Busch Lab

ZMP

im:7145024

Ensembl ID:
ENSDARG00000089139
ZFIN ID:
ZDB-GENE-050208-187
Human Orthologue:
C11orf74
Human Description:
chromosome 11 open reading frame 74 [Source:HGNC Symbol;Acc:25142]
Mouse Orthologue:
B230118H07Rik
Mouse Description:
RIKEN cDNA B230118H07 gene Gene [Source:MGI Symbol;Acc:MGI:1915420]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa15742 Nonsense Available for shipment Available now
sa45018 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15742
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000131193 Nonsense 19 229 1 6
Genomic Location (Zv9):
Chromosome 25 (position 9256177)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 8950840
GRCz11 25 9027908
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGTKTAGTTAATGTTTCAGCTATGAACAATCMCGACCAAGCCGTGGCT[G/T]AAGCTCTGGATCAGTTCTGCAACGCCCSGGAGCAAAYATACGAGCAGTTC
Long Flanking Sequence:
AGAATCTCCGATTTCAAGTCCGCCGAGTCCCTCCGAAGGGGATAAGGGCTTCCGCGATTGGGTGACGGTGGAACTCAAAGACGAGCTAGCGTTAGGCCTTCTGTAGAACCAGATGAGGCATCGTACTTGTACTTGCATAGTTTTTCCACCATAAGCTAGTATTTTAGAAACACATTCGAAGCAGAGATCACACAGTGTTTTGATATATGCCGCTGGTTTTATATCGTATAGCAGGAGATCGTCGGGAGCTCAAGCCAGACACGTCTTACTCCTTTGCCATGCAACCGGAAACCCAGCATGACAAGATTTTCTTTGTTTGGGTTGAACTAACTTTAACGTGGCATGGAAAATTGGCTTTCTGTACAGTTGGCTTTAATATAGTAACAGGCAAATATCAATCTTTCTGTATCTCTTCTTTTCTTAGTGTTTAAGAGAGGCTTGATGGGATGCCAGGTGTAGTTAATGTTTCAGCTATGAACAATCCCGACCAAGCCGTGGCT[G/T]AAGCTCTGGATCAGTTCTGCAACGCCCGGGAGCAAACATACGAGCAGTTCCTGTCCACTTTCACGTACCTGACTCCAGGTGATCATATTTAATACCACATACATCTTCTTTTCTCTGAAACATCCATTACTCCTTTGCCTGTGGACGTACTGTCGTATCCCATTGCAGAGAATGTGAGGGATCTGCGTTTGACTGCTCCTGGAGGACATAGAGACTTGTCCCGTAGAGAGATGGACAGCAGCCGAGAGCGACAACGAGTGGAGGAGGTGACAATGATGGAGGAGAGCATGCACCGACGGATGGGACAGGCCAACCGCTGCTCACCGACTGCTGATCAGGAAGAGGTCACAACCTTATAGATTTGACCCGCTCTGTCCGACAGTCTTTACCGGGAGAGGTTTAGCCAGACTTCTCCTTTACTTCCATCATTAAAGTGTTTAGCGTTAGCCGCTTTCCTGCTTATCTTTCACAGACCCACACTAATGTTAGAGATGCACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45018
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
ENSDART00000131193 Essential Splice Site 44 229 1 6
Genomic Location (Zv9):
Chromosome 25 (position 9256256)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 8950919
GRCz11 25 9027987
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGCAAACATACGAGCAGTTCCTGTCCACTTTCACGTACCTGACTCCAG[G/A]TGATCATATTTAATACCACATACATCTTCTTTTCTCTGAAACATCCATTA
Long Flanking Sequence:
GACGAGCTAGCGTTAGGCCTTCTGTAGAACCAGATGAGGCATCGTACTTGTACTTGCATAGTTTTTCCACCATAAGCTAGTATTTTAGAAACACATTCGAAGCAGAGATCACACAGTGTTTTGATATATGCCGCTGGTTTTATATCGTATAGCAGGAGATCGTCGGGAGCTCAAGCCAGACACGTCTTACTCCTTTGCCATGCAACCGGAAACCCAGCATGACAAGATTTTCTTTGTTTGGGTTGAACTAACTTTAACGTGGCATGGAAAATTGGCTTTCTGTACAGTTGGCTTTAATATAGTAACAGGCAAATATCAATCTTTCTGTATCTCTTCTTTTCTTAGTGTTTAAGAGAGGCTTGATGGGATGCCAGGTGTAGTTAATGTTTCAGCTATGAACAATCCCGACCAAGCCGTGGCTGAAGCTCTGGATCAGTTCTGCAACGCCCGGGAGCAAACATACGAGCAGTTCCTGTCCACTTTCACGTACCTGACTCCAG[G/A]TGATCATATTTAATACCACATACATCTTCTTTTCTCTGAAACATCCATTACTCCTTTGCCTGTGGACGTACTGTCGTATCCCATTGCAGAGAATGTGAGGGATCTGCGTTTGACTGCTCCTGGAGGACATAGAGACTTGTCCCGTAGAGAGATGGACAGCAGCCGAGAGCGACAACGAGTGGAGGAGGTGACAATGATGGAGGAGAGCATGCACCGACGGATGGGACAGGCCAACCGCTGCTCACCGACTGCTGATCAGGAAGAGGTCACAACCTTATAGATTTGACCCGCTCTGTCCGACAGTCTTTACCGGGAGAGGTTTAGCCAGACTTCTCCTTTACTTCCATCATTAAAGTGTTTAGCGTTAGCCGCTTTCCTGCTTATCTTTCACAGACCCACACTAATGTTAGAGATGCACAATATTGGAAAATTTGATTTGTGATATTTTTCTGCGATTACATTCTGCCTCTATTTGTAAAGAATTAATCATTTGGATTATT
Associated Phenotype:
Not determined