ZMP
zcchc7l
Ensembl ID:
ZFIN ID:
Description:
Zcchc7l protein [Source:UniProtKB/TrEMBL;Acc:Q4QRH2]
Human Orthologue:
ZCCHC7
Human Description:
zinc finger, CCHC domain containing 7 [Source:HGNC Symbol;Acc:26209]
Mouse Orthologue:
Zcchc7
Mouse Description:
zinc finger, CCHC domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:2442912]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39602 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8940 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14502 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39602
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 |
|---|---|---|---|---|---|
| ENSDART00000077799 | None | None | 347 | None | 7 |
| ENSDART00000102837 | Nonsense | 34 | 293 | 2 | 4 |
| ENSDART00000129066 | Nonsense | 34 | 627 | 2 | 9 |
| ENSDART00000142751 | Nonsense | 34 | 627 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 20544944)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21017040 |
| GRCz11 | 1 | 21709977 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCCATTTAGGGCTCTCCTTGAGATGTTCTCAGGGTTTCAGGAACGGTA[C/A]GACCATGAGGACGAGCTGTACAGGGATGAAGAAGACTCATCAGGTTTGTC
Long Flanking Sequence:
TATTTTTGTGCGCAAGCTGTGGAAATAACCCTAAGCTTATTGGGATTCCTTCCAAGGTGTGCGCTCAACAGACACATTTGATAAAACTATGGCCTTCATACCAAACTTTTTTTATTGACGATAAAATTGTAAATAAAGATTTTTTTATTGACAATAGTGTTCGGTCCGTAAATACTGATACCGTTTTATTGACCCAGCCTTATTTAATAATTTAAAAAGATTTAGAATGGTTTCTTTTGTTTTTATATTACGTATGTTTTGCAGGTCAGACTAAATAACCTATATGGTTATTTAAAACACTTAAGTAGACATTTCTTTACATTTAATATACTTATGTACATAGTATCATATTTGTAAATGTAACTTGATGCAAGAAGCACCAAAATGGGATACCTAGTTTTGACCTATACTAAACGTTACGGCCTCTAAATAACTCACGATCATGTTTGTTTTCCATTTAGGGCTCTCCTTGAGATGTTCTCAGGGTTTCAGGAACGGTA[C/A]GACCATGAGGACGAGCTGTACAGGGATGAAGAAGACTCATCAGGTTTGTCTGATTCGGACAGCGAGTTGGAATTCCGGCTTTATTCCCAGCTGCACTACAACGCAGAGTTCCAGGAAAACCATGAGGAATCAAGCAAAGTCCAACCATTGGTCCCACAAACTCAACTTCAGCCGGAAACCATGCCTCCTGCTCCACCTGTAGATGTTATCGTGATTGACTCAGGGCCAGATTCTTTTACAGTGTCAGACAGCACAGAGGATGATGAGAGTGTGTGTGCTAATAAAGTTCAGTCATTAAAACATTGTAAAAGGAAGTCACAGCCCAGTCGCTTCCGTTCACCTTCTCCGCCTCAGGTTCAAGCAGGAAGGAGCTCTCCAGATGATGTTGTGGTGCTGGATTCTGATTTAGAACAATCCTCTTCTGAATCTGAACCTCCTTTTGTGGAGGATTTGGACTCGGATACAGACTCTGATTCAGACTCTGATGGACTGGAGAACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8940
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 |
|---|---|---|---|---|---|
| ENSDART00000077799 | None | None | 347 | None | 7 |
| ENSDART00000102837 | Nonsense | 87 | 293 | 2 | 4 |
| ENSDART00000129066 | Nonsense | 87 | 627 | 2 | 9 |
| ENSDART00000142751 | Nonsense | 87 | 627 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 20544787)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21016883 |
| GRCz11 | 1 | 21709820 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTCCAGGAAAACCATGAGGAATCAAGCAAAGTCCAACCATTGGTCCCA[C/T]AAACTCAACTTCAGCYGGAAACCATGCCTCCTGCTCCACCTGTAGATGTT
