ZMP
dennd4a
Ensembl ID:
ZFIN ID:
Description:
C-myc promoter-binding protein [Source:RefSeq peptide;Acc:NP_001074458]
Human Orthologue:
DENND4A
Human Description:
DENN/MADD domain containing 4A [Source:HGNC Symbol;Acc:24321]
Mouse Orthologue:
Dennd4a
Mouse Description:
DENN/MADD domain containing 4A Gene [Source:MGI Symbol;Acc:MGI:2142979]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43085 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43084 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12574 | Nonsense | Available for shipment | Available now |
sa43083 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36626 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43085
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090922 | Nonsense | 513 | 1714 | 10 | 29 |
ENSDART00000090962 | Nonsense | 513 | 1674 | 10 | 28 |
ENSDART00000129591 | Nonsense | 513 | 1724 | 10 | 30 |
Genomic Location (Zv9):
Chromosome 18 (position 18866289)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 19096512 |
GRCz11 | 18 | 19085578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAGAGCGCAGATCCCTGACCTGGAAGATCCTGCCAAGAAAAGCCTGT[A/T]AACATCTGATCAACACCCTCAGCAATCTCCACCAGCAACTGGATGAGGGT
Long Flanking Sequence:
GACTTTTGATCTACAGAATTGCACTAAAGTCATCTTTTACCACATAAATTCCCCAAATAAACAGTAATTTCCACATACAGGTGATGATTAGTGTCTTTCGCACTGTATTATGTTTCAATTATGTTTCATGTCTCAAGAGACTCTTCGCAATAGCAAATATTTTTTGAGTGAAATTCTCAGTTACAGTGATCTTAATCTTCATGCAGATGTTTAAAAGATCAGGATAGAGATATATGAGCAGTGTGGAATGTCATAGTAAAGATAGGCTCTCAGTACCACCATGTGTTGAACACATGCTCTTGTGTTGTTTGTGTCATTATGCACCTAAAAGTTTGCAGACGTCGTAAAAGCTATATCAAAACTGTAAAGCTGTTGTTCACGGGCTTGGACCCGCTTTTCCGTTTGCTGTTTACTCTCTAAAATGATCAACATCTGTGACCTATTTCAGCAAAGAAGAGCGCAGATCCCTGACCTGGAAGATCCTGCCAAGAAAAGCCTGT[A/T]AACATCTGATCAACACCCTCAGCAATCTCCACCAGCAACTGGATGAGGGTTAGTGAGGCCAGGTCACAGTGGTGTTAACTGAGAAATGATTTCATTTGTCTGTCCCTTCGAGGGCGATATTAGTTCACTCGACTGCACACTTTAAATGGCCTTCCACTGTCCTTTTTGGTCTATGACAGTATCATTTTTATTACCTAACAATGTTTTATGAATGCTCGAGTGGGTCAGAGCAAAATGCAGTCATCCTTGAGATGTGATGAGATTTAGAGATGGGGTCAACAGGCTGGAGAAAGGCAGAGCAAGACACAGGTCTCTTATTTTTGAGTGCTTGGATATTATCTGATACCTGAGAGCTGATTGATGCTTTGGTTTTTGAACCAGACTTTGAACCCAATTATTAATGTGTTTTTGGTTCTTTAAAATGCCCTGTATGGAATGTACCATCTCGTAGAATCAGGCTTAAAGAGTTATTTACAGGGAAGCATGATGCATTTTTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43084
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 |
---|---|---|---|---|---|
ENSDART00000090922 | Nonsense | 811 | 1714 | 16 | 29 |
ENSDART00000090962 | Nonsense | 811 | 1674 | 16 | 28 |
ENSDART00000129591 | Nonsense | 820 | 1724 | 17 | 30 |
Genomic Location (Zv9):
Chromosome 18 (position 18852569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 19082792 |
GRCz11 | 18 | 19071858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTGTGATTTTGTGTTTAACGGTTTGTTTCTGGCCCTCTGGAGGTGTG[T/A]TATCGAGTGCTGATGCAGCTGTGTGGGCAATACGGTCAACCTGTTCTAGC
Long Flanking Sequence:
