Busch Lab

ZMP

elmod1

Ensembl ID:
ENSDARG00000062056
ZFIN ID:
ZDB-GENE-070112-262
Description:
ELMO domain-containing protein 1 [Source:RefSeq peptide;Acc:NP_001074150]
Human Orthologue:
ELMOD1
Human Description:
ELMO/CED-12 domain containing 1 [Source:HGNC Symbol;Acc:25334]
Mouse Orthologue:
Elmod1
Mouse Description:
ELMO domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:3583900]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
hu7879 Nonsense Available for shipment Available now
sa9697 Essential Splice Site Available for shipment Available now
sa37293 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
hu7879
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089246 Nonsense 226 230 8 8
ENSDART00000122389 None None 328 None 10
ENSDART00000134715 None None 327 None 11
ENSDART00000135410 None None 123 None 5
ENSDART00000139789 None None 141 None 7

The following transcripts of ENSDARG00000062056 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 21058912)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 22070405
GRCz11 21 22107041
KASP Assay ID:
554-2417.1 (used for ordering genotyping assays)
KASP Sequence:
AGGCTCATTTACAGTACATTGTTTTATCCCTCGAAAAAGCCCGCTAAATT[T/G]AAYTAATGCACTTTAAGAYGCCATTAAGCTTTAAATGCATGRGCAAAAAA
Long Flanking Sequence:
TTCAACAATGAAGTTAAGTAACTATTAGTTTGCTACAAATGTATGATCCGCAAAAAGACAGCCCGTCCCCTACTCAATGTACTGTACCATTTCAGTTGTAATTACATAAACATACTGAAATTAAAAGTCTCAACAACCTTTGATTCTTGCAGACTTTAACATACTTGAGGTGAAATATATTTCATTCACAGTTAGCTTGTTTTTAGTAGTCAGCATATAATTTTCCTTTTGCTAACGAACCAATAATCTAAATGCATTTCATACTATACATAATAACATACATGAGGTCAAATTTATTTTTGTAGTATACTTGAAGTAGTTTTATTGATTAGCAATAGATTTTCACATAGCCATGCTTTTTTTGTTTGTTTTTTGCAGGTATTTTGCAGAGCACGACAAAGCCACTGCTCTTCAAGTTCTTCATGACTCCTTGCAGCCCAAACACAGGTCAGGCTCATTTACAGTACATTGTTTTATCCCTCGAAAAAGCCCGCTAAATT[T/G]AACTAATGCACTTTAAGACGCCATTAAGCTTTAAATGCATGAGCAAAAAAGGGGTTTTTGTCATTGAAGCTTTTTATCAGTGTGTTATTTTATGTTGTGTGTGTGCACACCATGCATATTTAAAAAAAAAAAGATTTTTTTCATGCCATGTAATATCACACCTTCAGCATGCTTTCTCACCATAAAACACATCACACACCCACACATTCCTTTTTTTCTGTTCCTGCTTCTGCTTTATTCCCATCATCACTGTCATGCACAGGGACGTTTCCAAAGAAGAAGCCAGGTACATTTTTTCCTCTCTCAGTAAAAAAACTCATTTGATCATTTTGCCTCAGTCTAATGGCTATTTTTTGTTGTTGTTGTTTTTTAAATATCCAACCTCACCTCACTCTAAACACAAGGCATTTTGCTCCATTGTAACGTTGGTTAGTAGCTGCGAATGCTTTCTCTTTCTTTCCAGTGTGTAATTGTTGTCGTTTATTCAGTAGTTGGCTGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9697
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089246 None None 230 None 8
ENSDART00000122389 Essential Splice Site 226 328 8 10
ENSDART00000134715 Essential Splice Site 225 327 9 11
ENSDART00000135410 None None 123 None 5
ENSDART00000139789 None None 141 None 7

