Busch Lab

ZMP

si:dkey-3b8.4

Ensembl ID:
ENSDARG00000068398
ZFIN IDs:
ZDB-GENE-050419-24, ZDB-GENE-060531-22
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8DZ53]
Human Orthologue:
KIAA1377
Human Description:
KIAA1377 [Source:HGNC Symbol;Acc:29264]
Mouse Orthologue:
AK129341
Mouse Description:
cDNA sequence AK129341 Gene [Source:MGI Symbol;Acc:MGI:2680221]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa29070 Nonsense Mutation detected in F1 DNA Not yet available
sa29069 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36699 Nonsense Mutation detected in F1 DNA Not yet available
sa43154 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa29070
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
ENSDART00000098911 Nonsense 46 1084 2 12
ENSDART00000132315 Nonsense 23 1060 1 11
Genomic Location (Zv9):
Chromosome 18 (position 35747003)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 37426159
GRCz11 18 37407167
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAAACTGAAGATGAAAGGGAAGTGCTGTTACAGGAGCAGAGGTACTG[T/A]CGGGCTCGGGCTCGAAAGCTTTCTCTGGAAACTAATCGCAGAAGAAAGTA
Long Flanking Sequence:
TTGGATAAATTAAGTATCATACCAAAAGGACGTCATAAAGTCAGAGGTAGTACATGTTACCTGTTTGACGTTCCACCGGCTTTCTAGTCTTTACCTTGTTGTCATTCTTCAGTATTTTCCTTTTGAAACCTTTTGTTCCAGCTATGTTATTGCGCGATAAGATACAGTTTTGGCTATATGGATGAGATATTCGTTGTGTGGAGACCTGATATTTGGGATGTCAGTCATGGAGGACACACTTTATTACTCGTATCCTTTTTTGTGTATGAATTATATGTGGATATTGTAGTCTATTCAGCTGTAATTTACTGTAGCAAAACAACTGGCTTAGTTGATTATTTGTACAGATTTTTTTATGACTAACACTAAACAAACAAAGCACACATTATATATATATAGGAAGTACCTTCCTTAACTTTGCATCACATTAGCATCAGATCAGGTGTATATGGAGAAACTGAAGATGAAAGGGAAGTGCTGTTACAGGAGCAGAGGTACTG[T/A]CGGGCTCGGGCTCGAAAGCTTTCTCTGGAAACTAATCGCAGAAGAAAGTAAGTGTGACAAAAATGTATCTGATTTTATGTTGATTTCATTACTGCATGGGATTTTGGCTCATTTTATGGGTGGCTGATGAATTTACATCAAAGTGTATTTTATGTAAATTACATTATATTATTATATAAATTTGGTGTCAAAACATTTATCACTAAGTTAAGCAATTGCTGGAAAATTTCCACTAACTAATTTTTAAAACATTGTAGTGCAAAAATTAAAATAGCATTTTCATTAAAAATGTGCTCAATCTATTTATCTGTAAACATTTTTGTTTGTTTTTTTTTTACATTTGTGCACAATGTATGTAAACTTCAACACAAACATATTATTTTAGTTTTATTAAAAAATCTCCGGACTCATCTTTGTCAGTTAAAAGTAAATTTTCATAAAGATTTACATTTACAAAAATAACAAACATTTGCAATAGTACATTTATATGTATGTCTGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29069
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098911 Essential Splice Site 149 1084 None 12
ENSDART00000132315 Essential Splice Site 125 1060 None 11
Genomic Location (Zv9):
Chromosome 18 (position 35739771)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 37418927
GRCz11 18 37399935
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATACTCATCCATCTCAATTTTGGTCTGGTGCCTCCCCTGTTAGCAGG[T/C]ACGACATTACTGCCATCACAATATATCATAACGGGCAGAACTATTATAGT
Long Flanking Sequence:
TAAATAGAGAGTATTTCTTTGATTTTTGAGTAAACTATCCCTTTAATAAGCTGATATATTGGCATGCATGTAAACCGTCTGGCTGTTTTTCTATTTTCAGGGCTCTAGATGAGAAAAGAAAACAGTGGGATGTTCAGGAGCAGAGACTAAGGGAGAATATTCTACAACAGCGCCATCAGCAGGTCCAGGAGGCCACAGAGAACTTCCAAAGAGCTCATCTCCCGCCTTCCCAAAGGAAAAGACCCGGTATGTTCAGTGAAAAGTCAGGTGAACACTAATCCATGTGTTTACATGCACTGTGTTAGTAGTACTATAAGGTCAGTGTGTGTGTTGTAAACAGTCCGTCTGCCATAAACAGTAAATAGGGTGATTTGTGTTCTGCAGCAGCCTTTAAGAGAAGAACACCCAACCTTGACGAAGCACTTCATCATATTCAAGGCAGTCCACTCTTATATACTCATCCATCTCAATTTTGGTCTGGTGCCTCCCCTGTTAGCAGG[T/C]ACGACATTACTGCCATCACAATATATCATAACGGGCAGAACTATTATAGTCAGCTATTACTAAAACATAAAACTAAAGCCCTTTTATTACATCAAATAAAGTAAATGTTAACTGATATGAAACATTAAAAGCATTTAGCCTATTTTATTGCTGCTACAGAATTTTCAGTGTACATTAAAGGTTCTAATTTAACTTGATAGATTTAAATAACTACTGTAAAAATGGATTCTATTTTAAAATGGTAACACTTATTTTATTCTATAAAGATCATATTTCTTCACAATAAAAAAAAACATTCACACATAAAGAATTTATTTTTCTGAAAGGGATATTTGGCCAGAATAACAAAACTTTTAAGTAGTTTCACCAAATATTGCTTTCTTTATTCTTCTTAAGTTAAAACATTAAAATTTGCTTATCTAAAAAATGTATATACAGTGCTCAGCATATATATAACAACACCCCTCACAAATCTATCTTTTAAATTCATATTTTAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36699
