ZMP
ell
Ensembl ID:
ZFIN ID:
Description:
elongation factor RNA polymerase II [Source:RefSeq peptide;Acc:NP_956001]
Human Orthologue:
ELL
Human Description:
elongation factor RNA polymerase II [Source:HGNC Symbol;Acc:23114]
Mouse Orthologue:
Ell
Mouse Description:
elongation factor RNA polymerase II Gene [Source:MGI Symbol;Acc:MGI:109377]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11958 | Essential Splice Site | Available for shipment | Available now |
sa16550 | Essential Splice Site | Available for shipment | Available now |
sa12948 | Nonsense | Available for shipment | Available now |
sa43827 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11958
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032770 | Essential Splice Site | 45 | 597 | 1 | 11 |
ENSDART00000100642 | Essential Splice Site | 72 | 660 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 21244726)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20899402 |
GRCz11 | 22 | 20924380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGACAGACAGCGCTCTGCGGGCGTTTRAGGACTACCAGAGCAACAAG[G/A]TAAGACGCGCGTCGAGCGCAACGCGAGGCTGGATAAAYAGAGCTAACAGG
Long Flanking Sequence:
CACTGCCACGTTTTGAAATCCTCCCAGTATCCTAAAATAAATATAATAAAGCAAGGAAAATACTTTTTTTTCATTCCTTTTTACAAAACACTTATAAATGCATAGTAATACGTACTATTAAAGGACTTTAAGCGCATGTAATATCACTGACCAGGTAAAAGAACAGGTGAATCATTTTTGAACCGCTCGAAAGAACCGAGTCGCCGGGCTCCCCATCACTGGTCATCTCTCTCGTGATTACTGCGAGGCCACGCCCCTTCCCGCCTGTACGTAATTCACGCCGGATGAATATTCATACTCTCCGCTCGAGCTGCTTGTTGCGTTCACGGCAGAGGCGCGTGAGCGTGGTGGGAAATGCGAGCAAGATGGCGGCGTTGAAGGAGGAGCAGTGTTACGGACTGTCCTGTGGAAGAGTGAGCAATGGCAGCAAAATCTCCGTCTATCACGTCAAGCTGACAGACAGCGCTCTGCGGGCGTTTGAGGACTACCAGAGCAACAAG[G/A]TAAGACGCGCGTCGAGCGCAACGCGAGGCTGGATAAACAGAGCTAACAGGCTAACAGTGAACAGCAGGCGACAGTTATTTCCCTGCCTGACAGCAAATCACCCACTCAGCTCAACACATTCCCCTTAAAACGAGCAGGAACTTCGGTGTGGCGACCCAGTCCCTGCCCTTTGCTGTTGGTGGCTTCCTTATCAAGCACTTCTTGCGCCAATGAAGCCGTTAATTGAGCCCACAGCAGGTGATAAAAGAAAATAAGTTGTTAGATGTGTGTTGGTCTGGTGGCAGACTGTCTAGTTTGGTTTAAAGCACTTGGCTGCCAGGTTGGTGGAAAAACTGGAAGTGTGTGGGGAATATTTGGTTTTATTTCCCACCTTTATTTTAGACCCAGGAAGTCTTGGAAATTACGGATTATAAAGTTTTAATCATTTAAATTATAGGTTTACATATTTCTGGTTATGCTGGATTCACAACGGGGGGCCCTCAGCAAACTTGTTAATGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16550
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032770 | Essential Splice Site | 101 | 597 | 3 | 11 |
ENSDART00000100642 | Essential Splice Site | 128 | 660 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 21197280)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20851956 |
GRCz11 | 22 | 20876934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGACAATCCCCAGGGCAGCTTCGACTGCATTCAGCAGTACATTACAAG[G/A]TAAGAACAAAATTAAAYGTATMTTTYATTGTAGTGCTGTGATTWGTGATG
Long Flanking Sequence:
TTATTTTTATTTATCACCTTTTGATTTATTCATAATCTTTTTTTCCTTTTTTGTATTTTTTAGCTGTTCCTAATTGCATTTTATTATATATTTATTAATTCATTTATTAAGTCAAATTGTTTTTCTTATATTTGGTTTAGCATTTATTTAGATATTTTGATTTATTTAAAAAAAATGTTTTTATATTTCTGTAAAAGTGATACATTGAATCTTTTCTACCTAAATGAATGAATGAATAAACCTGATGAATCCATCTAATCTACCTAAAAGAACAAGTAAATCTGTGTGATCTCTCCTGCTGTAGCCGTCTGCTTTTAACATGCCTCTCGTCTCCCTCTCAGTGCTTATGTTGGCTGCTCTTCTCTTCTGTGTCAACAGAAAATCTCGATACCGCAGTCAGAGAATCCAAATGAGCTGCGAACGTTTACCTTCTACCTGTCCAATGTGGGCAAAGACAATCCCCAGGGCAGCTTCGACTGCATTCAGCAGTACATTACAAG[G/A]TAAGAACAAAATTAAACGTATCTTTCATTGTAGTGCTGTGATTTGTGATGAGCAGGAGCTTTTGTGTTAAGGAAATATTGCCATGAAAACAGTTGATTTGAGTTTGTCTAATGTTAAAACTGGTTGTGCTTGCATTCGTGGCATCATTACGAGCACCATCTGTTCCTTCCACTGTTCAGCTCTGGAGCAACACCAGAACACAGAGAATCAGTTCAGTTTGGTCAGTTCTCCAACCAAATGAGGAAGAATGCAAATCCATTCTTGATATATCTGCAGGCAGAAACAGCTTTTCATGCTCCTCTGAGATTTTGAGGCTTTGTGGCTTTTCATAACGTGTTTTTCACTATAATAAGAAAACTTTCAAAATATTCAATACAAAATACTTTAATTGTTTATTGCTTTTTAAATAATTTTCCACTTTAGCAGCTCTGCATACAGAAAACTGCAGTTTTATTCTTATCTGTTTTTACTGAGGGCTTTGTTCATTTATAATTTGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12948
