Busch Lab

ZMP

zgc:113421

Ensembl ID:
ENSDARG00000069397
ZFIN ID:
ZDB-GENE-050320-59
Description:
hypothetical protein LOC100148379 [Source:RefSeq peptide;Acc:NP_001139179]
Human Orthologue:
KIAA0913
Human Description:
KIAA0913 [Source:HGNC Symbol;Acc:23528]
Mouse Orthologue:
2310021P13Rik
Mouse Description:
RIKEN cDNA 2310021P13 gene Gene [Source:MGI Symbol;Acc:MGI:1919156]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa13957 Splice Site, Nonsense Available for shipment Available now
sa31922 Nonsense Available for shipment Available now
sa11173 Nonsense Available for shipment Available now
sa28097 Nonsense Mutation detected in F1 DNA Not yet available
sa7226 Essential Splice Site, Splice Site Mutation detected in F1 DNA Not yet available
sa22278 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa13957
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056432 Splice Site, Nonsense 371 1912 8 26
ENSDART00000133108 None None 196 None 4
ENSDART00000144612 None None 207 None 2

The following transcripts of ENSDARG00000069397 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 21992380)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 21721718
GRCz11 13 21852168
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCTGCACCTCTGTTAGAAATCCTCACCGAACAGTGTCTCACCCAYGAA[C/T]AGGTACAATTTCTGACTCAGCAACACTTCATTCATTCATTTATTCTGATG
Long Flanking Sequence:
GTCTATTTTCTCATTCTTTGTAAAAAAAAAAATGCACACCATGTGCTTCCTTTTTGTTTTTTCCTGACGATTGATTGAACAGATCCTACTGCTGGCCCTTCAGCCTCTGACCAGAGCACCTGGTATTTAGATGAGTCCACCCTCAGTGACAACATAAAGAAGACCCTGCACAAATTCTGTGGCCCTTCACCTGTTGTGTTTAGGTAAATATCACACTAAGAAGTATCTGTTTATACACACCTATATGTTAGAAGCACAACAGACAGAACTAACTGTTCCTTCGGTCTCTTGTTGTTCTCAGTGATGTGAACTCCATGTACCTGTCGTCCACTGAGCCTCCGGCAGCTGCTGAATGGGCTTGTCTGCTGAGGCCCCTGCGAGGCAGAGAGCCAGAGGGCATCTGGAATCTTTTGTCCATCGTCAGAGAGATGTTTAAGAGGCGAGACAGTAACGCTGCACCTCTGTTAGAAATCCTCACCGAACAGTGTCTCACCCACGAA[C/T]AGGTACAATTTCTGACTCAGCAACACTTCATTCATTCATTTATTCTGATGCAAACACTTGTCACATTTATGCTTGCACTAAGGCCAAAACAAATTCATAGTTGCGTTGGTTGCACTTTATTATACAGTATGTCAGCTTAACTTTAAAAAAGATATATATATATATATATATATAATATATATATATATAAGGTAGCTGGATAGGTTAATGGGATAGTTTATTTATTAATAGAAATTATAATCATTTACTCGTATTCGACTTGTTCTAAACCATCTGTTGAACTTAAAGGAAGATATACTGAAGAATGCTGAAAAAAAAACAGTCAGTGAATCCCATAGTAGCTGTATTTTACTTGTACTTAATATGGATGTCAATGGCATCCCCAAATAAATCAGAAAATCTTGTTTTATGTTTAACAGATAGAATGAAGGAATATCATAACTGTTTAGATCTACTTGATTGTGAATAAATGGTGAGGAAATTTTTGGGTGAACTATCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31922
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056432 Nonsense 432 1912 10 26
ENSDART00000133108 None None 196 None 4
ENSDART00000144612 None None 207 None 2

