ZMP
LOC100151213
Ensembl ID:
Human Orthologue:
ZNF407
Human Description:
zinc finger protein 407 [Source:HGNC Symbol;Acc:19904]
Mouse Orthologue:
Zfp407
Mouse Description:
zinc finger protein 407 Gene [Source:MGI Symbol;Acc:MGI:2685179]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13348 | Nonsense | Available for shipment | Available now |
sa19130 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10913 | Nonsense | Available for shipment | Available now |
sa45563 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42656 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13348
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 |
---|---|---|---|---|---|
ENSDART00000124065 | Nonsense | 137 | 1389 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 7946877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6792609 |
GRCz11 | 16 | 6733287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAGGTGCATCTGGAGAGTTCTTCAGTGTCTCTGTCAGAAGAGGACAAA[C/T]AATCGGATTGCTGCGTGGATGAAAACTCKGTGAAGGTTGTTGGAAACTCA
Long Flanking Sequence:
TTATTGTTATTATAAAATTTGTTATTTTCACAGGAAGGTTCATGGATCCTTCAAATAAAGTTTAGTAACATTCCTCCTTAACCGGCAGCATCATGGATGCTCCAAAACGGAAATTAAGGTCTGGAAAAGACATTTCAAAGGACAAAGGCCAGTCTAAGAGAAAAGCCAGTGATACTGGCACAGAAGATGTTTCCCCAGCACCTAAAAGTGCTAAAACTTCTGATGATTCAGGATATGTGTGTAATGAAGAAGAACATGAGCATGGTGAGACAGATACAGTGGGAGATCAGACAAGATCTATACAATCTAAAGAGTGTGACTCTTCAGAAACAAGCAATCCTTTAGTTTGTTCAGTGTGCAGTTTTGTTGCAAAAACTCAAACTGCACTGAAAATTCACTCAAAGCGGAAACACTCACAATTACAAGAAGCTGAAAACCAAACACACCTCTCAAAGGTGCATCTGGAGAGTTCTTCAGTGTCTCTGTCAGAAGAGGACAAA[C/T]AATCGGATTGCTGCGTGGATGAAAACTCTGTGAAGGTTGTTGGAAACTCAAGATCTAGTCCTACTCAGATGTTGCTGGAAATAGTTGAACCCACTTCATGTAGATCAGGAACTGATGGTGAAGGTACAAATGAGGCCAACATAGGTGGCGTTACAAATGATGGAATGGATGAGAATGATAAAAGTCAAAAGCATTCAACGTCTAATACTCCACAAACATTAGCAGTTGGACACAGTACAGACTCTCATAGAAAAGAGACAAATTGTGATAGCGAGGAATGCATGACCAGCAAGAGCAGCAAAAAGATGTTAGGAAATCAGCATTCGTTAAAGACAACAGCATTGTTGAAGCGTTCGACTGGAGGCAAGTCACAACATCAGTGTGGTAAGTGCACCTTCACAGCTGACAACTCCGTAATGTTAGCACAACACATTAAAACGCACCATCCGGTGGAGCACCGTTTCCACTGCAAGATTTGTCATTACTACACCACCACCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19130
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 |
---|---|---|---|---|---|
ENSDART00000124065 | Nonsense | 623 | 1389 | 1 | 8 |
ENSDART00000124065 | Nonsense | 623 | 1389 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 7948335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6794067 |
GRCz11 | 16 | 6734745 |
KASP Assay ID:
2260-9178.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGTGAGGAGAATTGTAATAACGAGAATGGAGAAAAGCAGTCTGACGAA[C/T]AGAGTACCTCTAAAGATAACGAAGAATCAGATCCAACCGTTTCTGATGTG
Long Flanking Sequence:
