ZMP
ZNF518A (1 of 2)
Ensembl ID:
Description:
zinc finger protein 518A [Source:HGNC Symbol;Acc:29009]
Human Orthologue:
ZNF518A
Human Description:
zinc finger protein 518A [Source:HGNC Symbol;Acc:29009]
Mouse Orthologue:
Zfp518a
Mouse Description:
zinc finger protein 518A Gene [Source:MGI Symbol;Acc:MGI:1919922]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa27974 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8549 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa42054 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15166 | Nonsense | Available for shipment | Available now |
| sa9134 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7224 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27974
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 |
|---|---|---|---|---|---|
| ENSDART00000115358 | Nonsense | 164 | 1254 | 1 | 3 |
| ENSDART00000126390 | Nonsense | 158 | 1250 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 30777141)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 29114078 |
| GRCz11 | 12 | 29228980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGAACAAGTGGAGACCAAATGAGGACAATTCATCTGGTCTAAAATTGT[T/A]GCTTAAAAAGTCTCCTCCAGGTGGAGGGTCCAGAGAATCACAGTGGATGT
Long Flanking Sequence:
TCCATGTAAGATGCAGCAGGGTGCAATCTTCTCTGGAAAAATACTGAGTTTTTGTTGCTCTGAGTGCAAAGACGACACCACTTACAGCCCTAACGACTTGTTGAAACATTTTCAAGGAGTACACAAGGGGACTCCTCCAACTTATCCTTGTGATTTATGCTTATTTGTCACCAATGAATTCTCATCTCTTCAGCGACATCGCATTGGGCATCGAAACACATTAGTCACGTGTGAGATTTGCAATGATGGGGTGCAGTATTCACTTCTTTTGCTTACCAGGCACTTTACAAGCTGCCACAGCCGTAATGGACAGTTTAGCTGTAAAAAATGTGAGTTCTCCACCCGAGATGCAGGAACCTTTGTTCAGCACATCCATCATCACAATGAACTCAATCACAACGCTCGCAGGGAGTACCTGAGCAAACATCTTACTCTGGCACATGGTGAGGAGATGAACAAGTGGAGACCAAATGAGGACAATTCATCTGGTCTAAAATTGT[T/A]GCTTAAAAAGTCTCCTCCAGGTGGAGGGTCCAGAGAATCACAGTGGATGTCAAAATATAACGCTATTCCTGGTGTAGGTCTTTTTGATCATAACGGCAGGTTGATTAATCCTGAAAAAACCTTGGAGGACACCCAGCAGTTTCTTGAAAGAGCCGTCGGGGTTAAAAAAGAGAGTAATAAATGGACAAAATCTCCCCTTAAAAGTGAGCCACAAATATTGCAGCTCATTCCATCAGCAACACAGCAACCAAAGTTACAAGAGCATGAGATTAGTCCTGGAAGTCCAGGACATGGCAATGGACTGACTGTTCTTATGGTAAAAAATAAAATTTCTATTCCACCAAACTGCACCACGCAAGTCATGGGCTTTAAGATGGTAGATGGCAAAAAGCATTTAGTTCTAAAGGTCATACCAACAAAACAAGAGGACTCCACTGAAAGTGAGGTTTTTGAGTCACATATTAGTGAAGATGAAAATAAACCAACCAGCAGTCCTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8549
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 |
|---|---|---|---|---|---|
| ENSDART00000115358 | Nonsense | 238 | 1254 | 1 | 3 |
| ENSDART00000126390 | Nonsense | 232 | 1250 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 30776920)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 29113857 |