The following transcripts of ENSDARG00000069397 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 21995980)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 21725318
GRCz11 13 21855768
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAAGTAAAACAATGTTTTTACTTCTCTATTTGTAACTCCTCAGGCGTT[T/A]GGAACTTGCTGCCCAACTAAAGCAGTGGCACCTGAAGGTGATCGAGATTG
Long Flanking Sequence:
AATATTAAAAAAATTATTTTAAACTGAGAAGATTAAATTAGCTGATAAAAACTTAACTGTAAGTTTTCCCCACAATTAAAGCTGACAAGTGCTAAAGTTTTCTTAATTGATGCTCAACAGAAATCTGTAATTTACTTAAAAAAAGGTACTCGAGGGTTTCACAAACGTTTAAAGAACTAGTGGTGTTTGTGACTTTGATTTAAAACAGGGATTTTCAACTCTGGCCCTTGAGGTCCACTTTCCTGCAGAGTTGAGTTCCAGCCCTAGTCAAACGAACAAGAAAAGCTAATCAAGGTATTCAGGATTATTGTTAAAGTTGCAGACAGGTGGGATTGACCAAAGTTGAATCTAAACTCTTCATGAGCAACTGTGAGAATACCTGTTCTAAATCAAACTCAGCACTGATTTTGAATGGCTCAGCTGAAGGATTTGGGGCTGTATTTGTTATCGCTCAAGTAAAACAATGTTTTTACTTCTCTATTTGTAACTCCTCAGGCGTT[T/A]GGAACTTGCTGCCCAACTAAAGCAGTGGCACCTGAAGGTGATCGAGATTGTGAAACGGGGGCAGCACCGCAAATCTCTCGACAAACTCTTCCAAGGCTTCAAACCAGCTGTGGAGTGTTGCTACTTCAACTGGGAAGTGGCGTACCCTTTACCTGGCATCACATATTGCAACGCAGATAAGAAAAACGTTTCATTTTGTTGGGCCAGGGCCATGCAGCAGCAGCGGGGCTTGAAAGCCATAAACAGCAGCGAAGCAGGAGAAGGAGCTCGCAGTGGGACATCAGAAGGCAATTCCTTAGAGCACAAATCACGGAGCAACTCCCATCTTCCCCAGCAGGAGGTGGCCGTGCGCCCCAAGGAGACCATTGTGAGCAAGAGGAAAGTTGTGTCGAATGTGAACAGTGGGAGTGTGCTGGTTTGTCTGGGCAGCAGAGTTCCTCTCTCACTTCCTGATGGAAGTAAAAGCATGTATAAAACTACTAACTCTTCCCCATCAGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11173
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056432 Nonsense 851 1912 11 26
ENSDART00000133108 None None 196 None 4
ENSDART00000144612 None None 207 None 2

The following transcripts of ENSDARG00000069397 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 22000272)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 21729610
GRCz11 13 21860060
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGCCTGTGCAGAGGCWCTCTATGCTCACGGCTACAGTAATGAAGCATG[T/A]CGACTAGCTGTCGAWCTTGCTCGAGATCTGCTGGCTAACCCTCCTGATCT
Long Flanking Sequence:
TTTTTTTTTCTTTTTTTTTCTTTGATTTCATTTCTACCAAGCCTGTTGCAAGCATTTATACTGCATTTTGTCTGCTTTGCTCTGCAATAATACTACTGAAATACTAGTAGGCAGTGGGGTTTCTATGCTACACTCATTACAGCTATACCAGCTTAACATAGTCAAATATTTTGAGAGGTGCGTATGAGGGTATGTGACTTTGTTAGGGCTACATCAGACCTTATACATATGCTCTGTACAGAAGTATTACGAAAAATCTAAATATTATGAAAAAAATGCTACAACACATTTTACCCAAGTTATTATATGTATCCTAATTTTTGGACCAGTTTTATTCCTTTGAATTGAAAACTAATTTTATTTTTCATAAATCAAAAGTCATTTTGATGTTTTTTTTTTTACTGAATTTCAAATTATTTAAAATGGTCTAATGGTGTGTTGCAGGTTCTGTTTGCCTGTGCAGAGGCTCTCTATGCTCACGGCTACAGTAATGAAGCATG[T/A]CGACTAGCTGTCGATCTTGCTCGAGATCTGCTGGCTAACCCTCCTGATCTGAAGGTGGAGCAGCCACAGACAAAGGTACTGAAACATGCTTTTACACCTCTTCCCCGGAGGTTAAAGCGATTACCTCTGCTCACCTTTGAGAACAAATCTTTCTTGTTTTTCTGTAGGGTAAAAAGAGTAAGGTGTCGACCACTAAACAGACACAGGTGGCCACCAACACCCTGTCTAAAGTAGCCTTCCTGCTGACAGTATTGAGTGAGAGGCTGGAGCTCCATAACCTGGCCTTCAACACTGGCATGTTCTCCCTGGAGCTGCAGAGGCCGCCAGCTTCTACTAAAGCTCTGGAGGTAAAGCTGACATCACAGTGGTCCAATCTGAAGATCTGTTAGTACAGTGATGTAGTTTGTTTAGACATTTATATCTTACATTACATTGTTTTAGATTCAGAGTTTATACAGTGGTGGAAAACCTGAAAAAGTCATGAAATTTTAACATGCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28097
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
ENSDART00000056432 Nonsense 905 1912 12 26
ENSDART00000133108 None None 196 None 4
ENSDART00000144612 None None 207 None 2

