Busch Lab

ZMP

rhoua

Ensembl ID:
ENSDARG00000019709
ZFIN ID:
ZDB-GENE-040618-3
Description:
rho-related GTP-binding protein RhoU [Source:RefSeq peptide;Acc:NP_001007444]
Human Orthologue:
RHOU
Human Description:
ras homolog gene family, member U [Source:HGNC Symbol;Acc:17794]
Mouse Orthologue:
Rhou
Mouse Description:
ras homolog gene family, member U Gene [Source:MGI Symbol;Acc:MGI:1916831]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa42201 Nonsense Mutation detected in F1 DNA Not yet available
sa42200 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa22288 Nonsense Available for shipment Available now
sa38938 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa42201
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046360 Nonsense 66 254 1 3
Genomic Location (Zv9):
Chromosome 13 (position 24602573)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 24248233
GRCz11 13 24378683
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACTTGTTGGGGATGGTGCAGTGGGTAAAACCAGTCTGATTGTGAGCTA[C/A]ACTACTAACGGATATCCCACAGAGTATGTCCCAACAGCGTTTGACAACTT
Long Flanking Sequence:
GTTCAGTTCAGTTTTAGAGAGGGCGGAGGAGGGCTCGTCTCATGAGGGCATAACGTCAGTGTACGTGTGGGCTTCCTATTTATTTTTGCTTCAGAGTTGATTTGTTTTATATCCAGACAAACCAAACACTTCTTGATTTGAGATGTAGCCTTTAGCAGACTGTTTTCCTCTACAATAAATGGACACCGCGGTGAAACCGGAGACTTGTGCTCCTCTCTCTCTCATTCACGAGCGACAAGTGAGATGATAAACTGCTGAAAGTGGCGTTAAGGCTCCGGGACGCTGTTTGCAGTGTTTGCAGCGATGCCTCCGCAGGGAGGAGGTGGAGAGTATAAGCCCGTTCCCGGTACGGTCGTGCCGCCGGTTCCGCCGCGGAGGCTGAGGAGCAGGGACCTGTCCTCTGCGGTCAAGAGTCGCTTTGGGACGGCGGCGGAGCGCAGGGTGAAGTGCGTACTTGTTGGGGATGGTGCAGTGGGTAAAACCAGTCTGATTGTGAGCTA[C/A]ACTACTAACGGATATCCCACAGAGTATGTCCCAACAGCGTTTGACAACTTTGCAGGTAAATATCACTCCAGCATTTAGAACCAAAAGAAAAAGGTAAATCTAAATTAAAATAATCTAATTAAAATAATATATTAATAGCCTAAATATATGGTAGCATCCAGCAATCGGTTAGAAAACCCAGTTTTAGTTGGTGCGACTAGTTTTAGTTGAATAAAGCTGACCAGTATGGTACAAAATGCTGATCAATTTAGACCAGTAATAAACTAGCTACTTACTGGTTAATTTATAATAATACTGTTAGTCAGTGTTTACTTATGAGATTTGCAAACTGTTAATTTTTTTTTGGAAGTAATAAGCTTGAACCTAAAACTTAGTTGTAATTTACAAACTCAATAAATACATTTTCACCTGGGAAACAAAAATGCCTATGCAATAGAAGAAAAAATATTTTGAATATTTGACAATTATTCAGATAAATGTTACTCAGGCACATTAAAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42200
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
ENSDART00000046360 Essential Splice Site 85 254 1 3
Genomic Location (Zv9):
Chromosome 13 (position 24602516)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 24248176
GRCz11 13 24378626
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGGATATCCCACAGAGTATGTCCCAACAGCGTTTGACAACTTTGCAGG[T/G]AAATATCACTCCAGCATTTAGAACCAAAAGAAAAAGGTAAATCTAAATTA
Long Flanking Sequence:
AGTGTACGTGTGGGCTTCCTATTTATTTTTGCTTCAGAGTTGATTTGTTTTATATCCAGACAAACCAAACACTTCTTGATTTGAGATGTAGCCTTTAGCAGACTGTTTTCCTCTACAATAAATGGACACCGCGGTGAAACCGGAGACTTGTGCTCCTCTCTCTCTCATTCACGAGCGACAAGTGAGATGATAAACTGCTGAAAGTGGCGTTAAGGCTCCGGGACGCTGTTTGCAGTGTTTGCAGCGATGCCTCCGCAGGGAGGAGGTGGAGAGTATAAGCCCGTTCCCGGTACGGTCGTGCCGCCGGTTCCGCCGCGGAGGCTGAGGAGCAGGGACCTGTCCTCTGCGGTCAAGAGTCGCTTTGGGACGGCGGCGGAGCGCAGGGTGAAGTGCGTACTTGTTGGGGATGGTGCAGTGGGTAAAACCAGTCTGATTGTGAGCTACACTACTAACGGATATCCCACAGAGTATGTCCCAACAGCGTTTGACAACTTTGCAGG[T/G]AAATATCACTCCAGCATTTAGAACCAAAAGAAAAAGGTAAATCTAAATTAAAATAATCTAATTAAAATAATATATTAATAGCCTAAATATATGGTAGCATCCAGCAATCGGTTAGAAAACCCAGTTTTAGTTGGTGCGACTAGTTTTAGTTGAATAAAGCTGACCAGTATGGTACAAAATGCTGATCAATTTAGACCAGTAATAAACTAGCTACTTACTGGTTAATTTATAATAATACTGTTAGTCAGTGTTTACTTATGAGATTTGCAAACTGTTAATTTTTTTTTGGAAGTAATAAGCTTGAACCTAAAACTTAGTTGTAATTTACAAACTCAATAAATACATTTTCACCTGGGAAACAAAAATGCCTATGCAATAGAAGAAAAAATATTTTGAATATTTGACAATTATTCAGATAAATGTTACTCAGGCACATTAAAACTATCTATCTGTCTGTCTTTCTATCTTGTTATAAAATATGATATATGCATTTTGGCAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22288
