Busch Lab

ZMP

ZNF507

Ensembl ID:
ENSDARG00000052164
Description:
zinc finger protein 507 [Source:HGNC Symbol;Acc:23783]
Human Orthologue:
ZNF507
Human Description:
zinc finger protein 507 [Source:HGNC Symbol;Acc:23783]
Mouse Orthologue:
Zfp507
Mouse Description:
zinc finger protein 507 Gene [Source:MGI Symbol;Acc:MGI:1916378]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa40988 Nonsense Mutation detected in F1 DNA Not yet available
sa40989 Nonsense Mutation detected in F1 DNA Not yet available
sa45292 Nonsense Mutation detected in F1 DNA Not yet available
sa34162 Nonsense Mutation detected in F1 DNA Not yet available
sa34163 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40988
Status:
Mutation detected in F1 DNA
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
ENSDART00000098942 Nonsense 34 910 1 8
Genomic Location (Zv9):
Chromosome 7 (position 48705538)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 46973157
GRCz11 7 47246236
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGGACACAGTCTTCATTCCCGACAGATGTCTTCTTGGTGTCGAGGAC[C/T]AGCAACGCCAGCAGCAGAAGCAGGCCGCTGACTCTCTTATTCAGGTCATT
Long Flanking Sequence:
CCACTTGTATCTTTGAACCTCAATAGACTTTTTTACATCTACATTACACACTGCATGAAAGATGATATTCAAAAAATCATAACACAAGCACTTTAAAACCATCTCTTAAAAACCAAAGTGATTTCTGCTTTTGTTTTAGAAACCACTTAATCTGTCATTGGAAAAAAAGGAAACAGCTGATGTACGAGACAGTAACTAGTGTGTGATATTTATAGATTTGTGAAGTAATGGCTATTCTTGTCAATATGTAAAGATGCCTCTGCTAGTTGACACACACTAAGCTTCAAAAGATTGTCAAAGCATTCCCCAACCAAATAGTTCTGCACTATATGTTTGCTGGCAGTAGAGATACTTGCTCAGTTGTGTTGGTTCTTATACCTTGTGTTGTTGCCGTTTTAGGAATGGAAGACAGCAGTGGTGTTGCTGTTCTTGTGCCTCACTCTAGAGGCCAGCAGGACACAGTCTTCATTCCCGACAGATGTCTTCTTGGTGTCGAGGAC[C/T]AGCAACGCCAGCAGCAGAAGCAGGCCGCTGACTCTCTTATTCAGGTCATTGAGAAGCTTAGCAAAATTGTGGAGAAGCGACCCAGACGATGCACCATCTCTGGGAAAAAGAGACCCCCAATTACTTGTGCTTCTGTAAGTGTTCCAGACATCAGGGATGACACTAAAGGGACCACACCTTCTAAGAAACCCAGAGAGCAAAGGGATGACCGCCTGGCATCCAGCAGCACAACTGGGCACTTGATCAAACAGGGGCCTTCAAGTCCAGGTGCCCGGACTGTTACGTGCTACCAGTGCAGTATGTGTCGATTTATATCTCCTACGTTGGAGCAGTTGAAAGAGCATCTGCTCTGTCATGACGAGCAGCACAGCGACCTCATCCTCATGTGTTCAGAATGCCAGTTCACTTCAAACCACCAAGAAGAAGTGGTAGCACATGTAAGACTCCATCTGGAGGAGGGCGACCATGCAAGATGCATCCTAGATGAGCAAGGAACAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40989
Status:
Mutation detected in F1 DNA
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
ENSDART00000098942 Nonsense 136 910 1 8
Genomic Location (Zv9):
Chromosome 7 (position 48705844)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 46973463
GRCz11 7 47246542
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCAAGTCCAGGTGCCCGGACTGTTACGTGCTACCAGTGCAGTATGTGT[C/T]GATTTATATCTCCTACGTTGGAGCAGTTGAAAGAGCATCTGCTCTGTCAT
Long Flanking Sequence:
CCAACCAAATAGTTCTGCACTATATGTTTGCTGGCAGTAGAGATACTTGCTCAGTTGTGTTGGTTCTTATACCTTGTGTTGTTGCCGTTTTAGGAATGGAAGACAGCAGTGGTGTTGCTGTTCTTGTGCCTCACTCTAGAGGCCAGCAGGACACAGTCTTCATTCCCGACAGATGTCTTCTTGGTGTCGAGGACCAGCAACGCCAGCAGCAGAAGCAGGCCGCTGACTCTCTTATTCAGGTCATTGAGAAGCTTAGCAAAATTGTGGAGAAGCGACCCAGACGATGCACCATCTCTGGGAAAAAGAGACCCCCAATTACTTGTGCTTCTGTAAGTGTTCCAGACATCAGGGATGACACTAAAGGGACCACACCTTCTAAGAAACCCAGAGAGCAAAGGGATGACCGCCTGGCATCCAGCAGCACAACTGGGCACTTGATCAAACAGGGGCCTTCAAGTCCAGGTGCCCGGACTGTTACGTGCTACCAGTGCAGTATGTGT[C/T]GATTTATATCTCCTACGTTGGAGCAGTTGAAAGAGCATCTGCTCTGTCATGACGAGCAGCACAGCGACCTCATCCTCATGTGTTCAGAATGCCAGTTCACTTCAAACCACCAAGAAGAAGTGGTAGCACATGTAAGACTCCATCTGGAGGAGGGCGACCATGCAAGATGCATCCTAGATGAGCAAGGAACAGAATTGGCAAGAAGCGTGCACCAGAAGACAGCGGTTTTGAGGGCAATCAGCTTGGAATCTGAGAAGACGTCCACACCGAAGAAGTGGTACAGCTTTGAGCAGGGTCGGTACCGTTGTCTCATCTGCAACTATGAATGCAGACAGCAGCGTAATCTGAAGACCCACGCATGGAAACATGCTGGCCTTGTTGACTGCTCGTACCCCATATTTGAAGATGAGACCGAATGTCCTGAGACTTTACAGAGCGCAAGTCCTCCTTTAATTCCACCCTGTAAAGAGGACACCATTGTTGTACTTGCAGCAGTTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45292
Status:
Mutation detected in F1 DNA
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
ENSDART00000098942 Nonsense 144 910 1 8
Genomic Location (Zv9):
Chromosome 7 (position 48705868)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 46973487
GRCz11 7 47246566
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACGTGCTACCAGTGCAGTATGTGTCGATTTATATCTCCTACGTTGGAG[C/T]AGTTGAAAGAGCATCTGCTCTGTCATGACGAGCAGCACAGCGACCTCATC
Long Flanking Sequence:
TGTTTGCTGGCAGTAGAGATACTTGCTCAGTTGTGTTGGTTCTTATACCTTGTGTTGTTGCCGTTTTAGGAATGGAAGACAGCAGTGGTGTTGCTGTTCTTGTGCCTCACTCTAGAGGCCAGCAGGACACAGTCTTCATTCCCGACAGATGTCTTCTTGGTGTCGAGGACCAGCAACGCCAGCAGCAGAAGCAGGCCGCTGACTCTCTTATTCAGGTCATTGAGAAGCTTAGCAAAATTGTGGAGAAGCGACCCAGACGATGCACCATCTCTGGGAAAAAGAGACCCCCAATTACTTGTGCTTCTGTAAGTGTTCCAGACATCAGGGATGACACTAAAGGGACCACACCTTCTAAGAAACCCAGAGAGCAAAGGGATGACCGCCTGGCATCCAGCAGCACAACTGGGCACTTGATCAAACAGGGGCCTTCAAGTCCAGGTGCCCGGACTGTTACGTGCTACCAGTGCAGTATGTGTCGATTTATATCTCCTACGTTGGAG[C/T]AGTTGAAAGAGCATCTGCTCTGTCATGACGAGCAGCACAGCGACCTCATCCTCATGTGTTCAGAATGCCAGTTCACTTCAAACCACCAAGAAGAAGTGGTAGCACATGTAAGACTCCATCTGGAGGAGGGCGACCATGCAAGATGCATCCTAGATGAGCAAGGAACAGAATTGGCAAGAAGCGTGCACCAGAAGACAGCGGTTTTGAGGGCAATCAGCTTGGAATCTGAGAAGACGTCCACACCGAAGAAGTGGTACAGCTTTGAGCAGGGTCGGTACCGTTGTCTCATCTGCAACTATGAATGCAGACAGCAGCGTAATCTGAAGACCCACGCATGGAAACATGCTGGCCTTGTTGACTGCTCGTACCCCATATTTGAAGATGAGACCGAATGTCCTGAGACTTTACAGAGCGCAAGTCCTCCTTTAATTCCACCCTGTAAAGAGGACACCATTGTTGTACTTGCAGCAGTTGGAGGAAAATCCCAGACCCTGCACAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34162
Status:
Mutation detected in F1 DNA
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
ENSDART00000098942 Nonsense 611 910 3 8
Genomic Location (Zv9):
Chromosome 7 (position 48707361)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 46974980
