Busch Lab

ZMP

si:dkey-7c22.1

Ensembl ID:
ENSDARG00000057255
ZFIN ID:
ZDB-GENE-060810-98
Human Orthologue:
KIAA0090
Human Description:
KIAA0090 [Source:HGNC Symbol;Acc:28957]
Mouse Orthologue:
C230096C10Rik
Mouse Description:
RIKEN cDNA C230096C10 gene Gene [Source:MGI Symbol;Acc:MGI:2443696]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa31087 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa43962 Nonsense Mutation detected in F1 DNA Not yet available
sa43963 Nonsense Mutation detected in F1 DNA Not yet available
sa29912 Nonsense Mutation detected in F1 DNA Not yet available
sa43964 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa37686 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa31087
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104268 Splice Site, Nonsense 31 964 2 22

The following transcripts of ENSDARG00000057255 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 21555731)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 21335038
GRCz11 23 21261589
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCATCCTGATCTGTCATCATGTGTTAACATCACTCTCATTTCTTCCAG[G/A]AGGCAACAGTACATCGGCAAGGTGCGTTTTGCCTTGTTTGATACTCATTC
Long Flanking Sequence:
ACATTTCCAAATCCCCTTAAAACCCAAGTAGCTGTTTATAGGCAGCTCTCGCGACTGCCTGATGTTAATTTGTTAAACTGCAGTTTACGCGGAGACATGAAATTAAATTAAAATAATGGTATATCAATAGTCAGCCTAAATCTGACATCATAAATAAAAGAAGAGCACATGATGACATATTTCTTGTTTAATTAAACGCTGACTGGTCGGGTCCTTAAGCGCAGAGCATTGTGGGAGTTGTTCCTCTGCAGCAATGGCTTGGCTTGTAGTCAGATTAGCAATATCGGTGTCTTTATTATATACTGCATCGGCGGTATTTGAAGACCAGGTTGGAAAGTTTGATTGGTACGTATCCGAGCTATAGTCGTGTGCTGCTTTGTCGTTTAATTCATTGAAAGATTAGTGCGACTATAACAGCCGGTACTTACTTCAGTCAGGCTGCTCCACCGGGCTCATCCTGATCTGTCATCATGTGTTAACATCACTCTCATTTCTTCCAG[G/A]AGGCAACAGTACATCGGCAAGGTGCGTTTTGCCTTGTTTGATACTCATTCTCAAGCGTCTAAAAAGCTCCTGGTGGCCACCGACAAGAACGTGTTTGCTTCCCTAAACTCAAGGACTGGAGACCTGTGTAAGTCTGTCTGCTAAATATGTTGTATTCCTTTATTAAATCGTATAGCTTTGTAGGCTTGTTCGTTTTTAGCTTTTCCCTTTCAAAGCCTTTTTTGTTTATTAGACTGACATAATTTGTCACAAGGTATTCACTGAAATGAATGAAGCTGTTCCATGTCTTGGTAAATGACCTTTGATTTGATAGGCTCACCTCTTCACATGTGTAATTAGTAGGAGGTTGTTTACTAACTTTTTTTTTTTTTTTTACTAAAAAGGATAGTCCACCCAAAATTATTGTTAGGTATTGGTATAGAGCTTAAGTTGGTTTTATATTCGCACATGCGTTCAGTGACAATTTGTGACATGCTCCCTATATTGTTTACTATGGTACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43962
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104268 Nonsense 386 964 11 22

