ZMP
megf10
Ensembl ID:
ZFIN IDs:
Human Orthologue:
MEGF10
Human Description:
multiple EGF-like-domains 10 [Source:HGNC Symbol;Acc:29634]
Mouse Orthologue:
Megf10
Mouse Description:
multiple EGF-like-domains 10 Gene [Source:MGI Symbol;Acc:MGI:2685177]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13029 | Nonsense | Available for shipment | Available now |
sa21693 | Nonsense | Available for shipment | Available now |
sa34869 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13029
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 |
---|---|---|---|---|---|
ENSDART00000043936 | Nonsense | 110 | 1119 | 5 | 25 |
The following transcripts of ENSDARG00000017229 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 16129082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 16142389 |
GRCz11 | 10 | 16100508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGACCTTACTCTCTCTTGTTTTCGCTGTAGCCCACTGTGCTGAGAAATG[T/A]GTGCATGGCCGCTGCGTGGCCCCCAACACCTGTCAGTGTGAGCCGGGCYG
Long Flanking Sequence:
AATTACCCTAACCTGCCTAGTTAACCTTATTAACCTAGTCAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAATGTCTTGAAAAATATCTAGTAAAATGTTATTTACTGCCATCATATCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTCTGATGTTTAGAAATGTGTTGAAATAATCTCTGTTAAACAGAAATTGGGGAAAAAAATAAACAGGGGGCTAATAATTCTGACTTTAACTGTATATGTGACAATCACAACCAGTTATAAGATTATCTGATGTTTGAGGTACACTTATAGAGCACAGGATTTGTGGCCAGTGAGTTTCCAGAAGAGACAGGGTTTCCTAGACTCATCGTCTCTTTGTACTGTATCTCATGGGTTTTATGTGGTTTCTGCTTGTGTTTGTTTGCTTGTCTCCTCATTGAAGGACTGAAACCTGACCTTACTCTCTCTTGTTTTCGCTGTAGCCCACTGTGCTGAGAAATG[T/A]GTGCATGGCCGCTGCGTGGCCCCCAACACCTGTCAGTGTGAGCCGGGCTGGGGAGGGGCTGACTGCTCCAGCGGTAAGTTCTGCAGCTGTGCCTGCCTATCTCTTTCTCTCTCACATACACTCTCTTTTTGTCTCTTGTATAATTAATCTGAACTCCATTTTTAGAGTCTTTAAACATGAATCTAATCGAGTGACAAAAGCCATTCAAAATTTTATGTGAACTTTGAAAAAAAATCAGATATAGATACTCTGTTACTTCATCAAAATCAGCAAGTGTAATCACAATCTCAATAATCAGCATTTTCACACATTTTTTGGTCTCATAGCAAATAGAATAAACTAAGTAATAGATAATTTCACAGCCAATTAGGTTTACTCAATTCACCTATACCAAGTGTCTTTGGACTGTGGGGGAAACTAGATATTTTTCAAGACATTCTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACCAGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21693
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043936 | Nonsense | 215 | 1119 | 6 | 25 |
The following transcripts of ENSDARG00000017229 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 16137788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 16151095 |
GRCz11 | 10 | 16109214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACATGCCACCACATCACAGGCGAATGCGTGTGCAGTCCAGGATACACA[G/T]GAGCATTGTAAGTTTACCTGCATTTTTTTTTGCAAACAATAGAAGATGGT
Long Flanking Sequence:
GAGGGGAGCTGGTTTTTCCCCCATTCCCACCTGCTGGGTTGTGGAGTCGATTGTCTCTGTTTTTGGGTCATGTTTGAATTGTCGAAGACATCAAATATTTGTGATATCTCATGTCTTACAACCTGCTTCAGGCATGAAAACTGTGCTCATCGTGCTGTGTGTATTATTACAATTGGAAAATCATGGTAAAGCACTGACTAATCACTATGGCGTACAGACTTTTGTCATAGAAGTGAAAATCAGCTTTGTGTCTTTGTGCAGCGTGTGACCGTGATCACTGGGGCCCACACTGCAGTAGCCGGTGTCAGTGTAAGAACGAGGCGCTGTGTAACCCCATCACTGGAGCGTGCATATGTGCACCCGGGTACCATGGCTGGCGATGTGAAGACCTCTGTGACCATTCCACTTATGGCAACAATTGCCAACAGAAATGTCTGTGCCAGAATAATGCTACATGCCACCACATCACAGGCGAATGCGTGTGCAGTCCAGGATACACA[G/T]GAGCATTGTAAGTTTACCTGCATTTTTTTTTGCAAACAATAGAAGATGGTGTTGGAAATACCGTGGCCATGGGAACTAAACCGATACCTTTAATTTAAGTTAGACTGGTAAATGCATAAATGTTTTGGTGTCTCTGTGCAGCTGTGAGGACTTGTGCCCTCCGGGAAAACATGGACAGCAATGTGAGGAGCGTTGTCCCTGTCAGAACGGTGGTGTGTGTCATCATGTGACTGGAGAATGTTCCTGTCCTGCTGGTTGGATGGTACGCCTGGCTGTTACAGTTCTGAATGTGGCTCTCGTAAATATTAAAACTGAAATTTATAAGTTATATAGTTTCATCATGTTTGGCACTATTATTGCAGTCATTATGAAATGTCTTTGCATTGGAGGAAACATTCCATTATCCATTATGTCAGTGTATTGATGTTACTTTCAGGGAATGGTGTGTGGACAACCCTGTCCGACGGGACGCTTTGGTAAGAACTGCTCACAGGAGTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34869
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043936 | Nonsense | 1090 | 1119 | 25 | 25 |
The following transcripts of ENSDARG00000017229 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 16189485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 16202792 |
GRCz11 | 10 | 16160911 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCACTTACAAACAACAACTGCAACGGGCCATTCTGTCAAGATCCATA[T/G]GACTTACCAAAGAATAGTCACATTCCATGTCATTATGACCTACTGCCTAC
Long Flanking Sequence:
AGCAAAAAGCTCAGCTGTTTAACTGTCAGCTCATGATTTGAATCCAACGCGGAAGAAAGTAGTTCCTTATACAAAAGGCTTTTTTGAGACTCTCCATGTTTAATTTTGTTTTTATATCCACGATTATACCTTTCAACTGTTGTATAAATTCAATATCACACTCGTAGCAGTGCGATATGGCTGTTTATCGGCACTGGTGGGGGCACTAAGGCACTTGGCATGCGGTCTTGTGCCAATGCACGCCTCCCACCAGTGCCGATATACACCTATATCGCTCTGCTACTCGTGTGATATTGCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATGCACATGAGCCTTTTATTGTTATTAAAAATGATGACATTTTTGTATTCTTTCTCTTTCTAGAGCCAACCATCAGTTCTGTCCAGGCACTTACAAACAACAACTGCAACGGGCCATTCTGTCAAGATCCATA[T/G]GACTTACCAAAGAATAGTCACATTCCATGTCATTATGACCTACTGCCTACAAGAGACAGCAGCCCATCACCCACAGAGGACAGCAAATAAACACTCGCAAACTTCATTAATGGACCATTACTGTGTTTATTGCTGTCTTGAATGTCATTCAACATTATAAAAGTTCTTAATCACGTCTGGCTTACATATTCAAAATGCCATAGTCTTACCCAGTATTCTGTGAGGAACAAGAGAACGATTGTTTTAGAGGAGGACGCTAATAATTGTAATTCATTCAAGCATATCATTCCATTCTTTTATAATAACACATCACACAAATCCCAGACAATCCTCCGTGTTTCTGATCAAGTATGTCAGATTTCAATTTCTGTTGTTTTTTCTTCCTTATAATATTTCGAATATTAGTACTGTTTATTGCAATCAGATTGTCCGAAAACATTTCAGGTTTACCAAAGGTTGACATGCCCTTATAAAGCATCATTAGTGTTGTATTTATATTG
Associated Phenotype:
Not determined