ZMP
LOC100332519
Ensembl ID:
Human Orthologue:
FRMPD4
Human Description:
FERM and PDZ domain containing 4 [Source:HGNC Symbol;Acc:29007]
Mouse Orthologue:
Frmpd4
Mouse Description:
FERM and PDZ domain containing 4 Gene [Source:MGI Symbol;Acc:MGI:3042378]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15687 | Essential Splice Site | Available for shipment | Available now |
sa21614 | Nonsense | Available for shipment | Available now |
sa12377 | Essential Splice Site | Available for shipment | Available now |
sa44716 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34787 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15687
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112441 | Essential Splice Site | 14 | 1130 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 56096482)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 54510866 |
GRCz11 | 9 | 54076779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KAAATGTTGCCTCAATTGATGTATTTTCCTCNNNNNNNTTTTTTTGTTTGTTTGTTT[T/A]GCAGTCASCTCTCGCAGTCCAGTTCTCTGGAGGAGGTGCGCGTTGATGYG
Long Flanking Sequence:
AACATTACCTGAACATGGCCAGACATAACCTGAACATAACCTGTTTTGGAGCCATATATGAAAATGCTCGACCTCCTTTAGTGGACATATGTTGTAAATCATTCCAAATTACACAAAAATACCTGAACATAACCTAAACATAGCCAGAACAAAACCTAAACATTACCTGAACATGGCCAGACATAAGCTGAACATAACCTGTTTTGGAGCCATATACGAAAATGCTCGACCTCCTTTAGTGTACATATGTTGTAAATCATTCCAAATTACACAAAATTACCTGAACATAACCTAAACATAGTCAGAACAAAACCTAAACATTACCTGAACATGGCCAGACATAAGCTGAACATAACCTGTTTTGGAGCCATATACGAAAATGCTCGACCTCCTTTAGTGGACATTTGTTGTAAATAATTCCAAATGACACAAAATTCATGGAAAATGCTTGAAATGTTGCCTCAATTGATGTATTTTCCTCTTTTTTTGTTTGTTTGTTT[T/A]GCAGTCACCTCTCGCAGTCCAGTTCTCTGGAGGAGGTGCGCGTTGATGTGGAGAAGTTTGTCCCTCCGGCACCGAGGAAGGTGGAGATGAGACGAGACCCGGTGCTCGGCTTTGGCTTCGTGGCGGGCAGTGAGAAACCTGTCGTGGTTCGATCTGTTACTCCAGGTACACAAATAACTAGATCAGCTACATTTATTGATATTAGTGATGCCAATGATATGTGTATATGATCTACACCATATATATATATATATATATATATTCATGTAAATAAACATATATAGACACGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCATTTATGTACATGTATGTATATGTATGTGTGTGTATATGAGCAATATCACACGAGTAGCAGTGCGATATAGCTGTATATCAGCACTGGTGGGAGGGGTGCACTGCTACAAGTGTGATATTGCGTTTATACAACAGTTCGACAGCACAATCGTGTTTATAAATAAGATAATCAAACACGGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21614
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 |
---|---|---|---|---|---|
ENSDART00000112441 | Nonsense | 64 | 1130 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 56096632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 54511016 |
GRCz11 | 9 | 54076929 |
KASP Assay ID:
2260-2620.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTGCTCGGCTTTGGCTTCGTGGCGGGCAGTGAGAAACCTGTCGTGGTT[C/T]GATCTGTTACTCCAGGTACACAAATAACTAGATCAGCTACATTTATTGAT
Long Flanking Sequence:
AAAACCTAAACATTACCTGAACATGGCCAGACATAAGCTGAACATAACCTGTTTTGGAGCCATATACGAAAATGCTCGACCTCCTTTAGTGTACATATGTTGTAAATCATTCCAAATTACACAAAATTACCTGAACATAACCTAAACATAGTCAGAACAAAACCTAAACATTACCTGAACATGGCCAGACATAAGCTGAACATAACCTGTTTTGGAGCCATATACGAAAATGCTCGACCTCCTTTAGTGGACATTTGTTGTAAATAATTCCAAATGACACAAAATTCATGGAAAATGCTTGAAATGTTGCCTCAATTGATGTATTTTCCTCTTTTTTTGTTTGTTTGTTTTGCAGTCACCTCTCGCAGTCCAGTTCTCTGGAGGAGGTGCGCGTTGATGTGGAGAAGTTTGTCCCTCCGGCACCGAGGAAGGTGGAGATGAGACGAGACCCGGTGCTCGGCTTTGGCTTCGTGGCGGGCAGTGAGAAACCTGTCGTGGTT[C/T]GATCTGTTACTCCAGGTACACAAATAACTAGATCAGCTACATTTATTGATATTAGTGATGCCAATGATATGTGTATATGATCTACACCATATATATATATATATATATATATTCATGTAAATAAACATATATAGACACGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCATTTATGTACATGTATGTATATGTATGTGTGTGTATATGAGCAATATCACACGAGTAGCAGTGCGATATAGCTGTATATCAGCACTGGTGGGAGGGGTGCACTGCTACAAGTGTGATATTGCGTTTATACAACAGTTCGACAGCACAATCGTGTTTATAAATAAGATAATCAAACACGGCGAGCCTAAAAACACCTTAATATTAAGAACTACTTTCTTCTGCCATTCATTCACATCTGCAGCTGACGTCAGAACAACAGAAGCCGTTACTCATTCACCAATGTCACTTTAGAACTAGTGTTTGAATGATTCTCTAGCGTAATGTCTAAAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12377
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112441 | Essential Splice Site | 391 | 1130 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 56121912)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 54536296 |
GRCz11 | 9 | 54102209 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGTGACCTGCGGCTGTATGGAGGACGAGTGTTCAAGTCTACACTGGTT[G/T]TAAGTGCANGAAAAAAACGGTGCACGACATTCACTACATACTGTATGAAAG
Long Flanking Sequence:
ATCAAAATAATTGAGTCCTTCAGGCTTGTTTGAAACCTACAGGTAAGTGTGTTGGAGCAGGGTTGGAACTAAACTGTGCAGGGCTTCGGCCCTCCAGCAATTGAGTTTGACACCCCTGACTTACATGATGAAAAATGATCGAGAAGTTGTAAAGAGTTTGACAGTTTTAATCAGAATTTGATCAACAGGTCAAATGCATTTATCTTTTGTTTTGAATGGGTTTATTAATTTGTTTATTTGTTTGTTTATTAATCAGACTAAACACCTTGTTAACACCTAAATAAAAAAAGAAGTGCTGAACTTTACCTTGTGTGTTTTTCTCATGGTCAAAAGGAGAAGCAGGAGTGTGTGTTTATGTTCTGGCCAGTTTCTGTTCTCTAATTGTTGTGGATTTCTGTTTTGTGTTGAAGCTGACGGCGTTACAGGCGAAGGTTCATTATCTGAAGTATTTGAGTGACCTGCGGCTGTATGGAGGACGAGTGTTCAAGTCTACACTGGTT[G/T]TAAGTGCAGAAAAAAACGGTGCACGACATTCACTACATACTGTATGAAAGAAGTGTTGAGGACACTTAAAGGAGTTTTAAACAGCCGTGTTACTTCAGAGTTCGTGTTACAGTCAGAATTATTTGCCGTCCTGTTCAATTGTAGTCTATTTATATTTTTTGGAGAGATACACATTTCTGAACATAATAGTTAATATTTCATTTCTAATCCCTGATTTCTTTTCTCTTTGTCATGATGACAGTAAATAATATTAGACTAGATATTCTTCAAGACACTATTATTCAGCTTAAAGTCACATTTAAAGGCTTCACTAGGGTAATTAGGGTAAAGTTGGGGTAATTAGGCAAGTTATTGTATAACAGTGGTTTATTCTGGAGACAATCCAAAACTAAAATTGCTTAAAGGGGCTAATAATATTGATCTTAAAACGGGTTTAAAAACATTAAAAACTGCTTTATTCTAGCCGAAATAAAACAAATAAGACTTCCTCCAGAAGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44716
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112441 | Nonsense | 622 | 1130 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 56132065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 54546449 |
GRCz11 | 9 | 54112362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAAGACATCCCAGAGGTCCTGGAGGAGCATCGGTATTTGTATGCACAA[C/T]AGAAGGACTACAAACCTCTGGAAGCGTCATTGGAGGTTGACGGTTTCCAA
Long Flanking Sequence:
TTCCTTCAACCTACAACATGAAAACACAAGGATTTAAATTATAAATATTTTACCTAATATTTGATGTAATCACTTCAGCATCACATTGACACTGCTGTCCTTTCTTTATTTATGTCTAAGGACACGACACGAGGATCAAGCACAACTACCAGGCAATCGACTGGAATTACGGTACCTGTGGTGGATGCAATGAGCCTCATCCTGAATACGCCGTCTGTGGACGAAGAGAGTGTGACATTTCCCCCAGTGAAATTCACCAGGCGCATCATATGCACGGGGACGAGAAAGCTGAAAGGCAGAGCAGAGGAAGCCACATGCATGCTCAGCCCTACTTCAACATCCCAAAAGGCAAACCTCAAGAATCGCCCAGAAGCGCCAAGGTGTCGTTCATATTTGGCGATCCTCCGCTGGACTCGGTGAACCCCCAAAATCTGGGATACCACAGACTGATGGAAGACATCCCAGAGGTCCTGGAGGAGCATCGGTATTTGTATGCACAA[C/T]AGAAGGACTACAAACCTCTGGAAGCGTCATTGGAGGTTGACGGTTTCCAATATGGTACCCATATGGTATACGGGGACGCCAAGATCTTCGGTACGACCGAGGGCATTGAGGAGCCTCTGCTGCATGATATCTGCTACGCCGAAACTACAGATGATGCAGAAGATGATGATGACATTAGTTGTGAGGAGGACATGATGATGATGATGGGAGAGATGAAGGACAAAGCGAACTCTCTGTTGTCACTTTCAGAATCAAGTGATGATATTATTGACCTTACTTCGCTGCCACCACCGCCTGAAGGGGACTACGAGGAGGACAGTGACGATCTGTTGGAGTCACTAAATTTGGCAATTGCCGCTCCACCACCAGGATTCAGAGATAGCTCGGATGAAGATGACCACCATGATAGAAAAATGGCGAAAAACGACATCCCTGTGTCGCTGATCGATTCCGTGCCGACGCAGGTTGCTGGTGGGAGCGAGGAAGTGTTTAATGATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34787
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112441 | Nonsense | 1003 | 1130 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 56133540)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 54547924 |
GRCz11 | 9 | 54113837 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCAAAGATTGCATATGATTCTGAATAATAAATCTGAAGAGCACATTTA[C/A]TCTGAGGTGGCTGGAGACAGCGCTCCATTACATGCAGACAGGGTTGCTCA
Long Flanking Sequence:
TCTGAAATGACGGAGAGTTCAGAGCTGGCCGCAGCTCAGAAACTCTCCGAAAACTCTCTGAAAATGTTTGTAGCCACAGCAGAGGGGTACCAAACTCTAGCTGAGGAGGAGACTGAATTCCGCTTGGCACCATCTCTAGATGATCCCCAGTCCTCTGCGGTCGCCAATCTCCGCTCAGACCACTTTGAGATGGAACCGGAAACAATGGAGACCAAGTCATTGACGGAGTACTTTAGCAAAATGCACAGGGATGTGATGAGGGGAATGGCACAGGGGAAGGTTGAGGAGCAGGACAGCGGGATGAAATCCAGTGCAGAAGCAGCAGCCCGACAGTTGAATATTGCAGAATCTGAAGATCTGGTTGGGATGTACAGCAACTTCAATGGGCGGGATTCCCAGTGTTCGGCTCCCTTTGACATGGAAAGTATGTCTTATGCCTTTCAGGGAAGCAATCAAAGATTGCATATGATTCTGAATAATAAATCTGAAGAGCACATTTA[C/A]TCTGAGGTGGCTGGAGACAGCGCTCCATTACATGCAGACAGGGTTGCTCAAAAGGTCAGTTTGGAGGACTCGATAGACTTGAATGCAAGTTCCCCCGCCAAAGAGCAGTATCTGGTCGAGCGAGCCCGGAGTGAACACCAACAAAGCAAGGGAGCTTCATCTGAACAAGAAGTGACCCGTTTGTACGAGTACCACTTGTCCAAAAGGATGTCATCTTTACAGAGCGAGGGTGTTCATTCCCTCCAGAGTTCCCAGTGTTCGTCCATTGATGCCGGCTGCAGTACGGGAAGCAGTAACTGCGTTACACCAATGGACTCTCCTCTGTGCACAGTAGATAGTGTCCATCTGCATACCGAGTCCTCTATGAAAGGTCTTGGATATACAAATCAGAATGTAGATGGAACTTTTTTGCGGAAGCACCACGGACAGGCTGGCGCAGAGTCAGGTCGAGAGGGAAGCCAAAGGTTGCCCAAGATCAGAGAAACTACAGGTACTGCAGG
Associated Phenotype:
Not determined