The following transcripts of ENSDARG00000062056 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 21058297)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 22069790
GRCz11 21 22106426
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATGAGCAAAGCTGAATGGGAAAAGAAGAAATTCRACAAAGCGATCGGG[T/C]GAGTTCAGAAAANNNNTTNNAAACTATTGTGCATACTCACATTGAGGTCCTGTT
Long Flanking Sequence:
CATATTTAAAAAAAAAAAGATTTTTTTCATGCCATGTAATATCACACCTTCAGCATGCTTTCTCACCATAAAACACATCACACACCCACACATTCCTTTTTTTCTGTTCCTGCTTCTGCTTTATTCCCATCATCACTGTCATGCACAGGGACGTTTCCAAAGAAGAAGCCAGGTACATTTTTTCCTCTCTCAGTAAAAAAACTCATTTGATCATTTTGCCTCAGTCTAATGGCTATTTTTTGTTGTTGTTGTTTTTTAAATATCCAACCTCACCTCACTCTAAACACAAGGCATTTTGCTCCATTGTAACGTTGGTTAGTAGCTGCGAATGCTTTCTCTTTCTTTCCAGTGTGTAATTGTTGTCGTTTATTCAGTAGTTGGCTGCATTATATTCAGTTTAAGATCAGGATTAAGTGGACATGTTATAACATTTTGGCTTTTCGTACAGCAAAATGAGCAAAGCTGAATGGGAAAAGAAGAAATTCGACAAAGCGATCGGG[T/C]GAGTTCAGAAAATTGCAAACTATTGTGCATACTCACATTGAGGTCCTGTTTACACCTGCTATTAAAGTGATAGTTCACTCAAAAAAATTCTGTCATCATTTACTCTCTCTGCACTTATTTCAAACCTGTTTGAGTTTCTTGCTTCTGCTGAACACAAAAGACGATATTTTGAAGAATTTTGGAAACCAGAAACCATTGACTTGCATAGTAATAATTTGTGTGTTATGGATATGAATTGCTGCTAGTTTCCCAAGTATCTTCTTCTGTGTTTAATTGAAAAAAGAAACTCAGTTGGTTTTGGAAGGATATTCCCAACCACGCCCCCCTTACCATTAGTTTGGTATGAGAAAATGATGTGCAAAAAGAAAGCTCCATCCCCTACAGTTTGAAGTTCATCAACATACGGCGATAAAAGCATTAGCAATTTCTAGTTCACATAGACTTTAAAGGTCTGATCACCTTAGCAACACATAGCAACAAAATAAAAAAAAGACTGTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37293
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089246 None None 230 None 8
ENSDART00000122389 Nonsense 254 328 9 10
ENSDART00000134715 Nonsense 253 327 10 11
ENSDART00000135410 None None 123 None 5
ENSDART00000139789 None None 141 None 7

The following transcripts of ENSDARG00000062056 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 21056469)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 22067962
GRCz11 21 22104598
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCTGGCCTATTCCCTGCTGGTGAGCGGAGCTCTGAAGACTCATCTGTA[T/A]AATGTGGCACCAGAGATGCCAAGCCTAGTGCACTTCCAACAGACCTTCTG
Long Flanking Sequence:
TATTTGATTAAAGATTCTGAGGGTGAATGAATTTTTACAAAATAATAAAGTGCACAGACACATGATTAAAACAAGCACTCCTATATACATCTAAAGAGTACATTTTTTCTTTAAATGTGAATGTTTGTGCAGTGTGTGCGTATTCATCACTCACTGTGTGAACTTGTGTGAACTCTGCTTTTGCGGCTGCGCTGATGTTTTGTGTGAGGATTTGAATCAGGCTCTTCTGCTTGTCATGAGCTTTCAGGATGCATTAGCTCTGATGTGTAGCATGAAGCCTGTTAAATCACTGCACACACACACATGCGCACACACACACATACTTAGACAAACACTGGCTGAGTCTTAGGATTTTATAATATTTATTTACACTAAACAAGTGTGTTTTGTGCTGACCCTCATCTTTTGTGGCGCAGATACTCTTTTGCTATAGTTGGCATAAACATCACAGATCTGGCCTATTCCCTGCTGGTGAGCGGAGCTCTGAAGACTCATCTGTA[T/A]AATGTGGCACCAGAGATGCCAAGCCTAGTGCACTTCCAACAGACCTTCTGTGAGTACTAATCATAATGTCGCCATTGTACTTGTTGTGAGAAAAGCTTTGTCTAAAAGATTTATGAAGAAACAAAACAAAACTATTACATAATTAGATATATAAAAATATATATACAATTAAAGGGATTAAAACTAAAAAATTTCCACACTTGCCAATTGCTGGTGACTTTTGAAACTTGTAAACATAACAGCCATTAAAAATGGACGTTATGTGCATTATTAATGTAATTTAATAATTATAGAAATTAAATAGTTATAAAAAAATTGTAAAAAAAATTATTGTAGTTTATATTTATATGTATTTATTTTACTTTACTTATTTTATATTTATTCTGTTAATATAGCAATAATAATAATATGAATTATTTTGTAAACATTAAATATATAATTGTATACATTATATTAATATGCACTCACCGGCCTTTTTATTAGGTTCACTTTACTAGTAC
Associated Phenotype:
Not determined