Busch Lab

ZMP

si:dkey-117k10.8

Ensembl ID:
ENSDARG00000052332
ZFIN ID:
ZDB-GENE-081105-171
Description:
Novel protein with a Zinc finger, C3HC4 type (RING finger) domain [Source:UniProtKB/TrEMBL;Acc:A9C3N

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41268 Nonsense Mutation detected in F1 DNA Not yet available
sa27249 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41268
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
ENSDART00000074163 Nonsense 197 627 7 12
ENSDART00000139266 Nonsense 25 350 2 7
Genomic Location (Zv9):
Chromosome 8 (position 41790612)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 39804192
GRCz11 8 39837966
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGATCCACTTACCAACTTCAGGGGTGGAGAAAATTATCCTTTGGATTA[T/A]AGGTAAGTTTCAGAATCATTTATTTTCTGTACTTTTAAGGCACGCTGTAT
Long Flanking Sequence:
TGTGTTTCCATTTTTGTACAAAGGTTTGTCTGCACATAAGACAACATGAGTCTGAAAGAAAAGAGTGAAAGGTGCCCATGTTTAACTGCTTTCTTATTTTTTTTGACCTGCTTGAATGCTGTAAAATAAAACTATCTCCTTGAAAAAAGATACAGTATATAGACATTCAAATACTCATATCGTATATTATTTTGTAGCGAGTATAAAAGAAAGAGAGCAAAATCACCCGAGTTTATCAAAGGAAACACAGACCTCAGTAAAGAAGAAAGTGGTCATGATGAACACAAAAATAAAAGGTAGGCTAAATAATTATGTGTGAGTACACATCCATGTTCTGGGGACTTATTGTGAGTTTTGACAAAATCATTAACATTGTCTGTCCTTAGAGTCAAATACGAGAGGGCACTCTCTCCTACCCCCAGTTGTATGTCTTTGAGATCAGAATGTTCAATGGATCCACTTACCAACTTCAGGGGTGGAGAAAATTATCCTTTGGATTA[T/A]AGGTAAGTTTCAGAATCATTTATTTTCTGTACTTTTAAGGCACGCTGTATGATTTTTTTTTTCTCATTAAAGTATAAAAAACACTAGAAAGATGTTGTGTATTTTGATGACTTATGTATTATACATTATGCTAAATGTTTCGAATAATGTTCAATTTCAGAGAAATAACCAGTTTAACTGGTAGCACCAAGGGCATAGATTTGCTCTTGACATTGGTAGGGACCTATGAATTCCCCCATTAGGCATTGTGATATAAGATTCTGGTGGGATGATAACTTTGGATAAAAATATGATATATTCATGTATTGTGACTACTGCTCTAAAATATGCTCTTTTTATATGTCTAGGTAAAAACCAACAACTTTTTCCCCATTGAACACAATATATTTTATTTTAAGAGACATTTTAAACATTTTGGAACAGTAAACATGTCAGGCTAAATAATTAAACTAAATCATTAACTTCTGCTGTCTTTGTTAGTTTCAAAAACATTGATTTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27249
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074163 Essential Splice Site 258 627 9 12
ENSDART00000139266 Essential Splice Site 86 350 4 7
Genomic Location (Zv9):
Chromosome 8 (position 41787716)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 39801296
GRCz11 8 39835070
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGACAGTCTCAACAAACAACAGCCAAATGGACAACACCTTCATGCTAAAG[T/A]AAGGGAATGTGTTACATGTGACCCTGAGACACAAAACCCAAAACTTTCTC
Long Flanking Sequence:
CATTTAGAATAGTCACCAATAGTGGTGTTTTGTTGGTTGCGTATCCTTAACTCTTGAGTTCCCTTATCATAAACAATTTTGAACAGTTGCTAATAGCATTTTATTGGTATGAACCTGAAAACAGTTTCTAGCAGTGTGAGCTTAACTGGTTGTCTCTTTATAGAGTAAAGCCAGAAAGAGCAGCTTCTCCTACAATCAGCTACATGTCTTTAAGAACAGACTGGTCTATGGATCCACCAAGCAACTTAAGAGATGTTCCTTTGGATACAAGGTGCATTTCATATATTTATTTACAGTGTTTTTGAATTTCTTTTAATAATTCTTTGATTTGTTATGGATCAAATATATAAATACTATTTAATGGACCAATATATAGATTAGAATTAATCAATATATGATACAACATGTAAAAAGATGCATTTTTCAGGATTAAGGAAGAAAATGAGACAGCGACAGTCTCAACAAACAACAGCCAAATGGACAACACCTTCATGCTAAAG[T/A]AAGGGAATGTGTTACATGTGACCCTGAGACACAAAACCCAAAACTTTCTCACTCTCGACCCCACTTGACTTACTCTTGCTCACTGATATATTCTGATTAAAAAATAAGCTCCAGGTCATTAGCATGATGTGATTAGTCATGAGACCCAGAGGGAGCCAACTGCATTCGACAACAGAAGCTGACATAAAACGATTTTCCAGCAGCATTGAATTTGTCACAGAAAACATCTGAGCAGTGGAGATGCAGATCGCGTCAACTTCTAACAGAAATAGCAAATGCTGACTTGGAAGACTTGGAATAAACTGCAACTGTAGTTGTGTCTGTCTGCTATATCCTGTGTTTTTGTATATTTACCAGCGGTTGTGTTTAGTGCTAGTAGCTGGATTAAGTGCGTAAAAATGTGTTTGTAGTGTAATGAAAGTAAAATAGTTTTGATTATAAAAACTCCCACTCCAATAGTGGCAAAAATATTACCCAATATGTCAACAATGGATAACCCC
Associated Phenotype:
Not determined