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
ENSDART00000046360 Nonsense 193 254 3 3
Genomic Location (Zv9):
Chromosome 13 (position 24596880)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 24242540
GRCz11 13 24372990
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGAGACCAGTTGAACCGCAGGATGCCAGCGTGTGCGCTGAAGAAGTC[C/T]AGGCTGTGTCGTACATGGAGTGTTCGGCGCTCACACAGAAAAACCTGAAG
Long Flanking Sequence:
ATGGAGAGTGCTCATAAACCACATATACAAGTGCACACACACACACACACACACACACACACACACACACACATAGATGTCAGGCCTATAAATGACTCAATATATTATGTAAAACACTTTTAAAAAAAAAACCTCTGGGCATTTTTCTGTCCACTGATTTTTGCAATTCAGAACATTAAGTGTTCATTTCTGATGTTTATTGCTTCTGAATGTTATTTTTTTTTTCCTTTGGGCAGGATGAGTTTGACAAGCTCCGGCCGCTGTGCTACACCAACGCTGACGTCTTCCTGCTCTGCTTCAGTGTGGTAAGTCCCTCCTCTTTCCAGAATGTGAGGGAAAAGTGGGTGCCTGAGATCCGCCGGCACTGCCCGCGGGCACCAATCCTGCTGGTCGGCACTCAGTCTGACCTTCGGGAGGACGTCAAAGTGCTCATCCAGCTGGCCCAGTACAAGGAGAGACCAGTTGAACCGCAGGATGCCAGCGTGTGCGCTGAAGAAGTC[C/T]AGGCTGTGTCGTACATGGAGTGTTCGGCGCTCACACAGAAAAACCTGAAGGAGGTGTTTGACACGGCTATAGTGGCCAGCATCCAATACTCGGACAGCCAGCAGCAGAAACGGCTAAAGAAGAGGACACCCGATAAAATGAGAAAGCTCTCCGAGTCCTGGTGGAAGAAATACTGCTGTTTGGCTTGAAGCGAGAGTATGATTGTATACTGTTTGACTGGAACTCACTTTTGCGGATAGAAAGAGACTGCTTTATGAGACCGTGTTAGTGGATTAACTGGAGCGCAGGTGGCTGTGAAATGAAAAGGATGGTTTGGAAAGAATCATAAAGACTCAAAGCTGTCGGCTACGTTTTGGAGTTAGGAAAGTCCCAGGTTAACCTCTAATACTCATGTGAACAATTCAAGACGAGAGCCATCTGTCTTTCTTTACCTTATCTCATGTTGAAGAGGGTTTCAAGTGGACTTAAGGGATGCTTTTCTATCAGGAGATCTAGTTTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38938
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
ENSDART00000046360 Nonsense 205 254 3 3
Genomic Location (Zv9):
Chromosome 13 (position 24596844)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 24242504
GRCz11 13 24372954
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCTGAAGAAGTCCAGGCTGTGTCGTACATGGAGTGTTCGGCGCTCACA[C/T]AGAAAAACCTGAAGGAGGTGTTTGACACGGCTATAGTGGCCAGCATCCAA
Long Flanking Sequence:
ACACACACACACACACACACACACACACACACACACATAGATGTCAGGCCTATAAATGACTCAATATATTATGTAAAACACTTTTAAAAAAAAAACCTCTGGGCATTTTTCTGTCCACTGATTTTTGCAATTCAGAACATTAAGTGTTCATTTCTGATGTTTATTGCTTCTGAATGTTATTTTTTTTTTCCTTTGGGCAGGATGAGTTTGACAAGCTCCGGCCGCTGTGCTACACCAACGCTGACGTCTTCCTGCTCTGCTTCAGTGTGGTAAGTCCCTCCTCTTTCCAGAATGTGAGGGAAAAGTGGGTGCCTGAGATCCGCCGGCACTGCCCGCGGGCACCAATCCTGCTGGTCGGCACTCAGTCTGACCTTCGGGAGGACGTCAAAGTGCTCATCCAGCTGGCCCAGTACAAGGAGAGACCAGTTGAACCGCAGGATGCCAGCGTGTGCGCTGAAGAAGTCCAGGCTGTGTCGTACATGGAGTGTTCGGCGCTCACA[C/T]AGAAAAACCTGAAGGAGGTGTTTGACACGGCTATAGTGGCCAGCATCCAATACTCGGACAGCCAGCAGCAGAAACGGCTAAAGAAGAGGACACCCGATAAAATGAGAAAGCTCTCCGAGTCCTGGTGGAAGAAATACTGCTGTTTGGCTTGAAGCGAGAGTATGATTGTATACTGTTTGACTGGAACTCACTTTTGCGGATAGAAAGAGACTGCTTTATGAGACCGTGTTAGTGGATTAACTGGAGCGCAGGTGGCTGTGAAATGAAAAGGATGGTTTGGAAAGAATCATAAAGACTCAAAGCTGTCGGCTACGTTTTGGAGTTAGGAAAGTCCCAGGTTAACCTCTAATACTCATGTGAACAATTCAAGACGAGAGCCATCTGTCTTTCTTTACCTTATCTCATGTTGAAGAGGGTTTCAAGTGGACTTAAGGGATGCTTTTCTATCAGGAGATCTAGTTTAGTCTGCCAGAATGTGCTTTTTTTAATTCAGGCTCTGT
Associated Phenotype:
Not determined