The following transcripts of ENSDARG00000069397 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 22000525)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 21729863
GRCz11 13 21860313
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGGTGGCCACCAACACCCTGTCTAAAGTAGCCTTCCTGCTGACAGTAT[T/A]GAGTGAGAGGCTGGAGCTCCATAACCTGGCCTTCAACACTGGCATGTTCT
Long Flanking Sequence:
AAATCTAAATATTATGAAAAAAATGCTACAACACATTTTACCCAAGTTATTATATGTATCCTAATTTTTGGACCAGTTTTATTCCTTTGAATTGAAAACTAATTTTATTTTTCATAAATCAAAAGTCATTTTGATGTTTTTTTTTTTACTGAATTTCAAATTATTTAAAATGGTCTAATGGTGTGTTGCAGGTTCTGTTTGCCTGTGCAGAGGCTCTCTATGCTCACGGCTACAGTAATGAAGCATGTCGACTAGCTGTCGATCTTGCTCGAGATCTGCTGGCTAACCCTCCTGATCTGAAGGTGGAGCAGCCACAGACAAAGGTACTGAAACATGCTTTTACACCTCTTCCCCGGAGGTTAAAGCGATTACCTCTGCTCACCTTTGAGAACAAATCTTTCTTGTTTTTCTGTAGGGTAAAAAGAGTAAGGTGTCGACCACTAAACAGACACAGGTGGCCACCAACACCCTGTCTAAAGTAGCCTTCCTGCTGACAGTAT[T/A]GAGTGAGAGGCTGGAGCTCCATAACCTGGCCTTCAACACTGGCATGTTCTCCCTGGAGCTGCAGAGGCCGCCAGCTTCTACTAAAGCTCTGGAGGTAAAGCTGACATCACAGTGGTCCAATCTGAAGATCTGTTAGTACAGTGATGTAGTTTGTTTAGACATTTATATCTTACATTACATTGTTTTAGATTCAGAGTTTATACAGTGGTGGAAAACCTGAAAAAGTCATGAAATTTTAACATGCTGTTTTCCAGGCCTGGAAAAGTTTTGAAAAACAGAAAAACCCACAATGTTTTGTAAAAGTCATGGAAATTAGTTTAAAAAAATATATAATATATATTATAAAATAAATTAAAATAGTATCCTTAAAAGTTGTTTTTCACATATATACTTGAATATTTGTCTTTACTCCTTTTCTGTCTATCCTCAAAAACATGCCCTCAGATTATTAGTGCTTTGTAAGCATTATCTAAATACATTTTACATCGATATAAAAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7226
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 > G
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056432 Splice Site None 1912 None 26
ENSDART00000133108 Essential Splice Site 151 196 4 4
ENSDART00000144612 None None 207 None 2

