ZMP
mcf2
Ensembl ID:
ZFIN ID:
Human Orthologue:
MCF2
Human Description:
MCF.2 cell line derived transforming sequence [Source:HGNC Symbol;Acc:6940]
Mouse Orthologue:
Mcf2
Mouse Description:
mcf.2 transforming sequence Gene [Source:MGI Symbol;Acc:MGI:96932]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35715 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28332 | Nonsense | Available for shipment | Available now |
sa11503 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35715
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034883 | Essential Splice Site | 252 | 1111 | 7 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33354093)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32143900 |
GRCz11 | 14 | 32484214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTGAGTTCCTCTTGCTATCCCACACTGAGAAATACAGGAGGCTTAAG[G/A]TAATTTAATGGTTGTGCATTTGCAACTTTAACACTCAACAGTTACTGGCC
Long Flanking Sequence:
AGCTTCTTCCAGCGCACCGTCACAGACCTCGGCTTCCGCTTTAGTCAAGAGGACTTCATGCTCAAAATGCCCGTAGGACTCATTGCAGACCCTAATTTTTTGTAATTCATGCTGTTTGGGAACTTCATTACCAACCCTGACCTGCATGTATGTCTGTTCAGGTGGTGATGCTGAGCTCGGTCACAGATCTGCTGCGGTACATTGATGAAAACCAGCTGACCTCCGAGTTTGGAGGGACTCTTGACTACTGCCACAGCGACTGGATTGTCCTGAGAACTGTAAGTACAGTGATGTCATTATATAAATACACAGAAACATCACATTATACTGAAGACGTTTGCTCTTTACAGGCTATTGAGAGTTTTGCAGTTATGGTTAAGGACATTGCTCAGATGCTGCAGGCGTTTGGTACAGAACTGGCCGAAACACAGTTATCAGAAGAGTGCAGCGCTATTGAGTTCCTCTTGCTATCCCACACTGAGAAATACAGGAGGCTTAAG[G/A]TAATTTAATGGTTGTGCATTTGCAACTTTAACACTCAACAGTTACTGGCCACATTATTAGGTACAGCTTGTTAGAAACTTGCTGTACTTTTTTTTTTTTTAGCAAAGTTCTTGAAACATTCTTTAAAAATTTTTTTATATCGACATGATAGCATCACACTCTTGGTTGGTAATGGGCTCACACGGACGCAGAGAAATCTACAGATTTTTACTTTTGTAAATGTGTATATTCATTCATTCATTCATTCATTCATTCATTTTCCTTCGGCTTAGTCCCTTATTCATCAGGGGTTGCCACAGCGGAATGAACAGCCAACTGTTCCAGCATATGTATAACACACCGAATGCCCTTCCAGCCGCAACCCAATAATGGGAAACACCCATACACTTTCACATTCACACACACATTCATACACTACAGTTGTACATACAATTTTGTTCATACAATTGACCTGAAGCGCATATCTTTGGGCTGTTGGGGAAACTGTAGCACCCAGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28332
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034883 | Nonsense | 455 | 1111 | 12 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33347807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32137614 |
GRCz11 | 14 | 32477928 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGTGATGATGGGGCTTATTTGTTGGCTAATCAGCAGGTAGAGAAATG[C/A]CAGTGTAAAGAGGGTGCACAGACAGCTCTGCGAGATATTGAGAAGTTCCA
Long Flanking Sequence:
GATCAAGTGTACTCGCGAGAGAGAGCGAATGTGCGCAAGGTATACCGAGTGTGTGTGCGCGCGAGAGAGAGACCAAAAGGCAATTAACGTTACTATTATTAATTACTATTACTAATACTACTATGTAATCAGAACTACTATTAAATCAGAAATCATTGTAATATGCTAATTTGGTGTTTCTTTTCTAACTGTGTTTCTTTACTTTTTCACGATTTTTTTGCTGAATTGAAATTTTAAAAGAATAATGTTTTATATAAATCTTCGCCAACATTATATCTGTACTCTCTCTTTTGCTCAACGTGTTCTTACAGAATTTCTAAAAAGTATCATATAAAAAAAGTAAACAAAAACTTGAACCCAAAATTTAAAAGTTATTATTGAAAATTGGCATTATTCCAGTGTTACATTATTTATATATCTTCACGTATTTTTGCTTTCCAGGCTCAGCGGTGGTGTGATGATGGGGCTTATTTGTTGGCTAATCAGCAGGTAGAGAAATG[C/A]CAGTGTAAAGAGGGTGCACAGACAGCTCTGCGAGATATTGAGAAGTTCCAGGAGGCGGCACCACCGCTTCTCACTGCTGGTGCTGATGTGCTCTTTCTTGAGTATGAGTCTGTGCTCACTCCTTATCTACAGGTGAACACCATCAGACTGCAAAAACTACACACAAACCGCATATTGGGCACTGTTATACACTAATCTCAATGCAGATCCAGGCACAACCACAACACGAGGGTGATGTTTCAGCCAGTTACAATTTTTGTGTCCTGCATCACTTTGTTAAAACAGCAATCACACGTGTGCTCATAGAGTATGTGAACCCATGGGCAGCAGGCCTGAAAATAAGGTGTTTAGGCCAAGGTTATAATAGTTTTGGAGTTGTCATTATTATTTTTTTTTTTTTTCGTTTGGACTTTTTGTTTTCAAATTCAGTTTAAGATTAGGTAGATTTACTTGTTTTTATTAGTTTTTATATTTTGAAATTGCTTAGTTTTTATTAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11503
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034883 | Nonsense | 926 | 1111 | 24 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33325610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32115417 |
GRCz11 | 14 | 32455731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAGGTAAAGATCGCCTGGCTGAATGAAATCAGAAAGATCCTGACCAAC[C/T]AGCAGAAACAGCTCAAAGGTCTYAACACATCACATTKCCTGTGATTTAAT
Long Flanking Sequence:
CGTTATATTTACAATTCAGACACTGAGTGATTCATATGAAGAAAATATATGGGTCCCATTTCAATTCTACATTGAATGTTGTGTTTTACAACATGTTGAGAAACATTTCAACTTAACAAATGCCAACATTTTTATATATGTTTAAAAGAAGGAGGGTCTATTCAATATTTCCCACTTTTTTTTTTTATTAAATTTACATTACACATCAAAGCTGCATAAATTAGAGGACCTTGAAGTGGTAAAATAAAAGCAACAGCATTAAATTATCCATAATTTTATTCATAAAACTGTTACATAGACGGCTATTATTTTTCTATACAATAAAATACATGAGATAGAGTTTTTAAAGCTCAAACAAGAACAAAAGACGAGTTACTCAATGGGCCGTAACCATAATTAACGTTTTATACATACCATTAATTTGAAAAAACTTCTTATAGGCACCCACTGTGGAGGTAAAGATCGCCTGGCTGAATGAAATCAGAAAGATCCTGACCAAC[C/T]AGCAGAAACAGCTCAAAGGTCTCAACACATCACATTTCCTGTGATTTAATATCGTTGTATTGTCTCCACAAGTGCTGTGAGTGATCTGTGATGTTCTGTGTTTCAGAAGAGCTGTGTCTGTCGACTGCAGTGTCCGAGCAGATGCAGATGCAGATTTCTCCTCCGCTGTCTGTCAGGTAAGAGTCCACCAGTGTCAACCATCTCTAATCCCTGATCATATCCACCCTCTACACACTCTCTCTCTTTCTTCTCCACCCTCTGGCTCAGACCAGCTTCTGCTGCTTTCAGCTCTGCCAGATCTCTCACAAAACACTACCTTCCCAAAAACCCTGCCCATAGATTTTGTTGCCCCCTCCTCTGCTTTAGCAATGCATAAGATGTGTAAGCAGAGCTCAAAATGAACTGTTTATCTGCCTAATTGACAGATACATTCTATACATTTCTAGATTTAGAGTTATTTATTTTTAGACATTTCTTTTTTTTTTTTTTAAGTACAATAA
Associated Phenotype:
Not determined