ZMP
slc2a11l
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 2 (facilitated glucose transporter), member 11-like [Source:RefSeq peptide;Ac
Human Orthologues:
AP000350.10, SLC2A11
Human Description:
solute carrier family 2 (facilitated glucose transporter), member 11 [Source:HGNC Symbol;Acc:14239]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34877 | Nonsense | Available for shipment | Available now |
sa21705 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34877
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 |
---|---|---|---|---|---|
ENSDART00000091357 | Nonsense | 5 | 504 | 1 | 12 |
ENSDART00000144847 | Nonsense | 5 | 504 | 1 | 12 |
The following transcripts of ENSDARG00000062873 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 17531707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17544053 |
GRCz11 | 10 | 17501487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCATACAGTAGAGCAGCACTTCACTGACACATACAATGACGGGGGCTT[T/A]ACGACAACTGGTACCATCACAACTATAAAATTACATGTTACTTTCATTAT
Long Flanking Sequence:
CTTAATTGTAGCAATTTTGTAATGGCACAACAGTTCACCAGGAGCACTTTAGCTGGCTGACTGAAAATTAAAAATCCATGTGCATATAGCCCACTGACATTGTGAATTAACAGCCAGGTCACTTTATCTGTGAAGACAAATTATCAATTGATTGCTGTTTTATTTATTTTGGTGGAAAGTGGAAAAGTGTTGGAGCTCAGTTTTATTTGTAAACTCTACTGTCACTTCATAAGCTGTGGAGACTGCTCTATTTTTAGCTTTACTAATTTTTGTCACAATTAATCTGCTTTCATTCACAGTACTCGAGAGACGTGTGAAGATAAACTCGGCTTGTACATTTTACCCTATTATGTCATCAAAAACTCATCCAAGCATGAAAAGTTACACATCAACTGTATGTCAGGCATTACTGTTTTTGCTTTGTCATCTTTCCTCTTTTCTTCACTCAGACTTCATACAGTAGAGCAGCACTTCACTGACACATACAATGACGGGGGCTT[T/A]ACGACAACTGGTACCATCACAACTATAAAATTACATGTTACTTTCATTATTCAGTTTTCACAAAAGTCTCTTTTTTTTCCAGACAAAAAGTCCTGTACTCGTTGCAGCCATTCTCATTGCAGGAATTGGAGGGACCTTCCAATACGGCTTCAATATTTCTGTCCTGAACTCCCCGTCACCCGTAAGTACCATTGTTTTTTTGGTAAAAAAAAAATCTTGTGGTGATTTAGTGTCTAAAATTAGTGGGATTGGAGGTAATCAGAATTAATTAAATGCATTTCTGCCACTTCTTTTAAAAAACATATTTGTAAAATGTATAAATACTCAGTCCATATCAGGGATTCTGGGTTGGTGCTTACAAAGTGCTGTGGTTTAATAAAATGAAATGAATGACACAATCAGCTGAGACTTGTGCTTATGTTGCTAGTTCATTAAAGAGCTGGTGAACAGCACCTGCCAGCAGCGCTATGGACACTCCCTGGAGCCCTGGGAACTGTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21705
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091357 | Nonsense | 369 | 504 | 10 | 12 |
ENSDART00000144847 | Nonsense | 369 | 504 | 10 | 12 |
The following transcripts of ENSDARG00000062873 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 17518219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17530565 |
GRCz11 | 10 | 17487999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTCCTGAGATTGGATTTGTCCGGTTCTGTTATAGGATTTTGTGTCCT[G/A]GATGCCATATTGCAGCATGGTCCTCATTTTCATATACATCTTCTTCTTCT
Long Flanking Sequence:
CTAATTAAACTAAAAGGGGGGCTGCAAGTATCAAGTATAACCAAAAATATATATATAAAAAAAACATAAAAGTATAATATAAGTTTATATAAATGGTCTCGTCAGCTTTAAATCTTTTTTTAATAGGGACTGAACCCATCAAACATCAAATATGAAAAAGAGTATCATACAAATATAATATAGTAAACGTAGTTAAATAAATTTCCGGTGTCAAAAAATTAAGTTGCATTTGATATAAATTATGTACTTTGTCTTTTAAATTCACTTGATTAGTGCTCTGTGAGACTGAAAGAGGAGAAAATAAGTCTAAAAAGTGTGGTGAATAAACAAAGACAATAAAAAAATGTAAATGTTTGGTAAGTTATTCATCAATAATCCAGTGAGCTACATGACAATGAAGAACTTTAAATTAACCAAAATTGTGTTAACTGTTATTAAAAAACATGCAGACTGTTCCTGAGATTGGATTTGTCCGGTTCTGTTATAGGATTTTGTGTCCT[G/A]GATGCCATATTGCAGCATGGTCCTCATTTTCATATACATCTTCTTCTTCTCTAGTGGACCAGGTACATCCACACATATTTCTCCTGTAATTTTATACATACTGAGAGAGTGCATCTCTGGTTTGTGTCATGTTGGTCTCAGCATTATTGTGGATTTCCTCCTTCATAGCTGGAGTGACAGCACCACTTCCTGGTGAGATTTTTACACAGTCCTACAAACCACCAGCATTTGTGGTTGCCTGTGTCCTCAACTGGATCGGACTCTTCCTAGTGGGCATGTTATTTCCTCTCATTGTGGTGAGTTATTCCACCTTAATAATGTCATGGCTTTATGACACTTTTTTGATCCTAAAGGTGAATTAGGGGAATCCAAAATGAAAACTATTGGTAACGCTTAATATAAAGCCTGTGTTTGTGATGTATTATCAGGACACTCTTAATGTATAACAATCAGAGAAGTAATTAATTGCTAAGTACATAATTATAATTGTTTTTAAAAAT
Associated Phenotype:
Not determined