The following transcripts of ENSDARG00000057255 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 21561236)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 21340543
GRCz11 23 21267094
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTAAATTGGTTTATCGGTTCTTTAGTTGTATGTCCACGCCTTCCTAAAA[A/T]AAGATGACTCGGTGGGCTACAGAGTCATGGTACAGACGGAAGACCTTACA
Long Flanking Sequence:
TTTTAGGTCCCTCTGGAATATTCACAGCACATTACAGATTAAATAAATTGTGATGCATTCTAGAAAATGCAGTCAATTCCTTATAGAACATAGTATTTTTGATTACTCTTTAACTCTCCGTTTGTTCTTTTGTACTTCAGTCTTATCTTGCTGCTTTTGCCACATCTGGAGAGAAGACAGTTGTTGCTGTGATGTCCCCAAAGAATGATACTGTAAGTCGCATATCAAAAATGTCTTTCTGTGTATGTATGTTGTTGTTTCTAAATCATTTGTTATTCTCACTCAAGGCCTGCAGCATCAATCTGTTCAGTGCTGACACTGGCCGCAGGCACCTTGACACAACCATTATCTACCACACAGACCCTTACGGAGGAAAACCAAATAAAGTAAGGAGTGATGCTGTAATTTTTCAAATTAAATAAAATGCTTCAAATCAAATTTTTGTTGTAAGTTAAATTGGTTTATCGGTTCTTTAGTTGTATGTCCACGCCTTCCTAAAA[A/T]AAGATGACTCGGTGGGCTACAGAGTCATGGTACAGACGGAAGACCTTACACTCACATTTCTGCAGCAGCCTGGTATGAACTACATTATGCCACAATTCCTTTTATTTTTATTTATATTTTTTATTTTTAACGAAAAATGTAAATAAATTACAAGATAATTCAATGAACCGTTGAAGTCAGAATTATTAGCTCCCTTTTTTTTTTTTTTTTTTTTTATATTTTCCAAATGATGTTTAACGGAGCAAAGACATTTTCACAGTATGTCTGATAATATTTTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTAGGCTGGAATAAAAGCAGTTTTAATTTTTTTAAAAACTATTTTAAGGTCAAAATTATTAGCCACTTTAAGCTATTTTTTTTTTCCAAAAGTCTACAGAACAAACTATTGTTTTACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACATAATTAAGCTAGTTAAGCCTTTAAATGTCTCATTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43963
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
ENSDART00000104268 Nonsense 408 964 11 22

The following transcripts of ENSDARG00000057255 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 21561302)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 21340609
GRCz11 23 21267160
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTACAGAGTCATGGTACAGACGGAAGACCTTACACTCACATTTCTGCAG[C/T]AGCCTGGTATGAACTACATTATGCCACAATTCCTTTTATTTTTATTTATA
Long Flanking Sequence:
ATGCAGTCAATTCCTTATAGAACATAGTATTTTTGATTACTCTTTAACTCTCCGTTTGTTCTTTTGTACTTCAGTCTTATCTTGCTGCTTTTGCCACATCTGGAGAGAAGACAGTTGTTGCTGTGATGTCCCCAAAGAATGATACTGTAAGTCGCATATCAAAAATGTCTTTCTGTGTATGTATGTTGTTGTTTCTAAATCATTTGTTATTCTCACTCAAGGCCTGCAGCATCAATCTGTTCAGTGCTGACACTGGCCGCAGGCACCTTGACACAACCATTATCTACCACACAGACCCTTACGGAGGAAAACCAAATAAAGTAAGGAGTGATGCTGTAATTTTTCAAATTAAATAAAATGCTTCAAATCAAATTTTTGTTGTAAGTTAAATTGGTTTATCGGTTCTTTAGTTGTATGTCCACGCCTTCCTAAAAAAAGATGACTCGGTGGGCTACAGAGTCATGGTACAGACGGAAGACCTTACACTCACATTTCTGCAG[C/T]AGCCTGGTATGAACTACATTATGCCACAATTCCTTTTATTTTTATTTATATTTTTTATTTTTAACGAAAAATGTAAATAAATTACAAGATAATTCAATGAACCGTTGAAGTCAGAATTATTAGCTCCCTTTTTTTTTTTTTTTTTTTTTATATTTTCCAAATGATGTTTAACGGAGCAAAGACATTTTCACAGTATGTCTGATAATATTTTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTAGGCTGGAATAAAAGCAGTTTTAATTTTTTTAAAAACTATTTTAAGGTCAAAATTATTAGCCACTTTAAGCTATTTTTTTTTTCCAAAAGTCTACAGAACAAACTATTGTTTTACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACATAATTAAGCTAGTTAAGCCTTTAAATGTCTCATTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTAAAATATTTTTTACTGTCTTCATGGCGAAGATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29912
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
ENSDART00000104268 Nonsense 465 964 13 22

