ZMP
igdcc4
Ensembl ID:
ZFIN ID:
Human Orthologue:
IGDCC4
Human Description:
immunoglobulin superfamily, DCC subclass, member 4 [Source:HGNC Symbol;Acc:13770]
Mouse Orthologue:
Igdcc4
Mouse Description:
immunoglobulin superfamily, DCC subclass, member 4 Gene [Source:MGI Symbol;Acc:MGI:1858497]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38621 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34101 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15443 | Nonsense | Available for shipment | Available now |
sa40929 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38620 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38621
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113467 | Essential Splice Site | 224 | 1246 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 33004479)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACACACACACACACACACACACACGCACTCATGATATGTCTGTGTGTA[G/T]GTCTGTCTCAGGAGAGTGAGGTGGTGATTGTGGCTCCGCCACAGAACTCT
Long Flanking Sequence:
TTTCAGTGTCACACCATCTTTCAGAAAACATCTATGCTGGTTTACTGCGTTAGAAGAATTTATAATTACTTCATTATTTCATAAATGCTTTATTTAAAAAGTTTTTAAAAATAGCACTTATTTAAAACAGTGATCTTTTTTAAATCCTTGAAATCTCACATGAATGCCTTTTCATCAGTTTTATACATCCTTGTTGAATAATATTATTAATTTATTTTTTTTAAATGCTTCTCTTTCACTTTCTTAATCTGTCTATCACACCATTTCCTCAATCCTATCTCACTCTATCTTTGTCACTTCCTGTGAGAATATTAGTTTACACTATCAGGTCAAATGCTAACTTAATTCTGCTTTCACTCAAATTGAAGTTTCTGTCTAATGGTGAACACTCTTTTATCCTGTCCACAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACGCACTCATGATATGTCTGTGTGTA[G/T]GTCTGTCTCAGGAGAGTGAGGTGGTGATTGTGGCTCCGCCACAGAACTCTACAGTAGTCATGGGACGTCCAGCTGTTATGGAGTGCATGGCTCAGGGTGAACCCAAACCCTTTGTGTCATGGAGCAGACAGGGTAAGATTTAACATGTTATACACAAATGCAACTGAATGCTTGTCTACTTTAACAGTCTGTAGCTTTTAAGAGCAGTAATTTGAACCAGGTGTGTACTGTGCACCTGAAGCTGGTCCATAAACAAGACTGTGACCTCACCCGATCAGTGTTGTCAAATTAAGAATGAATATGTAAAAAGACTTGAACTCAAATCTAAAATAGCTAAAATACACTGCCTGACAAAAGTCTTGTCACCCATCTAAGTTTTAGGAAAAACAAATAATAGCTTAACTTTTAGTTGATCATTTGGTATCAGAAGTGGCTTTTATGAAAGACAAAGGCCTCTAGATTACACGTATTTTACCAAAATAAAATATAATCATGTGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34101
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 |
---|---|---|---|---|---|
ENSDART00000113467 | Nonsense | 462 | 1246 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 32992198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 31386538 |
GRCz11 | 7 | 31657688 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAACGATAAATGTGCTTGTTTGTTTGCAGGCTCAGACAACATGGAGTA[T/A]CAGTTTGCGGTGAATAACGACACCACAGAGCTGCATGTGAAAGAACTGCT
Long Flanking Sequence:
ATGAAATAAATCAGTTATTGGAAATGAGTTAAAACTATTATGTTTAGAAATGCGTTAAAAAAAACTTCTCTACATTAAACAGAAATTGGGGAAAAATAAACAGGGGGCGAATAATTCTGACTTCAACTTTATGTAATAAAAACGTTAAAAGAAAATGACAAATATTGCTACATTGAGCATTTTCTATTTTCGGATTGTTGTAAAAAGTTTCTATGAGGCTCTTCCTGTTACCAGAGGTTACTTGAGTCCCTGTTTGACCTGCAGCCTTTTTCATTACTCTGAGTGTAGCCAGCTTAAGTGGATCAGTCCACAGAGAGAAATCCAGTCTCATTACTTTACCGAGGCCAATTCACTTCGTACTGTAGACCGCTGCTATTGATGGGGTCACTCTTCTCCACATTCGCATGCTCATACCCAAAGGACAACAATGTTTTGCTTTGGAGCAGGTTTTTAAACGATAAATGTGCTTGTTTGTTTGCAGGCTCAGACAACATGGAGTA[T/A]CAGTTTGCGGTGAATAACGACACCACAGAGCTGCATGTGAAAGAACTGCTCCCTCACACAGCCTACACGTTCTATGTAGTAGCCTATTCGCCCATGGGTGCCAGTCGCCCGTCTCTGCCTGTCACTGTGGAGATGCTGGAGGATGGTGAGCAATGAATAAAAGAGAGTGGTCAATATCATAAAGAAAGTAAATTGAGCTGCTGGCAATCAAACATGCTATTTCCTTGATATCTGCGCTGTGTTTAGACATGGCTATTTACTATATACTGTACATGGAATACCGGAGTAGCTTGCCCCGAAATTCTGTCATTATCTAGTTAGGTCCAACCCTGGTTCTACAGGTCCAATCCTGTTTGTGTTTATTTCTATTGTTGAATAGATTTTTTTAAAGAATCTTGGAAACCGCAAACCGTTGACATTGACTGCTGCTGTCAATGACTGCCGATTTCCAACGTTCTTCAAAATGTCTTATTTTGTGTTCAACAGACAATAAATCGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15443
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 |
---|---|---|---|---|---|
ENSDART00000113467 | Nonsense | 484 | 1246 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 32992132)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 31386472 |
GRCz11 | 7 | 31657622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAYGACACCACAGAGCTGCATGTGAAAGAACTGCTCCCTCACACAGCCTA[C/A]AYGTTCTATGTAGTRGCCTATTCGCCCATGGGTGCCAGTCGCCCGTCTCT
Long Flanking Sequence:
TCTCTACATTAAACAGAAATTGGGGAAAAATAAACAGGGGGCGAATAATTCTGACTTCAACTTTATGTAATAAAAACGTTAAAAGAAAATGACAAATATTGCTACATTGAGCATTTTCTATTTTCGGATTGTTGTAAAAAGTTTCTATGAGGCTCTTCCTGTTACCAGAGGTTACTTGAGTCCCTGTTTGACCTGCAGCCTTTTTCATTACTCTGAGTGTAGCCAGCTTAAGTGGATCAGTCCACAGAGAGAAATCCAGTCTCATTACTTTACCGAGGCCAATTCACTTCGTACTGTAGACCGCTGCTATTGATGGGGTCACTCTTCTCCACATTCGCATGCTCATACCCAAAGGACAACAATGTTTTGCTTTGGAGCAGGTTTTTAAACGATAAATGTGCTTGTTTGTTTGCAGGCTCAGACAACATGGAGTATCAGTTTGCGGTGAATAACGACACCACAGAGCTGCATGTGAAAGAACTGCTCCCTCACACAGCCTA[C/A]ACGTTCTATGTAGTAGCCTATTCGCCCATGGGTGCCAGTCGCCCGTCTCTGCCTGTCACTGTGGAGATGCTGGAGGATGGTGAGCAATGAATAAAAGAGAGTGGTCAATATCATAAAGAAAGTAAATTGAGCTGCTGGCAATCAAACATGCTATTTCCTTGATATCTGCGCTGTGTTTAGACATGGCTATTTACTATATACTGTACATGGAATACCGGAGTAGCTTGCCCCGAAATTCTGTCATTATCTAGTTAGGTCCAACCCTGGTTCTACAGGTCCAATCCTGTTTGTGTTTATTTCTATTGTTGAATAGATTTTTTTAAAGAATCTTGGAAACCGCAAACCGTTGACATTGACTGCTGCTGTCAATGACTGCCGATTTCCAACGTTCTTCAAAATGTCTTATTTTGTGTTCAACAGACAATAAATCGTACAGTAAATGCTTAGCTGGATTTATTTTGCCTTCCAATAACAACGCAAACTGACGTTGATATTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40929
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 |
---|---|---|---|---|---|
ENSDART00000113467 | Nonsense | 832 | 1246 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 32981500)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 31375840 |