CTCAGAGTCCCCAAAGCAACATCAGCCCTGAGACACATCAGTCCCATCAGCCCTGCTGCTATATTCCGTCGCTCCCAACAGGTTTATATTTTCAAACGCTAACCCATGATCCCACTTGTCAAATCTCTCCTCCTCCTCCTCACTAATGTCCTGATCCTCCCTCCGTAGGAGATCAAATCAGCCCAGCGGATGGCCAAAACCTACTCCTCCATCCCTCAGATGTGGTCTAAATGTCTCCTCAGGCACTGTCACGGTCTGTGGTTCATCTGTTTGCCTGCGTACGTCAGCGCGTGTCACTCTAAAGTGCGCGCTCTGCATACTGCTTACGATGTGCTAAGAAACATGCAGGACAAAAAGCTGCAGCCTCCAGATGAGGTACAGTCGCCTCTATTGATTGCTTTGATCATTTGCGAGTAGTGCTGCAGGTCTAGACTGCAGAATCTTGCACTTGTGTTGTGATTTTGTGTTTAACGGTTTGTTTCTGGCCCTCTGGAGGTGTG[T/A]TATCGAGTGCTGATGCAGCTGTGTGGGCAATACGGTCAACCTGTTCTAGCGGTTCGAGTCCTGTTTGAGATGAAGAAAGCCGGAGTTCAGCCTAACGCCATTACATATGGATACTACAACAGAGTGAGTGTAGTTTTCTCATGTTAAAATATACACATTCATTTCAAGGCCCATTTACATAAAAAATATAGTTATGAAAATAGCTGTAGAGATTACTATATAAGGTTCCACAGCGGCAGATGATACTGTTGTGTTAAATATTAGACTTCACTGAAGTTATCATGCTCATTAAAACAGAGTAGTTTATAGTTTATTAAATGGAAAAAATAAATAATGTGTTTTATGCTAGTGTGGCAGTAAAATGTGCTCCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12574
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 |
---|---|---|---|---|---|
ENSDART00000090922 | Nonsense | 885 | 1714 | 17 | 29 |
ENSDART00000090962 | Nonsense | 885 | 1674 | 17 | 28 |
ENSDART00000129591 | Nonsense | 894 | 1724 | 18 | 30 |
Genomic Location (Zv9):
Chromosome 18 (position 18849414)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 19079637 |
GRCz11 | 18 | 19068703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTGTGGGGAAAGCTGAGAAATGTKGTCCGGGGTGTGGTGCTGTTCAAA[C/T]AAGTATGGAGGAGGCAGACCACCCACCCSAAAKACACTCATCTTTCTGGT
Long Flanking Sequence:
GTTTGTAAAACCAGCTCTTCAAAATAAAAGAGAAGTGATTTATCTGTAGAGGTATGTTTTGCTAATTCTTCAGGACCTTCATCTGGCAGCAGATTTGGCATGTGACTTTGTTTTTCATGCCTGTTATCATTAGACAAAAGCATAGACCAGCAATCATCTCCCTGGGGATCGTTTTTGTGTGTGTGTGTGTTTTGGAAATTGTCCCAAAATACCAGGAGGACACACTGGCATAGATATAAGTCTGGGCAGCTGAGCGTTGCTCCAATTCTATCAGAGTAATTACAGCTAGTCCTTGACAAAGAACACAATCTACTTAAGATAATGAGAGGCATTGTACTGTAGAATTATTCAGCTAATCTGTATGTGAGTGTGTGTCTCTTACTGTAGCATTCTTCTCCCTTCAGGCCGTCCTGGAGAGCACATGGCCTTCTTCCACCAGAGGGGGATACTTCCTGTGGGGAAAGCTGAGAAATGTGGTCCGGGGTGTGGTGCTGTTCAAA[C/T]AAGTATGGAGGAGGCAGACCACCCACCCGAAAGACACTCATCTTTCTGGTAAAACCCCCAACTCTGTTGCACTTACTCTCCCCAAAAAAGCATTGATAGTCTCCTAATGCAATGTAAAAGCTACAAAATCCACCCAAGATGCTGGACAAAACAAATTTTCATAACATTTATTTAAATTACTAATGGATATTGTAAATATGACTATTTTGGGAAATGAGTGTTACTTAACAGCCAAATTGAAATCAGGCAAACCTCTAGATTTCAATTTTGATTGAGATTTCCACCTTTGAATATCTCATACAAACTATTCACTTTTGAGATTTCATTCTAGTTAGGAAGTTGCTTGTGTAGAGGGCAAGTTAGCTGACTTGATTTTAAAGAGTTTATTTTAGTGGAAATACTGTAGAGTTCATCAGCTACAAGCAGTTATTACTATAAGAACATATAGTTTAATAAAATATTAATACAAGTATTAAAACACACTCTGACCAATTTATCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43083
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 |
---|---|---|---|---|---|
ENSDART00000090922 | Nonsense | 890 | 1714 | 17 | 29 |
ENSDART00000090962 | Nonsense | 890 | 1674 | 17 | 28 |
ENSDART00000129591 | Nonsense | 899 | 1724 | 18 | 30 |
Genomic Location (Zv9):
Chromosome 18 (position 18849399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 19079622 |
