Busch Lab

ZMP

si:ch73-386h18.1

Ensembl ID:
ENSDARG00000073944
ZFIN IDs:
ZDB-GENE-050309-237, ZDB-GENE-050506-128
Human Orthologues:
ZFHX3, ZFHX4
Human Descriptions:
zinc finger homeobox 3 [Source:HGNC Symbol;Acc:777]
zinc finger homeobox 4 [Source:HGNC Symbol;Acc:30939]
Mouse Orthologues:
Zfhx3, Zfhx4
Mouse Descriptions:
zinc finger homeobox 3 Gene [Source:MGI Symbol;Acc:MGI:99948]
zinc finger homeodomain 4 Gene [Source:MGI Symbol;Acc:MGI:2137668]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa43032 Nonsense Mutation detected in F1 DNA Not yet available
sa6496 Nonsense Mutation detected in F1 DNA Not yet available
sa45626 Nonsense Mutation detected in F1 DNA Not yet available
sa45625 Nonsense Mutation detected in F1 DNA Not yet available
sa28966 Nonsense Mutation detected in F1 DNA Not yet available
sa36560 Nonsense Mutation detected in F1 DNA Not yet available
sa43031 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa43032
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
ENSDART00000113668 Nonsense 117 2962 1 10
ENSDART00000138972 None None 2329 None 5
ENSDART00000148008 Nonsense 266 980 1 2
Genomic Location (Zv9):
Chromosome 18 (position 5196388)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 5915284
GRCz11 18 6055649
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCCAGGCAACCTCCCACTCCTCTGTTTCCTAAAACCAAAAAGGAATTG[T/A]GAGTCTGTGGTACCACTTAACCTGGCATCTTCAAACTCTGTGAACAGCAC
Long Flanking Sequence:
GAGGATGTGGAGAGGCCTATTGGAGAGATATTGTACCAGCCTGATGGGTCCGCCTATGTGATGGACAGTAAACTTACAAGTGGTGCACCCTCCTCCTCATTAGGTGCCCCTACCTCCATTATAAGAACCTGTTTCATTTCTTTGTCTCAAAGCCCTACTCCACAGATTTTTCGTGTCTTCCAATTGCATAACCTTGGTGACAGTGATAGTCTAGCTCTGATGACCTGCCAATCCAAAGATAGTACTCCTGACGTGGCTGGATCATCAGAGACAGGGGTGATGTGGTCTGGTCCACCCAAACCCATCCTGATGTGCTTTTTGTGTCGGCTGTCTTTTGGCCGTTCACACTCATTTAGGGCTCATGCTTCTGTACAACACAACATCACCTTCAGTGATGAAGAACAACATCTGCTCTTGTTTAAGCACGCCTCTGCCATCTTACAGCCTGCCGGCCCAGGCAACCTCCCACTCCTCTGTTTCCTAAAACCAAAAAGGAATTG[T/A]GAGTCTGTGGTACCACTTAACCTGGCATCTTCAAACTCTGTGAACAGCACGGAGAACACAGCAAGACGGAAAGAGAACACAGAGCCTCTGACCTCTAAGCCAGGACTTTCTCTCCTGCCCTCTCCACCCAGAACCTCCCCTGCTACCTCAGTACCAAGCCCTGCCAAAGACCCTTCAACCCTGGGAAGAGAGGGCACTCAAAGAGGCAAGGTGGAAGAAATAAGGAAGGACGGAGAAAGTAGTGAGGAAGGAGAGAGGAGATTGTGTTTAGAGGTAGGCAGCACTGTAGATTGTAACAGTGCTCACAGTATTAGCAGCAGTAGCGGACAAGAGCACATTACTGAAGCTGCTCTGTCAAACCAAAGCATTTCAAAACCTCCAAACTCTGTAACAATAGCAACCAGCTTTATGAACAACACCAAAACCCTTACAGACTCTGAGTCAGAGTGTGGAACAAGCTTTAACTGCCACGACCCTGCACCTGCTTCCCTTGTTGTGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6496
