ZMP
si:ch211-250g4.1
Ensembl ID:
ZFIN ID:
Description:
disks large-associated protein 3 [Source:RefSeq peptide;Acc:NP_001038179]
Human Orthologue:
DLGAP3
Human Description:
discs, large (Drosophila) homolog-associated protein 3 [Source:HGNC Symbol;Acc:30368]
Mouse Orthologue:
Dlgap3
Mouse Description:
discs, large (Drosophila) homolog-associated protein 3 Gene [Source:MGI Symbol;Acc:MGI:3039563]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23571 | Nonsense | Available for shipment | Available now |
sa13263 | Nonsense | Available for shipment | Available now |
sa7460 | Missense | Mutation detected in F1 DNA | Not yet available |
sa23572 | Nonsense | Available for shipment | Available now |
sa7461 | Missense | Mutation detected in F1 DNA | Not yet available |
sa43323 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23571
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 |
---|---|---|---|---|---|
ENSDART00000103151 | Nonsense | 149 | 1059 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 39007951)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37871934 |
GRCz11 | 19 | 37459054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCGGAGCGAGAGTCCAAGTCGCATACGGCATTTGGTAAACTCTGTC[C/T]AGCGTCTTTTCGCCAAGTCTCATTCTCTAGAAGCACCCTCTAAACGTGAA
Long Flanking Sequence:
CCCTGTCGCGCCCACAGCGCCCCCTCTCGGCCCGGGCGGCCCACCATGCCCCGTCCATGAAGGGCTACCAAGTGAGTCGCAGTTTGTCACAGCATTCCTCTGGGCCTTGCTACTGCATGCCAGAGGATTGTGACACTGCAAGGGACTACATGCACCACCCTGACCATTACCAGGGACACAATGACCACCACTACTACCCACCCGGTGGGCCCCCTGAACCACTGGCCATGGTCCCATCTGGTGGAGGCACCTTCCCTCGCTCACACCCCAGTCAGCCGCAGCACTTTGACTCCACATGTGAAGAGTGTCTATCCTCGGCAGGGCACGGCCATGGTCATGGAGGAAAGATGCATCGTATCCCACCCAACCTTCTGGATCAATTTGAGAAACAGTTGCCCTTTCACCCTGATGGCTTTCACACCTTGCAGTACCAACGCACAGCCAGTGGGGAGCAGCGGAGCGAGAGTCCAAGTCGCATACGGCATTTGGTAAACTCTGTC[C/T]AGCGTCTTTTCGCCAAGTCTCATTCTCTAGAAGCACCCTCTAAACGTGAATTCAATGGGACTCGTGGAGGAGAGTACCGGGAAAGGGAAAGGGGGCACCGCAGCGGTGGTGAGGAAAGCGGCGGACATCATTATTCAGGAACACACCAGTCTCGGTCAGCTCGCCGTAACAAAAGCCGAGAACGGAGCAAGAGTGGAGACTCCCGCCATGAGTCTCGAAGTTCCCGTCACCGCAGTAAAACAGCCGGCTGGTGGAGCTCTGATGACAACCTGGACAGCGACAGCAGCTTTCTGGTGGGTGCAGGCAGGGGTGTTCGAGGTTATCCCACCGGACACGAGACCCTGGATGCTGCCATTCAGGAACTTACCTTAAGGAAATCTAAAGGTCCACCTCCTGGAGAGTGCTTGGCTTGCACCAATATAGCCATGACAGGGGACAGCGGACACTCTCTGAAGAGGAGCACGTGGTCATCCATGACGGTCAGTCAGGCTAGAGAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13263
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103151 | Nonsense | 232 | 1059 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 39008202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37872185 |