The following transcripts of ENSDARG00000069397 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 22004786)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 21734124
GRCz11 13 21864574
KASP Assay ID:
554-5275.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTAGTGGGCAAGATTAAATTCTTATTTCCTTACTCGTACYTTTGATTT[A/G]GCAGAAGGTGCGCAGTCGACCTCCTGTGATCAGCAGAGTGAAGCTGCACC
Long Flanking Sequence:
CTTCATGAGGGAGAGTGGAATGTTGCTGCTTCGATGAAACACAAGCCATGATACCATGCTTAAATTATTGCCTCATTTGATTCTTGTGTAGATTCTGGACAAGCTGCTTGACCGTGAGAGCCAGACCCATAAGCCGCAGACTCTGAGCTCGTTTTACTCTAGCAAACCGGCCACCAGCAGCCAGAAGAGCCCTTCCAAGCACGCCACCCACGGTGCCAGCGGAGCCACTGGGGGAGTGTCAAAGCACACCCCTACAGCAACATCAACTGCTGTGCAGGGCATGACCAGCGGGGGAGCTGCGGGCCAGCAGGGAGGTTTAGCTGGAGGTGTTCAGAGCACAGCCTCAGGAGAGAGTATCTCTGACAACAGAGATCAAGGTGAGCAATATCCACCAAACTGTTATGGGTAGACAACTCTGTTTCAGAGAGAAATACTGTGTCTTTATGAAGATTGTAGTGGGCAAGATTAAATTCTTATTTCCTTACTCGTACTTTTGATTT[A/G]GCAGAAGGTGCGCAGTCGACCTCCTGTGATCAGCAGAGTGAAGCTGCACCGTTCAAACCTGAGGGCACTGTGCCTAGTCGTCTGGCACTGGGGGGCCGTGGGGCATATGGCACCCGTTGCTGGGGGTCACCTGTGCGGCAGAAAAAGAAACACACTGGTAAGAGAAAGTGGAATTCACTCTTTTACTTTTGTATATGGTTATTTAATATATTGCTACATTTGGAAATTTTGCCAAGAAAGAAACAACTAAATTTAGTACTGATGCATGGCATTTAAGCAGACAGCTTTGATTCCAGTTTATCCCACATCATATATAAACATTTTTTTAGATTTTTTATTTTTTATTTTAAATGTTATTTATTTCATTATGCAATTAATTTATTAAACAATAAATAATAATTTAACAAGAAATCAGCATATTATAATAATTGGTAAATGACATACTAGAGCAGCATCACAAAAGCAGCACTGCAATACAGCTGTTTATCAGTACTGCTGTG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa7721
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056432 Nonsense 1340 1912 19 26
ENSDART00000133108 None None 196 None 4
ENSDART00000144612 None None 207 None 2

