Busch Lab

ZMP

znf644

Ensembl ID:
ENSDARG00000068920
ZFIN ID:
ZDB-GENE-030131-6244
Description:
Novel protein similar to vertebrate zinc finger protein 644 (ZNF644) [Source:UniProtKB/TrEMBL;Acc:A2
Human Orthologue:
ZNF644
Human Description:
zinc finger protein 644 [Source:HGNC Symbol;Acc:29222]
Mouse Orthologue:
Zfp644
Mouse Description:
zinc finger protein 644 Gene [Source:MGI Symbol;Acc:MGI:1277212]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa39815 Nonsense Mutation detected in F1 DNA Not yet available
sa30817 Nonsense Mutation detected in F1 DNA Not yet available
sa39816 Nonsense Mutation detected in F1 DNA Not yet available
sa39817 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39815
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099848 Nonsense 161 1169 1 5
ENSDART00000131630 Nonsense 161 1169 2 6
Genomic Location (Zv9):
Chromosome 2 (position 23022340)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22867574
GRCz11 2 22523225
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATATGGGGCTTTGATAACGAATCTCCAGAAGCCTCATTAGATAATTA[T/A]GATGATGCTAATGACCTTGGCTGGAATCCCCAACGAGAGTTTATGAAGTT
Long Flanking Sequence:
TCCTTAGGACAGTTAGGAATGTCTGCTTTGAAGGAAAGTGCCAAAGTAGAGGAAAATGACATCTCAATGTCAAGCATCTCTCAGGACCTTTTGAGCAACCAGTCATTCTCTGTAGAGGGGACTACATCAGGACCATCAGTGCATTGTCTTCACGAGACCATGGAGCTGCTGAGTGACCAAGGAGACCTCCTGTCCAGTGTTAGTTTCATAGACTCCATCTGTTCTGATGGACCAGCCAAGGCTGCTTACGTCAATGGATCCACATCACCACATATATCAGATGAAATATTGTTGGATATTTCAAAAAATGTACCAGGATTCCTTCCGAAATCATTGCACGCTCAGAATTCTGTGACAACCAACGTCCACTTTGAAGGAGCTGATCCACTCAGAAAAGAAGGGGAAATAACAATAAGGCAAACATTGACAGCAGAGGATGTTGAGAATAGGGGCATATGGGGCTTTGATAACGAATCTCCAGAAGCCTCATTAGATAATTA[T/A]GATGATGCTAATGACCTTGGCTGGAATCCCCAACGAGAGTTTATGAAGTTCTTGTGGGATGATGATAATGGTCTCGATATTGAAGAAAAACTGTCACCAGTTCCATCACCCATCAACCAGAAAAGAAGAGTTCCATCACCTATTGTTCATAAAAGAAGGAGACGTAAAGAGAAATTGGTGCTAAAAGTTGACCCTTCAGAGGACCCCTTCTCTGATTTGAATTTAGATTCAAAACAAGATCACCCTGGTGAAGGAAGCCCGATAGAGTTCGGTCCTGTAAAGAAGACTCGTTCACCAAGGAAACCCTCCAAACTACAGTCGCCCATTGTAAAGAACACCAAATATTTCAATGGAACTGCTGAGGCTGTTAAACATTTGTTTCCCAAACCAGCAAAAAAACCTTTAAGCAAGACTCAAAAAATAGGATTGATAAGAGAAACTTTGTCATCAGATTCTGAGGGACCTACATTTTTTCAACAAAACAATGATTTTAAAGAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30817
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099848 Nonsense 234 1169 1 5