GRCz11 7 47248059
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGTTGCTGTGTCTGGTGATGTTTCTACTGCAGACAGTCTGGTTGAATA[C/A]ATCGCTGGGAGCGAGAGGCCCTACCGCTGTAGATTGTGCCTCTACAGCAG
Long Flanking Sequence:
TCTCCCTCAGATGAAAATGTGCCACCAGTTCGCAGGAGGACTTACTCAGAGTCTCTTCGGCTGCATTCTTTGGCAGCAGAGGTCTTGGTGGCCATGCCCATGAGGGCCCCGGAGCTTAGCAAGACCACTGCAAAAGGTATACATGACCTGAGTACTCAAAGCCCTGATACAGGTCAGAGAATGGTGGAGACTGACACTGCCAACCCTAAATCATCCTCAGGAGAGCTCAATGGTGGAGAATCAACTGCTCTTATTAACCTTGGCCTCCAGGGTTCAAAAGATTCTCGAGAAGTGCTAGTCGAGGGACCTTCCAAGGCAGGCATCAGCATGTCTCTTTTAACAGTCATCGAGCGACTGCAGGAGCGTTCTGACCAAAACACTTCAGACGAGGACATTCTAAAGGAATTGCAGGACAATGCCCAGAGCCAACACGCTGGTGGAGTTCCTGGAGGTGTTGCTGTGTCTGGTGATGTTTCTACTGCAGACAGTCTGGTTGAATA[C/A]ATCGCTGGGAGCGAGAGGCCCTACCGCTGTAGATTGTGCCTCTACAGCAGCGGAAATAAGGGCTACATCAAGCAGCACCTACGTGTACATAGACAGAGACAGCCCTACCAGTGCCCCATCTGTGAGCATATAGCCTGTGACAGCAAGGACCTGGAACGTCACATGATCCACCACTTCAAGCCCCGCTTGTATAGCTGCAAACAGTGCACAGAGAGGTTCCATTACAAGGTGAGGAGAGAAATAAACCTGATTGGTGGAAATAAGCATTAAAGTGATTGTTCACCCAAAAATTTAAATTTACTCATTATTTACTCATCCTAAAGTGGTTCCGAACATTTATTTTTCCATTGAAAATGAGTGCGTTTCTGAAAACCATCATTAGCTAACTAAGGTTGCAAGTTCCATCGTTACAAACGTAGTTTGTTGATTTGGCATTTCCCAAATTCATCGTTCCAACGATCATTTGCAAGCTGCGTGGAAAACTTGTACGTTTCCAACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34163
Status:
Mutation detected in F1 DNA
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
ENSDART00000098942 Nonsense 792 910 6 8
Genomic Location (Zv9):
Chromosome 7 (position 48714303)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 46981922
GRCz11 7 47255001
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCCACCCACCCTCTCTCAAATCCCACATGTGGAAACATGCTGGAGAT[C/T]AGAATTATAACTATGAGCAAGTCAACAAGGCCATCAACGAGGCCATTTCC
Long Flanking Sequence:
GTTGTGTTTGCCGCAAGCAGCGCTTTGAGTTCCGCCTTTTTACAAACGGCCTTTCAATGCTCTTCAAATGTAGTACTCCAAACACACAGCCGCGCACACAAAAAGCACAAATTACTGTGAAAGCAAACACAATGCCTGACCCCACTTGGCAGGTGCTCCAGAAGGTCTTTTTTTTTCATAAACCGTGGCCTTGCGCCGCTCTAATTGTTTATTCTGCACCGCACGACCCCTGTAGGTGCTGCAGCTGTGATTTCGCCACTACTAATATGAATAGCCTGAAGAGCCACATGAAGAGACATCCGCAGGAACACCAGGCCATGCAGCTGCTGGAGCAGTACAGGTGAAGAGCAGACGGCGTGGAGGAGCCGGTGTGCAGAATTGTACTCCTCACGGACGTGGCTCATATAATCCTCTGTCTGTGTTACAGGTGCTCGCTGTGCGGTTACGTGTGCAGCCACCCACCCTCTCTCAAATCCCACATGTGGAAACATGCTGGAGAT[C/T]AGAATTATAACTATGAGCAAGTCAACAAGGCCATCAACGAGGCCATTTCCCAGAGCAGCCGGTGAGAATGCCCTTTAAATGTATATACAGTTAATGGGATTTGTTTTTGTTTATTTGCTTTATGGTTTTTGATTTTCGGTTAGGTGTTAAAGCTAATATCTTATGGGGTTTTTCCTAATCACATCAGTACTGCCCTTTAAACTTAATTTTGCAAAACAAAATGCTTCAACATTATTTGATCTCTTAATGTTTATTTGAAGTTAAAATGTTTTTTAAGTTATAATTAATACATTTGTTCAAATATTAGTAAGCTTAATATTGTTGTTATTATTATTATTGCTACTATTATTAATATTATTATTATTATGATTATTATAATAATAATAATTATTATTATTATTATTACTATTATTGTTGTTGTTATTGTTGTTATTACTATTATTATTATTACAATTATTATTATTATTATTATTATTATTGTTATTAATAATATTATTATT
Associated Phenotype:
Not determined