GAACTGGCAGTGGGGTTGTTCTGCTAAGTGCTGAGCAGTCGAGTCAGTCAAAGGCAAATGAGGCAGAAACGGTTGACAAAGTTGCAGATATTGAGATGTCTGTAGATGAAGTGGACAATACTGACTCCAGTGTTGTGGCATGTAAGAAAATCAAATATGACTCTGGAAACAATTGTTCTCAGTGCGACTTTGTTGCTCATTCGGCACAGTCTCTTGCGCTCCATGTGCGACGCAAGCACACAAAAGACTTTGAGTTTGTTTGTCTAGCGTGCTCCTATTACACTGTAACGCGCAGGGAGATGTTTAGGCACATGGCAACAGAAAAGCACAAGCAACAACGTGAGTGTTACTTGAAAAGACAAAGTAATGATCCTTCTGAAGACCCGGAAGTGATCACCGTTTTAGCATCCGCAAGTCCAACAACTAAAGATGCAGATCTTTCAGCGGACTTAAGTGAGGAGAATTGTAATAACGAGAATGGAGAAAAGCAGTCTGACGAA[C/T]AGAGTACCTCTAAAGATAACGAAGAATCAGATCCAACCGTTTCTGATGTGATCCAGTCAATAAAGATGGAGGATATGGTTGAGGAAAATGAGATGGACGAGGATGAAATTGCAGATTCGGGAGATGAAGGTCAATCTACTGAGAAACACCTTCGACTGACACAGTTAGATTCTTGCATATATCCCTTGAAAACTATTGCAGAGCACAAGCAGGCCTCACTTACTGGAGATGCAATTGCAGGTGGAGTAAACAAGCAGAGCATCAGAAAGCCTAAAACCCTTGACGCTAAAAATGCCAAGTCAATTCCACGTATACGCTGTGAAGACTGTGGATTTTTGGCAGATGGCATAAGTGGCCTAAACGTTCACATCTCCATGAAGCATCCATCCAAGGAGAAGAATTTCCATTGCTTGCTTTGCGGAAAGTCCTTTTATACGGACAGCAACCTGCAACAGCACTTGGGCAGTGCAGCGCACATGCGCAATGAGAACGGAAGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10913
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 |
---|---|---|---|---|---|
ENSDART00000124065 | Nonsense | 623 | 1389 | 1 | 8 |
ENSDART00000124065 | Nonsense | 623 | 1389 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 7948335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6794067 |
GRCz11 | 16 | 6734745 |
KASP Assay ID:
2260-9178.1 (used for ordering genotyping assays)
KASP Sequence:
TAARTGAGGAGAATTGTAATAACGAGAATGGAGAAAAGCAGTCTGACGAA[C/T]AGAGTACCTCTAAAGATAACGAAGAATCAGATCCAACCGTTTCTGATGTG
Long Flanking Sequence:
GAACTGGCAGTGGGGTTGTTCTGCTAAGTGCTGAGCAGTCGAGTCAGTCAAAGGCAAATGAGGCAGAAACGGTTGACAAAGTTGCAGATATTGAGATGTCTGTAGATGAAGTGGACAATACTGACTCCAGTGTTGTGGCATGTAAGAAAATCAAATATGACTCTGGAAACAATTGTTCTCAGTGCGACTTTGTTGCTCATTCGGCACAGTCTCTTGCGCTCCATGTGCGACGCAAGCACACAAAAGACTTTGAGTTTGTTTGTCTAGCGTGCTCCTATTACACTGTAACGCGCAGGGAGATGTTTAGGCACATGGCAACAGAAAAGCACAAGCAACAACGTGAGTGTTACTTGAAAAGACAAAGTAATGATCCTTCTGAAGACCCGGAAGTGATCACCGTTTTAGCATCCGCAAGTCCAACAACTAAAGATGCAGATCTTTCAGCGGACTTAAGTGAGGAGAATTGTAATAACGAGAATGGAGAAAAGCAGTCTGACGAA[C/T]AGAGTACCTCTAAAGATAACGAAGAATCAGATCCAACCGTTTCTGATGTGATCCAGTCAATAAAGATGGAGGATATGGTTGAGGAAAATGAGATGGACGAGGATGAAATTGCAGATTCGGGAGATGAAGGTCAATCTACTGAGAAACACCTTCGACTGACACAGTTAGATTCTTGCATATATCCCTTGAAAACTATTGCAGAGCACAAGCAGGCCTCACTTACTGGAGATGCAATTGCAGGTGGAGTAAACAAGCAGAGCATCAGAAAGCCTAAAACCCTTGACGCTAAAAATGCCAAGTCAATTCCACGTATACGCTGTGAAGACTGTGGATTTTTGGCAGATGGCATAAGTGGCCTAAACGTTCACATCTCCATGAAGCATCCATCCAAGGAGAAGAATTTCCATTGCTTGCTTTGCGGAAAGTCCTTTTATACGGACAGCAACCTGCAACAGCACTTGGGCAGTGCAGCGCACATGCGCAATGAGAACGGAAGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45563
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 |
---|---|---|---|---|---|
ENSDART00000124065 | Essential Splice Site | 876 | 1389 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 7950868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6796600 |
