ZMP
LOC100334424
Ensembl ID:
Human Orthologues:
TCEB3, TCEB3B, TCEB3C, TCEB3CL
Human Descriptions:
transcription elongation factor B (SIII), polypeptide 3 (110kDa, elongin A) [Source:HGNC Symbol;Acc:
transcription elongation factor B polypeptide 3B (elongin A2) [Source:HGNC Symbol;Acc:30771]
transcription elongation factor B polypeptide 3C (elongin A3) [Source:HGNC Symbol;Acc:24617]
transcription elongation factor B polypeptide 3C-like [Source:HGNC Symbol;Acc:31007]
transcription elongation factor B polypeptide 3B (elongin A2) [Source:HGNC Symbol;Acc:30771]
transcription elongation factor B polypeptide 3C (elongin A3) [Source:HGNC Symbol;Acc:24617]
transcription elongation factor B polypeptide 3C-like [Source:HGNC Symbol;Acc:31007]
Mouse Orthologue:
Tceb3
Mouse Description:
transcription elongation factor B (SIII), polypeptide 3 Gene [Source:MGI Symbol;Acc:MGI:1351315]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18370 | Nonsense | Available for shipment | Available now |
sa35400 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18370
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 |
---|---|---|---|---|---|
ENSDART00000113692 | Nonsense | 333 | 587 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 13 (position 2108647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2325228 |
GRCz11 | 13 | 2328797 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAMGTCCCTTTACCAATGAGTCTYCCTGAATGCGAGGATCTTTCTCAGTA[T/G]CAGTACTTCAGTGAAAAGAAAGGTGAGCGTTTTTATTTTTCWGTCYCTAA
Long Flanking Sequence:
ATGAATGAATTAATGAATGAATGTTATAGTATAAGTTCCATTGGATCAGTTAGGTAGACCAGTGTTTCCCAATCCTGTTCCTGGAGGCACACCAGCAGTACATATTTTGGATGTCTTCCCTATCTGACCCATTCATTTCAGGTTTTGGAGTCTCTTCTAATGTTCTGATTGGGGTTTGGTTAGGAAGGGGTTGAAAATGTGTACTGTCGGTGTGCTTTTTGGAACATGGTTGGGAAACACTGAGAATGTTGCGATATTTGATTTTAATTGCACAGCTTTTGTAATCTTAGTTTAGTTTTTTTTTTTAAGCGTCAGTATCCGGTTTAGTCCTAGTTTTATTAAGAAAACAGTGGCTAATATATTCTTTCTCTAAAGCAAGTCACGTTTGAGAAAAGGAGTAATTTGTGGCTTTATCTGCAGGTTCCTGAGCAGTCAGTGATGGACTTGCTGAACGTCCCTTTACCAATGAGTCTTCCTGAATGCGAGGATCTTTCTCAGTA[T/G]CAGTACTTCAGTGAAAAGAAAGGTGAGCGTTTTTATTTTTCTGTCCCTAATCTTGCAATGGATGATTTATGAAATGATTTTCAGAGTAATGAAATGCACTGGTGTATTTCTATTAAATATTGGTAGATAAAAGTGATCAGTTATTGGAGGTGAGTTATTAAAACTATTGTGGCACGCAAGCGTGGCTGTTCAGACTCGCACTGACACAAGGAGTCATGGGCTGCGTCTGAAACCGCATACTTCCATACTATATAGTACGCTAAAATCAGCATGCGAGCCGAGTAGTATGTCCGAATTCATAGAATTCGACAATCAGTATGCGGGAAGAACCCGGATGACTTACTACTTCCGGCGAGATTCTAAAGTGCGCATCCCATGCACGCTGCGCTATCCCATGATGACCCGTGAGAGAATTCGTGAATCGGAGAGGAGCGACACAACTGACGCAGGTAGGTCATGTGACCATGACAAAATGGAGGATGTAGTACGTCTGAATTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35400
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113692 | Essential Splice Site | 398 | 587 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 13 (position 2106002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2327873 |
GRCz11 | 13 | 2326152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACTCTGTACCAGCAGTGCATCCGAGCGCTGCAGAACAACATCGACTG[T/A]ACGTACAAAACACACCATGATGATCTTCAGCTCAATAATTTAAGAGTAAA
Long Flanking Sequence:
AGCAATTAGTGTATTACTATGAGTTATATTATTAAATATTTATGTTAAAGTTATCTAATAATTCCAGCCAGCTTTTAGTGAACTTGCAATATTGTCAAAACACAGAACTTTCAGTTGTTATATGTAATAAAGGCATTAAGAAGCAAGGCTTTGAACACCATTTCAGTGCCCAATAGTTAAATGATCTAATATGGGATCATAGTATTGTATAGAGTTCTGTAAGTGTTTATTTATTATTAGTTTAAACATTTAATTTATTTTTTATTTATTTATTTAAATTAAGAATTTGAAACTGTGAAGGTAAAACATTTTTTTATTTTTAATTCAGATGACAGAAGAGCGACTGAAGTGTGTGAGGATGAGGAGGCGGCGCCGATGTTCATTGGACAGCGGCTAAAGAATAAGATGCAGGTGTATTCGGGCAGCAAGATGGCATTTCTGCCCTCCATGATGACTCTGTACCAGCAGTGCATCCGAGCGCTGCAGAACAACATCGACTG[T/A]ACGTACAAAACACACCATGATGATCTTCAGCTCAATAATTTAAGAGTAAAGAAGCCTCATTCAGTGATGAACTAAATATATTGATTAAATAATAAAGAAACAAATCTAACTCTATAAAGAGAAATGTTTTAAAAAAAGCTTTGAGCATTGAAAGATCTTGAATTTGTCAGTTGTTGTTATTTATATGTTTGATTTATTTGTACAATGCATGATTTTTTTAAGAAACAGTGATGATTGTAAATAATAAATTATATACTTAATACAAGTATAATAGTAGCATAGCCAATGCTGCTGATACGGCATAAGTACCTAAAACCCAGAACTGGTGTAAACTAAACTGAAGCTTAATTGGCCAGCCAGTTAATTCAGCTTAATGGTACATGTTTTGCAGCTCTCTATGAAATTGGAGGAGTACCGTTTGAGATTTTGGAGCCAGTATTGGAGCGCTGCACGGCTGAACAGCTCCTGCGCATTGAGGAGTGCAATCCTGTGAGACTTGA
Associated Phenotype:
Not determined