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
ENSDART00000113668 Nonsense 560 2962 1 10
ENSDART00000138972 None None 2329 None 5
ENSDART00000148008 Nonsense 709 980 1 2
Genomic Location (Zv9):
Chromosome 18 (position 5195061)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 5916611
GRCz11 18 6056976
KASP Assay ID:
554-4678.1 (used for ordering genotyping assays)
KASP Sequence:
CGTGGCGGTGTGAAGTCTGCGACTATGAAACYAATGTGGCACGCAACCTC[C/T]GAATCCACATGACCAGTGAAAAGCACACACACAACGTGCTTCTACTGCAG
Long Flanking Sequence:
CTTACTCTTTTAGTATTCAGGCCTCTTTGGCACACACCAGAAACTCCTGCAAGACATTGAAGTGTCCAAAATGCAACTGGCACTACAAGTACCAGCAAACTCTCGAGGCCCATATGAAGGAGAAGCACCCGGAGTCGGAGACTGAACAGTGCCCATACTGCAGCAGTGGGCAGAGTCACCCACGCCTAGCAAGGGGTGAGACTTATTCTTGTGGATACAAGCCGTTCCGCTGCCAGGTCTGCCAATATTCCACCACTACTAAGGGCAACTTGAGCATCCACATGCAGTCTGACAAACACCTCAACAACATGCAGAGCCTGCAGTCACAGCCACAGCCCCATGCACACAGCCCAGCACCCCAGCCCAATCCTTTAACTCATTCCCTTCCTACTCTCACTCACCCGACTCGAGCCAACTCCCCATCTCCATCTAAGCTCCGGGGACGTGCTTCGTGGCGGTGTGAAGTCTGCGACTATGAAACCAATGTGGCACGCAACCTC[C/T]GAATCCACATGACCAGTGAAAAGCACACACACAACGTGCTTCTACTGCAGCAGAACCTGGCACACATGCAACGTCAACGAAAGCACAATGCCTCCGAGCTTTTCCGCCACTGCCAACCTCAATCCCAACTTCCCGACGCCATCACTTCTCTGTCTTGCCATGAAACGTCTTCACAGAAACTCTTTGAATGCATACTATGTGGCCGCTTTTCCTGTGACACCCTGGAGGAACTTAGTCAACACCTGACCATGCAGAGGTCATTACCCAGTTCCTATTGGAGGAGTACAACCGGAGACACCCATCACTGTCGGCTTTGTCATTACGCCACGCCATTGCGAGCTAATTTCCAACTGCACTGCCAGACAGACAAACATGTTCAGCGTTACCAGCTAGCTGCACATCTTCGAGAGGCCAGCAGTCAACAAGGAAACATCGAGGAAGAGGAAGAAGAGTGGCGCCTCAGGTGTGTTGCTGCTGGAAGCCAGGTGCAGCTCAGGTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45626
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
ENSDART00000113668 Nonsense 1195 2962 8 10
ENSDART00000138972 Nonsense 311 2329 4 5
ENSDART00000148008 None None 980 None 2
Genomic Location (Zv9):
Chromosome 18 (position 5177942)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 5933730
GRCz11 18 6074095
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGGATCTTCAGAAGAAGGCGGGTTGAAAGATGAGGAAGAATGTGATT[T/A]AGAGGAAAAACTAAGTCCTACAGACAATGATTCAATTGTGGTTAAAGATA
Long Flanking Sequence:
ACCTCACTTGGAGGCATCGAAAATTTATAAGCAACCATCAGAAGATGCAGAATCCACAAAAGAGAACAACGCGGCTTTTCCATGTTGGCATAAAGGCTGTAACAAAGTCTTTACATCCTCAAGTGCACTCCAGACACACTTCAACCAGATCCACAGCCAGAAATCTCAAACCGCAATATCTGATCGCCACATTTACAAGTACCGCTGCAATCAGTGCAGTCTGGCGTTCAAAACCCCCGAGAAGTTACAGCTCCATTCTCAGTACCACGCTATAAGAGCGGCGACCATGTGCTGCCTCTGTCAACGCAGTTTTCGGACAATGCAGGCCCTTCGAAAACACCTGGAAACAAGCCACCTGGAGCTAAGCGAAGCCCAGATACAACAGCTGTATGGTGGTTTAATGATGAATGGTGAGAGCCTCATCTCTGGAGATCAAACTTTTGGTGAAGAGGAGGGATCTTCAGAAGAAGGCGGGTTGAAAGATGAGGAAGAATGTGATT[T/A]AGAGGAAAAACTAAGTCCTACAGACAATGATTCAATTGTGGTTAAAGATAACGTTGAATGTGACTCCAAACAGCCCGTTTTGCCACTTCGAAAGGGCCCAAATATAACCATGGAGAAATTTCTGGACCCATCCAGGCCTTTCAAATGCACCGTTTGCAAGGAATCTTTCACACAGAAGAACATTCTCTTGGTTCACTACAACTCAGTATCACACTTGCACAAACTTAAACGGTCTCTGCAGGACACTCCAACTGGCTTGCAGGAGCCTGTAACCAATACAGATAACAAACCGTTTAAATGTAGCATTTGCAATGTAGCATATAGTCAAAGTTCAACCTTAGAGATTCACATGCGCTCTGTCTTGCACCAGACAAAAGCCCGGGCATCCAAGGTCGATTCATCCACTAGCTCTGAATCTGTTGGCCCTCCCCCAGGCAAAGCATTGTCCAGCACCCCTGTGTCCATGAAGTCTGCTACTCCCATGAACAATGGTGGACTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45625
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
ENSDART00000113668 None None 2962 None 10
ENSDART00000138972 Nonsense 518 2329 4 5
ENSDART00000148008 None None 980 None 2
Genomic Location (Zv9):
Chromosome 18 (position 5177322)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 5934350
GRCz11 18 6074715
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGAGAAAGAAGTTGGTAACCATGATTGATTCAGCTAGCAAGCAGCAA[C/T]AGGTGTCATTACAACAACAACAACAACAATCATTACAACAGCAACAGCAG
Long Flanking Sequence:
TTCTGGACCCATCCAGGCCTTTCAAATGCACCGTTTGCAAGGAATCTTTCACACAGAAGAACATTCTCTTGGTTCACTACAACTCAGTATCACACTTGCACAAACTTAAACGGTCTCTGCAGGACACTCCAACTGGCTTGCAGGAGCCTGTAACCAATACAGATAACAAACCGTTTAAATGTAGCATTTGCAATGTAGCATATAGTCAAAGTTCAACCTTAGAGATTCACATGCGCTCTGTCTTGCACCAGACAAAAGCCCGGGCATCCAAGGTCGATTCATCCACTAGCTCTGAATCTGTTGGCCCTCCCCCAGGCAAAGCATTGTCCAGCACCCCTGTGTCCATGAAGTCTGCTACTCCCATGAACAATGGTGGACTAAGCCACCAACAAAACACGGATCTCAATGGCACACCTGCAAACCCAGACACAAGCCATCCTTCGACATCTGATGTGAGAAAGAAGTTGGTAACCATGATTGATTCAGCTAGCAAGCAGCAA[C/T]AGGTGTCATTACAACAACAACAACAACAATCATTACAACAGCAACAGCAGCAGTTAGCCCAGGCTCAAGCCCATCTCCAGCAAGAGCTCCAAAAGAAGGCTGCTCTTCTTCAGTCTCATTTATTCAATCCCGCACTCCTACACCCTTTTCCTATGGCAACAGAGGCTCTTCTTCCAGTCCAACAGCAGCAACAATTGCTTCTTCCTTTTCTTATTCCAGGAGGAGAGTTCCGCATGAATCCAGAGGTAAGCCTTAAAGGCTCTGGGCTAAACTTAAGCACAATAATGCCTACTGTTAATCAGGATATTACTGAGGCTTCCAAAAACGATGGCGCAAAATATACTTCTAAACAGAAACAAAACGAAGATCTTGCTATTCATCCTGAAATTACTGAACAGAAACTGAGAAGTGATTCCCAGTGTGAAAATGACAAAGATGGACAAAAAAGTAACGAACGATCAACAGAAATTGACAATGTGGGCGCAAATGAAAAGCCCCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28966
