| Gene Summary for NIH-0778 |
|---|
| Functional Category: |
signal transduction-ion channel |
| Cell Location: |
integral membrane |
| OST #: |
|
| Mouse Nucleotide Accession #: |
NM_181317 |
| Human Nucleotide Accession #: |
BC034778 |
|
|
| Summary: |
| The mutated mouse gene is Kcns2 (K voltage-gated channel, subfamily S, 2), the ortholog of human KCNS2. Aliases include voltage-gated potassium channel 9.2 ; Kv9.2; and potassium voltage-gated channel, delayed-rectifier, subfamily S, member 2 |
|
| Phenotypic Summary for NIH-0778 |
|---|
| No Notable Phenotype |
| Mouse Gene Sequence Information |
|---|
 |
Nucleotide Reference: |
NM_181317 ACCESSION:NM_181317 NID: gi 73532785 ref NM_181317.3 Mus musculus K voltage-gated channel, subfamily S, 2 (Kcns2), mRNA |
|
Protein Reference: |
O35174 ACCESSION:O35174 NID: Mus musculus (Mouse). POTASSIUM CHANNEL ALPHA SUBUNIT. MOUSESPTRNRDB |
|
Entrez Gene: |
16539 |
| Human Gene Sequence Information |
|---|
|
Nucleotide Reference: |
BC034778 ACCESSION:BC034778 NID:21961636 Homo sapiens Homo sapiens, potassium voltage-gated channel, delayed-rectifier, subfamily S, member 2, clone MGC:34755 IMAGE:5175712, mRNA, complete cds. humRNA |
|
Protein Reference: |
Q9ULS6 ACCESSION:Q9ULS6 NID: Homo sapiens (Human). KIAA1144 PROTEIN (FRAGMENT). HUMANSPTRNRDB |
|
Entrez Gene: |
3788 |
| Mutation Information |
|---|
| Mutation Type: |
Homologous Recombination (standard) |
| Description: |
The single coding exon was targeted by homologous recombination (Accession: NM_008436). |
|
