Busch Lab

ZMP

zranb3

Ensembl ID:
ENSDARG00000088281
ZFIN ID:
ZDB-GENE-060712-1
Description:
Zranb3 protein [Source:UniProtKB/TrEMBL;Acc:Q6DC67]
Human Orthologue:
ZRANB3
Human Description:
zinc finger, RAN-binding domain containing 3 [Source:HGNC Symbol;Acc:25249]
Mouse Orthologue:
Zranb3
Mouse Description:
zinc finger, RAN-binding domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1918362]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa37454 Nonsense Mutation detected in F1 DNA Not yet available
sa45757 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa37454
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
ENSDART00000123231 Nonsense 152 269 4 6
ENSDART00000136408 Nonsense 147 264 3 5
Genomic Location (Zv9):
Chromosome 22 (position 12403748)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 12256989
GRCz11 22 12291037
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTTGACATCTTGCTCTTTCTTTCAGCTTTTCATGCAAATCGATGCTT[T/A]GTATCCGCGGAGGTTTGGAACCTGGAGTGACTACGCCAACAAATACTGCA
Long Flanking Sequence:
TCCCGCAAACTAAATCTACGTCAATGTGTACATAAAGACCTCTCAGGCTGGACTCTGGTGTGTAATAACGAGTCTCAACCTCCACTGCTTCTCTAATTCCTCTGAAACGTCTTGCCGGACTTATGAAAGACACCCTGTTTTCTTAATTCATCAAGATAATCGCTGTTTAGTTTATACTAATATGCACTGTGAGACTTTCTCTTAGAGGAAGCGCATTTGCATTTTATGAACTTAATACCTGATTTAATCAGCTTTAATCAGCAGAGTATTCGTCGGCGCCGGCTATAAACAGAATTCTGCTGACTAGTTTTCAATAAACTCCTGATTGCGCAGGTCTGAGGTCAGAACTTTAACAGTGTCCCCTCTTTTTAATGCTATTTGTTCCCATTTGGATGTTGCTGCTGTAAAGTTTGTTGTGCGTGTGTGTGTGTGATTTGTGGGGTGTCGCATTGATTTGACATCTTGCTCTTTCTTTCAGCTTTTCATGCAAATCGATGCTT[T/A]GTATCCGCGGAGGTTTGGAACCTGGAGTGACTACGCCAACAAATACTGCAACGCACATTATAGGTGAAAACCTTTCTTTTTATTGCACAATACGGCATTCAATTGACAGCTTAAAGGTCTCGTGAAGTGCTTTGAAATGTGCATTTTTATTCGATGTTTGACGTAATCTCAACCAAAACATGCAGAGGGTGGGACATAATATAGCTCCTCCCCTTTTAAACAAAAAACAGCCAACAGCGTTTTGTTTTATCATCGCTCTGCCATTGAGAAGTGTCTTGAAGGGGGCGGGGCATTTCTAGAAAGCAATTGATTGGTCGAAAGATTTGATGAGAAACTGAAGTATGAGGTGACATGAATAAAATCCTTGATCCATTTGGGTGGAAGTGATAAACTGAAAGCTTTACATGTTTATATCAGTTTTATATCTTCTAAAGACAATTTTTGTCTCTAGCTTATAAACATCCTAAAAACTAATATGGATACTAACATCTAAAAGACGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45757
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
ENSDART00000123231 Essential Splice Site 173 269 5 6
ENSDART00000136408 Essential Splice Site 168 264 4 5
Genomic Location (Zv9):
Chromosome 22 (position 12408147)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 12252590
GRCz11 22 12286638
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAAATGAGATGGATGTGAATTATGTGTGTGTGTGTGTTTTGTTTGCGC[A/T]GGTATTTCGGGGCCAGACGGCAGTGGGATTGTCGCGGCGCGTCTCATTTG
Long Flanking Sequence:
TTTTCTCTGTTAAGTTTACATTTTACACCAGTAACGACACACCTCCGGTTTCTTGAAATGCTATCTATCTAGACAGCTGAGTGGGTTTTGCTGCAGTGCTAATTTGTTTACGCGTATGTGTGTGTGTGTCTGTGTAACAGCAACATGAATGTGAAGCTCAGATATGAGTTGTGTCATGAAGGAGAGTGTTCACAACACATCTGAGAGGAGTTTTGTTCCTCTGTTCCTCTTCCTATCAAACCTACAGCGCAGAAATGAAATGACAGCGATTCACACAAGGGTCTCCGAGTACAAATTAATCTAGCGAGGAAAAAAAAAACACATGCGCGCACACACACACAAATTCCTGTCAATCATTCATATATGCGGCAGTACATGTAAAATATTCATAATTAAGTCTCTCACGCACACGTTTGGGACAGAGATGGTGTCGTTATGGTGAGGATTATGATGAAATGAGATGGATGTGAATTATGTGTGTGTGTGTGTTTTGTTTGCGC[A/T]GGTATTTCGGGGCCAGACGGCAGTGGGATTGTCGCGGCGCGTCTCATTTGGATGAGTTACACAAGCGTCTGAGTGAGATCATGATTCGCAGACTGAAGAATCAGGTGCTCACTCAACTGCCACCCAAAATACGCCAGCGAATTCCCTTTGACCTGCCCAAAGATGCAGCAAAGGTAAACCGTGACGCCACACATTCACAGTTGAGCATATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATCAATTACATTTATTTCTATCATGCTTTTTGCATTGTACAACGTTTCTAAGCCACATTACATTTACATTACTTGCATTATTAATAGTCTTTTACATTTTTATTATTTCTGTATATACAGTGTTGGGGGGTGGATTCAACACATCATTTTTTTTCTGGGAAAAATATTCTAAAGGAGCTATTGACATGGAATTGAACCAGATTTTGGTAAAAACCCAAACAAATCAAACATAAAAATATAC
Associated Phenotype:
Not determined