GRCz11 | 18 | 19068688 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAAATGTGGTCCGGGGTGTGGTGCTGTTCAAACAAGTATGGAGGAGG[C/T]AGACCACCCACCCGAAAGACACTCATCTTTCTGGTAAAACCCCCAACTCT
Long Flanking Sequence:
TCTTCAAAATAAAAGAGAAGTGATTTATCTGTAGAGGTATGTTTTGCTAATTCTTCAGGACCTTCATCTGGCAGCAGATTTGGCATGTGACTTTGTTTTTCATGCCTGTTATCATTAGACAAAAGCATAGACCAGCAATCATCTCCCTGGGGATCGTTTTTGTGTGTGTGTGTGTTTTGGAAATTGTCCCAAAATACCAGGAGGACACACTGGCATAGATATAAGTCTGGGCAGCTGAGCGTTGCTCCAATTCTATCAGAGTAATTACAGCTAGTCCTTGACAAAGAACACAATCTACTTAAGATAATGAGAGGCATTGTACTGTAGAATTATTCAGCTAATCTGTATGTGAGTGTGTGTCTCTTACTGTAGCATTCTTCTCCCTTCAGGCCGTCCTGGAGAGCACATGGCCTTCTTCCACCAGAGGGGGATACTTCCTGTGGGGAAAGCTGAGAAATGTGGTCCGGGGTGTGGTGCTGTTCAAACAAGTATGGAGGAGG[C/T]AGACCACCCACCCGAAAGACACTCATCTTTCTGGTAAAACCCCCAACTCTGTTGCACTTACTCTCCCCAAAAAAGCATTGATAGTCTCCTAATGCAATGTAAAAGCTACAAAATCCACCCAAGATGCTGGACAAAACAAATTTTCATAACATTTATTTAAATTACTAATGGATATTGTAAATATGACTATTTTGGGAAATGAGTGTTACTTAACAGCCAAATTGAAATCAGGCAAACCTCTAGATTTCAATTTTGATTGAGATTTCCACCTTTGAATATCTCATACAAACTATTCACTTTTGAGATTTCATTCTAGTTAGGAAGTTGCTTGTGTAGAGGGCAAGTTAGCTGACTTGATTTTAAAGAGTTTATTTTAGTGGAAATACTGTAGAGTTCATCAGCTACAAGCAGTTATTACTATAAGAACATATAGTTTAATAAAATATTAATACAAGTATTAAAACACACTCTGACCAATTTATCTGAATCAGTGAATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36626
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090922 | Nonsense | 963 | 1714 | 19 | 29 |
ENSDART00000090962 | Nonsense | 922 | 1674 | 18 | 28 |
ENSDART00000129591 | Nonsense | 972 | 1724 | 20 | 30 |
Genomic Location (Zv9):
Chromosome 18 (position 18841887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 19072110 |
GRCz11 | 18 | 19061176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGGGCTACGACTCTCTGTCTAAAGAGGAGGTGAGGTTTGGTGGAGGT[G/T]AAGAGCAGAACTCCTCTCCAGACATCAAGGAGAAGAAGGACAGAGACTCT
Long Flanking Sequence:
TTATCCTTTCCCTAGATTGATGAACATAATTGGTACTACTAGACCAACATAAATGAAACTAAAGTAAACTACCCTTATATAAGCTGTTTAACTCCTGTTAAAATAACTGCAAATAAGACCATGCAGTGATCTCAGAATGTTGAAAATCTGTTGTTCTCTAATTTTGATCTCCACTGTATTTATATACAGATTTGTATGGCAAATCTGTATATAAAAAAGGAAGAAGAAGACATCTTTCTGACATGAATATTTAATAAAGACGGTTGTTTTCCATATCTCTGTTACAAAGTGCTTTGTTGTTAATTGTCTCAAAAAGTGGGGATAACAAGCAAACGGCTGTTCTAAATGCTAAATCTTAACACTCACTGTATGTGTTTTGTGCATTTGTTTCCATTGTAAAATTAGCATTTTCAAACAAACCGGTATTTTCTTCTTTAGGGGGTCAGTCTGATCAGGGCTACGACTCTCTGTCTAAAGAGGAGGTGAGGTTTGGTGGAGGT[G/T]AAGAGCAGAACTCCTCTCCAGACATCAAGGAGAAGAAGGACAGAGACTCTTGTCCATGTGAGTAACACAGAATTCTGACCACCTTAAACTTACAAATAATGTAAATCAAATAATCTAAATTTTCTTGCCGTCATTTTGTCTCTGCATTGGAATCAACAACTCAAATTCTTTGTACAGTGCTCAGCATAATTGAGAACAGCCCATTTTGAAAATGAATATTTGTATCCATTTCTCAGTAAATATAGGCAATGTTTTTTGGTGCATTTAAACAAAGCAGATTTATTAAACAGATATATCTATTAAAATTATATTTTAGTCACCAAACATATTTAGAAATTGAAAGATATTACAATTAAATTCAAGCACAATATTGCAAAAAAAACATAACAACCTACAAAATTTTCATCGAAAATTTTCCTTTTTTTTTTTTTTTTTTGCTTCTCTTGATTTTTCCTCTTTTTTAAAATTATATTTAATATTTTTCTATAACATAAATTTGG
Associated Phenotype:
Not determined