| GRCz11 | 12 | 29228759 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGTAATAAATGGACAAAATCTCCCCTTAAAAGTGAGCCACAWATATTG[C/T]AGCKCATTCCATCAGCAACACAGCAACCAAAGTTACAAGAKCATGAGATT
Long Flanking Sequence:
TAGTCACGTGTGAGATTTGCAATGATGGGGTGCAGTATTCACTTCTTTTGCTTACCAGGCACTTTACAAGCTGCCACAGCCGTAATGGACAGTTTAGCTGTAAAAAATGTGAGTTCTCCACCCGAGATGCAGGAACCTTTGTTCAGCACATCCATCATCACAATGAACTCAATCACAACGCTCGCAGGGAGTACCTGAGCAAACATCTTACTCTGGCACATGGTGAGGAGATGAACAAGTGGAGACCAAATGAGGACAATTCATCTGGTCTAAAATTGTTGCTTAAAAAGTCTCCTCCAGGTGGAGGGTCCAGAGAATCACAGTGGATGTCAAAATATAACGCTATTCCTGGTGTAGGTCTTTTTGATCATAACGGCAGGTTGATTAATCCTGAAAAAACCTTGGAGGACACCCAGCAGTTTCTTGAAAGAGCCGTCGGGGTTAAAAAAGAGAGTAATAAATGGACAAAATCTCCCCTTAAAAGTGAGCCACAAATATTG[C/T]AGCTCATTCCATCAGCAACACAGCAACCAAAGTTACAAGAGCATGAGATTAGTCCTGGAAGTCCAGGACATGGCAATGGACTGACTGTTCTTATGGTAAAAAATAAAATTTCTATTCCACCAAACTGCACCACGCAAGTCATGGGCTTTAAGATGGTAGATGGCAAAAAGCATTTAGTTCTAAAGGTCATACCAACAAAACAAGAGGACTCCACTGAAAGTGAGGTTTTTGAGTCACATATTAGTGAAGATGAAAATAAACCAACCAGCAGTCCTTGCTCTTCATCAATAGCATCTCTTTTAAGTTTAGAGTCTGGAGAATCAAATGAAGCCTCTTTAATAGCGGAGGAGTCACACGAGGTTGAAAACCACATTGGCCACCATTACCCCTTGACAGAAGAGCACAAGGTTTACTTTGAGACCACAAGAAAGTCGGGGCAGGTTAATGAGGATGCTGAAATTGCACATAGTGTTAAAGTACTGTCAACAGCATCAAAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42054
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 |
|---|---|---|---|---|---|
| ENSDART00000115358 | Nonsense | 305 | 1254 | 1 | 3 |
| ENSDART00000126390 | Nonsense | 299 | 1250 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 30776719)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 29113656 |
| GRCz11 | 12 | 29228558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGGTAGATGGCAAAAAGCATTTAGTTCTAAAGGTCATACCAACAAAA[C/T]AAGAGGACTCCACTGAAAGTGAGGTTTTTGAGTCACATATTAGTGAAGAT
Long Flanking Sequence:
AACATCTTACTCTGGCACATGGTGAGGAGATGAACAAGTGGAGACCAAATGAGGACAATTCATCTGGTCTAAAATTGTTGCTTAAAAAGTCTCCTCCAGGTGGAGGGTCCAGAGAATCACAGTGGATGTCAAAATATAACGCTATTCCTGGTGTAGGTCTTTTTGATCATAACGGCAGGTTGATTAATCCTGAAAAAACCTTGGAGGACACCCAGCAGTTTCTTGAAAGAGCCGTCGGGGTTAAAAAAGAGAGTAATAAATGGACAAAATCTCCCCTTAAAAGTGAGCCACAAATATTGCAGCTCATTCCATCAGCAACACAGCAACCAAAGTTACAAGAGCATGAGATTAGTCCTGGAAGTCCAGGACATGGCAATGGACTGACTGTTCTTATGGTAAAAAATAAAATTTCTATTCCACCAAACTGCACCACGCAAGTCATGGGCTTTAAGATGGTAGATGGCAAAAAGCATTTAGTTCTAAAGGTCATACCAACAAAA[C/T]AAGAGGACTCCACTGAAAGTGAGGTTTTTGAGTCACATATTAGTGAAGATGAAAATAAACCAACCAGCAGTCCTTGCTCTTCATCAATAGCATCTCTTTTAAGTTTAGAGTCTGGAGAATCAAATGAAGCCTCTTTAATAGCGGAGGAGTCACACGAGGTTGAAAACCACATTGGCCACCATTACCCCTTGACAGAAGAGCACAAGGTTTACTTTGAGACCACAAGAAAGTCGGGGCAGGTTAATGAGGATGCTGAAATTGCACATAGTGTTAAAGTACTGTCAACAGCATCAAAAGATCGCTCGCTTTCCCTGTGTCCGAGCCATAGATCGAATGGGAGGTCATCGCCTCCTCCTCACGAGATGTCTTTCCTTTATCCAAGTGAAAAAAGACTCACTGATGATACCCAGACATCAAATTCAGCCACCACACTTTCTGATTTGCTGACGGCTCCAGTGAATGCATCCAAATGCAAGACTACAGCATTAGCTTCTCTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15166
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000115358 | Nonsense | 369 | 1254 | 2 | 3 |
| ENSDART00000126390 | Nonsense | 404 | 1250 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 30776402)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 29113339 |
| GRCz11 | 12 | 29228241 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGYTAAAGTACTKTCAACAGCATCAAAAGATCGCTCGCTTTCCCTGTG[T/A]CCGAGCCATAGATCGAATKGGAGGTCATCGCCTMCTCYYCACGAGATGTC
Long Flanking Sequence:
ACACAGCAACCAAAGTTACAAGAGCATGAGATTAGTCCTGGAAGTCCAGGACATGGCAATGGACTGACTGTTCTTATGGTAAAAAATAAAATTTCTATTCCACCAAACTGCACCACGCAAGTCATGGGCTTTAAGATGGTAGATGGCAAAAAGCATTTAGTTCTAAAGGTCATACCAACAAAACAAGAGGACTCCACTGAAAGTGAGGTTTTTGAGTCACATATTAGTGAAGATGAAAATAAACCAACCAGCAGTCCTTGCTCTTCATCAATAGCATCTCTTTTAAGTTTAGAGTCTGGAGAATCAAATGAAGCCTCTTTAATAGCGGAGGAGTCACACGAGGTTGAAAACCACATTGGCCACCATTACCCCTTGACAGAAGAGCACAAGGTTTACTTTGAGACCACAAGAAAGTCGGGGCAGGTTAATGAGGATGCTGAAATTGCACATAGTGTTAAAGTACTGTCAACAGCATCAAAAGATCGCTCGCTTTCCCTGTG[T/A]CCGAGCCATAGATCGAATGGGAGGTCATCGCCTCCTCCTCACGAGATGTCTTTCCTTTATCCAAGTGAAAAAAGACTCACTGATGATACCCAGACATCAAATTCAGCCACCACACTTTCTGATTTGCTGACGGCTCCAGTGAATGCATCCAAATGCAAGACTACAGCATTAGCTTCTCTAATGGACGAAGAATCCACACTTACTGATGCTGTTTCACATTCAAGGTCTGACTCTGAAATTTCTGTAGATGACAAGCCCACAAATGCTGATATCCTGAAATCTAAACTTCCAACTGCAGATGCAACATTTTCTAAAACGACTCTTATCCAGGAACCTCATTTTAGTTCTAAAGGTGGTGAATCATTTGAGAATAACAATGAACCTACTACAAGTTCTGTGGCTGAAGAAAGGCAAGGTCCTAATTCTGTCAAAGCTAAGACTTCACTATGTGAGGTGACTGACAAAAAGACCTGTGACGCAGAATTAGGAGAGAGCTCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9134
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 |
|---|---|---|---|---|---|
| ENSDART00000115358 | Nonsense | 504 | 1254 | 2 | 3 |
| ENSDART00000126390 | Nonsense | 475 | 1250 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 30775999)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 29112936 |
| GRCz11 | 12 | 29227838 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGTGAATCATTTGAGAATAAMAATGAACCTACTACAAGTTCTGTGRCT[G/T]AAGAAAGGCAAGGTCCTAATTCTGTCAAAGCTAAGACTTCACTATGTGAG
Long Flanking Sequence:
CCACAAGAAAGTCGGGGCAGGTTAATGAGGATGCTGAAATTGCACATAGTGTTAAAGTACTGTCAACAGCATCAAAAGATCGCTCGCTTTCCCTGTGTCCGAGCCATAGATCGAATGGGAGGTCATCGCCTCCTCCTCACGAGATGTCTTTCCTTTATCCAAGTGAAAAAAGACTCACTGATGATACCCAGACATCAAATTCAGCCACCACACTTTCTGATTTGCTGACGGCTCCAGTGAATGCATCCAAATGCAAGACTACAGCATTAGCTTCTCTAATGGACGAAGAATCCACACTTACTGATGCTGTTTCACATTCAAGGTCTGACTCTGAAATTTCTGTAGATGACAAGCCCACAAATGCTGATATCCTGAAATCTAAACTTCCAACTGCAGATGCAACATTTTCTAAAACGACTCTTATCCAGGAACCTCATTTTAGTTCTAAAGGTGGTGAATCATTTGAGAATAACAATGAACCTACTACAAGTTCTGTGGCT[G/T]AAGAAAGGCAAGGTCCTAATTCTGTCAAAGCTAAGACTTCACTATGTGAGGTGACTGACAAAAAGACCTGTGACGCAGAATTAGGAGAGAGCTCTCAGTTTTGTTCAAATGGCTTTTCTAACTCTCAAGCTTCAAACATTGTACTTGAAAATTCCACAGAGGTAATAAATAACAAAGCCACCGAGACAGACTCAAAAAATAAAACTAGTAAAGGTAAAACTGAATATAAAAATCCCAGAGATTCTCTCTCGGAGGTTGAAAACAACTTTCTAAATTCCCCAAGCCAAGAGGTCTTTAGTTTCCATAATTATTCTAAAGATACCTCTGGGAGCTCCCCTGAGTCAATGCAGCCTGAAGAAGACTCACAAGAACTTGAGGAAGAAGAGTGCGAGGAGGATTTTGGTGACTGGAGCTTGACTCTGCCAGCATCACCACCTCTTCCAGCTGAAGAAGATAGCAAGGAAGGACCTAATGAGAGTGATTTGGTCTCTGAAAGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7224
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000115358 | Missense | 917 | 1254 | 3 | 3 |
| ENSDART00000126390 | Essential Splice Site | 921 | 1250 | None | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 30774631)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 29111568 |
| GRCz11 | 12 | 29226470 |
KASP Assay ID:
554-5274.1 (used for ordering genotyping assays)
KASP Sequence:
TACAGGCTGGGAGACAAGCTTACTTGGTTAGATACATTTCTTCAGCTAAG[T/C]CAAGAATACTTTTGAACAGTACAGATGGACAAACCCTGAGTCAGGACAGC
Long Flanking Sequence:
CATATCCTGTGCCCGTTCAGCTAAAAAGCGGAGCGGGCTTCAAGCTGATAACTAAGGCCTGTTCTCCTAAAATTAATGTGTCCTATGTGAAACCGGGGATTGAAACGGCCTGCAAGACTAAGGGAGTAGCTCTCACATTAAATGGAGGTCGAATTGGCTTGTCTGCTCAAAGTTCAGGTCTTGAAAATAAAGGTGAAGCATCAGTCCAAACAGCACAAAGTGGAAACCGCTACTTTGTCAATGCCTCAGCCCTTAAAGCTTCAATTCTCTTATCAGGTGCTGTCAAGTCCTCATCTGGAGAACCAGCTGCTAATGTGCCACAGACTTGTTATTTAGTTCAGAGACCACTCCCTGTTAGTAGTGAGTCAACTGGTCCAAGTTCTAAGACTGTGCTTGCTACTCGCCCTGTATTGGCCGTGCCTGTGAATTCAGCAGATAAAGGTAGTTCATTACAGGCTGGGAGACAAGCTTACTTGGTTAGATACATTTCTTCAGCTAAG[T/C]CAAGAATACTTTTGAACAGTACAGATGGACAAACCCTGAGTCAGGACAGCCAAGTAAATGAGGCTGGCAAAAACCGTGTTTTCCTTAAGGTAGTTAGAGGACCCGATGGCACTAGATTTCTCTCCGCTCCATACAGCACTGCCAAAAAGCCAATATACCTTGCCACAAACTCTTTACAGTCACCCTACTTGTTAATGTCCTCAAATCAGTCTCTTAACAACACGTCTGCAGGTTTCAAAACTTCTACTAATCTCCAAGGTCTCACCCATAAACTCATCCCTGCGTCCCAGCTTCAACATGTTCTGCCCCAATCCAAAATTCAAATCAAAAGGATAAGCAGGGCTGATCATAATGGAGCATTACAGAAGTCACCACTTGTCCCCGGTTCCAACCGTCCACTAAGCCAAAGGAAACGGAGGCGAAGGGCTTCGTTAGAGGAAATGCGAGAGAGCTCAAAAATGAGGAGAGTCTCAAGCAAGTCGTCAGCTGAGAAAGATGCT
Associated Phenotype:
Not determined