The following transcripts of ENSDARG00000069397 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 22006666)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 21736004
GRCz11 13 21866454
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACTGTGCTGATTAAAGCTGGTGGAAACAGCTCMACCTCTATTTTCACT[C/T]AGCCCTCTGCCAGYGGAGGCCACCRGGGGCCACACCGCAACCTACATCTG
Long Flanking Sequence:
TGTTTTTAAGGTATGGCAAGCATAGACAGCAGTGCTCCAGAGACCACCTCAGACAGCTCTCCTACTCTCAGCCGACGACCTATTCGAGGAGGTTGGACCGCTACTTCCTGGGGGAGAGGTCAGGACAGCGACAGCATTAGCAGCTCTTCCTCTGATTCACTAGGCTCTTCATCATCCAGTGGCTCACGCAGAGCTGGAGGAGGAGCCAGAGCAAAGAGTACTGACACCAGCAGGTGAGACAAGCCTGTTTGTACCGTGCTCCATTATGTCAACAACAATTGTTAGCTCATTTATTTCCAGAACATATTCCCTGATTCAGTTTCTTTGCAGGTTATGACATGCATTATCTCTGTTTTTTTAGGTATAAAGGCCGTCGGCCCGAATGCCATGCTCCACACGTACCAAACCAGCCGTCTGAGGCAGCTGCCCATTTTTACTTTGAGCTGGCCAAGACTGTGCTGATTAAAGCTGGTGGAAACAGCTCCACCTCTATTTTCACT[C/T]AGCCCTCTGCCAGCGGAGGCCACCAGGGGCCACACCGCAACCTACATCTGTGTGCCTTTGAGATCGGCCTGTATGCCCTTGGCCTGCATAATTTTGTGTCTCCTAATTGGCTATCAAGAACGTATTCCTCACACGTATCCTGGATTACAGGTGAGAAACGATTGCTCTGCAGTGATTAAAAAAAGTACTATAGTACTACTACAGGGTTAGAAATAGATTAATGGTAAGAGATAGTTTGATGATGGGTAGATGGTTAAAAGATGAATGCTTGATTTATGGACAGATGCATCGTTAGTTATGGCTTATGATTGATAGATGCGAAGGATGATGGATTGGTAGATTGTATAGATAAATATGGGTGTAGATGATGGATGGATGGATGAATATGGTAGGATTGATGTCTGGATGGTTGTTTGAATATGGAAGGATGGATGGATATGGGTAGTTGATGCATGGATTGATGGATGATGGGGTTGTGAATTTAGAAGCGAAGACAGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22278
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056432 Nonsense 1513 1912 21 26
ENSDART00000133108 None None 196 None 4
ENSDART00000144612 Nonsense 21 207 1 2

The following transcripts of ENSDARG00000069397 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 22010539)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 21739877
GRCz11 13 21870327
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGTATTGGCTTTATGAACAAACCGTTGGCGGTGGTTCGGGATCTCAG[C/T]GAGAAGGTTCCGGACGCTGCGGGGCCAATGGTGGAGCTGGGAGAACGCCA
Long Flanking Sequence:
ATAAATACAATTTCATATTTAAGTTCTTCTGTTTTGTTTCCACAGGCCAGGCTATGGAGATTGGGAGTGCTGCTCTCAACATCCTGGTGGAATGCTGGGACGGGCACCTTACTCCTCCAGAGGTAGCATCATTGGCAGATCGTGCGTCGCGTGCACGTGATCCTAACATGGTGCGAGCTGCGGCAGAGCTGGCCTTGAGCTGCCTGCCTCATGCTCATGCCTTGAACCCCAATGAGATTCAGAGAGCCCTGGTGCAGTGCAAGGAGCAGGTACCATCCAGAAAAGCTCACATGCATTCTGTTTGACTGTAATCAGATTTTTATGCTTATCGAAATCATCTGCTTGTGGCTTTTCAGGACAATGTAATGCTGGAGAAAGCATGCATGGCCGTTGAGGAGGCTGCAAAAGGAGGTGGTGTTTATCCAGAGGTCCTATTCGAGGTGGCTCATCAGTGGTATTGGCTTTATGAACAAACCGTTGGCGGTGGTTCGGGATCTCAG[C/T]GAGAAGGTTCCGGACGCTGCGGGGCCAATGGTGGAGCTGGGAGAACGCCACCGGAAGGAGGCTGTGGTATTCTGGATAATACCGGAGCTTTGGATTCATCAGGTGTCTCTGCTGTAACTACAACAGTGACCGCAGCCGCGGTAGTACCTGTCATTTCTGTCGGCTCCACCATCTACCAATCTCATGCGCTGCCAGGCTCCGCCATGGCGCACACGCAAGGCCTGCATCCCTACACTACCATCCAAACACATCTGCCCACCGTCTGCACCCCACAGTACCTAGGCCACCCGCTTCAACACGTCCCCCGTCCTGCTGTCTTCCCTGTGTCTGGGGCGGCCTACCCACAAGTATGAGCTCTTTTATATAATTCATAGGCTGTAATTACATGTGCATAGAATTTTTATTCAGGGTGTAATATTGTTGGCCTGCACTTAACTGAAGGTGATAAATGCTAAATTTATACATTAACGTAGACATTTACTTGGCAGTCAGCGATGCTT
Associated Phenotype:
Not determined