The following transcripts of ENSDARG00000057255 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 21563632)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 21342939
GRCz11 23 21269490
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACGGACTGTTACCCATGGTTCTCAAGCGTCTCTCTTCCCAGTTCATCT[T/A]GCTACAGGCCTGGATGGCTCATCTCTGGAAACTTTTCTATGATGCCCGAA
Long Flanking Sequence:
TTTTACAGATAATGTTGAAAAGAAAGCATTTGAAAGCTGTTTTAATTCAGGTTTTATGTATGTATTGTGTGTATCTGTATATTTGTGTGTGTTATTTCAACCTGCACTATCTGTGTGTGATGTATGGCCAGTGTGTGTTGTTACCTGTGATGTTTCTGCTTTTTGCTTATCACTTGTCTCGCTCATCTGTCCTGTTTTCAGTGGCTTTCTTGCAATTTCTTTCTATATTTATTTCCTTGTGTGTTTTCTTTTGCCTATCTGCTGCATTCGGATCCAGCCATTCAAGGTATAGTAAAGAGCTTACTCTAATTTGCTGCTCTTCCTAATCACCTTTATGTATTTATTTTTTTTTTTCAGTGTCTCTTAACTTCTGGAAAAACGCATTTTGTCTCAAGAAGGTGTTTTCTTTGGTATGTCTGACACTCATCAGCGTGATCTCTTGTTTCCTGCAGACGGACTGTTACCCATGGTTCTCAAGCGTCTCTCTTCCCAGTTCATCT[T/A]GCTACAGGCCTGGATGGCTCATCTCTGGAAACTTTTCTATGATGCCCGAAAGCCCCGCAGCAGTGTGAAGAACGAGATCACCATAGACACACTGTCTCGTGACGAGTTCAACCTGCAGAAAATGATGGTAATGGTTACTGCCTCTGGGAAGGTAAGTTCACAAAATGGTTGTTGGTCTGTTGTTTTAGTTGTGCTGTCGGTAATCGAGGGGTGTTGTGTTTCTGCCCAGCTCTTTGGCATCGACAGTAGATCAGGGACTGTTTTGTGGAAGCAGTATTTAGAAAACATCAAGCCCAATTCGTTTTTCAAGCTCATTGTGCAAAGGACTACTGCCCACTTTCCACATCCACCACAGTGCACACTTCTTATAAAGGACCAGGTAAGGTTCTAATCTTTGTTCTGTATTGTTTGAGTTACTTATATCTTTTTTGTTTGTTTATTTATTTAATTAGCTTATAAAAACTATCTTTGTTTGATAGCTCATTGATTGGATTGTCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43964
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104268 Essential Splice Site 566 964 None 22

