTTGAACCCAATGCTATTACTTATGGATACTA[C/A]AACAAGGTATGGAAATTCTCACTAGTTTAAAGTGGACTACAGCACTAATCCTCAGAGCAATGAAGACTAGTGAATTTTTGCATACTGACACTGCAATACAGTATGGTATTATTTTAGCATTTTCTGTTACATATAATTTGCTTTGATTAGAATTTTTTTCTTCATAGCCCAAATTGCAAATGATTTAAATATGAATTAAATAATATTATGGAATTCATTTTTAAGATTTGCGCTGGTGCTTTGAACCTGAAGGCATGTTTATGGAATTGTCATCTTATTAAAGATAAATTAGTAAAATACTCTTCCGCTTAAGTATTTTCCAATAATCCACTATTAATCCACACCACACAACTCAGTTGATTAGAATGATTAATTAATGTTTTGTAATGTGAGGAAATTTGTCAGAAAAAAATCCATGGAGCCATTTGAACCCTAAACCTTTACTTCTGGACAAAATACTAGACCAATTAAATAGCAGATCTTTTCCCATCAAAATCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38651
Status:
Mutation detected in F1 DNA
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082930 | None | None | 633 | None | 16 |
ENSDART00000114722 | Nonsense | 869 | 1942 | 18 | 33 |
Genomic Location (Zv9):
Chromosome 7 (position 65607311)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58789051 |
GRCz11 | 7 | 59091481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATCTGTATATGATTCTGCATTGTCCAGGCTGTTCTGGAAAGTCCTTG[G/A]CCAAGCCGCAACCGTAGCGGTCTCTTCATGTGGACCAAAATGAGGAACCT
Long Flanking Sequence:
CACAGCTAATTACAGCTGGCATTTTCTTGGTTGGGCCCTGCACTGCAAAAAATGCTTTTCTTGCTTAGATTTTTTTTTCTCGTTTCTTGTCTAAATATTTAAAATTTCTTATATAAAGAAGCATTTTCTAAACAAGCAAAACATATTGTCTTGTTTTGCTTGTCTAGAAAACTCTTCTTGATTTAGGAATTTTTAGATATTTGGACTAGAAACAAGACAAAAAATCTAAGTAAGAAAAGCATTTTTTGCAGTGTGGGGCTCCGGCTGTACCCATCCCTCCCTTAAATTAATCAAGCTCTGTCTGTATTAGATTAGAATTATGCAGTTCTAGTGTTTTTCATGCCAAAGCAAAGATCTTTCATTTAATAACTTAAATATTTAGCATCTTAAATAAAATGGGTTCTTGTTGCTAGTGTGAACGGGGAGCATTGTAAATGTCATGGCAACCCCCTGATCTGTATATGATTCTGCATTGTCCAGGCTGTTCTGGAAAGTCCTTG[G/A]CCAAGCCGCAACCGTAGCGGTCTCTTCATGTGGACCAAAATGAGGAACCTTGTGCGAGGAGTGGTGCAGTTTAAACGGGCATTACGTGGGACCACTCTTCAAATAGGATCTTCTCTGAAAAGCACAGGTACAGGTTCTTCCTCCTTTCCCCCTCTTCTGGTGATTCTCTTCTGAGTCTCCATTTTGGTCAGAAAAGATGTCCTGTATTCCTGTCCTAATGCCTGACAGTAAATATTATTTAAACACAAGACAGTAAAAACATGATTAAATATTATGTTTTAATTGTAAGCGTACTGTTCAGAAATAGCAGGTAAAGAATTTATGTTTAAAGTTTTCAACAAGAAACACATTAGAATATGTTTAAATGTACATAATAATTGATTTAATAAGAAATACAACAAGCGTTTTTGTGCAATACTCATTTTATATAAGTTTAACATCATTATAATTAGTGACTGATATAATTTAGTTTGATTTTACGTTACCACTATAATGAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41064
Status:
Mutation detected in F1 DNA
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 |
---|---|---|---|---|---|
ENSDART00000082930 | None | None | 633 | None | 16 |
ENSDART00000114722 | Nonsense | 1819 | 1942 | 30 | 33 |
Genomic Location (Zv9):
Chromosome 7 (position 65592432)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58774172 |
GRCz11 | 7 | 59076602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGTGGGATAATGTCAACTTACATCAGGAGCCCACCGAGCCCCTCTAT[C/T]AGCTCTGGAGGACCTTCTGTGAGTAACTTTTGAGAATTATTTGTTCAGTG
Long Flanking Sequence:
TAAAGTGTTTTAATGCCCACAGGACATTGTTGTCTTGATTTGTTTATTTGCATTTTCTCTTAGGTAATCTATACACATAAGTTTCTTAGTCAGCACCCCATCATTTTCTGGAACCTGGTGTGGTATTTTCGTCGTTTAGACCTGCCCAGCATTCTGCCTGGACTCATTCTCACTTCTGAACACTGCAACAATGGAGTAAAGGTACTTGACCTTCATTCACACTGCTATACTCTTAATGAGTGCTCATTATGGAGCCTCAGGTTTTTCTCATTTAGATCAGTATAAAAATATAGCAGATGTTTGTTGAGCCATTATGTGCGTTTCAGCCCAGTAATTCTTGTTAAATGTATGTTGATATGAACCAACATAATAATGCACAGTTCTTTGTGTTGCTCCCAAAGCTGCCGCAGACATCTTTGTCTCAGGACAGTAAGCAGGTGTACGTGCAGCTGTTGTGGGATAATGTCAACTTACATCAGGAGCCCACCGAGCCCCTCTAT[C/T]AGCTCTGGAGGACCTTCTGTGAGTAACTTTTGAGAATTATTTGTTCAGTGTATGCATCAGCATGTTAATGTTTAATGAGACCGGTTTTAGGAACACCAAACAAAAATCATACTTCGTGTACGGCATGTGACATGTATGAACATTATTATATTTTGTCATACAGTGCAAAGGAAGGGAACTCTAGCCCCAACTGACCACCAGGAGACTCGGTCTTTGCTAAACAGCATTGTACGCAGCATTCAGATGAACGATGTTTACGGCCCCATCAATATGCTCATCCGGGAGATCAAGAAACATCCAGAAGTTAAACGCCAGAGGTTGGTCATGTATACTAGTTTTCTATACATGATTAGTGCAGTCTTAAATCCTTAAAGTATTCCTGAGTTGAATTACTTGATCTGCATTGATATTCCATTTATGTAACAGTTCAACGACATAATCGTGTATTTAAAAAAGAAAATTAAACAAAGAGTCTCGAAAATCCTTTTGTAAGAGAAACT
Associated Phenotype:
Not determined