ZMP
DCC
Ensembl ID:
Description:
deleted in colorectal carcinoma [Source:HGNC Symbol;Acc:2701]
Human Orthologue:
DCC
Human Description:
deleted in colorectal carcinoma [Source:HGNC Symbol;Acc:2701]
Mouse Orthologue:
Dcc
Mouse Description:
deleted in colorectal carcinoma Gene [Source:MGI Symbol;Acc:MGI:94869]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25288 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31409 | Nonsense | Available for shipment | Available now |
sa16961 | Nonsense | Available for shipment | Available now |
sa12693 | Essential Splice Site | Available for shipment | Available now |
sa13121 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25288
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126752 | Essential Splice Site | 53 | 895 | 2 | 32 |
Genomic Location (Zv9):
Chromosome 5 (position 97301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 146661 |
GRCz11 | 5 | 95609 |
KASP Assay ID:
554-7843.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTGGTATCCCCCTGAGCTCTCCTGATTGGCTATCGTGTGTGGTGTTC[A/G]GGATGGTGGTCATCTGCAGATTCTGGGTCTGGTGCGCTCAGATGAAGGCT
Long Flanking Sequence:
ATCGTCAACTCTGTTATCGTCAACTCTGTTATCGTCAACTCTGTTATCGTCAACTCTGTTATTGTCATCTATGTTATTGTCAACTCTGTTATCGTCAACTCTGTTATCCGTCATCTCTGTCATCGTCAACTCTGTTATCCGTCATCTCTGTTATCGTCAACTCTGTTATCGTCAACTTTGTTATCATCAACTTTGTTATCGTCAACTCTGTTATCGTCAACTTTGTTATTGTCAACTCTGTTATCCATCAAATGTGTAAAATCTGTTATGGTTTAAAAAAACGTGTAGCAACAGAATCAGGATGTTCTCGTTGAAGTGTTTTACTGTAAAATATATATTTGTGGTTTATAATTTCCAATTTAAATAAAATTAATTGAAAATGCTTGAAATGCACCTGGAAGTCCAAAATCCTGTATGCATGAGAGTCATAATAAATGTAAATGCATGAGCACATTGGTATCCCCCTGAGCTCTCCTGATTGGCTATCGTGTGTGGTGTTC[A/G]GGATGGTGGTCATCTGCAGATTCTGGGTCTGGTGCGCTCAGATGAAGGCTTTTATCAGTGCATCGCAGAGAATGAAGCGGGGAACAGTCAGGCCATGGCTCAACTCATCCTGCTGCAGCCCGGTAAGACACACACATGCGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATCTCCTGATCTGAGACCAGTGTCCTGCTGCAGCGCATTTAGAGTGCATTAGTGCCACAGGTCTGAGATCAGTGAGGAAGATCAGTGCTGCTATTCTGCTGTCCATCATTCAGCACCGCTGCCATCTGCGCACACACACACACACACACACACATGCATGCACATACAGGCATGTATATGCAAACACAAATACACAGACATACACACACACACAAAACCACTAAATTATGTAAACGTATACACACACACACACACACACACACAGGCACACACAATCACATGCATATACACTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31409
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 |
---|---|---|---|---|---|
ENSDART00000126752 | Nonsense | 281 | 895 | 6 | 32 |
Genomic Location (Zv9):
Chromosome 5 (position 79307)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 25772 |
GRCz11 | 5 | 77615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTACAGTTTGCGAGTGCTGGCGGTGAACCGACACGGCCCCGGGGTCT[C/A]GGATAAAGACACACTCATCACCACGCTCTCAGACGGTAAGAACATAACTC
Long Flanking Sequence:
CTCCTCCCCCTCCACTAACTTTTTAACTGTATGGAATGTGATTGGTAGTTAATGTGTTTTAAGGCTGGGGTTTTGTATGGCTCCTCCCCCTTCTCCTGTTCCTAACTGTATGGAATGTGATTGGTAGTTAATGTGTTCTAAGGTGGGGCTTGAGCATGACTCCTCCCCCCAGCTGATTTGAGATGTTTATGTTGATATTATGCTGCTTGTGTTTGTCAGAATGTGATTGCTAGGTAATGTGTTCTGAGGCGGGACTTAAACATGACTCCTCCCCGTTCTCCAGCTTTGTAGCTTTACGTAATGTCATTGGCAGTTATTATATTCTAAGGCTCCTCCAGCTGATGTGAGAGGTGTTTGTTTATGTTCATGTTGTGCTGTTTGTGTGTGTGCTGTTCAGAATGTGGAGGTGGTGGGTCAGAGCTACAGGATGGAGGGACTGAAGAAGTTCACTGAGTACAGTTTGCGAGTGCTGGCGGTGAACCGACACGGCCCCGGGGTCT[C/A]GGATAAAGACACACTCATCACCACGCTCTCAGACGGTAAGAACATAACTCAGCATTAACATTACCTTCTTTACATTCAACGTCTCTATAACAGGGGGTCTTAACAATTCAGAGTTGATCCATCTAGAGTAGTTATTATCTAATTAATATAACTAAAATAATAAGATTAAAAATGAACACTCTGGTCAGTGCCAATGGCGAAGTGAAAAGTGAACCGACACAGGCACTCTGGTGTTCACAGCAACCCGAGTTTGATTCCCACCTCGAGGTCCAATGCTGATCCTTCCCCTCTCTCTGCTCTCCACACTTTCCTGTCAATTCTCTCTACTGTCCTGTCCAATAAAGGTGAAAACCCCTAAAACTAATAATAATAAACAAGAGCAATCTGATTGTTCTGTGAAGCTGCTTGTTATAAAAATACTCAATGAGTTTTAACTATTTAACAATATTAATAAGAGATGAGCAGTGGATGCTGAAAGCACATATTTCAGTTATACTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16961
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 |
---|---|---|---|---|---|
ENSDART00000126752 | Nonsense | 674 | 895 | 27 | 32 |
Genomic Location (Zv9):
Chromosome 5 (position 52632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 171153 |
GRCz11 | 5 | 43356 |
KASP Assay ID:
2259-5299.1 (used for ordering genotyping assays)
KASP Sequence:
CTCATCAGGTGCTGGACCTCAATCTGGACACMGTCTACTATTTCCGCATC[C/T]AGGCCAAAAACGCTAAAGGAGTCGGGCCGYTGTCGGACCCCGTGCAGTAC
Long Flanking Sequence:
ATTTATATATATATATATATATATATATATATATATATATATATATATAAGAGTTTGTGTATTTATTTGTGTGTTTGTGTGTGTATACGAGTATGTTTGTGCATGTGTATTTATATAAGTCTGTGTATGTATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTTTATGTATATTTATGTGTGTGTGTGTGTGTGTGTGTCAGGTTTTATCCTCTACTACACGCTGGAGAAGAATCTGTGTGTGTGTGTTTGTGTGTGTATTTATGTATTTATTGTATGTTAATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGGGTTTATCCTCTACTACACGCTGGAGAAGAATCTGCCGATAGATGATTGGGTGATGGAGCCCATCAGTGGAGACAGGCTCACTCATCAGGTGCTGGACCTCAATCTGGACACCGTCTACTATTTCCGCATC[C/T]AGGCCAAAAACGCTAAAGGAGTCGGGCCGCTGTCGGACCCCGTGCAGTACAGGACCTCCAAAGGTGAGCTGTGCTGACTACAGAGGGCACTCGCTGCTCAAATCAATCCAGTTCACCTGTGTTTGTATAGTGTTTCCACAATCATCATCGCTCTATAGCTGCTACACAAACAGAGCACATCATTACTGGCATCACAGGCACACAAGAGGAGTTGTGTCGAGATGTGTCAGAGTATTGCCATTATTACTATTGTTATTGTTACATTTACAGTTACCATGACTTACTAAATATAATGTTAGAGTTATTAAATATATATTTTTACTAGTGCTGTCAGAATTAGCGAGTTAATGCATGCGATTCATTTGAGATATGTAATGCGTTGGGGCAATGCAGTGGTGCAGTAGGTAGTGCTGTCGCCCCATGGCAAGAAGGTCGATGGTTTGAGCCTTGGCTGGGCCAGGTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12693
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126752 | Essential Splice Site | 705 | 895 | 28 | 32 |
Genomic Location (Zv9):
Chromosome 5 (position 50130)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 168651 |
