ZMP
slc14a2
Ensembl ID:
ZFIN ID:
Description:
Facilitated urea transporterZgc:136632 [Source:UniProtKB/TrEMBL;Acc:Q533H0]
Human Orthologues:
SLC14A1, SLC14A2
Human Descriptions:
solute carrier family 14 (urea transporter), member 1 (Kidd blood group) [Source:HGNC Symbol;Acc:109
solute carrier family 14 (urea transporter), member 2 [Source:HGNC Symbol;Acc:10919]
solute carrier family 14 (urea transporter), member 2 [Source:HGNC Symbol;Acc:10919]
Mouse Orthologues:
Slc14a1, Slc14a2
Mouse Descriptions:
solute carrier family 14 (urea transporter), member 1 Gene [Source:MGI Symbol;Acc:MGI:1351654]
solute carrier family 14 (urea transporter), member 2 Gene [Source:MGI Symbol;Acc:MGI:1351653]
solute carrier family 14 (urea transporter), member 2 Gene [Source:MGI Symbol;Acc:MGI:1351653]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa7006 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20532 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7006
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073626 | Nonsense | 20 | 261 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 54987132)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 51521642 |
| GRCz11 | 5 | 52168235 |
KASP Assay ID:
554-5107.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCAATGTTTTAATAGAARAGTGACCCGCTGAATGTCACACATCTCTGC[A/T]AAACGTCTACTTCTACACAATATTCCAGTGCTCAAAACACAAAGGTGAGA
Long Flanking Sequence:
AGTACTAAAATGTTAATCCATATGCAGTCTATGTTATCTGCTTTTTTTATTTTTTATTTTGAGAAGAACGTGTTATAGTTATTTGGTAATTGCATACAAAGTTTCAAAAACCATAGAACGTTTTTTAATGCTTTTTAACAGCTTATCAGAATGAAAAAGCAAAGTGATTAGCAGAAACCTGCTCAAGCAACTTAGAATAGGACCAAACTAAGTCAGAGGAATGCAAAGTAAGATTTGAACTGCATGAATAGAGGTGGAGCAACGCAAACAGACCGGCACTATAAAACCATCAGATCTGTGGCTTCATGGACTTCATTGATTCTTTCTGCAACTGGCCTCATATATGCCTGGAACACATCTAACGAAGGTAGAAACACTCCTTTTTTCTCTCTCTCTGAATGTTATGTCAATTGAGTATGATAGTAACAAAACTTGAATTAAATTGAATAAAGTCAATGTTTTAATAGAAAAGTGACCCGCTGAATGTCACACATCTCTGC[A/T]AAACGTCTACTTCTACACAATATTCCAGTGCTCAAAACACAAAGGTGAGATTTTTCCTGTTCTCTTGTCTTTTGAAAAATTCCAGGAGGCAGAACACAGACGGATCCCTGCAAAGAATATTAAGTGTTTGTGTCTGTGAACATTTACAGGAGCTACAACCACTCATGGCAAATCCAGTCCACAAAATTACAGATGAGAAGAAACAGCAGGGACTCGAGAAGATCAATTCGGGCCAGAGGTTTAAAGCAAATCTCATAAAATGGGTCTCGTTTATTTCTGGAGACATGGCTGCGTTCGGAGAATGGATGAAAGGTACAGGAGTTTAAGCTAAATTGATGCTCGGTCAAGAGCCAAGCTTGAAAAAAACAACAAGAGCATTAATTCTGCAGTGAATAGTTGGCAGAAGAGTGTTTGTACATCTACTTTACGTTTAGATTGACAATGGAAAAGCCTAAGCATTCCTGTTTTCTTTATCTTAAAGATAAAAATGCAGCTTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20532
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 |
|---|---|---|---|---|---|
| ENSDART00000073626 | Nonsense | 150 | 261 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 54988433)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 51522934 |
| GRCz11 | 5 | 52169527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCTTTGTTGGAACCTTGTTTGCTACGATTTCTGCACTCATCCTCTGT[C/T]AGAACAGGTATTAACACAACTGGTCAATTATGAATGTCTAAATGTTTGAG
Long Flanking Sequence:
TACAAACAATTGAAACTACAGTTTTAAACCTGTGGGCATTTACAAGCTGACAGGTGTTTCTAAATCCTGCATTAAAGACCCAAGCTAGTCATTTAATGGTCTATTACTTTTGATACTTAACTACAAAATGCATTCACAGACACACAGATTAGTAGCAGTTATTAATTGTTTGGTTATTATTGTTATTAGTAATTGTTTTCACTGCAGGACATTTTTCATGGCATACACACATATCTCTTTAAACCTCTGCCCTCTGCAGACATCTGCAAAGACTTTATTGGTATCAACTATGTGCTTTCTCATGTTTACCCTGTTCAGGCCAGTTTATCTTGCTCCAAATTATGGACTGGGTGTTGCGTGGAGCGGCTCAGGTGATGTTTGTGAACAACCCACTCAGTGGTCTGATCATCTTTGCTGGACTGATCCTCCAGAACAGATGGTGGGCACTCAATGGCTTTGTTGGAACCTTGTTTGCTACGATTTCTGCACTCATCCTCTGT[C/T]AGAACAGGTATTAACACAACTGGTCAATTATGAATGTCTAAATGTTTGAGCAAGGTTTAAGTGTTGTGTTCCCTCAGAGGTGCAATTGCTGCTGGTCTGTATGGATATAACGGCATTTTGGTTGGTCTCCTGATGGCAGTTTTCTCAAATGCTGGAGATTGGTATTGGTGGCTTCTTCTTCCCAACATCTTCATGTCAATGGCATGGTGAGTTTGTGTCATGGCTCCTTCCAAGACTTATTTTAACTTGTAAGAAAGGAAATAGCTTAGAGCTGGAATGCACTTTGCAAGATTTGTAGTCTGTATGAGTTGATGCTGCTTAAAGTCAGAGCCACTCTGCAGATTCAGGGCAGAAAATTGTGTTGCATAATGATGAGTACAGACATTTTGGTTGACTAATATCGAACAATTTAAAAGATTTCTTTACTAAATGTAAATTTTATTTGTGATTCATGTTGCGGTTTGAAACTTTTTTGAACGTTTTTGTCAGTTTCTTAGTAT
Associated Phenotype:
Not determined