The following transcripts of ENSDARG00000057255 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 21566628)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 21345935
GRCz11 23 21272486
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTCAATACTGAATCTTATTTAAGAATGGACTGTATCTATTTATTTTT[A/T]GGATACAGGGCTTGGAAGCCTGTATGTCTTCAATCCCATCTTCGGCAAGA
Long Flanking Sequence:
CAAAATATTTAGCTCAGCCTTGTATGCTTAATTTGAACGAGATAAAAAATTCATCCTAAAACATAAATTAAATGTTAAAGAAAGCAAAAATGTAACTTTCTCATGCATCAATATTGTTAAATTTTTTATTTTATTGTATTTCTTGATAAGTAATGCTTCAATGAATGATCTGCCAGATAGAACTTTGATTCCAAGTGGTAAATGACTTTTTAGAATGGGAAGGGTTTGTCTGCATTTGCCTTGTTTTTGTTACCTCGATTTGAAAATATAATAGAATTTTCATTATTTACATTGAGTTCGTTTAACGTCTCTTTCATGTTATTGTATGAAAGAGAAATGTTACACACATTGTTTGCTATATGGAATGCCAAAACTTTGACGCTTAATATCTCAAAATCATTCAAATCACAGATAGAACCTTATAGTTCCAAGGTGATGAATTGTATTTATGTCTTCAATACTGAATCTTATTTAAGAATGGACTGTATCTATTTATTTTT[A/T]GGATACAGGGCTTGGAAGCCTGTATGTCTTCAATCCCATCTTCGGCAAGAAAAGTCAAATTAGTGTCCCAGCGTTACCCAGACCTATCCTTCAGTCTCTTCTGTTACCTGTCATCGACCAGGACTATTCTAAAGTCCTTCTACTTATTGATGATCAGAACAAAGTGGGTATCTGTTCTTCTGGCAAACGTTTTGTGTTTCTCAGAAACTTTATTTCCTATTTCCTATTTTATTTGTCATTCAGGTCACAGCATTTCCATCTACTAAGAATATTCTGCAGCAGCTTCAGGAGACTGCATCTTCCATATTTTTCTACCTAGTGGACTCCAACCAGGGAAAGCTGTCGGGTTTTCGTCTGCGCACGGTTTGCATTCACCATCAGAATCAAGCATACAGATGGAAAACGCATTTAATGTTGGTGTTCATTAGTGATTATTCATTTTTTTCGTTCAGGATTTGTCTACAGAACTGATCTGGGAAGTTGTTATCCCTACCGAGGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37686
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
ENSDART00000104268 Nonsense 650 964 16 22

The following transcripts of ENSDARG00000057255 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 21566962)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 21346269
GRCz11 23 21272820
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGGAGACTGCATCTTCCATATTTTTCTACCTAGTGGACTCCAACCAG[G/T]GAAAGCTGTCGGGTTTTCGTCTGCGCACGGTTTGCATTCACCATCAGAAT
Long Flanking Sequence:
AAATGTTACACACATTGTTTGCTATATGGAATGCCAAAACTTTGACGCTTAATATCTCAAAATCATTCAAATCACAGATAGAACCTTATAGTTCCAAGGTGATGAATTGTATTTATGTCTTCAATACTGAATCTTATTTAAGAATGGACTGTATCTATTTATTTTTAGGATACAGGGCTTGGAAGCCTGTATGTCTTCAATCCCATCTTCGGCAAGAAAAGTCAAATTAGTGTCCCAGCGTTACCCAGACCTATCCTTCAGTCTCTTCTGTTACCTGTCATCGACCAGGACTATTCTAAAGTCCTTCTACTTATTGATGATCAGAACAAAGTGGGTATCTGTTCTTCTGGCAAACGTTTTGTGTTTCTCAGAAACTTTATTTCCTATTTCCTATTTTATTTGTCATTCAGGTCACAGCATTTCCATCTACTAAGAATATTCTGCAGCAGCTTCAGGAGACTGCATCTTCCATATTTTTCTACCTAGTGGACTCCAACCAG[G/T]GAAAGCTGTCGGGTTTTCGTCTGCGCACGGTTTGCATTCACCATCAGAATCAAGCATACAGATGGAAAACGCATTTAATGTTGGTGTTCATTAGTGATTATTCATTTTTTTCGTTCAGGATTTGTCTACAGAACTGATCTGGGAAGTTGTTATCCCTACCGAGGTGCAGAAGATAGTGGCTGTCAAAGGGAAGCGTGCAAATGAACACGTGCATTCCCAAGGCAGAGTCATGGGGGATCGTAGCGTGCTCTACAAAGTACTGTTGACCTTGATTTACTGCTTTAATTGGCCAAATGAGATCAGACTTTTCTCTAATCATATATCCTCTCTCTTGTTGTTGGTCTGCAGTATCTGAACCCTAATCTCTTGGCTGTGATAACTGAAAGCACAGACACTCATCAGGAACGCAGCTTTGTTGGAATCTTCCTGATTGACGGTGTGACTGGCCGTATTGTGCATGAGGCTGTGCAGCGAAAGGCCAGAGGGCCAGTTCACTGTGT
Associated Phenotype:
Not determined