Long Flanking Sequence:
TGTTCGGTCCGTAAATACTGATACCGTTTTATTGACCCAGCCTTATTTAATAATTTAAAAAGATTTAGAATGGTTTCTTTTGTTTTTATATTACGTATGTTTTGCAGGTCAGACTAAATAACCTATATGGTTATTTAAAACACTTAAGTAGACATTTCTTTACATTTAATATACTTATGTACATAGTATCATATTTGTAAATGTAACTTGATGCAAGAAGCACCAAAATGGGATACCTAGTTTTGACCTATACTAAACGTTACGGCCTCTAAATAACTCACGATCATGTTTGTTTTCCATTTAGGGCTCTCCTTGAGATGTTCTCAGGGTTTCAGGAACGGTACGACCATGAGGACGAGCTGTACAGGGATGAAGAAGACTCATCAGGTTTGTCTGATTCGGACAGCGAGTTGGAATTCCGGCTTTATTCCCAGCTGCACTACAACGCAGAGTTCCAGGAAAACCATGAGGAATCAAGCAAAGTCCAACCATTGGTCCCA[C/T]AAACTCAACTTCAGCCGGAAACCATGCCTCCTGCTCCACCTGTAGATGTTATCGTGATTGACTCAGGGCCAGATTCTTTTACAGTGTCAGACAGCACAGAGGATGATGAGAGTGTGTGTGCTAATAAAGTTCAGTCATTAAAACATTGTAAAAGGAAGTCACAGCCCAGTCGCTTCCGTTCACCTTCTCCGCCTCAGGTTCAAGCAGGAAGGAGCTCTCCAGATGATGTTGTGGTGCTGGATTCTGATTTAGAACAATCCTCTTCTGAATCTGAACCTCCTTTTGTGGAGGATTTGGACTCGGATACAGACTCTGATTCAGACTCTGATGGACTGGAGAACTGGATGATTCTGGGCAAGGGGAGACAAGATGAAGATCAGAGCATCCAGCTGAACCTCGCGCAGAGTAGTTTTGTGAATACAGGTAAGGATTTTAAAAGTTTAAAGTCGCACTAAATCAGTGTTTCTCAATCATGTTCATGTTTTGGATGTCTCCTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14502
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 |
|---|---|---|---|---|---|
| ENSDART00000077799 | Nonsense | 209 | 347 | 6 | 7 |
| ENSDART00000102837 | None | None | 293 | None | 4 |
| ENSDART00000129066 | Nonsense | 491 | 627 | 9 | 9 |
| ENSDART00000142751 | Nonsense | 491 | 627 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 20395024)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 20919435 |
| GRCz11 | 1 | 21612372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCASCACACACCGAAGAAACGYATCGCACACACACCCAAACACAATCCA[C/T]AAACAAACCAACAAAACACACACTGGAGGGTCAAGCAGAACTCCAAAAAA
Long Flanking Sequence:
ATAAATTGCATTTCAAATTATATTAATTCCAGTAAAATTATATTAATTCAGTTTAAAGTTATATTAATTCCAATATTCATGTGACCTCATTAATCCCCATGATCTGAAATCATAAAGTATTTGTGTGTTTTCTGCAGCAATGCTCTCAGAGAAGGATGTACAATTGGTCCTATCCATCCTTGCCAGTTATCACCTATTATGACACAGTGAATGACATCAAATGCCGGGATTTCCGTCTGAAAAAGAAGGCCAGAGGTTTGTTAGATTCTGATCATTTCAGTTAAATAAACATTGTTGAGAGCTAAAGACTTAATGATGCGTTTCTTACAGAAATGCAGGACGCCGGACTGATTTCTCCTGATGGAGGCGTTGTAACATTTACCCCTCAACCACCCAGAAAGAAACAAAAAGTCAGCCACAGTCCACATCCGTACTCAAACAACACAAACAACCACCACACACCGAAGAAACGCATCGCACACACACCCAAACACAATCCA[C/T]AAACAAACCAACAAAACACACACTGGAGGGTCAAGCAGAACTCCAAAAAACCAGGACCCCACGGCAAAAACACCCCTCAAAGCAAAGAGTTCAAATCTCAAAATAAAGAAGCCAAGAACAAGAAAAGGAAAAAGAAAAAGGCTGCAGTTATAGATGAAGATGCCGACTTTCCCAGAGGTTCCAAAAAGAGCCCTCACAAGGCAGGTTTTCATTCGTCAACTCAAAAAGCCAATGTGAAGCCAGTGAAGCTGTTTGGAGTGGAGAAGAACCACATGAAGAAAAAAGACAAGTCGAAAAAGAAGGAGAGGATACAGAGAAAGAGACAACAAAAAGCGGCTAAAGATTCTGCCGCGTATCCCACTGATGAAAACCTCTTCCAGATTAAACAAAGAAAGGTAAAAAGAAGTAAATGAAATTGATCACACTTGTGTGATATCAGGTGATTCTCAAAGTTGGTTTTGCCCTTTTTCCATCCGATTAGTTTCATAGACTGTATTTTA
Associated Phenotype:
Not determined