ZMP
mcm3ap
Ensembl ID:
ZFIN ID:
Description:
MCM3 minichromosome maintenance deficient 3 (S. cerevisiae) associated protein [Source:UniProtKB/TrE
Human Orthologue:
MCM3AP
Human Description:
minichromosome maintenance complex component 3 associated protein [Source:HGNC Symbol;Acc:6946]
Mouse Orthologue:
Mcm3ap
Mouse Description:
minichromosome maintenance deficient 3 (S. cerevisiae) associated protein Gene [Source:MGI Symbol;Ac
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13572 | Nonsense | Available for shipment | Available now |
sa17895 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13572
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008053 | Nonsense | 722 | 2118 | 7 | 30 |
ENSDART00000056051 | Nonsense | 722 | 1820 | 8 | 26 |
ENSDART00000142512 | Nonsense | 722 | 2082 | 8 | 31 |
The following transcripts of ENSDARG00000021402 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 39517611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38655507 |
GRCz11 | 9 | 38465302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGACTTTTGAGTGGATTACATTATCACCTTCTGCTTAGGTGGATCATTA[T/A]GCTGCTAKCAAAGAGTATAGCAGGTCTTCAGCTGATCAGGAAGAACCTTT
Long Flanking Sequence:
GCATAATAAAGAAAAATAACTTTATTTAACAGTTTCTTCTTACAGTCAGTATACGGTGGATGTTTATGTTTCTCATATTACCTCAGATGTGCATGTGCTTAGTTTTAAACAGAGAATAAACTGTTGAATAAAGTAGTTATTTTTGTTTATGTGCACACAAAAGTATTACTGCTCTAGGCATATGGTATGTTTTGAGGGTGTTTTTGGTAACCTTCTGCACTTTAAACCAGTTAGGAACCTACATATGTATATGGAGGATGAGGGAGCTCTCACCTAAAGTAGCTTAATTTGTATTCTAAAGATGAACAAAGCTCTCAGCGATTTGGAATGACATGAGGGTGAGTAATTAATAACAAAATTATAATCAATTTGGTTATTACTACCTTTAAATGCTTGGATACCTTCAAAGATTTGTGTAGTCATTTGTGTGACAAACTTTGTGTGTCTTTGGTGACTTTTGAGTGGATTACATTATCACCTTCTGCTTAGGTGGATCATTA[T/A]GCTGCTATCAAAGAGTATAGCAGGTCTTCAGCTGATCAGGAAGAACCTTTACCTCATGAGCTTAGACCCCTTCCTGTGCTAAGCATGACTATGGACTACCTGGTGACTCAGATTATGGACCAGGGTGAAGGCAATTGCCGTGACTGGTATGACTTTGTCTGGAACAGAACCAGAGGCATTAGGAAGGTGGGCATTTAATTGCTTTTAATTGCTTCATTTACTATTGATTTGATTGTATTATTCATTTAAATATAAAAACTAATTGATTTAATATAAACTTCTTCTCTGTATTAAGTTTGTTACAATTTCTTCTTTTCTTGCAGGACATTACCCAGCAGCATCTGTGCGATCCAGAAACAGTATCTCTCATTGAGAAATGTACTCGTTTCCACATTCACTGCGCCCATCACCTCTGTCAGGAACCTATGATGTCTTTCGATGCCAAGATCAACAATGAGAATATGACAAAATGCCTGCAGAGTCTAAAGGAGATGTATCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17895
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008053 | Essential Splice Site | 1492 | 2118 | 20 | 30 |
ENSDART00000056051 | Essential Splice Site | 1456 | 1820 | 21 | 26 |
ENSDART00000142512 | Essential Splice Site | 1456 | 2082 | 21 | 31 |
The following transcripts of ENSDARG00000021402 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 39525917)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38663813 |
GRCz11 | 9 | 38473608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGACCAATATTAGGGGACAGACTCATGAAGTTTACATTTCTGTAAAGG[T/C]RAGCTTATAGWGTAAATANTTTGAAMAAATTTGATTATTATTTACTYCAT
Long Flanking Sequence:
CAGTTCATCAAATGAAAGTGTCCTATTACTACAATCTCTTAATGAGGTGAGGCACAGTGACAAGACGACTTGGAATAGATGTGCAGAATGCCGATAATTTATTTTTAATCTATGTGGCTGAATAATTGTTTGGCAGTGAGCGTGTATGGATGCCTCTTGACCTGCCCACACTTGTGGCAGAGAGCACTCCTAATGCACCTGACAGAATCTTCTGGAAAGCTACGCTTCTGATGCCAAGCAGCTGCGATAGTGACATAACCTTTGCCAGCAGGTGAGTATTGAAAAGATCGTAAAGTTTTTTAAAACACACAAGATAAAAACTGACTTGTGTTTGTTTCCATGCAGAATTCTGACAGATTGGCTTGAGGTTAAATTGGGTGGAGGAAATGAATCTGAAGAGAGTGAGAAACAATCAAAAGGGCAAGTGAAAACGCTGTGTGTCAGTCACAGCCTGACCAATATTAGGGGACAGACTCATGAAGTTTACATTTCTGTAAAGG[T/C]GAGCTTATAGAGTAAATAGTTTGAACAAATTTGATTATTATTTACTTCATTACATCAGTCCTACGCCTCAGTCACTTCAATATCACCATCATTAAGCTTGTGTGTGTGCATTTGCACAGGCATGCCATGGACCTTTGAGTGCAGAAGACCAGTGTCTGCTGGAGGAGCAGAAGGAGCTCCATGGTACCAATGCTCTGCTGATGCTGCTTCCCCCTGTTAACAGTGCTGGACAGGGGGAAGAAGAAGAAGAAGAAGAAGAGGAGGAGGACCTGCCACTGCTCTCTGCCCTCCTCCAGCTGAGGCAGGTACAGCAGGCCAGCTGCTGGCATTCTCCTCTACCACTGGCTGTGGTGGTCGCTGGCAACCAAATTGGTGATCAGGGTTTGGAACAAGGCAAGTAATAATCGAAAAGTTGGAAACACTTTATAATATCTACACACTATGAATCATTTGTTAAGCATTAGCAAATAGTTAATTCATTATCTGTTTAGCATTAACTC
Associated Phenotype:
Not determined