ZMP
rhcgl2
Ensembl ID:
ZFIN IDs:
Description:
Ammonium transporter Rh type C-like 2 [Source:UniProtKB/Swiss-Prot;Acc:Q8JI14]
Human Orthologue:
RHCG
Human Description:
Rh family, C glycoprotein [Source:HGNC Symbol;Acc:18140]
Mouse Orthologue:
Rhcg
Mouse Description:
Rhesus blood group-associated C glycoprotein Gene [Source:MGI Symbol;Acc:MGI:1888517]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16468 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16468
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 |
|---|---|---|---|---|---|
| ENSDART00000014573 | Nonsense | 145 | 329 | 3 | 12 |
| ENSDART00000048028 | Nonsense | 145 | 488 | 3 | 11 |
| ENSDART00000053518 | Nonsense | 145 | 488 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 25 (position 8792484)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 8516280 |
| GRCz11 | 25 | 8593348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTCATGACTGTTTACKSTGTGTTCAGMTTGATCAATGCAGATTTCTG[T/A]GYGGCCRGTTGTCTAATCGCATACGGTGCGGTGCTGGGGAAGGTCAGTCC
Long Flanking Sequence:
AACCATCAAGATTTTTACACTCTGTTGAAGTTTGTGGAAAAAACTCAATGTGTTTTAAATGCAAAACTACTCTGCCAGCAGGAGGCGCTTGTGGAAAATCAGAAGTACTGTAGCTGTTTTCACAGTAGCAGTTGAAGTCTAAGCATTGAACTCTCATGGTATTTTGTTGGGATTGTAAAAAAGTATGAATAAAAATAATAAATTAAAACTTTTCAGAAAAGTTTTTGTAAGTATAATTTCATATGTGTACTTGTCTACTGTCTGTATTTTGTATACTTTATGAATTCAGACACTCTTGACTCATAATGTTTTTTCTTATAAAAGGCTTTATAGTGTGTAATTATCTGATTCTGATCACAAATTATTTCATGCATGTGAAACATGGTATAATATGACTATCATGAGACTTTAAAGTCAATTTTGAGCTTTAATAAAATCGTAAATGAAAATTCTGTCATGACTGTTTACTCTGTGTTCAGATTGATCAATGCAGATTTCTG[T/A]GTGGCCAGTTGTCTAATCGCATACGGTGCGGTGCTGGGGAAGGTCAGTCCGGTTCAGCTGCTGGTCATGACACTGTTTGGGATCACGCTGTATGCTGTGGAGGAGTTCATCATCTTAAGTGTCCTCAACGTGAGTCTGATCTCGCTTTCACTATGGCCATTTTAAAAATATTTTGCAGTAACTTAAGTGCATATCTATAGTCGCTAAATTACATTCTCCTTTCAAAAGATTTTCTAATATGAGTGTATTTTAATATGTTTAGGAAACAGTTGTAGTTTTAATGTTTGTTTTATTGTTGAGATCAGCAATTACATTTCAAGTTTGAAGTTTGGTAAATTAGTTGTGTAATTATTTTTTGTGCATGTTTATGTGTGTATGCACAATATTTTAGTATCATAGTTGTGTGTTTGTCAATGAGAATATAACAAAGTTCAAACTTTATTGTCTTAAATGCACTTTTATAGCTGACAAGTTGTATTCTGCTTTCTAAGAAAGGATTT
Associated Phenotype:
Not determined