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 |
---|---|---|---|---|---|
ENSDART00000032770 | Nonsense | 318 | 597 | 8 | 11 |
ENSDART00000100642 | Nonsense | 345 | 660 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 21176548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20831224 |
GRCz11 | 22 | 20856202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAAGTTGTGTAATATTTGACTTCAGTTGAACACCCACAACCCCCAGAAA[C/T]GACCTGCAGCCGACTTCATCGATCCCCTGGCCAATAAGAAACCCAGAATA
Long Flanking Sequence:
GAATTTCTGTTTTTCTCTTTTTGGAAGAATAATGGAGGAACAAACTAACACATGCATGATTGAATGTAGCATGTTGTTTTTAATGGACCCTTTTCACAACACTGTTGTGACTCGTTTAATCCGAAATATTGATTGTTTTTTTTATATTTATGTACATTTATGTTTGTATTATATCATCTTTGCATCAAATTACCGCTTATGCGAAGTGTTTGATATGCAGAGTGTGTGGGCTGCCGTCTCGCACATTATTTTCCTTTTTTAAGGAAAGTCTTTACAAAGTTTTCACAAAGATCTGTTGTACTCTCCCATTCACTGCGTGCTAAATTTACCCAACTCTGACGACTTCCTCTACTGAGAAACCCAGAAATGTGAAAAGGGTCCATCTTCCCTCAAACTGCAACCAAGATGTTACATTTTCTCTTTTTCTTCCTCCAAGATCATGTACTGATATAAAGTTGTGTAATATTTGACTTCAGTTGAACACCCACAACCCCCAGAAA[C/T]GACCTGCAGCCGACTTCATCGATCCCCTGGCCAATAAGAAACCCAGAATATCGCATCTAGTCAGCAAGTCTACAGGACTCATCAATGGCAAGCTGAGCTCATCCAATGGAAAGGACACCTCTAGTTCTCAAGCAACTGAGACCTCGTCGAGCTCTCAGTTCCCTCCACTGGAGATCCCCCGACCCTTCGACCCCCTTTCAGATGTCAGCAACGACTCCAACGGCAGAGACTGTGAAGGTCAGGAGGCAGCGGTGGCAGAGAGACTAAGTCAGCCACCGTCATTCGCCCCTCGCTCCGCGACACAAGAGGAAAGGCAGACCTCCATGTCCCCACCCCACAGCAGTTTGGACAGCTCTCTGACCCAGACCACCCAACCCTCTCTGCACGGCAAGTCTAAGAAGAAGTCTAAAAAACACAAGGACAAAGATAAATCCAAAGACAAGGACAGGGATCGAGAGAGGGACGCGAAGAAGGAGAGGAGGGTTGATGAAGAGCGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43827
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032770 | Nonsense | 433 | 597 | 8 | 11 |
ENSDART00000100642 | Nonsense | 460 | 660 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 22 (position 21176202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20830878 |
GRCz11 | 22 | 20855856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGACACAAGAGGAAAGGCAGACCTCCATGTCCCCACCCCACAGCAGTT[T/A]GGACAGCTCTCTGACCCAGACCACCCAACCCTCTCTGCACGGCAAGTCTA
Long Flanking Sequence:
CTCTACTGAGAAACCCAGAAATGTGAAAAGGGTCCATCTTCCCTCAAACTGCAACCAAGATGTTACATTTTCTCTTTTTCTTCCTCCAAGATCATGTACTGATATAAAGTTGTGTAATATTTGACTTCAGTTGAACACCCACAACCCCCAGAAACGACCTGCAGCCGACTTCATCGATCCCCTGGCCAATAAGAAACCCAGAATATCGCATCTAGTCAGCAAGTCTACAGGACTCATCAATGGCAAGCTGAGCTCATCCAATGGAAAGGACACCTCTAGTTCTCAAGCAACTGAGACCTCGTCGAGCTCTCAGTTCCCTCCACTGGAGATCCCCCGACCCTTCGACCCCCTTTCAGATGTCAGCAACGACTCCAACGGCAGAGACTGTGAAGGTCAGGAGGCAGCGGTGGCAGAGAGACTAAGTCAGCCACCGTCATTCGCCCCTCGCTCCGCGACACAAGAGGAAAGGCAGACCTCCATGTCCCCACCCCACAGCAGTT[T/A]GGACAGCTCTCTGACCCAGACCACCCAACCCTCTCTGCACGGCAAGTCTAAGAAGAAGTCTAAAAAACACAAGGACAAAGATAAATCCAAAGACAAGGACAGGGATCGAGAGAGGGACGCGAAGAAGGAGAGGAGGGTTGATGAAGAGCGTGGCTTGGATCAAAGGAAACCCTGTGATGTCACGACGAGCGATAAGAGTACAGGTGAGGATCGGTTTCTCTGAATCATTTATCATGTCAAGGTCAGAAAACACCTCAGAGTTCCACACAATCTTTTGAATCTAATATATTACTTTACTTGGTGGTGACGGTGGGGTATCTTAGGGTAGTGTTTCTCAACCATGTTCCTGGAGGACCACCAACATTGCATGTTTTGGATGTCTCCTTCGTCTGTTACACACATTACAGATCTTTCAATCTCTGCTAAGGAGTTGATGATCATAATCAGGTGTGTTTGCTTAAGAAGATGTGCTGCACCCCAATTCGCACACTATCCGTCCT
Associated Phenotype:
Not determined