GRCz11 | 16 | 6737278 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTAATTTAAAGAGGAAAATTGAATGTCTTTTTAAAATTGTTTTTTTC[A/T]GGATCTAAACCGTTCAGGTGCAAGATCTGCAACTTTTCCACTGCTCAGCT
Long Flanking Sequence:
TGGCCAGATCTGTGCCTTGCCACAATTCTGTCTCTGAGCTCTTCAAGCAGTTCCTTTGACCTCATGATTCTCATTTGCTCTGACATACATTGTGAGCTGTAAGGTCTTCTATAGACAGGTGTGTGGTTTTCCTGATCAAGTCCAGATGGACTCATATGAAGGTGTAGGACCATCTCAAGGAGGATCAGAACAAATGGACAGCACCTGAGTTAAATATATGAGTGTCACAGCAAAGGGTCTGAATACTTAGGAGCATGTAATATTTAAGTTTTTCCTTTTTAATAAATCTGCAAAAAAAAAGTCAACAATTTTGTGTTTTTCTGTCAAAATGGGGTGCTGTGTGTACATTAATGAGGAAAAATCTACTTAAATGATTTTAGCAAATGGCTGCAATATAACAAAGAGTGAAAGATTTAAGGGGGTCTGAATACTTTCCATACTCACTGTTTTTGCTTAATTTAAAGAGGAAAATTGAATGTCTTTTTAAAATTGTTTTTTTC[A/T]GGATCTAAACCGTTCAGGTGCAAGATCTGCAACTTTTCCACTGCTCAGCTCGGGGATGCTCGCAACCATGTTAAGAGACATCTAGGCATGAGAGAGTACAAGTGTCACATCTGTGGGTGAGTTTAAGAGAGATGTGAGGGGGGAGATTAACCCCCTCACGACACTCTTAAGTTTAATATGATTTTTGTGTAGGACGTTTTATGAAGAAGAGTGCCTTTGCACCTCACAAACCCTTAAATAAACAAAGCAGGGGATGCTAAACATTTCTTTTATTTCACAAAAATAATGAAGCATACAGTAAGATGCGGATATTTGAATTTATAGGTTAATGGTGCTTTGGGAGAACTTTCAAATCTGAAGCTTGAAGGGTTTTTTAATCAAGGTGAAATGATTGCATGGATAATATAATGAGGGAAACTGTATCTCTCATTGGTATTATACAGCAATTATAATTAATGAATATTTGTTTTGGCTTTTAATTAGTTCATTTAAAAGTAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42656
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 |
---|---|---|---|---|---|
ENSDART00000124065 | Nonsense | 1188 | 1389 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 7959351)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6805083 |
GRCz11 | 16 | 6745761 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGGTGGCCATCGATCAGGCTCTGGAGCAGTCGGCCGCTGCCACTTTA[C/T]AGACCCTCGCCATGTCCAGCCAGCTGGCCGAAGTGCTGCACATCACCGAG
Long Flanking Sequence:
TCTTCTGTCGAACAGAAAGGAAGATCTTTTAAAGAAAGCTGAAATCCTGTAACCACTGATGTCCATAGGATTTGTTTTTCCGACTATAAAAGATAATGGTGACAGGTTTTGAGCTTTCTTCAAAATATCTTTGTTGATATAAAGGTTTGGAACCACTTGAGGGTTAGTAAATAGTGAGTAAATGTTCATTTTTGAGTAAACTATCTATTTAAATGACACCTCAGTTTCTCGTTAAGTGACCATGTTGAGTCAAAGAATGCATTTAACATCCCAATATGTCTTTCTACTCTCTTGTGTTTGTTGCAGGAATTGTATCCAAGTCCTATGAGTGTCGTCTGAAGGGTCAGGGGGCATCTTTTGTCCAGGCAGAAACTGTGTTTTCCCCTGAGGAGAGCGAACTGGGTTCTGAGGCAGTTCAGCAGGTCATCATCATCCAGGGCTACAGTGGAGGAGAGGTGGCCATCGATCAGGCTCTGGAGCAGTCGGCCGCTGCCACTTTA[C/T]AGACCCTCGCCATGTCCAGCCAGCTGGCCGAAGTGCTGCACATCACCGAGGACGGGCAGCTCATCACATCCGGTCAGGAAGTCTCTACAGGAGGCCAGACCACTCAATATGTCCTGGTGGAGTCATCCGGAGAAACCGTAGGAGAAGGAAGACCAGAAGTGGAGGCTGGACACAATGCATCTGAATCGTCTTCTGCTCTGGATGCTTTGCTTTGTGCTGTGACGGAGTTGGGCCAGCAGGCCTGCGCTGCTGAGGGAGAGATTTCCACCACTGCCGCGGCAGTGTCTGAAAGTCATCCAAAAGTGACGACCTCTCCAGCACAGAGCCAAAATGACGGGCAGGTATACGAGGAGAGGACAGAAGTGGGCATGGTGGCTCAGGTGGTGGGGTCTACCCATGAGCAACCGTCCGAGGAGATGCAAGAGGTGCTCCAGTTTGCAGCCAGTCAGCTGATGATGAAGGAAGGACTCACTCAAGTCATCGTCAATAATGAAGGGACG
Associated Phenotype:
Not determined