ZMP
zgc:113390
Ensembl ID:
ZFIN ID:
Description:
dermal papilla derived protein 13 [Source:RefSeq peptide;Acc:NP_001028898]
Human Orthologue:
C7orf10
Human Description:
chromosome 7 open reading frame 10 [Source:HGNC Symbol;Acc:16001]
Mouse Orthologue:
5033411D12Rik
Mouse Description:
RIKEN cDNA 5033411D12 gene Gene [Source:MGI Symbol;Acc:MGI:1923221]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25204 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa5985 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19338 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32472 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25204
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082503 | Essential Splice Site | 46 | 231 | 5 | 10 |
ENSDART00000089409 | Essential Splice Site | 46 | 231 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 24 (position 3380128)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 3270621 |
GRCz11 | 24 | 3302408 |
KASP Assay ID:
554-7699.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGTTGGGTTCCCCTTCCTGTTCATGATGTTTTTTTTTATATAATTGC[A/T]GAGCATTGCTGTTAACCTTAAATATCCAAAGGGGATCAAAGTTGTAACTG
Long Flanking Sequence:
GAGATGACACGAGAGCTTGGGGTCCTCCATTTCTGGGTGAAGAGAGTGCTTATTTTCTCAGTGTGAACAGGAACAAAAAGGTATAATCCTTGTTTTTGTAAATGTTGTATTTATACAGTTGAAGTCAAAACAATTATTATTATTAGCCCTCTTGTGATGTTTTTTTTATTTTTTTATTTTTTGGCAAATGTTTAACCGATTCAGGAATTTTTCACAGTATTTCCTATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTAATGGAGCTAGAATAAAAGCAGTTTTTAATTTTTTTAGGTTAAAATTATTAGCCCCCTTAAGCAATGTTGTTTTTTAATTGTCTACAGAACAAACCACTGTTATACAATGACTTGCCTAATTAACCTGATTGACCCAGTTAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGTATCTTGGAAAAATTCAGTTGGGTTCCCCTTCCTGTTCATGATGTTTTTTTTTATATAATTGC[A/T]GAGCATTGCTGTTAACCTTAAATATCCAAAGGGGATCAAAGTTGTAACTGAGGTAAGTACATCACACATTTTGTTTTGTTGTTGTTTGATTTATTTTGTTTTGCTCACCTTGCCTGTATATACACTACCTGACAAAAGTCTTGCCACCTATCCAAGTTTTAGGAACAACAAATAATTACTTCACTTCTAGTTGATCAAAAGTAGACATCTGCATTTAGACTCATTTGCTTTTAATGTTTATACAATAACATTTGTAATCTTTATTTTATATATGACTTACACCTTTTGATTTAAATACATTCCATCTTTTTTATTTTGTTTTGCACACCTTGCCTGTCTCACTTCATTGTCTTTTTTTGTCAGCTTGCCAAAATCTGTGATGTTCTTCTGGAGAATTATTTGCCCGGGAAGCTGGGTGAGATGGGACTTGGGTACGAGGAGTTGAGGAAAGTGGCGCCGCGGCTCATCTATTGCTCTATAACAGGTGCGCACAGTTTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5985
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082503 | Nonsense | 86 | 231 | 6 | 10 |
ENSDART00000089409 | Nonsense | 86 | 231 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 24 (position 3379693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 3270186 |
GRCz11 | 24 | 3301973 |
KASP Assay ID:
554-3650.1 (used for ordering genotyping assays)
KASP Sequence:
CTKCTGGAGAATTATTTGCCCGGGAAGCTGGGTGAGATGGGACTTGGGTA[C/A]GAGGAGTTGAGGAAAGTGGCGCCGCGGCTCATCTATTGYTCTATAACAGG
Long Flanking Sequence:
AGTATCTTGGAAAAATTCAGTTGGGTTCCCCTTCCTGTTCATGATGTTTTTTTTTATATAATTGCAGAGCATTGCTGTTAACCTTAAATATCCAAAGGGGATCAAAGTTGTAACTGAGGTAAGTACATCACACATTTTGTTTTGTTGTTGTTTGATTTATTTTGTTTTGCTCACCTTGCCTGTATATACACTACCTGACAAAAGTCTTGCCACCTATCCAAGTTTTAGGAACAACAAATAATTACTTCACTTCTAGTTGATCAAAAGTAGACATCTGCATTTAGACTCATTTGCTTTTAATGTTTATACAATAACATTTGTAATCTTTATTTTATATATGACTTACACCTTTTGATTTAAATACATTCCATCTTTTTTATTTTGTTTTGCACACCTTGCCTGTCTCACTTCATTGTCTTTTTTTGTCAGCTTGCCAAAATCTGTGATGTTCTTCTGGAGAATTATTTGCCCGGGAAGCTGGGTGAGATGGGACTTGGGTA[C/A]GAGGAGTTGAGGAAAGTGGCGCCGCGGCTCATCTATTGCTCTATAACAGGTGCGCACAGTTTTCACAAGATGCCAAAGCATCAACCTTATACTATTTTAAGATTTCTGCTTTAGTTATGACAAAGCGGCTTGATTTCTTTTTTTGTAGAAACTGTGTACAAACTTTATATTAGGGTACAGTTCTCACTATTAATAAACTACTGACTACGACTTTTATAGGTTAAGAAACTCGTAGTTTGCTGCATATTAATAGTCATTAAGGTAGTAGATGGGTTTAGGTATTGGGTAGGATTAGAGATGTAGAATAAGATCATGCAGAATATGTCATGTATACGCACTAATGAACTGGAAGTATTTAAAAAATAGGCAGGATATAAGACACTAGTTAATAAAGAGAATTGTTATTTATAATAAAGCATTGCTGAAACTGCAAGTAATATTACTTCTGAATACTGTAGTTAAGATTTTTTTATTTAAATAATATATTTTTTTACATTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19338
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 |
---|---|---|---|---|---|
ENSDART00000082503 | Nonsense | 89 | 231 | 6 | 10 |
ENSDART00000089409 | Nonsense | 89 | 231 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 24 (position 3379685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 3270178 |
GRCz11 | 24 | 3301965 |
KASP Assay ID:
554-6205.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATTATTTGCCCGGGAAGCTGGGTGAGATGGGACTTGGGTACGAGGAGT[T/A]GAGGAAAGTGGCGCCGCGGCTCATCTATTGCTCTATAACAGGTGCGCACA
Long Flanking Sequence:
GGAAAAATTCAGTTGGGTTCCCCTTCCTGTTCATGATGTTTTTTTTTATATAATTGCAGAGCATTGCTGTTAACCTTAAATATCCAAAGGGGATCAAAGTTGTAACTGAGGTAAGTACATCACACATTTTGTTTTGTTGTTGTTTGATTTATTTTGTTTTGCTCACCTTGCCTGTATATACACTACCTGACAAAAGTCTTGCCACCTATCCAAGTTTTAGGAACAACAAATAATTACTTCACTTCTAGTTGATCAAAAGTAGACATCTGCATTTAGACTCATTTGCTTTTAATGTTTATACAATAACATTTGTAATCTTTATTTTATATATGACTTACACCTTTTGATTTAAATACATTCCATCTTTTTTATTTTGTTTTGCACACCTTGCCTGTCTCACTTCATTGTCTTTTTTTGTCAGCTTGCCAAAATCTGTGATGTTCTTCTGGAGAATTATTTGCCCGGGAAGCTGGGTGAGATGGGACTTGGGTACGAGGAGT[T/A]GAGGAAAGTGGCGCCGCGGCTCATCTATTGCTCTATAACAGGTGCGCACAGTTTTCACAAGATGCCAAAGCATCAACCTTATACTATTTTAAGATTTCTGCTTTAGTTATGACAAAGCGGCTTGATTTCTTTTTTTGTAGAAACTGTGTACAAACTTTATATTAGGGTACAGTTCTCACTATTAATAAACTACTGACTACGACTTTTATAGGTTAAGAAACTCGTAGTTTGCTGCATATTAATAGTCATTAAGGTAGTAGATGGGTTTAGGTATTGGGTAGGATTAGAGATGTAGAATAAGATCATGCAGAATATGTCATGTATACGCACTAATGAACTGGAAGTATTTAAAAAATAGGCAGGATATAAGACACTAGTTAATAAAGAGAATTGTTATTTATAATAAAGCATTGCTGAAACTGCAAGTAATATTACTTCTGAATACTGTAGTTAAGATTTTTTTATTTAAATAATATATTTTTTTACATTTCAGAAGACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32472
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 |
---|---|---|---|---|---|
ENSDART00000082503 | Nonsense | 169 | 231 | 8 | 10 |
ENSDART00000089409 | Nonsense | 169 | 231 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 24 (position 3363210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 3253703 |
GRCz11 | 24 | 3285490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTCACGGAGCCATAATGGCCGCTTTGCTTCAGAGGCAGAAAACCGGA[C/T]GAGGCCTTCATATAGACTGCAATCTTCTGTCTTCACAGGTAATACTACTG
Long Flanking Sequence:
TATTGCGCATTATACAGTGCATCACTTTAAATAATTTACAGTATTAAGCATAAAAAGAAAAAAGTCTTTAAAACTGCTTTAGTTTAATAATATACCTCTGGTTCAACTACAAATCAGCTCTCTAAAATGTTTTATTTTTTCAGATATCATTCCTTCATTAACTAAACAAAAAAAAAAAAAAAAATGTGCTGAAGTGTGCTTATTTAATAACGACACACCTAACTATTGCACCATCACCACTGACCAATGGTAGTTAAAACAAGTTTACCAGCCTGAGTGAAGTTTTCCAATCATACCAGTTTGTTCTTCAGTTTCCATTAAAGGTTTTTGATTTTGAGTGCCGTTAGCAGTTTTAGGCCCTTTATGTCCTGTTGATTTATTTGTTCTGTTTTAAGGACGGGGATCCAGTCAGACCAGGTGTCGCTATGACAGATCTGGCCACTGGTTTATACACTCACGGAGCCATAATGGCCGCTTTGCTTCAGAGGCAGAAAACCGGA[C/T]GAGGCCTTCATATAGACTGCAATCTTCTGTCTTCACAGGTAATACTACTGTGACTTTATGACTACACTTTATTATTAAACACAACTTTATGTAAAAAAAGCATCTGATCAAAGTGACATGAATAGCTTTACATAATCTGCAATTAACATGTCGACAGGTCATAACATTATACATATTAATTTGGGACTTTAGACAATATCGGGCTGCTAGTTTATAGATCGATCTTTTCTTCGCATGAAACATTGACATTACAAACTAGATTTTTAAAAACATTTTATAGACATTTGATTCAAAAACAAAGTCTTTCACTTAAATCAGGGCTTTCAAACTCCTGTGAGTGTTCCTGGAGGGCCGACGCCCTGCACAGTTTAGTTCTAACCCTGTTTCAACACACTTACCTGTAAGTTTCAAACAAGCCTGAAGGACTCTATTAGTGTAATTAGGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCACAGCTGCGGCCCTCCAGGAACTG
Associated Phenotype:
Not determined