GRCz11 | 19 | 37459305 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCGCCATGAGTCTCGAAGTTCCCGTMACCGCAGTAAAACAGCCGGCTG[G/A]TGGAGCTCTGATGACAACCTGGACAGCGACAGCAGCTTTCWGGTGGGTGC
Long Flanking Sequence:
TTCCCTCGCTCACACCCCAGTCAGCCGCAGCACTTTGACTCCACATGTGAAGAGTGTCTATCCTCGGCAGGGCACGGCCATGGTCATGGAGGAAAGATGCATCGTATCCCACCCAACCTTCTGGATCAATTTGAGAAACAGTTGCCCTTTCACCCTGATGGCTTTCACACCTTGCAGTACCAACGCACAGCCAGTGGGGAGCAGCGGAGCGAGAGTCCAAGTCGCATACGGCATTTGGTAAACTCTGTCCAGCGTCTTTTCGCCAAGTCTCATTCTCTAGAAGCACCCTCTAAACGTGAATTCAATGGGACTCGTGGAGGAGAGTACCGGGAAAGGGAAAGGGGGCACCGCAGCGGTGGTGAGGAAAGCGGCGGACATCATTATTCAGGAACACACCAGTCTCGGTCAGCTCGCCGTAACAAAAGCCGAGAACGGAGCAAGAGTGGAGACTCCCGCCATGAGTCTCGAAGTTCCCGTCACCGCAGTAAAACAGCCGGCTG[G/A]TGGAGCTCTGATGACAACCTGGACAGCGACAGCAGCTTTCTGGTGGGTGCAGGCAGGGGTGTTCGAGGTTATCCCACCGGACACGAGACCCTGGATGCTGCCATTCAGGAACTTACCTTAAGGAAATCTAAAGGTCCACCTCCTGGAGAGTGCTTGGCTTGCACCAATATAGCCATGACAGGGGACAGCGGACACTCTCTGAAGAGGAGCACGTGGTCATCCATGACGGTCAGTCAGGCTAGAGAGGTCTATCCATCTTCACGTGGAGGAGGCGGAGGTCCAGGAGGAGGTGGAGGAGGATATGAGAAGGCATTAGTTCCCTTGGATCCCAAAATGAAGGAACGTTCACTACACCATCTGCAGGCAAGTACTTTCTCTAAATTATCCATCTAAAGCAGGGGTCACCAACCCTATTCCTGGAGAGCTACCTTCCTGCATATTTCAGTTGCAACCCTGACCAAACACACCTGTTTGTAATTATCAAGTGTGCTTTAGGTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7460
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103151 | Missense | 246 | 1059 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 39008243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37872226 |
GRCz11 | 19 | 37459346 |
KASP Assay ID:
554-4277.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCGGCTGGTGGAGCTCTGATGACAACCTGGACAGCGACAGCAGCTTTC[T/A]GGTGGGTGCAGGCAGGGGTGTTCGAGGTTATCCCACCGGACACGAGACCC
Long Flanking Sequence:
CACATGTGAAGAGTGTCTATCCTCGGCAGGGCACGGCCATGGTCATGGAGGAAAGATGCATCGTATCCCACCCAACCTTCTGGATCAATTTGAGAAACAGTTGCCCTTTCACCCTGATGGCTTTCACACCTTGCAGTACCAACGCACAGCCAGTGGGGAGCAGCGGAGCGAGAGTCCAAGTCGCATACGGCATTTGGTAAACTCTGTCCAGCGTCTTTTCGCCAAGTCTCATTCTCTAGAAGCACCCTCTAAACGTGAATTCAATGGGACTCGTGGAGGAGAGTACCGGGAAAGGGAAAGGGGGCACCGCAGCGGTGGTGAGGAAAGCGGCGGACATCATTATTCAGGAACACACCAGTCTCGGTCAGCTCGCCGTAACAAAAGCCGAGAACGGAGCAAGAGTGGAGACTCCCGCCATGAGTCTCGAAGTTCCCGTCACCGCAGTAAAACAGCCGGCTGGTGGAGCTCTGATGACAACCTGGACAGCGACAGCAGCTTTC[T/A]GGTGGGTGCAGGCAGGGGTGTTCGAGGTTATCCCACCGGACACGAGACCCTGGATGCTGCCATTCAGGAACTTACCTTAAGGAAATCTAAAGGTCCACCTCCTGGAGAGTGCTTGGCTTGCACCAATATAGCCATGACAGGGGACAGCGGACACTCTCTGAAGAGGAGCACGTGGTCATCCATGACGGTCAGTCAGGCTAGAGAGGTCTATCCATCTTCACGTGGAGGAGGCGGAGGTCCAGGAGGAGGTGGAGGAGGATATGAGAAGGCATTAGTTCCCTTGGATCCCAAAATGAAGGAACGTTCACTACACCATCTGCAGGCAAGTACTTTCTCTAAATTATCCATCTAAAGCAGGGGTCACCAACCCTATTCCTGGAGAGCTACCTTCCTGCATATTTCAGTTGCAACCCTGACCAAACACACCTGTTTGTAATTATCAAGTGTGCTTTAGGTACTATTAATTGGTTCAGGTGTGTTTGATCAGGGTTGGGACTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23572
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 |
---|---|---|---|---|---|
ENSDART00000103151 | Nonsense | 274 | 1059 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 39008326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37872309 |
GRCz11 | 19 | 37459429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCGGACACGAGACCCTGGATGCTGCCATTCAGGAACTTACCTTAAGG[A/T]AATCTAAAGGTCCACCTCCTGGAGAGTGCTTGGCTTGCACCAATATAGCC
Long Flanking Sequence:
ATCAATTTGAGAAACAGTTGCCCTTTCACCCTGATGGCTTTCACACCTTGCAGTACCAACGCACAGCCAGTGGGGAGCAGCGGAGCGAGAGTCCAAGTCGCATACGGCATTTGGTAAACTCTGTCCAGCGTCTTTTCGCCAAGTCTCATTCTCTAGAAGCACCCTCTAAACGTGAATTCAATGGGACTCGTGGAGGAGAGTACCGGGAAAGGGAAAGGGGGCACCGCAGCGGTGGTGAGGAAAGCGGCGGACATCATTATTCAGGAACACACCAGTCTCGGTCAGCTCGCCGTAACAAAAGCCGAGAACGGAGCAAGAGTGGAGACTCCCGCCATGAGTCTCGAAGTTCCCGTCACCGCAGTAAAACAGCCGGCTGGTGGAGCTCTGATGACAACCTGGACAGCGACAGCAGCTTTCTGGTGGGTGCAGGCAGGGGTGTTCGAGGTTATCCCACCGGACACGAGACCCTGGATGCTGCCATTCAGGAACTTACCTTAAGG[A/T]AATCTAAAGGTCCACCTCCTGGAGAGTGCTTGGCTTGCACCAATATAGCCATGACAGGGGACAGCGGACACTCTCTGAAGAGGAGCACGTGGTCATCCATGACGGTCAGTCAGGCTAGAGAGGTCTATCCATCTTCACGTGGAGGAGGCGGAGGTCCAGGAGGAGGTGGAGGAGGATATGAGAAGGCATTAGTTCCCTTGGATCCCAAAATGAAGGAACGTTCACTACACCATCTGCAGGCAAGTACTTTCTCTAAATTATCCATCTAAAGCAGGGGTCACCAACCCTATTCCTGGAGAGCTACCTTCCTGCATATTTCAGTTGCAACCCTGACCAAACACACCTGTTTGTAATTATCAAGTGTGCTTTAGGTACTATTAATTGGTTCAGGTGTGTTTGATCAGGGTTGGGACTGAATTCTGCAGGAAGGTAGATCTCCAGGAACAGGGTTGGTGACCCCTGATCTAAAGCAATGGTCTCAAACTCCTGGACGGCCACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7461
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103151 | Missense | 421 | 1059 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 39026779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37890762 |
GRCz11 | 19 | 37477882 |
KASP Assay ID:
554-4378.1 (used for ordering genotyping assays)
KASP Sequence:
CCCTCATTGCCCAGAGAGAAGCCTTCCGCCGCTCCGTCAGCATGGATCAA[C/T]GCTCCTCCACAACATCCAAGTCAGTCGTCAATTAATTTTAARTTTGTAGT
Long Flanking Sequence:
TTTATTAACAACTGTTTATAAAATTAAAAGTTTGCTACTGATTAGAACTTCAAGTGGCGATGAGGTCTTAAAAAAATCTGGCAAGGTCTTTAAAAAGTCTTAATAAGATATTGAAATCATCTTCAGGATCCCTGCATATACACTGTAGGGGTAAAAAATGTAATTGGCATTGGGCCTAACTGTTTAAAGATAAACCTCTGAATGGCAGCTCATCTGACCCCAAAGAAAGCTGCTTATGTTACTATAGAACAACTTCATCTTAGTAAAACCCGGGTGTATGTTCTGTGGATCTCTTGCAGGTGCCCTCAGATGACTGGTGTGGTGGTGGTCCATCCGACAGCGGTGGAGAGATTCCCTGCAGACGTATGCGCAGTGGCAGCTACATTAAGGCCATGGGGGATGATGACAGTGTTGACTCAGACACCAGCCCCAAAGCCTCACCCAAATCAGCCCTCATTGCCCAGAGAGAAGCCTTCCGCCGCTCCGTCAGCATGGATCAA[C/T]GCTCCTCCACAACATCCAAGTCAGTCGTCAATTAATTTTAAATTTGTAGTCATTTAGGATTAACACTGTTTGTTGAACTATTGGTATAAGGTACTGATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATATATATATATAATTGTACTGCTACAATATAAAAGTATAGCAAGAAGGTGTGTGTTTTATTTTAATGGGAAGTTTAAATGAGAAATATCAGCTGGAGCTTTACTGGTGTTCTCTTCTCCTCAGGTATTCATGTAAACAGTGTACAGATGCCTACCCAAACAGTCGAACCACACCTAAAGGTCACGCTCGCTCCCGCAGCTACACCCGCTCTCTGACCAGCGCTCAGGTATTACACAGTCAAACGGTACATAGTTCACATCATAGTAGATCACATAATATTCATATTGAGTTAATAAAGTTATTTGAATGTATTATTTTATAGAATAATCATTTAAGTCAGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43323
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 |
---|---|---|---|---|---|
ENSDART00000103151 | Nonsense | 850 | 1059 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 39037818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37901801 |
GRCz11 | 19 | 37488921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGAGGGCCCCCGGAGCCTCCCAGATTCAGGCCGAGCCTCGCCTTGCTTA[C/T]GAGATGGAGAGTTCTTCCTCCGGCTCCTGCAGACAGAGGTGGAGAGGATG
Long Flanking Sequence:
TATTGTTGCTTACCACAGAGTGAACACTCAACCTTGGAATTGATAGTATCATTCATCATATTTGAGCTACAGGAATGTCTATATATCAATCTGCTGGTAAGTTTAATGGTCATGTTGTTGTTTGTTCCAGACGAGCACGTTTCAAACGCTCCAACAGCGTAACGGCAAGTGTCCAGGCTGATCTTGAGACAGAAGGCTTTGGAGGACTGACCGTCCCCACTCAAGACAAGGGGCTGCAGTTTGGCTGCTCATTCCAGCGCCACTCATCTGAACCAGAATCAGCCAGTCAGTTTGCAGAGTATCGCACTGTACACACACAGGGCCAATGGGCCTACCGTGAGGATTACCACAGTGGGTACACCACTGAACCCGGCCCTCCAGAACTAAGGGCCCTGCCCCGCTCTCACTCCCCTCTGCCTCTGGCCCCCGAGCGTGGAGTGGGAGGATGGAGCGAGGGCCCCCGGAGCCTCCCAGATTCAGGCCGAGCCTCGCCTTGCTTA[C/T]GAGATGGAGAGTTCTTCCTCCGGCTCCTGCAGACAGAGGTGGAGAGGATGGAGGGATGGTGCCAGAACATGGAGAGAGAGGCAGAGACGAATGAATTGCCGGAAGAGGGTGAGTGAGGAATAGCGGAGATGATGGTTGGAGCATGGACAAACAGAATCAAAACACTCATTTTGATTTCACGGGGTCTTGAATCTGCTTTTTACCCCACAGAACAGTTCTTTCTGTCTAAATGCTGTTTGTTTCGCCCTCTGATTGGTGTTTTAGTGTTGGAACTCATCAGAGGAGCTGTCGGCAGTGCTCAGATGCTCATGTCACAAAGAGTCCAGCAGTTTTTCAGGATGTGCCAACAGAGTGTGGTGAGTGCTTTGTAATGCCTTTTGTTGTGGGCAAAAGAGACCTTACTTACTTTTTTCTGGAGCCTAAGTAAACTATGTAGTAAAGAAATACGCATAACATATAAAAAACAATAAATAAATAAATTATTTAGTTAGTTAACTTTT
Associated Phenotype:
Not determined