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
ENSDART00000098911 Nonsense 636 1084 6 12
ENSDART00000132315 Nonsense 612 1060 5 11
Genomic Location (Zv9):
Chromosome 18 (position 35731174)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 37410330
GRCz11 18 37391338
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGGCGACCCCAACAGACATGCTAACCTGCCTCAACAAACCCATAAA[C/T]AGCTTTCTGCAGATCACTCGGACCATGTGAATTTACTCACAGGGGTATCA
Long Flanking Sequence:
GTTCTTTACAGTTGCAAAAACACAAACCATATGTAGATGAAGCCCCCAGGCTCAAAGCAGAATCCAAACCACTGTGCATAGAGGAAGCTATAGGCATAGATCCTAAAAATGAAACGGATGTCACCAAATTGGCAAAAGCCGGAATGTTGAAGTCTTCCACAGGCACAGAGGAACCTAACAGAACACCTGCAGACCCCGTGACCCATTGTGCGCCAAACAACGTCAGATTCTTGAAAGGAATTCTTAAAAACCATTTAAAATCCAAATCCGCAAACGTCAAATTCACGTACACCCCTAGCCATTTGCTTTTCACCAAGGAAGTGGCCATTTTAATCCGGGACAGCGTAGAGCTGGCAAGGGCAAAACTCAATGAGCCTGAGAAAAAACGAAATATTAAGAAGAAACTGCGTTGGTTTGATGAAGTACATAGAGTTGAGGGGGAGGAACGAGTGTTTGGCGACCCCAACAGACATGCTAACCTGCCTCAACAAACCCATAAA[C/T]AGCTTTCTGCAGATCACTCGGACCATGTGAATTTACTCACAGGGGTATCAAAGAACATCTCCAGTAAGACCTCTGCTGTCCCTGCTGGGCCCCAATCCACTAGACATGCCTGGGCAGATGTAGGGCCCCAAGAAAGCCGTGCACAGGAGCATATCAAGGAGCCCACCTCTCAAAAAAGATCCCTCTGCATTGGGGGCCCAAGGACTCCCCGGAGAGTGCGCTCAGCCAGAGTCTCCTCGTGTCCCGTTACCTCCCGGGCCAGGAAGGGCACTATCATCAGGCCCCAATCTGCCAGAGAAGCACAACATGTGGCCAAGACCCAAGGGAAAAGCTTGGTACCTCGCCCCCCTCCAAAACCTGAAGTGGCGGAGGTTGACCTAGCTGAGTGTCCCGTGTACATTTCCAAGGCCGATGAAGGTGTACAGACAATGTACAAAGATGCTCCAGATCTCCAGAATGTAGTTTCTCCGCCTGTCCTCAGAACAGATGGTATCTGTGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43154
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098911 Essential Splice Site 916 1084 7 12
ENSDART00000132315 Essential Splice Site 892 1060 6 11
Genomic Location (Zv9):
Chromosome 18 (position 35728378)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 37407534
GRCz11 18 37388542
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAAAGGATCCTCAAGAATGGGGGGCTTTTTCTTGTCTTCCTCTAATG[G/A]TAAGGCTCTATAGGTTTATTTAATTAATGATGTCAAAGGGCATTCAGTGT
Long Flanking Sequence:
AGTTCAGCAGCTTTGTTTGAGCTATTAGAGGGATATTTTTCTAGAGTTTTTGGAATAGTGTTTTTTGGTGTTGGATCAATAGAGTGTGTTTTCTTTGGCCCTCAGCTCAGCGCTGCACCACTTGGGATTACTACTTGGTTGAAATTGATCCATTTAATGATGGACTGTTGCTCCTCAGGGGTCAATTATTTTTTTATAACATCAGGAAAAGTCGTTGTTTTGTCGACATAGACCTCAAGAACAGGAGAAGTGGCTTTCATACTTCGGGACCTTTAAGTTGAACTGTCTTCTTTCTTTTTTTGTCTTTTTTGTGTTCCTCTCTCTCTCCTTCTGAATTGATTTAGGTGACCCTCAAAGTTTTCTGGCTCACAATGGCCCGTTGTCTCCTTCGCCTCAAGTCTGTGCCAGTCTGTCCCATGTTACCATCAATGGTGATAGTCTGATCAATGGTGTCAAAGGATCCTCAAGAATGGGGGGCTTTTTCTTGTCTTCCTCTAATG[G/A]TAAGGCTCTATAGGTTTATTTAATTAATGATGTCAAAGGGCATTCAGTGTCCAAAAAGCTAGGTCATTTCCACCTGCCAGCTCATAATGTGATCAAATTGCTTATTGTTTCACTAGAGTTGTTTAAATTCACTTAAAGGAACAGTTGACCCAAAACAGAAAAGTCTGTCATCATTTACTCACCCTTCACTTGTCCCAAACCTGAGTGACTTTTTTTTCTGTTGAGCACAAAAGAAATAAATATTTTAAAGAAAGCTAGAAATTGGCAACCATTGACTTCAATAGTGTTGTTGTTTTTTTTTACTATGGATGTCAATGGTTTTTCAGCTTCAAAATAACTTCATTTTTGTTCAACTAATTAAAGAAACTTTGGGTTCTCTTGATGGTGAGTACATTTTCATTTTTGGGCGAGCTATCCTTTTAAATCCACAGAGCTTACTTATGTCCGTACCTCAAGAGGTTAAGCTTTAGATACTCTGGTGTAATAGCCTATCTTTGAGA
Associated Phenotype:
Not determined