Busch Lab

ZMP

LOC569740

Ensembl ID:
ENSDARG00000032372
Human Orthologue:
C9orf174
Human Description:
chromosome 9 open reading frame 174 [Source:HGNC Symbol;Acc:29303]
Mouse Orthologue:
E230008N13Rik
Mouse Description:
RIKEN cDNA E230008N13 gene Gene [Source:MGI Symbol;Acc:MGI:2685871]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa14782 Nonsense Available for shipment Available now
sa31476 Missense, Nonsense Available for shipment Available now
sa7004 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33713 Nonsense Available for shipment Available now
sa40557 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33712 Essential Splice Site Available for shipment Available now
sa38503 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14782
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042420 None None 1336 None 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 Nonsense 471 1502 15 39
Genomic Location (Zv9):
Chromosome 5 (position 52830916)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50498112
GRCz11 5 51144705
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTAMAATTTCACTCTTTSACATGTTYACTGAACATAGATANNNNNTGT[C/T]AAWTGTCTCACCCAACAGAGGAAAGAGGCCCAGCTGGATATGATGTTGGA
Long Flanking Sequence:
TGCCCCATACTGAATGAAACTCCAAACCATGATTTTTCCTTCACCAAACTTGACTGATTTCTATGAGAATCTTAGGTCCATGCTGATTCCAATAGGTATTCTCTAGTATTTTTGATGATTGAGATGCAGCTTAACAGATGGATCATTGGAAAAATCTACTTTCTGACACTTTTCCAAATAATCAACTAGAAGTCAACCTATTATTTGTTGCTCTTACAACTGGGATTGAAGACAAGACTTTTGTCAGGCAGTGTACATTCAAAATTCACTCACACTGTTTAGACCATAGTTTTGTAATGGTAGTAAAGTAAGAAATGTAGTAAAATCAAATTTTGTACACACTCAGACAAAACCTGATTTCACACACCAGAACTTTGTGACACTGGTCATCCAGAAACACATTTAGACACCACTTTATAATCAGTGCTTAAATAATGAGTGCTCAATCTTTTGTAAAATTTCACTCTTTGACATGTTCACTGAACATAGATACTGTATGT[C/T]AAATGTCTCACCCAACAGAGGAAAGAGGCCCAGCTGGATATGATGTTGGACAAACTCAGACAGGAAAGTTCAGAAGAAGCTCTGAAGGCCTCATTAGAGAAAATACTAACCTATTTGGAGGAAGTTAAGAATGGGTAACACACATTTAGATTTCTATAAATCATTTTTTGTTGTTATTGCACTGTATGATAAGCTACTGGAACTTAATAATGGAACAACGTTTCTGGCAAAAAAGAAAGAGAACCTAGATATTTTGTGGAAATATTTTCCTGCCTTGTTATTTAAGGTATGTGCAAACCTATGAAGAGGAAGTGGAAATTGTGGAGTATTATCCATCTACAGTACTGCAGGAACTACAAGCATACAGTCTTTCTGTTAGCCAGTTCTTCAGTGCTGAAGAGGTTTATGGTCAGGTACATATTTAACAAGAACAATGCTGTTATCTCTGTTTGTACTTGAACAAACATTGTTAAAATAACCTCTTTTTGTCATAGGACCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31476
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:
G > T
Consequence:
Missense, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042420 Nonsense 403 1336 11 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 Missense 492 1502 15 39
Genomic Location (Zv9):
Chromosome 5 (position 52830852)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50498048
GRCz11 5 51144641
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGAGGAAAGAGGCCCAGCTGGATATGATGTTGGACAAACTCAGACAG[G/T]AAAGTTCAGAAGAAGCTCTGAAGGCCTCATTAGAGAAAATACTAACCTAT
Long Flanking Sequence:
GAGAATCTTAGGTCCATGCTGATTCCAATAGGTATTCTCTAGTATTTTTGATGATTGAGATGCAGCTTAACAGATGGATCATTGGAAAAATCTACTTTCTGACACTTTTCCAAATAATCAACTAGAAGTCAACCTATTATTTGTTGCTCTTACAACTGGGATTGAAGACAAGACTTTTGTCAGGCAGTGTACATTCAAAATTCACTCACACTGTTTAGACCATAGTTTTGTAATGGTAGTAAAGTAAGAAATGTAGTAAAATCAAATTTTGTACACACTCAGACAAAACCTGATTTCACACACCAGAACTTTGTGACACTGGTCATCCAGAAACACATTTAGACACCACTTTATAATCAGTGCTTAAATAATGAGTGCTCAATCTTTTGTAAAATTTCACTCTTTGACATGTTCACTGAACATAGATACTGTATGTCAAATGTCTCACCCAACAGAGGAAAGAGGCCCAGCTGGATATGATGTTGGACAAACTCAGACAG[G/T]AAAGTTCAGAAGAAGCTCTGAAGGCCTCATTAGAGAAAATACTAACCTATTTGGAGGAAGTTAAGAATGGGTAACACACATTTAGATTTCTATAAATCATTTTTTGTTGTTATTGCACTGTATGATAAGCTACTGGAACTTAATAATGGAACAACGTTTCTGGCAAAAAAGAAAGAGAACCTAGATATTTTGTGGAAATATTTTCCTGCCTTGTTATTTAAGGTATGTGCAAACCTATGAAGAGGAAGTGGAAATTGTGGAGTATTATCCATCTACAGTACTGCAGGAACTACAAGCATACAGTCTTTCTGTTAGCCAGTTCTTCAGTGCTGAAGAGGTTTATGGTCAGGTACATATTTAACAAGAACAATGCTGTTATCTCTGTTTGTACTTGAACAAACATTGTTAAAATAACCTCTTTTTGTCATAGGACCATAAGGATTTTTGCCAAATTTATCCTTCTCTTAAACTTGGTGAGTTGAAAATGCATCTTTAGGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7004
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042420 Essential Splice Site 467 1336 None 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 None 562 1502 16 39
Genomic Location (Zv9):
Chromosome 5 (position 52830506)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50497702
GRCz11 5 51144295
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATACAGTSTTTYTGTTAGCCAGTTCTTYRGTGCTGAAGAGGTTTATGG[T/G]CRGGTACATATTTAACAWGAACAATGCTGTTATCTCTGTTTGTACTTGAA
Long Flanking Sequence:
CACTTTATAATCAGTGCTTAAATAATGAGTGCTCAATCTTTTGTAAAATTTCACTCTTTGACATGTTCACTGAACATAGATACTGTATGTCAAATGTCTCACCCAACAGAGGAAAGAGGCCCAGCTGGATATGATGTTGGACAAACTCAGACAGGAAAGTTCAGAAGAAGCTCTGAAGGCCTCATTAGAGAAAATACTAACCTATTTGGAGGAAGTTAAGAATGGGTAACACACATTTAGATTTCTATAAATCATTTTTTGTTGTTATTGCACTGTATGATAAGCTACTGGAACTTAATAATGGAACAACGTTTCTGGCAAAAAAGAAAGAGAACCTAGATATTTTGTGGAAATATTTTCCTGCCTTGTTATTTAAGGTATGTGCAAACCTATGAAGAGGAAGTGGAAATTGTGGAGTATTATCCATCTACAGTACTGCAGGAACTACAAGCATACAGTCTTTCTGTTAGCCAGTTCTTCAGTGCTGAAGAGGTTTATGG[T/G]CAGGTACATATTTAACAAGAACAATGCTGTTATCTCTGTTTGTACTTGAACAAACATTGTTAAAATAACCTCTTTTTGTCATAGGACCATAAGGATTTTTGCCAAATTTATCCTTCTCTTAAACTTGGTGAGTTGAAAATGCATCTTTAGGAGCTGTATTTTGTGACTGCCTGTAGATGTAATAACTATTTATTATGTTCATGTTGATGTTTACACAGATCAAAACATAAAAACTGGTAAAAACATAACACATAAAGATGCACCAAAGTCACATTTCAACAATCAAGAAAGCTCAAACTTCGACCTGTCCTGTGCAACGGTAAACAGGATGTGCACATGTTTGCTCATTTTAATTTTTCCATCTACATCAATAATTGAACTTCCTCTCCTTTGTAGGATGACCAACACTGTACGGCTTTAGCATTTTTATTCTCAAACACCAAGGAGACTCTGATCACTGCAAAAGGAAATGTGTACAGCTGCTCTGGGTTTCATACTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33713
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
ENSDART00000042420 Nonsense 726 1336 18 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 Nonsense 877 1502 23 39
Genomic Location (Zv9):
Chromosome 5 (position 52827469)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50494665
GRCz11 5 51141258
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGAGGGGGGGAATTTTACACCCCAGGAAATTGAGGTCTTTCAGTCA[C/T]AACTGGAAAAGATGGACAAGCGCATTGATACCGCAGAGGGGGCCGTGATA
Long Flanking Sequence:
AACTCCCAGACAGACTTACAAGAGTTACAGGTCCAGCTGAATAAACTGACTGAAGACTTTCAAATGCAAATCTACAAAAGAGAGAAAGATTTCATCGTTGGCACTAGTTCTGAAAAGTAAATAAATGCAAATACATTTTGTATAACGGTAATGATGTGTACAGTTTATGTAACAATCTGCTTTTTCTGGCCTTTTTTATTTACAGGCTAAATAGACTTTGGAACTCACTTCAATCCAGCCTGGACAAACTCATCAGTGTTATCCAGATTTCACAAAGAGACTTCAGACAAAAGATTGAGTTCAGGATGGAGGGTCTGAGGGAGTCAAATGTTCAGATAATGAGATCTTTTAAGTATGTGATCAATGTTCTCCGTATAAGTTTTTAGCATATTATGCAATGGATATTATTAAAGCCAAATGAAATAATCATTATCTATTCCACAAGATTGTTTTCTGAGGGGGGGAATTTTACACCCCAGGAAATTGAGGTCTTTCAGTCA[C/T]AACTGGAAAAGATGGACAAGCGCATTGATACCGCAGAGGGGGCCGTGATACAGGACATGGAGGATAGAGAATCAAAGTGTCTGGACCAGGTTGAGATTTTCAGCTCGTAAGTGAATCACTGTGATCATATACTACAGTCAGTGACTATCTGGTTTTTTTTGTTTGTTTTTTTGCTTAGGCCAAGGATATTTTCAGGAGGTTTGGGGAAAAATTCAGTTTTCATGCTAATGACCTGAAGTTTCTTGAAAAAATGCAACAAATTTTTACCAACACACGAGTCCAGATTAAGAGCGAGGTATGTACATAGTATCATTTAATGATATTTAATTTCTGTCATTCTGTGTTCATAATCTGCTGAATTTGTGCTTGTCTGTTCAGGCTTTGAAGAGTAACATGCAGAAAAAGATGATTGATAGCATGCTGCGTGATTTAAAACAAATGACTGCTGAGTATTACCAACCATGTCCTGATAAGAAGGTAAATGTCTTGAAGTGCCAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40557
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
ENSDART00000042420 Essential Splice Site 1002 1336 26 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 Essential Splice Site 1168 1502 31 39
Genomic Location (Zv9):
Chromosome 5 (position 52822163)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50489359
GRCz11 5 51135952
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGAAGTACCTTATTTTTGGCTCCAACCCCGAAGAGCAGAAGAACAGG[T/C]AAGTGCAACTGTGGTACTTATATATGATATGTTTTGCTTTGTTAATTTCA
Long Flanking Sequence:
CAGGGTTCCAATCAGGGTGACTAGACTTTATATTCTATACTGGACAATATTCCTGTTAAGTGACAAGACTTTTGTCAAAGAAAAGTCAGAACTTACTGTTCTAATTAAATAATTAAAAATCAAGATATCATACAATTTTATTTTGGTGAAATAAGTAATCTAGAGGCCTTGCTTTTCGTATAAGCAACTTCTGATACCAAATGATCAACTAGAGGTCAAGTTATTATTTGTTGTTCTTAAAACTTGGATAGGCGACAAGACTTTTGTCAGGTGGTGTATAGCTACAGTGTTCTACATCTTTTACTGTAATAGTTATTTCAATTCAGTGTACATTTAAAAATGGACATGCATGTGTGTTACAAATTTTTCTTGTTAAATTAACATTTTTAAATGTATTTCTTTGATGCAGTTCTATAAGTGTAAAGAGGTTGCCAAAACTTAACCGATTTGACAAGAAGTACCTTATTTTTGGCTCCAACCCCGAAGAGCAGAAGAACAGG[T/C]AAGTGCAACTGTGGTACTTATATATGATATGTTTTGCTTTGTTAATTTCATGTTTTTTTTTTAATCATTTTTAAAAATATGTTTGTTTCTTAGTGTTTGCTTCAAAACTTCAATTACTGGTATTCTGTGGAAAGCCAATGATATTCTTCTCATGGTGGCTGAGGTACTATAAACATAACAGTTTGTATGGTTTTTTTTTTTTTTTGGTGTATATTGTATATTTTTTTGTATGTAATTTACTATTCTGTAAATCACAATTAGGAGTTCTATAAGAAAGAGCGCCGCCCTATCACTCGTTCCGAGCAACTGCAGGAGACGTTTGATCAATGTGCAGAGGAGATACAGAAAAGACTTCTGGTCTACCAGAGCCAAGCACATGACTACCACAACAGCTGCCTGCAAGGTTCATTCTTAATGTTACTTGGAAAGGAAAAATATTACAATTCATTTTGAAGATATGATAATGTCAGTATTGAGATGGCTAAGTGGTTAGCAGCATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33712
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042420 Essential Splice Site 1210 1336 31 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 Essential Splice Site 1376 1502 36 39
ENSDART00000042420 Essential Splice Site 1210 1336 31 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 Essential Splice Site 1376 1502 36 39
Genomic Location (Zv9):
Chromosome 5 (position 52819422)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50486618
GRCz11 5 51133211
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTTCAGTTCGACAATCTCATTACCATCCATGAGGTTCAAGTGGGACG[T/A]AAGTCTATGTGGTTACACTATGGGAATGTAAAATGATGCCTCACCACCAG
Long Flanking Sequence:
ACAATGGTGATAACAGAGAAAAGTTCCCCAAAAGTTTCTCACATGTTCGTCACTGGGGAAGAAACCAATAACTGTCATGTCACAATATCAACCGTCTGCTTTATATATTTGTTAAATATTAAAGAAGTTTCTGCTTTTTGTGGTCTGCTGTAATAGAGAGAGCATAGTGGTCAGTTGCGTGTGCGTCTCAGTCACCCGGCTTGTGAGAGGGAACTCAAAGCGTTGGTGGAGGCTGAAGAGCAGAGACAGAGACATCACAGAGAGGCCATCCAGCATACCAGACAGGAACTTCAGGTTACTCAGACCTTCAGACTTGAGCTCACTAAGTCATTCTTCTGCCTTTGTTGCTCTTTTTGAGTGACTAAACTTGATTTTGTTTTTGGACAGGCCTGTGTCATCAAAAACGCCGAGGAATCTGTCACTGCTTTTGCCAGGTTGGCAGAGGCCCTGCTATTTCAGTTCGACAATCTCATTACCATCCATGAGGTTCAAGTGGGACG[T/A]AAGTCTATGTGGTTACACTATGGGAATGTAAAATGATGCCTCACCACCAGTTTGACATAAGAAGTGCTTTTGTTAATATATATATATATATATATATATATATATATATATATATATATATATATACACAGCTCAAAAAATAACTACAAGTCAATCACACTTCTCTGAAATTAAACATTAAACTGCCCCATTTAGGAGGAAAAATGGAACAGATTCAGGTTGTGCTGCCAAGTCATAGAGAATTAGCAAAACACCTCTAATAAAGGAGTGGTTCTGCAGGTGGTGACCACTGACCACTTTTCAGTTCCTTTGCTTTCTGGCAGATGTTTTGGTCACTTTTGAATGCTGGCGGTGCTTTCACTCTAGTGGTAGCATGAGATAGAGTCCACAACCCACACAAGTGGCTCATATAGTGCAGCTCATCAAGGATGGCAGATCAATGAGAGCTGTGGCAACAAAGTTTGCTGTGTCAGCGTAGTCACTACCTGGAGACAGGCCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38503
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
ENSDART00000042420 Essential Splice Site 1210 1336 31 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 Essential Splice Site 1376 1502 36 39
ENSDART00000042420 Essential Splice Site 1210 1336 31 34
ENSDART00000111120 None None 313 None 9
ENSDART00000130660 Essential Splice Site 1376 1502 36 39
Genomic Location (Zv9):
Chromosome 5 (position 52819422)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50486618
GRCz11 5 51133211
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTTCAGTTCGACAATCTCATTACCATCCATGAGGTTCAAGTGGGACG[T/A]AAGTCTATGTGGTTACACTATGGGAATGTAAAATGATGCCTCACCACCAG
Long Flanking Sequence:
ACAATGGTGATAACAGAGAAAAGTTCCCCAAAAGTTTCTCACATGTTCGTCACTGGGGAAGAAACCAATAACTGTCATGTCACAATATCAACCGTCTGCTTTATATATTTGTTAAATATTAAAGAAGTTTCTGCTTTTTGTGGTCTGCTGTAATAGAGAGAGCATAGTGGTCAGTTGCGTGTGCGTCTCAGTCACCCGGCTTGTGAGAGGGAACTCAAAGCGTTGGTGGAGGCTGAAGAGCAGAGACAGAGACATCACAGAGAGGCCATCCAGCATACCAGACAGGAACTTCAGGTTACTCAGACCTTCAGACTTGAGCTCACTAAGTCATTCTTCTGCCTTTGTTGCTCTTTTTGAGTGACTAAACTTGATTTTGTTTTTGGACAGGCCTGTGTCATCAAAAACGCCGAGGAATCTGTCACTGCTTTTGCCAGGTTGGCAGAGGCCCTGCTATTTCAGTTCGACAATCTCATTACCATCCATGAGGTTCAAGTGGGACG[T/C]AAGTCTATGTGGTTACACTATGGGAATGTAAAATGATGCCTCACCACCAGTTTGACATAAGAAGTGCTTTTGTTAATATATATATATATATATATATATATATATATATATATATATATATATATACACAGCTCAAAAAATAACTACAAGTCAATCACACTTCTCTGAAATTAAACATTAAACTGCCCCATTTAGGAGGAAAAATGGAACAGATTCAGGTTGTGCTGCCAAGTCATAGAGAATTAGCAAAACACCTCTAATAAAGGAGTGGTTCTGCAGGTGGTGACCACTGACCACTTTTCAGTTCCTTTGCTTTCTGGCAGATGTTTTGGTCACTTTTGAATGCTGGCGGTGCTTTCACTCTAGTGGTAGCATGAGATAGAGTCCACAACCCACACAAGTGGCTCATATAGTGCAGCTCATCAAGGATGGCAGATCAATGAGAGCTGTGGCAACAAAGTTTGCTGTGTCAGCGTAGTCACTACCTGGAGACAGGCCAG
Associated Phenotype:
Not determined