Busch Lab

ZMP

NP_001185682.1

Ensembl ID:
ENSDARG00000073962
Description:
hypothetical protein LOC564862 [Source:RefSeq peptide;Acc:NP_001185682]
Human Orthologue:
C15orf57
Human Description:
chromosome 15 open reading frame 57 [Source:HGNC Symbol;Acc:28295]
Mouse Orthologue:
Ccdc32
Mouse Description:
coiled-coil domain containing 32 Gene [Source:MGI Symbol;Acc:MGI:2685477]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa28883 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa28883
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
ENSDART00000114820 Nonsense 129 183 3 3
Genomic Location (Zv9):
Chromosome 17 (position 31287420)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 31211347
GRCz11 17 31228310
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATAAATGGTCTGCGTGTAATTATTCTGTCTTGGTATTCTTGTAGTGCTT[T/A]GGAGCAGTTCAAGCGCTGGCTGTCTCCTGAAAGAGTGGCCATCAATGCAG
Long Flanking Sequence:
TTTGAATTTAAAGCGACAATCACCAAAAATAATTAAATGTGGAGAATTTAGGCTGAAACTTTACATACACACTTAAGGATATCAAAGACTTATTTTACAAATAATAAAAAGAATTGGGGCATAATAGGTCCCCTTTAAAACATCTACAAGCTACTAAATGATTCCCCACTGGGGGCAATCAGTGAATTCCATGATTCATGTGGATTTTATGGTATTATACGAATCCTTCCAATAAAGAAATAATTAATTCTTGAAAGGTTTTGAAATTGACTATGCCAATTTGATATGCACTTCAAACCACTTTTTTGAAAAACAAAAGATTTTTACTACGATTCAAAGCTTCATAAAGCACCGAAAAAAGCAGACATCATTAAGAGACTGTGTTAATACAATGTGTTAAAAATGATATGACAAAGCACATAAGAACAGTTCCTGTCTGTGATTATGTTGAATAAATGGTCTGCGTGTAATTATTCTGTCTTGGTATTCTTGTAGTGCTT[T/A]GGAGCAGTTCAAGCGCTGGCTGTCTCCTGAAAGAGTGGCCATCAATGCAGAAGAGCTGGAGTACCTTCTCCTGCCCACACAGAACAGCGAGACCCCTGCCAGCTCCAGCCAAACTGACAAACCCTGTGTGGAGGAGGAGGAAGAGTGCCCGAGTCCAGAGAAATAATGACCATATCACAGCACAACCTGTATGCTGACCAGCAGTACAAGCGCATATTGTGATCCATTTAATGGGATAATATGTTTTACAGAAATAAATTAAGCTGGTGCTCGATTCAAGATGAATTATTGTACACATTTTTGTTGGTATATGAATAGATCAAATCTCTTTATTGGAGATATTATGCTTGCCAAGTAACATATTGTGTGGATGGAGGAAGCCAGTTTGTTATGAGAAAGTATGTGTATAAACAACATCACTACGTCATCATGTAACATTCCATGTATGTATCATCTGATGCATTTCTGTATGTGTTGATTTTTCTCCCGCCTGTAGTATT
Associated Phenotype:
Not determined