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
ENSDART00000113668 Nonsense 2158 2962 9 10
ENSDART00000138972 Nonsense 1296 2329 4 5
ENSDART00000148008 None None 980 None 2
Genomic Location (Zv9):
Chromosome 18 (position 5174988)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 5936684
GRCz11 18 6077049
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCTCACAAAAGATTTTTAGCCCTTTAGAGACTCCTGTATCTGAGCAA[C/T]AACAACAACAGAAACTATCCCAGGATATGAGCCCTTACAACTGCATTCAG
Long Flanking Sequence:
TTCAACGCATTTTTGATCTCATAAATCACCAGAAAAAGCAGTGTTACAAAGATGATGATGAGGAGTTGCAAAATAGTCTGAATGAAACTGCAGGGGAATATCAGGAGTCTCTTAGTCCAATATCTGGACCCTCTTGTTTAACACAAGCAACTTCTTGCTCAAGCCCCTCCAGCTCATCTGTGTCTAGTACTAATGTGAAGGCCACTGATTCTGAGCATAAGAACACAACAAGTGTCTACGGAGAGCTTAAACAAACAAATGAAACATCTTCTGAACCTAAACAGGCTGTTAGTATCAATTGTGAGTTTAAGGACACAGAAAACCGAATGCAGCAGCCAAAGCCTCTCTGTGAGGAGAACCAAAGCATAAGCACAGAGATTCAATCTCACTCATCTCCTAAACAACAAAAGATTTCCTGCACAGCATCTGAAACAAACCCAGCTCCATCACAGAGCTCACAAAAGATTTTTAGCCCTTTAGAGACTCCTGTATCTGAGCAA[C/T]AACAACAACAGAAACTATCCCAGGATATGAGCCCTTACAACTGCATTCAGTGTAAACTGAGCTTTCCCTCTTTTGAACACTGGCAGGAGCACCAGCAAATGCACTTCCTTACCCAAAGTTACTTTCCCACCCCACCATTCCTAGATCGTTCTGTAGACATGCCTCTTATGCTGTTTGATCCAGCTAACCCCCTACTTGCAAGGCATCTACTTTCAGGAACACTTTCCCAGATGGTAGCCAATCCCCCTGCAGTAACTTCTATTACTGATTCAACCATAAACTCACTGAAGAGGAAGCTTGAAGAGAAAGCAGGATCTAGTTCAGTGGAAAATGATTGGGAAAATAATGGGGACGAACCCCACCGCGACAAACGTATGAGGACCACCATAACACCAGAGCAGTTAGAGGTGTTATATCAGAAATATCTTTTGGACTCCAATCCTACACGCAAGATGCTTGACCACATCTCCAATGAGGTTGGTCTGAAGAAAAGAGTGGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36560
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113668 Nonsense 2494 2962 9 10
ENSDART00000138972 Nonsense 1632 2329 4 5
ENSDART00000148008 None None 980 None 2
Genomic Location (Zv9):
Chromosome 18 (position 5173980)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 5937692
GRCz11 18 6078057
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACAAACGATGAAGGAAATGACTCTCTAGAAGCTCAACATGGCAGTATT[G/T]AGCACATGTCTCCCAGCACCGAAAGGGAGGCTTCTTCTGAAAGTGATGAA
Long Flanking Sequence:
GGTTCCAGAACACCCGAGCTCGTGAGAGGAAAGGACAGTTTCGGGCATTGGGACCATCTCAAATCCATCGTCGCTGCCCATTCTGTCGAGCTCTCTTTAAAGCACAGACAGCTCTTGCAGCTCACATACGCTCACGTCACTGGCATGAAGCAAGGAATGCAGGCTACAGTATGGCAATGTCTAGTATGGGTCATGAGCAGGAAGGTTCTCCAGTCAAATCCGATCTCTTTGACTTTGCCACTTATTCTCAGTATTTGAACTCTACTGATGATGCAGATTCTTTAGCATGCAAGAGCATTGACCTGTCTTCACATCAGCAGCGCTTGAGTCCAAAACCTATCAAGGGTGAATGTATGGAGGAATTTGAGATGCCTTCCATGTCAGTTTATCAGACTTTTGAACAGAGCAAGCTCAATAGCCATGAGGCTAACACAAATACAACCCATGACCATACAAACGATGAAGGAAATGACTCTCTAGAAGCTCAACATGGCAGTATT[G/T]AGCACATGTCTCCCAGCACCGAAAGGGAGGCTTCTTCTGAAAGTGATGAAAAGATGTCTTCTGGATTGGTTAGTCCTGCAATGAGTTTTAATGCTAAAGATCTTGATAATGAGTTATTCTTGGATTACAGTGAGAATTCCAGTCTAGCTGATCCAGCTTCACCATGCCCTGGTAGCTCCAACAGTCAGAACTTTGATTATGACAGACATAACCAAAAACGCTACCGTACTCAAATGAGCAATCTGCAGGTAAAAGTGCTCAAAGCCTGCTTTAGTGACTATAAAACCCCAACAATGCTTGAGTGTGAAGCCTTGGGCAATGACATCGGACTTGCCAAAAGGGTGGTTCAGGTGTGGTTTCAGAATGCTCGTGCCAAGGAGAAAAAGGCCAAGCTTAGCCTAGCAAAGCAGTTTGGTACAGAAAGTACTTCAATTGACAGACCGAAGACAGAGTGTACTCTGTGCTCTGTTAAATACAGCAGCTCCTTGTCTATTCGTGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43031
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113668 Nonsense 2603 2962 9 10
ENSDART00000138972 Nonsense 1741 2329 4 5
ENSDART00000148008 None None 980 None 2
Genomic Location (Zv9):
Chromosome 18 (position 5173653)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 5938019
GRCz11 18 6078384
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATAAAACCCCAACAATGCTTGAGTGTGAAGCCTTGGGCAATGACATC[G/T]GACTTGCCAAAAGGGTGGTTCAGGTGTGGTTTCAGAATGCTCGTGCCAAG
Long Flanking Sequence:
GTCCAAAACCTATCAAGGGTGAATGTATGGAGGAATTTGAGATGCCTTCCATGTCAGTTTATCAGACTTTTGAACAGAGCAAGCTCAATAGCCATGAGGCTAACACAAATACAACCCATGACCATACAAACGATGAAGGAAATGACTCTCTAGAAGCTCAACATGGCAGTATTGAGCACATGTCTCCCAGCACCGAAAGGGAGGCTTCTTCTGAAAGTGATGAAAAGATGTCTTCTGGATTGGTTAGTCCTGCAATGAGTTTTAATGCTAAAGATCTTGATAATGAGTTATTCTTGGATTACAGTGAGAATTCCAGTCTAGCTGATCCAGCTTCACCATGCCCTGGTAGCTCCAACAGTCAGAACTTTGATTATGACAGACATAACCAAAAACGCTACCGTACTCAAATGAGCAATCTGCAGGTAAAAGTGCTCAAAGCCTGCTTTAGTGACTATAAAACCCCAACAATGCTTGAGTGTGAAGCCTTGGGCAATGACATC[G/T]GACTTGCCAAAAGGGTGGTTCAGGTGTGGTTTCAGAATGCTCGTGCCAAGGAGAAAAAGGCCAAGCTTAGCCTAGCAAAGCAGTTTGGTACAGAAAGTACTTCAATTGACAGACCGAAGACAGAGTGTACTCTGTGCTCTGTTAAATACAGCAGCTCCTTGTCTATTCGTGACCATGTCTTCTCCCAGCAACATCTTGCTAAAGTTAAAGAAGCCCTAGGTGGCCAGATGGAGAGGGACAGGGAATATTTGGGTTCAGTATCTACGCGTCAGCTGATGGCTCAGCAAGAGTTGGAGCAACTGAAAAAGACAAGTGATGTTTTGGGACATGTCCAACCACAAGCTATACTGGGCCTTAACCAAACTGCCCTTCATTGTCTGAGCCAGTCTTCAATGTATTCAGGTCTGCAGGCCCAGTGCATTGCAAACACACCAAGTGGTAGCAGCACAATGACTGCGGGGGTTTCTTCCATAAAAACAGGTATGTGGCTACTTTTTGTT
Associated Phenotype:
Not determined