GRCz11 | 7 | 31646990 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTGTGTTTTCCGACAGGACCCTCCTCTCCTGTGGACATGCAGT[T/A]AAGCGCTCTGGACTCGTTCTCAGTTCTGGTGAGCTGGCGCCCTCCGCTGG
Long Flanking Sequence:
TTTACTCATACTCTAGTGGTTTTAAACCTTTATGAGATTCTTTTTACTCTTAAACACAGAAGATATTTTGAAAAATGTTAGAAACCTGTAACCATTCACTTCCATAACAGGAAAAACAAATGGTTACAGGTTTTCAGCTTTCTTCAAAACATATTTTGTCTACAACAGAAGAAAGAAACTCATAAAGGTTTGAAGGGTGTGTAAATGATGACATCATTTTTCTTTCTGGGTGAACTATCCCTTTAAATAAAATAAATAAAAAGGAGATGTGCAATCTTTCTTTCATTTGGCACCAAATACAAATTTCTCTATGATTTGTACATATGTTGCTGCAATTAATTGCATTATATAAGTTGAAATAAAAGTTTCAGATGATTAAAATTCACAATTATTTGTGGTTCAATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTCCGACAGGACCCTCCTCTCCTGTGGACATGCAGT[T/A]AAGCGCTCTGGACTCGTTCTCAGTTCTGGTGAGCTGGCGCCCTCCGCTGGAGCCTAATGGAGTTGTCCTGACCTACTGGATTCTTTACACCCCCAACATCAGCCATCCAGATTACCAGTGGACAAACCTCACACATGATGGTCAGTCTGCACACACACAAACTAGCCAATGGTGTTGTACTTTGTCATTTCTTGTGGCTCTGACTCTTCCTCGTCCCTCAGGTTACGTGACTAGTGCAGAGGTGCCGGGCCTGATGAGCGGGACGCGTTATTATTTTAAGATGGGGGCCTGCACTGAGGTGGGAGTGGGACCATATTCACCCGTGAAGGATGTCTATACACCTCCCAAAAAATATGGTATGCATTCACTATTTGTGCAATGGATTGTTTTTTTTTTTTTTTGTTCAGGTTTTATTTTTTAAGGTTGTAATACTTTTTTATGGTCACCTTTTTTGTCCGAAACATGAAGATTATCAGTTTTTTCACTTTCACTTTTACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38620
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 |
---|---|---|---|---|---|
ENSDART00000113467 | Nonsense | 1098 | 1246 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 32963702)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 31358042 |
GRCz11 | 7 | 31629192 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGACACGTGGAGAGGTTGTATTCCCTCAGCAAGAACCAGGTGGAGGCT[G/T]AAGTCATCGTGCATTCACAGCTGTCCAACGCAACAGTTGACCAGGGGCCA
Long Flanking Sequence:
TATATATATATATATATATATATATATGGAAGTTGAAGTCTTATTAGGCCTAAGTGACATTTAAATGCTTAACAAAGTTAATTAGGCAAGTTAGAATAATTAAGCACTTCATTGTATAACAATGGTTTGTTCTGTAAATAATCTAAATAACCCCTAAGCTATAAATAAATAAATAAATAGCTTAAGGGGGCTAATAATATTGACCTTAAAATTATATTTAAAAAATAAAAAACTGCTTTTATTCTAGCCGAAATTAAACAATTAAGACTTTCCCCTGAAGAAAAAAAATATAGGACATACTGTGAAAAATAACTTGCTCTGTTAAATATCATTTGGGAAATAATTAAAAAAAATTAAATAAATAACAGGAGGACCAATAACTTGGACTTTAACTGTGTATATAATTATATTTTTCTTAATTATATATGTGTGATACTCCTTATTTGCAGAGTGGACACGTGGAGAGGTTGTATTCCCTCAGCAAGAACCAGGTGGAGGCT[G/T]AAGTCATCGTGCATTCACAGCTGTCCAACGCAACAGTTGACCAGGGGCCACAAAGCGACATGGAGCTCTGTCTGGAGTCTCCATCTTCCCAGCAGCCTTCTCCTGGAGAGAAGGCAACTCCATCAAGCCCTCACAGTGAGGACAACCATGAGACTCAATCACCATCCCCAACCCCCAGCACTCACATCTCTGAAGTACTGTCCAATCACAATGGACCATTCGAGAGTGGACCGATCGGTGCCAAAAACCAAGGAGTGGGGCTTACGAATGGCTTCCACTCATCCAAACCCCTTCGGTCAAAGGCAGAGACCCTGGAGAACGGGGCCCACAGACTGTGTCCCACAGGAAAGGTCCTGCCTTCACCGGGTCTCCCCGCTTCCCCTTCATCCTTCACCAGCTCTGGCCTTGTGCATTCTACCTCAGGGGCGCACAGCTATGTGTACCCCTAAGCTGGAGGGAAGAGAAATGTAATAAAAGTTGTTCTAGGACAACAGAGGAGG
Associated Phenotype:
Not determined