ZMP
si:ch211-39l18.5
Ensembl ID:
ZFIN ID:
Human Orthologues:
RP11-61P7.3, TMEFF1
Human Descriptions:
C9orf30-TMEFF1 fusion protein [Source:RefSeq peptide;Acc:NP_001185741]
transmembrane protein with EGF-like and two follistatin-like domains 1 [Source:HGNC Symbol;Acc:11866
transmembrane protein with EGF-like and two follistatin-like domains 1 [Source:HGNC Symbol;Acc:11866
Mouse Orthologue:
Tmeff1
Mouse Description:
transmembrane protein with EGF-like and two follistatin-like domains 1 Gene [Source:MGI Symbol;Acc:M
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19836 | Nonsense | Available for shipment | Available now |
sa18563 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19836
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 |
---|---|---|---|---|---|
ENSDART00000056441 | Nonsense | 205 | 326 | 6 | 9 |
The following transcripts of ENSDARG00000008191 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42285076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42334540 |
GRCz11 | 2 | 42183958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCCTGCCTGAAACAAGCTCAGATTAATGTCCGACACCTTGGACAGTG[T/A]TCAGGTAAACACAAATCCCGCATTAGACGAATCTTTACAATGCTAAATGG
Long Flanking Sequence:
ATAATTGTACACTGCACAGGTATAATACATTTATTTAATTATTCATTTTCATACATTAACATCCTAAAATCTAATTATTGATTCCTTATTATTGATTATCTAGTTACTGCAAATTGTAATATACAGTTTAAAAAAACTCAGTGAAAAAAAAACTACCGTGCTAAAATTCATCTTTAAATTCTTCATTTTCAAGTATTTGAATCTGGAAATTATGCAAATGTTTTCGGTTTTACTTCAATAAATTTTACATCACCTTATTTTATTTAAATTCTCACATCTTAATCGTTTATAAGCTTTTCATCTCACAAATCTCCATTTGAGGCAATCGTATCAGTAATATTTATCTGCTCTTCAAGGTGTGTGTGTAATATAGACTGCGGTGGCTACAATCTGAACCCAGTGTGTGGATCAGATGGACAGTCTTACAGTAATCCATGTCAGGTCAGAGAAGCTTCCTGCCTGAAACAAGCTCAGATTAATGTCCGACACCTTGGACAGTG[T/A]TCAGGTAAACACAAATCCCGCATTAGACGAATCTTTACAATGCTAAATGGAAATGCGGCATTATTCTGTGTTTGATTCATTCTATAGGTTCAGCTGTTCTAGTGGGCGGAGCTAATGTTGGCAGAGCGATGCCATGTCCTGAAATCAACAGCAGCTCATGTGTACATGGAACCTGTGAGATGAAAAATGATCTGGCAACATGCAGGTAGAACCAAACATACGCACAATACACACTTGTAAATTAGATGTCAAAATGATTAGCTCTCCTGTGAATTTTAATTTCAAGTATTTCCCAAATAATGTTTATCAAAGCAAGACATTTTTTAAAGTATTTCCTATAATATTTTTTCTTCTTGAAAAAGTCTGATTTGTTTTATTTCAGTATATATATAGTATAATATAGTATAATAGTATAATATATTTTCATTAAAAATAAAAGCAGCTTTTAGTTTTTAAAAAACCGCTTAAGGTCAATATTTTTAGCCCCCTTAGTTTTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18563
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 |
---|---|---|---|---|---|
ENSDART00000056441 | Nonsense | 256 | 326 | 8 | 9 |
The following transcripts of ENSDARG00000008191 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42285897)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42335361 |
GRCz11 | 2 | 42184779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTTGGKCTTGTCATTTAGGTGTAATTTGGGGTTTTCTGGCAAGYACTG[T/A]GAGCTAAGAGACTTCAGTGAGTTATATGTGGTGCCCAATGGACAGAAGCT
Long Flanking Sequence:
TTTTTAAAGTATTTCCTATAATATTTTTTCTTCTTGAAAAAGTCTGATTTGTTTTATTTCAGTATATATATAGTATAATATAGTATAATAGTATAATATATTTTCATTAAAAATAAAAGCAGCTTTTAGTTTTTAAAAAACCGCTTAAGGTCAATATTTTTAGCCCCCTTAGTTTTTGATTGTCTACAGAGCATTATTATACAATGACTTGCCTAATTAACCTAGTTAAGTCTCTAAATGTCACTTTAAGCTGAATACTAGTATCTTGAAAATATCTAATAAAACATTGTTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTTTTAGAAATGAGTTATTAAAACTATTATGTTTAGAAATGAGTTGAAAAAATCTTGGCTGATACTTTAATGACTAATAATTCAGAAGGGCTAATAATTCTGACTTCAGTTGTATGGGTTTGATGCGTTTTGGTCTTGTCATTTAGGTGTAATTTGGGGTTTTCTGGCAAGCACTG[T/A]GAGCTAAGAGACTTCAGTGAGTTATATGTGGTGCCCAATGGACAGAAGCTTCAGTACATCCTGATTGCTGCGATCATTGCCGCTGTACAGATCAGCATCATCATCGCTATCATAATATGCATCACAAGGTAAAACTTATCACATGAACGTGCACAGTGTTGGGGGAAGTTACTTTTGAAAGTAATGCATTACAATATTGAGTTACTCCACAAAAAAGTAACTAGTAACTTGTGTTACTTTTGAGTTACTTTTTCTGACCTGGCTGAGGATCTCTTTTAGAACTTGCAGGATTTTTTTCTTCTTCTATTTTTTTTATTAAAGAAACTCTGTAATTAATAATGCATTCCATAACCTTTGTTTACCTTAAAAACACATCAAAAAATAATAATGGAGGATAATGTTATTTTCCAAGCACTTCTGGCCCTCAATCTATATGCCTTATACAGATTAACCCTTAAAGACCTAGATGTATTTTGTGGGCACCTAATGGGCCTATATTA
Associated Phenotype:
Not determined