ENSDART00000131630 Nonsense 234 1169 2 6
ENSDART00000099848 Nonsense 234 1169 1 5
ENSDART00000131630 Nonsense 234 1169 2 6
Genomic Location (Zv9):
Chromosome 2 (position 23022558)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22867356
GRCz11 2 22523007
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAAATTGGTGCTAAAAGTTGACCCTTCAGAGGACCCCTTCTCTGATT[T/A]GAATTTAGATTCAAAACAAGATCACCCTGGTGAAGGAAGCCCGATAGAGT
Long Flanking Sequence:
CTGTTCTGATGGACCAGCCAAGGCTGCTTACGTCAATGGATCCACATCACCACATATATCAGATGAAATATTGTTGGATATTTCAAAAAATGTACCAGGATTCCTTCCGAAATCATTGCACGCTCAGAATTCTGTGACAACCAACGTCCACTTTGAAGGAGCTGATCCACTCAGAAAAGAAGGGGAAATAACAATAAGGCAAACATTGACAGCAGAGGATGTTGAGAATAGGGGCATATGGGGCTTTGATAACGAATCTCCAGAAGCCTCATTAGATAATTATGATGATGCTAATGACCTTGGCTGGAATCCCCAACGAGAGTTTATGAAGTTCTTGTGGGATGATGATAATGGTCTCGATATTGAAGAAAAACTGTCACCAGTTCCATCACCCATCAACCAGAAAAGAAGAGTTCCATCACCTATTGTTCATAAAAGAAGGAGACGTAAAGAGAAATTGGTGCTAAAAGTTGACCCTTCAGAGGACCCCTTCTCTGATT[T/A]GAATTTAGATTCAAAACAAGATCACCCTGGTGAAGGAAGCCCGATAGAGTTCGGTCCTGTAAAGAAGACTCGTTCACCAAGGAAACCCTCCAAACTACAGTCGCCCATTGTAAAGAACACCAAATATTTCAATGGAACTGCTGAGGCTGTTAAACATTTGTTTCCCAAACCAGCAAAAAAACCTTTAAGCAAGACTCAAAAAATAGGATTGATAAGAGAAACTTTGTCATCAGATTCTGAGGGACCTACATTTTTTCAACAAAACAATGATTTTAAAGAGAAGTCACTAGGACAAAATCAAATCACATGTAATAAAGACACAACTAGCTCAAAGCCATTCGTATGCAAGGAATGTGGACAGTGTTACTATGATCGAAGTTCACTGTTAAATCATATAAGTGTTCACCAGGACAAGGGAAAGAAACTAAATCAGTTCCATCAAATTAAAGATGAAGGTAAAGATGCAAAGTTGCAATGCCCCCAGTGTAATTTTGGAACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39816
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099848 Nonsense 234 1169 1 5
ENSDART00000131630 Nonsense 234 1169 2 6
ENSDART00000099848 Nonsense 234 1169 1 5
ENSDART00000131630 Nonsense 234 1169 2 6
Genomic Location (Zv9):
Chromosome 2 (position 23022558)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22867356
GRCz11 2 22523007
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAAATTGGTGCTAAAAGTTGACCCTTCAGAGGACCCCTTCTCTGATT[T/A]GAATTTAGATTCAAAACAAGATCACCCTGGTGAAGGAAGCCCGATAGAGT
Long Flanking Sequence:
CTGTTCTGATGGACCAGCCAAGGCTGCTTACGTCAATGGATCCACATCACCACATATATCAGATGAAATATTGTTGGATATTTCAAAAAATGTACCAGGATTCCTTCCGAAATCATTGCACGCTCAGAATTCTGTGACAACCAACGTCCACTTTGAAGGAGCTGATCCACTCAGAAAAGAAGGGGAAATAACAATAAGGCAAACATTGACAGCAGAGGATGTTGAGAATAGGGGCATATGGGGCTTTGATAACGAATCTCCAGAAGCCTCATTAGATAATTATGATGATGCTAATGACCTTGGCTGGAATCCCCAACGAGAGTTTATGAAGTTCTTGTGGGATGATGATAATGGTCTCGATATTGAAGAAAAACTGTCACCAGTTCCATCACCCATCAACCAGAAAAGAAGAGTTCCATCACCTATTGTTCATAAAAGAAGGAGACGTAAAGAGAAATTGGTGCTAAAAGTTGACCCTTCAGAGGACCCCTTCTCTGATT[T/A]GAATTTAGATTCAAAACAAGATCACCCTGGTGAAGGAAGCCCGATAGAGTTCGGTCCTGTAAAGAAGACTCGTTCACCAAGGAAACCCTCCAAACTACAGTCGCCCATTGTAAAGAACACCAAATATTTCAATGGAACTGCTGAGGCTGTTAAACATTTGTTTCCCAAACCAGCAAAAAAACCTTTAAGCAAGACTCAAAAAATAGGATTGATAAGAGAAACTTTGTCATCAGATTCTGAGGGACCTACATTTTTTCAACAAAACAATGATTTTAAAGAGAAGTCACTAGGACAAAATCAAATCACATGTAATAAAGACACAACTAGCTCAAAGCCATTCGTATGCAAGGAATGTGGACAGTGTTACTATGATCGAAGTTCACTGTTAAATCATATAAGTGTTCACCAGGACAAGGGAAAGAAACTAAATCAGTTCCATCAAATTAAAGATGAAGGTAAAGATGCAAAGTTGCAATGCCCCCAGTGTAATTTTGGAACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39817
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099848 Nonsense 914 1169 2 5
ENSDART00000131630 Nonsense 914 1169 3 6
Genomic Location (Zv9):
Chromosome 2 (position 23028495)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22861419
GRCz11 2 22517070
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGATTGGGCAAACCCACTTCCACTGCGTCCAAATCTCCAGTTATCATAT[T/A]GAAAGAATTGATGCGCGATAAGAAACAGTTCCAGCTAAAGCTGCAGGTTC
Long Flanking Sequence:
TTTTTAAATTGTCAGTCATGTAGAACTATTGTAGATCTTGCATGTATATAGTATAATTTTTCTTACTATAAAAGGCCAAATTTGCAGGTATCCAGGTTTCTTTTTTTCCTTAAAAGATAAATTTTTCAAAGTTTATTTTTTTTTTTTGTTATTTGCCACATGAAATGTTGTGGTGTAAGTTGGTGTAAGTCTAAGCCAGAATTCAGGCTGGTGTAGATTATCTAGGTCTGGACAGATTGGCTTATAATAAATAAGCAAATGTTGTAAATAAAGCTGATTTCAAATGGTTTCTTTGTTGTCTCTGATCCTGACAGAGGAGGACACGTCCCAGACTGATCATCCGGCAGAGCTGCCCACTGACTGCCAGCAGACAGAGCTCATCTGTCCTCTCTGTAGGGAGTGGTTTGACAATAGGACCGGGCTGTCCAATCATGTGAGAGGCCACCTAAAGCGATTGGGCAAACCCACTTCCACTGCGTCCAAATCTCCAGTTATCATAT[T/A]GAAAGAATTGATGCGCGATAAGAAACAGTTCCAGCTAAAGCTGCAGGTTCTTGAAAAGAAGTGCCGCACCACCAATACTTTCTATCCTGTTAGGCTGGGTAACGGACTGACATTTGCATCCACTGTCAAACGACAAAAAGATGACAAGGAGGAGAAAAAAAGGTTAGAGATTAATAAAGGCTCACCACCAAGTGATCTGATTGGTATTTTGAAGAAAAGAAGAGCCCACGAAGAGGCCAAAGCAAAGCATCAGTCCCTCACGGCAAAAAAGGCTCTTTCTTTAACTTCAGGGAAAGACTGTGGCCTTGAAATTCACACTTGCAAAGCAGTGCCAAGTTCACCAGGAGGTAATGTTTCATTTGTTTCAGTGATCACCTGTAAAAAAGGCTAAACGATGCAAAATGAAAGTTTTGTCACTTCACATTCTTATATATTTGACCAAACTCTCATGCTTTAAACATGAAACTGAAGGGAAAAATGATAATAATTTAAATTCTAAG
Associated Phenotype:
Not determined