Busch Lab

ZMP

smc4

Ensembl ID:
ENSDARG00000038882
ZFIN ID:
ZDB-GENE-020419-21
Description:
structural maintenance of chromosomes protein 4 [Source:RefSeq peptide;Acc:NP_775360]
Human Orthologue:
SMC4
Human Description:
structural maintenance of chromosomes 4 [Source:HGNC Symbol;Acc:14013]
Mouse Orthologue:
Smc4
Mouse Description:
structural maintenance of chromosomes 4 Gene [Source:MGI Symbol;Acc:MGI:1917349]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa35784 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa35784
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
ENSDART00000056765 Nonsense 416 1289 9 25
ENSDART00000130413 Nonsense 416 1289 9 24

The following transcripts of ENSDARG00000038882 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 1547171)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 1587056
GRCz11 15 1551965
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGCGAGAAGCTCAAACACACCAAGAGCAAAACCAAGAAACTGCAGAAA[C/T]AGCTTCAGAAAGACCAGGAGAAGGTGAGACTTTATGATGACCACAATCCA
Long Flanking Sequence:
TGTTCGTTGAGTTTAAATAGACACACGGTCACTGGAGTGTTTTAAAGCCACATAGATAAGTTGATTGATCAGCGGATCGCTTGTATGTCGGCTCATAAACAGACCAGCTGATTGACACAGCTTTGAAACACTCCAATGCTTATGTATCTGTGTTTACACTTGGTGAACCTTCACAGTCGTTTCTGTTGAGCATGTGAACACAATAGGCAATCGGTGGTGTTCAGGAACAAGCTCAACAGCGCTCAAATGTTAGCGGGAAATGGAGGTTTTTAAAATACCACTACTGATTGGTAACAAACTCCATACTTTGACAATCCTACTTGTATAGTTTCATAATTCAGGTATTTTGTGAATGTTGTTTTTCCTGCTAAAGAAAATTGACCAAGCTGACCAAGTACATCGAGAGCCAGAAGGAGAAGTTCACCCAGCTTGACCTGCAGGATGTGGAGGTGCGCGAGAAGCTCAAACACACCAAGAGCAAAACCAAGAAACTGCAGAAA[C/T]AGCTTCAGAAAGACCAGGAGAAGGTGAGACTTTATGATGACCACAATCCATGGTCTTGCAATACGAAATGGAGTCAGATCCAGATTGAATACCCTGATGGTCCATATCCGGAACAGAGTCTGGACTTTGAGAAGCCCTGCACTAGAGTGTTTATCATGCACATACAGTTGAATTCATAATTATTCACCCTCCTGTGAATTTTTTGTTTTCATTCTCAAATATTATCTCAAAATAATATTAAAGCCATTTTAAGGTCAATATTATTTGCCCCCTTAAGCAATATTTGTCTTGGATTGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGAACACTAGTGTCTTGAAGAATATCTAGTCTAATATTATGTGCTGTCATCATGACAAAGAAAATAAATCAGTTATTAGAGATGAGTTACTAAACTATTATAATTTGAAA
Associated Phenotype:
Not determined