GRCz11 | 5 | 40854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTGTCTCTCCTGTAGTTGAGCATCCGGATAAGAKGGCCAATGATCAAG[G/A]TAAGCTGATTCTCCCTCGTCATCTTTAATAAATCARCTCTGTGTTTTATC
Long Flanking Sequence:
GGCTGGAAACCAGCCTGGAAGTGGCCAAAACCCCTCTAAAACCAGCCTGGTCGACCAGCTAAAACCACCCAACCATCCTAGGCTGGTTTAGGCTGGATTTTTGAGCAGGGTGTTTAGACTGAAGTGTGTGTCTTTTGACTAAAGTGTGTCATTTTGCAAACAATCTAGGAGTTCTGCAAATTGAGTGTGCTGCTTGAAGAATTGTGATTATATTTTGAGATTGTGTGTAAACAACTGAAAAAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGAGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTAGATTTAAAGCAGTGCAAACACACTTATACTCTCTCCTTCTTCTCTCTCTCTGTCTCTCCTGTAGTTGAGCATCCGGATAAGATGGCCAATGATCAAG[G/A]TAAGCTGATTCTCCCTCGTCATCTTTAATAAATCAGCTCTGTGTTTTATCCACATGCATGCAGGACCCAGAGCTCTACTGTTTGTATATTCACTTGACACACACACACACACACACACACAGTTTTCTCATAGCAGATCAGTGGCTTCATTATGTTGAGGGCGCTCTTCATCTCTTATTTGTTTTCTGTTTCCTTTAATAGAGTCACGCTGAGGTGTGTTTTAGGGTTGGGTGTCCCAATGAGTTACAGGATGAGCAATTTAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGCAACTATTGTGTTTAACTGATGTTCAAAGCTTTTTTGAGGTTTAGGACTTAAAAACCGAGATTACGAGAGAAAACGAGACAGAATGACACACTCTAATACAGGCAGACAAAACTGTGTGTGTGCGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCATGTCTGTCTCCATGTGGGAGAGAGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13121
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 |
---|---|---|---|---|---|
ENSDART00000126752 | Nonsense | 848 | 895 | 31 | 32 |
Genomic Location (Zv9):
Chromosome 5 (position 41340)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 159861 |
GRCz11 | 5 | 32064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCARAGCTGCCAGGAGATCCCTCCAGTCAGCCACAGCCAATCAGAGAGC[C/T]AGATGGGCAGCAAGAGCAGCCACTCAGGTGAGGCTGCAGGCGGGCTGTGT
Long Flanking Sequence:
ACAAGTTCAGACCTCATTATCACCTGCCACACACACACTTCACATCCACTTCAGTCTGACAGCAGTAGCCCTGCAGACAAACAACATCATTATGTTCCACAAGAGCTGCGTTATTTTTACTGTCTGAGTGTGTGTACACCTCATATTCCTTATGCTGTGTAAAATGTCCCCACAAGTATAGTAATACCAGTAAATTTTGACCTTGTGGGGACATTTTTTGTCTCCTAAATCAGAGAATGTAAAAATGAAGATGTTTCCTGTGATTGTTGCTAACTCTGATGGGTGTGTGTGTGTGTGTGTGTAGGAAGCGTGCAACACACAGTGCAGGCAAGCGTAAGGGCAGCCAGAAAGACCTGCGTCCTCCAGACCTGTGGATCCACCATGAGGAGATGGAGCTGAAGAACATGGAGAAGCCCTCAGGCTCCGCCCCCTCCGGCCGAGACTCACCAATCCAGAGCTGCCAGGAGATCCCTCCAGTCAGCCACAGCCAATCAGAGAGC[C/T]AGATGGGCAGCAAGAGCAGCCACTCAGGTGAGGCTGCAGGCGGGCTGTGTGCATGCGTGTATGTGTGTGTATGTATGTATGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACATACACGTGTATATAGATGTGTGTGTGTGTCCTGCTGAAGGTGTGTGTGTGTGTGTGTTCAGGTGCGGATGCTGATGAATCCTCCAGCAGTATCTCCACATTAGAGAGATCTTTAGCTGCCAGAAGAGCGACGCGCACCAAGATGATGATTCCCATGGACTCACAGCCCAGCAACACACGTGAGCCTCAACACACACAAACACAGAATCACCCAAACATATGCAAATACACACAAAAATGCACTCACACAAACTAACAACACCAAACGAAGACACTCTCAANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined