ZMP
NP_998256.1
Ensembl ID:
Description:
engulfment and cell motility protein 1 [Source:RefSeq peptide;Acc:NP_998256]
Human Orthologue:
ELMO1
Human Description:
engulfment and cell motility 1 [Source:HGNC Symbol;Acc:16286]
Mouse Orthologue:
Elmo1
Mouse Description:
engulfment and cell motility 1, ced-12 homolog (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2153044]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23562 | Essential Splice Site | Available for shipment | Available now |
sa23561 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23562
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 |
---|---|---|---|---|---|
ENSDART00000006805 | Essential Splice Site | 260 | 726 | 10 | 22 |
ENSDART00000124214 | Essential Splice Site | 260 | 726 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 19 (position 35379122)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 34376603 |
GRCz11 | 19 | 33963723 |
KASP Assay ID:
2261-3500.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCAGTGATTAATGCACTGTTCCTCAAAGCCCCAGAGGAGAAGAGACAGG[T/C]ACAGCACACACACACAAACAAATCCTTTTTTATGTGCTTTTTCAGTTGTT
Long Flanking Sequence:
CATTGTCATTTTCAAATTGAGTTAGATGGATCCTACTTTGACCCACTTTTTTACGCAATATAGTATTGAGGGCCACAAAGTGTGTTAAGGAAGTATTAGCTAAAATTACCCCATGGACTGTTTATTTTACTAAACAGTTGTAAATTCCCTTTTTTTAGGTGTGTCTCTTTAAATGCAAATGAGCTGCTGCTCCCTGCCCCCTTCCATAAGAATAGCACATGCCTCAGATACTCCAACAGCAAGAACAACACATGTTTTAATGCATTGCCAGTAATAACTGCATATAAAAATACTCAATTTACACTATATATGCAATACTAGGCAAACAATGAAATTTTTGGTTATTTGTTGTTGTTGTTATTTGCTACTTTAATAGTATACTTTAATAGTCATTTGCATTTTTGTTCTCTCTGGCACCAGAACGGATCAGGACATTCAGACTTACACCATCGCAGTGATTAATGCACTGTTCCTCAAAGCCCCAGAGGAGAAGAGACAGG[T/C]ACAGCACACACACACAAACAAATCCTTTTTTATGTGCTTTTTCAGTTGTTCATTGTCGCCTAGACTAAATAATGACACCGTCTTCATTAGGCATGATGTGAGAAAATGTCAAGCAAATCTCCTGCTTGTCTGTCTAAATTTTCGTTCTAACAAGCTATGATTGTCAATAAACACAAACACATAATATTCTGCCCAATGGGTTTAAATTCCTGCTGCATGTGCAGGAATCAACATCATATTGCATATTAAACATCAGATATTTTATGTTTGAATGACTGCAGTTTGAATAAAGCAGGTTGTTGATATTAGAAATTTGAACATAGAACTAAAAACCATGCTGTTTTGTGGCTTTATAAAGAGGTGTTCACTCTCAACAATTTAGTGTGGTCAAGTGTACAGTACATGCTGCCATCTGAACTTTTTGTAAATTAAATAGAATTGAACTCTTGTCCAGTAAAATGTCACTCTTTTTAAATATTTCCCAAGTAACAGAGAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23561
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 |
---|---|---|---|---|---|
ENSDART00000006805 | Essential Splice Site | 433 | 726 | 15 | 22 |
ENSDART00000124214 | Essential Splice Site | 433 | 726 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 19 (position 35359824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 34357305 |
GRCz11 | 19 | 33944425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGAACTGACGAAAATGCTGTGTGAGATCCTCAAAGTGGGAGAACTTCG[T/C]AAGTGGCATCATTTAAAAATCTCTCGTCTATATTTGCATGAAAAATGCTG
Long Flanking Sequence:
TCCTGGATCAAAACAAACACAAGCACAGGTTGCCAGTCGAAGTCCCGCTACTGTCCACCGGAGGTTGCACTTCGGTCATGGACGCACACTTTCAGAGCCGTTCTGCATGAATGAATGAATAAAATATGCTGTTTTCCATCAAGGCCACCCCGGGTGCTGAAATATAATTGGCTAAACTGGCATTGGACGGGTTAAAATAACCAAAACAAAGACAGCGTTCCAGCACAGAAAACGCATTTTCAAAGCAGAATAACTGACTTCAGAACTGTTTTTCAGATAAACAAGAATGTTCACTTAGCATGTTTCTCGAATATCTGCAAACATATCATGATATTTTTATACTTTAGAAGAGTCAAAAACCAACATCCAGCACCTTTGTCTGTGTTACAGATTGTCCTGGAGAACAGCAGTCGTGAGGATAAACATGAGTGTCCGTTCGGCCGCAGCAGTATTGAACTGACGAAAATGCTGTGTGAGATCCTCAAAGTGGGAGAACTTCG[T/C]AAGTGGCATCATTTAAAAATCTCTCGTCTATATTTGCATGAAAAATGCTGAACTGACTCCAAGGAGGCCATAAAGGTGTGCATAAAAAGAAGTCATACATGGGTCATTTAGAAAAGTTAGAAAAACCCTTCATCCGATAAAAAATATCTATGATAGGAACACATTTGCTGGATAAATTCATGAGTGCGTATCAAGAAAGTCATGTTATTTTTTCATGTTCATGTTTTATTTTAATAATTCTGCAAAGGTCAAAATGAGTTTACTATTTTATTAGTGCTGTAAAATTATTAATTATGTTTATGTGTATTTGTGTGTCTGTCTATAAATACACATATTTGTCACAATAATAAATATATAAATAAATAAATAAATAGAGAAATAAAAGCTCAGATGCGAAGACCTCTAAATTCTGTCTGAAATTCTATTTTAAAATGAGCATAATTTTCAGGCTCCTTTGTATAAATTCAGTAATTTCATTTTTATAGCAAATAATACGTTCT
Associated Phenotype:
Not determined