ZMP
ZNF608
Ensembl ID:
Description:
zinc finger protein 608 [Source:HGNC Symbol;Acc:29238]
Human Orthologue:
ZNF608
Human Description:
zinc finger protein 608 [Source:HGNC Symbol;Acc:29238]
Mouse Orthologue:
Zfp608
Mouse Description:
zinc finger protein 608 Gene [Source:MGI Symbol;Acc:MGI:2442338]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41094 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25379 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34266 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41094
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112756 | Essential Splice Site | 355 | 1348 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 74645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 45804 |
GRCz11 | 8 | 224627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTGGGCACGCTTTTGGACTGTACCAAGCATGACTGGGCTCCACCAAG[G/A]TAATGTGCATAACACAAGTCAAAATTATGAGCCCTCCTGTGAAATCTAAA
Long Flanking Sequence:
CATATACACTCATTCACTATAGACAATTTAGCCTACCTAAGTCACCAGTACTGCATGTGTTTGGCCATGCCAACACGGGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCCGAGACTCAAACCAGCGACCTTCTTGCTGTGAGGCGACATCACTACCTACTGTGCCACCGTGTTGCCTTGCTCTGACTTATTGTTGCTATATTAGTTTTGTTTAATATAAATAATTTGTATTAATTATGTTTTTGTGTTTGATCTCTTTTCTTTGTCACGACTTGAATGAGCGGGTCGCATCAATCTATGCATGGCTAAAAATTCAACGTTTTTAAGTTTGATCATTGTGCAACATGTTTTCAACCTCTGCATGATATTGCTGAGGGACTCATGATTGTGTTTGATTTCAGGGGTTTTGGTTGTGAATGTCACATGGAGGAAACGGACCTATGTGGGCACGCTTTTGGACTGTACCAAGCATGACTGGGCTCCACCAAG[G/A]TAATGTGCATAACACAAGTCAAAATTATGAGCCCTCCTGTGAAATCTAAAGAGTCATCAGTGACGAAGCGGACAGGCCTGCAGGGCACGCACCGCAGGGGGGGCCCCGCGTGATTAGGGGGCCCCACGTCGTCGCAATCGCAATAATCAAACTCTTGGGAACAACTGTGGTCGGAACCAAAGTTCACAGGTCGGTGTTCTCTGAACTCCTCTCAAGGGGTGGACTACTTCATTCTGATTGTTTGCCGCCGAACCGCGTCATAGCTCATACCATAAAGTTGACTTGATTTCAACTCTCCTCGACGCCCACACAGGAGAAGACGCGCCTCTGTTTCTCGCCGCCGGTTCTCGTTATAAATGAATGACTTCTGGTTACTTTGACGCTCTCGCCGCTTTCGGTTTGTGATCGCTCCTCAGTTTGTGAAGGCTTCTACGCGTTGTCGCTCCATCCCGCCGCCTTTCCCCGCTCCTCAATTTGTGATCGCTCCCCTGCGTTGACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25379
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 |
---|---|---|---|---|---|
ENSDART00000112756 | Nonsense | 1108 | 1348 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 78563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49722 |
GRCz11 | 8 | 228545 |
KASP Assay ID:
554-7377.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCCTCTGGGTTTAGGCTTCAGAATCTCAGTCCTGGAGCCACTCTTAT[C/T]AGTCCAAATATGTGAAGCAGCAAAATCACGAGGTCAACAAGATCTCTGAG
Long Flanking Sequence:
GTGGAGTTGGACAAGCAGATGTCGTTTCAGCAGCAGGGGCGGCCAAAAGAGCAAGCGGTCCTCAAGGAGTCTGAAGACCTCAGTTTGGAGAGTTCAAACTCAAAATCAAATGTGGACACAAATGTAACATTTCTGAATGTAAGTTACTGATGTTACTTATCATTTACTGAGGAAATGTTCTAGTAAAAGACATTAACAGACTTCTAGAAATGTCCTTGATTATGGTGGGATAACAACCCAAACGCATGCTTGATTGTTTGGGGGGAATATGGTCCTTAATCATCAAACGATCGAGTATGCCAGGATTTTTTGATGATTGATTGAGATCATACTGATTTCTAAAGATTTTCCGCATATTAAACGCTTAATTTCGCAGGGCTACTGTTTCATAAGGGCTTCCCTGTAAGGTGTTTAATTTCCTTGGTTGTCAGACCCAAGTTTGACGGTAGATGTTCCTCTGGGTTTAGGCTTCAGAATCTCAGTCCTGGAGCCACTCTTAT[C/T]AGTCCAAATATGTGAAGCAGCAAAATCACGAGGTCAACAAGATCTCTGAGGAATTGAGTCTCAGTCCAGAAAAGGGGAAAGACTGGCACATAGAGCCTGAGTCCCGGCTGGAGGCTGAACTAAAGTGTGAGACGATTGCTGACGGTTCTGAAGAAAACACCCGGGCGGAGGGCGACGAAACATCAGGCGAGACGTCTGAAGACTCCGCAAGAACCGCCGCAGCATCACCCCAGCCGTCCTTCCTCCAGTATCAACACTCCTATCCGTATTTACACCTGTGCGAGACGGGCAGCAACGCATACAGAGTGATGTCTCCAGCTCTAGTGCACAATTACCCAGGTAATCATCTTCTGTACCGCGTAAACATGACACCAGAGGTGCTTGTATGAGAAACTGCTTGTAAAGAGTAAGCTGTGTGTGTTTTCCATTCTAGGTTTCCATTACCCTTTGTATGGAAAAACAGCAGGGAGGGAGGATTCAGAAGGGGCTCAAAGCAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34266
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 |
---|---|---|---|---|---|
ENSDART00000112756 | Nonsense | 1169 | 1348 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 78747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49906 |
GRCz11 | 8 | 228729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGCTGACGGTTCTGAAGAAAACACCCGGGCGGAGGGCGACGAAACAT[C/A]AGGCGAGACGTCTGAAGACTCCGCAAGAACCGCCGCAGCATCACCCCAGC
Long Flanking Sequence:
AAAAGACATTAACAGACTTCTAGAAATGTCCTTGATTATGGTGGGATAACAACCCAAACGCATGCTTGATTGTTTGGGGGGAATATGGTCCTTAATCATCAAACGATCGAGTATGCCAGGATTTTTTGATGATTGATTGAGATCATACTGATTTCTAAAGATTTTCCGCATATTAAACGCTTAATTTCGCAGGGCTACTGTTTCATAAGGGCTTCCCTGTAAGGTGTTTAATTTCCTTGGTTGTCAGACCCAAGTTTGACGGTAGATGTTCCTCTGGGTTTAGGCTTCAGAATCTCAGTCCTGGAGCCACTCTTATCAGTCCAAATATGTGAAGCAGCAAAATCACGAGGTCAACAAGATCTCTGAGGAATTGAGTCTCAGTCCAGAAAAGGGGAAAGACTGGCACATAGAGCCTGAGTCCCGGCTGGAGGCTGAACTAAAGTGTGAGACGATTGCTGACGGTTCTGAAGAAAACACCCGGGCGGAGGGCGACGAAACAT[C/A]AGGCGAGACGTCTGAAGACTCCGCAAGAACCGCCGCAGCATCACCCCAGCCGTCCTTCCTCCAGTATCAACACTCCTATCCGTATTTACACCTGTGCGAGACGGGCAGCAACGCATACAGAGTGATGTCTCCAGCTCTAGTGCACAATTACCCAGGTAATCATCTTCTGTACCGCGTAAACATGACACCAGAGGTGCTTGTATGAGAAACTGCTTGTAAAGAGTAAGCTGTGTGTGTTTTCCATTCTAGGTTTCCATTACCCTTTGTATGGAAAAACAGCAGGGAGGGAGGATTCAGAAGGGGCTCAAAGCAGTAAACCGGTGACAGATTCGACAGCATTAGAGCTTCTGTCACATCCACTCCTGCCTTATCACGGCAAATCTCCTGTTGTATGTATCTCACTACAAATAAATGACGATTTTAATAATAATAATGATGACCCTGGAGCACAAAACCAGTCTTATGCTGCACAAGTGAGTTTAATGTGGATTTGAAATTGT
Associated Phenotype:
Not determined